U.S. patent application number 15/430260 was filed with the patent office on 2017-06-01 for delivery, engineering and optimization of systems, methods and compositions for sequence manipulation and therapeutic applications.
The applicant listed for this patent is THE BROAD INSTITUTE INC., MASSACHUSETTS INSTITUTE OF TECHNOLOGY. Invention is credited to Feng ZHANG.
Application Number | 20170152528 15/430260 |
Document ID | / |
Family ID | 49883289 |
Filed Date | 2017-06-01 |
United States Patent
Application |
20170152528 |
Kind Code |
A1 |
ZHANG; Feng |
June 1, 2017 |
DELIVERY, ENGINEERING AND OPTIMIZATION OF SYSTEMS, METHODS AND
COMPOSITIONS FOR SEQUENCE MANIPULATION AND THERAPEUTIC
APPLICATIONS
Abstract
The invention provides for delivery, engineering and
optimization of systems, methods, and compositions for manipulation
of sequences and/or activities of target sequences. Provided are
delivery systems and tissues or organ which are targeted as sites
for delivery. Also provided are vectors and vector systems some of
which encode one or more components of a CRISPR complex, as well as
methods for the design and use of such vectors. Also provided are
methods of directing CRISPR complex formation in eukaryotic cells
to ensure enhanced specificity for target recognition and avoidance
of toxicity and to edit or modify a target site in a genomic locus
of interest to alter or improve the status of a disease or a
condition.
Inventors: |
ZHANG; Feng; (Cambridge,
MA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
THE BROAD INSTITUTE INC.
MASSACHUSETTS INSTITUTE OF TECHNOLOGY |
Cambridge
Cambridge |
MA
MA |
US
US |
|
|
Family ID: |
49883289 |
Appl. No.: |
15/430260 |
Filed: |
February 10, 2017 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14183512 |
Feb 18, 2014 |
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15430260 |
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14104837 |
Dec 12, 2013 |
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14183512 |
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61758468 |
Jan 30, 2013 |
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61769046 |
Feb 25, 2013 |
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61791409 |
Mar 15, 2013 |
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61802174 |
Mar 15, 2013 |
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61806375 |
Mar 28, 2013 |
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61814263 |
Apr 20, 2013 |
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61819803 |
May 6, 2013 |
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61828130 |
May 28, 2013 |
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61835931 |
Jun 17, 2013 |
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61836123 |
Jun 17, 2013 |
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61847537 |
Jul 17, 2013 |
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61736527 |
Dec 12, 2012 |
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61748427 |
Jan 2, 2013 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61P 7/00 20180101; A61P
35/00 20180101; A61P 1/16 20180101; C12N 15/8213 20130101; A61P
27/02 20180101; A01K 2217/05 20130101; C12N 15/85 20130101; A61P
21/00 20180101; A01K 2267/03 20130101; A61P 13/12 20180101; A61P
9/00 20180101; A61P 19/10 20180101; A01K 67/0275 20130101; A01K
2217/07 20130101; C12N 15/63 20130101; A61P 19/08 20180101; A61P
25/14 20180101; A61P 25/18 20180101; A61P 31/14 20180101; A61P
31/18 20180101; C12N 15/907 20130101; A01K 67/0278 20130101; C12N
15/102 20130101; C12N 2800/22 20130101; A01K 2217/072 20130101;
A61P 29/00 20180101; A61P 3/06 20180101; C12N 9/96 20130101; A01K
2227/105 20130101; C12N 15/8509 20130101; A61P 25/28 20180101; A61P
31/12 20180101; C12N 15/01 20130101; A61P 3/00 20180101; A61P 25/16
20180101; C12N 15/86 20130101; A01K 2217/052 20130101; A61P 11/00
20180101; C12N 9/22 20130101; C12N 15/90 20130101; A61P 35/02
20180101; A61P 37/02 20180101; A61P 43/00 20180101; A61P 25/00
20180101 |
International
Class: |
C12N 15/90 20060101
C12N015/90; C12N 9/22 20060101 C12N009/22; C12N 9/96 20060101
C12N009/96 |
Goverment Interests
STATEMENT AS TO FEDERALLY SPONSORED RESEARCH
[0004] This invention was made with government support under the
NIH Pioneer Award (1DP1MH100706) awarded by the National Institutes
of Health. The government has certain rights in the invention.
Claims
1. A method of altering expression of at least one gene product
comprising introducing into a eukaryotic cell containing and
expressing a DNA molecule having a target sequence and encoding the
gene product an engineered, non-naturally occurring Clustered
Regularly Interspaced Short Palindromic Repeats (CRISPR)-CRISPR
associated (Cas) system comprising one or more vectors comprising:
a) a first regulatory element operable in a eukaryotic cell
operably linked to at least one nucleotide sequence encoding a
CRISPR-Cas system guide RNA that hybridizes with the target
sequence, and b) a second regulatory element operable in a
eukaryotic cell operably linked to a nucleotide sequence encoding a
Type-II Cas9 protein, wherein components (a) and (b) are located on
same or different vectors of the system, whereby the guide RNA
targets the target sequence and the Cas9 protein generates at least
one site specific break in the DNA molecule, wherein the at least
one site specific break is repaired through a cellular repair
mechanism; and, wherein the Cas9 protein and the guide RNA do not
naturally occur together.
2. The method of claim 1, wherein the cellular repair mechanism is
Non-homologous end joining (NHEJ).
3. The method of claim 1, wherein the cellular repair mechanism is
Homology-directed repair (HDR).
4. The method of claim 1, wherein the Cas9 protein is a nickase
that generates a site specific break in only one strand of the DNA
molecule.
5. The method of claim 1, wherein the method further comprises the
insertion of a recombination template into the site specific break
in the DNA molecule.
6. The method of claim 1, wherein the expression of two or more
gene products is altered.
7. The method of claim 1, wherein the CRISPR-Cas system further
comprises one or more nuclear localization signal(s) (NLS(s)).
8. The method of claim 1, wherein the CRISPR-Cas system comprises a
trans-activating cr (tracr) sequence.
9. The method of claim 1, wherein the guide RNAs comprise a guide
sequence fused to a tracr sequence.
10. The method of claim 1, wherein the Cas9 protein is codon
optimized for expression in the eukaryotic cell.
11. The method of claim 1, wherein the eukaryotic cell is a
mammalian or human cell.
12. The method of claim 1, wherein the expression of one or more
gene products is increased.
13. The method of claim 1, wherein the expression of one or more
gene products is decreased.
14. The method of claim 1, wherein the one or more vectors are
viral vectors.
15. The method of claim 1, wherein the one or more viral vectors
are selected from the group consisting of retroviral, lentiviral,
adenoviral, adeno-associated and herpes simplex viral vectors.
16. A CRISPR-Cas system-mediated genome editing method comprising
introducing into a eukaryotic cell containing and expressing a DNA
molecule having a target sequence and encoding at least one gene
product an engineered, non-naturally occurring CRISPR-Cas system
comprising one or more vectors comprising: a) a first regulatory
element operable in a eukaryotic cell operably linked to at least
one nucleotide sequence encoding a CRISPR-Cas system guide RNA that
hybridizes with the target sequence, and b) a second regulatory
element operable in a eukaryotic cell operably linked to a
nucleotide sequence encoding a Type-II Cas9 protein, wherein
components (a) and (b) are located on same or different vectors of
the system, whereby expression of the at least one gene product is
altered through the CRISPR-Cas system acting as to the DNA molecule
comprising the guide RNA directing sequence-specific binding of the
CRISPR-Cas system, whereby the Cas9 protein generates at least one
site specific break in the DNA molecule, whereby there is genome
editing, and, wherein the Cas9 protein and the guide RNA do not
naturally occur together.
17. The method of claim 16, wherein the at least one site specific
break is repaired through a NHEJ cellular repair mechanism.
18. The method of claim 16, wherein the at least one site specific
break is repaired through a HDR cellular repair mechanism.
19. The method of claim 16, wherein the Cas9 protein is a nickase
that generates a site specific break in only one strand of the DNA
molecule.
20. The method of claim 16, wherein the method further comprises
the insertion of a recombination template into the site specific
break in the DNA molecule.
21. The method of claim 16, wherein the expression of two or more
gene products is altered.
22. The method of claim 16, wherein the CRISPR-Cas system further
comprises one or more NLS(s).
23. The method of claim 16, wherein the CRISPR-Cas system comprises
a tracr sequence.
24. The method of claim 16, wherein the Cas9 protein is codon
optimized for expression in the eukaryotic cell.
25. The method of claim 16, wherein the eukaryotic cell is a
mammalian or human cell.
26. The method of claim 16, wherein the expression of one or more
gene products is increased.
27. The method of claim 16, wherein the expression of one or more
gene products is decreased.
28. An engineered, programmable, non-naturally occurring Type II
CRISPR-Cas system comprising a Cas9 protein and at least one guide
RNA that targets and hybridizes to a target sequence of a DNA
molecule in a eukaryotic cell, wherein the DNA molecule encodes and
the eukaryotic cell expresses at least one gene product and the
Cas9 protein generates at least one site specific break in the DNA
molecule, wherein the at least one site specific break is repaired
through a cellular repair mechanism; and, wherein the Cas9 protein
and the guide RNA do not naturally occur together.
29. The CRISPR-Cas system of claim 28, wherein the cellular repair
mechanism is NHEJ.
30. The CRISPR-Cas system of claim 28, wherein the cellular repair
mechanism is HDR.
Description
RELATED APPLICATIONS AND INCORPORATION BY REFERENCE
[0001] This application is a continuation of U.S. application Ser.
No. 14/183,512 filed Feb. 18, 2014, which is a continuation of U.S.
application Ser. No. 14/104,837 filed Dec. 12, 2013 which claims
priority to US provisional patent application No. 61/736,527 filed
Dec. 12, 2012; 61/748,427 filed Jan. 2, 2013; 61/758,468 filed Jan.
30, 2013, 61/769,046 filed Feb. 25, 2013; 61/791,409 and 61/802,174
filed Mar. 15, 2013, 61/806,375 filed Mar. 28, 2013; 61/814,263
filed Apr. 20, 2013; 61/819,803 filed May 6, 2013; 61/828,130 filed
May 28, 2013; 61/835,931 and 61/836,123 filed Jun. 17, 2013 and
61/847,537 filed Jul. 17, 2013.
[0002] Reference is also made to US provisional patent application
No. 61/799,800 filed Mar. 15, 2013; 61/835,931, 61/835,936,
61/836,127, 61/836,101, 61/836,080 and 61/835,973 filed Jun. 17,
2013; 61/862,468 and 61/862,355 filed on Aug. 5, 2013; 61/871,301
filed on Aug. 28, 2013; 61/960,777 filed on Sep. 25, 2013 and
61/961,980 filed on Oct. 28, 2013.
[0003] The foregoing applications, and all documents cited therein
or during their prosecution ("appln cited documents") and all
documents cited or referenced in the appln cited documents, and all
documents cited or referenced herein ("herein cited documents"),
and all documents cited or referenced in herein cited documents,
together with any manufacturer's instructions, descriptions,
product specifications, and product sheets for any products
mentioned herein or in any document incorporated by reference
herein, are hereby incorporated herein by reference, and may be
employed in the practice of the invention. More specifically, all
referenced documents are incorporated by reference to the same
extent as if each individual document was specifically and
individually indicated to be incorporated by reference.
FIELD OF THE INVENTION
[0005] The present invention generally relates to the delivery,
engineering, optimization and therapeutic applications of systems,
methods, and compositions used for the control of gene expression
involving sequence targeting, such as genome perturbation or
gene-editing, that relate to Clustered Regularly Interspaced Short
Palindromic Repeats (CRISPR) and components thereof.
SEQUENCE LISTING
[0006] The instant application contains a Sequence Listing which
has been submitted electronically in ASCII format and is hereby
incorporated by reference in its entirety. Said ASCII copy, created
on Feb. 13, 2014, is named 44790.00.2041_SL.txt and is 211,772
bytes in size.
BACKGROUND OF THE INVENTION
[0007] Recent advances in genome sequencing techniques and analysis
methods have significantly accelerated the ability to catalog and
map genetic factors associated with a diverse range of biological
functions and diseases. Precise genome targeting technologies are
needed to enable systematic reverse engineering of causal genetic
variations by allowing selective perturbation of individual genetic
elements, as well as to advance synthetic biology,
biotechnological, and medical applications. Although genome-editing
techniques such as designer zinc fingers, transcription
activator-like effectors (TALEs), or homing meganucleases are
available for producing targeted genome perturbations, there
remains a need for new genome engineering technologies that are
affordable, easy to set up, scalable, and amenable to targeting
multiple positions within the eukaryotic genome.
SUMMARY OF THE INVENTION
[0008] The CRISPR-Cas system does not require the generation of
customized proteins to target specific sequences but rather a
single Cas enzyme can be programmed by a short RNA molecule to
recognize a specific DNA target. Adding the CRISPR-Cas system to
the repertoire of genome sequencing techniques and analysis methods
may significantly simplify the methodology and accelerate the
ability to catalog and map genetic factors associated with a
diverse range of biological functions and diseases. To utilize the
CRISPR-Cas system effectively for genome editing without
deleterious effects, it is critical to understand aspects of
engineering, optimization and cell-type/tissue/organ specific
delivery of these genome engineering tools, which are aspects of
the claimed invention.
[0009] There exists a pressing need for alternative and robust
systems and techniques for nucleic sequence targeting with a wide
array of applications. Aspects of this invention address this need
and provide related advantages. An exemplary CRISPR complex
comprises a CRISPR enzyme complexed with a guide sequence
hybridized to a target sequence within the target polynucleotide.
The guide sequence is linked to a tracr mate sequence, which in
turn hybridizes to a tracr sequence.
[0010] In one aspect, the invention provides methods for using one
or more elements of a CRISPR-Cas system. The CRISPR complex of the
invention provides an effective means for modifying a target
polynucleotide. The CRISPR complex of the invention has a wide
variety of utilities including modifying (e.g., deleting,
inserting, translocating, inactivating, activating) a target
polynucleotide in a multiplicity of cell types in various tissues
and organs. As such the CRISPR complex of the invention has a broad
spectrum of applications in, e.g., gene or genome editing, gene
therapy, drug discovery, drug screening, disease diagnosis, and
prognosis.
[0011] Aspects of the invention relate to Cas9 enzymes having
improved targeting specificity in a CRISPR-Cas9 system having guide
RNAs having optimal activity, smaller in length than wild-type Cas9
enzymes and nucleic acid molecules coding therefor, and chimeric
Cas9 enzymes, as well as methods of improving the target
specificity of a Cas9 enzyme or of designing a CRISPR-Cas9 system
comprising designing or preparing guide RNAs having optimal
activity and/or selecting or preparing a Cas9 enzyme having a
smaller size or length than wild-type Cas9 whereby packaging a
nucleic acid coding therefor into a delivery vector is more
advanced as there is less coding therefor in the delivery vector
than for wild-type Cas9, and/or generating chimeric Cas9
enzymes.
[0012] Also provided are uses of the present sequences, vectors,
enzymes or systems, in medicine. Also provided are uses of the same
in gene or genome editing.
[0013] In an additional aspect of the invention, a Cas9 enzyme may
comprise one or more mutations and may be used as a generic DNA
binding protein with or without fusion to a functional domain. The
mutations may be artificially introduced mutations or gain- or
loss-of-function mutations. The mutations may include but are not
limited to mutations in one of the catalytic domains (D10 and H840)
in the RuvC and HNH catalytic domains, respectively. Further
mutations have been characterized. In one aspect of the invention,
the transcriptional activation domain may be VP64. In other aspects
of the invention, the transcriptional repressor domain may be KRAB
or SID4X. Other aspects of the invention relate to the mutated Cas
9 enzyme being fused to domains which include but are not limited
to a transcriptional activator, repressor, a recombinase, a
transposase, a histone remodeler, a demethylase, a DNA
methyltransferase, a cryptochrome, a light inducible/controllable
domain or a chemically inducible/controllable domain.
[0014] In a further embodiment, the invention provides for methods
to generate mutant tracrRNA and direct repeat sequences or mutant
chimeric guide sequences that allow for enhancing performance of
these RNAs in cells. Aspects of the invention also provide for
selection of said sequences.
[0015] Aspects of the invention also provide for methods of
simplifying the cloning and delivery of components of the CRISPR
complex. In the preferred embodiment of the invention, a suitable
promoter, such as the U6 promoter, is amplified with a DNA oligo
and added onto the guide RNA. The resulting PCR product can then be
transfected into cells to drive expression of the guide RNA.
Aspects of the invention also relate to the guide RNA being
transcribed in vitro or ordered from a synthesis company and
directly transfected.
[0016] In one aspect, the invention provides for methods to improve
activity by using a more active polymerase. In a preferred
embodiment, the expression of guide RNAs under the control of the
T7 promoter is driven by the expression of the T7 polymerase in the
cell. In an advantageous embodiment, the cell is a eukaryotic cell.
In a preferred embodiment the eukaryotic cell is a human cell. In a
more preferred embodiment the human cell is a patient specific
cell.
[0017] In one aspect, the invention provides for methods of
reducing the toxicity of Cas enzymes. In certain aspects, the Cas
enzyme is any Cas9 as described herein, for instance any
naturally-occurring bacterial Cas9 as well as any chimaeras,
mutants, homologs or orthologs. In a preferred embodiment, the Cas9
is delivered into the cell in the form of mRNA. This allows for the
transient expression of the enzyme thereby reducing toxicity. In
another preferred embodiment, the invention also provides for
methods of expressing Cas9 under the control of an inducible
promoter, and the constructs used therein.
[0018] In another aspect, the invention provides for methods of
improving the in vivo applications of the CRISPR-Cas system. In the
preferred embodiment, the Cas enzyme is wildtype Cas9 or any of the
modified versions described herein, including any
naturally-occurring bacterial Cas9 as well as any chimaeras,
mutants, homologs or orthologs. An advantageous aspect of the
invention provides for the selection of Cas9 homologs that are
easily packaged into viral vectors for delivery. Cas9 orthologs
typically share the general organization of 3-4 RuvC domains and a
HNH domain. The 5' most RuvC domain cleaves the non-complementary
strand, and the HNH domain cleaves the complementary strand. All
notations are in reference to the guide sequence.
[0019] The catalytic residue in the 5' RuvC domain is identified
through homology comparison of the Cas9 of interest with other Cas9
orthologs (from S. pyogenes type II CRISPR locus, S. thermophilus
CRISPR locus 1, S. thermophilus CRISPR locus 3, and Franciscilla
novicida type II CRISPR locus), and the conserved Asp residue (D10)
is mutated to alanine to convert Cas9 into a complementary-strand
nicking enzyme. Similarly, the conserved His and Asn residues in
the HNH domains are mutated to Alanine to convert Cas9 into a
non-complementary-strand nicking enzyme. In some embodiments, both
sets of mutations may be made, to convert Cas9 into a non-cutting
enzyme.
[0020] In some embodiments, the CRISPR enzyme is a type I or III
CRISPR enzyme, preferably a type II CRISPR enzyme. This type II
CRISPR enzyme may be any Cas enzyme. A preferred Cas enzyme may be
identified as Cas9 as this can refer to the general class of
enzymes that share homology to the biggest nuclease with multiple
nuclease domains from the type II CRISPR system. Most preferably,
the Cas9 enzyme is from, or is derived from, spCas9 or saCas9. By
derived, Applicants mean that the derived enzyme is largely based,
in the sense of having a high degree of sequence homology with, a
wildtype enzyme, but that it has been mutated (modified) in some
way as described herein
[0021] It will be appreciated that the terms Cas and CRISPR enzyme
are generally used herein interchangeably, unless otherwise
apparent. As mentioned above, many of the residue numberings used
herein refer to the Cas9 enzyme from the type II CRISPR locus in
Streptococcus pyogenes. However, it will be appreciated that this
invention includes many more Cas9s from other species of microbes,
such as SpCas9, SaCas9, StlCas9 and so forth. Further examples are
provided herein. The skilled person will be able to determine
appropriate corresponding residues in Cas9 enzymes other than
SpCas9 by comparison of the relevant amino acid sequences. Thus,
where a specific amino acid replacement is referred to using the
SpCas9 numbering, then, unless the context makes it apparent this
is not intended to refer to other Cas9 enzymes, the disclosure is
intended to encompass corresponding modifications in other Cas9
enzymes.
[0022] An example of a codon optimized sequence, in this instance
optimized for humans (i.e. being optimized for expression in
humans) is provided herein, see the SaCas9 human codon optimized
sequence. Whilst this is preferred, it will be appreciated that
other examples are possible and codon optimization for a host
species is known.
[0023] In further embodiments, the invention provides for methods
of enhancing the function of Cas9 by generating chimeric Cas9
proteins. Chimeric Cas9 proteins chimeric Cas9s may be new Cas9
containing fragments from more than one naturally occurring Cas9.
These methods may comprise fusing N-terminal fragments of one Cas9
homolog with C-terminal fragments of another Cas9 homolog. These
methods also allow for the selection of new properties displayed by
the chimeric Cas9 proteins.
[0024] It will be appreciated that in the present methods, where
the organism is an animal or a plant, the modification may occur ex
vivo or in vitro, for instance in a cell culture and in some
instances not in vivo. In other embodiments, it may occur in
vivo.
[0025] In one aspect, the invention provides a method of modifying
an organism or a non-human organism by manipulation of a target
sequence in a genomic locus of interest comprising: delivering a
non-naturally occurring or engineered composition comprising:
A)-I. a CRISPR-Cas system chimeric RNA (chiRNA) polynucleotide
sequence, wherein the polynucleotide sequence comprises: (a) a
guide sequence capable of hybridizing to a target sequence in a
eukaryotic cell, (b) a tracr mate sequence, and (c) a tracr
sequence, and II. a polynucleotide sequence encoding a CRISPR
enzyme comprising at least one or more nuclear localization
sequences, wherein (a), (b) and (c) are arranged in a 5' to 3'
orientation, wherein when transcribed, the tracr mate sequence
hybridizes to the tracr sequence and the guide sequence directs
sequence-specific binding of a CRISPR complex to the target
sequence, and wherein the CRISPR complex comprises the CRISPR
enzyme complexed with (1) the guide sequence that is hybridized to
the target sequence, and (2) the tracr mate sequence that is
hybridized to the tracr sequence and the polynucleotide sequence
encoding a CRISPR enzyme is DNA or RNA, or (B) I. polynucleotides
comprising: (a) a guide sequence capable of hybridizing to a target
sequence in a eukaryotic cell, and (b) at least one or more tracr
mate sequences, II. a polynucleotide sequence encoding a CRISPR
enzyme, and III. a polynucleotide sequence comprising a tracr
sequence, wherein when transcribed, the tracr mate sequence
hybridizes to the tracr sequence and the guide sequence directs
sequence-specific binding of a CRISPR complex to the target
sequence, and wherein the CRISPR complex comprises the CRISPR
enzyme complexed with (1) the guide sequence that is hybridized to
the target sequence, and (2) the tracr mate sequence that is
hybridized to the tracr sequence, and the polynucleotide sequence
encoding a CRISPR enzyme is DNA or RNA.
[0026] Any or all of the polynucleotide sequence encoding a CRISPR
enzyme, guide sequence, tracr mate sequence or tracr sequence, may
be RNA. The polynucleotides encoding the sequence encoding a CRISPR
enzyme, the guide sequence, tracr mate sequence or tracr sequence
may be RNA and may be delivered via liposomes, nanoparticles,
exosomes, microvesicles, or a gene-gun.
[0027] It will be appreciated that where reference is made to a
polynucleotide, which is RNA and is said to `comprise` a feature
such a tracr mate sequence, the RNA sequence includes the feature.
Where the polynucleotide is DNA and is said to comprise a feature
such a tracr mate sequence, the DNA sequence is or can be
transcribed into the RNA including the feature at issue. Where the
feature is a protein, such as the CRISPR enzyme, the DNA or RNA
sequence referred to is, or can be, translated (and in the case of
DNA transcribed first).
[0028] Accordingly, in certain embodiments the invention provides a
method of modifying an organism, e.g., mammal including human or a
non-human mammal or organism by manipulation of a target sequence
in a genomic locus of interest comprising delivering a
non-naturally occurring or engineered composition comprising a
viral or plasmid vector system comprising one or more viral or
plasmid vectors operably encoding a composition for expression
thereof, wherein the composition comprises: (A) a non-naturally
occurring or engineered composition comprising a vector system
comprising one or more vectors comprising I. a first regulatory
element operably linked to a CRISPR-Cas system chimeric RNA
(chiRNA) polynucleotide sequence, wherein the polynucleotide
sequence comprises (a) a guide sequence capable of hybridizing to a
target sequence in a eukaryotic cell, (b) a tracr mate sequence,
and (c) a tracr sequence, and II. a second regulatory element
operably linked to an enzyme-coding sequence encoding a CRISPR
enzyme comprising at least one or more nuclear localization
sequences (or optionally at least one or more nuclear localization
sequences as some embodiments can involve no NLS), wherein (a), (b)
and (c) are arranged in a 5' to 3' orientation, wherein components
I and II are located on the same or different vectors of the
system, wherein when transcribed, the tracr mate sequence
hybridizes to the tracr sequence and the guide sequence directs
sequence-specific binding of a CRISPR complex to the target
sequence, and wherein the CRISPR complex comprises the CRISPR
enzyme complexed with (1) the guide sequence that is hybridized to
the target sequence, and (2) the tracr mate sequence that is
hybridized to the tracr sequence, or (B) a non-naturally occurring
or engineered composition comprising a vector system comprising one
or more vectors comprising I. a first regulatory element operably
linked to (a) a guide sequence capable of hybridizing to a target
sequence in a eukaryotic cell, and (b) at least one or more tracr
mate sequences, II. a second regulatory element operably linked to
an enzyme-coding sequence encoding a CRISPR enzyme, and III. a
third regulatory element operably linked to a tracr sequence,
wherein components I, II and III are located on the same or
different vectors of the system, wherein when transcribed, the
tracr mate sequence hybridizes to the tracr sequence and the guide
sequence directs sequence-specific binding of a CRISPR complex to
the target sequence, and wherein the CRISPR complex comprises the
CRISPR enzyme complexed with (1) the guide sequence that is
hybridized to the target sequence, and (2) the tracr mate sequence
that is hybridized to the tracr sequence. In some embodiments,
components I, II and III are located on the same vector. In other
embodiments, components I and II are located on the same vector,
while component III is located on another vector. In other
embodiments, components I and III are located on the same vector,
while component II is located on another vector. In other
embodiments, components II and III are located on the same vector,
while component I is located on another vector. In other
embodiments, each of components I, II and III is located on
different vectors. The invention also provides a viral or plasmid
vector system as described herein.
[0029] Preferably, the vector is a viral vector, such as a lenti-
or baculo- or preferably adeno-viral/adeno-associated viral
vectors, but other means of delivery are known (such as yeast
systems, microvesicles, gene guns/means of attaching vectors to
gold nanoparticles) and are provided. In some embodiments, one or
more of the viral or plasmid vectors may be delivered via
liposomes, nanoparticles, exosomes, microvesicles, or a
gene-gun.
[0030] By manipulation of a target sequence, Applicants also mean
the epigenetic manipulation of a target sequence. This may be of
the chromatin state of a target sequence, such as by modification
of the methylation state of the target sequence (i.e. addition or
removal of methylation or methylation patterns or CpG islands),
histone modification, increasing or reducing accessibility to the
target sequence, or by promoting 3D folding.
[0031] It will be appreciated that where reference is made to a
method of modifying an organism or mammal including human or a
non-human mammal or organism by manipulation of a target sequence
in a genomic locus of interest, this may apply to the organism (or
mammal) as a whole or just a single cell or population of cells
from that organism (if the organism is multicellular). In the case
of humans, for instance, Applicants envisage, inter alia, a single
cell or a population of cells and these may preferably be modified
ex vivo and then re-introduced. In this case, a biopsy or other
tissue or biological fluid sample may be necessary. Stem cells are
also particularly preferred in this regard. But, of course, in vivo
embodiments are also envisaged.
[0032] In certain embodiments the invention provides a method of
treating or inhibiting a condition caused by a defect in a target
sequence in a genomic locus of interest in a subject (e.g., mammal
or human) or a non-human subject (e.g., mammal) in need thereof
comprising modifying the subject or a non-human subject by
manipulation of the target sequence and wherein the condition is
susceptible to treatment or inhibition by manipulation of the
target sequence comprising providing treatment comprising:
delivering a non-naturally occurring or engineered composition
comprising an AAV or lentivirus vector system comprising one or
more AAV or lentivirus vectors operably encoding a composition for
expression thereof, wherein the target sequence is manipulated by
the composition when expressed, wherein the composition comprises:
(A) a non-naturally occurring or engineered composition comprising
a vector system comprising one or more vectors comprising I. a
first regulatory element operably linked to a CRISPR-Cas system
chimeric RNA (chiRNA) polynucleotide sequence, wherein the
polynucleotide sequence comprises (a) a guide sequence capable of
hybridizing to a target sequence in a eukaryotic cell, (b) a tracr
mate sequence, and (c) a tracr sequence, and II. a second
regulatory element operably linked to an enzyme-coding sequence
encoding a CRISPR enzyme comprising at least one or more nuclear
localization sequences (or optionally at least one or more nuclear
localization sequences as some embodiments can involve no NLS)
wherein (a), (b) and (c) are arranged in a 5' to 3' orientation,
wherein components I and II are located on the same or different
vectors of the system, wherein when transcribed, the tracr mate
sequence hybridizes to the tracr sequence and the guide sequence
directs sequence-specific binding of a CRISPR complex to the target
sequence, and wherein the CRISPR complex comprises the CRISPR
enzyme complexed with (1) the guide sequence that is hybridized to
the target sequence, and (2) the tracr mate sequence that is
hybridized to the tracr sequence, or (B) a non-naturally occurring
or engineered composition comprising a vector system comprising one
or more vectors comprising I. a first regulatory element operably
linked to (a) a guide sequence capable of hybridizing to a target
sequence in a eukaryotic cell, and (b) at least one or more tracr
mate sequences, II. a second regulatory element operably linked to
an enzyme-coding sequence encoding a CRISPR enzyme, and III. a
third regulatory element operably linked to a tracr sequence,
wherein components I, II and III are located on the same or
different vectors of the system, wherein when transcribed, the
tracr mate sequence hybridizes to the tracr sequence and the guide
sequence directs sequence-specific binding of a CRISPR complex to
the target sequence, and wherein the CRISPR complex comprises the
CRISPR enzyme complexed with (1) the guide sequence that is
hybridized to the target sequence, and (2) the tracr mate sequence
that is hybridized to the tracr sequence. In some embodiments,
components I, II and III are located on the same vector. In other
embodiments, components I and II are located on the same vector,
while component III is located on another vector. In other
embodiments, components I and III are located on the same vector,
while component II is located on another vector. In other
embodiments, components II and III are located on the same vector,
while component I is located on another vector. In other
embodiments, each of components I, II and III is located on
different vectors. The invention also provides a viral (e.g. AAV or
lentivirus) vector system as described herein, and can be part of a
vector system as described herein.
[0033] Some methods of the invention can include inducing
expression. In some methods of the invention the organism or
subject is a eukaryote (including mammal including human) or a
non-human eukaryote or a non-human animal or a non-human mammal. In
some embodiments, the organism or subject is a non-human animal,
and may be an arthropod, for example, an insect, or may be a
nematode. In some methods of the invention the organism or subject
is a plant. In some methods of the invention the organism or
subject is a mammal or a non-human mammal. A non-human mammal may
be for example a rodent (preferably a mouse or a rat), an ungulate,
or a primate. In some methods of the invention the organism or
subject is algae, including microalgae, or is a fungus. In some
methods of the invention the viral vector is an AAV or a
lentivirus, and can be part of a vector system as described herein.
In some methods of the invention the CRISPR enzyme is a Cas9. In
some methods of the invention the expression of the guide sequence
is under the control of the T7 promoter and is driven by the
expression of T7 polymerase.
[0034] The invention in some embodiments comprehends a method of
delivering a CRISPR enzyme comprising delivering to a cell mRNA
encoding the CRISPR enzyme. In some of these methods the CRISPR
enzyme is a Cas9.
[0035] The invention also provides methods of preparing the vector
systems of the invention, in particular the viral vector systems as
described herein. The invention in some embodiments comprehends a
method of preparing the AAV of the invention comprising
transfecting plasmid(s) containing or consisting essentially of
nucleic acid molecule(s) coding for the AAV into AAV-infected
cells, and supplying AAV rep and/or cap obligatory for replication
and packaging of the AAV. In some embodiments the AAV rep and/or
cap obligatory for replication and packaging of the AAV are
supplied by transfecting the cells with helper plasmid(s) or helper
virus(es). In some embodiments the helper virus is a poxvirus,
adenovirus, herpesvirus or baculovirus. In some embodiments the
poxvirus is a vaccinia virus. In some embodiments the cells are
mammalian cells. And in some embodiments the cells are insect cells
and the helper virus is baculovirus. In other embodiments, the
virus is a lentivirus.
[0036] In plants, pathogens are often host-specific. For example,
Fusarium oxyporum f. sp. lycopersici causes tomato wilt but attacks
only tomato, and F. oxysporum f. dianthii Puccinia graminis f. sp.
tritici attacks only wheat. Plants have existing and induced
defenses to resist most pathogens. Mutations and recombination
events across plant generations lead to genetic variability that
gives rise to susceptibility, especially as pathogens reproduce
with more frequency than plants. In plants there can be non-host
resistance, e.g., the host and pathogen are incompatible. There can
also be Horizontal Resistance, e.g., partial resistance against all
races of a pathogen, typically controlled by many genes and
Vertical Resistance, e.g., complete resistance to some races of a
pathogen but not to other races, typically controlled by a few
genes. In a Gene-for-Gene level, plants and pathogens evolve
together, and the genetic changes in one balance changes in other.
Accordingly, using Natural Variability, breeders combine most
useful genes for Yield, Quality, Uniformity, Hardiness, Resistance.
The sources of resistance genes include native or foreign
Varieties, Heirloom Varieties, Wild Plant Relatives, and Induced
Mutations, e.g., treating plant material with mutagenic agents.
Using the present invention, plant breeders are provided with a new
tool to induce mutations. Accordingly, one skilled in the art can
analyze the genome of sources of resistance genes, and in Varieties
having desired characteristics or traits employ the present
invention to induce the rise of resistance genes, with more
precision than previous mutagenic agents and hence accelerate and
improve plant breeding programs.
[0037] The invention further comprehends a composition of the
invention or a CRISPR enzyme thereof (including or alternatively
mRNA encoding the CRISPR enzyme) for use in medicine or in therapy.
In some embodiments the invention comprehends a composition
according to the invention or a CRISPR enzyme thereof (including or
alternatively mRNA encoding the CRISPR enzyme) for use in a method
according to the invention. In some embodiments the invention
provides for the use of a composition of the invention or a CRISPR
enzyme thereof (including or alternatively mRNA encoding the CRISPR
enzyme) in ex vivo gene or genome editing. In certain embodiments
the invention comprehends use of a composition of the invention or
a CRISPR enzyme thereof (including or alternatively mRNA encoding
the CRISPR enzyme) in the manufacture of a medicament for ex vivo
gene or genome editing or for use in a method according of the
invention. The invention comprehends in some embodiments a
composition of the invention or a CRISPR enzyme thereof (including
or alternatively mRNA encoding the CRISPR enzyme), wherein the
target sequence is flanked at its 3' end by a PAM (protospacer
adjacent motif) sequence comprising 5'-motif, especially where the
Cas9 is (or is derived from) S. pyogenes or S. aureus Cas9. For
example, a suitable PAM is 5'-NRG or 5'-NNGRR (where N is any
Nucleotide) for SpCas9 or SaCas9 enzymes (or derived enzymes),
respectively, as mentioned below.
[0038] It will be appreciated that SpCas9 or SaCas9 are those from
or derived from S. pyogenes or S. aureus Cas9.
[0039] Aspects of the invention comprehend improving the
specificity of a CRISPR enzyme, e.g. Cas9, mediated gene targeting
and reducing the likelihood of off-target modification by the
CRISPR enzyme, e.g. Cas9. The invention in some embodiments
comprehends a method of modifying an organism or a non-human
organism by minimizing off-target modifications by manipulation of
a first and a second target sequence on opposite strands of a DNA
duplex in a genomic locus of interest in a cell comprising
delivering a non-naturally occurring or engineered composition
comprising:
[0040] I. a first CRISPR-Cas system chimeric RNA (chiRNA)
polynucleotide sequence, wherein the first polynucleotide sequence
comprises:
(a) a first guide sequence capable of hybridizing to the first
target sequence, (b) a first tracr mate sequence, and (c) a first
tracr sequence,
[0041] II. a second CRISPR-Cas system chiRNA polynucleotide
sequence, wherein the second polynucleotide sequence comprises:
(a) a second guide sequence capable of hybridizing to the second
target sequence, (b) a second tracr mate sequence, and (c) a second
tracr sequence, and
[0042] III. a polynucleotide sequence encoding a CRISPR enzyme
comprising at least one or more nuclear localization sequences and
comprising one or more mutations, wherein (a), (b) and (c) are
arranged in a 5' to 3' orientation, wherein when transcribed, the
first and the second tracr mate sequence hybridize to the first and
second tracr sequence respectively and the first and the second
guide sequence directs sequence-specific binding of a first and a
second CRISPR complex to the first and second target sequences
respectively, wherein the first CRISPR complex comprises the CRISPR
enzyme complexed with (1) the first guide sequence that is
hybridized to the first target sequence, and (2) the first tracr
mate sequence that is hybridized to the first tracr sequence,
wherein the second CRISPR complex comprises the CRISPR enzyme
complexed with (1) the second guide sequence that is hybridized to
the second target sequence, and (2) the second tracr mate sequence
that is hybridized to the second tracr sequence, wherein the
polynucleotide sequence encoding a CRISPR enzyme is DNA or RNA, and
wherein the first guide sequence directs cleavage of one strand of
the DNA duplex near the first target sequence and the second guide
sequence directs cleavage of the other strand near the second
target sequence inducing a double strand break, thereby modifying
the organism or the non-human organism by minimizing off-target
modifications.
[0043] In some methods of the invention any or all of the
polynucleotide sequence encoding the CRISPR enzyme, the first and
the second guide sequence, the first and the second tracr mate
sequence or the first and the second tracr sequence, is/are RNA. In
further embodiments of the invention the polynucleotides encoding
the sequence encoding the CRISPR enzyme, the first and the second
guide sequence, the first and the second tracr mate sequence or the
first and the second tracr sequence, is/are RNA and are delivered
via liposomes, nanoparticles, exosomes, microvesicles, or a
gene-gun. In certain embodiments of the invention, the first and
second tracr mate sequence share 100% identity and/or the first and
second tracr sequence share 100% identity. In some embodiments, the
polynucleotides may be comprised within a vector system comprising
one or more vectors. In preferred embodiments of the invention the
CRISPR enzyme is a Cas9 enzyme, e.g. SpCas9. In an aspect of the
invention the CRISPR enzyme comprises one or more mutations in a
catalytic domain, wherein the one or more mutations are selected
from the group consisting of D10A, E762A, H840A, N854A, N863A and
D986A. In a highly preferred embodiment the CRISPR enzyme has the
D10A mutation. In preferred embodiments, the first CRISPR enzyme
has one or more mutations such that the enzyme is a complementary
strand nicking enzyme, and the second CRISPR enzyme has one or more
mutations such that the enzyme is a non-complementary strand
nicking enzyme. Alternatively the first enzyme may be a
non-complementary strand nicking enzyme, and the second enzyme may
be a complementary strand nicking enzyme.
[0044] In preferred methods of the invention the first guide
sequence directing cleavage of one strand of the DNA duplex near
the first target sequence and the second guide sequence directing
cleavage of the other strand near the second target sequence
results in a 5' overhang. In embodiments of the invention the 5'
overhang is at most 200 base pairs, preferably at most 100 base
pairs, or more preferably at most 50 base pairs. In embodiments of
the invention the 5' overhang is at least 26 base pairs, preferably
at least 30 base pairs or more preferably 34-50 base pairs.
[0045] The invention in some embodiments comprehends a method of
modifying an organism or a non-human organism by minimizing
off-target modifications by manipulation of a first and a second
target sequence on opposite strands of a DNA duplex in a genomic
locus of interest in a cell comprising delivering a non-naturally
occurring or engineered composition comprising a vector system
comprising one or more vectors comprising
[0046] I. a first regulatory element operably linked to
(a) a first guide sequence capable of hybridizing to the first
target sequence, and (b) at least one or more tracr mate
sequences,
[0047] II. a second regulatory element operably linked to
(a) a second guide sequence capable of hybridizing to the second
target sequence, and (b) at least one or more tracr mate
sequences,
[0048] III. a third regulatory element operably linked to an
enzyme-coding sequence encoding a CRISPR enzyme, and
[0049] IV. a fourth regulatory element operably linked to a tracr
sequence,
[0050] wherein components I, II, III and IV are located on the same
or different vectors of the system, when transcribed, the tracr
mate sequence hybridizes to the tracr sequence and the first and
the second guide sequence direct sequence-specific binding of a
first and a second CRISPR complex to the first and second target
sequences respectively, wherein the first CRISPR complex comprises
the CRISPR enzyme complexed with (1) the first guide sequence that
is hybridized to the first target sequence, and (2) the tracr mate
sequence that is hybridized to the tracr sequence, wherein the
second CRISPR complex comprises the CRISPR enzyme complexed with
(1) the second guide sequence that is hybridized to the second
target sequence, and (2) the tracr mate sequence that is hybridized
to the tracr sequence, wherein the polynucleotide sequence encoding
a CRISPR enzyme is DNA or RNA, and wherein the first guide sequence
directs cleavage of one strand of the DNA duplex near the first
target sequence and the second guide sequence directs cleavage of
the other strand near the second target sequence inducing a double
strand break, thereby modifying the organism or the non-human
organism by minimizing off-target modifications.
[0051] The invention also provides a vector system as described
herein. The system may comprise one, two, three or four different
vectors. Components I, II, III and IV may thus be located on one,
two, three or four different vectors, and all combinations for
possible locations of the components are herein envisaged, for
example: components I, II, III and IV can be located on the same
vector; components I, II, III and IV can each be located on
different vectors; components I, II, III and IV may be located on a
total of two or three different vectors, with all combinations of
locations envisaged, etc.
[0052] In some methods of the invention any or all of the
polynucleotide sequence encoding the CRISPR enzyme, the first and
the second guide sequence, the first and the second tracr mate
sequence or the first and the second tracr sequence, is/are RNA. In
further embodiments of the invention the first and second tracr
mate sequence share 100% identity and/or the first and second tracr
sequence share 100% identity. In preferred embodiments of the
invention the CRISPR enzyme is a Cas9 enzyme, e.g. SpCas9. In an
aspect of the invention the CRISPR enzyme comprises one or more
mutations in a catalytic domain, wherein the one or more mutations
are selected from the group consisting of D10A, E762A, H840A,
N854A, N863A and D986A. In a highly preferred embodiment the CRISPR
enzyme has the D10A mutation. In preferred embodiments, the first
CRISPR enzyme has one or more mutations such that the enzyme is a
complementary strand nicking enzyme, and the second CRISPR enzyme
has one or more mutations such that the enzyme is a
non-complementary strand nicking enzyme. Alternatively the first
enzyme may be a non-complementary strand nicking enzyme, and the
second enzyme may be a complementary strand nicking enzyme. In a
further embodiment of the invention, one or more of the viral
vectors are delivered via liposomes, nanoparticles, exosomes,
microvesicles, or a gene-gun.
[0053] In preferred methods of the invention the first guide
sequence directing cleavage of one strand of the DNA duplex near
the first target sequence and the second guide sequence directing
cleavage of other strand near the second target sequence results in
a 5' overhang. In embodiments of the invention the 5' overhang is
at most 200 base pairs, preferably at most 100 base pairs, or more
preferably at most 50 base pairs. In embodiments of the invention
the 5' overhang is at least 26 base pairs, preferably at least 30
base pairs or more preferably 34-50 base pairs.
[0054] The invention in some embodiments comprehends a method of
modifying a genomic locus of interest by minimizing off-target
modifications by introducing into a cell containing and expressing
a double stranded DNA molecule encoding a gene product of interest
an engineered, non-naturally occurring CRISPR-Cas system comprising
a Cas protein having one or more mutations and two guide RNAs that
target a first strand and a second strand of the DNA molecule
respectively, whereby the guide RNAs target the DNA molecule
encoding the gene product and the Cas protein nicks each of the
first strand and the second strand of the DNA molecule encoding the
gene product, whereby expression of the gene product is altered;
and, wherein the Cas protein and the two guide RNAs do not
naturally occur together.
[0055] In preferred methods of the invention the Cas protein
nicking each of the first strand and the second strand of the DNA
molecule encoding the gene product results in a 5' overhang. In
embodiments of the invention the 5' overhang is at most 200 base
pairs, preferably at most 100 base pairs, or more preferably at
most 50 base pairs. In embodiments of the invention the 5' overhang
is at least 26 base pairs, preferably at least 30 base pairs or
more preferably 34-50 base pairs.
[0056] Embodiments of the invention also comprehend the guide RNAs
comprising a guide sequence fused to a tracr mate sequence and a
tracr sequence. In an aspect of the invention the Cas protein is
codon optimized for expression in a eukaryotic cell, preferably a
mammalian cell or a human cell. In further embodiments of the
invention the Cas protein is a type II CRISPR-Cas protein, e.g. a
Cas 9 protein. In a highly preferred embodiment the Cas protein is
a Cas9 protein, e.g. SpCas9. In aspects of the invention the Cas
protein has one or more mutations selected from the group
consisting of D10A, E762A, H840A, N854A, N863A and D986A. In a
highly preferred embodiment the Cas protein has the D10A
mutation.
[0057] Aspects of the invention relate to the expression of the
gene product being decreased or a template polynucleotide being
further introduced into the DNA molecule encoding the gene product
or an intervening sequence being excised precisely by allowing the
two 5' overhangs to reanneal and ligate or the activity or function
of the gene product being altered or the expression of the gene
product being increased. In an embodiment of the invention, the
gene product is a protein.
[0058] The invention also comprehends an engineered, non-naturally
occurring CRISPR-Cas system comprising a Cas protein having one or
more mutations and two guide RNAs that target a first strand and a
second strand respectively of a double stranded DNA molecule
encoding a gene product in a cell, whereby the guide RNAs target
the DNA molecule encoding the gene product and the Cas protein
nicks each of the first strand and the second strand of the DNA
molecule encoding the gene product, whereby expression of the gene
product is altered, and, wherein the Cas protein and the two guide
RNAs do not naturally occur together.
[0059] In aspects of the invention the guide RNAs may comprise a
guide sequence fused to a tracr mate sequence and a tracr sequence.
In an embodiment of the invention the Cas protein is a type II
CRISPR-Cas protein. In an aspect of the invention the Cas protein
is codon optimized for expression in a eukaryotic cell, preferably
a mammalian cell or a human cell. In further embodiments of the
invention the Cas protein is a type II CRISPR-Cas protein, e.g. a
Cas 9 protein. In a highly preferred embodiment the Cas protein is
a Cas9 protein, e.g. SpCas9. In aspects of the invention the Cas
protein has one or more mutations selected from the group
consisting of D10A, E762A, H840A, N854A, N863A and D986A. In a
highly preferred embodiment the Cas protein has the D10A
mutation.
[0060] Aspects of the invention relate to the expression of the
gene product being decreased or a template polynucleotide being
further introduced into the DNA molecule encoding the gene product
or an intervening sequence being excised precisely by allowing the
two 5' overhangs to reanneal and ligate or the activity or function
of the gene product being altered or the expression of the gene
product being increased. In an embodiment of the invention, the
gene product is a protein.
[0061] The invention also comprehends an engineered, non-naturally
occurring vector system comprising one or more vectors
comprising:
a) a first regulatory element operably linked to each of two
CRISPR-Cas system guide RNAs that target a first strand and a
second strand respectively of a double stranded DNA molecule
encoding a gene product, b) a second regulatory element operably
linked to a Cas protein, wherein components (a) and (b) are located
on same or different vectors of the system, whereby the guide RNAs
target the DNA molecule encoding the gene product and the Cas
protein nicks each of the first strand and the second strand of the
DNA molecule encoding the gene product, whereby expression of the
gene product is altered; and, wherein the Cas protein and the two
guide RNAs do not naturally occur together.
[0062] In aspects of the invention the guide RNAs may comprise a
guide sequence fused to a tracr mate sequence and a tracr sequence.
In an embodiment of the invention the Cas protein is a type II
CRISPR-Cas protein. In an aspect of the invention the Cas protein
is codon optimized for expression in a eukaryotic cell, preferably
a mammalian cell or a human cell. In further embodiments of the
invention the Cas protein is a type II CRISPR-Cas protein, e.g. a
Cas 9 protein. In a highly preferred embodiment the Cas protein is
a Cas9 protein, e.g. SpCas9. In aspects of the invention the Cas
protein has one or more mutations selected from the group
consisting of D10A, E762A, H840A, N854A, N863A and D986A. In a
highly preferred embodiment the Cas protein has the D10A
mutation.
[0063] Aspects of the invention relate to the expression of the
gene product being decreased or a template polynucleotide being
further introduced into the DNA molecule encoding the gene product
or an intervening sequence being excised precisely by allowing the
two 5' overhangs to reanneal and ligate or the activity or function
of the gene product being altered or the expression of the gene
product being increased. In an embodiment of the invention, the
gene product is a protein. In preferred embodiments of the
invention the vectors of the system are viral vectors. In a further
embodiment, the vectors of the system are delivered via liposomes,
nanoparticles, exosomes, microvesicles, or a gene-gun.
[0064] In one aspect, the invention provides a method of modifying
a target polynucleotide in a eukaryotic cell. In some embodiments,
the method comprises allowing a CRISPR complex to bind to the
target polynucleotide to effect cleavage of said target
polynucleotide thereby modifying the target polynucleotide, wherein
the CRISPR complex comprises a CRISPR enzyme complexed with a guide
sequence hybridized to a target sequence within said target
polynucleotide, wherein said guide sequence is linked to a tracr
mate sequence which in turn hybridizes to a tracr sequence. In some
embodiments, said cleavage comprises cleaving one or two strands at
the location of the target sequence by said CRISPR enzyme. In some
embodiments, said cleavage results in decreased transcription of a
target gene. In some embodiments, the method further comprises
repairing said cleaved target polynucleotide by homologous
recombination with an exogenous template polynucleotide, wherein
said repair results in a mutation comprising an insertion,
deletion, or substitution of one or more nucleotides of said target
polynucleotide. In some embodiments, said mutation results in one
or more amino acid changes in a protein expressed from a gene
comprising the target sequence. In some embodiments, the method
further comprises delivering one or more vectors to said eukaryotic
cell, wherein the one or more vectors drive expression of one or
more of: the CRISPR enzyme, the guide sequence linked to the tracr
mate sequence, and the tracr sequence. In some embodiments, said
vectors are delivered to the eukaryotic cell in a subject. In some
embodiments, said modifying takes place in said eukaryotic cell in
a cell culture. In some embodiments, the method further comprises
isolating said eukaryotic cell from a subject prior to said
modifying. In some embodiments, the method further comprises
returning said eukaryotic cell and/or cells derived therefrom to
said subject.
[0065] In one aspect, the invention provides a method of modifying
expression of a polynucleotide in a eukaryotic cell. In some
embodiments, the method comprises allowing a CRISPR complex to bind
to the polynucleotide such that said binding results in increased
or decreased expression of said polynucleotide; wherein the CRISPR
complex comprises a CRISPR enzyme complexed with a guide sequence
hybridized to a target sequence within said polynucleotide, wherein
said guide sequence is linked to a tracr mate sequence which in
turn hybridizes to a tracr sequence. In some embodiments, the
method further comprises delivering one or more vectors to said
eukaryotic cells, wherein the one or more vectors drive expression
of one or more of: the CRISPR enzyme, the guide sequence linked to
the tracr mate sequence, and the tracr sequence.
[0066] In one aspect, the invention provides a method of generating
a model eukaryotic cell comprising a mutated disease gene. In some
embodiments, a disease gene is any gene associated with an increase
in the risk of having or developing a disease. In some embodiments,
the method comprises (a) introducing one or more vectors into a
eukaryotic cell, wherein the one or more vectors drive expression
of one or more of: a CRISPR enzyme, a guide sequence linked to a
tracr mate sequence, and a tracr sequence, and (b) allowing a
CRISPR complex to bind to a target polynucleotide to effect
cleavage of the target polynucleotide within said disease gene,
wherein the CRISPR complex comprises the CRISPR enzyme complexed
with (1) the guide sequence that is hybridized to the target
sequence within the target polynucleotide, and (2) the tracr mate
sequence that is hybridized to the tracr sequence, thereby
generating a model eukaryotic cell comprising a mutated disease
gene. In some embodiments, said cleavage comprises cleaving one or
two strands at the location of the target sequence by said CRISPR
enzyme. In some embodiments, said cleavage results in decreased
transcription of a target gene. In some embodiments, the method
further comprises repairing said cleaved target polynucleotide by
homologous recombination with an exogenous template polynucleotide,
wherein said repair results in a mutation comprising an insertion,
deletion, or substitution of one or more nucleotides of said target
polynucleotide. In some embodiments, said mutation results in one
or more amino acid changes in a protein expression from a gene
comprising the target sequence.
[0067] In one aspect the invention provides for a method of
selecting one or more prokaryotic cell(s) by introducing one or
more mutations in a gene in the one or more prokaryotic cell (s),
the method comprising: introducing one or more vectors into the
prokaryotic cell (s), wherein the one or more vectors drive
expression of one or more of: a CRISPR enzyme, a guide sequence
linked to a tracr mate sequence, a tracr sequence, and an editing
template; wherein the editing template comprises the one or more
mutations that abolish CRISPR enzyme cleavage, allowing homologous
recombination of the editing template with the target
polynucleotide in the cell(s) to be selected; allowing a CRISPR
complex to bind to a target polynucleotide to effect cleavage of
the target polynucleotide within said gene, wherein the CRISPR
complex comprises the CRISPR enzyme complexed with (1) the guide
sequence that is hybridized to the target sequence within the
target polynucleotide, and (2) the tracr mate sequence that is
hybridized to the tracr sequence, wherein binding of the CRISPR
complex to the target polynucleotide induces cell death, thereby
allowing one or more prokaryotic cell(s) in which one or more
mutations have been introduced to be selected. In a preferred
embodiment, the CRISPR enzyme is Cas9. In another aspect of the
invention the cell to be selected may be a eukaryotic cell. Aspects
of the invention allow for selection of specific cells without
requiring a selection marker or a two-step process that may include
a counter-selection system.
[0068] In one aspect, the invention provides for methods of
modifying a target polynucleotide in a eukaryotic cell. In some
embodiments, the method comprises allowing a CRISPR complex to bind
to the target polynucleotide to effect cleavage of said target
polynucleotide thereby modifying the target polynucleotide, wherein
the CRISPR complex comprises a CRISPR enzyme complexed with a guide
sequence hybridized to a target sequence within said target
polynucleotide, wherein said guide sequence is linked to a tracr
mate sequence which in turn hybridizes to a tracr sequence.
[0069] In other embodiments, this invention provides a method of
modifying expression of a polynucleotide in a eukaryotic cell. The
method comprises increasing or decreasing expression of a target
polynucleotide by using a CRISPR complex that binds to the
polynucleotide.
[0070] Where desired, to effect the modification of the expression
in a cell, one or more vectors comprising a tracr sequence, a guide
sequence linked to the tracr mate sequence, a sequence encoding a
CRISPR enzyme is delivered to a cell. In some methods, the one or
more vectors comprises a regulatory element operably linked to an
enzyme-coding sequence encoding said CRISPR enzyme comprising a
nuclear localization sequence; and a regulatory element operably
linked to a tracr mate sequence and one or more insertion sites for
inserting a guide sequence upstream of the tracr mate sequence.
When expressed, the guide sequence directs sequence-specific
binding of a CRISPR complex to a target sequence in a cell.
Typically, the CRISPR complex comprises a CRISPR enzyme complexed
with (1) the guide sequence that is hybridized to the target
sequence, and (2) the tracr mate sequence that is hybridized to the
tracr sequence.
[0071] In some methods, a target polynucleotide can be inactivated
to effect the modification of the expression in a cell. For
example, upon the binding of a CRISPR complex to a target sequence
in a cell, the target polynucleotide is inactivated such that the
sequence is not transcribed, the coded protein is not produced, or
the sequence does not function as the wild-type sequence does. For
example, a protein or microRNA coding sequence may be inactivated
such that the protein is not produced.
[0072] In certain embodiments, the CRISPR enzyme comprises one or
more mutations selected from the group consisting of D10A, E762A,
H840A, N854A, N863A or D986A and/or the one or more mutations is in
a RuvC1 or HNH domain of the CRISPR enzyme or is a mutation as
otherwise as discussed herein. In some embodiments, the CRISPR
enzyme has one or more mutations in a catalytic domain, wherein
when transcribed, the tracr mate sequence hybridizes to the tracr
sequence and the guide sequence directs sequence-specific binding
of a CRISPR complex to the target sequence, and wherein the enzyme
further comprises a functional domain. In some embodiments, the
functional domain is a transcriptional activation domain,
preferably VP64. In some embodiments, the functional domain is a
transcription repression domain, preferably KRAB. In some
embodiments, the transcription repression domain is SID, or
concatemers of SID (eg SID4X). In some embodiments, the functional
domain is an epigenetic modifying domain, such that an epigenetic
modifying enzyme is provided. In some embodiments, the functional
domain is an activation domain, which may be the P65 activation
domain.
[0073] In some embodiments, the CRISPR enzyme is a type I or III
CRISPR enzyme, but is preferably a type II CRISPR enzyme. This type
II CRISPR enzyme may be any Cas enzyme. A Cas enzyme may be
identified as Cas9 as this can refer to the general class of
enzymes that share homology to the biggest nuclease with multiple
nuclease domains from the type II CRISPR system. Most preferably,
the Cas9 enzyme is from, or is derived from, spCas9 or saCas9. By
derived, Applicants mean that the derived enzyme is largely based,
in the sense of having a high degree of sequence homology with, a
wildtype enzyme, but that it has been mutated (modified) in some
way as described herein.
[0074] It will be appreciated that the terms Cas and CRISPR enzyme
are generally used herein interchangeably, unless otherwise
apparent. As mentioned above, many of the residue numberings used
herein refer to the Cas9 enzyme from the type II CRISPR locus in
Streptococcus pyogenes. However, it will be appreciated that this
invention includes many more Cas9s from other species of microbes,
such as SpCas9, SaCa9, StlCas9 and so forth.
[0075] An example of a codon optimized sequence, in this instance
optimized for humans (i.e. being optimized for expression in
humans) is provided herein, see the SaCas9 human codon optimized
sequence. Whilst this is preferred, it will be appreciated that
other examples are possible and codon optimization for a host
species is known.
[0076] Preferably, delivery is in the form of a vector which may be
a viral vector, such as a lenti- or baculo- or preferably
adeno-viral/adeno-associated viral vectors, but other means of
delivery are known (such as yeast systems, microvesicles, gene
guns/means of attaching vectors to gold nanoparticles) and are
provided. A vector may mean not only a viral or yeast system (for
instance, where the nucleic acids of interest may be operably
linked to and under the control of (in terms of expression, such as
to ultimately provide a processed RNA) a promoter), but also direct
delivery of nucleic acids into a host cell. While in herein methods
the vector may be a viral vector and this is advantageously an AAV,
other viral vectors as herein discussed can be employed, such as
lentivirus. For example, baculoviruses may be used for expression
in insect cells. These insect cells may, in turn be useful for
producing large quantities of further vectors, such as AAV or
lentivirus vectors adapted for delivery of the present invention.
Also envisaged is a method of delivering the present CRISPR enzyme
comprising delivering to a cell mRNA encoding the CRISPR enzyme. It
will be appreciated that in certain embodiments the CRISPR enzyme
is truncated, and/or comprised of less than one thousand amino
acids or less than four thousand amino acids, and/or is a nuclease
or nickase, and/or is codon-optimized, and/or comprises one or more
mutations, and/or comprises a chimeric CRISPR enzyme, and/or the
other options as herein discussed. AAV and lentiviral vectors are
preferred.
[0077] In certain embodiments, the target sequence is flanked or
followed, at its 3' end, by a PAM suitable for the CRISPR enzyme,
typically a Cas and in particular a Cas9.
[0078] For example, a suitable PAM is 5'-NRG or 5'-NNGRR for SpCas9
or SaCas9 enzymes (or derived enzymes), respectively.
[0079] It will be appreciated that SpCas9 or SaCas9 are those from
or derived from S. pyogenes or S. aureus Cas9.
[0080] Accordingly, it is an object of the invention to not
encompass within the invention any previously known product,
process of making the product, or method of using the product such
that Applicants reserve the right and hereby disclose a disclaimer
of any previously known product, process, or method. It is further
noted that the invention does not intend to encompass within the
scope of the invention any product, process, or making of the
product or method of using the product, which does not meet the
written description and enablement requirements of the USPTO (35
U.S.C. .sctn.112, first paragraph) or the EPO (Article 83 of the
EPC), such that Applicants reserve the right and hereby disclose a
disclaimer of any previously described product, process of making
the product, or method of using the product.
[0081] It is noted that in this disclosure and particularly in the
claims and/or paragraphs, terms such as "comprises", "comprised",
"comprising" and the like can have the meaning attributed to it in
U.S. Patent law; e.g., they can mean "includes", "included",
"including", and the like; and that terms such as "consisting
essentially of" and "consists essentially of" have the meaning
ascribed to them in U.S. Patent law, e.g., they allow for elements
not explicitly recited, but exclude elements that are found in the
prior art or that affect a basic or novel characteristic of the
invention.
[0082] These and other embodiments are disclosed or are obvious
from and encompassed by, the following Detailed Description.
BRIEF DESCRIPTION OF THE DRAWINGS
[0083] The novel features of the invention are set forth with
particularity in the appended claims. A better understanding of the
features and advantages of the present invention will be obtained
by reference to the following detailed description that sets forth
illustrative embodiments, in which the principles of the invention
are utilized, and the accompanying drawings of which:
[0084] FIG. 1 shows a schematic model of the CRISPR system. The
Cas9 nuclease from Streptococcus pyogenes (yellow) is targeted to
genomic DNA by a synthetic guide RNA (sgRNA) consisting of a 20-nt
guide sequence (blue) and a scaffold (red). The guide sequence
base-pairs with the DNA target (blue), directly upstream of a
requisite 5'-NGG protospacer adjacent motif (PAM; magenta), and
Cas9 mediates a double-stranded break (DSB) .about.3 bp upstream of
the PAM (red triangle).
[0085] FIG. 2A-2F shows an exemplary CRISPR system, a possible
mechanism of action, an example adaptation for expression in
eukaryotic cells, and results of tests assessing nuclear
localization and CRISPR activity. FIG. 2C discloses SEQ ID NOS 212
and 213, respectively, in order of appearance. FIG. 2E discloses
SEQ ID NOS 214-216, respectively, in order of appearance. FIG. 2F
discloses SEQ ID NOS 217-221, respectively, in order of
appearance.
[0086] FIG. 3A-3D shows results of an evaluation of SpCas9
specificity for an example target. FIG. 3A discloses SEQ ID NOS
222, 215 and 223-233, respectively, in order of appearance. FIG. 3C
discloses SEQ ID NO: 222.
[0087] FIG. 4A-4G show an exemplary vector system and results for
its use in directing homologous recombination in eukaryotic cells.
FIG. 4E discloses SEQ ID NO: 234. FIG. 4F discloses SEQ ID NOS 235
and 236, respectively, in order of appearance. FIG. 4G discloses
SEQ ID NOS 237-241, respectively, in order of appearance.
[0088] FIG. 5 provides a table of protospacer sequences (SEQ ID NOS
93, 92, 91, 242-247, 95, 94 and 248-252, respectively, in order of
appearance) and summarizes modification efficiency results for
protospacer targets designed based on exemplary S. pyogenes and S.
thermophilus CRISPR systems with corresponding PAMs against loci in
human and mouse genomes. Cells were transfected with Cas9 and
either pre-crRNA/tracrRNA or chimeric RNA, and analyzed 72 hours
after transfection. Percent indels are calculated based on Surveyor
assay results from indicated cell lines (N=3 for all protospacer
targets, errors are S.E.M., N.D. indicates not detectable using the
Surveyor assay, and N.T. indicates not tested in this study).
[0089] FIG. 6A-6C shows a comparison of different tracrRNA
transcripts for Cas9-mediated gene targeting. FIG. 6A discloses SEQ
ID NOS 253 and 254, respectively, in order of appearance.
[0090] FIG. 7 shows a schematic of a surveyor nuclease assay for
detection of double strand break-induced micro-insertions and
-deletions.
[0091] FIG. 8A-8B shows exemplary bicistronic expression vectors
for expression of CRISPR system elements in eukaryotic cells. FIG.
8A discloses SEQ ID NOS 255-257, respectively, in order of
appearance. FIG. 8B discloses SEQ ID NOS 258, 182 and 183,
respectively, in order of appearance.
[0092] FIG. 9A-9C shows histograms of distances between adjacent S.
pyogenes SF370 locus 1 PAM (NGG) (FIG. 9A) and S. thermophilus LMD9
locus 2 PAM (NNAGAAW) (FIG. 9B) in the human genome; and distances
for each PAM by chromosome (Chr) (FIG. 9C).
[0093] FIG. 10A-10D shows an exemplary CRISPR system, an example
adaptation for expression in eukaryotic cells, and results of tests
assessing CRISPR activity. FIG. 10B discloses SEQ ID NOS 259 and
260, respectively, in order of appearance. FIG. 10C discloses SEQ
ID NO: 261.
[0094] FIG. 11A-11C shows exemplary manipulations of a CRISPR
system for targeting of genomic loci in mammalian cells. FIG. 1A
discloses SEQ ID NO: 262. FIG. 11B discloses SEQ ID NOS 263-265,
respectively, in order of appearance.
[0095] FIG. 12A-12B shows the results of a Northern blot analysis
of crRNA processing in mammalian cells. FIG. 12A discloses SEQ ID
NO: 266.
[0096] FIG. 13A-13B shows an exemplary selection of protospacers in
the human PVALB (SEQ ID NO: 267) and mouse Th loci (SEQ ID NO:
268).
[0097] FIG. 14 shows example protospacer and corresponding PAM
sequence targets of the S. thermophilus CRISPR system in the human
EMX1 locus. FIG. 14 discloses SEQ ID NO: 261.
[0098] FIG. 15 provides a table of sequences (SEQ ID NOS 269-276,
191-192 and 277-278, respectively, in order of appearance) for
primers and probes used for Surveyor, RFLP, genomic sequencing, and
Northern blot assays.
[0099] FIG. 16A-16C shows exemplary manipulation of a CRISPR system
with chimeric RNAs and results of SURVEYOR assays for system
activity in eukaryotic cells. FIG. 16A discloses SEQ ID NO:
279.
[0100] FIG. 17A-17B shows a graphical representation of the results
of SURVEYOR assays for CRISPR system activity in eukaryotic
cells.
[0101] FIG. 18 shows an exemplary visualization of some S. pyogenes
Cas9 target sites in the human genome using the UCSC genome
browser. FIG. 18 discloses SEQ ID NOS 280-358, respectively, in
order of appearance.
[0102] FIG. 19A-19D shows a circular depiction of the phylogenetic
analysis revealing five families of Cas9s, including three groups
of large Cas9s (.about.1400 amino acids) and two of small Cas9s
(.about.1100 amino acids).
[0103] FIG. 20A-20F shows the linear depiction of the phylogenetic
analysis revealing five families of Cas9s, including three groups
of large Cas9s (.about.1400 amino acids) and two of small Cas9s
(.about.1100 amino acids).
[0104] FIG. 21A-21D shows genome editing via homologous
recombination. (a) Schematic of SpCas9 nickase, with D10A mutation
in the RuvC I catalytic domain. (b) Schematic representing
homologous recombination (HR) at the human EMX1 locus using either
sense or antisense single stranded oligonucleotides as repair
templates. Red arrow above indicates sgRNA cleavage site; PCR
primers for genotyping (Tables J and K) are indicated as arrows in
right panel. (c) Sequence of region modified by HR. d, SURVEYOR
assay for wildtype (wt) and nickase (D10A) SpCas9-mediated indels
at the EMX1 target 1 locus (n=3). Arrows indicate positions of
expected fragment sizes. FIG. 21C discloses SEQ ID NOS 359-361,
359, 362 and 361, respectively, in order of appearance.
[0105] FIG. 22A-22B shows single vector designs for SpCas9. FIG.
22A discloses SEQ ID NOS 363-365, respectively, in order of
appearance. FIG. 22B discloses SEQ ID NO: 366.
[0106] FIG. 23 shows a graph representing the length distribution
of Cas9 orthologs.
[0107] FIG. 24A-24M shows sequences where the mutation points are
located within the SpCas9 gene. FIG. 24A-M discloses the nucleotide
sequence as SEQ ID NO: 367 and the amino acid sequence as SEQ ID
NO: 368.
[0108] FIG. 25A shows the Conditional Cas9, Rosa26 targeting vector
map.
[0109] FIG. 25B shows the Constitutive Cas9, Rosa26 targeting
vector map.
[0110] FIG. 26 shows a schematic of the important elements in the
Constitutive and Conditional Cas9 constructs.
[0111] FIG. 27 shows delivery and in vivo mouse brain Cas9
expression data.
[0112] FIG. 28A-28C shows RNA delivery of Cas9 and chimeric RNA
into cells (A) Delivery of a GFP reporter as either DNA or mRNA
into Neuro-2A cells. (B) Delivery of Cas9 and chimeric RNA against
the Icam2 gene as RNA results in cutting for one of two spacers
tested. (C) Delivery of Cas9 and chimeric RNA against the F7 gene
as RNA results in cutting for one of two spacers tested.
[0113] FIG. 29 shows how DNA double-strand break (DSB) repair
promotes gene editing. In the error-prone non-homologous end
joining (NHEJ) pathway, the ends of a DSB are processed by
endogenous DNA repair machineries and rejoined together, which can
result in random insertion/deletion (indel) mutations at the site
of junction. Indel mutations occurring within the coding region of
a gene can result in frame-shift and a premature stop codon,
leading to gene knockout. Alternatively, a repair template in the
form of a plasmid or single-stranded oligodeoxynucleotides (ssODN)
can be supplied to leverage the homology-directed repair (HDR)
pathway, which allows high fidelity and precise editing.
[0114] FIG. 30A-30C shows anticipated results for HDR in HEK and
HUES9 cells. (a) Either a targeting plasmid or an ssODN (sense or
antisense) with homology arms can be used to edit the sequence at a
target genomic locus cleaved by Cas9 (red triangle). To assay the
efficiency of HDR, we introduced a HindIII site (red bar) into the
target locus, which was PCR-amplified with primers that anneal
outside of the region of homology. Digestion of the PCR product
with HindIII reveals the occurrence of HDR events. (b) ssODNs,
oriented in either the sense or the antisense (s or a) direction
relative to the locus of interest, can be used in combination with
Cas9 to achieve efficient HDR-mediated editing at the target locus.
A minimal homology region of 40 bp, and preferably 90 bp, is
recommended on either side of the modification (red bar). (c)
Example of the effect of ssODNs on HDR in the EMX1 locus is shown
using both wild-type Cas9 and Cas9 nickase (D10A). Each ssODN
contains homology arms of 90 bp flanking a 12-bp insertion of two
restriction sites. FIG. 30B discloses SEQ ID NOS 359-361, 359, 362
and 361, respectively, in order of appearance.
[0115] FIG. 31A-31C shows the repair strategy for Cystic Fibrosis
delta F508 mutation. FIG. 31A discloses the nucleotide sequence as
SEQ ID NO: 371 and the amino acid sequence as 372. FIG. 31B
discloses SEQ ID NO: 279. FIG. 31C discloses the nucleotide
sequence as SEQ ID NO: 373 and the amino acid sequence as SEQ ID
NO: 374.
[0116] FIG. 32A-32B (a) shows a schematic of the GAA repeat
expansion in FXN intron 1 and (b) shows a schematic of the strategy
adopted to excise the GAA expansion region using the CRISPR/Cas
system.
[0117] FIG. 33 shows a screen for efficient SpCas9 mediated
targeting of Tet1-3 and Dnmt1, 3a and 3b gene loci. Surveyor assay
on DNA from transfected N2A cells demonstrates efficient DNA
cleavage by using different gRNAs.
[0118] FIG. 34 shows a strategy of multiplex genome targeting using
a 2-vector system in an AAV1/2 delivery system. Tet1-3 and Dnmt1,
3a and 3b gRNA under the control of the U6 promoter. GFP-KASH under
the control of the human synapsin promoter. Restriction sides shows
simple gRNA replacement strategy by subcloning. HA-tagged SpCas9
flanked by two nuclear localization signals (NLS) is shown. Both
vectors are delivered into the brain by AAV1/2 virus in a 1:1
ratio.
[0119] FIG. 35 shows verification of multiplex DNMT targeting
vector #1 functionality using Surveyor assay. N2A cells were
co-transfected with the DNMT targeting vector #1 (+) and the SpCas9
encoding vector for testing SpCas9 mediated cleavage of DNMTs genes
family loci. gRNA only (-) is negative control. Cells were
harvested for DNA purification and downstream processing 48 h after
transfection.
[0120] FIG. 36 shows verification of multiplex DNMT targeting
vector #2 functionality using Surveyor assay. N2A cells were
co-transfected with the DNMT targeting vector #1 (+) and the SpCas9
encoding vector for testing SpCas9 mediated cleavage of DNMTs genes
family loci. gRNA only (-) is negative control. Cells were
harvested for DNA purification and downstream processing 48 h after
transfection.
[0121] FIG. 37 shows schematic overview of short promoters and
short polyA versions used for HA-SpCas9 expression in vivo. Sizes
of the encoding region from L-ITR to R-ITR are shown on the
right.
[0122] FIG. 38 shows schematic overview of short promoters and
short polyA versions used for HA-SaCas9 expression in vivo. Sizes
of the encoding region from L-ITR to R-ITR are shown on the
right.
[0123] FIG. 39 shows expression of SpCas9 and SaCas9 in N2A cells.
Representative Western blot of HA-tagged SpCas9 and SaCas9 versions
under the control of different short promoters and with or short
polyA (spA) sequences. Tubulin is loading control. mCherry (mCh) is
a transfection control. Cells were harvested and further processed
for Western blotting 48 h after transfection.
[0124] FIG. 40 shows screen for efficient SaCas9 mediated targeting
of Tet3 gene locus. Surveyor assay on DNA from transfected N2A
cells demonstrates efficient DNA cleavage by using different gRNAs
with NNGGGT PUM sequence. GFP transfected cells and cells
expressing only SaCas9 are controls.
[0125] FIG. 41 shows expression of HA-SaCas9 in the mouse brain.
Animals were injected into dentate gyri with virus driving
expression of HA-SaCas9 under the control of human Synapsin
promoter. Animals were sacrificed 2 weeks after surgery. HA tag was
detected using rabbit monoclonal antibody C29F4 (Cell Signaling).
Cell nuclei stained in blue with DAPI stain.
[0126] FIG. 42 shows expression of SpCas9 and SaCas9 in cortical
primary neurons in culture 7 days after transduction.
Representative Western blot of HA-tagged SpCas9 and SaCas9 versions
under the control of different promoters and with bgh or short
polyA (spA) sequences. Tubulin is loading control.
[0127] FIG. 43 shows LIVE/DEAD stain of primary cortical neurons 7
days after transduction with AAV1 particles carrying SpCas9 with
different promoters and multiplex gRNAs constructs (example shown
on the last panel for DNMTs). Neurons after AAV transduction were
compared with control untransduced neurons. Red nuclei indicate
permeabilized, dead cells (second line of panels). Live cells are
marked in green color (third line of panels).
[0128] FIG. 44 shows LIVE/DEAD stain of primary cortical neurons 7
days after transduction with AAV1 particles carrying SaCas9 with
different promoters. Red nuclei indicate permeabilized, dead cells
(second line of panels). Live cells are marked in green color
(third line of panels).
[0129] FIG. 45 shows comparison of morphology of neurons after
transduction with AAV1 virus carrying SpCas9 and gRNA multiplexes
for TETs and DNMTs genes loci. Neurons without transduction are
shown as a control.
[0130] FIG. 46 shows verification of multiplex DNMT targeting
vector #1 functionality using Surveyor assay in primary cortical
neurons. Cells were co-transduced with the DNMT targeting vector #1
and the SpCas9 viruses with different promoters for testing SpCas9
mediated cleavage of DNMTs genes family loci.
[0131] FIG. 47 shows in vivo efficiency of SpCas9 cleavage in the
brain. Mice were injected with AAV1/2 virus carrying gRNA multiplex
targeting DNMT family genes loci together with SpCas9 viruses under
control of 2 different promoters: mouse Mecp2 and rat Map1b. Two
weeks after injection brain tissue was extracted and nuclei were
prepped and sorted using FACS, based on the GFP expression driven
by Synapsin promoter from gRNA multiplex construct. After gDNA
extraction Surveyor assay was run. + indicates GFP positive nuclei
and - control, GFP-negative nuclei from the same animal. Numbers on
the gel indicate assessed SpCas9 efficiency.
[0132] FIG. 48 shows purification of GFP-KASH labeled cell nuclei
from hippocampal neurons. The outer nuclear membrane (ONM) of the
cell nuclear membrane is tagged with a fusion of GFP and the KASH
protein transmembrane domain. Strong GFP expression in the brain
after one week of stereotactic surgery and AAV1/2 injection.
Density gradient centrifugation step to purify cell nuclei from
intact brain. Purified nuclei are shown. Chromatin stain by
Vybrant.RTM. DyeCycle.TM. Ruby Stain is shown in red, GFP labeled
nuclei are green. Representative FACS profile of GFP+ and GFP-cell
nuclei (Magenta: Vybrant.RTM. DyeCycle.TM. Ruby Stain, Green:
GFP).
[0133] FIG. 49 shows efficiency of SpCas9 cleavage in the mouse
brain. Mice were injected with AAV1/2 virus carrying gRNA multiplex
targeting TET family genes loci together with SpCas9 viruses under
control of 2 different promoters: mouse Mecp2 and rat Map1b. Three
weeks after injection brain tissue was extracted, nuclei were
prepped and sorted using FACS, based on the GFP expression driven
by Synapsin promoter from gRNA multiplex construct. After gDNA
extraction Surveyor assay was run. + indicates GFP positive nuclei
and - control, GFP-negative nuclei from the same animal. Numbers on
the gel indicate assessed SpCas9 efficiency.
[0134] FIG. 50 shows GFP-KASH expression in cortical neurons in
culture. Neurons were transduced with AAV1 virus carrying gRNA
multiplex constructs targeting TET genes loci. The strongest signal
localize around cells nuclei due to KASH domain localization.
[0135] FIG. 51 shows (top) a list of spacing (as indicated by the
pattern of arrangement for two PAM sequences) between pairs of
guide RNAs (SEQ ID NOS 375-391, respectively, in order of
appearance). Only guide RNA pairs satisfying patterns 1, 2, 3, 4
exhibited indels when used with SpCas9(D10A) nickase. (bottom) Gel
images showing that combination of SpCas9(D10A) with pairs of guide
RNA satisfying patterns 1, 2, 3, 4 led to the formation of indels
in the target site.
[0136] FIG. 52 shows a list of U6 reverse primer sequences (SEQ ID
NOS 392-438, respectively, in order of appearance) used to generate
U6-guide RNA expression casssettes. Each primer needs to be paired
with the U6 forward primer "gcactgagggcctatttcccatgattc" (SEQ ID
NO: 1) to generate amplicons containing U6 and the desired guide
RNA.
[0137] FIG. 53 shows a Genomic sequence map from the human Emx1
locus showing the locations of the 24 patterns listed in FIG. 33.
FIG. 53 discloses the nucleotide sequence as SEQ ID NO: 439 and the
amino acid sequences as SEQ ID NOS 440-443, respectively, in order
of appearance.
[0138] FIG. 54 shows on (right) a gel image indicating the
formation of indels at the target site when variable 5' overhangs
are present after cleavage by the Cas9 nickase targeted by
different pairs of guide RNAs. on (left) a table indicating the
lane numbers of the gel on the right and various parameters
including identifying the guide RNA pairs used and the length of
the 5' overhang present following cleavage by the Cas9 nickase.
[0139] FIG. 55 shows a Genomic sequence map from the human Emx1
locus showing the locations of the different pairs of guide RNAs
that result in the gel patterns of FIG. 54 (right) and which are
further described in Example 35. FIG. 55 discloses the nucleotide
sequence as SEQ ID NO: 439 and the amino acid sequences as SEQ ID
NOS 440-443, respectively, in order of appearance.
[0140] FIG. 56 shows staining of HA-SpCas9 in dorsal and ventral
hippocampus 8 weeks after injection of viruses encoding
Mecp2-HA-SpCas9 and 3.times.gRNA-TETS with Syn-KASH-GFP.
[0141] FIG. 57 shows Syn_GFP-KASH expression 8 weeks after
3.times.gRNA virus injection is specific for neurons (NeuN positive
cells) and not for glia cells (GFAP positive).
[0142] FIG. 58 shows behavior tests conducted 5 weeks after
CRISPR-mediated KD of TETs and DNMTs in dentate gyrus (ventral and
dorsal part) showed increased level of anxiety and learning
deficits. A) time spend in the open arm during elevated plus maze
test. B) open field test, time spent in the center of arena vs time
in the corners was measured. C) Novel object recognition test,
results were measured 3 h after familiarization phase. D) Barnes
maze; efficiency in finding escape within 3 days of training. E)
Barnes maze results. F) Freezing behavior during contextual fear
conditioning. G) Latency to first freezing episode during
contextual fear conditioning. H) Trace fear conditioning results
for TETs KD and DNMTs KD (I). Control--animals injected with SpCas9
virus and GFP-KASH construct without gRNAs. TETs--animals injected
with both SpCas9 and construct encoding gRNAs against Tet1, Tet2
and Tet3. DNMTs--animals injected with both SpCas9 and construct
encoding gRNAs against Dnmt1, Dnmt3a and Dnmt3b.
[0143] FIG. 59 shows cutting efficiency of Tet loci in the brain, 8
weeks after Mecp_SpCas9 virus injection in compare to control
animals injected with Mecp2_SpCas9 virus only.
[0144] FIG. 60 shows cutting efficiency of Dnmt loci in the brain,
8 weeks after Mecp_SpCas9 virus injection in compare to control
animals injected with Mecp2_SpCas9 virus only.
[0145] FIG. 61 shows Dnmt3a staining in the brain, 8 weeks after
stereotaxic injection of virus encoding Mecp2_SpCas9 and gRNAs
targeting Dnmt loci. Bottom panel shows magnification of ROI
indicated on the upper panel.
[0146] FIG. 62 shows staining of Syn_HA-SaCas9 in the dorsal
hippocampus, 4 weeks after injection of virus. First column shows
animal injected with Sa-Cas9 only, middle column animal injected
with both SaCas9 and gRNAs against TETs loci and the right column
represents animal injected with only gRNAs encoding virus. SaCas9
nuclear localization depends on the presence of gRNA.
[0147] FIG. 63A-63E shows SpCas9 in N2a cells. A) Targeting- and
SpCas9 expression vector. B) Western Blot analysis of N2a cells
expressing HA-tagged SpCas9 under the control of different
promoters. C) Cutting efficiency of Dnmt loci. D) Western blot
analysis demonstrating efficient knock down of Dnmt3a. e) Cutting
efficiency of Tet loci.
[0148] FIG. 64A-64D shows SpCas9 in primary neurons. A) Schematic
overview of SpCas9 cloning strategies used in this study. Short
promoters and short polyA for efficient packaging into AAV
delivering system. B) Schematic overview of combined multiplex
targeting and nuclear envelope labeling strategy. C) Western blot
analysis showing expression of HA-tagged SpCas9 under the control
of rMap1b and mMecp2 promoter and bGH and spA signal. D)
Immunocytochemistry demonstrating co-expression of SpCas9 and
GFP-KASH in primary neurons. SpCas9 under the control of the mMecp2
promoter is expressed in neurons (Map1b, NeuN) but not in astroglia
cells (GFAP).
[0149] FIG. 65A-65D shows knock down of Dnmt3a in primary neurons.
A) Immunocytochemistry demonstrating efficient knock down of Dnmt3a
after targeting with multiplex targeting vector and mMecp2-SpCas9.
B) Quantification of Dnmt3a antibody staining in control and
targeted neurons. C) Western blot analysis demonstrating reduced
Dnmt3a protein level. D) Quantification of Western Blot analysis
demonstrating a total knock down of Dnmt3a protein level of approx.
75% in a mixed primary neuron culture (neurons and astroglia).
[0150] FIG. 66A-66B shows knock down of Dnmt3a in vivo. A) Cutting
efficiency of Dnmt loci in the brain, 8 weeks after Mecp_SpCas9
virus injection in compare to control animals injected with
Mecp2_SpCas9 virus only. B) Western blot analysis showing reduced
Dnmt3a protein level in targeted neuronal nuclei (KASH-GFP
positive) compared to control nuclei (RubyDye positive) after
sorting cell nuclei using FACS.
[0151] FIG. 67A-67F shows expression of SaCas9 in primary neurons.
A) Size of SaCas9 expression vector using hSynapsin promoter and
bGH signal. B) Expression of SaCas9 in primary neurons (NeuN) but
not in astroglia (GFAP). C) Extranuclear localization of SaCas9 in
absence of gRNA. C' Higher magnification of SaCas9 positive neurons
shown in C). D) Nuclear localization of SaCas9 in presence of gRNA.
D') Higher magnification of SaCas9 positive neurons shown in D). E)
Western blot analysis demonstrating expression of HA-tagged SaCas9
and GFP-KASH. F) Cutting efficiency of Dnmt loci 1 week after AAV
infection.
[0152] FIG. 68A-68E shows gRNA dependent nuclear localization of
SaCas9. A) Confocal imaging analysis demonstrating extranuclear
localization of SaCas9 in absence of gRNA in primary neurons. B)
Nuclear localization of SaCas9 in presence of gRNA. C) Line Scan
analysis of confocal picture A) showing extranuclear localization
of SaCas9 in absence of gRNA (red, SaCas9 signal; blue, DAPI
signal, green, GFP-KASH signal. D) Line Scan analysis of confocal
picture B) showing nuclear localization of SaCas9 in presence of
gRNA (red, SaCas9 signal; blue, DAPI signal; green, GFP-KASH
signal). E) Subcellular localization of SaCas9 and SpCas9 under
conditions without (-) and with (+) gRNA in N2a cells. SaCas9
signal at 250 kDa in the cytoplasm fraction (Tubulin positive)
indicating dimerization of SaCas9 in the cytoplasm. In the presence
of gRNA a shift of SaCas9 protein into the nuclear fraction (Sun2
positive) is visible. SaCas9 signal at 100 kDa indicates a gRNA
dependent formation of SaCas9 homomers and transport into the cell
nucleus. In contrast, SpCas9 is mainly present as homomer and its
nuclear localization is independent of gRNA.
[0153] FIG. 69 shows an AAV-Sa-Cas9 vector, a liver-specific
AAV-Sa-Cas9 vector and an alternate AAV-Sa-Cas9 vector.
[0154] FIG. 70 shows data on optimized CMV-SaCas9-NLS-U6-sgRNA
vector (submitted vector design last time); new data compares
N'-term vs C'-term tagged SaCas9 and shows enhanced cleavage
efficiency using C'-term NLS tagging.
[0155] FIG. 71 shows SURVEYOR image showing indels generated by new
Pcsk9 targets.
[0156] FIG. 72 shows SaCas9 specificity: genome-wide off target
sites (GWOTs) are predicted based on 2 criteria: they contain 4 or
fewer mismatched bases to intended SaCas9 target and bear the least
restrictive PAM for SaCas9, NNGRR. HEK 293FT cells are transfected
with either SpCas9 or SaCas9 with their corresponding sgRNAs at a
target site (EMX1: TAGGGTTAGGGGCCCCAGGC (SEQ ID NO: 2)) that has
CGGGGT as a PAM (sequence including PAM disclosed as SEQ ID NO:
369) so that it can be cut by either SpCas9 (CGG) or SaCas9
(CGGGGT). DNAs from cells are harvested and analyzed for indels by
Illumina sequencing at on-target and 41 predicted off-target loci
(following protocols from Hsu et al. Nature Biotech 2013 and data
analysis pipeline developed by David Scott and Josh Weinstein).
[0157] FIG. 73 shows that that SaCas9 may have a higher level of
off-target activity than SpCas9 at certain loci.
[0158] The figures herein are for illustrative purposes only and
are not necessarily drawn to scale.
DETAILED DESCRIPTION OF THE INVENTION
[0159] The invention relates to the engineering and optimization of
systems, methods and compositions used for the control of gene
expression involving sequence targeting, such as genome
perturbation or gene-editing, that relate to the CRISPR-Cas system
and components thereof. In advantageous embodiments, the Cas enzyme
is Cas9.
[0160] An advantage of the present methods is that the CRISPR
system avoids off-target binding and its resulting side effects.
This is achieved using systems arranged to have a high degree of
sequence specificity for the target DNA.
[0161] Cas9
[0162] Cas9 optimization may be used to enhance function or to
develop new functions, one can generate chimeric Cas9 proteins.
Examples that the Applicants have generated are provided in Example
6. Chimeric Cas9 proteins can be made by combining fragments from
different Cas9 homologs. For example, two example chimeric Cas9
proteins from the Cas9s described herein. For example, Applicants
fused the N-term of St1Cas9 (fragment from this protein is in bold)
with C-term of SpCas9. The benefit of making chimeric Cas9s include
any or all of: reduced toxicity; improved expression in eukaryotic
cells; enhanced specificity; reduced molecular weight of protein,
for example, making the protein smaller by combining the smallest
domains from different Cas9 homologs; and/or altering the PAM
sequence requirement.
[0163] The Cas9 may be used as a generic DNA binding protein. For
example, and as shown in Example 7, Applicants used Cas9 as a
generic DNA binding protein by mutating the two catalytic domains
(D10 and H840) responsible for cleaving both strands of the DNA
target. In order to upregulate gene transcription at a target locus
Applicants fused a transcriptional activation domain (VP64) to
Cas9. Other transcriptional activation domains are known. As shown
in Example 17, transcriptional activation is possible. As also
shown in Example 17, gene repression (in this case of the
beta-catenin gene) is possible using a Cas9 repressor (DNA-binding
domain) that binds to the target gene sequence, thus repressing its
activity.
[0164] Cas9 and one or more guide RNA can be delivered using adeno
associated virus (AAV), lentivirus, adenovirus or other plasmid or
viral vector types, in particular, using formulations and doses
from, for example, U.S. Pat. No. 8,454,972 (formulations, doses for
adenovirus), U.S. Pat. No. 8,404,658 (formulations, doses for AAV)
and U.S. Pat. No. 5,846,946 (formulations, doses for DNA plasmids)
and from clinical trials and publications regarding the clinical
trials involving lentivirus, AAV and adenovirus. For examples, for
AAV, the route of administration, formulation and dose can be as in
U.S. Pat. No. 8,454,972 and as in clinical trials involving AAV.
For Adenovirus, the route of administration, formulation and dose
can be as in U.S. Pat. No. 8,404,658 and as in clinical trials
involving adenovirus. For plasmid delivery, the route of
administration, formulation and dose can be as in U.S. Pat. No.
5,846,946 and as in clinical studies involving plasmids. Doses may
be based on or extrapolated to an average 70 kg individual, and can
be adjusted for patients, subjects, mammals of different weight and
species. Frequency of administration is within the ambit of the
medical or veterinary practitioner (e.g., physician, veterinarian),
depending on usual factors including the age, sex, general health,
other conditions of the patient or subject and the particular
condition or symptoms being addressed.
[0165] The viral vectors can be injected into the tissue of
interest. For cell-type specific genome modification, the
expression of Cas9 can be driven by a cell-type specific promoter.
For example, liver-specific expression might use the Albumin
promoter and neuron-specific expression might use the Synapsin I
promoter.
[0166] Transgenic Animals and Plants
[0167] Transgenic animals are also provided. Preferred examples
include animals comprising Cas9, in terms of polynucleotides
encoding Cas9 or the protein itself. Mice, rats and rabbits are
preferred. To generate transgenic mice with the constructs, as
exemplified herein one may inject pure, linear DNA into the
pronucleus of a zygote from a pseudo pregnant female, e.g. a CB56
female. Founders may then be identified, genotyped, and backcrossed
to CB57 mice. The constructs may then be cloned and optionally
verified, for instance by Sanger sequencing. Knock outs are
envisaged where for instance one or more genes are knocked out in a
model. However, are knockins are also envisaged (alone or in
combination). An example knockin Cas9 mouse was generated and this
is exemplified, but Cas9 knockins are preferred. To generate a Cas9
knock in mice one may target the same constitutive and conditional
constructs to the Rosa26 locus, as described herein (FIGS. 25A-B
and 26). Methods of US Patent Publication Nos. 20120017290 and
20110265198 assigned to Sangamo BioSciences, Inc. directed to
targeting the Rosa locus may be modified to utilize the CRISPR Cas
system of the present invention. In another embodiment, the methods
of US Patent Publication No. 20130236946 assigned to Cellectis
directed to targeting the Rosa locus may also be modified to
utilize the CRISPR Cas system of the present invention.
[0168] Utility of the conditional Cas9 mouse: Applicants have shown
in 293 cells that the Cas9 conditional expression construct can be
activated by co-expression with Cre. Applicants also show that the
correctly targeted R1 mESCs can have active Cas9 when Cre is
expressed. Because Cas9 is followed by the P2A peptide cleavage
sequence and then EGFP Applicants identify successful expression by
observing EGFP. Applicants have shown Cas9 activation in mESCs.
This same concept is what makes the conditional Cas9 mouse so
useful. Applicants may cross their conditional Cas9 mouse with a
mouse that ubiquitously expresses Cre (ACTB-Cre line) and may
arrive at a mouse that expresses Cas9 in every cell. It should only
take the delivery of chimeric RNA to induce genome editing in
embryonic or adult mice. Interestingly, if the conditional Cas9
mouse is crossed with a mouse expressing Cre under a tissue
specific promoter, there should only be Cas9 in the tissues that
also express Cre. This approach may be used to edit the genome in
only precise tissues by delivering chimeric RNA to the same
tissue.
[0169] As mentioned above, transgenic animals are also provided, as
are transgenic plants, especially crops and algae. The transgenic
plants may be useful in applications outside of providing a disease
model. These may include food or feed production through expression
of, for instance, higher protein, carbohydrate, nutrient or vitamin
levels than would normally be seen in the wildtype. In this regard,
transgenic plants, especially pulses and tubers, and animals,
especially mammals such as livestock (cows, sheep, goats and pigs),
but also poultry and edible insects, are preferred.
[0170] Transgenic algae or other plants such as rape may be
particularly useful in the production of vegetable oils or biofuels
such as alcohols (especially methanol and ethanol), for instance.
These may be engineered to express or overexpress high levels of
oil or alcohols for use in the oil or biofuel industries.
[0171] Adeno Associated Virus (AAV)
[0172] In terms of in vivo delivery, AAV is advantageous over other
viral vectors for a couple of reasons:
[0173] Low toxicity (this may be due to the purification method not
requiring ultra centrifugation of cell particles that can activate
the immune response)
[0174] Low probability of causing insertional mutagenesis because
it doesn't integrate into the host genome.
[0175] AAV has a packaging limit of 4.5 or 4.75 Kb. This means that
Cas9 as well as a promoter and transcription terminator have to be
all fit into the same viral vector. Constructs larger than 4.5 or
4.75 Kb will lead to significantly reduced virus production. SpCas9
is quite large, the gene itself is over 4.1 Kb, which makes it
difficult for packing into AAV. Therefore embodiments of the
invention include utilizing homologs of Cas9 that are shorter. For
example:
TABLE-US-00001 Species Cas9 Size Corynebacter diphtheriae 3252
Eubacterium ventriosum 3321 Streptococcus pasteurianus 3390
Lactobacillus farciminis 3378 Sphaerochaeta globus 3537
Azospirillum B510 3504 Gluconacetobacter diazotrophicus 3150
Neisseria cinerea 3246 Roseburia intestinalis 3420 Parvibaculum
lavamentivorans 3111 Staphylococcus aureus 3159 Nitratifractor
salsuginis DSM 16511 3396 Campylobacter lari CF89-12 3009
Streptococcus thermophilus LMD-9 3396
[0176] These species are therefore, in general, preferred Cas9
species. Applicants have shown delivery and in vivo mouse brain
Cas9 expression data.
[0177] Two ways to package Cas9 coding nucleic acid molecules,
e.g., DNA, into viral vectors to mediate genome modification in
vivo are preferred:
[0178] To achieve NHEJ-mediated gene knockout:
[0179] Single Virus Vector:
[0180] Vector containing two or more expression cassettes:
[0181] Promoter-Cas9 coding nucleic acid molecule-terminator
[0182] Promoter-gRNA1-terminator
[0183] Promoter-gRNA2-terminator
[0184] Promoter-gRNA(N)-terminator (up to size limit of vector)
[0185] Double Virus Vector:
[0186] Vector 1 containing one expression cassette for driving the
expression of Cas9
[0187] Promoter-Cas9 coding nucleic acid molecule-terminator
[0188] Vector 2 containing one more expression cassettes for
driving the expression of one or more guideRNAs
[0189] Promoter-gRNA1-terminator
[0190] Promoter-gRNA(N)-terminator (up to size limit of vector)
[0191] To mediate homology-directed repair. In addition to the
single and double virus vector approaches described above, an
additional vector is used to deliver a homology-direct repair
template.
[0192] Promoter used to drive Cas9 coding nucleic acid molecule
expression can include:
[0193] AAV ITR can serve as a promoter: this is advantageous for
eliminating the need for an additional promoter element (which can
take up space in the vector). The additional space freed up can be
used to drive the expression of additional elements (gRNA, etc.).
Also, ITR activity is relatively weaker, so can be used to reduce
toxicity due to over expression of Cas9.
[0194] For ubiquitous expression, can use promoters: CMV, CAG, CBh,
PGK, SV40, Ferritin heavy or light chains, etc.
[0195] For brain expression, can use promoters: SynapsinI for all
neurons, CaMKIIalpha for excitatory neurons, GAD67 or GAD65 or VGAT
for GABAergic neurons, etc.
[0196] For liver expression, can use Albumin promoter.
[0197] For lung expression, can use SP-B.
[0198] For endothelial cells, can use ICAM.
[0199] For hematopoietic cells can use IFNbeta or CD45.
[0200] For Osteoblasts can use OG-2.
[0201] Promoter used to drive guide RNA can include:
[0202] Pol III promoters such as U6 or H1
[0203] Use of Pol II promoter and intronic cassettes to express
gRNA
[0204] As to AAV, the AAV can be AAV1, AAV2, AAV5 or any
combination thereof. One can select the AAV of the AAV with regard
to the cells to be targeted; e.g., one can select AAV serotypes 1,
2, 5 or a hybrid or capsid AAV1, AAV2, AAV5 or any combination
thereof for targeting brain or neuronal cells; and one can select
AAV4 for targeting cardiac tissue. AAV8 is useful for delivery to
the liver. The above promoters and vectors are preferred
individually.
[0205] RNA delivery is also a useful method of in vivo delivery.
FIG. 27 shows delivery and in vivo mouse brain Cas9 expression
data. It is possible to deliver Cas9 and gRNA (and, for instance,
HR repair template) into cells using liposomes or nanoparticles.
Thus delivery of the CRISPR enzyme, such as a Cas9 and/or delivery
of the RNAs of the invention may be in RNA form and via
microvesicles, liposomes or nanoparticles. For example, Cas9 mRNA
and gRNA can be packaged into liposomal particles for delivery in
vivo. Liposomal transfection reagents such as lipofectamine from
Life Technologies and other reagents on the market can effectively
deliver RNA molecules into the liver.
[0206] Enhancing NHEJ or HR efficiency is also helpful for
delivery. It is preferred that NHEJ efficiency is enhanced by
co-expressing end-processing enzymes such as Trex2 (Dumitrache et
al. Genetics. 2011 August, 188(4): 787-797). It is preferred that
HR efficiency is increased by transiently inhibiting NHEJ
machineries such as Ku70 and Ku86. HR efficiency can also be
increased by co-expressing prokaryotic or eukaryotic homologous
recombination enzymes such as RecBCD, RecA.
[0207] Various means of delivery are described herein, and further
discussed in this section.
[0208] Viral delivery: The CRISPR enzyme, for instance a Cas9,
and/or any of the present RNAs, for instance a guide RNA, can be
delivered using adeno associated virus (AAV), lentivirus,
adenovirus or other viral vector types, or combinations thereof.
Cas9 and one or more guide RNAs can be packaged into one or more
viral vectors. In some embodiments, the viral vector is delivered
to the tissue of interest by, for example, an intramuscular
injection, while other times the viral delivery is via intravenous,
transdermal, intranasal, oral, mucosal, or other delivery methods.
Such delivery may be either via a single dose, or multiple doses.
One skilled in the art understands that the actual dosage to be
delivered herein may vary greatly depending upon a variety of
factors, such as the vector chose, the target cell, organism, or
tissue, the general condition of the subject to be treated, the
degree of transformation/modification sought, the administration
route, the administration mode, the type of
transformation/modification sought, etc.
[0209] Such a dosage may further contain, for example, a carrier
(water, saline, ethanol, glycerol, lactose, sucrose, calcium
phosphate, gelatin, dextran, agar, pectin, peanut oil, sesame oil,
etc.), a diluent, a pharmaceutically-acceptable carrier (e.g.,
phosphate-buffered saline), a pharmaceutically-acceptable
excipient, an adjuvant to enhance antigenicity, an
immunostimulatory compound or molecule, and/or other compounds
known in the art. The adjuvant herein may contain a suspension of
minerals (alum, aluminum hydroxide, aluminum phosphate) on which
antigen is adsorbed; or water-in-oil emulsion in which antigen
solution is emulsified in oil (MF-59, Freund's incomplete
adjuvant), sometimes with the inclusion of killed mycobacteria
(Freund's complete adjuvant) to further enhance antigenicity
(inhibits degradation of antigen and/or causes influx of
macrophages). Adjuvants also include immunostimulatory molecules,
such as cytokines, costimulatory molecules, and for example,
immunostimulatory DNA or RNA molecules, such as CpG
oligonucleotides. Such a dosage formulation is readily
ascertainable by one skilled in the art. The dosage may further
contain one or more pharmaceutically acceptable salts such as, for
example, a mineral acid salt such as a hydrochloride, a
hydrobromide, a phosphate, a sulfate, etc.; and the salts of
organic acids such as acetates, propionates, malonates, benzoates,
etc. Additionally, auxiliary substances, such as wetting or
emulsifying agents, pH buffering substances, gels or gelling
materials, flavorings, colorants, microspheres, polymers,
suspension agents, etc. may also be present herein. In addition,
one or more other conventional pharmaceutical ingredients, such as
preservatives, humectants, suspending agents, surfactants,
antioxidants, anticaking agents, fillers, chelating agents, coating
agents, chemical stabilizers, etc. may also be present, especially
if the dosage form is a reconstitutable form. Suitable exemplary
ingredients include microcrystalline cellulose,
carboxymethylcellulose sodium, polysorbate 80, phenylethyl alcohol,
chlorobutanol, potassium sorbate, sorbic acid, sulfur dioxide,
propyl gallate, the parabens, ethyl vanillin, glycerin, phenol,
parachlorophenol, gelatin, albumin and a combination thereof. A
thorough discussion of pharmaceutically acceptable excipients is
available in REMINGTON'S PHARMACEUTICAL SCIENCES (Mack Pub. Co.,
N.J. 1991) which is incorporated by reference herein.
[0210] In an embodiment herein the delivery is via an adenovirus,
which may be at a single booster dose containing at least
1.times.10.sup.5 particles (also referred to as particle units, pu)
of adenoviral vector. In an embodiment herein, the dose preferably
is at least about 1.times.10.sup.6 particles (for example, about
1.times.10.sup.6-1.times.10.sup.12 particles), more preferably at
least about 1.times.10.sup.7 particles, more preferably at least
about 1.times.10.sup.8 particles (e.g., about
1.times.10.sup.8-1.times.10.sup.11 particles or about
1.times.10.sup.8-1.times.10.sup.12 particles), and most preferably
at least about 1.times.10.sup.0 particles (e.g., about
1*.times.10.sup.9-1.times.10.sup.10 particles or about
1.times.10.sup.9-1.times.10.sup.12 particles), or even at least
about 1.times.10.sup.10 particles (e.g., about
1.times.10-1.times.10.sup.12 particles) of the adenoviral vector.
Alternatively, the dose comprises no more than about
1.times.10.sup.14 particles, preferably no more than about
1.times.10.sup.13 particles, even more preferably no more than
about 1.times.10.sup.12 particles, even more preferably no more
than about 1.times.10.sup.11 particles, and most preferably no more
than about 1.times.10.sup.10 particles (e.g., no more than about
1.times.10.sup.9 articles). Thus, the dose may contain a single
dose of adenoviral vector with, for example, about 1.times.10.sup.6
particle units (pu), about 2.times.10.sup.6 pu, about
4.times.10.sup.6 pu, about 1.times.10.sup.7 pu, about
2.times.10.sup.7 pu, about 4.times.10.sup.7 pu, about
1.times.10.sup.8 pu, about 2.times.10.sup.8 pu, about
4.times.10.sup.8 pu, about 1.times.10.sup.9 pu, about
2.times.10.sup.9 pu, about 4.times.10.sup.9 pu, about
1.times.10.sup.10 pu, about 2.times.10.sup.10 pu, about
4.times.10.sup.10 pu, about 1.times.10.sup.11 pu, about
2.times.10.sup.1 pu, about 4.times.10.sup.11 pu, about
1.times.10.sup.12 pu, about 2.times.10.sup.12 pu, or about
4.times.10.sup.12 pu of adenoviral vector. See, for example, the
adenoviral vectors in U.S. Pat. No. 8,454,972 B2 to Nabel, et. al.,
granted on Jun. 4, 2013; incorporated by reference herein, and the
dosages at col 29, lines 36-58 thereof. In an embodiment herein,
the adenovirus is delivered via multiple doses.
[0211] In an embodiment herein, the delivery is via an AAV. A
therapeutically effective dosage for in vivo delivery of the AAV to
a human is believed to be in the range of from about 20 to about 50
ml of saline solution containing from about 1.times.10.sup.10 to
about 1.times.10.sup.10 functional AAV/ml solution. The dosage may
be adjusted to balance the therapeutic benefit against any side
effects. In an embodiment herein, the AAV dose is generally in the
range of concentrations of from about 1.times.10.sup.5 to
1.times.10.sup.50 genomes AAV, from about 1.times.10.sup.8 to
1.times.10.sup.20 genomes AAV, from about 1.times.10.sup.10 to
about 1.times.10.sup.16 genomes, or about 1.times.10.sup.11 to
about 1.times.10.sup.16 genomes AAV. A human dosage may be about
1.times.10.sup.13 genomes AAV. Such concentrations may be delivered
in from about 0.001 ml to about 100 ml, about 0.05 to about 50 ml,
or about 10 to about 25 ml of a carrier solution. Other effective
dosages can be readily established by one of ordinary skill in the
art through routine trials establishing dose response curves. See,
for example, U.S. Pat. No. 8,404,658 B2 to Hajjar, et al., granted
on Mar. 26, 2013, at col. 27, lines 45-60.
[0212] In an embodiment herein the delivery is via a plasmid. In
such plasmid compositions, the dosage should be a sufficient amount
of plasmid to elicit a response. For instance, suitable quantities
of plasmid DNA in plasmid compositions can be from about 0.1 to
about 2 mg, or from about 1 .mu.g to about 10 .mu.g.
[0213] The doses herein are based on an average 70 kg individual.
The frequency of administration is within the ambit of the medical
or veterinary practitioner (e.g., physician, veterinarian), or
scientist skilled in the art.
[0214] Lentivirus
[0215] Lentiviruses are complex retroviruses that have the ability
to infect and express their genes in both mitotic and post-mitotic
cells. The most commonly known lentivirus is the human
immunodeficiency virus (HIV), which uses the envelope glycoproteins
of other viruses to target a broad range of cell types.
[0216] Lentiviruses may be prepared as follows. After cloning
pCasES10 (which contains a lentiviral transfer plasmid backbone),
HEK293FT at low passage (p=5) were seeded in a T-75 flask to 50%
confluence the day before transfection in DMEM with 10% fetal
bovine serum and without antibiotics. After 20 hours, media was
changed to OptiMEM (serum-free) media and transfection was done 4
hours later. Cells were transfected with 10 .mu.g of lentiviral
transfer plasmid (pCasES10) and the following packaging plasmids: 5
.mu.g of pMD2.G (VSV-g pseudotype), and 7.5 ug of psPAX2
(gag/pol/rev/tat). Transfection was done in 4 mL OptiMEM with a
cationic lipid delivery agent (50 uL Lipofectamine 2000 and 100 ul
Plus reagent). After 6 hours, the media was changed to
antibiotic-free DMEM with 10% fetal bovine serum.
[0217] Lentivirus may be purified as follows. Viral supernatants
were harvested after 48 hours. Supernatants were first cleared of
debris and filtered through a 0.45 um low protein binding (PVDF)
filter. They were then spun in a ultracentrifuge for 2 hours at
24,000 rpm. Viral pellets were resuspended in 50 ul of DMEM
overnight at 4 C. They were then aliquotted and immediately frozen
at -80 C.
[0218] In another embodiment, minimal non-primate lentiviral
vectors based on the equine infectious anemia virus (EIAV) are also
contemplated, especially for ocular gene therapy (see, e.g.,
Balagaan, J Gene Med 2006; 8: 275-285, Published online 21 Nov.
2005 in Wiley InterScience (www.interscience.wiley.com). DOI:
10.1002/jgm.845). In another embodiment, RetinoStat.RTM., an equine
infectious anemia virus-based lentiviral gene therapy vector that
expresses angiostatic proteins endostain and angiostatin that is
delivered via a subretinal injection for the treatment of the web
form of age-related macular degeneration is also contemplated (see,
e.g., Binley et al., HUMAN GENE THERAPY 23:980-991 (September
2012)) may be modified for the CRISPR-Cas system of the present
invention.
[0219] In another embodiment, self-inactivating lentiviral vectors
with an siRNA targeting a common exon shared by HIV tat/rev, a
nucleolar-localizing TAR decoy, and an anti-CCR5-specific
hammerhead ribozyme (see, e.g., DiGiusto et al. (2010) Sci Transl
Med 2:36ra43) may be used/and or adapted to the CRISPR-Cas system
of the present invention. A minimum of 2.5.times.10.sup.6 CD34+
cells per kilogram patient weight may be collected and
prestimulated for 16 to 20 hours in X-VIVO 15 medium (Lonza)
containing 2 mML-glutamine, stem cell factor (100 ng/ml), Flt-3
ligand (Flt-3L) (100 ng/ml), and thrombopoietin (10 ng/ml)
(CellGenix) at a density of 2.times.10.sup.6 cells/ml.
Prestimulated cells may be transduced with lentiviral at a
multiplicity of infection of 5 for 16 to 24 hours in 75-cm.sup.2
tissue culture flasks coated with fibronectin (25 mg/cm.sup.2)
(RetroNectin, Takara Bio Inc.).
[0220] Lentiviral vectors have been disclosed as in the treatment
for Parkinson's Disease, see, e.g., US Patent Publication No.
20120295960 and U.S. Pat. Nos. 7,303,910 and 7,351,585. Lentiviral
vectors have also been disclosed for the treatment of ocular
diseases, see e.g., US Patent Publication Nos. 20060281180,
20090007284, US20110117189; US20090017543; US20070054961,
US20100317109. Lentiviral vectors have also been disclosed for
delivery to the train, see, e.g., US Patent Publication Nos.
US20110293571; US20110293571, US20040013648, US20070025970,
US20090111106 and U.S. Pat. No. 7,259,015.
[0221] RNA Delivery
[0222] RNA delivery: The CRISPR enzyme, for instance a Cas9, and/or
any of the present RNAs, for instance a guide RNA, can also be
delivered in the form of RNA. Cas9 mRNA can be generated using in
vitro transcription. For example, Cas9 mRNA can be synthesized
using a PCR cassette containing the following elements:
T7_promoter-kozak sequence (GCCACC)-Cas9-3' UTR from beta
globin-polyA tail (a string of 120 or more adenines). The cassette
can be used for transcription by T7 polymerase. Guide RNAs can also
be transcribed using in vitro transcription from a cassette
containing T7_promoter-GG-guide RNA sequence.
[0223] To enhance expression and reduce toxicity, the CRISPR enzyme
and/or guide RNA can be modified using pseudo-U or 5-Methyl-C.
[0224] mRNA delivery methods are especially promising for liver
delivery currently. In particular, for AAV8 is particularly
preferred for delivery to the liver.
[0225] Nanoparticles
[0226] CRISPR enzyme mRNA and guide RNA may be delivered
simultaneously using nanoparticles or lipid envelopes.
[0227] For example, Su X, Fricke J, Kavanagh D G, Irvine D J ("In
vitro and in vivo mRNA delivery using lipid-enveloped pH-responsive
polymer nanoparticles" Mol Pharm. 2011 Jun. 6; 8(3):774-87. doi:
10.1021/mp100390w. Epub 2011 Apr. 1) describes biodegradable
core-shell structured nanoparticles with a poly(.beta.-amino ester)
(PBAE) core enveloped by a phospholipid bilayer shell. These were
developed for in vivo mRNA delivery. The pH-responsive PBAE
component was chosen to promote endosome disruption, while the
lipid surface layer was selected to minimize toxicity of the
polycation core. Such are, therefore, preferred for delivering RNA
of the present invention.
[0228] In one embodiment, nanoparticles based on self assembling
bioadhesive polymers are contemplated, which may be applied to oral
delivery of peptides, intravenous delivery of peptides and nasal
delivery of peptides, all to the brain. Other embodiments, such as
oral absorption and ocular deliver of hydrophobic drugs are also
contemplated. The molecular envelope technology involves an
engineered polymer envelope which is protected and delivered to the
site of the disease (see, e.g., Mazza, M. et al. ACSNano, 2013.
7(2): 1016-1026; Siew, A., et al. Mol Pharm, 2012. 9(1):14-28;
Lalatsa, A., et al. J Contr Rel, 2012. 161(2):523-36; Lalatsa, A.,
et al., Mol Pharm, 2012. 9(6):1665-80; Lalatsa, A., et al. Mol
Pharm, 2012. 9(6):1764-74; Garrett, N. L., et al. J Biophotonics,
2012. 5(5-6):458-68; Garrett, N. L., et al. J Raman Spect, 2012.
43(5):681-688; Ahmad, S., et al. J Royal Soc Interface 2010. 7:
S423-33; Uchegbu, I. F. Expert Opin Drug Deliv, 2006. 3(5):629-40;
Qu, X., et al. Biomacromolecules, 2006. 7(12):3452-9 and Uchegbu,
I. F., et al. Int J Pharm, 2001. 224:185-199). Doses of about 5
mg/kg are contemplated, with single or multiple doses, depending on
the target tissue.
[0229] In one embodiment, nanoparticles that can deliver RNA to a
cancer cell to stop tumor growth developed by Dan Anderson's lab at
MIT may be used/and or adapted to the CRISPR Cas system of the
present invention. In particular, the Anderson lab developed fully
automated, combinatorial systems for the synthesis, purification,
characterization, and formulation of new biomaterials and
nanoformulations. See, e.g., Alabi et al., Proc Natl Acad Sci USA.
2013 Aug. 6; 110(32):12881-6; Zhang et al., Adv Mater. 2013 Sep. 6;
25(33):4641-5; Jiang et al., Nano Lett. 2013 Mar. 13;
13(3):1059-64; Karagiannis et al., ACS Nano. 2012 Oct. 23;
6(10):8484-7; Whitehead et al., ACS Nano. 2012 Aug. 28; 6(8):6922-9
and Lee et al., Nat Nanotechnol. 2012 Jun. 3; 7(6):389-93.
[0230] US patent application 20110293703 relates to lipidoid
compounds are also particularly useful in the administration of
polynucleotides, which may be applied to deliver the CRISPR Cas
system of the present invention. In one aspect, the aminoalcohol
lipidoid compounds are combined with an agent to be delivered to a
cell or a subject to form microparticles, nanoparticles, liposomes,
or micelles. The agent to be delivered by the particles, liposomes,
or micelles may be in the form of a gas, liquid, or solid, and the
agent may be a polynucleotide, protein, peptide, or small molecule.
The minoalcohol lipidoid compounds may be combined with other
aminoalcohol lipidoid compounds, polymers (synthetic or natural),
surfactants, cholesterol, carbohydrates, proteins, lipids, etc. to
form the particles. These particles may then optionally be combined
with a pharmaceutical excipient to form a pharmaceutical
composition.
[0231] US Patent Publication No. 0110293703 also provides methods
of preparing the aminoalcohol lipidoid compounds. One or more
equivalents of an amine are allowed to react with one or more
equivalents of an epoxide-terminated compound under suitable
conditions to form an aminoalcohol lipidoid compound of the present
invention. In certain embodiments, all the amino groups of the
amine are fully reacted with the epoxide-terminated compound to
form tertiary amines. In other embodiments, all the amino groups of
the amine are not fully reacted with the epoxide-terminated
compound to form tertiary amines thereby resulting in primary or
secondary amines in the aminoalcohol lipidoid compound. These
primary or secondary amines are left as is or may be reacted with
another electrophile such as a different epoxide-terminated
compound. As will be appreciated by one skilled in the art,
reacting an amine with less than excess of epoxide-terminated
compound will result in a plurality of different aminoalcohol
lipidoid compounds with various numbers of tails. Certain amines
may be fully functionalized with two epoxide-derived compound tails
while other molecules will not be completely functionalized with
epoxide-derived compound tails. For example, a diamine or polyamine
may include one, two, three, or four epoxide-derived compound tails
off the various amino moieties of the molecule resulting in
primary, secondary, and tertiary amines. In certain embodiments,
all the amino groups are not fully functionalized. In certain
embodiments, two of the same types of epoxide-terminated compounds
are used. In other embodiments, two or more different
epoxide-terminated compounds are used. The synthesis of the
aminoalcohol lipidoid compounds is performed with or without
solvent, and the synthesis may be performed at higher temperatures
ranging from 30.-100 C., preferably at approximately 50.-90 C. The
prepared aminoalcohol lipidoid compounds may be optionally
purified. For example, the mixture of aminoalcohol lipidoid
compounds may be purified to yield an aminoalcohol lipidoid
compound with a particular number of epoxide-derived compound
tails. Or the mixture may be purified to yield a particular stereo-
or regioisomer. The aminoalcohol lipidoid compounds may also be
alkylated using an alkyl halide (e.g., methyl iodide) or other
alkylating agent, and/or they may be acylated.
[0232] US Patent Publication No. 0110293703 also provides libraries
of aminoalcohol lipidoid compounds prepared by the inventive
methods. These aminoalcohol lipidoid compounds may be prepared
and/or screened using high-throughput techniques involving liquid
handlers, robots, microtiter plates, computers, etc. In certain
embodiments, the aminoalcohol lipidoid compounds are screened for
their ability to transfect polynucleotides or other agents (e.g.,
proteins, peptides, small molecules) into the cell.
[0233] US Patent Publication No. 20130302401 relates to a class of
poly(beta-amino alcohols) (PBAAs) has been prepared using
combinatorial polymerization. The inventive PBAAs may be used in
biotechnology and biomedical applications as coatings (such as
coatings of films or multilayer films for medical devices or
implants), additives, materials, excipients, non-biofouling agents,
micropatterning agents, and cellular encapsulation agents. When
used as surface coatings, these PBAAs elicited different levels of
inflammation, both in vitro and in vivo, depending on their
chemical structures. The large chemical diversity of this class of
materials allowed us to identify polymer coatings that inhibit
macrophage activation in vitro. Furthermore, these coatings reduce
the recruitment of inflammatory cells, and reduce fibrosis,
following the subcutaneous implantation of carboxylated polystyrene
microparticles. These polymers may be used to form polyelectrolyte
complex capsules for cell encapsulation. The invention may also
have many other biological applications such as antimicrobial
coatings, DNA or siRNA delivery, and stem cell tissue engineering.
The teachings of US Patent Publication No. 20130302401 may be
applied to the CRISPR Cas system of the present invention.
[0234] In another embodiment, lipid nanoparticles (LNPs) are
contemplated. In particular, an antitransthyretin small interfering
RNA encapsulated in lipid nanoparticles (see, e.g., Coelho et al.,
N Engl J Med 2013; 369:819-29) may be applied to the CRISPR Cas
system of the present invention. Doses of about 0.01 to about 1 mg
per kg of body weight administered intravenously are contemplated.
Medications to reduce the risk of infusion-related reactions are
contemplated, such as dexamethasone, acetampinophen,
diphenhydramine or cetirizine, and ranitidine are contemplated.
Multiple doses of about 0.3 mg per kilogram every 4 weeks for five
doses are also contemplated.
[0235] LNPs have been shown to be highly effective in delivering
siRNAs to the liver (see, e.g., Tabernero et al., Cancer Discovery,
April 2013, Vol. 3, No. 4, pages 363-470) and are therefore
contemplated for delivering CRISPR Cas to the liver. A dosage of
about four doses of 6 mg/kg of the LNP every two weeks may be
contemplated. Tabernero et al. demonstrated that tumor regression
was observed after the first 2 cycles of LNPs dosed at 0.7 mg/kg,
and by the end of 6 cycles the patient had achieved a partial
response with complete regression of the lymph node metastasis and
substantial shrinkage of the liver tumors. A complete response was
obtained after 40 doses in this patient, who has remained in
remission and completed treatment after receiving doses over 26
months. Two patients with RCC and extrahepatic sites of disease
including kidney, lung, and lymph nodes that were progressing
following prior therapy with VEGF pathway inhibitors had stable
disease at all sites for approximately 8 to 12 months, and a
patient with PNET and liver metastases continued on the extension
study for 18 months (36 doses) with stable disease.
[0236] However, the charge of the LNP must be taken into
consideration. As cationic lipids combined with negatively charged
lipids to induce nonbilayer structures that facilitate
intracellular delivery. Because charged LNPs are rapidly cleared
from circulation following intravenous injection, ionizable
cationic lipids with pKa values below 7 were developed (see, e.g.,
Rosin et al, Molecular Therapy, vol. 19, no. 12, pages 1286-2200,
December 2011). Negatively charged polymers such as siRNA
oligonucleotides may be loaded into LNPs at low pH values (e.g., pH
4) where the ionizable lipids display a positive charge. However,
at physiological pH values, the LNPs exhibit a low surface charge
compatible with longer circulation times. Four species of ionizable
cationic lipids have been focused upon, namely
1,2-dilineoyl-3-dimethylammonium-propane (DLinDAP),
1,2-dilinoleyloxy-3-N,N-dimethylaminopropane (DLinDMA),
1,2-dilinoleyloxy-keto-N,N-dimethyl-3-aminopropane (DLinKDMA), and
1,2-dilinoleyl-4-(2-dimethylaminoethyl)-[1,3]-dioxolane
(DLinKC2-DMA). It has been shown that LNP siRNA systems containing
these lipids exhibit remarkably different gene silencing properties
in hepatocytes in vivo, with potencies varying according to the
series DLinKC2-DMA>DLinKDMA>DLinDMA>>DLinDAP employing
a Factor VII gene silencing model (see, e.g., Rosin et al,
Molecular Therapy, vol. 19, no. 12, pages 1286-2200, December
2011). A dosage of 1 .mu.g/ml levels may be contemplated,
especially for a formulation containing DLinKC2-DMA.
[0237] Preparation of LNPs and CRISPR Cas encapsulation may be
used/and or adapted from Rosin et al, Molecular Therapy, vol. 19,
no. 12, pages 1286-2200, December 2011). The cationic lipids
1,2-dilineoyl-3-dimethylammonium-propane (DLinDAP),
1,2-dilinoleyloxy-3-N,N-dimethylaminopropane (DLinDMA),
1,2-dilinoleyloxyketo-N,N-dimethyl-3-aminopropane (DLinK-DMA),
1,2-dilinoleyl-4-(2-dimethylaminoethyl)-[1,3]-dioxolane
(DLinKC2-DMA), (3-o-[2''-(methoxypolyethyleneglycol 2000)
succinoyl]-1,2-dimyristoyl-sn-glycol (PEG-S-DMG), and
R-3-[(.omega.-methoxy-poly(ethylene glycol)2000)
carbamoyl]-1,2-dimyristyloxlpropyl-3-amine (PEG-C-DOMG) may be
provided by Tekmira Pharmaceuticals (Vancouver, Canada) or
synthesized. Cholesterol may be purchased from Sigma (St Louis,
Mo.). The specific CRISPR Cas RNA may be encapsulated in LNPs
containing DLinDAP, DLinDMA, DLinK-DMA, and DLinKC2-DMA (cationic
lipid: DSPC:CHOL:PEGS-DMG or PEG-C-DOMG at 40:10:40:10 molar
ratios). When required, 0.2% SP-DiOC18 (Invitrogen, Burlington,
Canada) may be incorporated to assess cellular uptake,
intracellular delivery, and biodistribution. Encapsulation may be
performed by dissolving lipid mixtures comprised of cationic lipid:
DSPC:cholesterol:PEG-c-DOMG (40:10:40:10 molar ratio) in ethanol to
a final lipid concentration of 10 mmol/l. This ethanol solution of
lipid may be added drop-wise to 50 mmol/l citrate, pH 4.0 to form
multilamellar vesicles to produce a final concentration of 30%
ethanol vol/vol. Large unilamellar vesicles may be formed following
extrusion of multilamellar vesicles through two stacked 80 nm
Nuclepore polycarbonate filters using the Extruder (Northern
Lipids, Vancouver, Canada). Encapsulation may be achieved by adding
RNA dissolved at 2 mg/ml in 50 mmol/l citrate, pH 4.0 containing
30% ethanol vol/vol drop-wise to extruded preformed large
unilamellar vesicles and incubation at 31.degree. C. for 30 minutes
with constant mixing to a final RNA/lipid weight ratio of 0.06/1
wt/wt. Removal of ethanol and neutralization of formulation buffer
were performed by dialysis against phosphate-buffered saline (PBS),
pH 7.4 for 16 hours using Spectra/Por 2 regenerated cellulose
dialysis membranes. Nanoparticle size distribution may be
determined by dynamic light scattering using a NICOMP 370 particle
sizer, the vesicle/intensity modes, and Gaussian fitting (Nicomp
Particle Sizing, Santa Barbara, Calif.). The particle size for all
three LNP systems may be .about.70 nm in diameter. siRNA
encapsulation efficiency may be determined by removal of free siRNA
using VivaPureD MiniH columns (Sartorius Stedim Biotech) from
samples collected before and after dialysis. The encapsulated RNA
may be extracted from the eluted nanoparticles and quantified at
260 nm. siRNA to lipid ratio was determined by measurement of
cholesterol content in vesicles using the Cholesterol E enzymatic
assay from Wako Chemicals USA (Richmond, Va.).
[0238] Preparation of large LNPs may be used/and or adapted from
Rosin et al, Molecular Therapy, vol. 19, no. 12, pages 1286-2200,
December 2011. A lipid premix solution (20.4 mg/ml total lipid
concentration) may be prepared in ethanol containing DLinKC2-DMA,
DSPC, and cholesterol at 50:10:38.5 molar ratios. Sodium acetate
may be added to the lipid premix at a molar ratio of 0.75:1 (sodium
acetate: DLinKC2-DMA). The lipids may be subsequently hydrated by
combining the mixture with 1.85 volumes of citrate buffer (10
mmol/l, pH 3.0) with vigorous stirring, resulting in spontaneous
liposome formation in aqueous buffer containing 35% ethanol. The
liposome solution may be incubated at 37.degree. C. to allow for
time-dependent increase in particle size. Aliquots may be removed
at various times during incubation to investigate changes in
liposome size by dynamic light scattering (Zetasizer Nano ZS,
Malvern Instruments, Worcestershire, UK). Once the desired particle
size is achieved, an aqueous PEG lipid solution (stock=10 mg/ml
PEG-DMG in 35% (vol/vol) ethanol) may be added to the liposome
mixture to yield a final PEG molar concentration of 3.5% of total
lipid. Upon addition of PEG-lipids, the liposomes should their
size, effectively quenching further growth. RNA may then be added
to the empty liposomes at an siRNA to total lipid ratio of
approximately 1:10 (wt:wt), followed by incubation for 30 minutes
at 37.degree. C. to form loaded LNPs. The mixture may be
subsequently dialyzed overnight in PBS and filtered with a
0.45-.mu.m syringe filter.
[0239] Spherical Nucleic Acid (SNA.TM.) constructs and other
nanoparticles (particularly gold nanoparticles) are also
contemplate as a means to delivery CRISPR/Cas system to intended
targets. Significant data show that AuraSense Therapeutics'
Spherical Nucleic Acid (SNA.TM.) constructs, based upon nucleic
acid-functionalized gold nanoparticles, are superior to alternative
platforms based on multiple key success factors, such as:
[0240] High in vivo stability. Due to their dense loading, a
majority of cargo (DNA or siRNA) remains bound to the constructs
inside cells, conferring nucleic acid stability and resistance to
enzymatic degradation.
[0241] Deliverability. For all cell types studied (e.g., neurons,
tumor cell lines, etc.) the constructs demonstrate a transfection
efficiency of 99% with no need for carriers or transfection
agents.
[0242] Therapeutic targeting. The unique target binding affinity
and specificity of the constructs allow exquisite specificity for
matched target sequences (i.e., limited off-target effects).
[0243] Superior efficacy. The constructs significantly outperform
leading conventional transfection reagents (Lipofectamine 2000 and
Cytofectin).
[0244] Low toxicity. The constructs can enter a variety of cultured
cells, primary cells, and tissues with no apparent toxicity.
[0245] No significant immune response. The constructs elicit
minimal changes in global gene expression as measured by
whole-genome microarray studies and cytokine-specific protein
assays.
[0246] Chemical tailorability. Any number of single or
combinatorial agents (e.g., proteins, peptides, small molecules)
can be used to tailor the surface of the constructs.
[0247] This platform for nucleic acid-based therapeutics may be
applicable to numerous disease states, including inflammation and
infectious disease, cancer, skin disorders and cardiovascular
disease.
[0248] Citable literature includes: Cutler et al., J. Am. Chem.
Soc. 2011 133:9254-9257, Hao et al., Small. 2011 7:3158-3162, Zhang
et al., ACS Nano. 2011 5:6962-6970, Cutler et al., J. Am. Chem.
Soc. 2012 134:1376-1391, Young et al., Nano Lett. 2012 12:3867-71,
Zheng et al., Proc. Natl. Acad. Sci. USA. 2012 109:11975-80,
Mirkin, Nanomedicine 2012 7:635-638 Zhang et al., J. Am. Chem. Soc.
2012 134:16488-1691, Weintraub, Nature 2013 495: S14-S16, Choi et
al., Proc. Natl. Acad. Sci. USA. 2013 110(19):7625-7630, Jensen et
al., Sci. Transl. Med. 5, 209ra152 (2013) and Mirkin, et al.,
Small, doi.org/10.1002/smll.201302143.
[0249] Self-assembling nanoparticles with siRNA may be constructed
with polyethyleneimine (PEI) that is PEGylated with an Arg-Gly-Asp
(RGD) peptide ligand attached at the distal end of the polyethylene
glycol (PEG), for example, as a means to target tumor
neovasculature expressing integrins and used to deliver siRNA
inhibiting vascular endothelial growth factor receptor-2 (VEGF R2)
expression and thereby tumor angiogenesis (see, e.g., Schiffelers
et al., Nucleic Acids Research, 2004, Vol. 32, No. 19). Nanoplexes
may be prepared by mixing equal volumes of aqueous solutions of
cationic polymer and nucleic acid to give a net molar excess of
ionizable nitrogen (polymer) to phosphate (nucleic acid) over the
range of 2 to 6. The electrostatic interactions between cationic
polymers and nucleic acid resulted in the formation of polyplexes
with average particle size distribution of about 100 nm, hence
referred to here as nanoplexes. A dosage of about 100 to 200 mg of
CRISPR Cas is envisioned for delivery in the self-assembling
nanoparticles of Schiffelers et al.
[0250] The nanoplexes of Bartlett et al. (PNAS, Sep. 25, 2007, vol.
104, no. 39) may also be applied to the present invention. The
nanoplexes of Bartlett et al. are prepared by mixing equal volumes
of aqueous solutions of cationic polymer and nucleic acid to give a
net molar excess of ionizable nitrogen (polymer) to phosphate
(nucleic acid) over the range of 2 to 6. The electrostatic
interactions between cationic polymers and nucleic acid resulted in
the formation of polyplexes with average particle size distribution
of about 100 nm, hence referred to here as nanoplexes. The
DOTA-siRNA of Bartlett et al. was synthesized as follows:
1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid
mono(N-hydroxysuccinimide ester) (DOTA-NHSester) was ordered from
Macrocyclics (Dallas, Tex.). The amine modified RNA sense strand
with a 100-fold molar excess of DOTA-NHS-ester in carbonate buffer
(pH 9) was added to a microcentrifuge tube. The contents were
reacted by stirring for 4 h at room temperature. The DOTA-RNAsense
conjugate was ethanol-precipitated, resuspended in water, and
annealed to the unmodified antisense strand to yield DOTA-siRNA.
All liquids were pretreated with Chelex-100 (Bio-Rad, Hercules,
Calif.) to remove trace metal contaminants. Tf-targeted and
nontargeted siRNA nanoparticles may be formed by using
cyclodextrin-containing polycations. Typically, nanoparticles were
formed in water at a charge ratio of 3 (+/-) and an siRNA
concentration of 0.5 g/liter. One percent of the adamantane-PEG
molecules on the surface of the targeted nanoparticles were
modified with Tf (adamantane-PEG-Tf). The nanoparticles were
suspended in a 5% (wt/vol) glucose carrier solution for
injection.
[0251] Davis et al. (Nature, Vol 464, 15 Apr. 2010) conducts a
siRNA clinical trial that uses a targeted nanoparticle-delivery
system (clinical trial registration number NCT00689065). Patients
with solid cancers refractory to standard-of-care therapies are
administered doses of targeted nanoparticles on days 1, 3, 8 and 10
of a 21-day cycle by a 30-min intravenous infusion. The
nanoparticles consist of a synthetic delivery system containing:
(1) a linear, cyclodextrin-based polymer (CDP), (2) a human
transferrin protein (TF) targeting ligand displayed on the exterior
of the nanoparticle to engage TF receptors (TFR) on the surface of
the cancer cells, (3) a hydrophilic polymer (polyethylene glycol
(PEG) used to promote nanoparticle stability in biological fluids),
and (4) siRNA designed to reduce the expression of the RRM2
(sequence used in the clinic was previously denoted siR2B+5). The
TFR has long been known to be upregulated in malignant cells, and
RRM2 is an established anti-cancer target. These nanoparticles
(clinical version denoted as CALAA-01) have been shown to be well
tolerated in multi-dosing studies in non-human primates. Although a
single patient with chronic myeloid leukaemia has been administered
siRNAby liposomal delivery, Davis et al.'s clinical trial is the
initial human trial to systemically deliver siRNA with a targeted
delivery system and to treat patients with solid cancer. To
ascertain whether the targeted delivery system can provide
effective delivery of functional siRNA to human tumours, Davis et
al. investigated biopsies from three patients from three different
dosing cohorts; patients A, B and C, all of whom had metastatic
melanoma and received CALAA-01 doses of 18, 24 and 30 mg m.sup.-2
siRNA, respectively. Similar doses may also be contemplated for the
CRISPR Cas system of the present invention. The delivery of the
invention may be achieved with nanoparticles containing a linear,
cyclodextrin-based polymer (CDP), a human transferrin protein (TF)
targeting ligand displayed on the exterior of the nanoparticle to
engage TF receptors (TFR) on the surface of the cancer cells and/or
a hydrophilic polymer (for example, polyethylene glycol (PEG) used
to promote nanoparticle stability in biological fluids).
[0252] Exosomes
[0253] Exosomes are endogenous nano-vesicles that transport RNAs
and proteins which can deliver short interfering (si)RNA to the
brain in mice. To reduce immunogenicity, Alvarez-Erviti et al.
(2011, Nat Biotechnol 29: 341) used self-derived dendritic cells
for exosome production. Targeting was achieved by engineering the
dendritic cells to express Lamp2b, an exosomal membrane protein,
fused to the neuron-specific RVG peptide3. Purified exosomes were
loaded with exogenous siRNA by electroporation. Intravenously
injected RVG-targeted exosomes delivered GAPDH siRNA specifically
to neurons, microglia, oligodendrocytes in the brain, resulting in
a specific gene knockdown. Pre-exposure to RVG exosomes did not
attenuate knockdown, and non-specific uptake in other tissues was
not observed. The therapeutic potential of exosome-mediated siRNA
delivery was demonstrated by the strong mRNA (60%) and protein
(62%) knockdown of BACE1, a therapeutic target in Alzheimer's
disease.
[0254] To obtain a pool of immunologically inert exosomes,
Alvarez-Erviti et al. harvested bone marrow from inbred C57BL/6
mice with a homogenous major histocompatibility complex (MHC)
haplotype. As immature dendritic cells produce large quantities of
exosomes devoid of T-cell activators such as MHC-II and CD86,
Alvarez-Erviti et al. selected for dendritic cells with
granulocyte/macrophage-colony stimulating factor (GM-CSF) for 7 d.
Exosomes were purified from the culture supernatant the following
day using well-established ultracentrifugation protocols. The
exosomes produced were physically homogenous, with a size
distribution peaking at 80 nm in diameter as determined by
nanoparticle tracking analysis (NTA) and electron microscopy.
Alvarez-Erviti et al. obtained 6-12 .mu.g of exosomes (measured
based on protein concentration) per 10.sup.6 cells.
[0255] Next, Alvarez-Erviti et al. investigated the possibility of
loading modified exosomes with exogenous cargoes using
electroporation protocols adapted for nanoscale applications. As
electroporation for membrane particles at the nanometer scale is
not well-characterized, nonspecific Cy5-labeled siRNA was used for
the empirical optimization of the electroporation protocol. The
amount of encapsulated siRNA was assayed after ultracentrifugation
and lysis of exosomes. Electroporation at 400 V and 125 .mu.F
resulted in the greatest retention of siRNA and was used for all
subsequent experiments.
[0256] Alvarez-Erviti et al. administered 150 .mu.g of each BACE1
siRNA encapsulated in 150 .mu.g of RVG exosomes to normal C57BL/6
mice and compared the knockdown efficiency to four controls:
untreated mice, mice injected with RVG exosomes only, mice injected
with BACE1 siRNA complexed to an in vivo cationic liposome reagent
and mice injected with BACE1 siRNA complexed to RVG-9R, the RVG pep
tide conjugated to 9 D-arginines that electrostatically binds to
the siRNA. Cortical tissue samples were analyzed 3 d after
administration and a significant protein knockdown (45%, P<0.05,
versus 62%, P<0.01) in both siRNA-RVG-9R-treated and siRNARVG
exosome-treated mice was observed, resulting from a significant
decrease in BACE1 mRNA levels (66% [+ or -] 15%, P<0.001 and 61%
[+ or -] 13% respectively, P<0.01). Moreover, Applicants
demonstrated a significant decrease (55%, P<0.05) in the total
[beta]-amyloid 1-42 levels, a main component of the amyloid plaques
in Alzheimer's pathology, in the RVG-exosome-treated animals. The
decrease observed was greater than the .beta.-amyloid 1-40 decrease
demonstrated in normal mice after intraventricular injection of
BACE1 inhibitors. Alvarez-Erviti et al. carried out 5'-rapid
amplification of cDNA ends (RACE) on BACE1 cleavage product, which
provided evidence of RNAi-mediated knockdown by the siRNA.
[0257] Finally, Alvarez-Erviti et al. investigated whether
siRNA-RVG exosomes induced immune responses in vivo by assessing
IL-6, IP-10, TNF.alpha. and IFN-.alpha. serum concentrations.
Following siRNA-RVG exosome treatment, nonsignificant changes in
all cytokines were registered similar to siRNA-transfection reagent
treatment in contrast to siRNA-RVG-9R, which potently stimulated
IL-6 secretion, confirming the immunologically inert profile of the
exosome treatment. Given that exosomes encapsulate only 20% of
siRNA, delivery with RVG-exosome appears to be more efficient than
RVG-9R delivery as comparable mRNA knockdown and greater protein
knockdown was achieved with fivefold less siRNA without the
corresponding level of immune stimulation. This experiment
demonstrated the therapeutic potential of RVG-exosome technology,
which is potentially suited for long-term silencing of genes
related to neurodegenerative diseases. The exosome delivery system
of Alvarez-Erviti et al. may be applied to deliver the CRISPR-Cas
system of the present invention to therapeutic targets, especially
neurodegenerative diseases. A dosage of about 100 to 1000 mg of
CRISPR Cas encapsulated in about 100 to 1000 mg of RVG exosomes may
be contemplated for the present invention.
[0258] E1-Andaloussi et al. (Nature Protocols 7,2112-2126(2012))
discloses how exosomes derived from cultured cells can be harnessed
for delivery of siRNA in vitro and in vivo. This protocol first
describes the generation of targeted exosomes through transfection
of an expression vector, comprising an exosomal protein fused with
a peptide ligand. Next, E1-Andaloussi et al. explain how to purify
and characterize exosomes from transfected cell supernatant. Next,
E1-Andaloussi et al. detail crucial steps for loading siRNA into
exosomes. Finally, E1-Andaloussi et al. outline how to use exosomes
to efficiently deliver siRNA in vitro and in vivo in mouse brain.
Examples of anticipated results in which exosome-mediated siRNA
delivery is evaluated by functional assays and imaging are also
provided. The entire protocol takes .about.3 weeks. Delivery or
administration according to the invention may be performed using
exosomes produced from self-derived dendritic cells.
[0259] In another embodiment, the plasma exosomes of Wahlgren et
al. (Nucleic Acids Research, 2012, Vol. 40, No. 17 e130) are
contemplated. Exosomes are nano-sized vesicles (30-90 nm in size)
produced by many cell types, including dendritic cells (DC), B
cells, T cells, mast cells, epithelial cells and tumor cells. These
vesicles are formed by inward budding of late endosomes and are
then released to the extracellular environment upon fusion with the
plasma membrane. Because exosomes naturally carry RNA between
cells, this property might be useful in gene therapy.
[0260] Exosomes from plasma are prepared by centrifugation of buffy
coat at 900 g for 20 min to isolate the plasma followed by
harvesting cell supernatants, centrifuging at 300 g for 10 min to
eliminate cells and at 16 500 g for 30 min followed by filtration
through a 0.22 mm filter. Exosomes are pelleted by
ultracentrifugation at 120 000 g for 70 min. Chemical transfection
of siRNA into exosomes is carried out according to the
manufacturer's instructions in RNAi Human/Mouse Starter Kit
(Quiagen, Hilden, Germany). siRNA is added to 100 ml PBS at a final
concentration of 2 mmol/ml. After adding HiPerFect transfection
reagent, the mixture is incubated for 10 min at RT. In order to
remove the excess of micelles, the exosomes are re-isolated using
aldehyde/sulfate latex beads. The chemical transfection of CRISPR
Cas into exosomes may be conducted similarly to siRNA. The exosomes
may be co-cultured with monocytes and lymphocytes isolated from the
peripheral blood of healthy donors. Therefore, it may be
contemplated that exosomes containing CRISPR Cas may be introduced
to monocytes and lymphocytes of and autologously reintroduced into
a human. Accordingly, delivery or administration according to the
invention may beperformed using plasma exosomes.
[0261] Liposomes
[0262] Delivery or administration according to the invention can be
performed with liposomes. Liposomes are spherical vesicle
structures composed of a uni- or multilamellar lipid bilayer
surrounding internal aqueous compartments and a relatively
impermeable outer lipophilic phospholipid bilayer. Liposomes have
gained considerable attention as drug delivery carriers because
they are biocompatible, nontoxic, can deliver both hydrophilic and
lipophilic drug molecules, protect their cargo from degradation by
plasma enzymes, and transport their load across biological
membranes and the blood brain barrier (BBB) (see, e.g., Spuch and
Navarro, Journal of Drug Delivery, vol. 2011, Article ID 469679, 12
pages, 2011. doi:10. 1155/2011/469679 for review).
[0263] Liposomes can be made from several different types of
lipids; however, phospholipids are most commonly used to generate
liposomes as drug carriers. Although liposome formation is
spontaneous when a lipid film is mixed with an aqueous solution, it
can also be expedited by applying force in the form of shaking by
using a homogenizer, sonicator, or an extrusion apparatus (see,
e.g., Spuch and Navarro, Journal of Drug Delivery, vol. 2011,
Article ID 469679, 12 pages, 2011. doi: 10.1155/2011/469679 for
review).
[0264] Several other additives may be added to liposomes in order
to modify their structure and properties. For instance, either
cholesterol or sphingomyelin may be added to the liposomal mixture
in order to help stabilize the liposomal structure and to prevent
the leakage of the liposomal inner cargo. Further, liposomes are
prepared from hydrogenated egg phosphatidylcholine or egg
phosphatidylcholine, cholesterol, and dicetyl phosphate, and their
mean vesicle sizes were adjusted to about 50 and 100 nm. (see,
e.g., Spuch and Navarro, Journal of Drug Delivery, vol. 2011,
Article ID 469679, 12 pages, 2011. doi:10.1155/2011/469679 for
review).
[0265] Conventional liposome formulation is mainly comprised of
natural phospholipids and lipids such as
1,2-distearoryl-sn-glycero-3-phosphatidyl choline (DSPC),
sphingomyelin, egg phosphatidylcholines and monosialoganglioside.
Since this formulation is made up of phospholipids only, liposomal
formulations have encountered many challenges, one of the ones
being the instability in plasma. Several attempts to overcome these
challenges have been made, specifically in the manipulation of the
lipid membrane. One of these attempts focused on the manipulation
of cholesterol. Addition of cholesterol to conventional
formulations reduces rapid release of the encapsulated bioactive
compound into the plasma or
1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE) increases the
stability (see, e.g., Spuch and Navarro, Journal of Drug Delivery,
vol. 2011, Article ID 469679, 12 pages, 2011.
doi:10.1155/2011/469679 for review).
[0266] In a particularly advantageous embodiment, Trojan Horse
liposomes (also known as Molecular Trojan Horses) are desirable and
protocols may be found at http://cshprotocols
cshlp.orgicontent/2010/4/pdb protS407 long. These particles allow
delivery of a transgene to the entire brain after an intravascular
injection. Without being bound by limitation, it is believed that
neutral lipid particles with specific antibodies conjugated to
surface allow crossing of the blood brain barrier via endocytosis.
Applicant postulates utilizing Trojan Horse Liposomes to deliver
the CRISPR family of nucleases to the brain via an intravascular
injection, which would allow whole brain transgenic animals without
the need for embryonic manipulation. About 1-5 g of DNA may be
contemplated for in vivo administration in liposomes.
[0267] In another embodiment, the CRISPR Cas system may be
administered in liposomes, such as a stable nucleic-acid-lipid
particle (SNALP) (see, e.g., Morrissey et al., Nature
Biotechnology, Vol. 23, No. 8, August 2005). Daily intravenous
injections of about 1, 3 or 5 mg/kg/day of a specific CRISPR Cas
targeted in a SNALP are contemplated. The daily treatment may be
over about three days and then weekly for about five weeks. In
another embodiment, a specific CRISPR Cas encapsulated SNALP)
administered by intravenous injection to at doses of abpit 1 or 2.5
mg/kg are also contemplated (see, e.g., Zimmerman et al., Nature
Letters, Vol. 441, 4 May 2006). The SNALP formulation may contain
the lipids 3-N-[(wmethoxypoly(ethylene glycol) 2000)
carbamoyl]-!,2-dimyristyloxy-propylamine (PEG-C-DMA),
1,2-dilinoleyloxy-N,N-dimethyl-3-aminopropane (DLinDMA),
1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC) and cholesterol,
in a 2:40:10:48 molar percent ratio (see, e.g., Zimmerman et al.,
Nature Letters, Vol. 441, 4 May 2006).
[0268] In another embodiment, stable nucleic-acid-lipid particles
(SNALPs) have proven to be effective delivery molecules to highly
vascularized HepG2-derived liver tumors but not in poorly
vascularized HCT-116 derived liver tumors (see, e.g., Li, Gene
Therapy (2012) 19, 775-780). The SNALP liposomes may be prepared by
formulating D-Lin-DMA and PEG-C-DMA with
distearoylphosphatidylcholine (DSPC), Cholesterol and siRNA using a
25:1 lipid/siRNA ratio and a 48/40/10/2 molar ratio of
Cholesterol/D-Lin-DMA/DSPC/PEG-C-DMA. The resulted SNALP liposomes
are about 80-100 nm in size.
[0269] In yet another embodiment, a SNALP may comprise synthetic
cholesterol (Sigma-Aldrich, St Louis, Mo., USA),
dipalmitoylphosphatidylcholine (Avanti Polar Lipids, Alabaster,
Ala., USA), 3-N-[(w-methoxy poly(ethylene
glycol)2000)carbamoyl]-1,2-dimyrestyloxypropylamine, and cationic
1,2-dilinoleyloxy-3-N,Ndimethylaminopropane (see, e.g., Geisbert et
al., Lancet 2010; 375: 1896-905). A dosage of about 2 mg/kg total
CRISPR Cas per dose administered as, for example, a bolus
intravenous infusion may be contemplated.
[0270] In yet another embodiment, a SNALP may comprise synthetic
cholesterol (Sigma-Aldrich),
1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC; Avanti Polar
Lipids Inc.), PEG-cDMA, and
1,2-dilinoleyloxy-3-(N;N-dimethyl)aminopropane (DLinDMA) (see,
e.g., Judge, J. Clin. Invest. 119:661-673 (2009)). Formulations
used for in vivo studies may comprise a final lipid/RNA mass ratio
of about 9:1.
[0271] The safety profile of RNAi nanomedicines has been reviewed
by Barros and Gollob of Alnylam Pharmaceuticals (see, e.g.,
Advanced Drug Delivery Reviews 64 (2012) 1730-1737). The stable
nucleic acid lipid particle (SNALP) is comprised of four different
lipids--an ionizable lipid (DLinDMA) that is cationic at low pH, a
neutral helper lipid, cholesterol, and a diffusible polyethylene
glycol (PEG)-lipid. The particle is approximately 80 nm in diameter
and is charge-neutral at physiologic pH. During formulation, the
ionizable lipid serves to condense lipid with the anionic siRNA
during particle formation. When positively charged under
increasingly acidic endosomal conditions, the ionizable lipid also
mediates the fusion of SNALP with the endosomal membrane enabling
release of siRNA into the cytoplasm. The PEG-lipid stabilizes the
particle and reduces aggregation during formulation, and
subsequently provides a neutral hydrophilic exterior that improves
pharmacokinetic properties.
[0272] To date, two clinical programs have been initiated using
SNALPsiRNA formulations. Tekmira Pharmaceuticals recently completed
a phase I single-dose study of SNALP-ApoB in adult volunteers with
elevated LDL cholesterol. ApoB is predominantly expressed in the
liver and jejunum and is essential for the assembly and secretion
of VLDL and LDL. Seventeen subjects received a single dose of
SNALP-ApoB (dose escalation across 7 dose levels). There was no
evidence of liver toxicity (anticipated as the potential
dose-limiting toxicity based on preclinical studies). One (of two)
subjects at the highest dose experienced flu-like symptoms
consistent with immune system stimulation, and the decision was
made to conclude the trial.
[0273] Alnylam Pharmaceuticals has similarly advanced ALN-TTR01,
which employs the SNALP technology described above and targets
hepatocyte production of both mutant and wild-type TTR to treat TTR
amyloidosis (ATTR). Three ATTR syndromes have been described:
familial amyloidotic polyneuropathy (FAP) and familial amyloidotic
cardiomyopathy (FAC)--both caused by autosomal dominant mutations
in TTR; and senile systemic amyloidosis (SSA) cause by wildtype
TTR. A placebo-controlled, single dose-escalation phase I trial of
ALN-TTR01 was recently completed in patients with ATTR. ALN-TTR01
was administered as a 15-minute IV infusion to 31 patients (23 with
study drug and 8 with placebo) within a dose range of 0.01 to 1.0
mg/kg (based on siRNA). Treatmentwaswell tolerated with no
significant increases in liver function tests. Infusion-related
reactions were noted in 3 of 23 patients at .gtoreq.0.4 mg/kg; all
responded to slowing of the infusion rate and all continued on
study. Minimal and transient elevations of serum cytokines IL-6,
IP-10 and IL-1ra were noted in two patients at the highest dose of
1 mg/kg (as anticipated from preclinical and NHP studies). Lowering
of serum TTR, the expected pharmacodynamics effect of ALN-TTR01,
was observed at 1 mg/kg.
[0274] In yet another embodiment, a SNALP may be made by
solubilizing a cationic lipid, DSPC, cholesterol and PEG-lipid were
solubilized in ethanol at a molar ratio of 40:10:40:10,
respectively (see, Semple et al., Nature Niotechnology, Volume 28
Number 2 Feb. 2010, pp. 172-177). The lipid mixture was added to an
aqueous buffer (50 mM citrate, pH 4) with mixing to a final ethanol
and lipid concentration of 30% (vol/vol) and 6.1 mg/ml,
respectively, and allowed to equilibrate at 22.degree. C. for 2 min
before extrusion. The hydrated lipids were extruded through two
stacked 80 nm pore-sized filters (Nuclepore) at 22.degree. C. using
a Lipex Extruder (Northern Lipids) until a vesicle diameter of
70-90 nm, as determined by dynamic light scattering analysis, was
obtained. This generally required 1-3 passes. The siRNA
(solubilized in a 50 mM citrate, pH 4 aqueous solution containing
30% ethanol) was added to the pre-equilibrated (35.degree. C.)
vesicles at a rate of .about.5 ml/min with mixing. After a final
target siRNA/lipid ratio of 0.06 (wt/wt) was reached, the mixture
was incubated for a further 30 min at 35.degree. C. to allow
vesicle reorganization and encapsulation of the siRNA. The ethanol
was then removed and the external buffer replaced with PBS (155 mM
NaCl, 3 mM Na2HPO4, 1 mM KH2PO4, pH 7.5) by either dialysis or
tangential flow diafiltration. siRNA were encapsulated in SNALP
using a controlled step-wise dilution method process. The lipid
constituents of KC2-SNALP were DLin-KC2-DMA (cationic lipid),
dipalmitoylphosphatidylcholine (DPPC; Avanti Polar Lipids),
synthetic cholesterol (Sigma) and PEG-C-DMA used at a molar ratio
of 57.1:7.1:34.3:1.4. Upon formation of the loaded particles, SNALP
were dialyzed against PBS and filter sterilized through a 0.2 .mu.m
filter before use. Mean particle sizes were 75-85 nm and 90-95% of
the siRNA was encapsulated within the lipid particles. The final
siRNA/lipid ratio in formulations used for in vivo testing was
.about.0.15 (wt/wt). LNP-siRNA systems containing Factor VII siRNA
were diluted to the appropriate concentrations in sterile PBS
immediately before use and the formulations were administered
intravenously through the lateral tail vein in a total volume of 10
ml/kg. This method may be extrapolated to the CRISPR Cas system of
the present invention.
[0275] Other Lipids
[0276] Other cationic lipids, such as amino lipid
2,2-dilinoleyl-4-dimethylaminoethyl-[1,3]-dioxolane (DLin-KC2-DMA)
may be utilized to encapsulate CRISPR Cas similar to SiRNA (see,
e.g., Jayaraman, Angew. Chem. Int. Ed. 2012, 51, 8529-8533). A
preformed vesicle with the following lipid composition may be
contemplated: amino lipid, distearoylphosphatidylcholine (DSPC),
cholesterol and (R)-2,3-bis(octadecyloxy) propyl-1-(methoxy
poly(ethylene glycol)2000)propylcarbamate (PEG-lipid) in the molar
ratio 40/10/40/10, respectively, and a FVII siRNA/total lipid ratio
of approximately 0.05 (w/w). To ensure a narrow particle size
distribution in the range of 70-90 nm and a low polydispersity
index of 0.11_0.04 (n=56), the particles may be extruded up to
three times through 80 nm membranes prior to adding the CRISPR Cas
RNA. Particles containing the highly potent amino lipid 16 may be
used, in which the molar ratio of the four lipid components 16,
DSPC, cholesterol and PEG-lipid (50/10/38.5/1.5) which may be
further optimized to enhance in vivo activity.
[0277] Michael S D Kormann et al. ("Expression of therapeutic
proteins after delivery of chemically modified mRNA in mice: Nature
Biotechnology, Volume:29, Pages: 154-157 (2011) Published online 9
Jan. 2011) describes the use of lipid envelopes to deliver RNA. Use
of lipid envelopes is also preferred in the present invention.
[0278] In another embodiment, lipids may be formulated with the
CRISPR Cas system of the present invention to form lipid
nanoparticles (LNPs). Lipids include, but are not limited to,
DLin-KC2-DMA4, C12-200 and colipids disteroylphosphatidyl choline,
cholesterol, and PEG-DMG may be formulated with CRISPR Cas instead
of siRNA (see, e.g., Novobrantseva, Molecular Therapy-Nucleic Acids
(2012) 1, e4: doi: 10.1038/mtna.2011.3) using a spontaneous vesicle
formation procedure. The component molar ratio may be about
50/10/38.5/1.5 (DLin-KC2-DMA or C12-200/disteroylphosphatidyl
choline/cholesterol/PEG-DMG). The final lipid:siRNA weight ratio
may be .about.12:1 and 9:1 in the case of DLin-KC2-DMA and C12-200
lipid nanoparticles (LNPs), respectively. The formulations may have
mean particle diameters of .about.80 nm with >90% entrapment
efficiency. A 3 mg/kg dose may be contemplated.
[0279] Tekmira has a portfolio of approximately 95 patent families,
in the U.S. and abroad, that are directed to various aspects of
LNPs and LNP formulations (see, e.g., U.S. Pat. Nos. 7,982,027;
7,799,565; 8,058,069; 8,283,333; 7,901,708; 7,745,651; 7,803,397;
8,101,741; 8,188,263; 7,915,399; 8,236,943 and 7,838,658 and
European Pat. Nos. 1766035; 1519714; 1781593 and 1664316), all of
which may be used/and or adapted to the present invention.
[0280] The CRISPR Cas system may be delivered encapsulated in PLGA
Microspheres such as that further described in US published
applications 20130252281 and 20130245107 and 20130244279 (assigned
to Moderna Therapeutics) which relate to aspects of formulation of
compositions comprising modified nucleic acid molecules which may
encode a protein, a protein precursor, or a partially or fully
processed form of the protein or a protein precursor. The
formulation may have a molar ratio 50:10:38.5:1.5-3.0 (cationic
lipid:fusogenic lipid:cholesterol:PEG lipid). The PEG lipid may be
selected from, but is not limited to PEG-c-DOMG, PEG-DMG. The
fusogenic lipid may be DSPC. See also, Schrum et al., Delivery and
Formulation of Engineered Nucleic Acids, US published application
20120251618.
[0281] Nanomerics' technology addresses bioavailability challenges
for a broad range of therapeutics, including low molecular weight
hydrophobic drugs, peptides, and nucleic acid based therapeutics
(plasmid, siRNA, miRNA). Specific administration routes for which
the technology has demonstrated clear advantages include the oral
route, transport across the blood-brain-barrier, delivery to solid
tumours, as well as to the eye. See, e.g., Mazza et al., 2013, ACS
Nano. 2013 Feb. 26; 7(2):1016-26; Uchegbu and Siew, 2013, J Pharm
Sci. 102(2):305-10 and Lalatsa et al., 2012, J Control Release.
2012 Jul. 20; 161(2):523-36.
[0282] US Patent Publication No. 20050019923 describes cationic
dendrimers for delivering bioactive molecules, such as
polynucleotide molecules, peptides and polypeptides and/or
pharmaceutical agents, to a mammalian body. The dendrimers are
suitable for targeting the delivery of the bioactive molecules to,
for example, the liver, spleen, lung, kidney or heart. Dendrimers
are synthetic 3-dimensional macromolecules that are prepared in a
step-wise fashion from simple branched monomer units, the nature
and functionality of which can be easily controlled and varied.
Dendrimers are synthesised from the repeated addition of building
blocks to a multifunctional core (divergent approach to synthesis),
or towards a multifunctional core (convergent approach to
synthesis) and each addition of a 3-dimensional shell of building
blocks leads to the formation of a higher generation of the
dendrimers. Polypropylenimine dendrimers start from a diaminobutane
core to which is added twice the number of amino groups by a double
Michael addition of acrylonitrile to the primary amines followed by
the hydrogenation of the nitriles. This results in a doubling of
the amino groups. Polypropylenimine dendrimers contain 100%
protonable nitrogens and up to 64 terminal amino groups (generation
5, DAB 64). Protonable groups are usually amine groups which are
able to accept protons at neutral pH. The use of dendrimers as gene
delivery agents has largely focused on the use of the
polyamidoamine. and phosphorous containing compounds with a mixture
of amine/amide or N--P(O.sub.2)S as the conjugating units
respectively with no work being reported on the use of the lower
generation polypropylenimine dendrimers for gene delivery.
Polypropylenimine dendrimers have also been studied as pH sensitive
controlled release systems for drug delivery and for their
encapsulation of guest molecules when chemically modified by
peripheral amino acid groups. The cytotoxicity and interaction of
polypropylenimine dendrimers with DNA as well as the transfection
efficacy of DAB 64 has also been studied.
[0283] US Patent Publication No. 20050019923 is based upon the
observation that, contrary to earlier reports, cationic dendrimers,
such as polypropylenimine dendrimers, display suitable properties,
such as specific targeting and low toxicity, for use in the
targeted delivery of bioactive molecules, such as genetic material.
In addition, derivatives of the cationic dendrimer also display
suitable properties for the targeted delivery of bioactive
molecules. See also, Bioactive Polymers, US published application
20080267903, which discloses "Various polymers, including cationic
polyamine polymers and dendrimeric polymers, are shown to possess
anti-proliferative activity, and may therefore be useful for
treatment of disorders characterised by undesirable cellular
proliferation such as neoplasms and tumours, inflammatory disorders
(including autoimmune disorders), psoriasis and atherosclerosis.
The polymers may be used alone as active agents, or as delivery
vehicles for other therapeutic agents, such as drug molecules or
nucleic acids for gene therapy. In such cases, the polymers' own
intrinsic anti-tumour activity may complement the activity of the
agent to be delivered."
[0284] Supercharged Proteins
[0285] Supercharged proteins are a class of engineered or naturally
occurring proteins with unusually high positive or negative net
theoretical charge. Both supernegatively and superpositively
charged proteins exhibit a remarkable ability to withstand
thermally or chemically induced aggregation. Superpositively
charged proteins are also able to penetrate mammalian cells.
Associating cargo with these proteins, such as plasmid DNA, siRNA,
or other proteins, can enable the functional delivery of these
macromolecules into mammalian cells both in vitro and in vivo.
David Liu's lab reported the creation and characterization of
supercharged proteins in 2007 (Lawrence et al., 2007, Journal of
the American Chemical Society 129, 10110-10112).
[0286] The nonviral delivery of siRNA and plasmid DNA into
mammalian cells are valuable both for research and therapeutic
applications (Akinc et al., 2010, Nat. Biotech. 26, 561-569).
Purified +36 GFP protein (or other superpositively charged protein)
is mixed with siRNAs in the appropriate serum-free media and
allowed to complex prior addition to cells. Inclusion of serum at
this stage inhibits formation of the supercharged protein-siRNA
complexes and reduces the effectiveness of the treatment. The
following protocol has been found to be effective for a variety of
cell lines (McNaughton et al., 2009, Proc. Natl. Acad. Sci. USA
106, 6111-6116). However, pilot experiments varying the dose of
protein and siRNA should be performed to optimize the procedure for
specific cell lines.
[0287] (1) One day before treatment, plate 1.times.10.sup.5 cells
per well in a 48-well plate.
[0288] (2) On the day of treatment, dilute purified +36 GFP protein
in serumfree media to a final concentration 200 nM. Add siRNA to a
final concentration of 50 nM. Vortex to mix and incubate at room
temperature for 10 min.
[0289] (3) During incubation, aspirate media from cells and wash
once with PBS.
[0290] (4) Following incubation of +36 GFP and siRNA, add the
protein-siRNA complexes to cells.
[0291] (5) Incubate cells with complexes at 37 C for 4 h.
[0292] (6) Following incubation, aspirate the media and wash three
times with 20 U/mL heparin PBS. Incubate cells with
serum-containing media for a further 48 h or longer depending upon
the assay for knockdown.
[0293] (7) Analyze cells by immunoblot, qPCR, phenotypic assay, or
other appropriate method.
[0294] David Liu's lab has further found +36 GFP to be an effective
plasmid delivery reagent in a range of cells. As plasmid DNA is a
larger cargo than siRNA, proportionately more +36 GFP protein is
required to effectively complex plasmids. For effective plasmid
delivery Applicants have developed a variant of +36 GFP bearing a
C-terminal HA2 peptide tag, a known endosome-disrupting peptide
derived from the influenza virus hemagglutinin protein. The
following protocol has been effective in a variety of cells, but as
above it is advised that plasmid DNA and supercharged protein doses
be optimized for specific cell lines and delivery applications.
[0295] (1) One day before treatment, plate 1.times.10.sup.5 per
well in a 48-well plate.
[0296] (2) On the day of treatment, dilute purified 36 GFP protein
in serumfree media to a final concentration 2 mM. Add 1 mg of
plasmid DNA. Vortex to mix and incubate at room temperature for 10
min.
[0297] (3) During incubation, aspirate media from cells and wash
once with PBS.
[0298] (4) Following incubation of 36 GFP and plasmid DNA, gently
add the protein-DNA complexes to cells.
[0299] (5) Incubate cells with complexes at 37 C for 4 h.
[0300] (6) Following incubation, aspirate the media and wash with
PBS. Incubate cells in serum-containing media and incubate for a
further 24-48 h.
[0301] (7) Analyze plasmid delivery (e.g., by plasmid-driven gene
expression) as appropriate.
[0302] See also, e.g., McNaughton et al., Proc. Natl. Acad. Sci.
USA 106, 6111-6116 (2009); Cronican et al., ACS Chemical Biology 5,
747-752 (2010); Cronican et al., Chemistry & Biology 18,
833-838 (2011); Thompson et al., Methods in Enzymology 503, 293-319
(2012); Thompson, D. B., et al., Chemistry & Biology 19 (7),
831-843 (2012). The methods of the super charged proteins may be
used and/or adapted for delivery of the CRISPR Cas system of the
present invention.
[0303] Implantable Devices
[0304] In another embodiment, implantable devices are also
contemplated for delivery of the CRISPR Cas system. For example, US
Patent Publication 20110195123 discloses an implantable medical
device which elutes a drug locally and in prolonged period is
provided, including several types of such a device, the treatment
modes of implementation and methods of implantation. The device
comprising of polymeric substrate, such as a matrix for example,
that is used as the device body, and drugs, and in some cases
additional scaffolding materials, such as metals or additional
polymers, and materials to enhance visibility and imaging. The
selection of drug is based on the advantageous of releasing drug
locally and in prolonged period, where drug is released directly to
the extracellular matrix (ECM) of the diseased area such as tumor,
inflammation, degeneration or for symptomatic objectives, or to
injured smooth muscle cells, or for prevention. One kind of drug is
the gene silencing drugs based on RNA interference (RNAi),
including but not limited to si RNA, sh RNA, or antisense RNA/DNA,
ribozyme and nucleoside analogs. Therefore, this system may be
used/and or adapted to the CRISPR Cas system of the present
invention. The modes of implantation in some embodiments are
existing implantation procedures that are developed and used today
for other treatments, including brachytherapy and needle biopsy. In
such cases the dimensions of the new implant described in this
invention are similar to the original implant. Typically a few
devices are implanted during the same treatment procedure.
[0305] As described in US Patent Publication 20110195123, there is
provided a drug delivery implantable or insertable system,
including systems applicable to a cavity such as the abdominal
cavity and/or any other type of administration in which the drug
delivery system is not anchored or attached, comprising a biostable
and/or degradable and/or bioabsorbable polymeric substrate, which
may for example optionally be a matrix. It should be noted that the
term "insertion" also includes implantation. The drug delivery
system is preferably implemented as a "Loder" as described in US
Patent Publication 20110195123.
[0306] The polymer or plurality of polymers are biocompatible,
incorporating an agent and/or plurality of agents, enabling the
release of agent at a controlled rate, wherein the total volume of
the polymeric substrate, such as a matrix for example, in some
embodiments is optionally and preferably no greater than a maximum
volume that permits a therapeutic level of the agent to be reached.
As a non-limiting example, such a volume is preferably within the
range of 0.1 m.sup.3 to 1000 mm.sup.3, as required by the volume
for the agent load. The Loder may optionally be larger, for example
when incorporated with a device whose size is determined by
functionality, for example and without limitation, a knee joint, an
intra-uterine or cervical ring and the like.
[0307] The drug delivery system (for delivering the composition) is
designed in some embodiments to preferably employ degradable
polymers, wherein the main release mechanism is bulk erosion; or in
some embodiments, non degradable, or slowly degraded polymers are
used, wherein the main release mechanism is diffusion rather than
bulk erosion, so that the outer part functions as membrane, and its
internal part functions as a drug reservoir, which practically is
not affected by the surroundings for an extended period (for
example from about a week to about a few months). Combinations of
different polymers with different release mechanisms may also
optionally be used. The concentration gradient at the surface is
preferably maintained effectively constant during a significant
period of the total drug releasing period, and therefore the
diffusion rate is effectively constant (termed "zero mode"
diffusion). By the term "constant" it is meant a diffusion rate
that is preferably maintained above the lower threshold of
therapeutic effectiveness, but which may still optionally feature
an initial burst and/or fluctuate, for example increasing and
decreasing to a certain degree. The diffusion rate is preferably so
maintained for a prolonged period, and it can be considered
constant to a certain level to optimize the therapeutically
effective period, for example the effective silencing period.
[0308] The drug delivery system optionally and preferably is
designed to shield the nucleotide based therapeutic agent from
degradation, whether chemical in nature or due to attack from
enzymes and other factors in the body of the subject.
[0309] The drug delivery system as described in US Patent
Publication 20110195123 is optionally associated with sensing
and/or activation appliances that are operated at and/or after
implantation of the device, by non and/or minimally invasive
methods of activation and/or acceleration/deceleration, for example
optionally including but not limited to thermal heating and
cooling, laser beams, and ultrasonic, including focused ultrasound
and/or RF (radiofrequency) methods or devices.
[0310] According to some embodiments of US Patent Publication
20110195123, the site for local delivery may optionally include
target sites characterized by high abnormal proliferation of cells,
and suppressed apoptosis, including tumors, active and or chronic
inflammation and infection including autoimmune diseases states,
degenerating tissue including muscle and nervous tissue, chronic
pain, degenerative sites, and location of bone fractures and other
wound locations for enhancement of regeneration of tissue, and
injured cardiac, smooth and striated muscle. The site for local
delivery also may optionally include sites enabling performing
preventive activities including pregnancy, prevention of infection
and aging.
[0311] The site for implantation of the composition, or target
site, preferably features a radius, area and/or volume that is
sufficiently small for targeted local delivery. For example, the
target site optionally has a diameter in a range of from about 0.1
mm to about 5 cm.
[0312] The location of the target site is preferably selected for
maximum therapeutic efficacy. For example, the composition of the
drug delivery system (optionally with a device for implantation as
described above) is optionally and preferably implanted within or
in the proximity of a tumor environment, or the blood supply
associated thereof.
[0313] For example the composition (optionally with the device) is
optionally implanted within or in the proximity to pancreas,
prostate, breast, liver, via the nipple, within the vascular system
and so forth.
[0314] The target location is optionally selected from the group
consisting of (as non-limiting examples only, as optionally any
site within the body may be suitable for implanting a Loder): 1.
brain at degenerative sites like in Parkinson or Alzheimer disease
at the basal ganglia, white and gray matter; 2. spine as in the
case of amyotrophic lateral sclerosis (ALS); 3. uterine cervix to
prevent HPV infection; 4. active and chronic inflammatory joints;
5. dermis as in the case of psoriasis; 6. sympathetic and sensoric
nervous sites for analgesic effect; 7. Intra osseous implantation;
8. acute and chronic infection sites; 9. Intra vaginal; 10. Inner
ear--auditory system, labyrinth of the inner ear, vestibular
system; 11. Intra tracheal; 12. Intra-cardiac; coronary,
epicardiac; 13. urinary bladder; 14. biliary system; 15.
parenchymal tissue including and not limited to the kidney, liver,
spleen; 16. lymph nodes; 17. salivary glands; 18. dental gums; 19.
Intra-articular (into joints); 20. Intra-ocular; 21. Brain tissue;
22. Brain ventricles; 23. Cavities, including abdominal cavity (for
example but without limitation, for ovary cancer); 24. Intra
esophageal and 25. Intra rectal.
[0315] Optionally insertion of the system (for example a device
containing the composition) is associated with injection of
material to the ECM at the target site and the vicinity of that
site to affect local pH and/or temperature and/or other biological
factors affecting the diffusion of the drug and/or drug kinetics in
the ECM, of the target site and the vicinity of such a site.
[0316] Optionally, according to some embodiments, the release of
said agent could be associated with sensing and/or activation
appliances that are operated prior and/or at and/or after
insertion, by non and/or minimally invasive and/or else methods of
activation and/or acceleration/deceleration, including laser beam,
radiation, thermal heating and cooling, and ultrasonic, including
focused ultrasound and/or RF (radiofrequency) methods or devices,
and chemical activators.
[0317] According to other embodiments of US Patent Publication
20110195123, the drug preferably comprises a gene silencing
biological RNAi drug, for example for localized cancer cases in
breast, pancreas, brain, kidney, bladder, lung, and prostate as
described below. Moreover, many drugs other than siRNA are
applicable to be encapsulated in Loder, and can be used in
association with this invention, as long as such drugs can be
encapsulated with the Loder substrate, such as a matrix for
example. Such drugs include approved drugs that are delivered today
by methods other than of this invention, including Amphotericin B
for fungal infection; antibiotics such as in osteomyelitis; pain
killers such as narcotics; anti degenerative such as in Alzheimer
or Parkinson diseases in a Loder implanted in the vicinity of the
spine in the case of back pain. Such a system may be used and/or
adapted to deliver the CRISPR Cas system of the present
invention.
[0318] For example, for specific applications such as prevention of
growth or regrowth of smooth muscle cells (that are injured during
a stenting procedure and as a result tend to proliferate), the drug
may optionally be siRNA that silence smooth muscle cells, including
H19 silencing, or a drug selected from the group consisting of
taxol, rapamycin and rapamycin-analogs. In such cases the Loder is
preferably either a Drug Eluting Stent (DES), with prolonged
release at constant rate, or a dedicated device that is implanted
separately, in association to the stent. All of this may be
used/and or adapted to the CRISPR Cas system of the present
invention.
[0319] As another example of a specific application, neuro and
muscular degenerative diseases develop due to abnormal gene
expression. Local delivery of silencing RNAs may have therapeutic
properties for interfering with such abnormal gene expression.
Local delivery of anti apoptotic, anti inflammatory and anti
degenerative drugs including small drugs and macromolecules may
also optionally be therapeutic. In such cases the Loder is applied
for prolonged release at constant rate and/or through a dedicated
device that is implanted separately. All of this may be used and/or
adapted to the CRISPR Cas system of the present invention.
[0320] As yet another example of a specific application,
psychiatric and cognitive disorders are treated with gene
modifiers. Gene knockdown with silencing RNA is a treatment option.
Loders locally delivering nucleotide based agents to central
nervous system sites are therapeutic options for psychiatric and
cognitive disorders including but not limited to psychosis,
bi-polar diseases, neurotic disorders and behavioral maladies. The
Loders could also deliver locally drugs including small drugs and
macromolecules upon implantation at specific brain sites. All of
this may be used and/or adapted to the CRISPR Cas system of the
present invention.
[0321] As another example of a specific application, silencing of
innate and/or adaptive immune mediators at local sites enables the
prevention of organ transplant rejection. Local delivery of
silencing RNAs and immunomodulating reagents with the Loder
implanted into the transplanted organ and/or the implanted site
renders local immune suppression by repelling immune cells such as
CD8 activated against the transplanted organ. All of this may be
used/and or adapted to the CRISPR Cas system of the present
invention.
[0322] As another example of a specific application, vascular
growth factors including VEGFs and angiogenin and others are
essential for neovascularization. Local delivery of the factors,
peptides, peptidomimetics, or suppressing their repressors is an
important therapeutic modality; silencing the repressors and local
delivery of the factors, peptides, macromolecules and small drugs
stimulating angiogenesis with the Loder is therapeutic for
peripheral, systemic and cardiac vascular disease.
[0323] The method of insertion, such as implantation, may
optionally already be used for other types of tissue implantation
and/or for insertions and/or for sampling tissues, optionally
without modifications, or alternatively optionally only with
non-major modifications in such methods. Such methods optionally
include but are not limited to brachytherapy methods, biopsy,
endoscopy with and/or without ultrasound, such as ERCP,
stereotactic methods into the brain tissue, Laparoscopy, including
implantation with a laparoscope into joints, abdominal organs, the
bladder wall and body cavities.
[0324] CRISPR Enzyme mRNA and Guide RNA
[0325] CRISPR enzyme mRNA and guide RNA might also be delivered
separately. CRISPR enzyme mRNA can be delivered prior to the guide
RNA to give time for CRISPR enzyme to be expressed. CRISPR enzyme
mRNA might be administered 1-12 hours (preferably around 2-6 hours)
prior to the administration of guide RNA.
[0326] Alternatively, CRISPR enzyme mRNA and guide RNA can be
administered together. Advantageously, a second booster dose of
guide RNA can be administered 1-12 hours (preferably around 2-6
hours) after the initial administration of CRISPR enzyme mRNA+guide
RNA.
[0327] Additional administrations of CRISPR enzyme mRNA and/or
guide RNA might be useful to achieve the most efficient levels of
genome modification.
[0328] For minimization of toxicity and off-target effect, it will
be important to control the concentration of CRISPR enzyme mRNA and
guide RNA delivered. Optimal concentrations of CRISPR enzyme mRNA
and guide RNA can be determined by testing different concentrations
in a cellular or animal model and using deep sequencing the analyze
the extent of modification at potential off-target genomic loci.
For example, for the guide sequence targeting
5'-GAGTCCGAGCAGAAGAAGAA-3' (SEQ ID NO: 3) in the EMX1 gene of the
human genome, deep sequencing can be used to assess the level of
modification at the following two off-target loci, 1:
5'-GAGTCCTAGCAGGAGAAGAA-3' (SEQ ID NO: 4) and 2:
5'-GAGTCTAAGCAGAAGAAGAA-3' (SEQ ID NO: 5). The concentration that
gives the highest level of on-target modification while minimizing
the level of off-target modification should be chosen for in vivo
delivery.
[0329] Alternatively, to minimize the level of toxicity and
off-target effect, CRISPR enzyme nickase mRNA (for example S.
pyogenes Cas9 with the D10A mutation) can be delivered with a pair
of guide RNAs targeting a site of interest. The two guide RNAs need
to be spaced as follows. Guide sequences in red (single underline)
and blue (double underline) respectively (these examples are based
on the PAM requirement for Streptococcus pyogenes Cas9).
TABLE-US-00002 Over- hang Guide RNA design length (guide sequence
and (bp) PAM color coded) 14
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN NNNNNNGGNNNNNNNNNNNNNN-3'
(SEQ ID NO: 6) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
NNNNNNCCNNNNNNNNNNNNNN-5' (SEQ ID NO: 7) 13
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN NNNNNGGNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 8) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
NNNNNCCNNNNNNNNNNNNNNN-5' (SEQ ID NO: 9) 12
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN NNNNGGNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 10) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
NNNNNCCNNNNNNNNNNNNNNN-5' (SEQ ID NO: 11) 11
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN NNNGGNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 12) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
NNNCCNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 13) 10
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN NNGGNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 14) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
NNCCNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 15) 9
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN NGGNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 16) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
NCCNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 17) 8
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNN GGNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 18) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNN
CCNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 19) 7
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNNG GNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 20) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNNC
CNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 21) 6
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNNGG NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 22) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNNCC
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 23) 5
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNNGGN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 24) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNNCCN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 25) 4
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNNGGNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 26) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNCCNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 27) 3
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNNGGNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 28) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNCCNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 29) 2
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNNGGNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 30) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNCCNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 31) 1
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNNGGNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 32) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNCCNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 33) blunt
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNNGGNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 34) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNNCCNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 35) 1
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNNGGNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 36) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNNCCNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 37) 2
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNNGGNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 38) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNNCCNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 39) 3
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNNGGNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 40) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNNCCNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 41) 4
5'-NNNNNNNNNNNNNNNNNNNNCCNNNNGGNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 42) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNNCCNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 43) 5
5'-NNNNNNNNNNNNNNNNNNNNCCNNNGGNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 44) 3'-NNNNNNNNNNNNNNNNNNNNGGNNNCCNNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 45) 6
5'-NNNNNNNNNNNNNNNNNNNNCCNNGGNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 46) 3'-NNNNNNNNNNNNNNNNNNNNGGNNCCNNNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 47) 7
5'-NNNNNNNNNNNNNNNNNNNNCCNGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 48) 3'-NNNNNNNNNNNNNNNNNNNNGGNCCNNNNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 49) 8
5'-NNNNNNNNNNNNNNNNNNNNCCGGNNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 50) 3'-NNNNNNNNNNNNNNNNNNNNGGCCNNNNNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 51) 12
5'-NNNNNNNNNNNNNNNNNNNNNNNGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 52) 3'-NNNNNNNNNNNNNNNNNNNNNNNCCGGNNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 53) 13
5'-NNNNNNNNNNNNNNNNNNNNNNCGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 54) 3'-NNNNNNNNNNNNNNNNNNNNNNNCCNGGNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 55) 14
5'-NNNNNNNNNNNNNNNNNNNNNNCGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 54) 3'-NNNNNNNNNNNNNNNNNNNNNNNCCNGGNNNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 56) 15
5'-NNNNNNNNNNNNNNNNNNNNNNCGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 54) 3'-NNNNNNNNNNNNNNNNNNNNNNNCCNNNGGNNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 57) 16
5'-NNNNNNNNNNNNNNNNNNNNNNCGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 54) 3'-NNNNNNNNNNNNNNNNNNNNNNNCCNNNNGGNNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 58) 17
5'-NNNNNNNNNNNNNNNNNNNNNNCGGNNNNNNNNNNNNN NNNNNNNNNNNNNNNNNNNNNN-3'
(SEQ ID NO: 54) 3'-NNNNNNNNNNNNNNNNNNNNNNNCCNNNNNGGNNNNNN
NNNNNNNNNNNNNNNNNNNNNN-5' (SEQ ID NO: 59)
[0330] Further interrogation of the system have given Applicants
evidence of the 5' overhang (see, e.g., Ran et al., Cell. 2013 Sep.
12; 154(6):1380-9 and U.S. Provisional Patent Application Ser. No.
61/871,301 filed Aug. 28, 2013). Applicants have further identified
parameters that relate to efficient cleavage by the Cas9 nickase
mutant when combined with two guide RNAs and these parameters
include but are not limited to the length of the 5' overhang. In
embodiments of the invention the 5' overhang is at most 200 base
pairs, preferably at most 100 base pairs, or more preferably at
most 50 base pairs. In embodiments of the invention the 5' overhang
is at least 26 base pairs, preferably at least 30 base pairs or
more preferably 34-50 base pairs or 1-34 base pairs. In other
preferred methods of the invention the first guide sequence
directing cleavage of one strand of the DNA duplex near the first
target sequence and the second guide sequence directing cleavage of
other strand near the second target sequence results in a blunt cut
or a 3' overhang. In embodiments of the invention the 3' overhang
is at most 150, 100 or 25 base pairs or at least 15, 10 or 1 base
pairs. In preferred embodiments the 3' overhang is 1-100
basepairs.
[0331] Aspects of the invention relate to the expression of the
gene product being decreased or a template polynucleotide being
further introduced into the DNA molecule encoding the gene product
or an intervening sequence being excised precisely by allowing the
two 5' overhangs to reanneal and ligate or the activity or function
of the gene product being altered or the expression of the gene
product being increased. In an embodiment of the invention, the
gene product is a protein.
[0332] Only sgRNA pairs creating 5' overhangs with less than 8 bp
overlap between the guide sequences (offset greater than -8 bp)
were able to mediate detectable indel formation. Importantly, each
guide used in these assays is able to efficiently induce indels
when paired with wildtype Cas9, indicating that the relative
positions of the guide pairs are the most important parameters in
predicting double nicking activity.
[0333] Since Cas9n and Cas9H840A nick opposite strands of DNA,
substitution of Cas9n with Cas9H840A with a given sgRNA pair should
result in the inversion of the overhang type. For example, a pair
of sgRNAs that will generate a 5' overhang with Cas9n should in
principle generate the corresponding 3' overhang instead.
Therefore, sgRNA pairs that lead to the generation of a 3' overhang
with Cas9n might be used with Cas9H840A to generate a 5' overhang.
Unexpectedly, Applicants tested Cas9H840A with a set of sgRNA pairs
designed to generate both 5' and 3' overhangs (offset range from
-278 to +58 bp), but were unable to observe indel formation.
Further work may be needed to identify the necessary design rules
for sgRNA pairing to allow double nicking by Cas9H840A.
[0334] Liver, Proprotein Convertase Subtilisin Kexin 9 (PCSK9)
[0335] Proprotein convertase subtilisin kexin 9 (PCSK9) is a member
of the subtilisin serine protease family. PCSK9 is primarily
expressed by the liver and is critical for the down regulation of
hepatocyte LDL receptor expression. LDL-C levels in plasma are
highly elevated in humans with gain of function mutations in PCSK9,
classifying them as having severe hypercholesterolemia. Therefore,
PCSK9 is an attractive target for CRISPR. PCS9K-targeted CRISPR may
be formulated in a lipid particle and for example administered at
about 15, 45, 90, 150, 250 and 400 .mu.g/kg intraveneously (see,
e.g.,
http://www.ainylam.comicapellaiwp-content/uploads/2013/08/ALN-PCS02-001-P-
rotocol-Lancet.pdf).
[0336] Bailey et al. (J Mol Med (Berl). 1999 January; 77(1):244-9)
discloses insulin delivery by ex-vivo somatic cell gene therapy
involves the removal of non-B-cell somatic cells (e.g. fibroblasts)
from a diabetic patient, and genetically altering them in vitro to
produce and secrete insulin. The cells can be grown in culture and
returned to the donor as a source of insulin replacement. Cells
modified in this way could be evaluated before implantation, and
reserve stocks could be cryopreserved. By using the patient's own
cells, the procedure should obviate the need for immunosuppression
and overcome the problem of tissue supply, while avoiding a
recurrence of cell destruction. Ex-vivo somatic cell gene therapy
requires an accessible and robust cell type that is amenable to
multiple transfections and subject to controlled proliferation.
Special problems associated with the use of non-B-cell somatic
cells include the processing of proinsulin to insulin, and the
conferment of sensitivity to glucose-stimulated proinsulin
biosynthesis and regulated insulin release. Preliminary studies
using fibroblasts, pituitary cells, kidney (COS) cells and ovarian
(CHO) cells suggest that these challenges could be met, and that
ex-vivo somatic cell gene therapy offers a feasible approach to
insulin replacement therapy. The system of Bailey et al. may be
used/and or adapted to the CRISPR Cas system of the present
invention for delivery to the liver.
[0337] The methods of Sato et al. (Nature Biotechnology Volume 26
Number 4 Apr. 2008, Pages 431-442) may be applied to the CRISPR Cas
system of the present invention for delivery to the liver. Sato et
al. found that treatments with the siRNA-bearing vitamin A-coupled
liposomes almost completely resolved liver fibrosis and prolonged
survival in rats with otherwise lethal dimethylnitrosamine-induced
liver cirrhosis in a dose- and duration-dependent manner. Cationic
liposomes (Lipotrust) containing
O,O'-ditetradecanoyl-N-(a-trimethylammonioacetyl) diethanolamine
chloride (DC-6-14) as a cationic lipid, cholesterol and
dioleoylphosphatidylethanolamine at a molar ratio of 4:3:3 (which
has shown high transfection efficiency under serumcontaining
conditions for in vitro and in vivo gene delivery) were purchased
from Hokkaido System Science. The liposomes were manufactured using
a freeze-dried empty liposomes method and prepared at a
concentration of 1 mM (DC-16-4) by addition of double-distilled
water (DDW) to the lyophilized lipid mixture under vortexing before
use. To prepare VA-coupled liposomes, 200 nmol of vitamin A
(retinol, Sigma) dissolved in DMSO was mixed with the liposome
suspensions (100 nmol as DC-16-4) by vortexing in a 1.5 ml tube at
25 1 C. To prepare VA-coupled liposomes carrying siRNAgp46
(VA-lip-siRNAgp46), a solution of siRNAgp46 (580 pmol/ml in DDW)
was added to the retinol-coupled liposome solution with stirring at
25 C. The ratio of siRNA to DC-16-4 was 1:11.5 (mol/mol) and the
siRNA to liposome ratio (wt/wt) was 1:1. Any free vitamin A or
siRNA that was not taken up by liposomes were separated from
liposomal preparations using a micropartition system (VIVASPIN 2
concentrator 30,000 MWCO PES, VIVASCIENCE). The liposomal
suspension was added to the filters and centrifuged at 1,500 g for
5 min 3 times at 25 1 C. Fractions were collected and the material
trapped in the filter was reconstituted with PBS to achieve the
desired dose for in vitro or in vivo use. Three injections of 0.75
mg/kg siRNA were given every other day to rats. The system of Sato
et al. may be used/and or adapted to the CRISPR Cas system of the
present invention for delivery to the liver by delivering about 0.5
to 1 mg/kg of CRISPR Cas RNA in the liposomes as described by Sato
et al. to humans.
[0338] The methods of Rozema et al. (PNAS, Aug. 7, 2007, vol. 104,
no. 32) for a vehicle for the delivery of siRNA to hepatocytes both
in vitro and in vivo, which Rozema et al. have named siRNA Dynamic
PolyConjugates may also be applied to the present invention. Key
features of the Dynamic Poly-Conjugate technology include a
membrane-active polymer, the ability to reversibly mask the
activity of this polymer until it reaches the acidic environment of
endosomes, and the ability to target this modified polymer and its
siRNA cargo specifically to hepatocytes in vivo after simple,
low-pressure i.v. injection. SATA-modified siRNAs are synthesized
by reaction of 5' aminemodified siRNA with 1 weight equivalents (wt
eq) of Nsuccinimidyl-S-acetylthioacetate (SATA) reagent (Pierce)
and 0.36 wt eq of NaHCO.sub.3 in water at 4.degree. C. for 16 h.
The modified siRNAs are then precipitated by the addition of 9 vol
of ethanol and incubation at 80.degree. C. for 2 h. The precipitate
is resuspended in 1.times.siRNA buffer (Dharmacon) and quantified
by measuring absorbance at the 260-nm wavelength. PBAVE (30 mg/ml
in 5 mMTAPS, pH 9) is modified by addition of 1.5 wt % SMPT
(Pierce). After a 1-h incubation, 0.8 mg of SMPT-PBAVE was added to
400 .mu.l of isotonic glucose solution containing 5 mM TAPS (pH 9).
To this solution was added 50 .mu.g of SATA-modified siRNA. For the
dose-response experiments where [PBAVE] was constant, different
amounts of siRNA are added. The mixture is then incubated for 16 h.
To the solution is then added 5.6 mg of Hepes free base followed by
a mixture of 3.7 mg of CDM-NAG and 1.9 mg of CDM-PEG. The solution
is then incubated for at least 1 h at room temperature before
injection. CDM-PEG and CDM-NAG are synthesized from the acid
chloride generated by using oxalyl chloride. To the acid chloride
is added 1.1 molar equivalents polyethylene glycol monomethyl ether
(molecular weight average of 450) to generate CDM-PEG or
(aminoethoxy)ethoxy-2-(acetylamino)-2-deoxy-.beta.-D-glucopyranoside
to generate CDM-NAG. The final product is purified by using
reverse-phase HPLC with a 0.1% TFA water/acetonitrile gradient.
About 25 to 50 .mu.g of siRNA was delivered to mice. The system of
Rozema et al. may be applied to the CRISPR Cas system of the
present invention for delivery to the liver, for example by
envisioning a dosage of about 50 to about 200 mg of CRISPR Cas for
delivery to a human.
[0339] Bone
[0340] Oakes and Lieberman (Clin Orthop Relat Res. 2000 October;
(379 Suppl): S101-12) discusses delivery of genes to the bone. By
transferring genes into cells at a specific anatomic site, the
osteoinductive properties of growth factors can be used at
physiologic doses for a sustained period to facilitate a more
significant healing response. The specific anatomic site, the
quality of the bone, and the soft-tissue envelope, influences the
selection of the target cells for regional gene therapy. Gene
therapy vectors delivered to a treatment site in osteoconductive
carriers have yielded promising results. Several investigators have
shown exciting results using ex vivo and in vivo regional gene
therapy in animal models. Such a system may be used/and or adapted
to the CRISPR Cas system for delivery to the bone.
[0341] Brain
[0342] Delivery options for the brain include encapsulation of
CRISPR enzyme and guide RNA in the form of either DNA or RNA into
liposomes and conjugating to molecular Trojan horses for
trans-blood brain barrier (BBB) delivery. Molecular Trojan horses
have been shown to be effective for delivery of B-gal expression
vectors into the brain of non-human primates. The same approach can
be used to delivery vectors containing CRISPR enzyme and guide RNA.
For instance, Xia C F and Boado R J, Pardridge W M
("Antibody-mediated targeting of siRNA via the human insulin
receptor using avidin-biotin technology." Mol Pharm. 2009 May-June;
6(3):747-51. doi: 10.1021/mp800194) describes how delivery of short
interfering RNA (siRNA) to cells in culture, and in vivo, is
possible with combined use of a receptor-specific monoclonal
antibody (mAb) and avidin-biotin technology. The authors also
report that because the bond between the targeting mAb and the
siRNA is stable with avidin-biotin technology, and RNAi effects at
distant sites such as brain are observed in vivo following an
intravenous administration of the targeted siRNA.
[0343] Zhang et al. (Mol Ther. 2003 January; 7(1):11-8.)) describe
how expression plasmids encoding reporters such as luciferase were
encapsulated in the interior of an "artificial virus" comprised of
an 85 nm pegylated immunoliposome, which was targeted to the rhesus
monkey brain in vivo with a monoclonal antibody (MAb) to the human
insulin receptor (HIR). The HIRMAb enables the liposome carrying
the exogenous gene to undergo transcytosis across the blood-brain
barrier and endocytosis across the neuronal plasma membrane
following intravenous injection. The level of luciferase gene
expression in the brain was 50-fold higher in the rhesus monkey as
compared to the rat. Widespread neuronal expression of the
beta-galactosidase gene in primate brain was demonstrated by both
histochemistry and confocal microscopy. The authors indicate that
this approach makes feasible reversible adult transgenics in 24
hours. Accordingly, the use of immunoliposome is preferred. These
may be used in conjunction with antibodies to target specific
tissues or cell surface proteins.
[0344] Other means of delivery or RNA are also preferred, such as
via nanoparticles (Cho, S., Goldberg, M., Son, S., Xu, Q., Yang,
F., Mei, Y., Bogatyrev, S., Langer, R. and Anderson, D., Lipid-like
nanoparticles for small interfering RNA delivery to endothelial
cells, Advanced Functional Materials, 19: 3112-3118, 2010) or
exosomes (Schroeder, A., Levins, C., Cortez, C., Langer, R., and
Anderson, D., Lipid-based nanotherapeutics for siRNA delivery,
Journal of Internal Medicine, 267: 9-21, 2010, PMID: 20059641).
[0345] Indeed, exosomes have been shown to be particularly useful
in delivery siRNA, a system with some parallels to the CRISPR
system. For instance, E1-Andaloussi S, et al. ("Exosome-mediated
delivery of siRNA in vitro and in vivo." Nat Protoc. 2012 December;
7(12):2112-26. doi: 10.1038/nprot.2012.131. Epub 2012 Nov. 15.)
describe how exosomes are promising tools for drug delivery across
different biological barriers and can be harnessed for delivery of
siRNA in vitro and in vivo. Their approach is to generate targeted
exosomes through transfection of an expression vector, comprising
an exosomal protein fused with a peptide ligand. The exosomes are
then purify and characterized from transfected cell supernatant,
then siRNA is loaded into the exosomes. Delivery or administration
according to the invention can be performed with exosomes, in
particular but not limited to the brain.
[0346] Vitamin E (.alpha.-tocopherol) may be conjugated with CRISPR
Cas and delivered to the brain along with high density lipoprotein
(HDL), for example in a similar manner as was done by Uno et al.
(HUMAN GENE THERAPY 22:711-719 (June 2011)) for delivering
short-interfering RNA (siRNA) to the brain. Mice were infused via
Osmotic minipumps (model 1007D; Alzet, Cupertino, Calif.) filled
with phosphate-buffered saline (PBS) or free TocsiBACE or
Toc-siBACE/HDL and connected with Brain Infusion Kit 3 (Alzet). A
brain-infusion cannula was placed about 0.5 mm posterior to the
bregma at midline for infusion into the dorsal third ventricle. Uno
et al. found that as little as 3 nmol of Toc-siRNA with HDL could
induce a target reduction in comparable degree by the same ICV
infusion method. A similar dosage of CRISPR Cas conjugated to
.alpha.-tocopherol and co-administered with HDL targeted to the
brain may be contemplated for humans in the present invention, for
example, about 3 nmol to about 3 .mu.mol of CRISPR Cas targeted to
the brain may becontemplated.
[0347] Zou et al. ((HUMAN GENE THERAPY 22:465-475 (April 2011))
describes a method of lentiviral-mediated delivery of short-hairpin
RNAs targeting PKC.gamma. for in vivo gene silencing in the spinal
cord of rats. Zou et al. administered about 10 pCl of a recombinant
lentivirus having a titer of 1.times.10.sup.9 transducing units
(TU)/ml by an intrathecal catheter. A similar dosage of CRISPR Cas
expressed in a lentiviral vector targeted to the brain may be
contemplated for humans in the present invention, for example,
about 10-50 ml of CRISPR Cas targeted to the brain in a lentivirus
having a titer of 1.times.10.sup.9 transducing units (TU)/ml may
becontemplated.
[0348] Targeted Deletion, Therapeutic Applications
[0349] Targeted deletion of genes is preferred. Examples are
exemplified in Example 18. Preferred are, therefore, genes involved
in cholesterol biosynthesis, fatty acid biosynthesis, and other
metabolic disorders, genes encoding mis-folded proteins involved in
amyloid and other diseases, oncogenes leading to cellular
transformation, latent viral genes, and genes leading to
dominant-negative disorders, amongst other disorders. As
exemplified here. Applicants prefer gene delivery of a CRISPR-Cas
system to the liver, brain, ocular, epithelial, hematopoetic, or
another tissue of a subject or a patient in need thereof, suffering
from metabolic disorders, amyloidosis and protein-aggregation
related diseases, cellular transformation arising from genetic
mutations and translocations, dominant negative effects of gene
mutations, latent viral infections, and other related symptoms,
using either viral or nanoparticle delivery system.
[0350] Therapeutic applications of the CRISPR-Cas system include
Glaucoma, Amyloidosis, and Huntington's disease. These are
exemplified in Example 20 and the features described therein are
preferred alone or in combination.
[0351] Another example of a polyglutamine expansion disease that
may be treated by the present invention includes spinocerebellar
ataxia type 1 (SCA1). Upon intracerebellar injection, recombinant
adenoassociated virus (AAV) vectors expressing short hairpin RNAs
profoundly improve motor coordination, restored cerebellar
morphology and resolved characteristic ataxin-1 inclusions in
Purkinje cells of SCA1 mice (see, e.g., Xia et al., Nature
Medicine, Vol. 10, No. 8, August 2004). In particular, AAV1 and
AAV5 vectors are preferred and AAV titers of about
1.times.10.sup.12 vector genomes/ml are desirable.
[0352] As an example, chronic infection by HIV-1 may be treated or
prevented. In order to accomplish this, one may generate CRISPR-Cas
guide RNAs that target the vast majority of the HIV-1 genome while
taking into account HIV-1 strain variants for maximal coverage and
effectiveness. One may accomplish delivery of the CRISPR-Cas system
by conventional adenoviral or lentiviral-mediated infection of the
host immune system. Depending on approach, host immune cells could
be a) isolated, transduced with CRISPR-Cas, selected, and
re-introduced in to the host or b) transduced in vivo by systemic
delivery of the CRISPR-Cas system. The first approach allows for
generation of a resistant immune population whereas the second is
more likely to target latent viral reservoirs within the host. This
is discussed in more detail in the Examples section.
[0353] In another example, US Patent Publication No. 20130171732
assigned to Sangamo BioSciences, Inc. relates to insertion of an
anti-HIV transgene into the genome, methods of which may be applied
to the CRISPR Cas system of the present invention. In another
embodiment, the CXCR4 gene may be targeted and the TALE system of
US Patent Publication No. 20100291048 assigned to Sangamo
BioSciences, Inc. may be modified to the CRISPR Cas system of the
present invention. The method of US Patent Publication Nos.
20130137104 and 20130122591 assigned to Sangamo BioSciences, Inc.
and US Patent Publication No. 20100146651 assigned to Cellectis may
be more generally applicable for transgene expression as it
involves modifying a hypoxanthine-guanine phosphoribosyltransferase
(HPRT) locus for increasing the frequency of gene modification.
[0354] It is also envisaged that the present invention generates a
gene knockout cell library. Each cell may have a single gene
knocked out. This is exemplified in Example 23.
[0355] One may make a library of ES cells where each cell has a
single gene knocked out, and the entire library of ES cells will
have every single gene knocked out. This library is useful for the
screening of gene function in cellular processes as well as
diseases. To make this cell library, one may integrate Cas9 driven
by an inducible promoter (e.g. doxycycline inducible promoter) into
the ES cell. In addition, one may integrate a single guide RNA
targeting a specific gene in the ES cell. To make the ES cell
library, one may simply mix ES cells with a library of genes
encoding guide RNAs targeting each gene in the human genome. One
may first introduce a single BxB1 attB site into the AAVS1 locus of
the human ES cell. Then one may use the BxB1 integrase to
facilitate the integration of individual guide RNA genes into the
BxB1 attB site in AAVS1 locus. To facilitate integration, each
guide RNA gene may be contained on a plasmid that carries of a
single attP site. This way BxB1 will recombine the attB site in the
genome with the attP site on the guide RNA containing plasmid. To
generate the cell library, one may take the library of cells that
have single guide RNAs integrated and induce Cas9 expression. After
induction, Cas9 mediates double strand break at sites specified by
the guide RNA.
[0356] Chronic administration of protein therapeutics may elicit
unacceptable immune responses to the specific protein. The
immunogenicity of protein drugs can be ascribed to a few
immunodominant helper T lymphocyte (HTL) epitopes. Reducing the MHC
binding affinity of these HTL epitopes contained within these
proteins can generate drugs with lower immunogenicity (Tangri S, et
al. ("Rationally engineered therapeutic proteins with reduced
immunogenicity" J Immunol. 2005 Mar. 15; 174(6):3187-96.) In the
present invention, the immunogenicity of the CRISPR enzyme in
particular may be reduced following the approach first set out in
Tangri et al with respect to erythropoietin and subsequently
developed. Accordingly, directed evolution or rational design may
be used to reduce the immunogenicity of the CRISPR enzyme (for
instance a Cas9) in the host species (human or other species).
[0357] In Example 28, Applicants used 3 guideRNAs of interest and
able to visualize efficient DNA cleavage in vivo occurring only in
a small subset of cells. Essentially, what Applicants have shown
here is targeted in vivo cleavage. In particular, this provides
proof of concept that specific targeting in higher organisms such
as mammals can also be achieved. It also highlights multiplex
aspect in that multiple guide sequences (i.e. separate targets) can
be used simultaneously (in the sense of co-delivery). In other
words, Applicants used a multiple approach, with several different
sequences targeted at the same time, but independently.
[0358] A suitable example of a protocol for producing AAV, a
preferred vector of the invention is provided in Example 34.
[0359] Trinucleotide repeat disorders are preferred conditions to
be treated. These are also exemplified herein.
[0360] For example, US Patent Publication No. 20110016540,
describes use of zinc finger nucleases to genetically modify cells,
animals and proteins associated with trinucleotide repeat expansion
disorders. Trinucleotide repeat expansion disorders are complex,
progressive disorders that involve developmental neurobiology and
often affect cognition as well as sensori-motor functions.
[0361] Trinucleotide repeat expansion proteins are a diverse set of
proteins associated with susceptibility for developing a
trinucleotide repeat expansion disorder, the presence of a
trinucleotide repeat expansion disorder, the severity of a
trinucleotide repeat expansion disorder or any combination thereof.
Trinucleotide repeat expansion disorders are divided into two
categories determined by the type of repeat. The most common repeat
is the triplet CAG, which, when present in the coding region of a
gene, codes for the amino acid glutamine (Q). Therefore, these
disorders are referred to as the polyglutamine (polyQ) disorders
and comprise the following diseases: Huntington Disease (HD);
Spinobulbar Muscular Atrophy (SBMA); Spinocerebellar Ataxias (SCA
types 1, 2, 3, 6, 7, and 17); and Dentatorubro-Pallidoluysian
Atrophy (DRPLA). The remaining trinucleotide repeat expansion
disorders either do not involve the CAG triplet or the CAG triplet
is not in the coding region of the gene and are, therefore,
referred to as the non-polyglutamine disorders. The
non-polyglutamine disorders comprise Fragile X Syndrome (FRAXA);
Fragile XE Mental Retardation (FRAXE); Friedreich Ataxia (FRDA);
Myotonic Dystrophy (DM); and Spinocerebellar Ataxias (SCA types 8,
and 12).
[0362] The proteins associated with trinucleotide repeat expansion
disorders are typically selected based on an experimental
association of the protein associated with a trinucleotide repeat
expansion disorder to a trinucleotide repeat expansion disorder.
For example, the production rate or circulating concentration of a
protein associated with a trinucleotide repeat expansion disorder
may be elevated or depressed in a population having a trinucleotide
repeat expansion disorder relative to a population lacking the
trinucleotide repeat expansion disorder. Differences in protein
levels may be assessed using proteomic techniques including but not
limited to Western blot, immunohistochemical staining, enzyme
linked immunosorbent assay (ELISA), and mass spectrometry.
Alternatively, the proteins associated with trinucleotide repeat
expansion disorders may be identified by obtaining gene expression
profiles of the genes encoding the proteins using genomic
techniques including but not limited to DNA microarray analysis,
serial analysis of gene expression (SAGE), and quantitative
real-time polymerase chain reaction (Q-PCR).
[0363] Non-limiting examples of proteins associated with
trinucleotide repeat expansion disorders include AR (androgen
receptor), FMR1 (fragile X mental retardation 1), HTT (huntingtin),
DMPK (dystrophia myotonica-protein kinase), FXN (frataxin), ATXN2
(ataxin 2), ATN1 (atrophin 1), FEN1 (flap structure-specific
endonuclease 1), TNRC6A (trinucleotide repeat containing 6A),
PABPN1 (poly(A) binding protein, nuclear 1), JPH3 (junctophilin 3),
MED15 (mediator complex subunit 15), ATXN1 (ataxin 1), ATXN3
(ataxin 3), TBP (TATA box binding protein), CACNAIA (calcium
channel, voltage-dependent, P/Q type, alpha 1A subunit), ATXN80S
(ATXN8 opposite strand (non-protein coding)), PPP2R2B (protein
phosphatase 2, regulatory subunit B, beta), ATXN7 (ataxin 7),
TNRC6B (trinucleotide repeat containing 6B), TNRC6C (trinucleotide
repeat containing 6C), CELF3 (CUGBP, Elav-like family member 3),
MAB21L1 (mab-21-like 1 (C. elegans)), MSH2 (mutS homolog 2, colon
cancer, nonpolyposis type 1 (E. coli)), TMEMI85A (transmembrane
protein 185A), SIX5 (SIX homeobox 5), CNPY3 (canopy 3 homolog
(zebrafish)), FRAXE (fragile site, folic acid type, rare,
fra(XXq28) E), GNB2 (guanine nucleotide binding protein (G
protein), beta polypeptide 2), RPL14 (ribosomal protein L14), ATXN8
(ataxin 8), INSR (insulin receptor), TTR (transthyretin), EP400
(EIA binding protein p400), GIGYF2 (GRB10 interacting GYF protein
2), OGG1 (8-oxoguanine DNA glycosylase), STCI (stanniocalcin 1),
CNDPI (carnosine dipeptidase 1 (metallopeptidase M20 family)),
C10orf2 (chromosome 10 open reading frame 2), MAML3 mastermind-like
3 (Drosophila), DKC1 (dyskeratosis congenita 1, dyskerin), PAXIP1
(PAX interacting (with transcription-activation domain) protein 1),
CASK (calcium/calmodulin-dependent serine protein kinase (MAGUK
family)), MAPT (microtubule-associated protein tau), SP1 (Sp1
transcription factor), POLG (polymerase (DNA directed), gamma),
AFF2 (AF4/FMR2 family, member 2), THBS1 (thrombospondin 1), TP53
(tumor protein p53), ESR1 (estrogen receptor 1), CGGBP1 (CGG
triplet repeat binding protein 1), ABTI (activator of basal
transcription 1), KLK3 (kallikrein-related peptidase 3), PRNP
(prion protein), JUN (jun oncogene), KCNN3 (potassium
intermediate/small conductance calcium-activated channel, subfamily
N, member 3), BAX (BCL2-associated X protein), FRAXA (fragile site,
folic acid type, rare, fra(XXq27.3) A (macroorchidism, mental
retardation)), KBTBD10 (kelch repeat and BTB (POZ) domain
containing 10), MBNL1 (muscleblind-like (Drosophila)), RAD51 (RAD51
homolog (RecA homolog, E. coli) (S. cerevisiae)), NCOA3 (nuclear
receptor coactivator 3), ERDA1 (expanded repeat domain, CAG/CTG 1),
TSC1 (tuberous sclerosis 1), COMP (cartilage oligomeric matrix
protein), GCLC (glutamate-cysteine ligase, catalytic subunit), RRAD
(Ras-related associated with diabetes), MSH3 (mutS homolog 3 (E.
coli)), DRD2 (dopamine receptor D2), CD44 (CD44 molecule (Indian
blood group)), CTCF (CCCTC-binding factor (zinc finger protein)),
CCND1 (cyclin D1), CLSPN (claspin homolog (Xenopus laevis)), MEF2A
(myocyte enhancer factor 2A), PTPRU (protein tyrosine phosphatase,
receptor type, U), GAPDH (glyceraldehyde-3-phosphate
dehydrogenase), TRIM22 (tripartite motif-containing 22), WT1 (Wilms
tumor 1), AHR (aryl hydrocarbon receptor), GPX1 (glutathione
peroxidase 1), TPMT (thiopurine S-methyltransferase), NDP (Norrie
disease (pseudoglioma)), ARX (aristaless related homeobox), MUS81
(MUS81 endonuclease homolog (S. cerevisiae)), TYR (tyrosinase
(oculocutaneous albinism IA)), EGR1 (early growth response 1), UNG
(uracil-DNA glycosylase), NUMBL (numb homolog (Drosophila)-like),
FABP2 (fatty acid binding protein 2, intestinal), EN2 (engrailed
homeobox 2), CRYGC (crystallin, gamma C), SRP14 (signal recognition
particle 14 kDa (homologous Alu RNA binding protein)), CRYGB
(crystallin, gamma B), PDCD1 (programmed cell death 1), HOXA1
(homeobox A1), ATXN2L (ataxin 2-like), PMS2 (PMS2 postmeiotic
segregation increased 2 (S. cerevisiae)), GLA (galactosidase,
alpha), CBL (Cas-Br-M (murine) ecotropic retroviral transforming
sequence), FTH1 (ferritin, heavy polypeptide 1), IL12RB2
(interleukin 12 receptor, beta 2), OTX2 (orthodenticle homeobox 2),
HOXA5 (homeobox A5), POLG2 (polymerase (DNA directed), gamma 2,
accessory subunit), DLX2 (distal-less homeobox 2), SIRPA
(signal-regulatory protein alpha), OTX1 (orthodenticle homeobox 1),
AHRR (aryl-hydrocarbon receptor repressor), MANF (mesencephalic
astrocyte-derived neurotrophic factor), TMEM158 (transmembrane
protein 158 (gene/pseudogene)), and ENSG00000078687.
[0364] Preferred proteins associated with trinucleotide repeat
expansion disorders include HTT (Huntingtin), AR (androgen
receptor), FXN (frataxin), Atxn3 (ataxin), Atxn1 (ataxin), Atxn2
(ataxin), Atxn7 (ataxin), Atxn10 (ataxin), DMPK (dystrophia
myotonica-protein kinase), Atn1 (atrophin 1), CBP (creb binding
protein), VLDLR (very low density lipoprotein receptor), and any
combination thereof.
[0365] According to another aspect, a method of gene therapy for
the treatment of a subject having a mutation in the CFTR gene is
provided and comprises administering a therapeutically effective
amount of a CRISPR-Cas gene therapy particle, optionally via a
biocompatible pharmaceutical carrier, to the cells of a subject.
Preferably, the target DNA comprises the mutation deltaF508. In
general, it is of preferred that the mutation is repaired to the
wildtype. In this case, the mutation is a deletion of the three
nucleotides that comprise the codon for phenylalanine (F) at
position 508. Accordingly, repair in this instance requires
reintroduction of the missing codon into the mutant.
[0366] To implement this Gene Repair Strategy, it is preferred that
an adenovirus/AAV vector system is introduced into the host cell,
cells or patient. Preferably, the system comprises a Cas9 (or Cas9
nickase) and the guide RNA along with a adenovirus/AAV vector
system comprising the homology repair template containing the F508
residue. This may be introduced into the subject via one of the
methods of delivery discussed earlier. The CRISPR-Cas system may be
guided by the CFTRdelta 508 chimeric guide RNA. It targets a
specific site of the CFTR genomic locus to be nicked or cleaved.
After cleavage, the repair template is inserted into the cleavage
site via homologous recombination correcting the deletion that
results in cystic fibrosis or causes cystic fibrosis related
symptoms. This strategy to direct delivery and provide systemic
introduction of CRISPR systems with appropriate guide RNAs can be
employed to target genetic mutations to edit or otherwise
manipulate genes that cause metabolic, liver, kidney and protein
diseases and disorders such as those in Table B.
[0367] Genome Editing
[0368] The CRISPR/Cas9 systems of the present invention can be used
to correct genetic mutations that were previously attempted with
limited success using TALEN and ZFN. For example, WO2013163628 A2,
Genetic Correction of Mutated Genes, published application of Duke
University describes efforts to correct, for example, a frameshift
mutation which causes a premature stop codon and a truncated gene
product that can be corrected via nuclease mediated non-homologous
end joining such as those responsible for Duchenne Muscular
Dystrophy, ("DMD") a recessive, fatal, X-linked disorder that
results in muscle degeneration due to mutations in the dystrophin
gene. The majority of dystrophin mutations that cause DMD are
deletions of exons that disrupt the reading frame and cause
premature translation termination in the dystrophin gene.
Dystrophin is a cytoplasmic protein that provides structural
stability to the dystroglycan complex of the cell membrane that is
responsible for regulating muscle cell integrity and function. The
dystrophin gene or "DMD gene" as used interchangeably herein is 2.2
megabases at locus Xp21. The primary transcription measures about
2,400 kb with the mature mRNA being about 14 kb. 79 exons code for
the protein which is over 3500 amino acids. Exon 51 is frequently
adjacent to frame-disrupting deletions in DMD patients and has been
targeted in clinical trials for oligonucleotide-based exon
skipping. A clinical trial for the exon 51 skipping compound
eteplirsen recently reported a significant functional benefit
across 48 weeks, with an average of 47% dystrophin positive fibers
compared to baseline. Mutations in exon 51 are ideally suited for
permanent correction by NHEJ-based genome editing.
[0369] The methods of US Patent Publication No. 20130145487
assigned to Cellectis, which relates to meganuclease variants to
cleave a target sequence from the human dystrophin gene (DMD), may
also be modified to for the CRISPR Cas system of the present
invention.
[0370] Blood
[0371] The present invention also contemplates delivering the
CRISPR-Cas system to the blood.
[0372] The plasma exosomes of Wahlgren et al. (Nucleic Acids
Research, 2012, Vol. 40, No. 17 e130) were previously described and
may be utilized to deliver the CRISPR Cas system to the blood.
[0373] The CRISPR Cas system of the present invention is also
contemplated to treat hemoglobinopathies, such as thalassemias and
sickle cell disease. See, e.g., International Patent Publication
No. WO 2013/126794 for potential targets that may be targeted by
the CRISPR Cas system of the present invention.
[0374] US Patent Publication Nos. 20110225664, 20110091441,
20100229252, 20090271881 and 20090222937 assigned to Cellectis,
relates to CREI variants, wherein at least one of the two I-CreI
monomers has at least two substitutions, one in each of the two
functional subdomains of the LAGLIDADG core domain (SEQ ID NO: 60)
situated respectively from positions 26 to 40 and 44 to 77 of
I-CreI, said variant being able to cleave a DNA target sequence
from the human interleukin-2 receptor gamma chain (IL2RG) gene also
named common cytokine receptor gamma chain gene or gamma C gene.
The target sequences identified in US Patent Publication Nos.
20110225664, 20110091441, 20100229252, 20090271881 and 20090222937
may be utilized for the CRISPR Cas system of the present
invention.
[0375] Severe Combined Immune Deficiency (SCID) results from a
defect in lymphocytes T maturation, always associated with a
functional defect in lymphocytes B (Cavazzana-Calvo et al., Annu.
Rev. Med., 2005, 56, 585-602; Fischer et al., Immunol. Rev., 2005,
203, 98-109). Overall incidence is estimated to 1 in 75 000 births.
Patients with untreated SCID are subject to multiple opportunist
micro-organism infections, and do generally not live beyond one
year. SCID can be treated by allogenic hematopoietic stem cell
transfer, from a familial donor. Histocompatibility with the donor
can vary widely. In the case of Adenosine Deaminase (ADA)
deficiency, one of the SCID forms, patients can be treated by
injection of recombinant Adenosine Deaminase enzyme.
[0376] Since the ADA gene has been shown to be mutated in SCID
patients (Giblett et al., Lancet, 1972, 2, 1067-1069), several
other genes involved in SCID have been identified (Cavazzana-Calvo
et al., Annu. Rev. Med., 2005, 56, 585-602; Fischer et al.,
Immunol. Rev., 2005, 203, 98-109). There are four major causes for
SCID: (i) the most frequent form of SCID, SCID-X1 (X-linked SCID or
X-SCID), is caused by mutation in the IL2RG gene, resulting in the
absence of mature T lymphocytes and NK cells. IL2RG encodes the
gamma C protein (Noguchi, et al., Cell, 1993, 73, 147-157), a
common component of at least five interleukin receptor complexes.
These receptors activate several targets through the JAK3 kinase
(Macchi et al., Nature, 1995, 377, 65-68), which inactivation
results in the same syndrome as gamma C inactivation; (ii) mutation
in the ADA gene results in a defect in purine metabolism that is
lethal for lymphocyte precursors, which in turn results in the
quasi absence of B, T and NK cells; (iii) V(D)J recombination is an
essential step in the maturation of immunoglobulins and T
lymphocytes receptors (TCRs). Mutations in Recombination Activating
Gene 1 and 2 (RAG1 and RAG2) and Artemis, three genes involved in
this process, result in the absence of mature T and B lymphocytes;
and (iv) Mutations in other genes such as CD45, involved in T cell
specific signaling have also been reported, although they represent
a minority of cases (Cavazzana-Calvo et al., Annu. Rev. Med., 2005,
56, 585-602; Fischer et al., Immunol. Rev., 2005, 203, 98-109).
[0377] Since when their genetic bases have been identified, the
different SCID forms have become a paradigm for gene therapy
approaches (Fischer et al., Immunol. Rev., 2005, 203, 98-109) for
two major reasons. First, as in all blood diseases, an ex vivo
treatment can be envisioned. Hematopoietic Stem Cells (HSCs) can be
recovered from bone marrow, and keep their pluripotent properties
for a few cell divisions. Therefore, they can be treated in vitro,
and then reinjected into the patient, where they repopulate the
bone marrow. Second, since the maturation of lymphocytes is
impaired in SCID patients, corrected cells have a selective
advantage. Therefore, a small number of corrected cells can restore
a functional immune system. This hypothesis was validated several
times by (i) the partial restoration of immune functions associated
with the reversion of mutations in SCID patients (Hirschhorn et
al., Nat. Genet., 1996, 13, 290-295; Stephan et al., N. Engl. J.
Med., 1996, 335, 1563-1567; Bousso et al., Proc. Natl., Acad. Sci.
USA, 2000, 97, 274-278; Wada et al., Proc. Natl. Acad. Sci. USA,
2001, 98, 8697-8702; Nishikomori et al., Blood, 2004, 103,
4565-4572), (ii) the correction of SCID-X1 deficiencies in vitro in
hematopoietic cells (Candotti et al., Blood, 1996, 87, 3097-3102;
Cavazzana-Calvo et al., Blood, 1996, Blood, 88, 3901-3909; Taylor
et al., Blood, 1996, 87, 3103-3107; Hacein-Bey et al., Blood, 1998,
92, 4090-4097), (iii) the correction of SCID-X1 (Soudais et al.,
Blood, 2000, 95, 3071-3077; Tsai et al., Blood, 2002, 100, 72-79),
JAK-3 (Bunting et al., Nat. Med., 1998, 4, 58-64; Bunting et al.,
Hum. Gene Ther., 2000, 11, 2353-2364) and RAG2 (Yates et al.,
Blood, 2002, 100, 3942-3949) deficiencies in vivo in animal models
and (iv) by the result of gene therapy clinical trials
(Cavazzana-Calvo et al., Science, 2000, 288, 669-672; Aiuti et al.,
Nat. Med., 2002; 8, 423-425; Gaspar et al., Lancet, 2004, 364,
2181-2187).
[0378] US Patent Publication No. 20110182867 assigned to the
Children's Medical Center Corporation and the President and Fellows
of Harvard College relates to methods and uses of modulating fetal
hemoglobin expression (HbF) in a hematopoietic progenitor cells via
inhibitors of BCL11A expression or activity, such as RNAi and
antibodies. The targets disclosed in US Patent Publication No.
20110182867, such as BCL11A, may be targeted by the CRISPR Cas
system of the present invention for modulating fetal hemoglobin
expression. See also Bauer et al. (Science 11 Oct. 2013: Vol. 342
no. 6155 pp. 253-257) and Xu et al. (Science 18 Nov. 2011: Vol. 334
no. 6058 pp. 993-996) for additional BCL11A targets.
[0379] Ears
[0380] The present invention also contemplates delivering the
CRISPR-Cas system to one or both ears.
[0381] Researchers are looking into whether gene therapy could be
used to aid current deafness treatments--namely, cochlear implants.
Deafness is often caused by lost or damaged hair cells that cannot
relay signals to auditory neurons. In such cases, cochlear implants
may be used to respond to sound and transmit electrical signals to
the nerve cells. But these neurons often degenerate and retract
from the cochlea as fewer growth factors are released by impaired
hair cells.
[0382] US patent application 20120328580 describes injection of a
pharmaceutical composition into the ear (e.g., auricular
administration), such as into the luminae of the cochlea (e.g., the
Scala media, Sc vestibulae, and Sc tympani), e.g., using a syringe,
e.g., a single-dose syringe. For example, one or more of the
compounds described herein can be administered by intratympanic
injection (e.g., into the middle ear), and/or injections into the
outer, middle, and/or inner ear. Such methods are routinely used in
the art, for example, for the administration of steroids and
antibiotics into human ears. Injection can be, for example, through
the round window of the ear or through the cochlear capsule. Other
inner ear administration methods are known in the art (see, e.g.,
Salt and Plontke, Drug Discovery Today, 10:1299-1306, 2005).
[0383] In another mode of administration, the pharmaceutical
composition can be administered in situ, via a catheter or pump. A
catheter or pump can, for example, direct a pharmaceutical
composition into the cochlear luminae or the round window of the
ear and/or the lumen of the colon. Exemplary drug delivery
apparatus and methods suitable for administering one or more of the
compounds described herein into an ear, e.g., a human ear, are
described by McKenna et al., (U.S. Publication No. 2006/0030837)
and Jacobsen et al., (U.S. Pat. No. 7,206,639). In some
embodiments, a catheter or pump can be positioned, e.g., in the ear
(e.g., the outer, middle, and/or inner ear) of a patient during a
surgical procedure. In some embodiments, a catheter or pump can be
positioned, e.g., in the ear (e.g., the outer, middle, and/or inner
ear) of a patient without the need for a surgical procedure.
[0384] Alternatively or in addition, one or more of the compounds
described herein can be administered in combination with a
mechanical device such as a cochlear implant or a hearing aid,
which is worn in the outer ear. An exemplary cochlear implant that
is suitable for use with the present invention is described by Edge
et al., (U.S. Publication No. 2007/0093878).
[0385] In some embodiments, the modes of administration described
above may be combined in any order and can be simultaneous or
interspersed.
[0386] Alternatively or in addition, the present invention may be
administered according to any of the Food and Drug Administration
approved methods, for example, as described in CDER Data Standards
Manual, version number 004 (which is available at
fda.give/cder/dsm/DRG/drg00301.htm).
[0387] In general, the cell therapy methods described in US patent
application 20120328580 can be used to promote complete or partial
differentiation of a cell to or towards a mature cell type of the
inner ear (e.g., a hair cell) in vitro. Cells resulting from such
methods can then be transplanted or implanted into a patient in
need of such treatment. The cell culture methods required to
practice these methods, including methods for identifying and
selecting suitable cell types, methods for promoting complete or
partial differentiation of selected cells, methods for identifying
complete or partially differentiated cell types, and methods for
implanting complete or partially differentiated cells are described
below.
[0388] Cells suitable for use in the present invention include, but
are not limited to, cells that are capable of differentiating
completely or partially into a mature cell of the inner ear, e.g.,
a hair cell (e.g., an inner and/or outer hair cell), when
contacted, e.g., in vitro, with one or more of the compounds
described herein. Exemplary cells that are capable of
differentiating into a hair cell include, but are not limited to
stem cells (e.g., inner ear stem cells, adult stem cells, bone
marrow derived stem cells, embryonic stem cells, mesenchymal stem
cells, skin stem cells, iPS cells, and fat derived stem cells),
progenitor cells (e.g., inner ear progenitor cells), support cells
(e.g., Deiters' cells, pillar cells, inner phalangeal cells, tectal
cells and Hensen's cells), and/or germ cells. The use of stem cells
for the replacement of inner ear sensory cells is described in Li
et al., (U.S. Publication No. 2005/0287127) and Li et al., (U.S.
patent Ser. No. 11/953,797). The use of bone marrow derived stem
cells for the replacement of inner ear sensory cells is described
in Edge et al., PCT/US2007/084654. iPS cells are described, e.g.,
at Takahashi et al., Cell, Volume 131, Issue 5, Pages 861-872
(2007); Takahashi and Yamanaka, Cell 126, 663-76 (2006); Okita et
al., Nature 448, 260-262 (2007); Yu, J. et al., Science
318(5858):1917-1920 (2007); Nakagawa et al., Nat. Biotechnol.
26:101-106 (2008); and Zaehres and Scholer, Cell 131(5):834-835
(2007).
[0389] Such suitable cells can be identified by analyzing (e.g.,
qualitatively or quantitatively) the presence of one or more tissue
specific genes. For example, gene expression can be detected by
detecting the protein product of one or more tissue-specific genes.
Protein detection techniques involve staining proteins (e.g., using
cell extracts or whole cells) using antibodies against the
appropriate antigen. In this case, the appropriate antigen is the
protein product of the tissue-specific gene expression. Although,
in principle, a first antibody (i.e., the antibody that binds the
antigen) can be labeled, it is more common (and improves the
visualization) to use a second antibody directed against the first
(e.g., an anti-IgG). This second antibody is conjugated either with
fluorochromes, or appropriate enzymes for colorimetric reactions,
or gold beads (for electron microscopy), or with the biotin-avidin
system, so that the location of the primary antibody, and thus the
antigen, can be recognized.
[0390] The CRISPR Cas molecules of the present invention may be
delivered to the ear by direct application of pharmaceutical
composition to the outer ear, with compositions modified from US
Published application, 20110142917. In some embodiments the
pharmaceutical composition is applied to the ear canal. Delivery to
the ear may also be refereed to as aural or otic delivery.
[0391] In some embodiments the RNA molecules of the invention are
delivered in liposome or lipofectin formulations and the like and
can be prepared by methods well known to those skilled in the art.
Such methods are described, for example, in U.S. Pat. Nos.
5,593,972, 5,589,466, and 5,580,859, which are herein incorporated
by reference.
[0392] Delivery systems aimed specifically at the enhanced and
improved delivery of siRNA into mammalian cells have been
developed, (see, for example, Shen et al FEBS Let. 2003,
539:111-114; Xia et al., Nat. Biotech. 2002, 20:1006-1010; Reich et
al., Mol. Vision. 2003, 9: 210-216; Sorensen et al., J. Mol. Biol.
2003, 327: 761-766; Lewis et al., Nat. Gen. 2002, 32: 107-108 and
Simeoni et al., NAR 2003, 31, 11: 2717-2724) and may be applied to
the present invention, siRNA has recently been successfully used
for inhibition of gene expression in primates (see for example.
Tolentino et al., Retina 24(4):660 which may also be applied to the
present invention.
[0393] Qi et al. discloses methods for efficient siRNA transfection
to the inner ear through the intact round window by a novel
proteidic delivery technology which may be applied to the CRISPR
Cas system of the present invention (see, e.g., Qi et al., Gene
Therapy (2013), 1-9). In particular, a TAT double stranded
RNA-binding domains (TAT-DRBDs), which can transfect Cy3-labeled
siRNA into cells of the inner ear, including the inner and outer
hair cells, crista ampullaris, macula utriculi and macula sacculi,
through intact round-window permeation was successful for
delivering double stranded siRNAs in vivo for treating various
inner ear ailments and preservation of hearing function. About 40
.mu.l of 10 mM RNA may be contemplated as the dosage for
administration to the ear.
[0394] According to Rejali et al. (Hear Res. 2007 June;
228(1-2):180-7), cochlear implant function can be improved by good
preservation of the spiral ganglion neurons, which are the target
of electrical stimulation by the implant and brain derived
neurotrophic factor (BDNF) has previously been shown to enhance
spiral ganglion survival in experimentally deafened ears. Rejali et
al. tested a modified design of the cochlear implant electrode that
includes a coating of fibroblast cells transduced by a viral vector
with a BDNF gene insert. To accomplish this type of ex vivo gene
transfer, Rejali et al. transduced guinea pig fibroblasts with an
adenovirus with a BDNF gene cassette insert, and determined that
these cells secreted BDNF and then attached BDNF-secreting cells to
the cochlear implant electrode via an agarose gel, and implanted
the electrode in the scala tympani. Rejali et al. determined that
the BDNF expressing electrodes were able to preserve significantly
more spiral ganglion neurons in the basal turns of the cochlea
after 48 days of implantation when compared to control electrodes
and demonstrated the feasibility of combining cochlear implant
therapy with ex vivo gene transfer for enhancing spiral ganglion
neuron survival. Such a system may be applied to the CRISPR Cas
system of the present invention for delivery to the ear.
[0395] Mukherjea et al. (Antioxidants & Redox Signaling, Volume
13, Number 5, 2010) document that knockdown of NOX3 using short
interfering (si) RNA abrogated cisplatin ototoxicity, as evidenced
by protection of OHCs from damage and reduced threshold shifts in
auditory brainstem responses (ABRs). Different doses of siNOX3
(0.3, 0.6, and 0.9 .mu.g) were administered to rats and NOX3
expression was evaluated by real time RT-PCR. The lowest dose of
NOX3 siRNA used (0.3 .mu.g) did not show any inhibition of NOX3
mRNA when compared to transtympanic administration of scrambled
siRNA or untreated cochleae. However, administration of the higher
doses of NOX3 siRNA (0.6 and 0.9 .mu.g) reduced NOX3 expression
compared to control scrambled siRNA. Such a system may be applied
to the CRISPR Cas system of the present invention for transtympanic
administration with a dosage of about 2 mg to about 4 mg of CRISPR
Cas for administration to a human.
[0396] Jung et al. (Molecular Therapy, vol. 21 no. 4, 834-841 April
2013) demonstrate that Hes5 levels in the utricle decreased after
the application of siRNA and that the number of hair cells in these
utricles was significantly larger than following control treatment.
The data suggest that siRNA technology may be useful for inducing
repair and regeneration in the inner ear and that the Notch
signaling pathway is a potentially useful target for specific gene
expression inhibition. Jung et al. injected 8 .mu.g of Hes5 siRNA
in 2 .mu.l volume, prepared by adding sterile normal saline to the
lyophilized siRNA to a vestibular epithelium of the ear. Such a
system may be applied to the CRISPR Cas system of the present
invention for administration to the vestibular epithelium of the
ear with a dosage of about 1 to about 30 mg of CRISPR Cas for
administration to a human.
[0397] Eyes
[0398] The present invention also contemplates delivering the
CRISPR-Cas system to one or both eyes.
[0399] In yet another aspect of the invention, the CRISPR-Cas
system may be used to correct ocular defects that arise from
several genetic mutations further described in Genetic Diseases of
the Eye, Second Edition, edited by Elias I. Traboulsi, Oxford
University Press, 2012.
[0400] For administration to the eye, lentiviral vectors, in
particular equine infectious anemia viruses (EIAV) are particularly
preferred.
[0401] In another embodiment, minimal non-primate lentiviral
vectors based on the equine infectious anemia virus (EIAV) are also
contemplated, especially for ocular gene therapy (see, e.g.,
Balagaan, J Gene Med 2006; 8: 275-285, Published online 21 Nov.
2005 in Wiley InterScience (www.interscience.wiley.com). DOI:
10.1002/jgm.845). The vectors are contemplated to have
cytomegalovirus (CMV) promoter driving expression of the target
gene. Intracameral, subretinal, intraocular and intravitreal
injections are all contemplated (see, e.g., Balagaan, J Gene Med
2006; 8: 275-285, Published online 21 Nov. 2005 in Wiley
InterScience (www.interscience.wiley.com). DOI: 10.1002/jgm.845).
Intraocular injections may be performed with the aid of an
operating microscope. For subretinal and intravitreal injections,
eyes may be prolapsed by gentle digital pressure and fundi
visualised using a contact lens system consisting of a drop of a
coupling medium solution on the cornea covered with a glass
microscope slide coverslip. For subretinal injections, the tip of a
10-mm 34-gauge needle, mounted on a 5-.mu.l Hamilton syringe may be
advanced under direct visualisation through the superior equatorial
sclera tangentially towards the posterior pole until the aperture
of the needle was visible in the subretinal space. Then, 2 .mu.l of
vector suspension may be injected to produce a superior bullous
retinal detachment, thus confirming subretinal vector
administration. This approach creates a self-sealing sclerotomy
allowing the vector suspension to be retained in the subretinal
space until it is absorbed by the RPE, usually within 48 h of the
procedure. This procedure may be repeated in the inferior
hemisphere to produce an inferior retinal detachment. This
technique results in the exposure of approximately 70% of
neurosensory retina and RPE to the vector suspension. For
intravitreal injections, the needle tip may be advanced through the
sclera 1 mm posterior to the corneoscleral limbus and 2 .mu.l of
vector suspension injected into the vitreous cavity. For
intracameral injections, the needle tip may be advanced through a
corneoscleral limbal paracentesis, directed towards the central
cornea, and 2 .mu.l of vector suspension may be injected. For
intracameral injections, the needle tip may be advanced through a
corneoscleral limbal paracentesis, directed towards the central
cornea, and 2 .mu.l of vector suspension may be injected. These
vectors may be injected at titres of either 1.0-1.4.times.10.sup.10
or 1.0-1.4.times.10.sup.9 transducing units (TU)/ml.
[0402] In another embodiment, RetinoStat.RTM., an equine infectious
anemia virus-based lentiviral gene therapy vector that expresses
angiostatic proteins endostain and angiostatin that is delivered
via a subretinal injection for the treatment of the web form of
age-related macular degeneration is also contemplated (see, e.g.,
Binley et al., HUMAN GENE THERAPY 23:980-991 (September 2012)).
Such a vector may be modified for the CRISPR-Cas system of the
present invention. Each eye may be treated with either
RetinoStat.RTM. at a dose of 1.1.times.10.sup.5 transducing units
per eye (TU/eye) in a total volume of 100 .mu.l.
[0403] In another embodiment, an E1-, partial E3-, E4-deleted
adenoviral vector may be contemplated for delivery to the eye.
Twenty-eight patients with advanced neovascular age-related macular
degeneration (AMD) were given a single intravitreous injection of
an E1-, partial E3-, E4-deleted adenoviral vector expressing human
pigment ep-ithelium-derived factor (AdPEDF.11) (see, e.g.,
Campochiaro et al., Human Gene Therapy 17:167-176 (February 2006)).
Doses ranging from 10.sup.6 to 10.sup.9.5 particle units (PU) were
investigated and there were no serious adverse events related to
AdPEDF.11 and no dose-limiting toxicities (see, e.g., Campochiaro
et al., Human Gene Therapy 17:167-176 (February 2006)). Adenoviral
vector-mediated ocular gene transfer appears to be a viable
approach for the treatment of ocular disorders and could be applied
to the CRISPR Cas system.
[0404] In another embodiment, the sd-rxRNA.RTM. system of RXi
Pharmaceuticals may be used/and or adapted for delivering CRISPR
Cas to the eye. In this system, a single intravitreal
administration of 3 .mu.g of sd-rxRNA results in sequence-specific
reduction of PPIB mRNA levels for 14 days. The the sd-rxRNA.RTM.
system may be applied to the CRISPR Cas system of the present
invention, contemplating a dose of about 3 to 20 mg of CRISPR
administered to a human.
[0405] Millington-Ward et al. (Molecular Therapy, vol. 19 no. 4,
642-649 April 2011) describes adeno-associated virus (AAV) vectors
to deliver an RNA interference (RNAi)-based rhodopsin suppressor
and a codon-modified rhodopsin replacement gene resistant to
suppression due to nucleotide alterations at degenerate positions
over the RNAi target site. An injection of either
6.0.times.10.sup.9 vp or 1.8.times.10.sup.10 vp AAV were
subretinally injected into the eyes by Millington-Ward et al. The
AAV vectors of Millington-Ward et al. may be applied to the CRISPR
Cas system of the present invention, contemplating a dose of about
2.times.10.sup.11 to about 6.times.10.sup.13 vp administered to a
human.
[0406] Dalkara et al. (Sci Transl Med 5, 189ra76 (2013)) also
relates to in vivo directed evolution to fashion an AAV vector that
delivers wild-type versions of defective genes throughout the
retina after noninjurious injection into the eyes' vitreous humor.
Dalkara describes a a 7mer peptide display library and an AAV
library constructed by DNA shuffling of cap genes from AAV1, 2, 4,
5, 6, 8, and 9. The rcAAV libraries and rAAV vectors expressing GFP
under a CAG or Rho promoter were packaged and and
deoxyribonuclease-resistant genomic titers were obtained through
quantitative PCR. The libraries were pooled, and two rounds of
evolution were performed, each consisting of initial library
diversification followed by three in vivo selection steps. In each
such step, P30 rho-GFP mice were intravitreally injected with 2 ml
of iodixanol-purified, phosphate-buffered saline (PBS)-dialyzed
library with a genomic titer of about 1.times.10.sup.12 vg/ml. The
AAV vectors of Dalkara et al. may be applied to the CRISPR Cas
system of the present invention, contemplating a dose of about
1.times.10.sup.15 to about 1.times.10.sup.16 vg/ml administered to
a human.
[0407] In another embodiment, the rhodopsin gene may be targeted
for the treatment of retinitis pigmentosa (RP), wherein the system
of US Patent Publication No. 20120204282 assigned to Sangamo
BioSciences, Inc. may be modified in accordance of the CRISPR Cas
system of the present invention.
[0408] In another embodiment, the methods of US Patent Publication
No. 20130183282 assigned to Cellectis, which is directed to methods
of cleaving a target sequence from the human rhodopsin gene, may
also be modified to the CRISPR Cas system of the present
invention.
[0409] US Patent Publication No. 20130202678 assigned to Academia
Sinica relates to methods for treating retinopathies and
sight-threatening ophthalmologic disorders relating to delivering
of the Puf-A gene (which is expressed in retinal ganglion and
pigmented cells of eye tissues and displays a unique anti-apoptotic
activity) to the sub-retinal or intravitreal space in the eye. In
particular, desirable targets are zgc:193933, prdm1a, spata2,
tex10, rbb4, ddx3, zp2.2, Blimp-1 and HtrA2, all of which may be
targeted by the CRISPR Cas system of the present invention.
[0410] Wu (Cell Stem Cell, 13:659-62, 2013) designed a guide RNA
that led Cas9 to a single base pair mutation that causes cataracts
in mice, where it induced DNA cleavage. Then using either the other
wild-type allele or oligos given to the zygotes repair mechanisms
corrected the sequence of the broken allele and corrected the
cataract-causing genetic defect in mutant mouse.
[0411] US Patent Publication No. 20120159653, describes use of zinc
finger nucleases to genetically modify cells, animals and proteins
associated with macular degeration (MD). Macular degeneration (MD)
is the primary cause of visual impairment in the elderly, but is
also a hallmark symptom of childhood diseases such as Stargardt
disease, Sorsby fundus, and fatal childhood neurodegenerative
diseases, with an age of onset as young as infancy. Macular
degeneration results in a loss of vision in the center of the
visual field (the macula) because of damage to the retina.
Currently existing animal models do not recapitulate major
hallmarks of the disease as it is observed in humans. The available
animal models comprising mutant genes encoding proteins associated
with MD also produce highly variable phenotypes, making
translations to human disease and therapy development
problematic.
[0412] One aspect of US Patent Publication No. 20120159653 relates
to editing of any chromosomal sequences that encode proteins
associated with MD which may be applied to the CRISPR Cas system of
the present invention. The proteins associated with MD are
typically selected based on an experimental association of the
protein associated with MD to an MD disorder. For example, the
production rate or circulating concentration of a protein
associated with MD may be elevated or depressed in a population
having an MD disorder relative to a population lacking the MD
disorder. Differences in protein levels may be assessed using
proteomic techniques including but not limited to Western blot,
immunohistochemical staining, enzyme linked immunosorbent assay
(ELISA), and mass spectrometry. Alternatively, the proteins
associated with MD may be identified by obtaining gene expression
profiles of the genes encoding the proteins using genomic
techniques including but not limited to DNA microarray analysis,
serial analysis of gene expression (SAGE), and quantitative
real-time polymerase chain reaction (Q-PCR).
[0413] By way of non-limiting example, proteins associated with MD
include but are not limited to the following proteins: (ABCA4)
ATP-binding cassette, sub-family A (ABC1), member 4 ACHM1
achromatopsia (rod monochromacy) 1 ApoE Apolipoprotein E (ApoE)
C1QTNF5 (CTRP5) C1q and tumor necrosis factor related protein 5
(CIQTNF5) C2 Complement component 2 (C2) C3 Complement components
(C3) CCL2 Chemokine (C-C motif) Ligand 2 (CCL2) CCR2 Chemokine (C-C
motif) receptor 2 (CCR2) CD36 Cluster of Differentiation 36 CFB
Complement factor B CFH Complement factor CFH H CFHRI complement
factor H-related 1 CFHR3 complement factor H-related 3 CNGB3 cyclic
nucleotide gated channel beta 3 CP ceruloplasmin (CP) CRP C
reactive protein (CRP) CST3 cystatin C or cystatin 3 (CST3) CTSD
Cathepsin D (CTSD) CX3CR1 chemokine (C-X3-C motif) receptor 1
ELOVL4 Elongation of very long chain fatty acids 4 ERCC6 excision
repair cross-complementing rodent repair deficiency,
complementation group 6 FBLN5 Fibulin-5 FBLN5 Fibulin 5 FBLN6
Fibulin 6 FSCN2 fascin (FSCN2) HMCN1 Hemicentrin 1 HMCN1 hemicentin
1 HTRA1 HtrA serine peptidase 1 (HTRA1) HTRA1 HtrA serine peptidase
1 IL-6 Interleukin 6 IL-8 Interleukin 8 LOC387715 Hypothetical
protein PLEKHA1 Pleckstrin homology domain-containing family A
member 1 (PLEKHA1) PROM1 Prominin 1(PROM1 or CD133) PRPH2
Peripherin-2 RPGR retinitis pigmentosa GTPase regulator SERPING1
serpin peptidase inhibitor. clade G, member 1 (C1-inhibitor) TCOF1
Treacle TIMP3 Metalloproteinase inhibitor 3 (TIMP3) TLR3 Toll-like
receptor 3
[0414] The identity of the protein associated with MD whose
chromosomal sequence is edited can and will vary. In preferred
embodiments, the proteins associated with MD whose chromosomal
sequence is edited may be the ATP-binding cassette, sub-family A
(ABC1) member 4 protein (ABCA4) encoded by the ABCR gene, the
apolipoprotein E protein (APOE) encoded by the APOE gene, the
chemokine (C-C motif) Ligand 2 protein (CCL2) encoded by the CCL2
gene, the chemokine (C-C motif) receptor 2 protein (CCR2) encoded
by the CCR2 gene, the ceruloplasmin protein (CP) encoded by the CP
gene, the cathepsin D protein (CTSD) encoded by the CTSD gene, or
the metalloproteinase inhibitor 3 protein (TIMP3) encoded by the
TIMP3 gene. In an exemplary embodiment, the genetically modified
animal is a rat, and the edited chromosomal sequence encoding the
protein associated with MD may be: (ABCA4) ATP-binding cassette,
NM_000350 sub-family A (ABC1), member 4 APOE Apolipoprotein E
NM_138828 (APOE) CCL2 Chemokine (C-C NM_031530 motif) Ligand 2
(CCL2) CCR2 Chemokine (C-C NM_021866 motif) receptor 2 (CCR2) CP
ceruloplasmin (CP) NM_012532 CTSD Cathepsin D (CTSD) NM_134334
TIMP3 Metalloproteinase NM_012886 inhibitor 3 (TIMP3) The animal or
cell may comprise 1, 2, 3, 4, 5, 6, 7 or more disrupted chromosomal
sequences encoding a protein associated with MD and zero, 1, 2, 3,
4, 5, 6, 7 or more chromosomally integrated sequences encoding the
disrupted protein associated with MD.
[0415] The edited or integrated chromosomal sequence may be
modified to encode an altered protein associated with MD. Several
mutations in MD-related chromosomal sequences have been associated
with MD. Non-limiting examples of mutations in chromosomal
sequences associated with MD include those that may cause MD
including in the ABCR protein, E471K (i.e. glutamate at position
471 is changed to lysine), R1129L (i.e. arginine at position 1129
is changed to leucine), T1428M (i.e. threonine at position 1428 is
changed to methionine), R1517S (i.e. arginine at position 1517 is
changed to serine), I11562T (i.e. isoleucine at position 1562 is
changed to threonine), and G1578R (i.e. glycine at position 1578 is
changed to arginine); in the CCR2 protein, V64I (i.e. valine at
position 192 is changed to isoleucine); in CP protein, G969B (i.e.
glycine at position 969 is changed to asparagine or aspartate); in
TIMP3 protein, S156C (i.e. serine at position 156 is changed to
cysteine), G166C (i.e. glycine at position 166 is changed to
cysteine), G167C (i.e. glycine at position 167 is changed to
cysteine), Y168C (i.e. tyrosine at position 168 is changed to
cysteine), S170C (i.e. serine at position 170 is changed to
cysteine), Y172C (i.e. tyrosine at position 172 is changed to
cysteine) and S181C (i.e. serine at position 181 is changed to
cysteine). Other associations of genetic variants in MD-associated
genes and disease are known in the art.
[0416] Heart
[0417] The present invention also contemplates delivering the
CRISPR-Cas system to the heart. For the heart, a myocardium tropic
adena-associated virus (AAVM) is preferred, in particular AAVM41
which showed preferential gene transfer in the heart (see, e.g.,
Lin-Yanga et al., PNAS, Mar. 10, 2009, vol. 106, no. 10).
Administration may be systemic or local. A dosage of about
1-10.times.10.sup.14 vector genomes are contemplated for systemic
administration. See also, e.g., Eulalio et al. (2012) Nature 492:
376 and Somasuntharam et al. (2013) Biomaterials 34: 7790.
[0418] For example, US Patent Publication No. 20110023139,
describes use of zinc finger nucleases to genetically modify cells,
animals and proteins associated with cardiovascular disease.
Cardiovascular diseases generally include high blood pressure,
heart attacks, heart failure, and stroke and TIA. Any chromosomal
sequence involved in cardiovascular disease or the protein encoded
by any chromosomal sequence involved in cardiovascular disease may
be utilized in the methods described in this disclosure. The
cardiovascular-related proteins are typically selected based on an
experimental association of the cardiovascular-related protein to
the development of cardiovascular disease. For example, the
production rate or circulating concentration of a
cardiovascular-related protein may be elevated or depressed in a
population having a cardiovascular disorder relative to a
population lacking the cardiovascular disorder. Differences in
protein levels may be assessed using proteomic techniques including
but not limited to Western blot, immunohistochemical staining,
enzyme linked immunosorbent assay (ELISA), and mass spectrometry.
Alternatively, the cardiovascular-related proteins may be
identified by obtaining gene expression profiles of the genes
encoding the proteins using genomic techniques including but not
limited to DNA microarray analysis, serial analysis of gene
expression (SAGE), and quantitative real-time polymerase chain
reaction (Q-PCR).
[0419] By way of example, the chromosomal sequence may comprise,
but is not limited to, ILIB (interleukin 1, beta), XDH (xanthine
dehydrogenase), TP53 (tumor protein p53), PTGIS (prostaglandin 12
(prostacyclin) synthase), MB (myoglobin), IL4 (interleukin 4),
ANGPT1 (angiopoietin 1), ABCG8 (ATP-binding cassette, sub-family G
(WHITE), member 8), CTSK (cathepsin K), PTGIR (prostaglandin 12
(prostacyclin) receptor (IP)), KCNJ11 (potassium
inwardly-rectifying channel, subfamily J, member 11), INS
(insulin), CRP (C-reactive protein, pentraxin-related), PDGFRB
(platelet-derived growth factor receptor, beta polypeptide). CCNA2
(cyclin A2), PDGFB (platelet-derived growth factor beta polypeptide
(simian sarcoma viral (v-sis) oncogene homolog)), KCNJ5 (potassium
inwardly-rectifying channel, subfamily J, member 5), KCNN3
(potassium intermediate/small conductance calcium-activated
channel, subfamily N, member 3), CAPN10 (calpain 10), PTGES
(prostaglandin E synthase), ADRA2B (adrenergic, alpha-2B-,
receptor), ABCG5 (ATP-binding cassette, sub-family G (WHITE),
member 5), PRDX2 (peroxiredoxin 2), CAPN5 (calpain 5), PARP14 (poly
(ADP-ribose) polymerase family, member 14), MEX3C (mex-3 homolog C
(C. elegans)), ACE angiotensin I converting enzyme
(peptidyl-dipeptidase A) 1), TNF (tumor necrosis factor (TNF
superfamily, member 2)), IL6 (interleukin 6 (interferon, beta 2)),
STN (statin), SERPINE1 (serpin peptidase inhibitor, clade E (nexin,
plasminogen activator inhibitor type 1), member 1), ALB (albumin),
ADIPOQ (adiponectin, C1Q and collagen domain containing), APOB
(apolipoprotein B (including Ag(x) antigen)), APOE (apolipoprotein
E), LEP (leptin), MTHFR (5,10-methylenetetrahydrofolate reductase
(NADPH)), APOA1 (apolipoprotein A-I), EDN1 (endothelin 1), NPPB
(natriuretic peptide precursor B), NOS3 (nitric oxide synthase 3
(endothelial cell)), PPARG (peroxisome proliferator-activated
receptor gamma), PLAT (plasminogen activator, tissue), PTGS2
(prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase
and cyclooxygenase)), CETP (cholesteryl ester transfer protein,
plasma), AGTR1 (angiotensin II receptor, type 1), HMGCR
(3-hydroxy-3-methylglutaryl-Coenzyme A reductase), IGF1
(insulin-like growth factor 1 (somatomedin C)), SELE (selectin E),
REN (renin), PPARA (peroxisome proliferator-activated receptor
alpha), PON1 (paraoxonase 1), KNG1 (kininogen 1), CCL2 (chemokine
(C-C motif) ligand 2), LPL (lipoprotein lipase), VWF (von
Willebrand factor), F2 (coagulation factor II (thrombin)), ICAM1
(intercellular adhesion molecule 1), TGFB1 (transforming growth
factor, beta 1), NPPA (natriuretic peptide precursor A), IL10
(interleukin 10), EPO (erythropoietin), SOD1 (superoxide dismutase
1, soluble), VCAM1 (vascular cell adhesion molecule 1), IFNG
(interferon, gamma), LPA (lipoprotein, Lp(a)), MPO
(myeloperoxidase), ESR1 (estrogen receptor 1), MAPK1
(mitogen-activated protein kinase 1), HP (haptoglobin), F3
(coagulation factor III (thromboplastin, tissue factor)), CST3
(cystatin C), COG2 (component of oligomeric golgi complex 2), MMP9
(matrix metallopeptidase 9 (gelatinase B, 92 kDa gelatinase, 92 kDa
type IV collagenase)), SERPINC1 (serpin peptidase inhibitor, clade
C (antithrombin), member 1), F8 (coagulation factor VIII,
procoagulant component), HMOX1 (heme oxygenase (decycling) 1),
APOC3 (apolipoprotein C-III), IL8 (interleukin 8), PROK1
(prokineticin 1), CBS (cystathionine-beta-synthase), NOS2 (nitric
oxide synthase 2, inducible), TLR4 (toll-like receptor 4), SELP
(selectin P (granule membrane protein 140 kDa, antigen CD62)),
ABCA1 (ATP-binding cassette, sub-family A (ABC1), member 1), AGT
(angiotensinogen (serpin peptidase inhibitor, clade A, member 8)),
LDLR (low density lipoprotein receptor), GPT (glutamic-pyruvate
transaminase (alanine aminotransferase)), VEGFA (vascular
endothelial growth factor A), NR3C2 (nuclear receptor subfamily 3,
group C, member 2), IL18 (interleukin 18 (interferon-gamma-inducing
factor)), NOS1 (nitric oxide synthase 1 (neuronal)), NR3C1 (nuclear
receptor subfamily 3, group C, member 1 (glucocorticoid receptor)),
FGB (fibrinogen beta chain), HGF (hepatocyte growth factor
(hepapoietin A; scatter factor)), IL1A (interleukin 1, alpha), RETN
(resistin), AKT1 (v-akt murine thymoma viral oncogene homolog 1),
LIPC (lipase, hepatic), HSPD1 (heat shock 60 kDa protein 1
(chaperonin)), MAPK14 (mitogen-activated protein kinase 14), SPP1
(secreted phosphoprotein 1), ITGB3 (integrin, beta 3 (platelet
glycoprotein 111a, antigen CD61)), CAT (catalase), UTS2 (urotensin
2), THBD (thrombomodulin), F10 (coagulation factor X), CP
(ceruloplasmin (ferroxidase)), TNFRSF11B (tumor necrosis factor
receptor superfamily, member 11b), EDNRA (endothelin receptor type
A), EGFR (epidermal growth factor receptor (erythroblastic leukemia
viral (v-erb-b) oncogene homolog, avian)), MMP2 (matrix
metallopeptidase 2 (gelatinase A, 72 kDa gelatinase, 72 kDa type IV
collagenase)), PLG (plasminogen), NPY (neuropeptide Y), RHOD (ras
homolog gene family, member D), MAPK8 (mitogen-activated protein
kinase 8), MYC (v-myc myelocytomatosis viral oncogene homolog
(avian)), FN1 (fibronectin 1), CMA1 (chymase 1, mast cell), PLAU
(plasminogen activator, urokinase), GNB3 (guanine nucleotide
binding protein (G protein), beta polypeptide 3), ADRB2
(adrenergic, beta-2-, receptor, surface), APOA5 (apolipoprotein
A-V), SOD2 (superoxide dismutase 2, mitochondrial), F5 (coagulation
factor V (proaccelerin, labile factor)), VDR (vitamin D
(1,25-dihydroxyvitamin D3) receptor), ALOX5 (arachidonate
5-lipoxygenase), HLA-DRB1 (major histocompatibility complex, class
II, DR beta 1), PARP1 (poly (ADP-ribose) polymerase 1), CD40LG
(CD40 ligand), PON2 (paraoxonase 2), AGER (advanced glycosylation
end product-specific receptor), IRS1 (insulin receptor substrate
1), PTGS1 (prostaglandin-endoperoxide synthase 1 (prostaglandin G/H
synthase and cyclooxygenase)), ECE1 (endothelin converting enzyme
1), F7 (coagulation factor VII (serum prothrombin conversion
accelerator)), URN (interleukin 1 receptor antagonist), EPHX2
(epoxide hydrolase 2, cytoplasmic), IGFBP1 (insulin-like growth
factor binding protein 1), MAPK10 (mitogen-activated protein kinase
10), FAS (Fas (TNF receptor superfamily, member 6)), ABCB1
(ATP-binding cassette, sub-family B (MDR/TAP), member 1), JUN (jun
oncogene), IGFBP3 (insulin-like growth factor binding protein 3),
CD14 (CD14 molecule), PDE5A (phosphodiesterase 5A, cGMP-specific),
AGTR2 (angiotensin II receptor, type 2), CD40 (CD40 molecule, TNF
receptor superfamily member 5), LCAT (lecithin-cholesterol
acyltransferase), CCR5 (chemokine (C-C motif) receptor 5), MMP1
(matrix metallopeptidase 1 (interstitial collagenase)), TIMP1 (TIMP
metallopeptidase inhibitor 1), ADM (adrenomedullin), DYT10
(dystonia 10), STAT3 (signal transducer and activator of
transcription 3 (acute-phase response factor)), MMP3 (matrix
metallopeptidase 3 (stromelysin 1, progelatinase)), ELN (elastin),
USF1 (upstream transcription factor 1), CFH (complement factor H),
HSPA4 (heat shock 70 kDa protein 4), MMP12 (matrix metallopeptidase
12 (macrophage elastase)), MME (membrane metallo-endopeptidase),
F2R (coagulation factor II (thrombin) receptor), SELL (selectin L),
CTSB (cathepsin B), ANXA5 (annexin A5), ADRB1 (adrenergic, beta-1-,
receptor), CYBA (cytochrome b-245, alpha polypeptide), FGA
(fibrinogen alpha chain), GGT1 (gamma-glutamyltransferase 1), LIPG
(lipase, endothelial), HIF1A (hypoxia inducible factor 1, alpha
subunit (basic helix-loop-helix transcription factor)), CXCR4
(chemokine (C-X-C motif) receptor 4), PROC (protein C (inactivator
of coagulation factors Va and VIIIa)), SCARB1 (scavenger receptor
class B, member 1), CD79A (CD79a molecule,
immunoglobulin-associated alpha), PLTP (phospholipid transfer
protein), ADD1 (adducin 1 (alpha)), FGG (fibrinogen gamma chain),
SAA1 (serum amyloid A1), KCNH2 (potassium voltage-gated channel,
subfamily H (eag-related), member 2), DPP4 (dipeptidyl-peptidase
4), G6PD (glucose-6-phosphate dehydrogenase), NPR1 (natriuretic
peptide receptor A/guanylate cyclase A (atrionatriuretic peptide
receptor A)), VTN (vitronectin), KIAA0101 (KIAA0101), FOS (FBJ
murine osteosarcoma viral oncogene homolog), TLR2 (toll-like
receptor 2), PPIG (peptidylprolyl isomerase G (cyclophilin G)),
IL1R (interleukin 1 receptor, type I), AR (androgen receptor),
CYP1A1 (cytochrome P450, family 1, subfamily A, polypeptide 1),
SERPINA1 (serpin peptidase inhibitor, clade A (alpha-1
antiproteinase, antitrypsin), member 1), MTR
(5-methyltetrahydrofolate-homocysteine methyltransferase), RBP4
(retinol binding protein 4, plasma), APOA4 (apolipoprotein A-IV),
CDKN2A (cyclin-dependent kinase inhibitor 2A (melanoma, p16,
inhibits CDK4)), FGF2 (fibroblast growth factor 2 (basic)), EDNRB
(endothelin receptor type B), ITGA2 (integrin, alpha 2 (CD49B,
alpha 2 subunit of VLA-2 receptor)), CABIN1 (calcineurin binding
protein 1), SHBG (sex hormone-binding globulin), HMGB1
(high-mobility group box 1), HSP90B2P (heat shock protein 90 kDa
beta (Grp94), member 2 (pseudogene)), CYP3A4 (cytochrome P450,
family 3, subfamily A, polypeptide 4), GJA1 (gap junction protein,
alpha 1, 43 kDa), CAV1 (caveolin 1, caveolae protein, 22 kDa), ESR2
(estrogen receptor 2 (ER beta)), LTA (lymphotoxin alpha (TNF
superfamily, member 1)), GDF15 (growth differentiation factor 15),
BDNF (brain-derived neurotrophic factor), CYP2D6 (cytochrome P450,
family 2, subfamily D, polypeptide 6), NGF (nerve growth factor
(beta polypeptide)), SP1 (Sp1 transcription factor), TGIF1
(TGFB-induced factor homeobox 1), SRC (v-src sarcoma
(Schmidt-Ruppin A-2) viral oncogene homolog (avian)), EGF
(epidermal growth factor (beta-urogastrone)), PIK3CG
(phosphoinositide-3-kinase, catalytic, gamma polypeptide), HLA-A
(major histocompatibility complex, class I, A), KCNQ1 (potassium
voltage-gated channel, KQT-like subfamily, member 1), CNR1
(cannabinoid receptor 1 (brain)), FBN1 (fibrillin 1), CHKA (choline
kinase alpha), BEST1 (bestrophin 1), APP (amyloid beta (A4)
precursor protein), CTNNB1 (catenin (cadherin-associated protein),
beta 1, 88 kDa), IL2 (interleukin 2), CD36 (CD36 molecule
(thrombospondin receptor)), PRKAB1 (protein kinase, AMP-activated,
beta 1 non-catalytic subunit), TPO (thyroid peroxidase), ALDH7A1
(aldehyde dehydrogenase 7 family, member A1), CX3CR1 (chemokine
(C-X3-C motif) receptor 1), TH (tyrosine hydroxylase), F9
(coagulation factor IX), GH1 (growth hormone 1), TF (transferrin),
HFE (hemochromatosis), IL17A (interleukin 17A), PTEN (phosphatase
and tensin homolog), GSTM1 (glutathione S-transferase mu 1), DMD
(dystrophin), GATA4 (GATA binding protein 4), F13A1 (coagulation
factor XIII, A1 polypeptide), TTR (transthyretin), FABP4 (fatty
acid binding protein 4, adipocyte), PON3 (paraoxonase 3), APOC1
(apolipoprotein C-I), INSR (insulin receptor), TNFRSF1B (tumor
necrosis factor receptor superfamily, member 1B), HTR2A
(5-hydroxytryptamine (serotonin) receptor 2A), CSF3 (colony
stimulating factor 3 (granulocyte)), CYP2C9 (cytochrome P450,
family 2, subfamily C, polypeptide 9), TXN (thioredoxin), CYP11B2
(cytochrome P450, family 11, subfamily B, polypeptide 2), PTH
(parathyroid hormone), CSF2 (colony stimulating factor 2
(granulocyte-macrophage)), KDR (kinase insert domain receptor (a
type III receptor tyrosine kinase)), PLA2G2A (phospholipase A2,
group IIA (platelets, synovial fluid)), B2M (beta-2-microglobulin),
THBS1 (thrombospondin 1), GCG (glucagon), RHOA (ras homolog gene
family, member A), ALDH2 (aldehyde dehydrogenase 2 family
(mitochondrial)), TCF7L2 (transcription factor 7-like 2 (T-cell
specific, HMG-box)), BDKRB2 (bradykinin receptor B2), NFE2L2
(nuclear factor (erythroid-derived 2)-like 2), NOTCH1 (Notch
homolog 1, translocation-associated (Drosophila)). UGT1A1 (UDP
glucuronosyltransferase 1 family, polypeptide A1), IFNA1
(interferon, alpha 1), PPARD (peroxisome proliferator-activated
receptor delta), SIRT1 (sirtuin (silent mating type information
regulation 2 homolog) 1 (S. cerevisiae)), GNRH1
(gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)),
PAPPA (pregnancy-associated plasma protein A, pappalysin 1), ARR3
(arrestin 3, retinal (X-arrestin)), NPPC (natriuretic peptide
precursor C), AHSP (alpha hemoglobin stabilizing protein), PTK2
(PTK2 protein tyrosine kinase 2), IL13 (interleukin 13), MTOR
(mechanistic target of rapamycin (serine/threonine kinase)), ITGB2
(integrin, beta 2 (complement component 3 receptor 3 and 4
subunit)), GSTT1 (glutathione S-transferase theta 1), IL6ST
(interleukin 6 signal transducer (gp130, oncostatin M receptor)),
CPB2 (carboxypeptidase B2 (plasma)), CYP1A2 (cytochrome P450,
family 1, subfamily A, polypeptide 2), HNF4A (hepatocyte nuclear
factor 4, alpha), SLC6A4 (solute carrier family 6 (neurotransmitter
transporter, serotonin), member 4), PLA2G6 (phospholipase A2, group
VI (cytosolic, calcium-independent)), TNFSF11 (tumor necrosis
factor (ligand) superfamily, member 11), SLC8A1 (solute carrier
family 8 (sodium/calcium exchanger), member 1), F2RL1 (coagulation
factor II (thrombin) receptor-like 1), AKRJA1 (aldo-keto reductase
family 1, member A1 (aldehyde reductase)), ALDH9A1 (aldehyde
dehydrogenase 9 family, member A1), BGLAP (bone
gamma-carboxyglutamate (gla) protein), MTTP (microsomal
triglyceride transfer protein), MTRR
(5-methyltetrahydrofolate-homocysteine methyltransferase
reductase), SULT1A3 (sulfotransferase family, cytosolic, 1A,
phenol-preferring, member 3), RAGE (renal tumor antigen), C4B
(complement component 4B (Chido blood group), P2RY12 (purinergic
receptor P2Y, G-protein coupled, 12), RNLS (renalase, FAD-dependent
amine oxidase), CREB1 (cAMP responsive element binding protein 1),
POMC (proopiomelanocortin), RAC1 (ras-related C3 botulinum toxin
substrate 1 (rho family, small GTP binding protein Rac1)), LMNA
(lamin NC), CD59 (CD59 molecule, complement regulatory protein),
SCN5A (sodium channel, voltage-gated, type V, alpha subunit),
CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1), MIF
(macrophage migration inhibitory factor (glycosylation-inhibiting
factor)), MMP13 (matrix metallopeptidase 13 (collagenase 3)), TIMP2
(TIMP metallopeptidase inhibitor 2), CYP19A1 (cytochrome P450,
family 19, subfamily A, polypeptide 1), CYP21A2 (cytochrome P450,
family 21, subfamily A, polypeptide 2), PTPN22 (protein tyrosine
phosphatase, non-receptor type 22 (lymphoid)), MYH14 (myosin, heavy
chain 14, non-muscle), MBL2 (mannose-binding lectin (protein C) 2,
soluble (opsonic defect)), SELPLG (selectin P ligand), AOC3 (amine
oxidase, copper containing 3 (vascular adhesion protein 1)), CTSL1
(cathepsin L1), PCNA (proliferating cell nuclear antigen), IGF2
(insulin-like growth factor 2 (somatomedin A)), ITGB1 (integrin,
beta 1 (fibronectin receptor, beta polypeptide, antigen CD29
includes MDF2, MSK12)), CAST (calpastatin), CXCL12 (chemokine
(C-X-C motif) ligand 12 (stromal cell-derived factor 1)), IGHE
(immunoglobulin heavy constant epsilon), KCNE1 (potassium
voltage-gated channel, Isk-related family, member 1), TFRC
(transferrin receptor (p90, CD71)), COL1A1 (collagen, type I, alpha
1), COL1A2 (collagen, type I, alpha 2), IL2RB (interleukin 2
receptor, beta), PLA2G10 (phospholipase A2, group X), ANGPT2
(angiopoietin 2), PROCR (protein C receptor, endothelial (EPCR)),
NOX4 (NADPH oxidase 4), HAMP (hepcidin antimicrobial peptide),
PTPN11 (protein tyrosine phosphatase, non-receptor type 11), SLC2A
(solute carrier family 2 (facilitated glucose transporter), member
1), IL2RA (interleukin 2 receptor, alpha), CCL5 (chemokine (C-C
motif) ligand 5), IRF1 (interferon regulatory factor 1), CFLAR
(CASP8 and FADD-like apoptosis regulator), CALCA
(calcitonin-related polypeptide alpha), EIF4E (eukaryotic
translation initiation factor 4E), GSTP1 (glutathione S-transferase
pi 1), JAK2 (Janus kinase 2), CYP3A5 (cytochrome P450, family 3,
subfamily A, polypeptide 5), HSPG2 (heparan sulfate proteoglycan
2), CCL3 (chemokine (C-C motif) ligand 3), MYD88 (myeloid
differentiation primary response gene (88)), VIP (vasoactive
intestinal peptide), SOAT1 (sterol O-acyltransferase 1), ADRBK1
(adrenergic, beta, receptor kinase 1), NR4A2 (nuclear receptor
subfamily 4, group A, member 2), MMP8 (matrix metallopeptidase 8
(neutrophil collagenase)), NPR2 (natriuretic peptide receptor
B/guanylate cyclase B (atrionatriuretic peptide receptor B)), GCH1
(GTP cyclohydrolase 1), EPRS (glutamyl-prolyl-tRNA synthetase),
PPARGC1A (peroxisome proliferator-activated receptor gamma,
coactivator I alpha), F12 (coagulation factor XII (Hageman
factor)), PECAM1 (platelet/endothelial cell adhesion molecule),
CCL4 (chemokine (C-C motif) ligand 4), SERPINA3 (serpin peptidase
inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member
3), CASR (calcium-sensing receptor), GJA5 (gap junction protein,
alpha 5, 40 kDa), FABP2 (fatty acid binding protein 2, intestinal),
TTF2 (transcription termination factor, RNA polymerase II), PROS1
(protein S (alpha)), CTF1 (cardiotrophin 1), SGCB (sarcoglycan,
beta (43 kDa dystrophin-associated glycoprotein)), YME1L1
(YME1-like 1 (
S. cerevisiae)), CAMP (cathelicidin antimicrobial peptide), ZC3H12A
(zinc finger CCCH-type containing 12A), AKR1B1 (aldo-keto reductase
family 1, member B1 (aldose reductase)), DES (desmin), MMP7 (matrix
metallopeptidase 7 (matrilysin, uterine)), AHR (aryl hydrocarbon
receptor), CSF1 (colony stimulating factor 1 (macrophage)), HDAC9
(histone deacetylase 9), CTGF (connective tissue growth factor),
KCNMA1 (potassium large conductance calcium-activated channel,
subfamily M, alpha member 1), UGTIA (UDP glucuronosyltransferase 1
family, polypeptide A complex locus), PRKCA (protein kinase C,
alpha), COMT (catechol-.beta.-methyltransferase), S100B (S100
calcium binding protein B), EGR1 (early growth response 1), PRL
(prolactin), IL15 (interleukin 15), DRD4 (dopamine receptor D4),
CAMK2G (calcium/calmodulin-dependent protein kinase II gamma),
SLC22A2 (solute carrier family 22 (organic cation transporter),
member 2), CCL11 (chemokine (C-C motif) ligand 11), PGF (B321
placental growth factor), THPO (thrombopoietin), GP6 (glycoprotein
VI (platelet)), TACR1 (tachykinin receptor 1), NTS (neurotensin),
HNF1A (HNF1 homeobox A), SST (somatostatin), KCND1 (potassium
voltage-gated channel, Sha1-related subfamily, member 1), LOC646627
(phospholipase inhibitor), TBXAS1 (thromboxane A synthase 1
(platelet)), CYP2J2 (cytochrome P450, family 2, subfamily J,
polypeptide 2), TBXA2R (thromboxane A2 receptor), ADH1C (alcohol
dehydrogenase 1C (class I), gamma polypeptide), ALOX12
(arachidonate 12-lipoxygenase), AHSG (alpha-2-HS-glycoprotein),
BHMT (betaine-homocysteine methyltransferase), GJA4 (gap junction
protein, alpha 4, 37 kDa), SLC25A4 (solute carrier family 25
(mitochondrial carrier, adenine nucleotide translocator), member
4), ACLY (ATP citrate lyase), ALOXSAP (arachidonate
5-lipoxygenase-activating protein), NUMA1 (nuclear mitotic
apparatus protein 1), CYP27B1 (cytochrome P450, family 27,
subfamily B, polypeptide 1), CYSLTR2 (cysteinyl leukotriene
receptor 2), SOD3 (superoxide dismutase 3, extracellular), LTC4S
(leukotriene C4 synthase), UCN (urocortin), GHRL (ghrelin/obestatin
prepropeptide), APOC2 (apolipoprotein C-II), CLEC4A (C-type lectin
domain family 4, member A), KBTBD10 (kelch repeat and BTB (POZ)
domain containing 10), TNC (tenascin C), TYMS (thymidylate
synthetase), SHC1 (SHC (Src homology 2 domain containing)
transforming protein 1), LRP1 (low density lipoprotein
receptor-related protein 1), SOCS3 (suppressor of cytokine
signaling 3), ADH1B (alcohol dehydrogenase 1B (class I), beta
polypeptide), KLK3 (kallikrein-related peptidase 3), HSD11B1
(hydroxysteroid (11-beta) dehydrogenase 1), VKORC1 (vitamin K
epoxide reductase complex, subunit 1), SERPINB2 (serpin peptidase
inhibitor, clade B (ovalbumin), member 2), TNS1 (tensin 1), RNF19A
(ring finger protein 19A), EPOR (erythropoietin receptor), ITGAM
(integrin, alpha M (complement component 3 receptor 3 subunit)),
PITX2 (paired-like homeodomain 2), MAPK7 (mitogen-activated protein
kinase 7), FCGR3A (Fc fragment of IgG, low affinity 111a, receptor
(CD16a)), LEPR (leptin receptor), ENG (endoglin), GPX1 (glutathione
peroxidase 1), GOT2 (glutamic-oxaloacetic transaminase 2,
mitochondrial (aspartate aminotransferase 2)), HRH1 (histamine
receptor H1), NR112 (nuclear receptor subfamily 1, group I, member
2), CRH (corticotropin releasing hormone), HTR1A
(5-hydroxytryptamine (serotonin) receptor 1A), VDAC1
(voltage-dependent anion channel 1), HPSE (heparanase), SFTPD
(surfactant protein D), TAP2 (transporter 2, ATP-binding cassette,
sub-family B (MDR/TAP)), RNF123 (ring finger protein 123), PTK2B
(PTK2B protein tyrosine kinase 2 beta), NTRK2 (neurotrophic
tyrosine kinase, receptor, type 2), IL6R (interleukin 6 receptor),
ACHE (acetylcholinesterase (Yt blood group)). GLP1R (glucagon-like
peptide 1 receptor), GHR (growth hormone receptor), GSR
(glutathione reductase), NQO1 (NAD(P)H dehydrogenase, quinone 1),
NR5A1 (nuclear receptor subfamily 5, group A, member 1), GJB2 (gap
junction protein, beta 2, 26 kDa), SLC9A1 (solute carrier family 9
(sodium/hydrogen exchanger), member 1), MAOA (monoamine oxidase A),
PCSK9 (proprotein convertase subtilisin/kexin type 9), FCGR2A (Fc
fragment of IgG, low affinity Ha, receptor (CD32)), SERPINF1
(serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment
epithelium derived factor), member 1), EDN3 (endothelin 3), DHFR
(dihydrofolate reductase), GAS6 (growth arrest-specific 6), SMPD1
(sphingomyelin phosphodiesterase 1, acid lysosomal), UCP2
(uncoupling protein 2 (mitochondrial, proton carrier)), TFAP2A
(transcription factor AP-2 alpha (activating enhancer binding
protein 2 alpha)), C4BPA (complement component 4 binding protein,
alpha), SERPINF2 (serpin peptidase inhibitor, clade F (alpha-2
antiplasmin, pigment epithelium derived factor), member 2), TYMP
(thymidine phosphorylase), ALPP (alkaline phosphatase, placental
(Regan isozyme)), CXCR2 (chemokine (C-X-C motif) receptor 2),
SLC39A3 (solute carrier family 39 (zinc transporter), member 3),
ABCG2 (ATP-binding cassette, sub-family G (WHITE), member 2), ADA
(adenosine deaminase), JAK3 (Janus kinase 3), HSPA1A (heat shock 70
kDa protein 1A), FASN (fatty acid synthase), FGF1 (fibroblast
growth factor 1 (acidic)), F11 (coagulation factor XI), ATP7A
(ATPase, Cu++ transporting, alpha polypeptide), CR1 (complement
component (3b/4b) receptor 1 (Knops blood group)), GFAP (glial
fibrillary acidic protein), ROCK1 (Rho-associated, coiled-coil
containing protein kinase 1), MECP2 (methyl CpG binding protein 2
(Rett syndrome)), MYLK (myosin light chain kinase), BCHE
(butyrylcholinesterase), LIPE (lipase, hormone-sensitive), PRDX5
(peroxiredoxin 5), ADORA1 (adenosine A1 receptor), WRN (Werner
syndrome, RecQ helicase-like), CXCR3 (chemokine (C-X-C motif)
receptor 3), CD81 (CD81 molecule), SMAD7 (SMAD family member 7),
LAMC2 (laminin, gamma 2), MAP3K5 (mitogen-activated protein kinase
kinase kinase 5), CHGA (chromogranin A (parathyroid secretory
protein 1)), IAPP (islet amyloid polypeptide), RHO (rhodopsin),
ENPP1 (ectonucleotide pyrophosphatase/phosphodiesterase 1), PTHLH
(parathyroid hormone-like hormone), NRG1 (neuregulin 1), VEGFC
(vascular endothelial growth factor C), ENPEP (glutamyl
aminopeptidase (aminopeptidase A)), CEBPB (CCAAT/enhancer binding
protein (C/EBP), beta), NAGLU (N-acetylglucosaminidase, alpha-),
F2RL3 (coagulation factor II (thrombin) receptor-like 3), CX3CL1
(chemokine (C-X3-C motif) ligand 1), BDKRB1 (bradykinin receptor
B1), ADAMTS13 (ADAM metallopeptidase with thrombospondin type 1
motif, 13), ELANE (elastase, neutrophil expressed), ENPP2
(ectonucleotide pyrophosphatase/phosphodiesterase 2), CISH
(cytokine inducible SH2-containing protein), GAST (gastrin), MYOC
(myocilin, trabecular meshwork inducible glucocorticoid response),
ATP1A2 (ATPase, Na+/K+ transporting, alpha 2 polypeptide), NF1
(neurofibromin 1), GJB1 (gap junction protein, beta 1, 32 kDa),
MEF2A (myocyte enhancer factor 2A), VCL (vinculin), BMPR2 (bone
morphogenetic protein receptor, type II (serine/threonine kinase)),
TUBB (tubulin, beta), CDC42 (cell division cycle 42 (GTP binding
protein, 25 kDa)), KRT18 (keratin 18), HSF1 (heat shock
transcription factor 1), MYB (v-myb myeloblastosis viral oncogene
homolog (avian)), PRKAA2 (protein kinase, AMP-activated, alpha 2
catalytic subunit), ROCK2 (Rho-associated, coiled-coil containing
protein kinase 2), TFP1 (tissue factor pathway inhibitor
(lipoprotein-associated coagulation inhibitor)), PRKG1 (protein
kinase, cGMP-dependent, type I), BMP2 (bone morphogenetic protein
2), CTNND1 (catenin (cadherin-associated protein), delta 1), CTH
(cystathionase (cystathionine gamma-lyase)), CTSS (cathepsin S),
VAV2 (vav 2 guanine nucleotide exchange factor), NPY2R
(neuropeptide Y receptor Y2), IGFBP2 (insulin-like growth factor
binding protein 2, 36 kDa), CD28 (CD28 molecule), GSTA1
(glutathione S-transferase alpha 1), PPIA (peptidylprolyl isomerase
A (cyclophilin A)), APOH (apolipoprotein H (beta-2-glycoprotein
I)), S100A8 (S100 calcium binding protein A8), IL11 (interleukin
11), ALOX15 (arachidonate 15-lipoxygenase), FBLN1 (fibulin 1),
NR1H3 (nuclear receptor subfamily 1, group H, member 3), SCD
(stearoyl-CoA desaturase (delta-9-desaturase)), GIP (gastric
inhibitory polypeptide), CHGB (chromogranin B (secretogranin 1)),
PRKCB (protein kinase C, beta), SRD5A1 (steroid-5-alpha-reductase,
alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase
alpha 1)), HSD11B2 (hydroxysteroid (11-beta) dehydrogenase 2),
CALCRL (calcitonin receptor-like), GALNT2
(UDP-N-acetyl-alpha-D-galactosamine:polypeptide
N-acetylgalactosaminyltransferase 2 (GalNAc-T2)), ANGPTL4
(angiopoietin-like 4), KCNN4 (potassium intermediate/small
conductance calcium-activated channel, subfamily N, member 4),
PIK3C2A (phosphoinositide-3-kinase, class 2, alpha polypeptide),
HBEGF (heparin-binding EGF-like growth factor), CYP7A1 (cytochrome
P450, family 7, subfamily A, polypeptide 1), HLA-DRB5 (major
histocompatibility complex, class II, DR beta 5), BNIP3
(BCL2/adenovirus E1B 19 kDa interacting protein 3), GCKR
(glucokinase (hexokinase 4) regulator), S100A12 (S100 calcium
binding protein A12), PADI4 (peptidyl arginine deiminase, type IV),
HSPA14 (heat shock 70 kDa protein 14), CXCR1 (chemokine (C-X-C
motif) receptor 1), H19 (H19, imprinted maternally expressed
transcript (non-protein coding)), KRTAP19-3 (keratin associated
protein 19-3), IDDM2 (insulin-dependent diabetes mellitus 2), RAC2
(ras-related C3 botulinum toxin substrate 2 (rho family, small GTP
binding protein Rac2)), RYR1 (ryanodine receptor 1 (skeletal)),
CLOCK (clock homolog (mouse)), NGFR (nerve growth factor receptor
(TNFR superfamily, member 16)), DBH (dopamine beta-hydroxylase
(dopamine beta-monooxygenase)), CHRNA4 (cholinergic receptor,
nicotinic, alpha 4), CACNA1C (calcium channel, voltage-dependent, L
type, alpha 1C subunit), PRKAG2 (protein kinase, AMP-activated,
gamma 2 non-catalytic subunit), CHAT (choline acetyltransferase),
PTGDS (prostaglandin D2 synthase 21 kDa (brain)), NR1H2 (nuclear
receptor subfamily 1, group H, member 2), TEK (TEK tyrosine kinase,
endothelial), VEGFB (vascular endothelial growth factor B), MEF2C
(myocyte enhancer factor 2C), MAPKAPK2 (mitogen-activated protein
kinase-activated protein kinase 2), TNFRSF11A (tumor necrosis
factor receptor superfamily, member 11a, NFKB activator), HSPA9
(heat shock 70 kDa protein 9 (mortalin)), CYSLTR1 (cysteinyl
leukotriene receptor 1), MAT1A (methionine adenosyltransferase I,
alpha), OPRL1 (opiate receptor-like 1), IMPA1 (inositol(myo)-1 (or
4)-monophosphatase 1), CLCN2 (chloride channel 2), DLD
(dihydrolipoamide dehydrogenase), PSMA6 (proteasome (prosome,
macropain) subunit, alpha type, 6), PSMB8 (proteasome (prosome,
macropain) subunit, beta type, 8 (large multifunctional peptidase
7)), CHI3L1 (chitinase 3-like 1 (cartilage glycoprotein-39)),
ALDH1B1 (aldehyde dehydrogenase 1 family, member B1), PARP2 (poly
(ADP-ribose) polymerase 2), STAR (steroidogenic acute regulatory
protein), LBP (lipopolysaccharide binding protein), ABCC6
(ATP-binding cassette, sub-family C(CFTR/MRP), member 6), RGS2
(regulator of G-protein signaling 2, 24 kDa), EFNB2 (ephrin-B2),
GJB6 (gap junction protein, beta 6, 30 kDa), APOA2 (apolipoprotein
A-II), AMPD1 (adenosine monophosphate deaminase 1), DYSF
(dysferlin, limb girdle muscular dystrophy 2B (autosomal
recessive)), FDFT1 (farnesyl-diphosphate farnesyltransferase 1),
EDN2 (endothelin 2), CCR6 (chemokine (C-C motif) receptor 6), GJB3
(gap junction protein, beta 3, 31 kDa), IL1RL1 (interleukin 1
receptor-like 1), ENTPD1 (ectonucleoside triphosphate
diphosphohydrolase 1), BBS4 (Bardet-Biedl syndrome 4), CELSR2
(cadherin, EGF LAG seven-pass G-type receptor 2 (flamingo homolog,
Drosophila)), F11R (F11 receptor), RAPGEF3 (Rap guanine nucleotide
exchange factor (GEF) 3), HYAL1 (hyaluronoglucosaminidase 1),
ZNF259 (zinc finger protein 259), ATOX1 (ATX1 antioxidant protein 1
homolog (yeast)), ATF6 (activating transcription factor 6), KHK
(ketohexokinase (fructokinase)), SAT1 (spermidine/spermine
N1-acetyltransferase 1), GGH (gamma-glutamyl hydrolase (conjugase,
folylpolygammaglutamyl hydrolase)), TIMP4 (TIMP metallopeptidase
inhibitor 4), SLC4A4 (solute carrier family 4, sodium bicarbonate
cotransporter, member 4), PDE2A (phosphodiesterase 2A,
cGMP-stimulated), PDE3B (phosphodiesterase 3B, cGMP-inhibited),
FADS1 (fatty acid desaturase 1), FADS2 (fatty acid desaturase 2),
TMSB4X (thymosin beta 4, X-linked), TXNIP (thioredoxin interacting
protein), LIMS 1 (LIM and senescent cell antigen-like domains 1),
RHOB (ras homolog gene family, member B), LY96 (lymphocyte antigen
96), FOXO1 (forkhead box 01), PNPLA2 (patatin-like phospholipase
domain containing 2), TRH (thyrotropin-releasing hormone), GJC1
(gap junction protein, gamma 1, 45 kDa), SLC17A5 (solute carrier
family 17 (anion/sugar transporter), member 5), FTO (fat mass and
obesity associated), GJD2 (gap junction protein, delta 2, 36 kDa),
PSRC1 (proline/serine-rich coiled-coil 1), CASP12 (caspase 12
(gene/pseudogene)), GPBAR1 (G protein-coupled bile acid receptor
1), PXK (PX domain containing serine/threonine kinase), IL33
(interleukin 33), TRIB1 (tribbles homolog 1 (Drosophila)), PBX4
(pre-B-cell leukemia homeobox 4), NUPR1 (nuclear protein,
transcriptional regulator, 1), 15-Septmeber (15 kDa selenoprotein),
CILP2 (cartilage intermediate layer protein 2), TERC (telomerase
RNA component), GGT2 (gamma-glutamyltransferase 2), MT-CO1
(mitochondrially encoded cytochrome c oxidase I), and UOX (urate
oxidase, pseudogene).
[0420] In an additional embodiment, the chromosomal sequence may
further be selected from Pon1 (paraoxonase 1), LDLR (LDL receptor),
ApoE (Apolipoprotein E), Apo B-100 (Apolipoprotein B-100), ApoA
(Apolipoprotein(a)), ApoA1 (Apolipoprotein A1), CBS (Cystathione
B-synthase), Glycoprotein IIb/IIb, MTHRF
(5,10-methylenetetrahydrofolate reductase (NADPH), and combinations
thereof. In one iteration, the chromosomal sequences and proteins
encoded by chromosomal sequences involved in cardiovascular disease
may be chosen from Cacna1C, Sod1, Pten, Ppar(alpha), Apo E, Leptin,
and combinations thereof.
[0421] Kidneys
[0422] The present invention also contemplates delivering the
CRISPR-Cas system to the kidney. Delivery strategies to induce
cellular uptake of the therapeutic nucleic acid include physical
force or vector systems such as viral-, lipid- or complex-based
delivery, or nanocarriers. From the initial applications with less
possible clinical relevance, when nucleic acids were addressed to
renal cells with hydrodynamic high pressure injection systemically,
a wide range of gene therapeutic viral and non-viral carriers have
been applied already to target posttranscriptional events in
different animal kidney disease models in vivo (Csaba Revesz and
Peter Hamar (2011). Delivery Methods to Target RNAs in the Kidney,
Gene Therapy Applications, Prof. Chunsheng Kang (Ed.), ISBN:
978-953-307-541-9, InTech, Available from:
http://www.intechopen.com/books/gene-therapy-applications/delivery-method-
s-to-target-rnas-in-the-kidney). Delivery methods to the kidney are
summarized as follows:
TABLE-US-00003 Delivery Functional method Carrier Target RNA
Disease Model assays Author Hydrodynamic/ TransIT In Vivo
p85.alpha. Acute renal Ischemia- Uptake, Larson et al., Lipid Gene
Delivery injury reperfusion bio- Surgery, (August System, DOTAP
distribution 2007), Vol. 142, No. 2, pp. (262-269) Hydrodynamic/
Lipofectamine Fas Acute Ischemia- Blood urea Hamar et al., Lipid
2000 renal reperfusion nitrogen, Fas Proc Natl Acad Sci, injury
Immuno- (October 2004), histochemistry Vol. 101, apoptosis, No. 41,
pp. histological (14883-14888) scoring Hydrodynamic n.a. Apoptosis
Acute Ischemia- n.a. Zheng et al., Am J cascade renal reperfusion
Pathol, (October elements injury 2008), Vol. 173, No. 4, pp.
(973-980) Hydrodynamic n.a. Nuclear factor Acute Ischemia- n.a.
Feng et al., kappa-b renal reperfusion Transplantation, (NFkB)
injury (May 2009), Vol. 87, No. 9, pp. (1283-1289) Hydrodynamic/
Lipofectamine Apoptosis, Acute Ischemia- Apoptosis Xie & Guo,
Viral 2000 antagonizing renal reperfusion oxidative stress, Am Soc
Nephrol, transcription injury caspase activation, (December 2006),
factor (AATF) membrane lipid Vol. 17, No. 12, peroxidation pp.
(3336-3346) Hydrodynamic pBAsi mU6 Neo/ Gremlin Diabetic
Streptozotozin- Proteinuria, Q. Zhang et al., TransIt-EE
nephropathy induced serum creatinine, PloS ONE, Hydrodynamic
diabetes glomerular and (July 2010) Delivery System tubular
diameter, Vol. 5, collagen type No. 7, e11709, IV/BMP7 pp. (1-13)
expression Viral/Lipid pSUPER TGF-.beta. type II Interstitial
Unilateral .alpha.-SMA Kushibikia et al., J vector/ receptor renal
fibrosis urethral expression, Controlled Release, Lipofectamine
obstruction collagen content, (July 2005), Vol. 105 No. 3, pp.
(318-331) Viral Adeno- Mineral Hyper-tension Cold-induced blood
pressure, Wang et al., associated corticoid caused renal
hypertension serum albumin, Gene Therapy, virus-2 receptor damage
serum urea (July 2006), nitrogen, serum Vol. 13, creatinine, kidney
No. 14, pp. weight, urinary (1097-1103) sodium Hydrodynamic/ pU6
vector Luciferace n.a. n.a. uptake Kobayashi et al., Viral Journal
of Pharmacology and Experimental Therapeutics, (February 2004) Vol.
308, No. 2. pp. (688-693) Lipid Lipoproteins, apoB1, apoM n.a. n.a.
Uptake, binding Wolfrum et al., albumin affinity to Nature
lipoproteins Biotechnology, and albumin (September 2007), Vol. 25,
No. 10, pp. (1149-1157) Lipid Lipofectamine2000 p53 Acute Ischemic
and Histological Molitoris et al., renal cisplatin- scoring, J Am
Soc Neprol, injury induced acute apoptosis (August 2009), injury
Vol. 20, No. 8 pp. (1754-1764) Lipid DOTAP/DOPE, COX-2 Breast
MDA-MB- Cell Mikhaylova et al., DOTAP/DOPE/ adeno- 231 breast
viability, Cancer Gene Therapy DOPE-PEG2000 carcinoma cancer uptake
(March 2011), xenograft- Vol. 16, No. 3, pp. bearing (217-226)
mouse Lipid Cholesterol 12/15- Diabetic Strep- Albuminuria, Yuan et
al., lipoxygenase nephro- tozotozin- urinary Am J Physiol pathy
induced creatinine, Renal Physiol, diabetes histology, (June 2008),
type I and IV Vol. 295, pp. collagen, (F605-F617) TGF-.beta.,
fibronectin, plasminogen activator inhibitor 1 Lipid Lipofectamine
Mitochondrial Diabetic Strep- Cell proliferation Y. Zhang et al.,
2000 membrane 44 neuro- tozotozin- and apoptosis, J Am Soc Neprol,
(TIM44) pathy induced histology, ROS, (April 2006), diabetes
mitochondrial Vol. 17, import of Mn-SOD No. 4, pp. and glutathione
(1090-1101) peroxidase, cellular membrane polarization
Hydrodynamic/ Proteolipo-some RLIP76 Renal Caki-2 kidney uptake
Singhal et al. Lipid carcinoma cancer Cancer Res. xenograft- (May
2009), bearing Vol. 69, No. 10 mouse pp. (4244-4251) Polymer
PEGylated Luciferase n.a. n.a. Uptake, Malek et al., PEI pGL3
biodistribution, Toxicology erthrocyte and Applied aggregation
Pharmacology (April 2009), Vol. 236, No. 1, pp. (97-108) Polymer
PEGylated MAPK1 Lupus Glomerulo- Proteinuria, Shimizu et al.,
poly-L-lysine glomerulo- nephritis glomerulosclerosis, J Am Soc
nephritis TGF-.beta., Nephrology, fibronectin, (April 2010),
plasminogen Vol. 21, No. 4, activator pp. (622-633) inhibitor 1
Polymer/ Hyaluronic acid/ VEGF Kidney B16F1 Biodistribution, Jiang
et al., Nano Quantum dot/ cancer/ melanoma citotoxicity, Molecular
particle PEI melanoma tumor- tumor volume, Pharmaceutics, bearing
endocytosis (May-June 2009) mouse Vol. 6, No. 3, pp. (727-737)
Polymer/ PEGylated GAPDH n.a. n.a. cell viability, Cao et al, Nano
polycapro- uptake J Controlled particle lactone Release, nanofiber
(June 2010), Vol. 144, No. 2, pp. (203-212) Aptamer Spiegelmer CC
Glomerulo- Uninephrecto- urinary albumin, Ninichuk et al., mNOX-E36
chemokine sclerosis mized urinary creatinine, Am J Pathol, ligand 2
mouse histopathology, (March 2008), glomerular Vol. 172, filtration
rate, No. 3, pp, macrophage count, (628-637) serum Ccl2, Mac-2+,
Ki-67+ Aptamer Aptamer vasopressin Congestive n.a. Binding affinity
Purschke et al., NOX-F37 (AVP) heart to D-AVP, Proc Natl Acad Sci,
failure Inhibition of (March 2006), AVP Signaling, Vol. 103, No.
13, Urine osmolality, pp. (5173-5178) and sodium concentration,
[0423] Yuan et al. (Am J Physiol Renal Physiol 295: F605-F617,
2008) investigated whether in vivo delivery of small interfering
RNAs (siRNAs) targeting the 12/15-lipoxygenase (12/15-LO) pathway
of arachidonate acid metabolism can ameliorate renal injury and
diabetic nephropathy (DN) in a streptozotocininjected mouse model
of type 1 diabetes. To achieve greater in vivo access and siRNA
expression in the kidney, Yuan et al. used double-stranded 12/15-LO
siRNA oligonucleotides conjugated with cholesterol. About 400 .mu.g
of siRNA was injected subcutaneously into mice. The method of Yuang
et al. may be applied to the CRISPR Cas system of the present
invention contemplating a 1-2 g subcutaneous injection of CRISPR
Cas conjugated with cholesterol to a human for delivery to the
kidneys.
[0424] Molitoris et al. (J Am Soc Nephrol 20: 1754-1764, 2009)
exploited proximal tubule cells (PTCs), as the site of
oligonucleotide reabsorption within the kidney to test the efficacy
of siRNA targeted to p53, a pivotal protein in the apoptotic
pathway, to prevent kidney injury. Naked synthetic siRNA to p53
injected intravenously 4 h after ischemic injury maximally
protected both PTCs and kidney function. Molitoris et al.'s data
indicates that rapid delivery of siRNA to proximal tubule cells
follows intravenous administration. For dose-response analysis,
rats were injected with doses of siP53, 0.33; 1, 3, or 5 mg/kg,
given at the same four time points, resulting in cumulative doses
of 1.32; 4, 12, and 20 mg/kg, respectively. All siRNA doses tested
produced a SCr reducing effect on day one with higher doses being
effective over approximately five days compared with PBS-treated
ischemic control rats. The 12 and 20 mg/kg cumulative doses
provided the best protective effect. The method of Molitoris et al.
may be applied to the CRISPR Cas system of the present invention
contemplating 12 and 20 mg/kg cumulative doses to a human for
delivery to the kidneys.
[0425] Thompson et al. (Nucleic Acid Therapeutics, Volume 22,
Number 4, 2012) reports the toxicological and pharmacokinetic
properties of the synthetic, small interfering RNA I5NP following
intravenous administration in rodents and nonhuman primates. I5NP
is designed to act via the RNA interference (RNAi) pathway to
temporarily inhibit expression of the pro-apoptotic protein p53 and
is being developed to protect cells from acute ischemia/reperfusion
injuries such as acute kidney injury that can occur during major
cardiac surgery and delayed graft function that can occur following
renal transplantation. Doses of 800 mg/kg I5NP in rodents, and
1,000 mg/kg I5NP in nonhuman primates, were required to elicit
adverse effects, which in the monkey were isolated to direct
effects on the blood that included a sub-clinical activation of
complement and slightly increased clotting times. In the rat, no
additional adverse effects were observed with a rat analogue of
I5NP, indicating that the effects likely represent class effects of
synthetic RNA duplexes rather than toxicity related to the intended
pharmacologic activity of I5NP. Taken together, these data support
clinical testing of intravenous administration of I5NP for the
preservation of renal function following acute ischemia/reperfusion
injury. The no observed adverse effect level (NOAEL) in the monkey
was 500 mg/kg. No effects on cardiovascular, respiratory, and
neurologic parameters were observed in monkeys following i.v.
administration at dose levels up to 25 mg/kg. Therefore, a similar
dosage may be contemplated for intravenous administration of CRISPR
Cas to the kidneys of a human.
[0426] Shimizu et al. (J Am Soc Nephrol 21: 622-633, 2010)
developed a system to target delivery of siRNAs to glomeruli via
poly(ethylene glycol)-poly(L-lysine)-based vehicles. The
siRNA/nanocarrier complex was approximately 10 to 20 nm in
diameter, a size that would allow it to move across the fenestrated
endothelium to access to the mesangium. After intraperitoneal
injection of fluorescence-labeled siRNA/nanocarrier complexes,
Shimizu et al. detected siRNAs in the blood circulation for a
prolonged time. Repeated intraperitoneal administration of a
mitogen-activated protein kinase 1 (MAPK1) siRNA/nanocarrier
complex suppressed glomerular MAPK1 mRNA and protein expression in
a mouse model of glomerulonephritis. For the investigation of siRNA
accumulation, Cy5-labeled siRNAs complexed with PIC nanocarriers
(0.5 ml, 5 nmol of siRNA content), naked Cy5-labeled siRNAs (0.5
ml, 5 nmol), or Cy5-labeled siRNAs encapsulated in HVJ-E (0.5 ml, 5
nmol of siRNA content) were administrated to BALB-c mice. The
method of Shimizu et al. may be applied to the CRISPR Cas system of
the present invention contemplating a dose of about of 10-20
.mu.mol CRISPR Cas complexed with nanocarriers in about 1-2 liters
to a human for intraperitoneal administration and delivery to the
kidneys.
[0427] Lungs
[0428] The present invention also contemplates delivering the
CRISPR-Cas system to one or both lungs.
[0429] Although AAV-2-based vectors were originally proposed for
CFTR delivery to CF airways, other serotypes such as AAV-1, AAV-5,
AAV-6, and AAV-9 exhibit improved gene transfer efficiency in a
variety of models of the lung epithelium (see, e.g., Li et al.,
Molecular Therapy, vol. 17 no. 12, 2067-277 December 2009). AAV-1
was demonstrated to be .about.100-fold more efficient than AAV-2
and AAV-5 at transducing human airway epithelial cells in vitro, 5
although AAV-1 transduced murine tracheal airway epithelia in vivo
with an efficiency equal to that of AAV-5. Other studies have shown
that AAV-5 is 50-fold more efficient than AAV-2 at gene delivery to
human airway epithelium (HAE) in vitro and significantly more
efficient in the mouse lung airway epithelium in vivo. AAV-6 has
also been shown to be more efficient than AAV-2 in human airway
epithelial cells in vitro and murine airways in vivo.8 The more
recent isolate, AAV-9, was shown to display greater gene transfer
efficiency than AAV-5 in murine nasal and alveolar epithelia in
vivo with gene expression detected for over 9 months suggesting AAV
may enable long-term gene expression in vivo, a desirable property
for a CFTR gene delivery vector. Furthermore, it was demonstrated
that AAV-9 could be readministered to the murine lung with no loss
of CFTR expression and minimal immune consequences. CF and non-CF
HAE cultures may be inoculated on the apical surface with 100 .mu.l
of AAV vectors for hours (see, e.g., Li et al., Molecular Therapy,
vol. 17 no. 12, 2067-277 December 2009). The MOI may vary from
1.times.10.sup.3 to 4.times.10.sup.5 vector genomes/cell, depending
on virus concentration and purposes of the experiments. The above
cited vectors are contemplated for the delivery and/or
administration of the invention.
[0430] Zamora et al. (Am J Respir Crit Care Med Vol 183. pp
531-538, 2011) reported an example of the application of an RNA
interference therapeutic to the treatment of human infectious
disease and also a randomized trial of an antiviral drug in
respiratory syncytial virus (RSV)-infected lung transplant
recipients. Zamora et al. performed a randomized, double-blind,
placebocontrolled trial in LTX recipients with RSV respiratory
tract infection. Patients were permitted to receive standard of
care for RSV. Aerosolized ALN-RSV01 (0.6 mg/kg) or placebo was
administered daily for 3 days. This study demonstrates that an RNAi
therapeutic targeting RSV can be safely administered to LTX
recipients with RSV infection. Three daily doses of ALN-RSV01 did
not result in any exacerbation of respiratory tract symptoms or
impairment of lung function and did not exhibit any systemic
proinflammatory effects, such as induction of cytokines or CRP.
Pharmacokinetics showed only low, transient systemic exposure after
inhalation, consistent with preclinical animal data showing that
ALN-RSV01, administered intravenously or by inhalation, is rapidly
cleared from the circulation through exonucleasemediated digestion
and renal excretion. The method of Zamora et al. may be applied to
the CRISPR Cas system of the present invention and an aerosolized
CRISPR Cas, for example with a dosage of 0.6 mg/kg, may be
contemplated for the present invention.
[0431] For an example of CFTRdelta508 chimeric guide RNA, see
Example 22 which demonstrates gene transfer or gene delivery of a
CRISPR-Cas system in airways of subject or a patient in need
thereof, suffering from cystic fibrosis or from cystic fibrosis
(CF) related symptoms, using adeno-associated virus (AAV)
particles. In particular, they exemplify a repair strategy for
Cystic Fibrosis delta F508 mutation. This type of strategy should
apply across all organisms. With particular reference to CF,
suitable patients may include: Human, non-primate human, canine,
feline, bovine, equine and other domestic animals. In this
instance, Applicants utilized a CRISPR-Cas system comprising a Cas9
enzyme to target deltaF508 or other CFTR-inducing mutations.
[0432] The treated subjects in this instance receive
pharmaceutically effective amount of aerosolized AAV vector system
per lung endobronchially delivered while spontaneously breathing.
As such, aerosolized delivery is preferred for AAV delivery in
general. An adenovirus or an AAV particle may be used for delivery.
Suitable gene constructs, each operably linked to one or more
regulatory sequences, may be cloned into the delivery vector. In
this instance, the following constructs are provided as examples:
Cbh or EF1a promoter for Cas9, U6 or H1 promoter for chimeric guide
RNA): A preferred arrangement is to use a CFTRdelta508 targeting
chimeric guide, a repair template for deltaF508 mutation and a
codon optimized Cas9 enzyme (preferred Cas9s are those with
nuclease or nickase activity) with optionally one or more nuclear
localization signal or sequence(s) (NLS(s)), e.g., two (2) NLSs.
Constructs without NLS are also envisaged.
[0433] In order to identify the Cas9 target site, Applicants
analyzed the human CFTR genomic locus and identified the Cas9
target site. Preferably, in general and in this CF case, the PAM
may contain a NGG or a NNAGAAW motif.
[0434] Accordingly, in the case of CF, the present method comprises
manipulation of a target sequence in a genomic locus of interest
comprising delivering a non-naturally occurring or engineered
composition comprising a viral vector system comprising one or more
viral vectors operably encoding a composition for expression
thereof, wherein the composition comprises:
a non-naturally occurring or engineered composition comprising a
vector system comprising one or more vectors comprising I. a first
regulatory element operably linked to a CRISPR-Cas system chimeric
RNA (chiRNA) polynucleotide sequence, wherein the polynucleotide
sequence comprises (a) a guide sequence capable of hybridizing to
the CF target sequence in a suitable mammalian cell, (b) a tracr
mate sequence, and (c) a tracr sequence, and II. a second
regulatory element operably linked to an enzyme-coding sequence
encoding a CRISPR enzyme comprising at least one or more nuclear
localization sequences, wherein (a), (b) and (c) are arranged in a
5' to 3' orientation, wherein components I and II are located on
the same or different vectors of the system, wherein when
transcribed, the tracr mate sequence hybridizes to the tracr
sequence and the guide sequence directs sequence-specific binding
of a CRISPR complex to the target sequence, and wherein the CRISPR
complex comprises the CRISPR enzyme complexed with (1) the guide
sequence that is hybridized to the target sequence, and (2) the
tracr mate sequence that is hybridized to the tracr sequence. In
respect of CF, preferred target DNA sequences comprise the
CFTRdelta508 mutation. A preferred PAM is described above. A
preferred CRISPR enzyme is any Cas (described herein, but
particularly that described in Example 22).
[0435] Alternatives to CF include any genetic disorder and examples
of these are well known. Another preferred method or use of the
invention is for correcting defects in the EMP2A and EMP2B genes
that have been identified to be associated with Lafora disease.
[0436] In some embodiments, a "guide sequence" may be distinct from
"guide RNA". A guide sequence may refer to an approx. 20 bp
sequence, within the guide RNA, that specifies the target site.
[0437] In some embodiments, the Cas9 is (or is derived from)
SpCas9. In such embodiments, preferred mutations are at any or all
or positions 10, 762, 840, 854, 863 and/or 986 of SpCas9 or
corresponding positions in other Cas9s (which may be ascertained
for instance by standard sequence comparison tools. In particular,
any or all of the following mutations are preferred in SpCas9:
D10A, E762A, H840A, N854A, N863A and/or D986A; as well as
conservative substitution for any of the replacement amino acids is
also envisaged. The same (or conservative substitutions of these
mutations) at corresponding positions in other Cas9s are also
preferred. Particularly preferred are D10 and H840 in SpCas9.
However, in other Cas9s, residues corresponding to SpCas9 D10 and
H840 are also preferred. These are advantageous as they provide
nickase activity. Such mutations may be applied to all aspects of
the present invention, not only treatment of CF.
[0438] Schwank et al. (Cell Stem Cell, 13:653-58, 2013) used
CRISPR/Cas9 to correct a defect associated with cystic fibrosis in
human stem cells. The team's target was the gene for an ion
channel, cystic fibrosis transmembrane conductor receptor (CFTR). A
deletion in CFTR causes the protein to misfold in cystic fibrosis
patients. Using cultured intestinal stem cells developed from cell
samples from two children with cystic fibrosis, Schwank et al. were
able to correct the defect using CRISPR along with a donor plasmid
containing the reparative sequence to be inserted. The researchers
then grew the cells into intestinal "organoids," or miniature guts,
and showed that they functioned normally. In this case, about half
of clonal organoids underwent the proper genetic correction.
[0439] Muscles
[0440] The present invention also contemplates delivering the
CRISPR-Cas system to muscle(s).
[0441] Bortolanza et al. (Molecular Therapy vol. 19 no. 11,
2055-264 November 2011) shows that systemic delivery of RNA
interference expression cassettes in the FRG1 mouse, after the
onset of facioscapulohumeral muscular dystrophy (FSHD), led to a
dose-dependent long-term FRG1 knockdown without signs of toxicity.
Bortolanza et al. found that a single intravenous injection of
5.times.10.sup.12 vg of rAAV6-sh1FRG1 rescues muscle histopathology
and muscle function of FRG1 mice. In detail, 200 .mu.l containing
2.times.10.sup.12 or 5.times.10.sup.12 vg of vector in
physiological solution were injected into the tail vein using a
25-gauge Terumo syringe. The method of Bortolanza et al. may be
applied to an AAV expressing CRISPR Cas and injected into humans at
a dosage of about 2.times.10.sup.15 or 2.times.10.sup.16 vg of
vector.
[0442] Dumonceaux et al. (Molecular Therapy vol. 18 no. 5, 881-887
May 2010) inhibit the myostatin pathway using the technique of RNA
interference directed against the myostatin receptor AcvRIIb mRNA
(sh-AcvRIIb). The restoration of a quasi-dystrophin was mediated by
the vectorized U7 exon-skipping technique (U7-DYS).
Adeno-associated vectors carrying either the sh-AcvrIIb construct
alone, the U7-DYS construct alone, or a combination of both
constructs were injected in the tibialis anterior (TA) muscle of
dystrophic mdx mice. The injections were performed with 10.sup.11
AAV viral genomes. The method of Dumonceaux et al. may be applied
to an AAV expressing CRISPR Cas and injected into humans, for
example, at a dosage of about 10.sup.14 to about 10.sup.15 vg of
vector.
[0443] Kinouchi et al. (Gene Therapy (2008) 15, 1126-1130) report
the effectiveness of in vivo siRNA delivery into skeletal muscles
of normal or diseased mice through nanoparticle formation of
chemically unmodified siRNAs with atelocollagen (ATCOL).
ATCOL-mediated local application of siRNA targeting myostatin, a
negative regulator of skeletal muscle growth, in mouse skeletal
muscles or intravenously, caused a marked increase in the muscle
mass within a few weeks after application. These results imply that
ATCOL-mediated application of siRNAs is a powerful tool for future
therapeutic use for diseases including muscular atrophy. Mst-siRNAs
(final concentration, 10 mM) were mixed with ATCOL (final
concentration for local administration, 0.5%) (AteloGene, Kohken,
Tokyo, Japan) according to the manufacturer's instructions. After
anesthesia of mice (20-week-old male C57BL/6) by Nembutal (25
mg/kg, i.p.), the Mst-siRNA/ATCOL complex was injected into the
masseter and biceps femoris muscles. The method of Kinouchi et al.
may be applied to CRISPR Cas and injected into a human, for
example, at a dosage of about 500 to 1000 ml of a 40 .mu.M solution
into the muscle.
[0444] Hagstrom et al. (Molecular Therapy Vol. 10, No. 2, August
2004) describe an intravascular, nonviral methodology that enables
efficient and repeatable delivery of nucleic acids to muscle cells
(myofibers) throughout the limb muscles of mammals. The procedure
involves the injection of naked plasmid DNA or siRNA into a distal
vein of a limb that is transiently isolated by a tourniquet or
blood pressure cuff. Nucleic acid delivery to myofibers is
facilitated by its rapid injection in sufficient volume to enable
extravasation of the nucleic acid solution into muscle tissue. High
levels of transgene expression in skeletal muscle were achieved in
both small and large animals with minimal toxicity. Evidence of
siRNA delivery to limb muscle was also obtained. For plasmid DNA
intravenous injection into a rhesus monkey, a threeway stopcock was
connected to two syringe pumps (Model PHD 2000; Harvard
Instruments), each loaded with a single syringe. Five minutes after
a papaverine injection, pDNA (15.5 to 25.7 mg in 40-100 ml saline)
was injected at a rate of 1.7 or 2.0 ml/s. This could be scaled up
for plasmid DNA expressing CRISPR Cas of the present invention with
an injection of about 300 to 500 mg in 800 to 2000 ml saline for a
human. For adenoviral vector injections into a rat,
2.times.10.sup.9 infectious particles were injected in 3 ml of
normal saline solution (NSS). This could be scaled up for an
adenoviral vector expressing CRISPR Cas of the present invention
with an injection of about 1.times.10.sup.13 infectious particles
were injected in 10 liters of NSS for a human. For siRNA, a rat was
injected into the great saphenous vein with 12.5 .mu.g of a siRNA
and a primate was injected injected into the great saphenous vein
with 750 .mu.g of a siRNA. This could be scaled up for a CRISPR Cas
of the present invention, for example, with an injection of about
15 to about 50 mg into the great saphenous vein of a human.
[0445] Skin
[0446] The present invention also contemplates delivering the
CRISPR-Cas system to the skin.
[0447] Hickerson et al. (Molecular Therapy--Nucleic Acids (2013) 2,
e129) relates to a motorized microneedle array skin delivery device
for delivering self-delivery (sd)-siRNA to human and murine skin.
The primary challenge to translating siRNA-based skin therapeutics
to the clinic is the development of effective delivery systems.
Substantial effort has been invested in a variety of skin delivery
technologies with limited success. In a clinical study in which
skin was treated with siRNA, the exquisite pain associated with the
hypodermic needle injection precluded enrollment of additional
patients in the trial, highlighting the need for improved, more
"patient-friendly" (i.e., little or no pain) delivery approaches.
Microneedles represent an efficient way to deliver large charged
cargos including siRNAs across the primary barrier, the stratum
corneum, and are generally regarded as less painful than
conventional hypodermic needles. Motorized "stamp type" microneedle
devices, including the motorized microneedle array (MMNA) device
used by Hickerson et al., have been shown to be safe in hairless
mice studies and cause little or no pain as evidenced by (i)
widespread use in the cosmetic industry and (ii) limited testing in
which nearly all volunteers found use of the device to be much less
painful than a flushot, suggesting siRNA delivery using this device
will result in much less pain than was experienced in the previous
clinical trial using hypodermic needle injections. The MMNA device
(marketed as Triple-M or Tri-M by Bomtech Electronic Co, Seoul,
South Korea) was adapted for delivery of siRNA to mouse and human
skin. sd-siRNA solution (up to 300 .mu.l of 0.1 mg/ml RNA) was
introduced into the chamber of the disposable Tri-M needle
cartridge (Bomtech), which was set to a depth of 0.1 mm. For
treating human skin, deidentified skin (obtained immediately
following surgical procedures) was manually stretched and pinned to
a cork platform before treatment. All intradermal injections were
performed using an insulin syringe with a 28-gauge 0.5-inch needle.
The MMNA device and method of Hickerson et al. could be used and/or
adapted to deliver the CRISPR Cas of the present invention, for
example, at a dosage of up to 300 .mu.l of 0.1 mg/ml CRISPR Cas to
the skin.
[0448] Leachman et al. (Molecular Therapy, vol. 18 no. 2, 442-446
February 2010) relates to a phase Ib clinical trial for treatment
of a rare skin disorder pachyonychia congenita (PC), an autosomal
dominant syndrome that includes a disabling plantar keratoderma,
utilizing the first short-interfering RNA (siRNA)-based therapeutic
for skin. This siRNA, called TD101, specifically and potently
targets the keratin 6a (K6a) N171K mutant mRNA without affecting
wild-type K6a mRNA. The dose-escalation schedule is presented
below:
TABLE-US-00004 Dose Concentration of Total dose Week no. Days
Volume (ml) TD101 (mg/ml) TD101 (mg) 1 1-2 1-7 0.1 1.0 0.10 2 3-4
8-14 0.25 1.0 0.25 3 5-6 15-21 0.50 1.0 0.50 4 7-8 22-28 1.0 1.0
1.0 5 9-10 29-35 1.5 1.0 1.5 6 11-12 36-42 2.0 1.0 2.0 7 13-14
43-49 2.0 1.5 3.0 8 15-16 50-56 2.0 2.0 4.0 9 17-18 57-63 2.0 2.5
5.0 10 19-20 64-70 2.0 3.0 6.0 11 21-22 71-77 2.0 3.5 7.0 12 23-24
78-84 2.0 4.0 8.0 13 25-26 85-91 2.0 4.5 9.0 14 27-28 92-98 2.0 5.0
10.0 15 29-30 99-105 2.0 6.0 12.0 16 31-32 106-112 2.0 7.0 14.0 17
33 113-119 2.0 8.5 17.0
[0449] Initially, 0.1 ml of a 1.0 mg/ml solution of TD101 or
vehicle alone (Dulbecco's phosphate-buffered saline without calcium
or magnesium) was administered to symmetric calluses. Six rising
dose-volumes were completed without an adverse reaction to the
increases: 0.1, 0.25, 0.5, 1.0, 1.5, and 2.0 ml of a 1.0 mg/ml
solution of TD101 solution per injection. As the highest planned
volume (2.0 ml) was well tolerated, the concentration of TD101 was
then increased each week from 1 mg/ml up to a final concentration
of 8.5 mg/ml. Similar dosages are contemplated for the
administration of a CRISPR Cas that specifically and potently
targets the keratin 6a (K6a) N171K mutant mRNA.
[0450] Zheng et al. (PNAS, Jul. 24, 2012, vol. 109, no. 30,
11975-11980) show that spherical nucleic acid nanoparticle
conjugates (SNA-NCs), gold cores surrounded by a dense shell of
highly oriented, covalently immobilized siRNA, freely penetrate
almost 100% of keratinocytes in vitro, mouse skin, and human
epidermis within hours after application. Zheng et al. demonstrated
that a single application of 25 nM epidermal growth factor receptor
(EGFR) SNA-NCs for 60 h demonstrate effective gene knockdown in
human skin. A similar dosage may be contemplated for CRISPR Cas
immobilized in SNA-NCs for administration to the skin.
[0451] Hepatitis Viruses
[0452] The present invention may also be applied to treat hepatitis
B virus (HBV). However, the CRISPR Cas system must be adapted to
avoid the shortcomings of RNAi, such as the risk of oversatring
endogenous small RNA pathways, by for example, optimizing dose and
sequence (see, e.g., Grimm et al., Nature vol. 441, 26 May 2006).
For example, low doses, such as about 1-10.times.10.sup.14
particles per humane are contemplated.
[0453] In another embodiment, the CRISPR Cas system directed
against HBV may be administered in liposomes, such as a stable
nucleic-acid-lipid particle (SNALP) (see, e.g., Morrissey et al.,
Nature Biotechnology, Vol. 23, No. 8, August 2005). Daily
intravenous injections of about 1, 3 or 5 mg/kg/day of CRISPR Cas
targeted to HBV RNA in a SNALP are contemplated. The daily
treatment may be over about three days and then weekly for about
five weeks.
[0454] In another embodiment, the system of Chen et al. (Gene
Therapy (2007) 14, 11-19) may be used/and or adapted for the CRISPR
Cas system of the present invention. Chen et al. use a
double-stranded adenoassociated virus 8-pseudotyped vector
(dsAAV2/8) to deliver shRNA. A single administration of dsAAV2/8
vector (1.times.10.sup.12 vector genomes per mouse), carrying
HBV-specific shRNA, effectively suppressed the steady level of HBV
protein, mRNA and replicative DNA in liver of HBV transgenic mice,
leading to up to 2-3 log.sub.10 decrease in HBV load in the
circulation. Significant HBV suppression sustained for at least 120
days after vector administration. The therapeutic effect of shRNA
was target sequence dependent and did not involve activation of
interferon. For the present invention, a CRISPR Cas system directed
to HBV may be cloned into an AAV vector, such as a dsAAV2/8 vector
and administered to a human, for example, at a dosage of about
1.times.10.sup.15 vector genomes to about 1.times.10.sup.16 vector
genomes per human.
[0455] In another embodiment, the method of Wooddell et al.
(Molecular Therapy vol. 21 no. 5, 973-985 May 2013) may be used/and
or adapted to the CRISPR Cas system of the present invention.
Woodell et al. show that simple coinjection of a
hepatocyte-targeted, N-acetylgalactosamine-conjugated melittin-like
peptide (NAG-MLP) with a liver-tropic cholesterol-conjugated siRNA
(chol-siRNA) targeting coagulation factor VII (F7) results in
efficient F7 knockdown in mice and nonhuman primates without
changes in clinical chemistry or induction of cytokines. Using
transient and transgenic mouse models of HBV infection, Wooddell et
al. show that a single coinjection of NAG-MLP with potent
chol-siRNAs targeting conserved HBV sequences resulted in multilog
repression of viral RNA, proteins, and viral DNA with long duration
of effect. Intraveinous coinjections, for example, of about 6 mg/kg
of NAG-MLP and 6 mg/kg of HBV specific CRISPR Cas may be envisioned
for the present invention. In the alternative, about 3 mg/kg of
NAG-MLP and 3 mg/kg of HBV specific CRISPR Cas may be delivered on
day one, followed by administration of about about 2-3 mg/kg of
NAG-MLP and 2-3 mg/kg of HBV specific CRISPR Cas two weeks
later.
[0456] The present invention may also be applied to treat hepatitis
C virus (HCV). The methods of Roelvinki et al. (Molecular Therapy
vol. 20 no. 9, 1737-1749 September 2012) may be applied to the
CRISPR Cas system. For example, an AAV vector such as AAV8 may be a
contemplated vector and for example a dosage of about
1.25.times.10.sup.1 to 1.25.times.10.sup.13 vector genomes per
kilogram body weight (vg/kg) may be contemplated.
[0457] It will be readily apparent that a host of other diseases
can be treated in a similar fashion. Some examples of genetic
diseases caused by mutations are provided herein, but many more are
known. The above strategy can be applied to these diseases.
[0458] Huntington's Disease (HD)
[0459] RNA interference (RNAi) offers therapeutic potential for
this disorder by reducing the expression of HIT, the
disease-causing gene of Huntington's disease (see, e.g., McBride et
al., Molecular Therapy vol. 19 no. 12 Dec. 2011, pp. 2152-2162),
therefore Applicant postulates that it may be used/and or adapted
to the CRISPR-Cas system. The CRISPR-Cas system may be generated
using an algorithm to reduce the off-targeting potential of
antisense sequences. The CRISPR-Cas sequences may target either a
sequence in exon 52 of mouse, rhesus or human huntingtin and
expressed in a viral vector, such as AAV. Animals, including
humans, may be injected with about three microinjections per
hemisphere (six injections total): the first 1 mm rostral to the
anterior commissure (12 .mu.l) and the two remaining injections (12
.mu.l and 10 .mu.l, respectively) spaced 3 and 6 mm caudal to the
first injection with 1e12 vg/ml of AAV at a rate of about 1
.mu.l/minute, and the needle was left in place for an additional 5
minutes to allow the injectate to diffuse from the needle tip.
[0460] DiFiglia et al. (PNAS, Oct. 23, 2007, vol. 104, no. 43,
17204-17209) observed that single administration into the adult
striatum of an siRNA targeting Htt can silence mutant Htt,
attenuate neuronal pathology, and delay the abnormal behavioral
phenotype observed in a rapid-onset, viral transgenic mouse model
of HD. DiFiglia injected mice intrastriatally with 2 .mu.l of
Cy3-labeled cc-siRNA-Htt or unconjugated siRNA-Htt at 10 .mu.M. A
similar dosage of CRISPR Cas targeted to Htt may be contemplated
for humans in the present invention, for example, about 5-10 ml of
10 .mu.M CRISPR Cas targeted to Htt may be injected
intrastriatally.
[0461] In another example, Boudreau et al. (Molecular Therapy vol.
17 no. 6 Jun. 2009) injects 5 .mu.l of recombinant AAV serotype 2/1
vectors expressing htt-specific RNAi virus (at 4.times.10.sup.12
viral genomes/ml) into the straiatum. A similar dosage of CRISPR
Cas targeted to Htt may be contemplated for humans in the present
invention, for example, about 10-20 ml of 4.times.10.sup.12 viral
genomes/ml) CRISPR Cas targeted to Htt may be injected
intrastriatally.
[0462] In another example, a CRISPR Cas targeted to HTT may be
administered continuously (see, e.g., Yu et al., Cell 150, 895-908,
Aug. 31, 2012). Yu et al. utilizes osmotic pumps delivering 0.25
ml/hr (Model 2004) to deliver 300 mg/day of ss-siRNA or
phosphate-buffered saline (PBS) (Sigma Aldrich) for 28 days, and
pumps designed to deliver 0.5 .mu.l/hr (Model 2002) were used to
deliver 75 mg/day of the positive control MOE ASO for 14 days.
Pumps (Durect Corporation) were filled with ss-siRNA or MOE diluted
in sterile PBS and then incubated at 37 C for 24 or 48 (Model 2004)
hours prior to implantation. Mice were anesthetized with 2.5%
isofluorane, and a midline incision was made at the base of the
skull. Using stereotaxic guides, a cannula was implanted into the
right lateral ventricle and secured with Loctite adhesive. A
catheter attached to an Alzet osmotic mini pump was attached to the
cannula, and the pump was placed subcutaneously in the midscapular
area. The incision was closed with 5.0 nylon sutures. A similar
dosage of CRISPR Cas targeted to Htt may be contemplated for humans
in the present invention, for example, about 500 to 1000 g/day
CRISPR Cas targeted to Htt may be administered.
[0463] In another example of continuous infusion, Stiles et al.
(Experimental Neurology 233 (2012) 463-471) implanted an
intraparenchymal catheter with a titanium needle tip into the right
putamen. The catheter was connected to a SynchroMed.RTM. II Pump
(Medtronic Neurological, Minneapolis, Minn.) subcutaneously
implanted in the abdomen. After a 7 day infusion of phosphate
buffered saline at 6 .mu.L/day, pumps were re-filled with test
article and programmed for continuous delivery for 7 days. About
2.3 to 11.52 mg/d of siRNA were infused at varying infusion rates
of about 0.1 to 0.5 .mu.L/min. A similar dosage of CRISPR Cas
targeted to Htt may be contemplated for humans in the present
invention, for example, about 20 to 200 mg/day CRISPR Cas targeted
to Htt may be administered.
[0464] In another example, the methods of US Patent Publication No.
20130253040 assigned to Sangamo may also be also be adapted from
TALES to the CRISPR Cas system of the present invention for
treating Huntington's Disease.
[0465] Nucleic Acids, Amino Acids and Proteins
[0466] The invention uses nucleic acids to bind target DNA
sequences. This is advantageous as nucleic acids are much easier
and cheaper to produce than proteins, and the specificity can be
varied according to the length of the stretch where homology is
sought. Complex 3-D positioning of multiple fingers, for example is
not required.
[0467] The terms "polynucleotide", "nucleotide", "nucleotide
sequence", "nucleic acid" and "oligonucleotide" are used
interchangeably. They refer to a polymeric form of nucleotides of
any length, either deoxyribonucleotides or ribonucleotides, or
analogs thereof. Polynucleotides may have any three dimensional
structure, and may perform any function, known or unknown. The
following are non-limiting examples of polynucleotides: coding or
non-coding regions of a gene or gene fragment, loci (locus) defined
from linkage analysis, exons, introns, messenger RNA (mRNA),
transfer RNA, ribosomal RNA, short interfering RNA (siRNA),
short-hairpin RNA (shRNA), micro-RNA (miRNA), ribozymes, cDNA,
recombinant polynucleotides, branched polynucleotides, plasmids,
vectors, isolated DNA of any sequence, isolated RNA of any
sequence, nucleic acid probes, and primers. The term also
encompasses nucleic-acid-like structures with synthetic backbones,
see, e.g., Eckstein, 1991; Baserga et al., 1992; Milligan, 1993; WO
97/03211; WO 96/39154; Mata, 1997; Strauss-Soukup, 1997; and
Samstag, 1996. A polynucleotide may comprise one or more modified
nucleotides, such as methylated nucleotides and nucleotide analogs.
If present, modifications to the nucleotide structure may be
imparted before or after assembly of the polymer. The sequence of
nucleotides may be interrupted by non-nucleotide components. A
polynucleotide may be further modified after polymerization, such
as by conjugation with a labeling component.
[0468] As used herein the term "wild type" is a term of the art
understood by skilled persons and means the typical form of an
organism, strain, gene or characteristic as it occurs in nature as
distinguished from mutant or variant forms.
[0469] As used herein the term "variant" should be taken to mean
the exhibition of qualities that have a pattern that deviates from
what occurs in nature.
[0470] The terms "non-naturally occurring" or "engineered" are used
interchangeably and indicate the involvement of the hand of man.
The terms, when referring to nucleic acid molecules or polypeptides
mean that the nucleic acid molecule or the polypeptide is at least
substantially free from at least one other component with which
they are naturally associated in nature and as found in nature.
[0471] "Complementarity" refers to the ability of a nucleic acid to
form hydrogen bond(s) with another nucleic acid sequence by either
traditional Watson-Crick base pairing or other non-traditional
types. A percent complementarity indicates the percentage of
residues in a nucleic acid molecule which can form hydrogen bonds
(e.g., Watson-Crick base pairing) with a second nucleic acid
sequence (e.g., 5, 6, 7, 8, 9, 10 out of 10 being 50%, 60%, 700%,
80%, 90%, and 100% complementary). "Perfectly complementary" means
that all the contiguous residues of a nucleic acid sequence will
hydrogen bond with the same number of contiguous residues in a
second nucleic acid sequence. "Substantially complementary" as used
herein refers to a degree of complementarity that is at least 60%,
65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100% over a
region of 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22,
23, 24, 25, 30, 35, 40, 45, 50, or more nucleotides, or refers to
two nucleic acids that hybridize under stringent conditions.
[0472] As used herein, "stringent conditions" for hybridization
refer to conditions under which a nucleic acid having
complementarity to a target sequence predominantly hybridizes with
the target sequence, and substantially does not hybridize to
non-target sequences. Stringent conditions are generally
sequence-dependent, and vary depending on a number of factors. In
general, the longer the sequence, the higher the temperature at
which the sequence specifically hybridizes to its target sequence.
Non-limiting examples of stringent conditions are described in
detail in Tijssen (1993), Laboratory Techniques In Biochemistry And
Molecular Biology-Hybridization With Nucleic Acid Probes Part I,
Second Chapter "Overview of principles of hybridization and the
strategy of nucleic acid probe assay", Elsevier, N.Y. Where
reference is made to a polynucleotide sequence, then complementary
or partially complementary sequences are also envisaged. These are
preferably capable of hybridising to the reference sequence under
highly stringent conditions. Generally, in order to maximize the
hybridization rate, relatively low-stringency hybridization
conditions are selected: about 20 to 25.degree. C. lower than the
thermal melting point (T.sub.m). The T.sub.m is the temperature at
which 50% of specific target sequence hybridizes to a perfectly
complementary probe in solution at a defined ionic strength and pH.
Generally, in order to require at least about 85% nucleotide
complementarity of hybridized sequences, highly stringent washing
conditions are selected to be about 5 to 15.degree. C. lower than
the T.sub.m. In order to require at least about 70% nucleotide
complementarity of hybridized sequences, moderately-stringent
washing conditions are selected to be about 15 to 30.degree. C.
lower than the T.sub.m. Highly permissive (very low stringency)
washing conditions may be as low as 50.degree. C. below the
T.sub.m, allowing a high level of mis-matching between hybridized
sequences. Those skilled in the art will recognize that other
physical and chemical parameters in the hybridization and wash
stages can also be altered to affect the outcome of a detectable
hybridization signal from a specific level of homology between
target and probe sequences. Preferred highly stringent conditions
comprise incubation in 500/% formamide, 5.times.SSC, and 1% SDS at
42.degree. C., or incubation in 5.times.SSC and 1% SDS at
65.degree. C., with wash in 0.2.times.SSC and 0.1% SDS at
65.degree. C.
[0473] "Hybridization" refers to a reaction in which one or more
polynucleotides react to form a complex that is stabilized via
hydrogen bonding between the bases of the nucleotide residues. The
hydrogen bonding may occur by Watson Crick base pairing, Hoogstein
binding, or in any other sequence specific manner. The complex may
comprise two strands forming a duplex structure, three or more
strands forming a multi stranded complex, a single self-hybridizing
strand, or any combination of these. A hybridization reaction may
constitute a step in a more extensive process, such as the
initiation of PCR, or the cleavage of a polynucleotide by an
enzyme. A sequence capable of hybridizing with a given sequence is
referred to as the "complement" of the given sequence.
[0474] As used herein, the term "genomic locus" or "locus" (plural
loci) is the specific location of a gene or DNA sequence on a
chromosome. A "gene" refers to stretches of DNA or RNA that encode
a polypeptide or an RNA chain that has functional role to play in
an organism and hence is the molecular unit of heredity in living
organisms. For the purpose of this invention it may be considered
that genes include regions which regulate the production of the
gene product, whether or not such regulatory sequences are adjacent
to coding and/or transcribed sequences. Accordingly, a gene
includes, but is not necessarily limited to, promoter sequences,
terminators, translational regulatory sequences such as ribosome
binding sites and internal ribosome entry sites, enhancers,
silencers, insulators, boundary elements, replication origins,
matrix attachment sites and locus control regions.
[0475] As used herein, "expression of a genomic locus" or "gene
expression" is the process by which information from a gene is used
in the synthesis of a functional gene product. The products of gene
expression are often proteins, but in non-protein coding genes such
as rRNA genes or tRNA genes, the product is functional RNA. The
process of gene expression is used by all known life--eukaryotes
(including multicellular organisms), prokaryotes (bacteria and
archaea) and viruses to generate functional products to survive. As
used herein "expression" of a gene or nucleic acid encompasses not
only cellular gene expression, but also the transcription and
translation of nucleic acid(s) in cloning systems and in any other
context. As used herein, "expression" also refers to the process by
which a polynucleotide is transcribed from a DNA template (such as
into and mRNA or other RNA transcript) and/or the process by which
a transcribed mRNA is subsequently translated into peptides,
polypeptides, or proteins. Transcripts and encoded polypeptides may
be collectively referred to as "gene product." If the
polynucleotide is derived from genomic DNA, expression may include
splicing of the mRNA in a eukaryotic cell.
[0476] The terms "polypeptide", "peptide" and "protein" are used
interchangeably herein to refer to polymers of amino acids of any
length. The polymer may be linear or branched, it may comprise
modified amino acids, and it may be interrupted by non amino acids.
The terms also encompass an amino acid polymer that has been
modified; for example, disulfide bond formation, glycosylation,
lipidation, acetylation, phosphorylation, or any other
manipulation, such as conjugation with a labeling component. As
used herein the term "amino acid" includes natural and/or unnatural
or synthetic amino acids, including glycine and both the D or L
optical isomers, and amino acid analogs and peptidomimetics.
[0477] As used herein, the term "domain" or "protein domain" refers
to a part of a protein sequence that may exist and function
independently of the rest of the protein chain.
[0478] As described in aspects of the invention, sequence identity
is related to sequence homology. Homology comparisons may be
conducted by eye, or more usually, with the aid of readily
available sequence comparison programs. These commercially
available computer programs may calculate percent (%) homology
between two or more sequences and may also calculate the sequence
identity shared by two or more amino acid or nucleic acid
sequences. In some preferred embodiments, the capping region of the
dTALEs described herein have sequences that are at least 95%
identical or share identity to the capping region amino acid
sequences provided herein.
[0479] Sequence homologies may be generated by any of a number of
computer programs known in the art, for example BLAST or FASTA,
etc. A suitable computer program for carrying out such an alignment
is the GCG Wisconsin Bestfit package (University of Wisconsin,
U.S.A; Devereux et al., 1984, Nucleic Acids Research 12:387).
Examples of other software than may perform sequence comparisons
include, but are not limited to, the BLAST package (see Ausubel et
al., 1999 ibid--Chapter 18), FASTA (Atschul et al., 1990, J. Mol.
Biol., 403-410) and the GENEWORKS suite of comparison tools. Both
BLAST and FASTA are available for offline and online searching (see
Ausubel et al., 1999 ibid, pages 7-58 to 7-60). However it is
preferred to use the GCG Bestfit program.
[0480] Percentage (%) sequence homology may be calculated over
contiguous sequences, i.e., one sequence is aligned with the other
sequence and each amino acid or nucleotide in one sequence is
directly compared with the corresponding amino acid or nucleotide
in the other sequence, one residue at a time. This is called an
"ungapped" alignment. Typically, such ungapped alignments are
performed only over a relatively short number of residues.
[0481] Although this is a very simple and consistent method, it
fails to take into consideration that, for example, in an otherwise
identical pair of sequences, one insertion or deletion may cause
the following amino acid residues to be put out of alignment, thus
potentially resulting in a large reduction in % homology when a
global alignment is performed. Consequently, most sequence
comparison methods are designed to produce optimal alignments that
take into consideration possible insertions and deletions without
unduly penalizing the overall homology or identity score. This is
achieved by inserting "gaps" in the sequence alignment to try to
maximize local homology or identity.
[0482] However, these more complex methods assign "gap penalties"
to each gap that occurs in the alignment so that, for the same
number of identical amino acids, a sequence alignment with as few
gaps as possible--reflecting higher relatedness between the two
compared sequences--may achieve a higher score than one with many
gaps. "Affinity gap costs" are typically used that charge a
relatively high cost for the existence of a gap and a smaller
penalty for each subsequent residue in the gap. This is the most
commonly used gap scoring system. High gap penalties may, of
course, produce optimized alignments with fewer gaps. Most
alignment programs allow the gap penalties to be modified. However,
it is preferred to use the default values when using such software
for sequence comparisons. For example, when using the GCG Wisconsin
Bestfit package the default gap penalty for amino acid sequences is
-12 for a gap and -4 for each extension.
[0483] Calculation of maximum % homology therefore first requires
the production of an optimal alignment, taking into consideration
gap penalties. A suitable computer program for carrying out such an
alignment is the GCG Wisconsin Bestfit package (Devereux et al.,
1984 Nuc. Acids Research 12 p 387). Examples of other software than
may perform sequence comparisons include, but are not limited to,
the BLAST package (see Ausubel et al., 1999 Short Protocols in
Molecular Biology, 4.sup.th Ed.--Chapter 18), FASTA (Altschul et
al., 1990 J. Mol. Biol. 403-410) and the GENEWORKS suite of
comparison tools. Both BLAST and FASTA are available for offline
and online searching (see Ausubel et al., 1999, Short Protocols in
Molecular Biology, pages 7-58 to 7-60). However, for some
applications, it is preferred to use the GCG Bestfit program. A new
tool, called BLAST 2 Sequences is also available for comparing
protein and nucleotide sequences (see FEMS Microbiol Lett. 1999
174(2): 247-50; FEMS Microbiol Lett. 1999 177(1): 187-8 and the
website of the National Center for Biotechnology information at the
website of the National Institutes for Health).
[0484] Although the final % homology may be measured in terms of
identity, the alignment process itself is typically not based on an
all-or-nothing pair comparison. Instead, a scaled similarity score
matrix is generally used that assigns scores to each pair-wise
comparison based on chemical similarity or evolutionary distance.
An example of such a matrix commonly used is the BLOSUM62
matrix--the default matrix for the BLAST suite of programs. GCG
Wisconsin programs generally use either the public default values
or a custom symbol comparison table, if supplied (see user manual
for further details). For some applications, it is preferred to use
the public default values for the GCG package, or in the case of
other software, the default matrix, such as BLOSUM62.
[0485] Alternatively, percentage homologies may be calculated using
the multiple alignment feature in DNASIS.TM. (Hitachi Software),
based on an algorithm, analogous to CLUSTAL (Higgins D G &
Sharp P M (1988), Gene 73(1), 237-244). Once the software has
produced an optimal alignment, it is possible to calculate %
homology, preferably % sequence identity. The software typically
does this as part of the sequence comparison and generates a
numerical result.
[0486] The sequences may also have deletions, insertions or
substitutions of amino acid residues which produce a silent change
and result in a functionally equivalent substance. Deliberate amino
acid substitutions may be made on the basis of similarity in amino
acid properties (such as polarity, charge, solubility,
hydrophobicity, hydrophilicity, and/or the amphipathic nature of
the residues) and it is therefore useful to group amino acids
together in functional groups. Amino acids may be grouped together
based on the properties of their side chains alone. However, it is
more useful to include mutation data as well. The sets of amino
acids thus derived are likely to be conserved for structural
reasons. These sets may be described in the form of a Venn diagram
(Livingstone C. D. and Barton G. J. (1993) "Protein sequence
alignments: a strategy for the hierarchical analysis of residue
conservation" Comput. Appl. Biosci. 9: 745-756) (Taylor W. R.
(1986) "The classification of amino acid conservation" J. Theor.
Biol. 119; 205-218). Conservative substitutions may be made, for
example according to the table below which describes a generally
accepted Venn diagram grouping of amino acids.
TABLE-US-00005 Set Sub-set Hydrophobic F W Y H K M I L V A G C
Aromatic F W Y H Aliphatic I L V Polar W Y H K R E D C S T N Q
Charged H K R E D Positively H K R charged Negatively E D charged
Small V C A G S P T N D Tiny A G S
[0487] Embodiments of the invention include sequences (both
polynucleotide or polypeptide) which may comprise homologous
substitution (substitution and replacement are both used herein to
mean the interchange of an existing amino acid residue or
nucleotide, with an alternative residue or nucleotide) that may
occur i.e., like-for-like substitution in the case of amino acids
such as basic for basic, acidic for acidic, polar for polar, etc.
Non-homologous substitution may also occur i.e., from one class of
residue to another or alternatively involving the inclusion of
unnatural amino acids such as ornithine (hereinafter referred to as
Z), diaminobutyric acid ornithine (hereinafter referred to as B),
norleucine ornithine (hereinafter referred to as O), pyriylalanine,
thienylalanine, naphthylalanine and phenylglycine.
[0488] Variant amino acid sequences may include suitable spacer
groups that may be inserted between any two amino acid residues of
the sequence including alkyl groups such as methyl, ethyl or propyl
groups in addition to amino acid spacers such as glycine or
J3-alanine residues. A further form of variation, which involves
the presence of one or more amino acid residues in peptoid form,
may be well understood by those skilled in the art. For the
avoidance of doubt, "the peptoid form" is used to refer to variant
amino acid residues wherein the .alpha.-carbon substituent group is
on the residue's nitrogen atom rather than the .alpha.-carbon.
Processes for preparing peptides in the peptoid form are known in
the art, for example Simon R J et al., PNAS (1992) 89(20),
9367-9371 and Horwell D C, Trends Biotechnol. (1995) 13(4),
132-134.
[0489] The practice of the present invention employs, unless
otherwise indicated, conventional techniques of immunology,
biochemistry, chemistry, molecular biology, microbiology, cell
biology, genomics and recombinant DNA, which are within the skill
of the art. See Sambrook, Fritsch and Maniatis, MOLECULAR CLONING:
A LABORATORY MANUAL, 2nd edition (1989); CURRENT PROTOCOLS IN
MOLECULAR BIOLOGY (F. M. Ausubel, et al. eds., (1987)); the series
METHODS IN ENZYMOLOGY (Academic Press, Inc.): PCR 2: A PRACTICAL
APPROACH (M. J. MacPherson, B. D. Hames and G. R. Taylor eds.
(1995)), Harlow and Lane, eds. (1988) ANTIBODIES, A LABORATORY
MANUAL, and ANIMAL CELL CULTURE (R. I. Freshney, ed. (1987)).
[0490] Vectors
[0491] In one aspect, the invention provides for vectors that are
used in the engineering and optimization of CRISPR-Cas systems.
[0492] A used herein, a "vector" is a tool that allows or
facilitates the transfer of an entity from one environment to
another. It is a replicon, such as a plasmid, phage, or cosmid,
into which another DNA segment may be inserted so as to bring about
the replication of the inserted segment. Generally, a vector is
capable of replication when associated with the proper control
elements. In general, the term "vector" refers to a nucleic acid
molecule capable of transporting another nucleic acid to which it
has been linked. Vectors include, but are not limited to, nucleic
acid molecules that are single-stranded, double-stranded, or
partially double-stranded: nucleic acid molecules that comprise one
or more free ends, no free ends (e.g. circular); nucleic acid
molecules that comprise DNA, RNA, or both; and other varieties of
polynucleotides known in the art. One type of vector is a
"plasmid," which refers to a circular double stranded DNA loop into
which additional DNA segments can be inserted, such as by standard
molecular cloning techniques. Another type of vector is a viral
vector, wherein virally-derived DNA or RNA sequences are present in
the vector for packaging into a virus (e.g. retroviruses,
replication defective retroviruses, adenoviruses, replication
defective adenoviruses, and adeno-associated viruses (AAVs)). Viral
vectors also include polynucleotides carried by a virus for
transfection into a host cell. Certain vectors are capable of
autonomous replication in a host cell into which they are
introduced (e.g. bacterial vectors having a bacterial origin of
replication and episomal mammalian vectors). Other vectors (e.g.,
non-episomal mammalian vectors) are integrated into the genome of a
host cell upon introduction into the host cell, and thereby are
replicated along with the host genome. Moreover, certain vectors
are capable of directing the expression of genes to which they are
operatively-linked. Such vectors are referred to herein as
"expression vectors." Common expression vectors of utility in
recombinant DNA techniques are often in the form of plasmids.
[0493] Recombinant expression vectors can comprise a nucleic acid
of the invention in a form suitable for expression of the nucleic
acid in a host cell, which means that the recombinant expression
vectors include one or more regulatory elements, which may be
selected on the basis of the host cells to be used for expression,
that is operatively-linked to the nucleic acid sequence to be
expressed. Within a recombinant expression vector, "operably
linked" is intended to mean that the nucleotide sequence of
interest is linked to the regulatory element(s) in a manner that
allows for expression of the nucleotide sequence (e.g. in an in
vitro transcription/translation system or in a host cell when the
vector is introduced into the host cell). With regards to
recombination and cloning methods, mention is made of U.S. patent
application Ser. No. 10/815,730, published Sep. 2, 2004 as US
2004-0171156 A1, the contents of which are herein incorporated by
reference in their entirety.
[0494] Aspects of the invention relate to bicistronic vectors for
chimeric RNA and Cas9. Bicistronic expression vectors for chimeric
RNA and Cas9 are preferred. In general and particularly in this
embodiment Cas9 is preferably driven by the CBh promoter. The
chimeric RNA may preferably be driven by a U6 promoter. Ideally the
two are combined. The chimeric guide RNA typically consists of a 20
bp guide sequence (Ns) and this may be joined to the tracr sequence
(running from the first "U" of the lower strand to the end of the
transcript). The tracr sequence may be truncated at various
positions as indicated. The guide and tracr sequences are separated
by the tracr-mate sequence, which may be GUUUUAGAGCUA (SEQ ID NO:
61). This may be followed by the loop sequence GAAA as shown. Both
of these are preferred examples. Applicants have demonstrated
Cas9-mediated indels at the human EMX1 and PVALB loci by SURVEYOR
assays. ChiRNAs are indicated by their "+n" designation, and crRNA
refers to a hybrid RNA where guide and tracr sequences are
expressed as separate transcripts. Throughout this application,
chimeric RNA may also be called single guide, or synthetic guide
RNA (sgRNA). The loop is preferably GAAA, but it is not limited to
this sequence or indeed to being only 4 bp in length. Indeed,
preferred loop forming sequences for use in hairpin structures are
four nucleotides in length, and most preferably have the sequence
GAAA. However, longer or shorter loop sequences may be used, as may
alternative sequences. The sequences preferably include a
nucleotide triplet (for example, AAA), and an additional nucleotide
(for example C or G). Examples of loop forming sequences include
CAAA and AAAG.
[0495] The term "regulatory element" is intended to include
promoters, enhancers, internal ribosomal entry sites (IRES), and
other expression control elements (e.g. transcription termination
signals, such as polyadenylation signals and poly-U sequences).
Such regulatory elements are described, for example, in Goeddel,
GENE EXPRESSION TECHNOLOGY: METHODS IN ENZYMOLOGY 185, Academic
Press, San Diego, Calif. (1990). Regulatory elements include those
that direct constitutive expression of a nucleotide sequence in
many types of host cell and those that direct expression of the
nucleotide sequence only in certain host cells (e.g.,
tissue-specific regulatory sequences). A tissue-specific promoter
may direct expression primarily in a desired tissue of interest,
such as muscle, neuron, bone, skin, blood, specific organs (e.g.
liver, pancreas), or particular cell types (e.g. lymphocytes).
Regulatory elements may also direct expression in a
temporal-dependent manner, such as in a cell-cycle dependent or
developmental stage-dependent manner, which may or may not also be
tissue or cell-type specific. In some embodiments, a vector
comprises one or more pol III promoter (e.g. 1, 2, 3, 4, 5, or more
pol III promoters), one or more pol II promoters (e.g. 1, 2, 3, 4,
5, or more pol II promoters), one or more pol I promoters (e.g. 1,
2, 3, 4, 5, or more pol I promoters), or combinations thereof.
Examples of pol III promoters include, but are not limited to, U6
and H1 promoters. Examples of pol II promoters include, but are not
limited to, the retroviral Rous sarcoma virus (RSV) LTR promoter
(optionally with the RSV enhancer), the cytomegalovirus (CMV)
promoter (optionally with the CMV enhancer) [see, e.g., Boshart et
al, Cell, 41:521-530 (1985)], the SV40 promoter, the dihydrofolate
reductase promoter, the .beta.-actin promoter, the phosphoglycerol
kinase (PGK) promoter, and the EF1.alpha. promoter. Also
encompassed by the term "regulatory element" are enhancer elements,
such as WPRE; CMV enhancers; the R-U5' segment in LTR of HTLV-I
(Mol. Cell. Biol., Vol. 8(1), p. 466-472, 1988); SV40 enhancer; and
the intron sequence between exons 2 and 3 of rabbit .beta.-globin
(Proc. Natl. Acad. Sci. USA., Vol. 78(3), p. 1527-31, 1981). It
will be appreciated by those skilled in the art that the design of
the expression vector can depend on such factors as the choice of
the host cell to be transformed, the level of expression desired,
etc. A vector can be introduced into host cells to thereby produce
transcripts, proteins, or peptides, including fusion proteins or
peptides, encoded by nucleic acids as described herein (e.g.,
clustered regularly interspersed short palindromic repeats (CRISPR)
transcripts, proteins, enzymes, mutant forms thereof, fusion
proteins thereof, etc.). With regards to regulatory sequences,
mention is made of U.S. patent application Ser. No. 10/491,026, the
contents of which are incorporated by reference herein in their
entirety. With regards to promoters, mention is made of PCT
publication WO 2011/028929 and U.S. application Ser. No.
12/511,940, the contents of which are incorporated by reference
herein in their entirety.
[0496] Vectors can be designed for expression of CRISPR transcripts
(e.g. nucleic acid transcripts, proteins, or enzymes) in
prokaryotic or eukaryotic cells. For example, CRISPR transcripts
can be expressed in bacterial cells such as Escherichia coli,
insect cells (using baculovirus expression vectors), yeast cells,
or mammalian cells. Suitable host cells are discussed further in
Goeddel, GENE EXPRESSION TECHNOLOGY: METHODS IN ENZYMOLOGY 185,
Academic Press, San Diego, Calif. (1990). Alternatively, the
recombinant expression vector can be transcribed and translated in
vitro, for example using T7 promoter regulatory sequences and T7
polymerase.
[0497] Vectors may be introduced and propagated in a prokaryote or
prokaryotic cell. In some embodiments, a prokaryote is used to
amplify copies of a vector to be introduced into a eukaryotic cell
or as an intermediate vector in the production of a vector to be
introduced into a eukaryotic cell (e.g. amplifying a plasmid as
part of a viral vector packaging system). In some embodiments, a
prokaryote is used to amplify copies of a vector and express one or
more nucleic acids, such as to provide a source of one or more
proteins for delivery to a host cell or host organism. Expression
of proteins in prokaryotes is most often carried out in Escherichia
coli with vectors containing constitutive or inducible promoters
directing the expression of either fusion or non-fusion proteins.
Fusion vectors add a number of amino acids to a protein encoded
therein, such as to the amino terminus of the recombinant protein.
Such fusion vectors may serve one or more purposes, such as: (i) to
increase expression of recombinant protein; (ii) to increase the
solubility of the recombinant protein; and (iii) to aid in the
purification of the recombinant protein by acting as a ligand in
affinity purification. Often, in fusion expression vectors, a
proteolytic cleavage site is introduced at the junction of the
fusion moiety and the recombinant protein to enable separation of
the recombinant protein from the fusion moiety subsequent to
purification of the fusion protein. Such enzymes, and their cognate
recognition sequences, include Factor Xa, thrombin and
enterokinase. Example fusion expression vectors include pGEX
(Pharmacia Biotech Inc; Smith and Johnson, 1988. Gene 67: 31-40),
pMAL (New England Biolabs, Beverly, Mass.) and pRIT5 (Pharmacia,
Piscataway, N.J.) that fuse glutathione S-transferase (GST),
maltose E binding protein, or protein A, respectively, to the
target recombinant protein.
[0498] Examples of suitable inducible non-fusion E. coli expression
vectors include pTrc (Amrann et al., (1988) Gene 69:301-315) and
pET 11d (Studier et al., GENE EXPRESSION TECHNOLOGY: METHODS IN
ENZYMOLOGY 185, Academic Press, San Diego, Calif. (1990)
60-89).
[0499] In some embodiments, a vector is a yeast expression vector.
Examples of vectors for expression in yeast Saccharomyces cerivisae
include pYepSecl (Baldari, et al., 1987. EMBO J. 6: 229-234), pMFa
(Kuijan and Herskowitz, 1982. Cell 30: 933-943), pJRY88 (Schultz et
al., 1987. Gene 54: 113-123), pYES2 (Invitrogen Corporation, San
Diego, Calif.), and picZ (InVitrogen Corp, San Diego, Calif.).
[0500] In some embodiments, a vector drives protein expression in
insect cells using baculovirus expression vectors. Baculovirus
vectors available for expression of proteins in cultured insect
cells (e.g., SF9 cells) include the pAc series (Smith, et al.,
1983. Mol. Cell. Biol. 3: 2156-2165) and the pVL series (Lucklow
and Summers, 1989. Virology 170: 31-39).
[0501] In some embodiments, a vector is capable of driving
expression of one or more sequences in mammalian cells using a
mammalian expression vector. Examples of mammalian expression
vectors include pCDM8 (Seed, 1987. Nature 329: 840) and pMT2PC
(Kaufman, et al., 1987. EMBO J. 6: 187-195). When used in mammalian
cells, the expression vector's control functions are typically
provided by one or more regulatory elements. For example, commonly
used promoters are derived from polyoma, adenovirus 2,
cytomegalovirus, simian virus 40, and others disclosed herein and
known in the art. For other suitable expression systems for both
prokaryotic and eukaryotic cells see, e.g., Chapters 16 and 17 of
Sambrook, et al., MOLECULAR CLONING: A LABORATORY MANUAL. 2nd ed.,
Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press,
Cold Spring Harbor, N.Y., 1989.
[0502] In some embodiments, the recombinant mammalian expression
vector is capable of directing expression of the nucleic acid
preferentially in a particular cell type (e.g., tissue-specific
regulatory elements are used to express the nucleic acid).
Tissue-specific regulatory elements are known in the art.
Non-limiting examples of suitable tissue-specific promoters include
the albumin promoter (liver-specific; Pinkert, et al., 1987. Genes
Dev. 1: 268-277), lymphoid-specific promoters (Calame and Eaton,
1988. Adv. Immunol. 43: 235-275), in particular promoters of T cell
receptors (Winoto and Baltimore, 1989. EMBO J. 8: 729-733) and
immunoglobulins (Baneiji, et al., 1983. Cell 33: 729-740; Queen and
Baltimore, 1983. Cell 33: 741-748), neuron-specific promoters
(e.g., the neurofilament promoter; Byrne and Ruddle, 1989. Proc.
Natl. Acad. Sci. USA 86: 5473-5477), pancreas-specific promoters
(Edlund, et al., 1985. Science 230: 912-916), and mammary
gland-specific promoters (e.g., milk whey promoter; U.S. Pat. No.
4,873,316 and European Application Publication No. 264,166).
Developmentally-regulated promoters are also encompassed, e.g., the
murine hox promoters (Kessel and Gruss, 1990. Science 249: 374-379)
and the .alpha.-fetoprotein promoter (Campes and Tilghman, 1989.
Genes Dev. 3: 537-546). With regards to these prokaryotic and
eukaryotic vectors, mention is made of U.S. Pat. No. 6,750,059, the
contents of which are incorporated by reference herein in their
entirety. Other embodiments of the invention may relate to the use
of viral vectors, with regards to which mention is made of U.S.
patent application Ser. No. 13/092,085, the contents of which are
incorporated by reference herein in their entirety. Tissue-specific
regulatory elements are known in the art and in this regard,
mention is made of U.S. Pat. No. 7,776,321, the contents of which
are incorporated by reference herein in their entirety.
[0503] Regulatory Elements
[0504] In some embodiments, a regulatory element is operably linked
to one or more elements of a CRISPR system so as to drive
expression of the one or more elements of the CRISPR system. In
general, CRISPRs (Clustered Regularly Interspaced Short Palindromic
Repeats), also known as SPIDRs (SPacer Interspersed Direct
Repeats), constitute a family of DNA loci that are usually specific
to a particular bacterial species. The CRISPR locus comprises a
distinct class of interspersed short sequence repeats (SSRs) that
were recognized in E. coli (Ishino et al., J. Bacteriol.,
169:5429-5433 [1987]; and Nakata et al., J. Bacteriol.,
171:3553-3556 [1989]), and associated genes. Similar interspersed
SSRs have been identified in Haloferax mediterranei, Streptococcus
pyogenes, Anabaena, and Mycobacterium tuberculosis (See, Groenen et
al., Mol. Microbiol., 10:1057-1065 [1993]; Hoe et al., Emerg.
Infect. Dis., 5:254-263 [1999]; Masepohl et al., Biochim. Biophys.
Acta 1307:26-30 [1996]; and Mojica et al., Mol. Microbiol.,
17:85-93 [1995]). The CRISPR loci typically differ from other SSRs
by the structure of the repeats, which have been termed short
regularly spaced repeats (SRSRs) (Janssen et al., OMICS J. Integ.
Biol., 6:23-33 [2002]; and Mojica et al., Mol. Microbiol.,
36:244-246 [2000]). In general, the repeats are short elements that
occur in clusters that are regularly spaced by unique intervening
sequences with a substantially constant length (Mojica et al.,
[2000], supra). Although the repeat sequences are highly conserved
between strains, the number of interspersed repeats and the
sequences of the spacer regions typically differ from strain to
strain (van Embden et al., J. Bacteriol., 182:2393-2401 [2000]).
CRISPR loci have been identified in more than 40 prokaryotes (See
e.g., Jansen et al., Mol. Microbiol., 43:1565-1575 [2002]; and
Mojica et al., [2005]) including, but not limited to Aeropyrum,
Pyrobaculum, Sulfolobus, Archaeoglobus, Halocarcula,
Methanobacterium, Methanococcus, Methanosarcina, Methanopyrus,
Pyrococcus, Picrophilus, Thermoplasma, Corynebacterium,
Mycobacterium, Streptomyces, Aquifex, Porphyromonas, Chlorobium,
Thermus, Bacillus, Listeria, Staphylococcus, Clostridium,
Thermoanaerobacter, Mycoplasma, Fusobacterium, Azarcus,
Chromobacterium, Neisseria, Nitrosomonas, Desulfovibrio, Geobacter,
Myxococcus, Campylobacter, Wolinella, Acinetobacter, Erwinia,
Escherichia, Legionella, Methylococcus, Pasteurella,
Photobacterium, Salmonella, Xanthomonas, Yersinia, Treponema, and
Thermotoga.
[0505] In general, "CRISPR system" refers collectively to
transcripts and other elements involved in the expression of or
directing the activity of CRISPR-associated ("Cas") genes,
including sequences encoding a Cas gene, a tracr (trans-activating
CRISPR) sequence (e.g. tracrRNA or an active partial tracrRNA), a
tracr-mate sequence (encompassing a "direct repeat" and a
tracrRNA-processed partial direct repeat in the context of an
endogenous CRISPR system), a guide sequence (also referred to as a
"spacer" in the context of an endogenous CRISPR system), or other
sequences and transcripts from a CRISPR locus. In embodiments of
the invention the terms guide sequence and guide RNA are used
interchangeably. In some embodiments, one or more elements of a
CRISPR system is derived from a type I, type II, or type III CRISPR
system. In some embodiments, one or more elements of a CRISPR
system is derived from a particular organism comprising an
endogenous CRISPR system, such as Streptococcus pyogenes. In
general, a CRISPR system is characterized by elements that promote
the formation of a CRISPR complex at the site of a target sequence
(also referred to as a protospacer in the context of an endogenous
CRISPR system). In the context of formation of a CRISPR complex,
"target sequence" refers to a sequence to which a guide sequence is
designed to have complementarity, where hybridization between a
target sequence and a guide sequence promotes the formation of a
CRISPR complex. A target sequence may comprise any polynucleotide,
such as DNA or RNA polynucleotides. In some embodiments, a target
sequence is located in the nucleus or cytoplasm of a cell.
[0506] In some embodiments, direct repeats may be identified in
silico by searching for repetitive motifs that fulfill any or all
of the following criteria:
[0507] 1. found in a 2 Kb window of genomic sequence flanking the
type II CRISPR locus;
[0508] 2. span from 20 to 50 bp; and
[0509] 3. interspaced by 20 to 50 bp.
[0510] In some embodiments, 2 of these criteria may be used, for
instance 1 and 2, 2 and 3, or 1 and 3. In some embodiments, all 3
criteria may be used.
[0511] In some embodiments, candidate tracrRNA may be subsequently
predicted by sequences that fulfill any or all of the following
criteria:
[0512] 1. sequence homology to direct repeats (motif search in
Geneious with up to 18-bp mismatches);
[0513] 2. presence of a predicted Rho-independent transcriptional
terminator in direction of transcription; and
[0514] 3. stable hairpin secondary structure between tracrRNA and
direct repeat.
[0515] In some embodiments, 2 of these criteria may be used, for
instance 1 and 2, 2 and 3, or 1 and 3. In some embodiments, all 3
criteria may be used.
[0516] In some embodiments, chimeric synthetic guide RNAs (sgRNAs)
designs may incorporate at least 12 bp of duplex structure between
the direct repeat and tracrRNA.
[0517] In preferred embodiments of the invention, the CRISPR system
is a type II CRISPR system and the Cas enzyme is Cas9, which
catalyzes DNA cleavage. Enzymatic action by Cas9 derived from
Streptococcus pyogenes or any closely related Cas9 generates double
stranded breaks at target site sequences which hybridize to 20
nucleotides of the guide sequence and that have a
protospacer-adjacent motif (PAM) sequence (examples include NGG/NRG
or a PAM that can be determined as described herein) following the
20 nucleotides of the target sequence. CRISPR activity through Cas9
for site-specific DNA recognition and cleavage is defined by the
guide sequence, the tracr sequence that hybridizes in part to the
guide sequence and the PAM sequence. More aspects of the CRISPR
system are described in Karginov and Hannon, The CRISPR system:
small RNA-guided defence in bacteria and archaea, Mole Cell 2010,
Jan. 15; 37(1): 7.
[0518] The type II CRISPR locus from Streptococcus pyogenes SF370,
which contains a cluster of four genes Cas9, Cas1, Cas2, and Csn1,
as well as two non-coding RNA elements, tracrRNA and a
characteristic array of repetitive sequences (direct repeats)
interspaced by short stretches of non-repetitive sequences
(spacers, about 30 bp each). In this system, targeted DNA
double-strand break (DSB) is generated in four sequential steps
(FIG. 2A). First, two non-coding RNAs, the pre-crRNA array and
tracrRNA, are transcribed from the CRISPR locus. Second, tracrRNA
hybridizes to the direct repeats of pre-crRNA, which is then
processed into mature crRNAs containing individual spacer
sequences. Third, the mature crRNA:tracrRNA complex directs Cas9 to
the DNA target consisting of the protospacer and the corresponding
PAM via heteroduplex formation between the spacer region of the
crRNA and the protospacer DNA. Finally, Cas9 mediates cleavage of
target DNA upstream of PAM to create a DSB within the protospacer
(FIG. 2A). FIG. 2B demonstrates the nuclear localization of the
codon optimized Cas9. To promote precise transcriptional
initiation, the RNA polymerase III-based U6 promoter was selected
to drive the expression of tracrRNA (FIG. 2C). Similarly, a U6
promoter-based construct was developed to express a pre-crRNA array
consisting of a single spacer flanked by two direct repeats (DRs,
also encompassed by the term "tracr-mate sequences"; FIG. 2C). The
initial spacer was designed to target a 33-base-pair (bp) target
site (30-bp protospacer plus a 3-bp CRISPR motif (PAM) sequence
satisfying the NGG recognition motif of Cas9) in the human EMX1
locus (FIG. 2C), a key gene in the development of the cerebral
cortex.
[0519] Typically, in the context of an endogenous CRISPR system,
formation of a CRISPR complex (comprising a guide sequence
hybridized to a target sequence and complexed with one or more Cas
proteins) results in cleavage of one or both strands in or near
(e.g. within 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 50, or more base
pairs from) the target sequence. Without wishing to be bound by
theory, the tracr sequence, which may comprise or consist of all or
a portion of a wild-type tracr sequence (e.g. about or more than
about 20, 26, 32, 45, 48, 54, 63, 67, 85, or more nucleotides of a
wild-type tracr sequence), may also form part of a CRISPR complex,
such as by hybridization along at least a portion of the tracr
sequence to all or a portion of a tracr mate sequence that is
operably linked to the guide sequence. In some embodiments, one or
more vectors driving expression of one or more elements of a CRISPR
system are introduced into a host cell such that expression of the
elements of the CRISPR system direct formation of a CRISPR complex
at one or more target sites. For example, a Cas enzyme, a guide
sequence linked to a tracr-mate sequence, and a tracr sequence
could each be operably linked to separate regulatory elements on
separate vectors. Alternatively, two or more of the elements
expressed from the same or different regulatory elements, may be
combined in a single vector, with one or more additional vectors
providing any components of the CRISPR system not included in the
first vector. CRISPR system elements that are combined in a single
vector may be arranged in any suitable orientation, such as one
element located 5' with respect to ("upstream" of) or 3' with
respect to ("downstream" of) a second element. The coding sequence
of one element may be located on the same or opposite strand of the
coding sequence of a second element, and oriented in the same or
opposite direction. In some embodiments, a single promoter drives
expression of a transcript encoding a CRISPR enzyme and one or more
of the guide sequence, tracr mate sequence (optionally operably
linked to the guide sequence), and a tracr sequence embedded within
one or more intron sequences (e.g. each in a different intron, two
or more in at least one intron, or all in a single intron). In some
embodiments, the CRISPR enzyme, guide sequence, tracr mate
sequence, and tracr sequence are operably linked to and expressed
from the same promoter.
[0520] In some embodiments, a vector comprises one or more
insertion sites, such as a restriction endonuclease recognition
sequence (also referred to as a "cloning site"). In some
embodiments, one or more insertion sites (e.g. about or more than
about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more insertion sites) are
located upstream and/or downstream of one or more sequence elements
of one or more vectors. In some embodiments, a vector comprises an
insertion site upstream of a tracr mate sequence, and optionally
downstream of a regulatory element operably linked to the tracr
mate sequence, such that following insertion of a guide sequence
into the insertion site and upon expression the guide sequence
directs sequence-specific binding of a CRISPR complex to a target
sequence in a eukaryotic cell. In some embodiments, a vector
comprises two or more insertion sites, each insertion site being
located between two tracr mate sequences so as to allow insertion
of a guide sequence at each site. In such an arrangement, the two
or more guide sequences may comprise two or more copies of a single
guide sequence, two or more different guide sequences, or
combinations of these. When multiple different guide sequences are
used, a single expression construct may be used to target CRISPR
activity to multiple different, corresponding target sequences
within a cell. For example, a single vector may comprise about or
more than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, or more
guide sequences. In some embodiments, about or more than about 1,
2, 3, 4, 5, 6, 7, 8, 9, 10, or more such guide-sequence-containing
vectors may be provided, and optionally delivered to a cell.
[0521] In some embodiments, a vector comprises a regulatory element
operably linked to an enzyme-coding sequence encoding a CRISPR
enzyme, such as a Cas protein. Non-limiting examples of Cas
proteins include Cas1, Cas1B, Cas2, Cas3, Cas4, Cas5, Cas6, Cas7,
Cas8, Cas9 (also known as Csn1 and Csx12), Cas10, Csy1, Csy2, Csy3,
Cse1, Cse2, Csc1, Csc2, Csa5, Csn2, Csm2, Csm3, Csm4, Csm5, Csm6,
Cmr1, Cmr3, Cmr4, Cmr5, Cmr6, Csb1, Csb2, Csb3, Csx17, Csx14,
Csx10, Csx16, CsaX, Csx3, Csx1, Csx15, Csf1, Csf2, Csf3, Csf4,
homologues thereof, or modified versions thereof. In some
embodiments, the unmodified CRISPR enzyme has DNA cleavage
activity, such as Cas9. In some embodiments, the CRISPR enzyme
directs cleavage of one or both strands at the location of a target
sequence, such as within the target sequence and/or within the
complement of the target sequence. In some embodiments, the CRISPR
enzyme directs cleavage of one or both strands within about 1, 2,
3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 50, 100, 200, 500, or more
base pairs from the first or last nucleotide of a target sequence.
In some embodiments, a vector encodes a CRISPR enzyme that is
mutated to with respect to a corresponding wild-type enzyme such
that the mutated CRISPR enzyme lacks the ability to cleave one or
both strands of a target polynucleotide containing a target
sequence. For example, an aspartate-to-alanine substitution (D10A)
in the RuvC I catalytic domain of Cas9 from S. pyogenes converts
Cas9 from a nuclease that cleaves both strands to a nickase
(cleaves a single strand). Other examples of mutations that render
Cas9 a nickase include, without limitation, H840A, N854A, and
N863A. As a further example, two or more catalytic domains of Cas9
(RuvC I, RuvC II, and RuvC III or the HNH domain) may be mutated to
produce a mutated Cas9 substantially lacking all DNA cleavage
activity. In some embodiments, a D10A mutation is combined with one
or more of H840A, N854A, or N863A mutations to produce a Cas9
enzyme substantially lacking all DNA cleavage activity. In some
embodiments, a CRISPR enzyme is considered to substantially lack
all DNA cleavage activity when the DNA cleavage activity of the
mutated enzyme is less than about 25%, 10%, 5%, 1%, 0.1%, 0.01%, or
lower with respect to its non-mutated form. Where the enzyme is not
SpCas9, mutations may be made at any or all residues corresponding
to positions 10, 762, 840, 854, 863 and/or 986 of SpCas9 (which may
be ascertained for instance by standard sequence comparison tools.
In particular, any or all of the following mutations are preferred
in SpCas9: D10A, E762A, H840A, N854A, N863A and/or D986A; as well
as conservative substitution for any of the replacement amino acids
is also envisaged. The same (or conservative substitutions of these
mutations) at corresponding positions in other Cas9s are also
preferred. Particularly preferred are D10 and H840 in SpCas9.
However, in other Cas9s, residues corresponding to SpCas9 D10 and
H840 are also preferred.
[0522] An aspartate-to-alanine substitution (D10A) in the RuvC I
catalytic domain of SpCas9 was engineered to convert the nuclease
into a nickase (SpCas9n) (see e.g. Sapranauskas et al., 2011,
Nucleic Acis Research, 39: 9275; Gasiunas et al., 2012, Proc. Natl.
Acad. Sci. USA, 109:E2579), such that nicked genomic DNA undergoes
the high-fidelity homology-directed repair (HDR). Surveyor assay
confirmed that SpCas9n does not generate indels at the EMX1
protospacer target. Co-expression of EMX1-targeting chimeric crRNA
(having the tracrRNA component as well) with SpCas9 produced indels
in the target site, whereas co-expression with SpCas9n did not
(n=3). Moreover, sequencing of 327 amplicons did not detect any
indels induced by SpCas9n. The same locus was selected to test
CRISPR-mediated HR by co-transfecting HEK 293FT cells with the
chimeric RNA targeting EMX1, hSpCas9 or hSpCas9n, as well as a HR
template to introduce a pair of restriction sites (HindIII and
NheI) near the protospacer.
[0523] Preferred orthologs are described herein. A Cas enzyme may
be identified Cas9 as this can refer to the general class of
enzymes that share homology to the biggest nuclease with multiple
nuclease domains from the type II CRISPR system. Most preferably,
the Cas9 enzyme is from, or is derived from, spCas9 or saCas9. By
derived, Applicants mean that the derived enzyme is largely based,
in the sense of having a high degree of sequence homology with, a
wildtype enzyme, but that it has been mutated (modified) in some
way as described herein.
[0524] It will be appreciated that the terms Cas and CRISPR enzyme
are generally used herein interchangeably, unless otherwise
apparent. As mentioned above, many of the residue numberings used
herein refer to the Cas9 enzyme from the type II CRISPR locus in
Streptococcus pyogenes. However, it will be appreciated that this
invention includes many more Cas9s from other species of microbes,
such as SpCas9, SaCa9, StlCas9 and so forth.
[0525] Codon Optimization
[0526] An example of a codon optimized sequence, in this instance
optimized for humans (i.e. being optimized for expression in
humans) is provided herein, see the SaCas9 human codon optimized
sequence. Whilst this is preferred, it will be appreciated that
other examples are possible and codon optimization for a host
species is known.
[0527] In some embodiments, an enzyme coding sequence encoding a
CRISPR enzyme is codon optimized for expression in particular
cells, such as eukaryotic cells. The eukaryotic cells may be those
of or derived from a particular organism, such as a mammal,
including but not limited to human, mouse, rat, rabbit, dog, or
non-human mammal or primate. In some embodiments, processes for
modifying the germ line genetic identity of human beings and/or
processes for modifying the genetic identity of animals which are
likely to cause them suffering without any substantial medical
benefit to man or animal, and also animals resulting from such
processes, may be excluded.
[0528] In general, codon optimization refers to a process of
modifying a nucleic acid sequence for enhanced expression in the
host cells of interest by replacing at least one codon (e.g. about
or more than about 1, 2, 3, 4, 5, 10, 15, 20, 25, 50, or more
codons) of the native sequence with codons that are more frequently
or most frequently used in the genes of that host cell while
maintaining the native amino acid sequence. Various species exhibit
particular bias for certain codons of a particular amino acid.
Codon bias (differences in codon usage between organisms) often
correlates with the efficiency of translation of messenger RNA
(mRNA), which is in turn believed to be dependent on, among other
things, the properties of the codons being translated and the
availability of particular transfer RNA (tRNA) molecules. The
predominance of selected tRNAs in a cell is generally a reflection
of the codons used most frequently in peptide synthesis.
Accordingly, genes can be tailored for optimal gene expression in a
given organism based on codon optimization. Codon usage tables are
readily available, for example, at the "Codon Usage Database"
available at www.kazusa.orjp/codon/(visited Jul. 9, 2002), and
these tables can be adapted in a number of ways. See Nakamura, Y.,
et al. "Codon usage tabulated from the international DNA sequence
databases: status for the year 2000" Nucl. Acids Res. 28:292
(2000). Computer algorithms for codon optimizing a particular
sequence for expression in a particular host cell are also
available, such as Gene Forge (Aptagen; Jacobus, Pa.), are also
available. In some embodiments, one or more codons (e.g. 1, 2, 3,
4, 5, 10, 15, 20, 25, 50, or more, or all codons) in a sequence
encoding a CRISPR enzyme correspond to the most frequently used
codon for a particular amino acid.
[0529] Nuclear Localization Sequences (NLSs)
[0530] In some embodiments, a vector encodes a CRISPR enzyme
comprising one or more nuclear localization sequences (NLSs), such
as about or more than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more
NLSs. In some embodiments, the CRISPR enzyme comprises about or
more than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more NLSs at or
near the amino-terminus, about or more than about 1, 2, 3, 4, 5, 6,
7, 8, 9, 10, or more NLSs at or near the carboxy-terminus, or a
combination of these (e.g. one or more NLS at the amino-terminus
and one or more NLS at the carboxy terminus). When more than one
NLS is present, each may be selected independently of the others,
such that a single NLS may be present in more than one copy and/or
in combination with one or more other NLSs present in one or more
copies. In a preferred embodiment of the invention, the CRISPR
enzyme comprises at most 6 NLSs. In some embodiments, an NLS is
considered near the N- or C-terminus when the nearest amino acid of
the NLS is within about 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 40, 50,
or more amino acids along the polypeptide chain from the N- or
C-terminus. Non-limiting examples of NLSs include an NLS sequence
derived from: the NLS of the SV40 virus large T-antigen, having the
amino acid sequence PKKKRKV (SEQ ID NO: 62); the NLS from
nucleoplasmin (e.g. the nucleoplasmin bipartite NLS with the
sequence KRPAATKKAGQAKKKK (SEQ ID NO: 63)); the c-myc NLS having
the amino acid sequence PAAKRVKLD (SEQ ID NO: 64) or RQRRNELKRSP
(SEQ ID NO: 65); the hRNPA1 M9 NLS having the sequence
NQSSNFGPMKGGNFGGRSSGPYGGGGQYFAKPRNQGGY (SEQ ID NO: 66); the
sequence RMRIZFKNKGKDTAELRRRRVEVSVELRKAKKDEQILKRRNV (SEQ ID NO: 67)
of the IBB domain from importin-alpha; the sequences VSRKRPRP (SEQ
ID NO: 68) and PPKKARED (SEQ ID NO: 69) of the myoma T protein; the
sequence PQPKKKPL (SEQ ID NO: 70) of human p53; the sequence
SALIKKKKKMAP (SEQ ID NO: 71) of mouse c-abl IV; the sequences DRLRR
(SEQ ID NO: 72) and PKQKKRK (SEQ ID NO: 73) of the influenza virus
NS1; the sequence RKLKKKIKKL (SEQ ID NO: 74) of the Hepatitis virus
delta antigen: the sequence REKKKFLKRR (SEQ ID NO: 75) of the mouse
Mx1 protein; the sequence KRKGDEVDGVDEVAKKKSKK (SEQ ID NO: 76) of
the human poly(ADP-ribose) polymerase; and the sequence
RKCLQAGMNLEARKTKK (SEQ ID NO: 77) of the steroid hormone receptors
(human) glucocorticoid.
[0531] In general, the one or more NLSs are of sufficient strength
to drive accumulation of the CRISPR enzyme in a detectable amount
in the nucleus of a eukaryotic cell. In general, strength of
nuclear localization activity may derive from the number of NLSs in
the CRISPR enzyme, the particular NLS(s) used, or a combination of
these factors. Detection of accumulation in the nucleus may be
performed by any suitable technique. For example, a detectable
marker may be fused to the CRISPR enzyme, such that location within
a cell may be visualized, such as in combination with a means for
detecting the location of the nucleus (e.g. a stain specific for
the nucleus such as DAPI). Cell nuclei may also be isolated from
cells, the contents of which may then be analyzed by any suitable
process for detecting protein, such as immunohistochemistry,
Western blot, or enzyme activity assay. Accumulation in the nucleus
may also be determined indirectly, such as by an assay for the
effect of CRISPR complex formation (e.g. assay for DNA cleavage or
mutation at the target sequence, or assay for altered gene
expression activity affected by CRISPR complex formation and/or
CRISPR enzyme activity), as compared to a control no exposed to the
CRISPR enzyme or complex, or exposed to a CRISPR enzyme lacking the
one or more NLSs.
[0532] Guide Sequence
[0533] In general, a guide sequence is any polynucleotide sequence
having sufficient complementarity with a target polynucleotide
sequence to hybridize with the target sequence and direct
sequence-specific binding of a CRISPR complex to the target
sequence. In some embodiments, the degree of complementarity
between a guide sequence and its corresponding target sequence,
when optimally aligned using a suitable alignment algorithm, is
about or more than about 50%, 60%, 75%, 80%, 85%, 90%, 95%, 97.5%,
99%, or more. Optimal alignment may be determined with the use of
any suitable algorithm for aligning sequences, non-limiting example
of which include the Smith-Waterman algorithm, the Needleman-Wunsch
algorithm, algorithms based on the Burrows-Wheeler Transform (e.g.
the Burrows Wheeler Aligner), ClustalW, Clustal X, BLAT, Novoalign
(Novocraft Technologies; available at www.novocraft.com), ELAND
(Illumina, San Diego, Calif.), SOAP (available at
soap.genomics.org.cn), and Maq (available at maq.sourceforge.net).
In some embodiments, a guide sequence is about or more than about
5, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25,
26, 27, 28, 29, 30, 35, 40, 45, 50, 75, or more nucleotides in
length. In some embodiments, a guide sequence is less than about
75, 50, 45, 40, 35, 30, 25, 20, 15, 12, or fewer nucleotides in
length. The ability of a guide sequence to direct sequence-specific
binding of a CRISPR complex to a target sequence may be assessed by
any suitable assay. For example, the components of a CRISPR system
sufficient to form a CRISPR complex, including the guide sequence
to be tested, may be provided to a host cell having the
corresponding target sequence, such as by transfection with vectors
encoding the components of the CRISPR sequence, followed by an
assessment of preferential cleavage within the target sequence,
such as by Surveyor assay as described herein. Similarly, cleavage
of a target polynucleotide sequence may be evaluated in a test tube
by providing the target sequence, components of a CRISPR complex,
including the guide sequence to be tested and a control guide
sequence different from the test guide sequence, and comparing
binding or rate of cleavage at the target sequence between the test
and control guide sequence reactions. Other assays are possible,
and will occur to those skilled in the art.
[0534] A guide sequence may be selected to target any target
sequence. In some embodiments, the target sequence is a sequence
within a genome of a cell. Exemplary target sequences include those
that are unique in the target genome. For example, for the S.
pyogenes Cas9, a unique target sequence in a genome may include a
Cas9 target site of the form MMMMMMMMNNNNNNNNNNNNXGG where
NNNNNNNNNNNNXGG (N is A, G, T, or C; and X can be anything) has a
single occurrence in the genome. A unique target sequence in a
genome may include an S. pyogenes Cas9 target site of the form
MMMMMMMMMGG where NNNNNNNNNNNXGG (N is A, G, T, or C; and X can be
anything) has a single occurrence in the genome. For the S.
thermophilus CRISPR1 Cas9, a unique target sequence in a genome may
include a Cas9 target site of the form MMMMMMMMNNNNNNNNNNNNXXAGAAW
(SEQ ID NO: 78) where NNNNNNNNNNNNXXAGAAW (SEQ ID NO: 79) (N is A,
G, T, or C; X can be anything; and W is A or T) has a single
occurrence in the genome. A unique target sequence in a genome may
include an S. thermophilus CRISPR1 Cas9 target site of the form
MMMMMMMMMNNNNNNNNNNNXXAGAAW (SEQ ID NO: 80) where
NNNNNNNNNNNXXAGAAW (SEQ ID NO: 81) (N is A, G, T, or C; X can be
anything; and W is A or T) has a single occurrence in the genome.
For the S. pyogenes Cas9, a unique target sequence in a genome may
include a Cas9 target site of the form MMMMMMMMGGXG where
NNNNNNNNNNNNXGGXG (N is A, G, T, or C; and X can be anything) has a
single occurrence in the genome. A unique target sequence in a
genome may include an S. pyogenes Cas9 target site of the form
MMMMMMMMMMNNNNNNNNNNNXGGXG where NNNNNNNNNNNXGGXG (N is A, G, T, or
C; and X can be anything) has a single occurrence in the genome. In
each of these sequences "M" may be A, G, T, or C, and need not be
considered in identifying a sequence as unique.
[0535] In some embodiments, a guide sequence is selected to reduce
the degree secondary structure within the guide sequence. In some
embodiments, about or less than about 75%, 50%, 40%, 30%, 25%, 20%,
15%, 10%, 5%, 1%, or fewer of the nucleotides of the guide sequence
participate in self-complementary base pairing when optimally
folded. Optimal folding may be determined by any suitable
polynucleotide folding algorithm. Some programs are based on
calculating the minimal Gibbs free energy. An example of one such
algorithm is mFold, as described by Zuker and Stiegler (Nucleic
Acids Res. 9 (1981), 133-148). Another example folding algorithm is
the online webserver RNAfold, developed at Institute for
Theoretical Chemistry at the University of Vienna, using the
centroid structure prediction algorithm (see e.g. A. R. Gruber el
al., 2008, Cell 106(1): 23-24; and PA Carr and GM Church, 2009,
Nature Biotechnology 27(12): 1151-62).
[0536] Tracr Mate Sequence
[0537] In general, a tracr mate sequence includes any sequence that
has sufficient complementarity with a tracr sequence to promote one
or more of: (1) excision of a guide sequence flanked by tracr mate
sequences in a cell containing the corresponding tracr sequence;
and (2) formation of a CRISPR complex at a target sequence, wherein
the CRISPR complex comprises the tracr mate sequence hybridized to
the tracr sequence. In general, degree of complementarity is with
reference to the optimal alignment of the tracr mate sequence and
tracr sequence, along the length of the shorter of the two
sequences. Optimal alignment may be determined by any suitable
alignment algorithm, and may further account for secondary
structures, such as self-complementarity within either the tracr
sequence or tracr mate sequence. In some embodiments, the degree of
complementarity between the tracr sequence and tracr mate sequence
along the length of the shorter of the two when optimally aligned
is about or more than about 25%, 30%, 40%, 50%, 60%, 700%, 800%,
90%, 95%, 97.5%, 99%, or higher. In some embodiments, the tracr
sequence is about or more than about 5, 6, 7, 8, 9, 10, 11, 12, 13,
14, 15, 16, 17, 18, 19, 20, 25, 30, 40, 50, or more nucleotides in
length. In some embodiments, the tracr sequence and tracr mate
sequence are contained within a single transcript, such that
hybridization between the two produces a transcript having a
secondary structure, such as a hairpin. In an embodiment of the
invention, the transcript or transcribed polynucleotide sequence
has at least two or more hairpins. In preferred embodiments, the
transcript has two, three, four or five hairpins. In a further
embodiment of the invention, the transcript has at most five
hairpins. In a hairpin structure the portion of the sequence 5' of
the final "N" and upstream of the loop corresponds to the tracr
mate sequence, and the portion of the sequence 3' of the loop
corresponds to the tracr sequence Further non-limiting examples of
single polynucleotides comprising a guide sequence, a tracr mate
sequence, and a tracr sequence are as follows (listed 5' to 3'),
where "N" represents a base of a guide sequence, the first block of
lower case letters represent the tracr mate sequence, and the
second block of lower case letters represent the tracr sequence,
and the final poly-T sequence represents the transcription
terminator: (1)
NNNNNNNNNNNNNNNNNNNNgtttttgtactctcaagatttaGAAAtaaatcttgcagaagctacaaagataa
ggcttcatgccgaaatcaacaccctgtcattttatggcagggtgttttcgttatttaaTTTTTT
(SEQ ID NO: 82); (2) gNNNNNN NNNNNNNNNNN
gtactctcaGAAAtgcagaagctacaaagataaggcttcatgccg
aaatcaacaccctgtcattttatggcagggtgttttcgttatttaaTTTTTT (SEQ ID NO:
83); (3) NNN NN
NNNNNNNNNNgtttttgtactctcaGAAAtgcagaagctacaaagataaggcttcatgccg
aaatcaacaccctgtcattttatggcagggtgtTTTTTT (SEQ ID NO: 84); (4)
NNNNNNNNNNNNNNNNNNNNgttttagagctaGAAAtagcaagttaaaataaggctagtccgttatcaactt
gaaaaagtggcaccgagtcggtgcTTTTTT (SEQ ID NO: 85); (5)
NNNNNNNNNNNNNNNNNNNNgttttagagctaGAAATAGcaagttaaaataaggctagtccgttatcaac
ttgaaaaagtgTTTTTTT (SEQ ID NO: 86); and (6)
NgttttagagctagAAATAGcaagttaaaataaggctagtccgttatcaTT TTTTTT (SEQ ID
NO: 87). In some embodiments, sequences (1) to (3) are used in
combination with Cas9 from S. thermophilus CRISPR1. In some
embodiments, sequences (4) to (6) are used in combination with Cas9
from S. pyogenes. In some embodiments, the tracr sequence is a
separate transcript from a transcript comprising the tracr mate
sequence.
[0538] Recombination Template
[0539] In some embodiments, a recombination template is also
provided. A recombination template may be a component of another
vector as described herein, contained in a separate vector, or
provided as a separate polynucleotide. In some embodiments, a
recombination template is designed to serve as a template in
homologous recombination, such as within or near a target sequence
nicked or cleaved by a CRISPR enzyme as a part of a CRISPR complex.
A template polynucleotide may be of any suitable length, such as
about or more than about 10, 15, 20, 25, 50, 75, 100, 150, 200,
500, 1000, or more nucleotides in length. In some embodiments, the
template polynucleotide is complementary to a portion of a
polynucleotide comprising the target sequence. When optimally
aligned, a template polynucleotide might overlap with one or more
nucleotides of a target sequences (e.g. about or more than about 1,
5, 10, 15, 20, or more nucleotides). In some embodiments, when a
template sequence and a polynucleotide comprising a target sequence
are optimally aligned, the nearest nucleotide of the template
polynucleotide is within about 1, 5, 10, 15, 20, 25, 50, 75, 100,
200, 300, 400, 500, 1000, 5000, 10000, or more nucleotides from the
target sequence.
[0540] Fusion Protein
[0541] In some embodiments, the CRISPR enzyme is part of a fusion
protein comprising one or more heterologous protein domains (e.g.
about or more than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more
domains in addition to the CRISPR enzyme). A CRISPR enzyme fusion
protein may comprise any additional protein sequence, and
optionally a linker sequence between any two domains. Examples of
protein domains that may be fused to a CRISPR enzyme include,
without limitation, epitope tags, reporter gene sequences, and
protein domains having one or more of the following activities:
methylase activity, demethylase activity, transcription activation
activity, transcription repression activity, transcription release
factor activity, histone modification activity, RNA cleavage
activity and nucleic acid binding activity. Non-limiting examples
of epitope tags include histidine (His) tags, V5 tags, FLAG tags,
influenza hemagglutinin (HA) tags, Myc tags, VSV-G tags, and
thioredoxin (Trx) tags. Examples of reporter genes include, but are
not limited to, glutathione-S-transferase (GST), horseradish
peroxidase (HRP), chloramphenicol acetyltransferase (CAT)
beta-galactosidase, beta-glucuronidase, luciferase, green
fluorescent protein (GFP), HcRed, DsRed, cyan fluorescent protein
(CFP), yellow fluorescent protein (YFP), and autofluorescent
proteins including blue fluorescent protein (BFP). A CRISPR enzyme
may be fused to a gene sequence encoding a protein or a fragment of
a protein that bind DNA molecules or bind other cellular molecules,
including but not limited to maltose binding protein (MBP), S-tag,
Lex A DNA binding domain (DBD) fusions, GALA DNA binding domain
fusions, and herpes simplex virus (HSV) BP16 protein fusions.
Additional domains that may form part of a fusion protein
comprising a CRISPR enzyme are described in US20110059502,
incorporated herein by reference. In some embodiments, a tagged
CRISPR enzyme is used to identify the location of a target
sequence.
[0542] Inducible System
[0543] In some embodiments, a CRISPR enzyme may form a component of
an inducible system. The inducible nature of the system would allow
for spatiotemporal control of gene editing or gene expression using
a form of energy. The form of energy may include but is not limited
to electromagnetic radiation, sound energy, chemical energy and
thermal energy. Examples of inducible system include tetracycline
inducible promoters (Tet-On or Tet-Off), small molecule two-hybrid
transcription activations systems (FKBP, ABA, etc), or light
inducible systems (Phytochrome, LOV domains, or cryptochrome). In
one embodiment, the CRISPR enzyme may be a part of a Light
Inducible Transcriptional Effector (LITE) to direct changes in
transcriptional activity in a sequence-specific manner. The
components of a light may include a CRISPR enzyme, a
light-responsive cytochrome heterodimer (e.g. from Arabidopsis
thaliana), and a transcriptional activation/repression domain.
Further examples of inducible DNA binding proteins and methods for
their use are provided in U.S. 61/736,465 and U.S. 61/721,283,
which is hereby incorporated by reference in its entirety.
[0544] Delivery
[0545] In some aspects, the invention provides methods comprising
delivering one or more polynucleotides, such as or one or more
vectors as described herein, one or more transcripts thereof,
and/or one or proteins transcribed therefrom, to a host cell. In
some aspects, the invention further provides cells produced by such
methods, and animals comprising or produced from such cells. In
some embodiments, a CRISPR enzyme in combination with (and
optionally complexed with) a guide sequence is delivered to a cell.
Conventional viral and non-viral based gene transfer methods can be
used to introduce nucleic acids in mammalian cells or target
tissues. Such methods can be used to administer nucleic acids
encoding components of a CRISPR system to cells in culture, or in a
host organism. Non-viral vector delivery systems include DNA
plasmids, RNA (e.g. a transcript of a vector described herein),
naked nucleic acid, and nucleic acid complexed with a delivery
vehicle, such as a liposome. Viral vector delivery systems include
DNA and RNA viruses, which have either episomal or integrated
genomes after delivery to the cell. For a review of gene therapy
procedures, see Anderson, Science 256:808-813 (1992); Nabel &
Felgner, TIBTECH 11:211-217 (1993); Mitani & Caskey, TIBTECH
11:162-166 (1993); Dillon, TIBTECH 11:167-175 (1993); Miller,
Nature 357:455-460 (1992); Van Brunt, Biotechnology 6(10):1149-1154
(1988); Vigne, Restorative Neurology and Neuroscience 8:35-36
(1995); Kremer & Perricaudet, British Medical Bulletin
51(1):31-44 (1995); Haddada et al., in Current Topics in
Microbiology and Immunology Doerfler and Bohm (eds) (1995); and Yu
et al., Gene Therapy 1:13-26 (1994).
[0546] Methods of non-viral delivery of nucleic acids include
lipofection, microinjection, biolistics, virosomes, liposomes,
immunoliposomes, polycation or lipid:nucleic acid conjugates, naked
DNA, artificial virions, and agent-enhanced uptake of DNA.
Lipofection is described in e.g., U.S. Pat. Nos. 5,049,386,
4,946,787; and 4,897,355) and lipofection reagents are sold
commercially (e.g., Transfectam.TM. and Lipofectin.TM.). Cationic
and neutral lipids that are suitable for efficient
receptor-recognition lipofection of polynucleotides include those
of Felgner, WO 91/17424; WO 91/16024. Delivery can be to cells
(e.g. in vitro or ex vivo administration) or target tissues (e.g.
in vivo administration).
[0547] The preparation of lipid:nucleic acid complexes, including
targeted liposomes such as immunolipid complexes, is well known to
one of skill in the art (see, e.g., Crystal, Science 270:404-410
(1995); Blaese et al., Cancer Gene Ther. 2:291-297 (1995); Behr et
al., Bioconjugate Chem. 5:382-389 (1994); Remy et al., Bioconjugate
Chem. 5:647-654 (1994); Gao et al., Gene Therapy 2:710-722 (1995);
Ahmad et al., Cancer Res. 52:4817-4820 (1992); U.S. Pat. Nos.
4,186,183, 4,217,344, 4,235,871, 4,261,975, 4,485,054, 4,501,728,
4,774,085, 4,837,028, and 4,946,787).
[0548] The use of RNA or DNA viral based systems for the delivery
of nucleic acids take advantage of highly evolved processes for
targeting a virus to specific cells in the body and trafficking the
viral payload to the nucleus. Viral vectors can be administered
directly to patients (in vivo) or they can be used to treat cells
in vitro, and the modified cells may optionally be administered to
patients (ex vivo). Conventional viral based systems could include
retroviral, lentivirus, adenoviral, adeno-associated and herpes
simplex virus vectors for gene transfer. Integration in the host
genome is possible with the retrovirus, lentivirus, and
adeno-associated virus gene transfer methods, often resulting in
long term expression of the inserted transgene. Additionally, high
transduction efficiencies have been observed in many different cell
types and target tissues.
[0549] The tropism of a retrovirus can be altered by incorporating
foreign envelope proteins, expanding the potential target
population of target cells. Lentiviral vectors are retroviral
vectors that are able to transduce or infect non-dividing cells and
typically produce high viral titers. Selection of a retroviral gene
transfer system would therefore depend on the target tissue.
Retroviral vectors are comprised of cis-acting long terminal
repeats with packaging capacity for up to 6-10 kb of foreign
sequence. The minimum cis-acting LTRs are sufficient for
replication and packaging of the vectors, which are then used to
integrate the therapeutic gene into the target cell to provide
permanent transgene expression. Widely used retroviral vectors
include those based upon murine leukemia virus (MuLV), gibbon ape
leukemia virus (GaLV), Simian Immuno deficiency virus (SIV), human
immuno deficiency virus (HIV), and combinations thereof (see, e.g.,
Buchscher et al., J. Virol. 66:2731-2739 (1992); Johann et al., J.
Virol. 66:1635-1640 (1992); Sommnerfelt et al., Virol. 176:58-59
(1990); Wilson et al., J. Virol. 63:2374-2378 (1989); Miller et
al., J. Virol. 65:2220-2224 (1991); PCT/US94/05700).
[0550] In another embodiment, Cocal vesiculovirus envelope
pseudotyped retroviral vector particles are contemplated (see,
e.g., US Patent Publication No. 20120164118 assigned to the Fred
Hutchinson Cancer Research Center). Cocal virus is in the
Vesiculovirus genus, and is a causative agent of vesicular
stomatitis in mammals. Cocal virus was originally isolated from
mites in Trinidad (Jonkers et al., Am. J. Vet. Res. 25:236-242
(1964)), and infections have been identified in Trinidad, Brazil,
and Argentina from insects, cattle, and horses. Many of the
vesiculoviruses that infect mammals have been isolated from
naturally infected arthropods, suggesting that they are
vector-borne. Antibodies to vesiculoviruses are common among people
living in rural areas where the viruses are endemic and
laboratory-acquired; infections in humans usually result in
influenza-like symptoms. The Cocal virus envelope glycoprotein
shares 71.5% identity at the amino acid level with VSV-G Indiana,
and phylogenetic comparison of the envelope gene of vesiculoviruses
shows that Cocal virus is serologically distinct from, but most
closely related to, VSV-G Indiana strains among the
vesiculoviruses. Jonkers et al., Am. J. Vet. Res. 25:236-242 (1964)
and Travassos da Rosa et al., Am. J. Tropical Med. & Hygiene
33:999-1006 (1984). The Cocal vesiculovirus envelope pseudotyped
retroviral vector particles may include for example, lentiviral,
alpharetroviral, betaretroviral, gammaretroviral, deltaretroviral,
and epsilonretroviral vector particles that may comprise retroviral
Gag, Pol, and/or one or more accessory protein(s) and a Cocal
vesiculovirus envelope protein. Within certain aspects of these
embodiments, the Gag, Pol, and accessory proteins are lentiviral
and/or gammaretroviral.
[0551] In applications where transient expression is preferred,
adenoviral based systems may be used. Adenoviral based vectors are
capable of very high transduction efficiency in many cell types and
do not require cell division. With such vectors, high titer and
levels of expression have been obtained. This vector can be
produced in large quantities in a relatively simple system.
[0552] Adeno-associated virus ("AAV") vectors may also be used to
transduce cells with target nucleic acids, e.g., in the in vitro
production of nucleic acids and peptides, and for in vivo and ex
vivo gene therapy procedures (see, e.g., West et al., Virology
160:38-47 (1987); U.S. Pat. No. 4,797,368; WO 93/24641; Kotin,
Human Gene Therapy 5:793-801 (1994); Muzyczka, J. Clin. Invest.
94:1351 (1994). Construction of recombinant AAV vectors are
described in a number of publications, including U.S. Pat. No.
5,173,414; Tratschin et al., Mol. Cell. Biol. 5:3251-3260 (1985);
Tratschin, et al., Mol. Cell. Biol. 4:2072-2081 (1984); Hermonat
& Muzyczka, PNAS 81:6466-6470 (1984); and Samulski et al., J.
Virol. 63:03822-3828 (1989).
[0553] Packaging cells are typically used to form virus particles
that are capable of infecting a host cell. Such cells include 293
cells, which package adenovirus, and .psi..sup.2 cells or PA317
cells, which package retrovirus. Viral vectors used in gene therapy
are usually generated by producer a cell line that packages a
nucleic acid vector into a viral particle. The vectors typically
contain the minimal viral sequences required for packaging and
subsequent integration into a host, other viral sequences being
replaced by an expression cassette for the polynucleotide(s) to be
expressed. The missing viral functions are typically supplied in
trans by the packaging cell line. For example, AAV vectors used in
gene therapy typically only possess ITR sequences from the AAV
genome which are required for packaging and integration into the
host genome. Viral DNA is packaged in a cell line, which contains a
helper plasmid encoding the other AAV genes, namely rep and cap,
but lacking ITR sequences. The cell line may also infected with
adenovirus as a helper. The helper virus promotes replication of
the AAV vector and expression of AAV genes from the helper plasmid.
The helper plasmid is not packaged in significant amounts due to a
lack of ITR sequences. Contamination with adenovirus can be reduced
by, e.g., heat treatment to which adenovirus is more sensitive than
AAV.
[0554] Accordingly, AAV is considered an ideal candidate for use as
a transducing vector. Such AAV transducing vectors can comprise
sufficient cis-acting functions to replicate in the presence of
adenovirus or herpesvirus or poxvirus (e.g., vaccinia virus) helper
functions provided in trans. Recombinant AAV (rAAV) can be used to
carry exogenous genes into cells of a variety of lineages. In these
vectors, the AAV cap and/or rep genes are deleted from the viral
genome and replaced with a DNA segment of choice. Current AAV
vectors may accommodate up to 4300 bases of inserted DNA.
[0555] There are a number of ways to produce rAAV, and the
invention provides rAAV and methods for preparing rAAV. For
example, plasmid(s) containing or consisting essentially of the
desired viral construct are transfected into AAV-infected cells. In
addition, a second or additional helper plasmid is cotransfected
into these cells to provide the AAV rep and/or cap genes which are
obligatory for replication and packaging of the recombinant viral
construct. Under these conditions, the rep and/or cap proteins of
AAV act in trans to stimulate replication and packaging of the rAAV
construct. Two to Three days after transfection, rAAV is harvested.
Traditionally rAAV is harvested from the cells along with
adenovirus. The contaminating adenovirus is then inactivated by
heat treatment. In the instant invention, rAAV is advantageously
harvested not from the cells themselves, but from cell supernatant.
Accordingly, in an initial aspect the invention provides for
preparing rAAV, and in addition to the foregoing, rAAV can be
prepared by a method that comprises or consists essentially of:
infecting susceptible cells with a rAAV containing exogenous DNA
including DNA for expression, and helper virus (e.g., adenovirus,
herpesvirus, poxvirus such as vaccinia virus) wherein the rAAV
lacks functioning cap and/or rep (and the helper virus (e.g.,
adenovirus, herpesvirus, poxvirus such as vaccinia virus) provides
the cap and/or rev function that the rAAV lacks); or infecting
susceptible cells with a rAAV containing exogenous DNA including
DNA for expression, wherein the recombinant lacks functioning cap
and/or rep, and transfecting said cells with a plasmid supplying
cap and/or rep function that the rAAV lacks; or infecting
susceptible cells with a rAAV containing exogenous DNA including
DNA for expression, wherein the recombinant lacks functioning cap
and/or rep, wherein said cells supply cap and/or rep function that
the recombinant lacks; or transfecting the susceptible cells with
an AAV lacking functioning cap and/or rep and plasmids for
inserting exogenous DNA into the recombinant so that the exogenous
DNA is expressed by the recombinant and for supplying rep and/or
cap functions whereby transfection results in an rAAV containing
the exogenous DNA including DNA for expression that lacks
functioning cap and/or rep.
[0556] The rAAV can be from an AAV as herein described, and
advantageously can be an rAAV1, rAAV2, AAV5 or rAAV having hybrid
or capsid which may comprise AAV1, AAV2, AAV5 or any combination
thereof. One can select the AAV of the rAAV with regard to the
cells to be targeted by the rAAV; e.g., one can select AAV
serotypes 1, 2, 5 or a hybrid or capsid AAV1, AAV2, AAV5 or any
combination thereof for targeting brain or neuronal cells; and one
can select AAV4 for targeting cardiac tissue.
[0557] In addition to 293 cells, other cells that can be used in
the practice of the invention and the relative infectivity of
certain AAV serotypes in vitro as to these cells (see Grimm, D. et
al, J. Virol. 82: 5887-5911 (2008)) are as follows:
TABLE-US-00006 Cell Line AAV-1 AAV-2 AAV-3 AAV-4 AAV-5 AAV-6 AAV-8
AAV-9 Huh-7 13 100 2.5 0.0 0.1 10 0.7 0.0 HEK293 25 100 2.5 0.1 0.1
5 0.7 0.1 HeLa 3 100 2.0 0.1 6.7 1 0.2 0.1 HepG2 3 100 16.7 0.3 1.7
5 0.3 ND Hep1A 20 100 0.2 1.0 0.1 1 0.2 0.0 911 17 100 11 0.2 0.1
17 0.1 ND CHO 100 100 14 1.4 333 50 10 1.0 COS 33 100 33 3.3 5.0 14
2.0 0.5 MeWo 10 100 20 0.3 6.7 10 1.0 0.2 NIH3T3 10 100 2.9 2.9 0.3
10 0.3 ND A549 14 100 20 ND 0.5 10 0.5 0.1 HT1180 20 100 10 0.1 0.3
33 0.5 0.1 Monocytes 1111 100 ND ND 125 1429 ND ND Immature DC 2500
100 ND ND 222 2857 ND ND Mature DC 2222 100 ND ND 333 3333 ND
ND
[0558] The invention provides rAAV that contains or consists
essentially of an exogenous nucleic acid molecule encoding a CRISPR
(Clustered Regularly Interspaced Short Palindromic Repeats) system,
e.g., a plurality of cassettes comprising or consisting a first
cassette comprising or consisting essentially of a promoter, a
nucleic acid molecule encoding a CRISPR-associated (Cas) protein
(putative nuclease or helicase proteins), e.g., Cas9 and a
terminator, and a two, or more, advantageously up to the packaging
size limit of the vector, e.g., in total (including the first
cassette) five, cassettes comprising or consisting essentially of a
promoter, nucleic acid molecule encoding guide RNA (gRNA) and a
terminator (e.g., each cassette schematically represented as
Promoter-gRNA1-terminator, Promoter-gRNA2-terminator . . .
Promoter-gRNA(N)-terminator (where N is a number that can be
inserted that is at an upper limit of the packaging size limit of
the vector), or two or more individual rAAVs, each containing one
or more than one cassette of a CRISPR system, e.g., a first rAAV
containing the first cassette comprising or consisting essentially
of a promoter, a nucleic acid molecule encoding Cas, e.g., Cas9 and
a terminator, and a second rAAV containing a plurality, four,
cassettes comprising or consisting essentially of a promoter,
nucleic acid molecule encoding guide RNA (gRNA) and a terminator
(e.g., each cassette schematically represented as
Promoter-gRNA1-terminator, Promoter-gRNA2-terminator . . .
Promoter-gRNA(N)-terminator (where N is a number that can be
inserted that is at an upper limit of the packaging size limit of
the vector). As rAAV is a DNA virus, the nucleic acid molecules in
the herein discussion concerning AAV or rAAV are advantageously
DNA. The promoter is in some embodiments advantageously human
Synapsin I promoter (hSyn).
[0559] Additional methods for the delivery of nucleic acids to
cells are known to those skilled in the art. See, for example,
US20030087817, incorporated herein by reference.
[0560] In some embodiments, a host cell is transiently or
non-transiently transfected with one or more vectors described
herein. In some embodiments, a cell is transfected as it naturally
occurs in a subject. In some embodiments, a cell that is
transfected is taken from a subject. In some embodiments, the cell
is derived from cells taken from a subject, such as a cell line. A
wide variety of cell lines for tissue culture are known in the art.
Examples of cell lines include, but are not limited to, C8161,
CCRF-CEM, MOLT, mIMCD-3, NHDF, HeLa-S3, Huh1, Huh4, Huh7, HUVEC,
HASMC, HEKn, HEKa, MiaPaCell, Panc1, PC-3, TF1, CTLL-2, C1R, Rat6,
CV1, RPTE, A10, T24, J82, A375, ARH-77, Calu1, SW480, SW620, SKOV3,
SK-UT, CaCo2, P388D1, SEM-K2, WEHI-231, HB56, TIB55, Jurkat,
J45.01, LRMB, Bcl-1, BC-3, IC21, DLD2, Raw264.7, NRK, NRK-52E,
MRC5, MEF, Hep G2, HeLa B, HeLa T4, COS, COS-1, COS-6, COS-M6A,
BS-C-1 monkey kidney epithelial, BALB/3T3 mouse embryo fibroblast,
3T3 Swiss, 3T3-L1, 132-d5 human fetal fibroblasts; 10.1 mouse
fibroblasts, 293-T, 3T3, 721, 9L, A2780, A2780ADR, A2780cis, A172,
A20, A253, A431, A-549, ALC, B16, B35, BCP-1 cells, BEAS-2B,
bEnd.3, BHK-21, BR 293, BxPC3, C3H-10T1/2, C6/36, Cal-27, CHO,
CHO-7, CHO-IR, CHO-K1, CHO-K2, CHO-T, CHO Dhfr -/-, COR-L23,
COR-L23/CPR, COR-L23/5010, COR-L23/R23, COS-7, COV-434, CML T1,
CMT, CT26, D17, DH82, DU145, DuCaP, EL4, EM2, EM3, EMT6/AR1,
EMT6/AR10.0, FM3, H1299, H69, HB54, HB55, HCA2, HEK-293, HeLa,
Hepa1c1c7, HL-60, HMEC, HT-29, Jurkat, JY cells, K562 cells, Ku812,
KCL22, KG1, KYO1, LNCap, Ma-Me1 1-48, MC-38, MCF-7, MCF-10A,
MDA-MB-231, MDA-MB-468, MDA-MB-435, MDCK II, MDCK II, MOR/0.2R,
MONO-MAC 6, MTD-1A, MyEnd, NCI-H69/CPR, NCI-H69/LX10, NCI-H69/LX20,
NCI-H69/LX4, NIH-3T3, NALM-1, NW-145, OPCN/OPCT cell lines, Peer,
PNT-1A/PNT 2, RenCa, RIN-5F, RMA/RMAS, Saos-2 cells, Sf-9, SkBr3,
T2, T-47D, T84, THP1 cell line, U373, U87, U937, VCaP, Vero cells,
WM39, WT-49, X63, YAC-1, YAR, and transgenic varieties thereof.
Cell lines are available from a variety of sources known to those
with skill in the art (see, e.g., the American Type Culture
Collection (ATCC) (Manassas, Va.)). In some embodiments, a cell
transfected with one or more vectors described herein is used to
establish a new cell line comprising one or more vector-derived
sequences. In some embodiments, a cell transiently transfected with
the components of a CRISPR system as described herein (such as by
transient transfection of one or more vectors, or transfection with
RNA), and modified through the activity of a CRISPR complex, is
used to establish a new cell line comprising cells containing the
modification but lacking any other exogenous sequence. In some
embodiments, cells transiently or non-transiently transfected with
one or more vectors described herein, or cell lines derived from
such cells are used in assessing one or more test compounds.
[0561] In some embodiments, one or more vectors described herein
are used to produce a non-human transgenic animal or transgenic
plant. In some embodiments, the transgenic animal is a mammal, such
as a mouse, rat, or rabbit. Methods for producing transgenic
animals and plants are known in the art, and generally begin with a
method of cell transfection, such as described herein.
[0562] In another embodiment, a fluid delivery device with an array
of needles (see, e.g., US Patent Publication No. 20110230839
assigned to the Fred Hutchinson Cancer Research Center) may be
contemplated for delivery of CRISPR Cas to solid tissue. A device
of US Patent Publication No. 20110230839 for delivery of a fluid to
a solid tissue may comprise a plurality of needles arranged in an
array; a plurality of reservoirs, each in fluid communication with
a respective one of the plurality of needles; and a plurality of
actuators operatively coupled to respective ones of the plurality
of reservoirs and configured to control a fluid pressure within the
reservoir. In certain embodiments each of the plurality of
actuators may comprise one of a plurality of plungers, a first end
of each of the plurality of plungers being received in a respective
one of the plurality of reservoirs, and in certain further
embodiments the plungers of the plurality of plungers are
operatively coupled together at respective second ends so as to be
simultaneously depressable. Certain still further embodiments may
comprise a plunger driver configured to depress all of the
plurality of plungers at a selectively variable rate. In other
embodiments each of the plurality of actuators may comprise one of
a plurality of fluid transmission lines having first and second
ends, a first end of each of the plurality of fluid transmission
lines being coupled to a respective one of the plurality of
reservoirs. In other embodiments the device may comprise a fluid
pressure source, and each of the plurality of actuators comprises a
fluid coupling between the fluid pressure source and a respective
one of the plurality of reservoirs. In further embodiments the
fluid pressure source may comprise at least one of a compressor, a
vacuum accumulator, a peristaltic pump, a master cylinder, a
microfluidic pump, and a valve. In another embodiment, each of the
plurality of needles may comprise a plurality of ports distributed
along its length.
[0563] Modifying a Target
[0564] In one aspect, the invention provides for methods of
modifying a target polynucleotide in a eukaryotic cell, which may
be in vivo, ex vivo or in vitro. In some embodiments, the method
comprises sampling a cell or population of cells from a human or
non-human animal, or a plant, and modifying the cell or cells.
Culturing may occur at any stage ex vivo. The cell or cells may
even be re-introduced into the non-human animal or plant. For
re-introduced cells it is particularly preferred that the cells are
stem cells.
[0565] In some embodiments, the method comprises allowing a CRISPR
complex to bind to the target polynucleotide to effect cleavage of
said target polynucleotide thereby modifying the target
polynucleotide, wherein the CRISPR complex comprises a CRISPR
enzyme complexed with a guide sequence hybridized to a target
sequence within said target polynucleotide, wherein said guide
sequence is linked to a tracr mate sequence which in turn
hybridizes to a tracr sequence.
[0566] In one aspect, the invention provides a method of modifying
expression of a polynucleotide in a eukaryotic cell. In some
embodiments, the method comprises allowing a CRISPR complex to bind
to the polynucleotide such that said binding results in increased
or decreased expression of said polynucleotide; wherein the CRISPR
complex comprises a CRISPR enzyme complexed with a guide sequence
hybridized to a target sequence within said polynucleotide, wherein
said guide sequence is linked to a tracr mate sequence which in
turn hybridizes to a tracr sequence. Similar considerations and
conditions apply as above for methods of modifying a target
polynucleotide. In fact, these sampling, culturing and
re-introduction options apply across the aspects of the present
invention.
[0567] Indeed, in any aspect of the invention, the CRISPR complex
may comprise a CRISPR enzyme complexed with a guide sequence
hybridized to a target sequence, wherein said guide sequence may be
linked to a tracr mate sequence which in turn may hybridize to a
tracr sequence. Similar considerations and conditions apply as
above for methods of modifying a target polynucleotide.
[0568] Kits
[0569] In one aspect, the invention provides kits containing any
one or more of the elements disclosed in the above methods and
compositions. Elements may be provided individually or in
combinations, and may be provided in any suitable container, such
as a vial, a bottle, or a tube. In some embodiments, the kit
includes instructions in one or more languages, for example in more
than one language.
[0570] In some embodiments, a kit comprises one or more reagents
for use in a process utilizing one or more of the elements
described herein. Reagents may be provided in any suitable
container. For example, a kit may provide one or more reaction or
storage buffers. Reagents may be provided in a form that is usable
in a particular assay, or in a form that requires addition of one
or more other components before use (e.g. in concentrate or
lyophilized form). A buffer can be any buffer, including but not
limited to a sodium carbonate buffer, a sodium bicarbonate buffer,
a borate buffer, a Tris buffer, a MOPS buffer, a HEPES buffer, and
combinations thereof. In some embodiments, the buffer is alkaline.
In some embodiments, the buffer has a pH from about 7 to about 10.
In some embodiments, the kit comprises one or more oligonucleotides
corresponding to a guide sequence for insertion into a vector so as
to operably link the guide sequence and a regulatory element. In
some embodiments, the kit comprises a homologous recombination
template polynucleotide. In some embodiments, the kit comprises one
or more of the vectors and/or one or more of the polynucleotides
described herein. The kit may advantageously allows to provide all
elements of the systems of the invention.
[0571] CRISPR Complex
[0572] In one aspect, the invention provides methods for using one
or more elements of a CRISPR system. The CRISPR complex of the
invention provides an effective means for modifying a target
polynucleotide. The CRISPR complex of the invention has a wide
variety of utility including modifying (e.g., deleting, inserting,
translocating, inactivating, activating) a target polynucleotide in
a multiplicity of cell types. As such the CRISPR complex of the
invention has a broad spectrum of applications in, e.g., gene
therapy, drug screening, disease diagnosis, and prognosis. An
exemplary CRISPR complex comprises a CRISPR enzyme complexed with a
guide sequence hybridized to a target sequence within the target
polynucleotide. The guide sequence is linked to a tracr mate
sequence, which in turn hybridizes to a tracr sequence.
[0573] In one embodiment, this invention provides a method of
cleaving a target polynucleotide. The method comprises modifying a
target polynucleotide using a CRISPR complex that binds to the
target polynucleotide and effect cleavage of said target
polynucleotide. Typically, the CRISPR complex of the invention,
when introduced into a cell, creates a break (e.g., a single or a
double strand break) in the genome sequence. For example, the
method can be used to cleave a disease gene in a cell.
[0574] The break created by the CRISPR complex can be repaired by a
repair processes such as the error prone non-homologous end joining
(NHEJ) pathway or the high fidelity homology-directed repair (HDR)
(FIG. 29). During these repair process, an exogenous polynucleotide
template can be introduced into the genome sequence. In some
methods, the HDR process is used modify genome sequence. For
example, an exogenous polynucleotide template comprising a sequence
to be integrated flanked by an upstream sequence and a downstream
sequence is introduced into a cell. The upstream and downstream
sequences share sequence similarity with either side of the site of
integration in the chromosome.
[0575] Where desired, a donor polynucleotide can be DNA, e.g., a
DNA plasmid, a bacterial artificial chromosome (BAC), a yeast
artificial chromosome (YAC), a viral vector, a linear piece of DNA,
a PCR fragment, a naked nucleic acid, or a nucleic acid complexed
with a delivery vehicle such as a liposome or poloxamer.
[0576] The exogenous polynucleotide template comprises a sequence
to be integrated (e.g., a mutated gene). The sequence for
integration may be a sequence endogenous or exogenous to the cell.
Examples of a sequence to be integrated include polynucleotides
encoding a protein or a non-coding RNA (e.g., a microRNA). Thus,
the sequence for integration may be operably linked to an
appropriate control sequence or sequences. Alternatively, the
sequence to be integrated may provide a regulatory function.
[0577] The upstream and downstream sequences in the exogenous
polynucleotide template are selected to promote recombination
between the chromosomal sequence of interest and the donor
polynucleotide. The upstream sequence is a nucleic acid sequence
that shares sequence similarity with the genome sequence upstream
of the targeted site for integration. Similarly, the downstream
sequence is a nucleic acid sequence that shares sequence similarity
with the chromosomal sequence downstream of the targeted site of
integration. The upstream and downstream sequences in the exogenous
polynucleotide template can have 75%, 80%, 85%, 90%, 95%, or 100%
sequence identity with the targeted genome sequence. Preferably,
the upstream and downstream sequences in the exogenous
polynucleotide template have about 95%, 96%, 97%, 98%, 99%, or 100%
sequence identity with the targeted genome sequence. In some
methods, the upstream and downstream sequences in the exogenous
polynucleotide template have about 99% or 100% sequence identity
with the targeted genome sequence.
[0578] An upstream or downstream sequence may comprise from about
20 bp to about 2500 bp, for example, about 50, 100, 200, 300, 400,
500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400, 1500, 1600,
1700, 1800, 1900, 2000, 2100, 2200, 2300, 2400, or 2500 bp. In some
methods, the exemplary upstream or downstream sequence have about
200 bp to about 2000 bp, about 600 bp to about 1000 bp, or more
particularly about 700 bp to about 1000 bp.
[0579] In some methods, the exogenous polynucleotide template may
further comprise a marker. Such a marker may make it easy to screen
for targeted integrations. Examples of suitable markers include
restriction sites, fluorescent proteins, or selectable markers. The
exogenous polynucleotide template of the invention can be
constructed using recombinant techniques (see, for example,
Sambrook et al., 2001 and Ausubel et al., 1996).
[0580] In an exemplary method for modifying a target polynucleotide
by integrating an exogenous polynucleotide template, a double
stranded break is introduced into the genome sequence by the CRISPR
complex, the break is repaired via homologous recombination an
exogenous polynucleotide template such that the template is
integrated into the genome. The presence of a double-stranded break
facilitates integration of the template.
[0581] In other embodiments, this invention provides a method of
modifying expression of a polynucleotide in a eukaryotic cell. The
method comprises increasing or decreasing expression of a target
polynucleotide by using a CRISPR complex that binds to the
polynucleotide.
[0582] In some methods, a target polynucleotide can be inactivated
to effect the modification of the expression in a cell. For
example, upon the binding of a CRISPR complex to a target sequence
in a cell, the target polynucleotide is inactivated such that the
sequence is not transcribed, the coded protein is not produced, or
the sequence does not function as the wild-type sequence does. For
example, a protein or microRNA coding sequence may be inactivated
such that the protein is not produced.
[0583] In some methods, a control sequence can be inactivated such
that it no longer functions as a control sequence. As used herein,
"control sequence" refers to any nucleic acid sequence that effects
the transcription, translation, or accessibility of a nucleic acid
sequence. Examples of a control sequence include, a promoter, a
transcription terminator, and an enhancer are control
sequences.
[0584] The inactivated target sequence may include a deletion
mutation (i.e., deletion of one or more nucleotides), an insertion
mutation (i.e., insertion of one or more nucleotides), or a
nonsense mutation (i.e., substitution of a single nucleotide for
another nucleotide such that a stop codon is introduced). In some
methods, the inactivation of a target sequence results in
"knock-out" of the target sequence.
[0585] Disease Models
[0586] A method of the invention may be used to create a plant, an
animal or cell that may be used as a disease model. As used herein,
"disease" refers to a disease, disorder, or indication in a
subject. For example, a method of the invention may be used to
create an animal or cell that comprises a modification in one or
more nucleic acid sequences associated with a disease, or a plant,
animal or cell in which the expression of one or more nucleic acid
sequences associated with a disease are altered. Such a nucleic
acid sequence may encode a disease associated protein sequence or
may be a disease associated control sequence. Accordingly, it is
understood that in embodiments of the invention, a plant, subject,
patient, organism or cell can be a non-human subject, patient,
organism or cell. Thus, the invention provides a plant, animal or
cell, produced by the present methods, or a progeny thereof. The
progeny may be a clone of the produced plant or animal, or may
result from sexual reproduction by crossing with other individuals
of the same species to introgress further desirable traits into
their offspring. The cell may be in vivo or ex vivo in the cases of
multicellular organisms, particularly animals or plants. In the
instance where the cell is in cultured, a cell line may be
established if appropriate culturing conditions are met and
preferably if the cell is suitably adapted for this purpose (for
instance a stem cell). Bacterial cell lines produced by the
invention are also envisaged. Hence, cell lines are also
envisaged.
[0587] In some methods, the disease model can be used to study the
effects of mutations on the animal or cell and development and/or
progression of the disease using measures commonly used in the
study of the disease. Alternatively, such a disease model is useful
for studying the effect of a pharmaceutically active compound on
the disease.
[0588] In some methods, the disease model can be used to assess the
efficacy of a potential gene therapy strategy. That is, a
disease-associated gene or polynucleotide can be modified such that
the disease development and/or progression is inhibited or reduced.
In particular, the method comprises modifying a disease-associated
gene or polynucleotide such that an altered protein is produced
and, as a result, the animal or cell has an altered response.
Accordingly, in some methods, a genetically modified animal may be
compared with an animal predisposed to development of the disease
such that the effect of the gene therapy event may be assessed.
[0589] In another embodiment, this invention provides a method of
developing a biologically active agent that modulates a cell
signaling event associated with a disease gene. The method
comprises contacting a test compound with a cell comprising one or
more vectors that drive expression of one or more of a CRISPR
enzyme, a guide sequence linked to a tracr mate sequence, and a
tracr sequence; and detecting a change in a readout that is
indicative of a reduction or an augmentation of a cell signaling
event associated with, e.g., a mutation in a disease gene contained
in the cell.
[0590] A cell model or animal model can be constructed in
combination with the method of the invention for screening a
cellular function change. Such a model may be used to study the
effects of a genome sequence modified by the CRISPR complex of the
invention on a cellular function of interest. For example, a
cellular function model may be used to study the effect of a
modified genome sequence on intracellular signaling or
extracellular signaling. Alternatively, a cellular function model
may be used to study the effects of a modified genome sequence on
sensory perception. In some such models, one or more genome
sequences associated with a signaling biochemical pathway in the
model are modified.
[0591] Several disease models have been specifically investigated.
These include de novo autism risk genes CHD8, KATNAL2, and SCN2A;
and the syndromic autism (Angelman Syndrome) gene UBE3A. These
genes and resulting autism models are of course preferred, but
serve to show the broad applicability of the invention across genes
and corresponding models.
[0592] An altered expression of one or more genome sequences
associated with a signaling biochemical pathway can be determined
by assaying for a difference in the mRNA levels of the
corresponding genes between the test model cell and a control cell,
when they are contacted with a candidate agent. Alternatively, the
differential expression of the sequences associated with a
signaling biochemical pathway is determined by detecting a
difference in the level of the encoded polypeptide or gene
product.
[0593] To assay for an agent-induced alteration in the level of
mRNA transcripts or corresponding polynucleotides, nucleic acid
contained in a sample is first extracted according to standard
methods in the art. For instance, mRNA can be isolated using
various lytic enzymes or chemical solutions according to the
procedures set forth in Sambrook et al. (1989), or extracted by
nucleic-acid-binding resins following the accompanying instructions
provided by the manufacturers. The mRNA contained in the extracted
nucleic acid sample is then detected by amplification procedures or
conventional hybridization assays (e.g. Northern blot analysis)
according to methods widely known in the art or based on the
methods exemplified herein.
[0594] For purpose of this invention, amplification means any
method employing a primer and a polymerase capable of replicating a
target sequence with reasonable fidelity. Amplification may be
carried out by natural or recombinant DNA polymerases such as
TaqGold.TM., T7 DNA polymerase, Klenow fragment of E. coli DNA
polymerase, and reverse transcriptase. A preferred amplification
method is PCR. In particular, the isolated RNA can be subjected to
a reverse transcription assay that is coupled with a quantitative
polymerase chain reaction (RT-PCR) in order to quantify the
expression level of a sequence associated with a signaling
biochemical pathway.
[0595] Detection of the gene expression level can be conducted in
real time in an amplification assay. In one aspect, the amplified
products can be directly visualized with fluorescent DNA-binding
agents including but not limited to DNA intercalators and DNA
groove binders. Because the amount of the intercalators
incorporated into the double-stranded DNA molecules is typically
proportional to the amount of the amplified DNA products, one can
conveniently determine the amount of the amplified products by
quantifying the fluorescence of the intercalated dye using
conventional optical systems in the art. DNA-binding dye suitable
for this application include SYBR green, SYBR blue, DAPI, propidium
iodine, Hoeste, SYBR gold, ethidium bromide, acridines, proflavine,
acridine orange, acriflavine, fluorcoumanin, ellipticine,
daunomycin, chloroquine, distamycin D, chromomycin, homidium,
mithramycin, ruthenium polypyridyls, anthramycin, and the like.
[0596] In another aspect, other fluorescent labels such as sequence
specific probes can be employed in the amplification reaction to
facilitate the detection and quantification of the amplified
products. Probe-based quantitative amplification relies on the
sequence-specific detection of a desired amplified product. It
utilizes fluorescent, target-specific probes (e.g., TaqMan.RTM.
probes) resulting in increased specificity and sensitivity. Methods
for performing probe-based quantitative amplification are well
established in the art and are taught in U.S. Pat. No.
5,210,015.
[0597] In yet another aspect, conventional hybridization assays
using hybridization probes that share sequence homology with
sequences associated with a signaling biochemical pathway can be
performed. Typically, probes are allowed to form stable complexes
with the sequences associated with a signaling biochemical pathway
contained within the biological sample derived from the test
subject in a hybridization reaction. It will be appreciated by one
of skill in the art that where antisense is used as the probe
nucleic acid, the target polynucleotides provided in the sample are
chosen to be complementary to sequences of the antisense nucleic
acids. Conversely, where the nucleotide probe is a sense nucleic
acid, the target polynucleotide is selected to be complementary to
sequences of the sense nucleic acid.
[0598] Hybridization can be performed under conditions of various
stringency. Suitable hybridization conditions for the practice of
the present invention are such that the recognition interaction
between the probe and sequences associated with a signaling
biochemical pathway is both sufficiently specific and sufficiently
stable. Conditions that increase the stringency of a hybridization
reaction are widely known and published in the art. See, for
example, (Sambrook, et al., (1989), Nonradioactive In Situ
Hybridization Application Manual, Boehringer Mannheim, second
edition). The hybridization assay can be formed using probes
immobilized on any solid support, including but are not limited to
nitrocellulose, glass, silicon, and a variety of gene arrays. A
preferred hybridization assay is conducted on high-density gene
chips as described in U.S. Pat. No. 5,445,934.
[0599] For a convenient detection of the probe-target complexes
formed during the hybridization assay, the nucleotide probes are
conjugated to a detectable label. Detectable labels suitable for
use in the present invention include any composition detectable by
photochemical, biochemical, spectroscopic, immunochemical,
electrical, optical or chemical means. A wide variety of
appropriate detectable labels are known in the art, which include
fluorescent or chemiluminescent labels, radioactive isotope labels,
enzymatic or other ligands. In preferred embodiments, one will
likely desire to employ a fluorescent label or an enzyme tag, such
as digoxigenin, .beta.-galactosidase, urease, alkaline phosphatase
or peroxidase, avidin/biotin complex.
[0600] The detection methods used to detect or quantify the
hybridization intensity will typically depend upon the label
selected above. For example, radiolabels may be detected using
photographic film or a phosphoimager. Fluorescent markers may be
detected and quantified using a photodetector to detect emitted
light. Enzymatic labels are typically detected by providing the
enzyme with a substrate and measuring the reaction product produced
by the action of the enzyme on the substrate; and finally
colorimetric labels are detected by simply visualizing the colored
label.
[0601] An agent-induced change in expression of sequences
associated with a signaling biochemical pathway can also be
determined by examining the corresponding gene products.
Determining the protein level typically involves a) contacting the
protein contained in a biological sample with an agent that
specifically bind to a protein associated with a signaling
biochemical pathway; and (b) identifying any agent:protein complex
so formed. In one aspect of this embodiment, the agent that
specifically binds a protein associated with a signaling
biochemical pathway is an antibody, preferably a monoclonal
antibody.
[0602] The reaction is performed by contacting the agent with a
sample of the proteins associated with a signaling biochemical
pathway derived from the test samples under conditions that will
allow a complex to form between the agent and the proteins
associated with a signaling biochemical pathway. The formation of
the complex can be detected directly or indirectly according to
standard procedures in the art. In the direct detection method, the
agents are supplied with a detectable label and unreacted agents
may be removed from the complex; the amount of remaining label
thereby indicating the amount of complex formed. For such method,
it is preferable to select labels that remain attached to the
agents even during stringent washing conditions. It is preferable
that the label does not interfere with the binding reaction. In the
alternative, an indirect detection procedure may use an agent that
contains a label introduced either chemically or enzymatically. A
desirable label generally does not interfere with binding or the
stability of the resulting agent:polypeptide complex. However, the
label is typically designed to be accessible to an antibody for an
effective binding and hence generating a detectable signal.
[0603] A wide variety of labels suitable for detecting protein
levels are known in the art. Non-limiting examples include
radioisotopes, enzymes, colloidal metals, fluorescent compounds,
bioluminescent compounds, and chemiluminescent compounds.
[0604] The amount of agent:polypeptide complexes formed during the
binding reaction can be quantified by standard quantitative assays.
As illustrated above, the formation of agent:polypeptide complex
can be measured directly by the amount of label remained at the
site of binding. In an alternative, the protein associated with a
signaling biochemical pathway is tested for its ability to compete
with a labeled analog for binding sites on the specific agent. In
this competitive assay, the amount of label captured is inversely
proportional to the amount of protein sequences associated with a
signaling biochemical pathway present in a test sample.
[0605] A number of techniques for protein analysis based on the
general principles outlined above are available in the art. They
include but are not limited to radioimmunoassays, ELISA (enzyme
linked immunoradiometric assays), "sandwich" immunoassays,
immunoradiometric assays, in situ immunoassays (using e.g.,
colloidal gold, enzyme or radioisotope labels), western blot
analysis, immunoprecipitation assays, immunofluorescent assays, and
SDS-PAGE.
[0606] Antibodies that specifically recognize or bind to proteins
associated with a signaling biochemical pathway are preferable for
conducting the aforementioned protein analyses. Where desired,
antibodies that recognize a specific type of post-translational
modifications (e.g., signaling biochemical pathway inducible
modifications) can be used. Post-translational modifications
include but are not limited to glycosylation, lipidation,
acetylation, and phosphorylation. These antibodies may be purchased
from commercial vendors. For example, anti-phosphotyrosine
antibodies that specifically recognize tyrosine-phosphorylated
proteins are available from a number of vendors including
Invitrogen and Perkin Elmer. Anti-phosphotyrosine antibodies are
particularly useful in detecting proteins that are differentially
phosphorylated on their tyrosine residues in response to an ER
stress. Such proteins include but are not limited to eukaryotic
translation initiation factor 2 alpha (eF-2a). Alternatively, these
antibodies can be generated using conventional polyclonal or
monoclonal antibody technologies by immunizing a host animal or an
antibody-producing cell with a target protein that exhibits the
desired post-translational modification.
[0607] In practicing the subject method, it may be desirable to
discern the expression pattern of an protein associated with a
signaling biochemical pathway in different bodily tissue, in
different cell types, and/or in different subcellular structures.
These studies can be performed with the use of tissue-specific,
cell-specific or subcellular structure specific antibodies capable
of binding to protein markers that are preferentially expressed in
certain tissues, cell types, or subcellular structures.
[0608] An altered expression of a gene associated with a signaling
biochemical pathway can also be determined by examining a change in
activity of the gene product relative to a control cell. The assay
for an agent-induced change in the activity of a protein associated
with a signaling biochemical pathway will dependent on the
biological activity and/or the signal transduction pathway that is
under investigation. For example, where the protein is a kinase, a
change in its ability to phosphorylate the downstream substrate(s)
can be determined by a variety of assays known in the art.
Representative assays include but are not limited to immunoblotting
and immunoprecipitation with antibodies such as
anti-phosphotyrosine antibodies that recognize phosphorylated
proteins. In addition, kinase activity can be detected by high
throughput chemiluminescent assays such as AlphaScreen.TM.
(available from Perkin Elmer) and eTag.TM. assay (Chan-Hui, et al.
(2003) Clinical Immunology 111: 162-174).
[0609] Where the protein associated with a signaling biochemical
pathway is part of a signaling cascade leading to a fluctuation of
intracellular pH condition, pH sensitive molecules such as
fluorescent pH dyes can be used as the reporter molecules. In
another example where the protein associated with a signaling
biochemical pathway is an ion channel, fluctuations in membrane
potential and/or intracellular ion concentration can be monitored.
A number of commercial kits and high-throughput devices are
particularly suited for a rapid and robust screening for modulators
of ion channels. Representative instruments include FLIPR.TM.
(Molecular Devices, Inc.) and VIPR (Aurora Biosciences). These
instruments are capable of detecting reactions in over 1000 sample
wells of a microplate simultaneously, and providing real-time
measurement and functional data within a second or even a
minisecond.
[0610] In practicing any of the methods disclosed herein, a
suitable vector can be introduced to a cell or an embryo via one or
more methods known in the art, including without limitation,
microinjection, electroporation, sonoporation, biolistics, calcium
phosphate-mediated transfection, cationic transfection, liposome
transfection, dendrimer transfection, heat shock transfection,
nucleofection transfection, magnetofection, lipofection,
impalefection, optical transfection, proprietary agent-enhanced
uptake of nucleic acids, and delivery via liposomes,
immunoliposomes, virosomes, or artificial virions. In some methods,
the vector is introduced into an embryo by microinjection. The
vector or vectors may be microinjected into the nucleus or the
cytoplasm of the embryo. In some methods, the vector or vectors may
be introduced into a cell by nucleofection.
[0611] The target polynucleotide of a CRISPR complex can be any
polynucleotide endogenous or exogenous to the eukaryotic cell. For
example, the target polynucleotide can be a polynucleotide residing
in the nucleus of the eukaryotic cell. The target polynucleotide
can be a sequence coding a gene product (e.g., a protein) or a
non-coding sequence (e.g., a regulatory polynucleotide or a junk
DNA).
[0612] Examples of target polynucleotides include a sequence
associated with a signaling biochemical pathway, e.g., a signaling
biochemical pathway-associated gene or polynucleotide. Examples of
target polynucleotides include a disease associated gene or
polynucleotide. A "disease-associated" gene or polynucleotide
refers to any gene or polynucleotide which is yielding
transcription or translation products at an abnormal level or in an
abnormal form in cells derived from a disease-affected tissues
compared with tissues or cells of a non disease control. It may be
a gene that becomes expressed at an abnormally high level; it may
be a gene that becomes expressed at an abnormally low level, where
the altered expression correlates with the occurrence and/or
progression of the disease. A disease-associated gene also refers
to a gene possessing mutation(s) or genetic variation that is
directly responsible or is in linkage disequilibrium with a gene(s)
that is responsible for the etiology of a disease. The transcribed
or translated products may be known or unknown, and may be at a
normal or abnormal level.
[0613] The target polynucleotide of a CRISPR complex can be any
polynucleotide endogenous or exogenous to the eukaryotic cell. For
example, the target polynucleotide can be a polynucleotide residing
in the nucleus of the eukaryotic cell. The target polynucleotide
can be a sequence coding a gene product (e.g., a protein) or a
non-coding sequence (e.g., a regulatory polynucleotide or a junk
DNA). Without wishing to be bound by theory, it is believed that
the target sequence should be associated with a PAM (protospacer
adjacent motif); that is, a short sequence recognized by the CRISPR
complex. The precise sequence and length requirements for the PAM
differ depending on the CRISPR enzyme used, but PAMs are typically
2-5 base pair sequences adjacent the protospacer (that is, the
target sequence) Examples of PAM sequences are given in the
examples section below, and the skilled person will be able to
identify further PAM sequences for use with a given CRISPR
enzyme.
[0614] The target polynucleotide of a CRISPR complex may include a
number of disease-associated genes and polynucleotides as well as
signaling biochemical pathway-associated genes and polynucleotides
as listed in U.S. provisional patent applications 61/736,527 and
61/748,427 having Broad reference BI-2011/008/W SGR Docket No.
44063-701.101 and BI-2011/008/WSGR Docket No. 44063-701.102
respectively, both entitled SYSTEMS METHODS AND COMPOSITIONS FOR
SEQUENCE MANIPULATION filed on Dec. 12, 2012 and Jan. 2, 2013,
respectively, the contents of all of which are herein incorporated
by reference in their entirety.
[0615] Examples of target polynucleotides include a sequence
associated with a signaling biochemical pathway, e.g., a signaling
biochemical pathway-associated gene or polynucleotide. Examples of
target polynucleotides include a disease associated gene or
polynucleotide. A "disease-associated" gene or polynucleotide
refers to any gene or polynucleotide which is yielding
transcription or translation products at an abnormal level or in an
abnormal form in cells derived from a disease-affected tissues
compared with tissues or cells of a non disease control. It may be
a gene that becomes expressed at an abnormally high level; it may
be a gene that becomes expressed at an abnormally low level, where
the altered expression correlates with the occurrence and/or
progression of the disease. A disease-associated gene also refers
to a gene possessing mutation(s) or genetic variation that is
directly responsible or is in linkage disequilibrium with a gene(s)
that is responsible for the etiology of a disease. The transcribed
or translated products may be known or unknown, and may be at a
normal or abnormal level.
[0616] Examples of disease-associated genes and polynucleotides are
listed in Tables A and B. Disease specific information is available
from McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins
University (Baltimore, Md.) and National Center for Biotechnology
Information, National Library of Medicine (Bethesda, Md.),
available on the World Wide Web. Examples of signaling biochemical
pathway-associated genes and polynucleotides are listed in Table
C.
[0617] Mutations in these genes and pathways can result in
production of improper proteins or proteins in improper amounts
which affect function. Further examples of genes, diseases and
proteins are hereby incorporated by reference from U.S. Provisional
application 61/736,527 filed Dec. 12, 2012. Such genes, proteins
and pathways may be the target polynucleotide of a CRISPR
complex.
TABLE-US-00007 TABLE A DISEASE/DISORDERS GENE(S) Neoplasia PTEN;
ATM; ATR; EGFR; ERBB2; ERBB3; ERBB4; Notch1; Notch2; Notch3;
Notch4; AKT; AKT2; AKT3; HIF; HIF1a; HIF3a; Met; HRG; Bcl2; PPAR
alpha; PPAR gamma; WT1 (Wilms Tumor); FGF Receptor Family members
(5 members: 1, 2, 3, 4, 5); CDKN2a; APC; RB (retinoblastoma); MEN1;
VHL; BRCA1; BRCA2; AR (Androgen Receptor); TSG101; IGF; IGF
Receptor; Igf1 (4 variants); Igf2 (3 variants); Igf 1 Receptor; Igf
2 Receptor; Bax; Bcl2; caspases family (9 members: 1, 2, 3, 4, 6,
7, 8, 9, 12); Kras; Apc Age-related Macular Abcr; Ccl2; Cc2; cp
(ceruloplasmin); Timp3; cathepsinD; Degeneration Vldlr; Ccr2
Schizophrenia Neuregulin1 (Nrg1); Erb4 (receptor for Neuregulin);
Complexin1 (Cplx1); Tph1 Tryptophan hydroxylase; Tph2 Tryptophan
hydroxylase 2; Neurexin 1; GSK3; GSK3a; GSK3b Disorders 5-HTT
(Slc6a4); COMT; DRD (Drd1a); SLC6A3; DAOA; DTNBP1; Dao (Dao1)
Trinucleotide Repeat HTT (Huntington's Dx); SBMA/SMAX1/AR
(Kennedy's Disorders Dx); FXN/X25 (Friedrich's Ataxia); ATX3
(Machado- Joseph's Dx); ATXN1 and ATXN2 (spinocerebellar ataxias);
DMPK (myotonic dystrophy); Atrophin-1 and Atn1 (DRPLA Dx); CBP
(Creb-BP - global instability); VLDLR (Alzheimer's); Atxn7; Atxn10
Fragile X Syndrome FMR2; FXR1; FXR2; mGLUR5 Secretase Related APH-1
(alpha and beta); Presenilin (Psen1); nicastrin Disorders (Ncstn);
PEN-2 Others Nos1; Parp1; Nat1; Nat2 Prion - related disorders Prp
ALS SOD1; ALS2; STEX; FUS; TARDBP; VEGF (VEGF-a; VEGF-b; VEGF-c)
Drug addiction Prkce (alcohol); Drd2; Drd4; ABAT (alcohol); GRIA2;
Grm5; Grin1; Htr1b; Grin2a; Drd3; Pdyn; Gria1 (alcohol) Autism
Mecp2; BZRAP1; MDGA2; Sema5A; Neurexin 1; Fragile X (FMR2 (AFF2);
FXR1; FXR2; Mglur5) Alzheimer's Disease E1; CHIP; UCH; UBB; Tau;
LRP; PICALM; Clusterin; PS1; SORL1; CR1; Vldlr; Uba1; Uba3; CHIP28
(Aqp1, Aquaporin 1); Uchl1; Uchl3; APP Inflammation IL-10; IL-1
(IL-1a; IL-1b); IL-13; IL-17 (IL-17a (CTLA8); IL- 17b; IL-17c;
IL-17d; IL-17f); II-23; Cx3cr1; ptpn22; TNFa; NOD2/CARD15 for IBD;
IL-6; IL-12 (IL-12a; IL-12b); CTLA4; Cx3cl1 Parkinson's Disease
x-Synuclein; DJ-1; LRRK2; Parkin; PINK1
TABLE-US-00008 TABLE B Blood and Anemia (CDAN1, CDA1, RPS19, DBA,
PKLR, PK1, NT5C3, UMPH1, coagulation diseases PSN1, RHAG, RH50A,
NRAMP2, SPTB, ALAS2, ANH1, ASB, and disorders ABCB7, ABC7, ASAT);
Bare lymphocyte syndrome (TAPBP, TPSN, TAP2, ABCB3, PSF2, RING11,
MHC2TA, C2TA, RFX5, RFXAP, RFX5), Bleeding disorders (TBXA2R,
P2RX1, P2X1); Factor H and factor H-like 1 (HF1, CFH, HUS); Factor
V and factor VIII (MCFD2); Factor VII deficiency (F7); Factor X
deficiency (F10); Factor XI deficiency (F11); Factor XII deficiency
(F12, HAF); Factor XIIIA deficiency (F13A1, F13A); Factor XIIIB
deficiency (F13B); Fanconi anemia (FANCA, FACA, FA1, FA, FAA,
FAAP95, FAAP90, FLJ34064, FANCB, FANCC, FACC, BRCA2, FANCD1,
FANCD2, FANCD, FACD, FAD, FANCE, FACE, FANCF, XRCC9, FANCG, BRIP1,
BACH1, FANCJ, PHF9, FANCL, FANCM, KIAA1596); Hemophagocytic
lymphohistiocytosis disorders (PRF1, HPLH2, UNC13D, MUNC13-4,
HPLH3, HLH3, FHL3); Hemophilia A (F8, F8C, HEMA); Hemophilia B (F9,
HEMB), Hemorrhagic disorders (PI, ATT, F5); Leukocyde deficiencies
and disorders (ITGB2, CD18, LCAMB, LAD, EIF2B1, EIF2BA, EIF2B2,
EIF2B3, EIF2B5, LVWM, CACH, CLE, EIF2B4); Sickle cell anemia (HBB);
Thalassemia (HBA2, HBB, HBD, LCRB, HBA1). Cell dysregulation B-cell
non-Hodgkin lymphoma (BCL7A, BCL7); Leukemia (TAL1, and oncology
TCL5, SCL, TAL2, FLT3, NBS1, NBS, ZNFN1A1, IK1, LYF1, diseases and
disorders HOXD4, HOX4B, BCR, CML, PHL, ALL, ARNT, KRAS2, RASK2,
GMPS, AF10, ARHGEF12, LARG, KIAA0382, CALM, CLTH, CEBPA, CEBP,
CHIC2, BTL, FLT3, KIT, PBT, LPP, NPM1, NUP214, D9S46E, CAN, CAIN,
RUNX1, CBFA2, AML1, WHSC1L1, NSD3, FLT3, AF1Q, NPM1, NUMA1, ZNF145,
PLZF, PML, MYL, STAT5B, AF10, CALM, CLTH, ARL11, ARLTS1, P2RX7,
P2X7, BCR, CML, PHL, ALL, GRAF, NF1, VRNF, WSS, NFNS, PTPN11,
PTP2C, SHP2, NS1, BCL2, CCND1, PRAD1, BCL1, TCRA, GATA1, GF1,
ERYF1, NFE1, ABL1, NQO1, DIA4, NMOR1, NUP214, D9S46E, CAN, CAIN).
Inflammation and AIDS (KIR3DL1, NKAT3, NKB1, AMB11, KIR3DS1, IFNG,
CXCL12, immune related SDF1); Autoimmune lymphoproliferative
syndrome (TNFRSF6, APT1, diseases and disorders FAS, CD95, ALPS1A);
Combined immunodeficiency, (IL2RG, SCIDX1, SCIDX, IMD4); HIV-1
(CCL5, SCYA5, D17S136E, TCP228), HIV susceptibility or infection
(IL10, CSIF, CMKBR2, CCR2, CMKBR5, CCCKR5 (CCR5));
Immunodeficiencies (CD3E, CD3G, AICDA, AID, HIGM2, TNFRSF5, CD40,
UNG, DGU, HIGM4, TNFSF5, CD40LG, HIGM1, IGM, FOXP3, IPEX, AIID,
XPID, PIDX, TNFRSF14B, TACI); Inflammation (IL-10, IL-1 (IL-1a,
IL-1b), IL-13, IL-17 (IL-17a (CTLA8), IL-17b, IL-17c, IL-17d,
IL-17f), II-23, Cx3cr1, ptpn22, TNFa, NOD2/CARD15 for IBD, IL-6,
IL-12 (IL-12a, IL-12b), CTLA4, Cx3cl1); Severe combined
immunodeficiencies (SCIDs)(JAK3, JAKL, DCLRE1C, ARTEMIS, SCIDA,
RAG1, RAG2, ADA, PTPRC, CD45, LCA, IL7R, CD3D, T3D, IL2RG, SCIDX1,
SCIDX, IMD4). Metabolic, liver, Amyloid neuropathy (TTR, PALB);
Amyloidosis (APOA1, APP, AAA, kidney and protein CVAP, AD1, GSN,
FGA, LYZ, TTR, PALB); Cirrhosis (KRT18, KRT8, diseases and
disorders CIRH1A, NAIC, TEX292, KIAA1988); Cystic fibrosis (CFTR,
ABCC7, CF, MRP7); Glycogen storage diseases (SLC2A2, GLUT2, G6PC,
G6PT, G6PT1, GAA, LAMP2, LAMPB, AGL, GDE, GBE1, GYS2, PYGL, PFKM);
Hepatic adenoma, 142330 (TCF1, HNF1A, MODY3), Hepatic failure,
early onset, and neurologic disorder (SCOD1, SCO1), Hepatic lipase
deficiency (LIPC), Hepatoblastoma, cancer and carcinomas (CTNNB1,
PDGFRL, PDGRL, PRLTS, AXIN1, AXIN, CTNNB1, TP53, P53, LFS1, IGF2R,
MPRI, MET, CASP8, MCH5; Medullary cystic kidney disease (UMOD,
HNFJ, FJHN, MCKD2, ADMCKD2); Phenylketonuria (PAH, PKU1, QDPR,
DHPR, PTS); Polycystic kidney and hepatic disease (FCYT, PKHD1,
ARPKD, PKD1, PKD2, PKD4, PKDTS, PRKCSH, G19P1, PCLD, SEC63).
Muscular/Skeletal Becker muscular dystrophy (DMD, BMD, MYF6),
Duchenne Muscular diseases and disorders Dystrophy (DMD, BMD);
Emery-Dreifuss muscular dystrophy (LMNA, LMN1, EMD2, FPLD, CMD1A,
HGPS, LGMD1B, LMNA, LMN1, EMD2, FPLD, CMD1A); Facioscapulohumeral
muscular dystrophy (FSHMD1A, FSHD1A); Muscular dystrophy (FKRP,
MDC1C, LGMD2I, LAMA2, LAMM, LARGE, KIAA0609, MDC1D, FCMD, TTID,
MYOT, CAPN3, CANP3, DYSF, LGMD2B, SGCG, LGMD2C, DMDA1, SCG3, SGCA,
ADL, DAG2, LGMD2D, DMDA2, SGCB, LGMD2E, SGCD, SGD, LGMD2F, CMD1L,
TCAP, LGMD2G, CMD1N, TRIM32, HT2A, LGMD2H, FKRP, MDC1C, LGMD2I,
TTN, CMD1G, TMD, LGMD2J, POMT1, CAV3, LGMD1C, SEPN1, SELN, RSMD1,
PLEC1, PLTN, EBS1); Osteopetrosis (LRP5, BMND1, LRP7, LR3, OPPG,
VBCH2, CLCN7, CLC7, OPTA2, OSTM1, GL, TCIRG1, TIRC7, OC116, OPTB1);
Muscular atrophy (VAPB, VAPC, ALS8, SMN1, SMA1, SMA2, SMA3, SMA4,
BSCL2, SPG17, GARS, SMAD1, CMT2D, HEXB, IGHMBP2, SMUBP2, CATF1,
SMARD1). Neurological and ALS (SOD1, ALS2, STEX, FUS, TARDBP, VEGF
(VEGF-a, VEGF-b, neuronal diseases and VEGF-c); Alzheimer disease
(APP, AAA, CVAP, AD1, APOE, AD2, disorders PSEN2, AD4, STM2, APBB2,
FE65L1, NOS3, PLAU, URK, ACE, DCP1, ACE1, MPO, PACIP1, PAXIP1L,
PTIP, A2M, BLMH, BMH, PSEN1, AD3); Autism (Mecp2, BZRAP1, MDGA2,
Sema5A, Neurexin1, GLO1, MECP2, RTT, PPMX, MRX16, MRX79, NLGN3,
NLGN4, KIAA1260, AUTSX2); Fragile X Syndrome (FMR2, FXR1, FXR2,
mGLUR5); Huntington's disease and disease like disorders (HD, IT15,
PRNP, PRIP, JPH3, JP3, HDL2, TBP, SCA17); Parkinson disease (NR4A2,
NURR1, NOT, TINUR, SNCAIP, TBP, SCA17, SNCA, NACP, PARK1, PARK4,
DJ1, PARK7, LRRK2, PARK8, PINK1, PARK6, UCHL1, PARK5, SNCA, NACP,
PARK1, PARK4, PRKN, PARK2, PDJ, DBH, NDUFV2); Rett syndrome (MECP2,
RTT, PPMX, MRX16, MRX79, CDKL5, STK9, MECP2, RTT, PPMX, MRX16,
MRX79, x-Synuclein, DJ-1); Schizophrenia (Neuregulin1 (Nrg1), Erb4
(receptor for Neuregulin), Complexin1 (Cplx1), Tph1 Tryptophan
hydroxylase, Tph2, Tryptophan hydroxylase 2, Neurexin 1, GSK3,
GSK3a, GSK3b, 5-HTT (Slc6a4), COMT, DRD (Drd1a), SLC6A3, DAOA,
DTNBP1, Dao (Dao1)); Secretase Related Disorders (APH-1 (alpha and
beta), Presenilin (Psen1), nicastrin, (Ncstn), PEN-2, Nos1, Parp1,
Nat1, Nat2); Trinucleotide Repeat Disorders (HTT (Huntington's Dx),
SBMA/SMAX1/AR (Kennedy's Dx), FXN/X25 (Friedrich's Ataxia), ATX3
(Machado-Joseph's Dx), ATXN1 and ATXN2 (spinocerebellar ataxias),
DMPK (myotonic dystrophy), Atrophin-1 and Atn1 (DRPLA Dx), CBP
(Creb-BP-global instability), VLDLR (Alzheimer's), Atxn7, Atxn10).
Occular diseases and Age-related macular degeneration (Abcr, Ccl2,
Cc2, cp (ceruloplasmin), disorders Timp3, cathepsinD, Vldlr, Ccr2);
Cataract (CRYAA, CRYA1, CRYBB2, CRYB2, PITX3, BFSP2, CP49, CP47,
CRYAA, CRYA1, PAX6, AN2, MGDA, CRYBA1, CRYB1, CRYGC, CRYG3, CCL,
LIM2, MP19, CRYGD, CRYG4, BFSP2, CP49, CP47, HSF4, CTM, HSF4, CTM,
MIP, AQP0, CRYAB, CRYA2, CTPP2, CRYBB1, CRYGD, CRYG4, CRYBB2,
CRYB2, CRYGC, CRYG3, CCL, CRYAA, CRYA1, GJA8, CX50, CAE1, GJA3,
CX46, CZP3, CAE3, CCM1, CAM, KRIT1); Corneal clouding and dystrophy
(APOA1, TGFBI, CSD2, CDGG1, CSD, BIGH3, CDG2, TACSTD2, TROP2, M1S1,
VSX1, RINX, PPCD, PPD, KTCN, COL8A2, FECD, PPCD2, PIP5K3, CFD);
Cornea plana congenital (KERA, CNA2); Glaucoma (MYOC, TIGR, GLC1A,
JOAG, GPOA, OPTN, GLC1E, FIP2, HYPL, NRP, CYP1B1, GLC3A, OPA1, NTG,
NPG, CYP1B1, GLC3A); Leber congenital amaurosis (CRB1, RP12, CRX,
CORD2, CRD, RPGRIP1, LCA6, CORD9, RPE65, RP20, AIPL1, LCA4, GUCY2D,
GUC2D, LCA1, CORD6, RDH12, LCA3); Macular dystrophy (ELOVL4, ADMD,
STGD2, STGD3, RDS, RP7, PRPH2, PRPH, AVMD, AOFMD, VMD2).
TABLE-US-00009 TABLE C CELLULAR FUNCTION GENES PI3K/AKT Signaling
PRKCE; ITGAM; ITGA5; IRAK1; PRKAA2; EIF2AK2; PTEN; EIF4E; PRKCZ;
GRK6; MAPK1; TSC1; PLK1; AKT2; IKBKB; PIK3CA; CDK8; CDKN1B; NFKB2;
BCL2; PIK3CB; PPP2R1A; MAPK8; BCL2L1; MAPK3; TSC2; ITGA1; KRAS;
EIF4EBP1; RELA; PRKCD; NOS3; PRKAA1; MAPK9; CDK2; PPP2CA; PIM1;
ITGB7; YWHAZ; ILK; TP53; RAF1; IKBKG; RELB; DYRK1A; CDKN1A; ITGB1;
MAP2K2; JAK1; AKT1; JAK2; PIK3R1; CHUK; PDPK1; PPP2R5C; CTNNB1;
MAP2K1; NFKB1; PAK3; ITGB3; CCND1; GSK3A; FRAP1; SFN; ITGA2; TTK;
CSNK1A1; BRAF; GSK3B; AKT3; FOXO1; SGK; HSP90AA1; RPS6KB1 ERK/MAPK
Signaling PRKCE; ITGAM; ITGA5; HSPB1; IRAK1; PRKAA2; EIF2AK2; RAC1;
RAP1A; TLN1; EIF4E; ELK1; GRK6; MAPK1; RAC2; PLK1; AKT2; PIK3CA;
CDK8; CREB1; PRKCI; PTK2; FOS; RPS6KA4; PIK3CB; PPP2R1A; PIK3C3;
MAPK8; MAPK3; ITGA1; ETS1; KRAS; MYCN; EIF4EBP1; PPARG; PRKCD;
PRKAA1; MAPK9; SRC; CDK2; PPP2CA; PIM1; PIK3C2A; ITGB7; YWHAZ;
PPP1CC; KSR1; PXN; RAF1; FYN; DYRK1A; ITGB1; MAP2K2; PAK4; PIK3R1;
STAT3; PPP2R5C; MAP2K1; PAK3; ITGB3; ESR1; ITGA2; MYC; TTK;
CSNK1A1; CRKL; BRAF; ATF4; PRKCA; SRF; STAT1; SGK Glucocorticoid
Receptor RAC1; TAF4B; EP300; SMAD2; TRAF6; PCAF; ELK1; Signaling
MAPK1; SMAD3; AKT2; IKBKB; NCOR2; UBE2I; PIK3CA; CREB1; FOS; HSPA5;
NFKB2; BCL2; MAP3K14; STAT5B; PIK3CB; PIK3C3; MAPK8; BCL2L1; MAPK3;
TSC22D3; MAPK10; NRIP1; KRAS; MAPK13; RELA; STAT5A; MAPK9; NOS2A;
PBX1; NR3C1; PIK3C2A; CDKN1C; TRAF2; SERPINE1; NCOA3; MAPK14; TNF;
RAF1; IKBKG; MAP3K7; CREBBP; CDKN1A; MAP2K2; JAK1; IL8; NCOA2;
AKT1; JAK2; PIK3R1; CHUK; STAT3; MAP2K1; NFKB1; TGFBR1; ESR1;
SMAD4; CEBPB; JUN; AR; AKT3; CCL2; MMP1; STAT1; IL6; HSP90AA1
Axonal Guidance PRKCE; ITGAM; ROCK1; ITGA5; CXCR4; ADAM12;
Signaling IGF1; RAC1; RAP1A; EIF4E; PRKCZ; NRP1; NTRK2; ARHGEF7;
SMO; ROCK2; MAPK1; PGF; RAC2; PTPN11; GNAS; AKT2; PIK3CA; ERBB2;
PRKCI; PTK2; CFL1; GNAQ; PIK3CB; CXCL12; PIK3C3; WNT11; PRKD1;
GNB2L1; ABL1; MAPK3; ITGA1; KRAS; RHOA; PRKCD; PIK3C2A; ITGB7;
GLI2; PXN; VASP; RAF1; FYN; ITGB1; MAP2K2; PAK4; ADAM17; AKT1;
PIK3R1; GLI1; WNT5A; ADAM10; MAP2K1; PAK3; ITGB3; CDC42; VEGFA;
ITGA2; EPHA8; CRKL; RND1; GSK3B; AKT3; PRKCA Ephrin Receptor PRKCE;
ITGAM; ROCK1; ITGA5; CXCR4; IRAK1; Signaling PRKAA2; EIF2AK2; RAC1;
RAP1A; GRK6; ROCK2; MAPK1; PGF; RAC2; PTPN11; GNAS; PLK1; AKT2;
DOK1; CDK8; CREB1; PTK2; CFL1; GNAQ; MAP3K14; CXCL12; MAPK8;
GNB2L1; ABL1; MAPK3; ITGA1; KRAS; RHOA; PRKCD; PRKAA1; MAPK9; SRC;
CDK2; PIM1; ITGB7; PXN; RAF1; FYN; DYRK1A; ITGB1; MAP2K2; PAK4;
AKT1; JAK2; STAT3; ADAM10; MAP2K1; PAK3; ITGB3; CDC42; VEGFA;
ITGA2; EPHA8; TTK; CSNK1A1; CRKL; BRAF; PTPN13; ATF4; AKT3; SGK
Actin Cytoskeleton ACTN4; PRKCE; ITGAM; ROCK1; ITGA5; IRAK1;
Signaling PRKAA2; EIF2AK2; RAC1; INS; ARHGEF7; GRK6; ROCK2; MAPK1;
RAC2; PLK1; AKT2; PIK3CA; CDK8; PTK2; CFL1; PIK3CB; MYH9; DIAPH1;
PIK3C3; MAPK8; F2R; MAPK3; SLC9A1; ITGA1; KRAS; RHOA; PRKCD;
PRKAA1; MAPK9; CDK2; PIM1; PIK3C2A; ITGB7; PPP1CC; PXN; VIL2; RAF1;
GSN; DYRK1A; ITGB1; MAP2K2; PAK4; PIP5K1A; PIK3R1; MAP2K1; PAK3;
ITGB3; CDC42; APC; ITGA2; TTK; CSNK1A1; CRKL; BRAF; VAV3; SGK
Huntington's Disease PRKCE; IGF1; EP300; RCOR1; PRKCZ; HDAC4; TGM2;
Signaling MAPK1; CAPNS1; AKT2; EGFR; NCOR2; SP1; CAPN2; PIK3CA;
HDAC5; CREB1; PRKCI; HSPA5; REST; GNAQ; PIK3CB; PIK3C3; MAPK8;
IGF1R; PRKD1; GNB2L1; BCL2L1; CAPN1; MAPK3; CASP8; HDAC2; HDAC7A;
PRKCD; HDAC11; MAPK9; HDAC9; PIK3C2A; HDAC3; TP53; CASP9; CREBBP;
AKT1; PIK3R1; PDPK1; CASP1; APAF1; FRAP1; CASP2; JUN; BAX; ATF4;
AKT3; PRKCA; CLTC; SGK; HDAC6; CASP3 Apoptosis Signaling PRKCE;
ROCK1; BID; IRAK1; PRKAA2; EIF2AK2; BAK1; BIRC4; GRK6; MAPK1;
CAPNS1; PLK1; AKT2; IKBKB; CAPN2; CDK8; FAS; NFKB2; BCL2; MAP3K14;
MAPK8; BCL2L1; CAPN1; MAPK3; CASP8; KRAS; RELA; PRKCD; PRKAA1;
MAPK9; CDK2; PIM1; TP53; TNF; RAF1; IKBKG; RELB; CASP9; DYRK1A;
MAP2K2; CHUK; APAF1; MAP2K1; NFKB1; PAK3; LMNA; CASP2; BIRC2; TTK;
CSNK1A1; BRAF; BAX; PRKCA; SGK; CASP3; BIRC3; PARP1 B Cell Receptor
RAC1; PTEN; LYN; ELK1; MAPK1; RAC2; PTPN11; Signaling AKT2; IKBKB;
PIK3CA; CREB1; SYK; NFKB2; CAMK2A; MAP3K14; PIK3CB; PIK3C3; MAPK8;
BCL2L1; ABL1; MAPK3; ETS1; KRAS; MAPK13; RELA; PTPN6; MAPK9; EGR1;
PIK3C2A; BTK; MAPK14; RAF1; IKBKG; RELB; MAP3K7; MAP2K2; AKT1;
PIK3R1; CHUK; MAP2K1; NFKB1; CDC42; GSK3A; FRAP1; BCL6; BCL10; JUN;
GSK3B; ATF4; AKT3; VAV3; RPS6KB1 Leukocyte Extravasation ACTN4;
CD44; PRKCE; ITGAM; ROCK1; CXCR4; CYBA; Signaling RAC1; RAP1A;
PRKCZ; ROCK2; RAC2; PTPN11; MMP14; PIK3CA; PRKCI; PTK2; PIK3CB;
CXCL12; PIK3C3; MAPK8; PRKD1; ABL1; MAPK10; CYBB; MAPK13; RHOA;
PRKCD; MAPK9; SRC; PIK3C2A; BTK; MAPK14; NOX1; PXN; VIL2; VASP;
ITGB1; MAP2K2; CTNND1; PIK3R1; CTNNB1; CLDN1; CDC42; F11R; ITK;
CRKL; VAV3; CTTN; PRKCA; MMP1; MMP9 Integrin Signaling ACTN4;
ITGAM; ROCK1; ITGA5; RAC1; PTEN; RAP1A; TLN1; ARHGEF7; MAPK1; RAC2;
CAPNS1; AKT2; CAPN2; PIK3CA; PTK2; PIK3CB; PIK3C3; MAPK8; CAV1;
CAPN1; ABL1; MAPK3; ITGA1; KRAS; RHOA; SRC; PIK3C2A; ITGB7; PPP1CC;
ILK; PXN; VASP; RAF1; FYN; ITGB1; MAP2K2; PAK4; AKT1; PIK3R1; TNK2;
MAP2K1; PAK3; ITGB3; CDC42; RND3; ITGA2; CRKL; BRAF; GSK3B; AKT3
Acute Phase Response IRAK1; SOD2; MYD88; TRAF6; ELK1; MAPK1;
PTPN11; Signaling AKT2; IKBKB; PIK3CA; FOS; NFKB2; MAP3K14; PIK3CB;
MAPK8; RIPK1; MAPK3; IL6ST; KRAS; MAPK13; IL6R; RELA; SOCS1; MAPK9;
FTL; NR3C1; TRAF2; SERPINE1; MAPK14; TNF; RAF1; PDK1; IKBKG; RELB;
MAP3K7; MAP2K2; AKT1; JAK2; PIK3R1; CHUK; STAT3; MAP2K1; NFKB1;
FRAP1; CEBPB; JUN; AKT3; IL1R1; IL6 PTEN Signaling ITGAM; ITGA5;
RAC1; PTEN; PRKCZ; BCL2L11; MAPK1; RAC2; AKT2; EGFR; IKBKB; CBL;
PIK3CA; CDKN1B; PTK2; NFKB2; BCL2; PIK3CB; BCL2L1; MAPK3; ITGA1;
KRAS; ITGB7; ILK; PDGFRB; INSR; RAF1; IKBKG; CASP9; CDKN1A; ITGB1;
MAP2K2; AKT1; PIK3R1; CHUK; PDGFRA; PDPK1; MAP2K1; NFKB1; ITGB3;
CDC42; CCND1; GSK3A; ITGA2; GSK3B; AKT3; FOXO1; CASP3; RPS6KB1 p53
Signaling PTEN; EP300; BBC3; PCAF; FASN; BRCA1; GADD45A; BIRC5;
AKT2; PIK3CA; CHEK1; TP53INP1; BCL2; PIK3CB; PIK3C3; MAPK8; THBS1;
ATR; BCL2L1; E2F1; PMAIP1; CHEK2; TNFRSF10B; TP73; RB1; HDAC9;
CDK2; PIK3C2A; MAPK14; TP53; LRDD; CDKN1A; HIPK2; AKT1; PIK3R1;
RRM2B; APAF1; CTNNB1; SIRT1; CCND1; PRKDC; ATM; SFN; CDKN2A; JUN;
SNAI2; GSK3B; BAX; AKT3 Aryl Hydrocarbon HSPB1; EP300; FASN; TGM2;
RXRA; MAPK1; NQO1; Receptor Signaling NCOR2; SP1; ARNT; CDKN1B;
FOS; CHEK1; SMARCA4; NFKB2; MAPK8; ALDH1A1; ATR; E2F1; MAPK3;
NRIP1; CHEK2; RELA; TP73; GSTP1; RB1; SRC; CDK2; AHR; NFE2L2;
NCOA3; TP53; TNF; CDKN1A; NCOA2; APAF1; NFKB1; CCND1; ATM; ESR1;
CDKN2A; MYC; JUN; ESR2; BAX; IL6; CYP1B1; HSP90AA1 Xenobiotic
Metabolism PRKCE; EP300; PRKCZ; RXRA; MAPK1; NQO1; Signaling NCOR2;
PIK3CA; ARNT; PRKCI; NFKB2; CAMK2A; PIK3CB; PPP2R1A; PIK3C3; MAPK8;
PRKD1; ALDH1A1; MAPK3; NRIP1; KRAS; MAPK13; PRKCD; GSTP1; MAPK9;
NOS2A; ABCB1; AHR; PPP2CA; FTL; NFE2L2; PIK3C2A; PPARGC1A; MAPK14;
TNF; RAF1; CREBBP; MAP2K2; PIK3R1; PPP2R5C; MAP2K1; NFKB1; KEAP1;
PRKCA; EIF2AK3; IL6; CYP1B1; HSP90AA1 SAPK/JNK Signaling PRKCE;
IRAK1; PRKAA2; EIF2AK2; RAC1; ELK1; GRK6; MAPK1; GADD45A; RAC2;
PLK1; AKT2; PIK3CA; FADD; CDK8; PIK3CB; PIK3C3; MAPK8; RIPK1;
GNB2L1; IRS1; MAPK3; MAPK10; DAXX; KRAS; PRKCD; PRKAA1; MAPK9;
CDK2; PIM1; PIK3C2A; TRAF2; TP53; LCK; MAP3K7; DYRK1A; MAP2K2;
PIK3R1; MAP2K1; PAK3; CDC42; JUN; TTK; CSNK1A1; CRKL; BRAF; SGK
PPAr/RXR Signaling PRKAA2; EP300; INS; SMAD2; TRAF6; PPARA; FASN;
RXRA; MAPK1; SMAD3; GNAS; IKBKB; NCOR2; ABCA1; GNAQ; NFKB2;
MAP3K14; STAT5B; MAPK8; IRS1; MAPK3; KRAS; RELA; PRKAA1; PPARGC1A;
NCOA3; MAPK14; INSR; RAF1; IKBKG; RELB; MAP3K7; CREBBP; MAP2K2;
JAK2; CHUK; MAP2K1; NFKB1; TGFBR1; SMAD4; JUN; IL1R1; PRKCA; IL6;
HSP90AA1; ADIPOQ NF-KB Signaling IRAK1; EIF2AK2; EP300; INS; MYD88;
PRKCZ; TRAF6; TBK1; AKT2; EGFR; IKBKB; PIK3CA; BTRC; NFKB2;
MAP3K14; PIK3CB; PIK3C3; MAPK8; RIPK1; HDAC2; KRAS; RELA; PIK3C2A;
TRAF2; TLR4; PDGFRB; TNF; INSR; LCK; IKBKG; RELB; MAP3K7; CREBBP;
AKT1; PIK3R1; CHUK; PDGFRA; NFKB1; TLR2; BCL10; GSK3B; AKT3;
TNFAIP3; IL1R1 Neuregulin Signaling ERBB4; PRKCE; ITGAM; ITGA5;
PTEN; PRKCZ; ELK1; MAPK1; PTPN11; AKT2; EGFR; ERBB2; PRKCI; CDKN1B;
STAT5B; PRKD1; MAPK3; ITGA1; KRAS; PRKCD; STAT5A; SRC; ITGB7; RAF1;
ITGB1; MAP2K2; ADAM17; AKT1; PIK3R1; PDPK1; MAP2K1; ITGB3; EREG;
FRAP1; PSEN1; ITGA2; MYC; NRG1; CRKL; AKT3; PRKCA; HSP90AA1;
RPS6KB1 Wnt & Beta catenin CD44; EP300; LRP6; DVL3; CSNK1E;
GJA1; SMO; Signaling AKT2; PIN1; CDH1; BTRC; GNAQ; MARK2; PPP2R1A;
WNT11; SRC; DKK1; PPP2CA; SOX6; SFRP2; ILK; LEF1; SOX9; TP53;
MAP3K7; CREBBP; TCF7L2; AKT1; PPP2R5C; WNT5A; LRP5; CTNNB1; TGFBR1;
CCND1; GSK3A; DVL1; APC; CDKN2A; MYC; CSNK1A1; GSK3B; AKT3; SOX2
Insulin Receptor PTEN; INS; EIF4E; PTPN1; PRKCZ; MAPK1; TSC1;
Signaling PTPN11; AKT2; CBL; PIK3CA; PRKCI; PIK3CB; PIK3C3; MAPK8;
IRS1; MAPK3; TSC2; KRAS; EIF4EBP1; SLC2A4; PIK3C2A; PPP1CC; INSR;
RAF1; FYN; MAP2K2; JAK1; AKT1; JAK2; PIK3R1; PDPK1; MAP2K1; GSK3A;
FRAP1; CRKL; GSK3B; AKT3; FOXO1; SGK; RPS6KB1 IL-6 Signaling HSPB1;
TRAF6; MAPKAPK2; ELK1; MAPK1; PTPN11; IKBKB; FOS; NFKB2; MAP3K14;
MAPK8; MAPK3; MAPK10; IL6ST; KRAS; MAPK13; IL6R; RELA; SOCS1;
MAPK9; ABCB1; TRAF2; MAPK14; TNF; RAF1; IKBKG; RELB; MAP3K7;
MAP2K2; IL8; JAK2; CHUK; STAT3; MAP2K1; NFKB1; CEBPB; JUN; IL1R1;
SRF; IL6 Hepatic Cholestasis PRKCE; IRAK1; INS; MYD88; PRKCZ;
TRAF6; PPARA; RXRA; IKBKB; PRKCI; NFKB2; MAP3K14; MAPK8; PRKD1;
MAPK10; RELA; PRKCD; MAPK9; ABCB1; TRAF2; TLR4; TNF; INSR; IKBKG;
RELB; MAP3K7; IL8; CHUK; NR1H2; TJP2; NFKB1; ESR1; SREBF1; FGFR4;
JUN; IL1R1; PRKCA; IL6 IGF-1 Signaling IGF1; PRKCZ; ELK1; MAPK1;
PTPN11; NEDD4; AKT2; PIK3CA; PRKCI; PTK2; FOS; PIK3CB; PIK3C3;
MAPK8; IGF1R; IRS1; MAPK3; IGFBP7; KRAS; PIK3C2A; YWHAZ; PXN; RAF1;
CASP9; MAP2K2; AKT1; PIK3R1; PDPK1; MAP2K1; IGFBP2; SFN; JUN;
CYR61; AKT3; FOXO1; SRF; CTGF; RPS6KB1 NRF2-mediated PRKCE; EP300;
SOD2; PRKCZ; MAPK1; SQSTM1; Oxidative Stress Response NQO1; PIK3CA;
PRKCI; FOS; PIK3CB; PIK3C3; MAPK8; PRKD1; MAPK3; KRAS; PRKCD;
GSTP1; MAPK9; FTL; NFE2L2; PIK3C2A; MAPK14; RAF1; MAP3K7; CREBBP;
MAP2K2; AKT1; PIK3R1; MAP2K1; PPIB; JUN; KEAP1; GSK3B; ATF4; PRKCA;
EIF2AK3; HSP90AA1 Hepatic Fibrosis/Hepatic EDN1; IGF1; KDR; FLT1;
SMAD2; FGFR1; MET; PGF; Stellate Cell Activation SMAD3; EGFR; FAS;
CSF1; NFKB2; BCL2; MYH9; IGF1R; IL6R; RELA; TLR4; PDGFRB; TNF;
RELB; IL8; PDGFRA; NFKB1; TGFBR1; SMAD4; VEGFA; BAX; IL1R1; CCL2;
HGF; MMP1; STAT1; IL6; CTGF; MMP9 PPAR Signaling EP300; INS; TRAF6;
PPARA; RXRA; MAPK1; IKBKB; NCOR2; FOS; NFKB2; MAP3K14; STAT5B;
MAPK3; NRIP1; KRAS; PPARG; RELA; STAT5A; TRAF2; PPARGC1A; PDGFRB;
TNF; INSR; RAF1; IKBKG; RELB; MAP3K7; CREBBP; MAP2K2; CHUK; PDGFRA;
MAP2K1; NFKB1; JUN; IL1R1; HSP90AA1 Fc Epsilon RI Signaling PRKCE;
RAC1; PRKCZ; LYN; MAPK1; RAC2; PTPN11; AKT2; PIK3CA; SYK; PRKCI;
PIK3CB; PIK3C3; MAPK8; PRKD1; MAPK3; MAPK10; KRAS; MAPK13; PRKCD;
MAPK9; PIK3C2A; BTK; MAPK14; TNF; RAF1; FYN; MAP2K2; AKT1; PIK3R1;
PDPK1; MAP2K1; AKT3; VAV3; PRKCA G-Protein Coupled PRKCE; RAP1A;
RGS16; MAPK1; GNAS; AKT2; IKBKB; Receptor Signaling PIK3CA; CREB1;
GNAQ; NFKB2; CAMK2A; PIK3CB; PIK3C3; MAPK3; KRAS; RELA; SRC;
PIK3C2A; RAF1; IKBKG; RELB; FYN; MAP2K2; AKT1; PIK3R1; CHUK;
PDPK1; STAT3; MAP2K1; NFKB1; BRAF; ATF4; AKT3; PRKCA Inositol
Phosphate PRKCE; IRAK1; PRKAA2; EIF2AK2; PTEN; GRK6; Metabolism
MAPK1; PLK1; AKT2; PIK3CA; CDK8; PIK3CB; PIK3C3; MAPK8; MAPK3;
PRKCD; PRKAA1; MAPK9; CDK2; PIM1; PIK3C2A; DYRK1A; MAP2K2; PIP5K1A;
PIK3R1; MAP2K1; PAK3; ATM; TTK; CSNK1A1; BRAF; SGK PDGF Signaling
EIF2AK2; ELK1; ABL2; MAPK1; PIK3CA; FOS; PIK3CB; PIK3C3; MAPK8;
CAV1; ABL1; MAPK3; KRAS; SRC; PIK3C2A; PDGFRB; RAF1; MAP2K2; JAK1;
JAK2; PIK3R1; PDGFRA; STAT3; SPHK1; MAP2K1; MYC; JUN; CRKL; PRKCA;
SRF; STAT1; SPHK2 VEGF Signaling ACTN4; ROCK1; KDR; FLT1; ROCK2;
MAPK1; PGF; AKT2; PIK3CA; ARNT; PTK2; BCL2; PIK3CB; PIK3C3; BCL2L1;
MAPK3; KRAS; HIF1A; NOS3; PIK3C2A; PXN; RAF1; MAP2K2; ELAVL1; AKT1;
PIK3R1; MAP2K1; SFN; VEGFA; AKT3; FOXO1; PRKCA Natural Killer Cell
PRKCE; RAC1; PRKCZ; MAPK1; RAC2; PTPN11; Signaling KIR2DL3; AKT2;
PIK3CA; SYK; PRKCI; PIK3CB; PIK3C3; PRKD1; MAPK3; KRAS; PRKCD;
PTPN6; PIK3C2A; LCK; RAF1; FYN; MAP2K2; PAK4; AKT1; PIK3R1; MAP2K1;
PAK3; AKT3; VAV3; PRKCA Cell Cycle: G1/S HDAC4; SMAD3; SUV39H1;
HDAC5; CDKN1B; BTRC; Checkpoint Regulation ATR; ABL1; E2F1; HDAC2;
HDAC7A; RB1; HDAC11; HDAC9; CDK2; E2F2; HDAC3; TP53; CDKN1A; CCND1;
E2F4; ATM; RBL2; SMAD4; CDKN2A; MYC; NRG1; GSK3B; RBL1; HDAC6 T
Cell Receptor RAC1; ELK1; MAPK1; IKBKB; CBL; PIK3CA; FOS; Signaling
NFKB2; PIK3CB; PIK3C3; MAPK8; MAPK3; KRAS; RELA; PIK3C2A; BTK; LCK;
RAF1; IKBKG; RELB; FYN; MAP2K2; PIK3R1; CHUK; MAP2K1; NFKB1; ITK;
BCL10; JUN; VAV3 Death Receptor Signaling CRADD; HSPB1; BID; BIRC4;
TBK1; IKBKB; FADD; FAS; NFKB2; BCL2; MAP3K14; MAPK8; RIPK1; CASP8;
DAXX; TNFRSF10B; RELA; TRAF2; TNF; IKBKG; RELB; CASP9; CHUK; APAF1;
NFKB1; CASP2; BIRC2; CASP3; BIRC3 FGF Signaling RAC1; FGFR1; MET;
MAPKAPK2; MAPK1; PTPN11; AKT2; PIK3CA; CREB1; PIK3CB; PIK3C3;
MAPK8; MAPK3; MAPK13; PTPN6; PIK3C2A; MAPK14; RAF1; AKT1; PIK3R1;
STAT3; MAP2K1; FGFR4; CRKL; ATF4; AKT3; PRKCA; HGF GM-CSF Signaling
LYN; ELK1; MAPK1; PTPN11; AKT2; PIK3CA; CAMK2A; STAT5B; PIK3CB;
PIK3C3; GNB2L1; BCL2L1; MAPK3; ETS1; KRAS; RUNX1; PIM1; PIK3C2A;
RAF1; MAP2K2; AKT1; JAK2; PIK3R1; STAT3; MAP2K1; CCND1; AKT3; STAT1
Amyotrophic Lateral BID; IGF1; RAC1; BIRC4; PGF; CAPNS1; CAPN2;
Sclerosis Signaling PIK3CA; BCL2; PIK3CB; PIK3C3; BCL2L1; CAPN1;
PIK3C2A; TP53; CASP9; PIK3R1; RAB5A; CASP1; APAF1; VEGFA; BIRC2;
BAX; AKT3; CASP3; BIRC3 JAK/Stat Signaling PTPN1; MAPK1; PTPN11;
AKT2; PIK3CA; STAT5B; PIK3CB; PIK3C3; MAPK3; KRAS; SOCS1; STAT5A;
PTPN6; PIK3C2A; RAF1; CDKN1A; MAP2K2; JAK1; AKT1; JAK2; PIK3R1;
STAT3; MAP2K1; FRAP1; AKT3; STAT1 Nicotinate and PRKCE; IRAK1;
PRKAA2; EIF2AK2; GRK6; MAPK1; Nicotinamide Metabolism PLK1; AKT2;
CDK8; MAPK8; MAPK3; PRKCD; PRKAA1; PBEF1; MAPK9; CDK2; PIM1;
DYRK1A; MAP2K2; MAP2K1; PAK3; NT5E; TTK; CSNK1A1; BRAF; SGK
Chemokine Signaling CXCR4; ROCK2; MAPK1; PTK2; FOS; CFL1; GNAQ;
CAMK2A; CXCL12; MAPK8; MAPK3; KRAS; MAPK13; RHOA; CCR3; SRC;
PPP1CC; MAPK14; NOX1; RAF1; MAP2K2; MAP2K1; JUN; CCL2; PRKCA IL-2
Signaling ELK1; MAPK1; PTPN11; AKT2; PIK3CA; SYK; FOS; STAT5B;
PIK3CB; PIK3C3; MAPK8; MAPK3; KRAS; SOCS1; STAT5A; PIK3C2A; LCK;
RAF1; MAP2K2; JAK1; AKT1; PIK3R1; MAP2K1; JUN; AKT3 Synaptic Long
Term PRKCE; IGF1; PRKCZ; PRDX6; LYN; MAPK1; GNAS; Depression PRKCI;
GNAQ; PPP2R1A; IGF1R; PRKD1; MAPK3; KRAS; GRN; PRKCD; NOS3; NOS2A;
PPP2CA; YWHAZ; RAF1; MAP2K2; PPP2R5C; MAP2K1; PRKCA Estrogen
Receptor TAF4B; EP300; CARM1; PCAF; MAPK1; NCOR2; Signaling
SMARCA4; MAPK3; NRIP1; KRAS; SRC; NR3C1; HDAC3; PPARGC1A; RBM9;
NCOA3; RAF1; CREBBP; MAP2K2; NCOA2; MAP2K1; PRKDC; ESR1; ESR2
Protein Ubiquitination TRAF6; SMURF1; BIRC4; BRCA1; UCHL1; NEDD4;
Pathway CBL; UBE2I; BTRC; HSPA5; USP7; USP10; FBXW7; USP9X; STUB1;
USP22; B2M; BIRC2; PARK2; USP8; USP1; VHL; HSP90AA1; BIRC3 IL-10
Signaling TRAF6; CCR1; ELK1; IKBKB; SP1; FOS; NFKB2; MAP3K14;
MAPK8; MAPK13; RELA; MAPK14; TNF; IKBKG; RELB; MAP3K7; JAK1; CHUK;
STAT3; NFKB1; JUN; IL1R1; IL6 VDR/RXR Activation PRKCE; EP300;
PRKCZ; RXRA; GADD45A; HES1; NCOR2; SP1; PRKCI; CDKN1B; PRKD1;
PRKCD; RUNX2; KLF4; YY1; NCOA3; CDKN1A; NCOA2; SPP1; LRP5; CEBPB;
FOXO1; PRKCA TGF-beta Signaling EP300; SMAD2; SMURF1; MAPK1; SMAD3;
SMAD1; FOS; MAPK8; MAPK3; KRAS; MAPK9; RUNX2; SERPINE1; RAF1;
MAP3K7; CREBBP; MAP2K2; MAP2K1; TGFBR1; SMAD4; JUN; SMAD5 Toll-like
Receptor IRAK1; EIF2AK2; MYD88; TRAF6; PPARA; ELK1; Signaling
IKBKB; FOS; NFKB2; MAP3K14; MAPK8; MAPK13; RELA; TLR4; MAPK14;
IKBKG; RELB; MAP3K7; CHUK; NFKB1; TLR2; JUN p38 MAPK Signaling
HSPB1; IRAK1; TRAF6; MAPKAPK2; ELK1; FADD; FAS; CREB1; DDIT3;
RPS6KA4; DAXX; MAPK13; TRAF2; MAPK14; TNF; MAP3K7; TGFBR1; MYC;
ATF4; IL1R1; SRF; STAT1 Neurotrophin/TRK NTRK2; MAPK1; PTPN11;
PIK3CA; CREB1; FOS; Signaling PIK3CB; PIK3C3; MAPK8; MAPK3; KRAS;
PIK3C2A; RAF1; MAP2K2; AKT1; PIK3R1; PDPK1; MAP2K1; CDC42; JUN;
ATF4 FXR/RXR Activation INS; PPARA; FASN; RXRA; AKT2; SDC1; MAPK8;
APOB; MAPK10; PPARG; MTTP; MAPK9; PPARGC1A; TNF; CREBBP; AKT1;
SREBF1; FGFR4; AKT3; FOXO1 Synaptic Long Term PRKCE; RAP1A; EP300;
PRKCZ; MAPK1; CREB1; Potentiation PRKCI; GNAQ; CAMK2A; PRKD1;
MAPK3; KRAS; PRKCD; PPP1CC; RAF1; CREBBP; MAP2K2; MAP2K1; ATF4;
PRKCA Calcium Signaling RAP1A; EP300; HDAC4; MAPK1; HDAC5; CREB1;
CAMK2A; MYH9; MAPK3; HDAC2; HDAC7A; HDAC11; HDAC9; HDAC3; CREBBP;
CALR; CAMKK2; ATF4; HDAC6 EGF Signaling ELK1; MAPK1; EGFR; PIK3CA;
FOS; PIK3CB; PIK3C3; MAPK8; MAPK3; PIK3C2A; RAF1; JAK1; PIK3R1;
STAT3; MAP2K1; JUN; PRKCA; SRF; STAT1 Hypoxia Signaling in the
EDN1; PTEN; EP300; NQO1; UBE2I; CREB1; ARNT; Cardiovascular System
HIF1A; SLC2A4; NOS3; TP53; LDHA; AKT1; ATM; VEGFA; JUN; ATF4; VHL;
HSP90AA1 LPS/IL-1 Mediated IRAK1; MYD88; TRAF6; PPARA; RXRA; ABCA1;
Inhibition of RXR Function MAPK8; ALDH1A1; GSTP1; MAPK9; ABCB1;
TRAF2; TLR4; TNF; MAP3K7; NR1H2; SREBF1; JUN; IL1R1 LXR/RXR
Activation FASN; RXRA; NCOR2; ABCA1; NFKB2; IRF3; RELA; NOS2A;
TLR4; TNF; RELB; LDLR; NR1H2; NFKB1; SREBF1; IL1R1; CCL2; IL6; MMP9
Amyloid Processing PRKCE; CSNK1E; MAPK1; CAPNS1; AKT2; CAPN2;
CAPN1; MAPK3; MAPK13; MAPT; MAPK14; AKT1; PSEN1; CSNK1A1; GSK3B;
AKT3; APP IL-4 Signaling AKT2; PIK3CA; PIK3CB; PIK3C3; IRS1; KRAS;
SOCS1; PTPN6; NR3C1; PIK3C2A; JAK1; AKT1; JAK2; PIK3R1; FRAP1;
AKT3; RPS6KB1 Cell Cycle: G2/M DNA EP300; PCAF; BRCA1; GADD45A;
PLK1; BTRC; Damage Checkpoint CHEK1; ATR; CHEK2; YWHAZ; TP53;
CDKN1A; Regulation PRKDC; ATM; SFN; CDKN2A Nitric Oxide Signaling
in KDR; FLT1; PGF; AKT2; PIK3CA; PIK3CB; PIK3C3; the Cardiovascular
System CAV1; PRKCD; NOS3; PIK3C2A; AKT1; PIK3R1; VEGFA; AKT3;
HSP90AA1 Purine Metabolism NME2; SMARCA4; MYH9; RRM2; ADAR;
EIF2AK4; PKM2; ENTPD1; RAD51; RRM2B; TJP2; RAD51C; NT5E; POLD1;
NME1 cAMP-mediated RAP1A; MAPK1; GNAS; CREB1; CAMK2A; MAPK3;
Signaling SRC; RAF1; MAP2K2; STAT3; MAP2K1; BRAF; ATF4
Mitochondrial SOD2; MAPK8; CASP8; MAPK10; MAPK9; CASP9; Dysfunction
PARK7; PSEN1; PARK2; APP; CASP3 Notch Signaling HES1; JAG1; NUMB;
NOTCH4; ADAM17; NOTCH2; PSEN1; NOTCH3; NOTCH1; DLL4 Endoplasmic
Reticulum HSPA5; MAPK8; XBP1; TRAF2; ATF6; CASP9; ATF4; Stress
Pathway EIF2AK3; CASP3 Pyrimidine Metabolism NME2; AICDA; RRM2;
EIF2AK4; ENTPD1; RRM2B; NT5E; POLD1; NME1 Parkinson's Signaling
UCHL1; MAPK8; MAPK13; MAPK14; CASP9; PARK7; PARK2; CASP3 Cardiac
& Beta GNAS; GNAQ; PPP2R1A; GNB2L1; PPP2CA; PPP1CC; Adrenergic
Signaling PPP2R5C Glycolysis/Gluconeogenesis HK2; GCK; GPI;
ALDH1A1; PKM2; LDHA; HK1 Interferon Signaling IRF1; SOCS1; JAK1;
JAK2; IFITM1; STAT1; IFIT3 Sonic Hedgehog ARRB2; SMO; GLI2; DYRK1A;
GLI1; GSK3B; DYRK1B Signaling Glycerophospholipid PLD1; GRN; GPAM;
YWHAZ; SPHK1; SPHK2 Metabolism Phospholipid PRDX6; PLD1; GRN;
YWHAZ; SPHK1; SPHK2 Degradation Tryptophan Metabolism SIAH2; PRMT5;
NEDD4; ALDH1A1; CYP1B1; SIAH1 Lysine Degradation SUV39H1; EHMT2;
NSD1; SETD7; PPP2R5C Nucleotide Excision ERCC5; ERCC4; XPA; XPC;
ERCC1 Repair Pathway Starch and Sucrose UCHL1; HK2; GCK; GPI; HK1
Metabolism Aminosugars Metabolism NQO1; HK2; GCK; HK1 Arachidonic
Acid PRDX6; GRN; YWHAZ; CYP1B1 Metabolism Circadian Rhythm CSNK1E;
CREB1; ATF4; NR1D1 Signaling Coagulation System BDKRB1; F2R;
SERPINE1; F3 Dopamine Receptor PPP2R1A; PPP2CA; PPP1CC; PPP2R5C
Signaling Glutathione Metabolism IDH2; GSTP1; ANPEP; IDH1
Glycerolipid Metabolism ALDH1A1; GPAM; SPHK1; SPHK2 Linoleic Acid
PRDX6; GRN; YWHAZ; CYP1B1 Metabolism Methionine Metabolism DNMT1;
DNMT3B; AHCY; DNMT3A Pyruvate Metabolism GLO1; ALDH1A1; PKM2; LDHA
Arginine and Proline ALDH1A1; NOS3; NOS2A Metabolism Eicosanoid
Signaling PRDX6; GRN; YWHAZ Fructose and Mannose HK2; GCK; HK1
Metabolism Galactose Metabolism HK2; GCK; HK1 Stilbene, Coumarine
and PRDX6; PRDX1; TYR Lignin Biosynthesis Antigen Presentation
CALR; B2M Pathway Biosynthesis of Steroids NQO1; DHCR7 Butanoate
Metabolism ALDH1A1; NLGN1 Citrate Cycle IDH2; IDH1 Fatty Acid
Metabolism ALDH1A1; CYP1B1 Glycerophospholipid PRDX6; CHKA
Metabolism Histidine Metabolism PRMT5; ALDH1A1 Inositol Metabolism
ERO1L; APEX1 Metabolism of GSTP1; CYP1B1 Xenobiotics by Cytochrome
p450 Methane Metabolism PRDX6; PRDX1 Phenylalanine PRDX6; PRDX1
Metabolism Propanoate Metabolism ALDH1A1; LDHA Selenoamino Acid
PRMT5; AHCY Metabolism Sphingolipid Metabolism SPHK1; SPHK2
Aminophosphonate PRMT5 Metabolism Androgen and Estrogen PRMT5
Metabolism Ascorbate and Aldarate ALDH1A1 Metabolism Bile Acid
Biosynthesis ALDH1A1 Cysteine Metabolism LDHA Fatty Acid
Biosynthesis FASN Glutamate Receptor GNB2L1 Signaling NRF2-mediated
PRDX1 Oxidative Stress Response Pentose Phosphate GPI Pathway
Pentose and Glucuronate UCHL1 Interconversions Retinol Metabolism
ALDH1A1 Riboflavin Metabolism TYR Tyrosine Metabolism PRMT5, TYR
Ubiquinone Biosynthesis PRMT5 Valine, Leucine and ALDH1A1
Isoleucine Degradation Glycine, Serine and CHKA Threonine
Metabolism Lysine Degradation ALDH1A1 Pain/Taste TRPM5; TRPA1
Pain TRPM7; TRPC5; TRPC6; TRPC1; Cnr1; cnr2; Grk2; Trpa1; Pomc;
Cgrp; Crf; Pka; Era; Nr2b; TRPM5; Prkaca; Prkacb; Prkar1a; Prkar2a
Mitochondrial Function AIF; CytC; SMAC (Diablo); Aifm-1; Aifm-2
Developmental BMP-4; Chordin (Chrd); Noggin (Nog); WNT (Wnt2;
Neurology Wnt2b; Wnt3a; Wnt4; Wnt5a; Wnt6; Wnt7b; Wnt8b; Wnt9a;
Wnt9b; Wnt10a; Wnt10b; Wnt16); beta-catenin; Dkk-1; Frizzled
related proteins; Otx-2; Gbx2; FGF-8; Reelin; Dab1; unc-86 (Pou4f1
or Brn3a); Numb; Reln
[0618] Embodiments of the invention also relate to methods and
compositions related to knocking out genes, amplifying genes and
repairing particular mutations associated with DNA repeat
instability and neurological disorders (Robert D. Wells, Tetsuo
Ashizawa, Genetic Instabilities and Neurological Diseases, Second
Edition, Academic Press, Oct. 13, 2011--Medical). Specific aspects
of tandem repeat sequences have been found to be responsible for
more than twenty human diseases (New insights into repeat
instability: role of RNA*DNA hybrids. McIvor E I, Polak U,
Napierala M. RNA Biol. 2010 September-October; 7(5):551-8). The
CRISPR-Cas system may be harnessed to correct these defects of
genomic instability.
[0619] A further aspect of the invention relates to utilizing the
CRISPR-Cas system for correcting defects in the EMP2A and EMP2B
genes that have been identified to be associated with Lafora
disease. Lafora disease is an autosomal recessive condition which
is characterized by progressive myoclonus epilepsy which may start
as epileptic seizures in adolescence. A few cases of the disease
may be caused by mutations in genes yet to be identified. The
disease causes seizures, muscle spasms, difficulty walking,
dementia, and eventually death. There is currently no therapy that
has proven effective against disease progression. Other genetic
abnormalities associated with epilepsy may also be targeted by the
CRISPR-Cas system and the underlying genetics is further described
in Genetics of Epilepsy and Genetic Epilepsies, edited by Giuliano
Avanzini, Jeffrey L. Noebels, Mariani Foundation Paediatric
Neurology:20; 2009).
[0620] The methods of US Patent Publication No. 20110158957
assigned to Sangamo BioSciences, Inc. involved in inactivating T
cell receptor (TCR) genes may also be modified to the CRISPR Cas
system of the present invention. In another example, the methods of
US Patent Publication No. 20100311124 assigned to Sangamo
BioSciences, Inc. and US Patent Publication No. 20110225664
assigned to Cellectis, which are both involved in inactivating
glutamine synthetase gene expression genes may also be modified to
the CRISPR Cas system of the present invention.
[0621] Several further aspects of the invention relate to
correcting defects associated with a wide range of genetic diseases
which are further described on the website of the National
Institutes of Health under the topic subsection Genetic Disorders
(website at health.nih.gov/topic/GeneticDisorders). The genetic
brain diseases may include but are not limited to
Adrenoleukodystrophy, Agenesis of the Corpus Callosum, Aicardi
Syndrome, Alpers' Disease, Alzheimer's Disease, Barth Syndrome,
Batten Disease, CADASIL, Cerebellar Degeneration, Fabry's Disease,
Gerstmann-Straussler-Scheinker Disease, Huntington's Disease and
other Triplet Repeat Disorders, Leigh's Disease, Lesch-Nyhan
Syndrome, Menkes Disease, Mitochondrial Myopathies and NINDS
Colpocephaly. These diseases are further described on the website
of the National Institutes of Health under the subsection Genetic
Brain Disorders.
[0622] In some embodiments, the condition may be neoplasia. In some
embodiments, where the condition is neoplasia, the genes to be
targeted are any of those listed in Table A (in this case PTEN and
so forth). In some embodiments, the condition may be Age-related
Macular Degeneration. In some embodiments, the condition may be a
Schizophrenic Disorder. In some embodiments, the condition may be a
Trinucleotide Repeat Disorder. In some embodiments, the condition
may be Fragile X Syndrome. In some embodiments, the condition may
be a Secretase Related Disorder. In some embodiments, the condition
may be a Prion-related disorder. In some embodiments, the condition
may be ALS. In some embodiments, the condition may be a drug
addiction. In some embodiments, the condition may be Autism. In
some embodiments, the condition may be Alzheimer's Disease. In some
embodiments, the condition may be inflammation. In some
embodiments, the condition may be Parkinson's Disease.
[0623] For example, US Patent Publication No. 20110023145,
describes use of zinc finger nucleases to genetically modify cells,
animals and proteins associated with autism spectrum disorders
(ASD). Autism spectrum disorders (ASDs) are a group of disorders
characterized by qualitative impairment in social interaction and
communication, and restricted repetitive and stereotyped patterns
of behavior, interests, and activities. The three disorders,
autism, Asperger syndrome (AS) and pervasive developmental
disorder--not otherwise specified (PDD-NOS) are a continuum of the
same disorder with varying degrees of severity, associated
intellectual functioning and medical conditions. ASDs are
predominantly genetically determined disorders with a heritability
of around 90%.
[0624] US Patent Publication No. 20110023145 comprises editing of
any chromosomal sequences that encode proteins associated with ASD
which may be applied to the CRISPR Cas system of the present
invention. The proteins associated with ASD are typically selected
based on an experimental association of the protein associated with
ASD to an incidence or indication of an ASD. For example, the
production rate or circulating concentration of a protein
associated with ASD may be elevated or depressed in a population
having an ASD relative to a population lacking the ASD. Differences
in protein levels may be assessed using proteomic techniques
including but not limited to Western blot, immunohistochemical
staining, enzyme linked immunosorbent assay (ELISA), and mass
spectrometry. Alternatively, the proteins associated with ASD may
be identified by obtaining gene expression profiles of the genes
encoding the proteins using genomic techniques including but not
limited to DNA microarray analysis, serial analysis of gene
expression (SAGE), and quantitative real-time polymerase chain
reaction (Q-PCR).
[0625] Non limiting examples of disease states or disorders that
may be associated with proteins associated with ASD include autism,
Asperger syndrome (AS), pervasive developmental disorder--not
otherwise specified (PDD-NOS), Rett's syndrome, tuberous sclerosis,
phenylketonuria, Smith-Lemli-Opitz syndrome and fragile X syndrome.
By way of non-limiting example, proteins associated with ASD
include but are not limited to the following proteins: ATP10C
aminophospholipid-MET MET receptor transporting ATPase tyrosine
kinase (ATP10C) BZRAP1 MGLUR5 (GRM5) Metabotropic glutamate
receptor 5 (MGLUR5) CDH10 Cadherin-10 MGLUR6 (GRM6) Metabotropic
glutamate receptor 6 (MGLUR6) CDH9 Cadherin-9 NLGN1 Neuroligin-1
CNTN4 Contactin-4 NLGN2 Neuroligin-2 CNTNAP2 Contactin-associated
SEMA5A Neuroligin-3 protein-like 2 (CNTNAP2) DHCR7
7-dehydrocholesterol NLGN4X Neuroligin-4 X-reductase (DHCR7) linked
DOC2A Double C2-like domain-NLGN4Y Neuroligin-4 Y-containing
protein alpha linked DPP6 Dipeptidyl NLGN5 Neuroligin-5
aminopeptidase-like protein 6 EN2 engrailed 2 (EN2) NRCAM Neuronal
cell adhesion molecule (NRCAM) MDGA2 fragile X mental retardation
NRXN1 Neurexin-1 1 (MDGA2) FMR2 (AFF2) AF4/FMR2 family member 2
OR4M2 Olfactory receptor (AFF2) 4M2 FOXP2 Forkhead box protein P2
OR4N4 Olfactory receptor (FOXP2) 4N4 FXR1 Fragile X mental OXTR
oxytocin receptor retardation, autosomal (OXTR) homolog 1 (FXR1)
FXR2 Fragile X mental PAH phenylalanine retardation, autosomal
hydroxylase (PAH) homolog 2 (FXR2) GABRA1 Gamma-aminobutyric acid
PTEN Phosphatase and receptor subunit alpha-1 tensin homologue
(GABRA1) (PTEN) GABRA5 GABAA (.gamma.-aminobutyric PTPRZ1
Receptor-type acid) receptor alpha 5 tyrosine-protein subunit
(GABRA5) phosphatase zeta (PTPRZ1) GABRB1 Gamma-aminobutyric acid
RELN Reelin receptor subunit beta-1 (GABRB1) GABRB3 GABAA
(.gamma.-aminobutyric RPL10 60S ribosomal acid) receptor .beta.3
subunit protein L10 (GABRB3) GABRG1 Gamma-aminobutyric acid SEMA5A
Semaphorin-5A receptor subunit gamma-1 (SEMA5A) (GABRG1) HIRIP3
HIRA-interacting protein 3 SEZ6L2 seizure related 6 homolog
(mouse)-like 2 HOXA1 Homeobox protein Hox-A1 SHANK3 SH3 and
multiple (HOXA1) ankyrin repeat domains 3 (SHANK3) IL6
Interleukin-6 SHBZRAP1 SH3 and multiple ankyrin repeat domains 3
(SHBZRAP1) LAMB1 Laminin subunit beta-1 SLC6A4 Serotonin (LAMB1)
transporter (SERT) MAPK3 Mitogen-activated protein TAS2R1 Taste
receptor kinase 3 type 2 member 1 TAS2R1 MAZ Myc-associated zinc
finger TSC1 Tuberous sclerosis protein protein 1 MDGA2 MAM domain
containing TSC2 Tuberous sclerosis glycosylphosphatidylinositol
protein 2 anchor 2 (MDGA2) MECP2 Methyl CpG binding UBE3A Ubiquitin
protein protein 2 (MECP2) ligase E3A (UBE3A) MECP2 methyl CpG
binding WNT2 Wingless-type protein 2 (MECP2) MMTV integration site
family, member 2 (WNT2)
[0626] The identity of the protein associated with ASD whose
chromosomal sequence is edited can and will vary. In preferred
embodiments, the proteins associated with ASD whose chromosomal
sequence is edited may be the benzodiazapine receptor (peripheral)
associated protein 1 (BZRAP1) encoded by the BZRAP1 gene, the
AF4/FMR2 family member 2 protein (AFF2) encoded by the AFF2 gene
(also termed MFR2), the fragile X mental retardation autosomal
homolog 1 protein (FXR1) encoded by the FXR1 gene, the fragile X
mental retardation autosomal homolog 2 protein (FXR2) encoded by
the FXR2 gene, the MAM domain containing
glycosylphosphatidylinositol anchor 2 protein (MDGA2) encoded by
the MDGA2 gene, the methyl CpG binding protein 2 (MECP2) encoded by
the MECP2 gene, the metabotropic glutamate receptor 5 (MGLUR5)
encoded by the MGLUR5-1 gene (also termed GRM5), the neurexin 1
protein encoded by the NRXN1 gene, or the semaphorin-5A protein
(SEMA5A) encoded by the SEMA5A gene. In an exemplary embodiment,
the genetically modified animal is a rat, and the edited
chromosomal sequence encoding the protein associated with ASD is as
listed below: BZRAP1 benzodiazapine receptor XM_002727789,
(peripheral) associated XM_213427, protein 1 (BZRAP1) XM_002724533,
XM_001081125 AFF2 (FMR2) AF4/FMR2 family member 2 XM_219832, (AFF2)
XM_001054673 FXR1 Fragile X mental NM_001012179 retardation,
autosomal homolog 1 (FXR1) FXR2 Fragile X mental NM_001100647
retardation, autosomal homolog 2 (FXR2) MDGA2 MAM domain containing
NM_199269 glycosylphosphatidylinositol anchor 2 (MDGA2) MECP2
Methyl CpG binding NM_022673 protein 2 (MECP2) MGLUR5 Metabotropic
glutamate NM_017012 (GRM5) receptor 5 (MGLUR5) NRXN1 Neurexin-1
NM_021767 SEMA5A Semaphorin-5A (SEMA5A) NM 001107659
[0627] Exemplary animals or cells may comprise one, two, three,
four, five, six, seven, eight, or nine or more inactivated
chromosomal sequences encoding a protein associated with ASD, and
zero, one, two, three, four, five, six, seven, eight, nine or more
chromosomally integrated sequences encoding proteins associated
with ASD. The edited or integrated chromosomal sequence may be
modified to encode an altered protein associated with ASD.
Non-limiting examples of mutations in proteins associated with ASD
include the L18Q mutation in neurexin 1 where the leucine at
position 18 is replaced with a glutamine, the R451C mutation in
neuroligin 3 where the arginine at position 451 is replaced with a
cysteine, the R87W mutation in neuroligin 4 where the arginine at
position 87 is replaced with a tryptophan, and the I425V mutation
in serotonin transporter where the isoleucine at position 425 is
replaced with a valine. A number of other mutations and chromosomal
rearrangements in ASD-related chromosomal sequences have been
associated with ASD and are known in the art. See, for example,
Freitag et al. (2010) Eur. Child. Adolesc. Psychiatry 19:169-178,
and Bucan et al. (2009) PLoS Genetics 5: e1000536, the disclosure
of which is incorporated by reference herein in its entirety.
[0628] Examples of proteins associated with Parkinson's disease
include but are not limited to .alpha.-synuclein, DJ-1, LRRK2,
PINK1, Parkin, UCHL1, Synphilin-1, and NURR1.
[0629] Examples of addiction-related proteins may include ABAT for
example.
[0630] Examples of inflammation-related proteins may include the
monocyte chemoattractant protein-1 (MCP1) encoded by the Ccr2 gene,
the C-C chemokine receptor type 5 (CCR5) encoded by the Ccr5 gene,
the IgG receptor IIB (FCGR2b, also termed CD32) encoded by the
Fcgr2b gene, or the Fc epsilon R1g (FCER1g) protein encoded by the
Fcer1g gene, for example.
[0631] Examples of cardiovascular diseases associated proteins may
include IL1B (interleukin 1, beta), XDH (xanthine dehydrogenase),
TP53 (tumor protein p53), PTGIS (prostaglandin 12 (prostacyclin)
synthase), MB (myoglobin), IL4 (interleukin 4), ANGPT1
(angiopoietin 1), ABCG8 (ATP-binding cassette, sub-family G
(WHITE), member 8), or CTSK (cathepsin K), for example.
[0632] For example, US Patent Publication No. 20110023153,
describes use of zinc finger nucleases to genetically modify cells,
animals and proteins associated with Alzheimer's Disease. Once
modified cells and animals may be further tested using known
methods to study the effects of the targeted mutations on the
development and/or progression of AD using measures commonly used
in the study of AD--such as, without limitation, learning and
memory, anxiety, depression, addiction, and sensory motor functions
as well as assays that measure behavioral, functional,
pathological, metaboloic and biochemical function.
[0633] The present disclosure comprises editing of any chromosomal
sequences that encode proteins associated with AD. The AD-related
proteins are typically selected based on an experimental
association of the AD-related protein to an AD disorder. For
example, the production rate or circulating concentration of an
AD-related protein may be elevated or depressed in a population
having an AD disorder relative to a population lacking the AD
disorder. Differences in protein levels may be assessed using
proteomic techniques including but not limited to Western blot,
immunohistochemical staining, enzyme linked immunosorbent assay
(ELISA), and mass spectrometry. Alternatively, the AD-related
proteins may be identified by obtaining gene expression profiles of
the genes encoding the proteins using genomic techniques including
but not limited to DNA microarray analysis, serial analysis of gene
expression (SAGE), and quantitative real-time polymerase chain
reaction (Q-PCR).
[0634] Examples of Alzheimer's disease associated proteins may
include the very low density lipoprotein receptor protein (VLDLR)
encoded by the VLDLR gene, the ubiquitin-like modifier activating
enzyme 1 (UBA1) encoded by the UBA1 gene, or the NEDD8-activating
enzyme E1 catalytic subunit protein (UBE1C) encoded by the UBA3
gene, for example.
[0635] By way of non-limiting example, proteins associated with AD
include but are not limited to the proteins listed as follows:
Chromosomal Sequence Encoded Protein ALAS2 Delta-aminolevulinate
synthase 2 (ALAS2) ABCA1 ATP-binding cassette transporter (ABCA1)
ACE Angiotensin 1-converting enzyme (ACE) APOE Apolipoprotein E
precursor (APOE) APP amyloid precursor protein (APP) AQP1 aquaporin
1 protein (AQP1) BIN1 Myc box-dependent-interacting protein 1 or
bridging integrator 1 protein (BIN1) BDNF brain-derived
neurotrophic factor (BDNF) BTNL8 Butyrophilin-like protein 8
(BTNL8) C10RF49 chromosome 1 open reading frame 49 CDH4 Cadherin-4
CHRNB2 Neuronal acetylcholine receptor subunit beta-2 CKLFSF2
CKLF-like MARVEL transmembrane domain-containing protein 2
(CKLFSF2) CLEC4E C-type lectin domain family 4, member e (CLEC4E)
CLU clusterin protein (also known as apoplipoprotein J) CR1
Erythrocyte complement receptor 1 (CR1, also known as CD35, C3b/C4b
receptor and immune adherence receptor) CR1L Erythrocyte complement
receptor 1 (CR1L) CSF3R granulocyte colony-stimulating factor 3
receptor (CSF3R) CST3 Cystatin C or cystatin 3 CYP2C Cytochrome
P450 2C DAPK1 Death-associated protein kinase 1 (DAPK1) ESR1
Estrogen receptor 1 FCAR Fc fragment of IgA receptor (FCAR, also
known as CD89) FCGR3B Fc fragment of IgG, low affinity IIIb,
receptor (FCGR3B or CD16b) FFA2 Free fatty acid receptor 2 (FFA2)
FGA Fibrinogen (Factor I) GAB2 GRB2-associated-binding protein 2
(GAB2) GAB2 GRB2-associated-binding protein 2 (GAB2) GALP
Galanin-like peptide GAPDHS Glyceraldehyde-3-phosphate
dehydrogenase, spermatogenic (GAPDHS) GMPB GMBP HP Haptoglobin (HP)
HTR7 5-hydroxytryptamine (serotonin) receptor 7 (adenylate
cyclase-coupled) IDE Insulin degrading enzyme IF127 IF127 IFI6
Interferon, alpha-inducible protein 6 (IFI6) IFIT2
Interferon-induced protein with tetratricopeptide repeats 2 (IFIT2)
IL1RN interleukin-1 receptor antagonist (IL-1RA) IL8RA Interleukin
8 receptor, alpha (IL8RA or CD181) IL8RB Interleukin 8 receptor,
beta (IL8RB) JAG1 Jagged 1 (JAG1) KCNJ15 Potassium
inwardly-rectifying channel, subfamily J, member 15 (KCNJ15) LRP6
Low-density lipoprotein receptor-related protein 6 (LRP6) MAPT
microtubule-associated protein tau (MAPT) MARK4 MAP/microtubule
affinity-regulating kinase 4 (MARK4) MPHOSPH1 M-phase
phosphoprotein 1 MTHFR 5,10-methyl enetetrahydrofolate reductase
MX2 Interferon-induced GTP-binding protein Mx2 NBN Nibrin, also
known as NBN NCSTN Nicastrin NIACR2 Niacin receptor 2 (NIACR2, also
known as GPR109B) NMNAT3 nicotinamide nucleotide
adenylyltransferase 3 NTM Neurotrimin (or HNT) ORM1 Orosmucoid 1
(ORM1) or Alpha-1-acid glycoprotein 1 P2RY13 P2Y purinoceptor 13
(P2RY13) PBEF1 Nicotinamide phosphoribosyltransferase (NAmPRTase or
Nampt) also known as pre-B-cell colony-enhancing factor 1 (PBEF1)
or visfatin PCK1 Phosphoenolpyruvate carboxykinase PICALM
phosphatidylinositol binding clathrin assembly protein (PICALM)
PLAU Urokinase-type plasminogen activator (PLAU) PLXNC1 Plexin C1
(PLXNC1) PRNP Prion protein PSEN1 presenilin 1 protein (PSEN1)
PSEN2 presenilin 2 protein (PSEN2) PTPRA protein tyrosine
phosphatase receptor type A protein (PTPRA) RALGPS2 Ra1 GEF with PH
domain and SH3 binding motif 2 (RALGPS2) RGSL2 regulator of
G-protein signaling like 2 (RGSL2) SELENBP1 Selenium binding
protein 1 (SELNBP1) SLC25A37 Mitoferrin-1 SORL1 sortilin-related
receptor L(DLR class) A repeats-containing protein (SORL1) TF
Transferrin TFAM Mitochondrial transcription factor A TNF Tumor
necrosis factor TNFRSF10C Tumor necrosis factor receptor
superfamily member 10C (TNFRSF10C) TNFSF10 Tumor necrosis factor
receptor superfamily, (TRAIL) member 10a (TNFSF10) UBA1
ubiquitin-like modifier activating enzyme 1 (UBA1) UBA3
NEDD8-activating enzyme E1 catalytic subunit protein (UBE1C) UBB
ubiquitin B protein (UBB) UBQLN1 Ubiquilin-1 UCHL1 ubiquitin
carboxyl-terminal esterase L1 protein (UCHL1) UCHL3 ubiquitin
carboxyl-terminal hydrolase isozyme L3 protein (UCHL3) VLDLR very
low density lipoprotein receptor protein (VLDLR)
[0636] In exemplary embodiments, the proteins associated with AD
whose chromosomal sequence is edited may be the very low density
lipoprotein receptor protein (VLDLR) encoded by the VLDLR gene, the
ubiquitin-like modifier activating enzyme 1 (UBA1) encoded by the
UBA1 gene, the NEDD8-activating enzyme E1 catalytic subunit protein
(UBE1C) encoded by the UBA3 gene, the aquaporin 1 protein (AQP1)
encoded by the AQP1 gene, the ubiquitin carboxyl-terminal esterase
L1 protein (UCHL1) encoded by the UCHL1 gene, the ubiquitin
carboxyl-terminal hydrolase isozyme L3 protein (UCHL3) encoded by
the UCHL3 gene, the ubiquitin B protein (UBB) encoded by the UBB
gene, the microtubule-associated protein tau (MAPT) encoded by the
MAPT gene, the protein tyrosine phosphatase receptor type A protein
(PTPRA) encoded by the PTPRA gene, the phosphatidylinositol binding
clathrin assembly protein (PICALM) encoded by the PICALM gene, the
clusterin protein (also known as apoplipoprotein J) encoded by the
CLU gene, the presenilin 1 protein encoded by the PSEN1 gene, the
presenilin 2 protein encoded by the PSEN2 gene, the
sortilin-related receptor L(DLR class) A repeats-containing protein
(SORL1) protein encoded by the SORL1 gene, the amyloid precursor
protein (APP) encoded by the APP gene, the Apolipoprotein E
precursor (APOE) encoded by the APOE gene, or the brain-derived
neurotrophic factor (BDNF) encoded by the BDNF gene. In an
exemplary embodiment, the genetically modified animal is a rat, and
the edited chromosomal sequence encoding the protein associated
with AD is as as follows: APP amyloid precursor protein (APP)
NM_019288 AQP1 aquaporin 1 protein (AQP1) NM_012778 BDNF
Brain-derived neurotrophic factor NM_012513 CLU clusterin protein
(also known as NM_053021 apoplipoprotein J) MAPT
microtubule-associated protein NM_017212 tau (MAPT) PICALM
phosphatidylinositol binding NM_053554 clathrin assembly protein
(PICALM) PSEN1 presenilin 1 protein (PSEN1) NM_019163 PSEN2
presenilin 2 protein (PSEN2) NM_031087 PTPRA protein tyrosine
phosphatase NM_012763 receptor type A protein (PTPRA) SORL1
sortilin-related receptor L(DLR NM_053519, class) A
repeats-containing XM_001065506, protein (SORL1) XM_217115 UBA1
ubiquitin-like modifier activating NM_001014080 enzyme 1 (UBA1)
UBA3 NEDD8-activating enzyme E1 NM_057205 catalytic subunit protein
(UBE1C) UBB ubiquitin B protein (UBB) NM_138895 UCHL1 ubiquitin
carboxyl-terminal NM_017237 esterase L1 protein (UCHL1) UCHL3
ubiquitin carboxyl-terminal NM_001110165 hydrolase isozyme L3
protein (UCHL3) VLDLR very low density lipoprotein NM_013155
receptor protein (VLDLR)
[0637] The animal or cell may comprise 1, 2, 3, 4, 5, 6, 7, 8, 9,
10, 11, 12, 13, 14, 15 or more disrupted chromosomal sequences
encoding a protein associated with AD and zero, 1, 2, 3, 4, 5, 6,
7, 8, 9, 10, 11, 12, 13, 14, 15 or more chromosomally integrated
sequences encoding a protein associated with AD.
[0638] The edited or integrated chromosomal sequence may be
modified to encode an altered protein associated with AD. A number
of mutations in AD-related chromosomal sequences have been
associated with AD. For instance, the V7171 (i.e. valine at
position 717 is changed to isoleucine) missense mutation in APP
causes familial AD. Multiple mutations in the presenilin-1 protein,
such as H163R (i.e. histidine at position 163 is changed to
arginine), A246E (i.e. alanine at position 246 is changed to
glutamate), L286V (i.e. leucine at position 286 is changed to
valine) and C410Y (i.e. cysteine at position 410 is changed to
tyrosine) cause familial Alzheimer's type 3. Mutations in the
presenilin-2 protein, such as N141 I (i.e. asparagine at position
141 is changed to isoleucine), M239V (i.e. methionine at position
239 is changed to valine), and D439A (i.e. aspartate at position
439 is changed to alanine) cause familial Alzheimer's type 4. Other
associations of genetic variants in AD-associated genes and disease
are known in the art. See, for example, Waring et al. (2008) Arch.
Neurol. 65:329-334, the disclosure of which is incorporated by
reference herein in its entirety.
[0639] Examples of proteins associated Autism Spectrum Disorder may
include the benzodiazapine receptor (peripheral) associated protein
1 (BZRAP1) encoded by the BZRAP1 gene, the AF4/FMR2 family member 2
protein (AFF2) encoded by the AFF2 gene (also termed MFR2), the
fragile X mental retardation autosomal homolog 1 protein (FXR1)
encoded by the FXR1 gene, or the fragile X mental retardation
autosomal homolog 2 protein (FXR2) encoded by the FXR2 gene, for
example.
[0640] Examples of proteins associated Macular Degeneration may
include the ATP-binding cassette, sub-family A (ABC1) member 4
protein (ABCA4) encoded by the ABCR gene, the apolipoprotein E
protein (APOE) encoded by the APOE gene, or the chemokine (C-C
motif) Ligand 2 protein (CCL2) encoded by the CCL2 gene, for
example.
[0641] Examples of proteins associated Schizophrenia may include
NRG1, ErbB4, CPLX1, TPH1, TPH2, NRXN1, GSK3A, BDNF, DISC1, GSK3B,
and combinations thereof.
[0642] Examples of proteins involved in tumor suppression may
include ATM (ataxia telangiectasia mutated), ATR (ataxia
telangiectasia and Rad3 related), EGFR (epidermal growth factor
receptor), ERBB2 (v-erb-b2 erythroblastic leukemia viral oncogene
homolog 2), ERBB3 (v-erb-b2 erythroblastic leukemia viral oncogene
homolog 3), ERBB4 (v-erb-b2 erythroblastic leukemia viral oncogene
homolog 4), Notch 1. Notch2, Notch 3, or Notch 4, for example.
[0643] Examples of proteins associated with a secretase disorder
may include PSENEN (presenilin enhancer 2 homolog (C. elegans)),
CTSB (cathepsin B), PSEN1 (presenilin 1), APP (amyloid beta (A4)
precursor protein), APH1B (anterior pharynx defective 1 homolog B
(C. elegans)), PSEN2 (presenilin 2 (Alzheimer disease 4)), or BACE1
(beta-site APP-cleaving enzyme 1), for example.
[0644] For example, US Patent Publication No. 20110023146,
describes use of zinc finger nucleases to genetically modify cells,
animals and proteins associated with secretase-associated
disorders. Secretases are essential for processing pre-proteins
into their biologically active forms. Defects in various components
of the secretase pathways contribute to many disorders,
particularly those with hallmark amyloidogenesis or amyloid
plaques, such as Alzheimer's disease (AD).
[0645] A secretase disorder and the proteins associated with these
disorders are a diverse set of proteins that effect susceptibility
for numerous disorders, the presence of the disorder, the severity
of the disorder, or any combination thereof. The present disclosure
comprises editing of any chromosomal sequences that encode proteins
associated with a secretase disorder. The proteins associated with
a secretase disorder are typically selected based on an
experimental association of the secretase-related proteins with the
development of a secretase disorder. For example, the production
rate or circulating concentration of a protein associated with a
secretase disorder may be elevated or depressed in a population
with a secretase disorder relative to a population without a
secretase disorder. Differences in protein levels may be assessed
using proteomic techniques including but not limited to Western
blot, immunohistochemical staining, enzyme linked immunosorbent
assay (ELISA), and mass spectrometry. Alternatively, the protein
associated with a secretase disorder may be identified by obtaining
gene expression profiles of the genes encoding the proteins using
genomic techniques including but not limited to DNA microarray
analysis, serial analysis of gene expression (SAGE), and
quantitative real-time polymerase chain reaction (Q-PCR).
[0646] By way of non-limiting example, proteins associated with a
secretase disorder include PSENEN (presenilin enhancer 2 homolog
(C. elegans)), CTSB (cathepsin B), PSEN1 (presenilin 1), APP
(amyloid beta (A4) precursor protein), APH1B (anterior pharynx
defective 1 homolog B (C. elegans)), PSEN2 (presenilin 2 (Alzheimer
disease 4)), BACE1 (beta-site APP-cleaving enzyme 1), ITM2B
(integral membrane protein 2B), CTSD (cathepsin D), NOTCH1 (Notch
homolog 1, translocation-associated (Drosophila)), TNF (tumor
necrosis factor (TNF superfamily, member 2)), INS (insulin), DYT10
(dystonia 10), ADAM17 (ADAM metallopeptidase domain 17), APOE
(apolipoprotein E), ACE (angiotensin I converting enzyme
(peptidyl-dipeptidase A) 1), STN (statin), TP53 (tumor protein
p53), IL6 (interleukin 6 (interferon, beta 2)), NGFR (nerve growth
factor receptor (TNFR superfamily, member 16)), IL1B (interleukin
1, beta), ACHE (acetylcholinesterase (Yt blood group)), CTNNB1
(catenin (cadherin-associated protein), beta 1, 88 kDa), IGF1
(insulin-like growth factor 1 (somatomedin C)), IFNG (interferon,
gamma), NRG1 (neuregulin 1), CASP3 (caspase 3, apoptosis-related
cysteine peptidase), MAPK1 (mitogen-activated protein kinase 1),
CDH1 (cadherin 1, type 1, E-cadherin (epithelial)), APBB1 (amyloid
beta (A4) precursor protein-binding, family B, member 1 (Fe65)),
HMGCR (3-hydroxy-3-methylglutaryl-Coenzyme A reductase), CREB1
(cAMP responsive element binding protein 1), PTGS2
(prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase
and cyclooxygenase)), HES1 (hairy and enhancer of split 1,
(Drosophila)), CAT (catalase), TGFB1 (transforming growth factor,
beta 1), ENO2 (enolase 2 (gamma, neuronal)), ERBB4 (v-erb-a
erythroblastic leukemia viral oncogene homolog 4 (avian)), TRAPPC10
(trafficking protein particle complex 10), MAOB (monoamine oxidase
B), NGF (nerve growth factor (beta polypeptide)), MMP12 (matrix
metallopeptidase 12 (macrophage elastase)), JAG1 (jagged 1
(Alagille syndrome)), CD40LG (CD40 ligand), PPARG (peroxisome
proliferator-activated receptor gamma), FGF2 (fibroblast growth
factor 2 (basic)), IL3 (interleukin 3 (colony-stimulating factor,
multiple)), LRP1 (low density lipoprotein receptor-related protein
1), NOTCH4 (Notch homolog 4 (Drosophila)), MAPK8 (mitogen-activated
protein kinase 8), PREP (prolyl endopeptidase), NOTCH3 (Notch
homolog 3 (Drosophila)), PRNP (prion protein), CTSG (cathepsin G),
EGF (epidermal growth factor (beta-urogastrone)), REN (renin), CD44
(CD44 molecule (Indian blood group)), SELP (selectin P (granule
membrane protein 140 kDa, antigen CD62)), GHR (growth hormone
receptor), ADCYAP1 (adenylate cyclase activating polypeptide 1
(pituitary)), INSR (insulin receptor), GFAP (glial fibrillary
acidic protein), MMP3 (matrix metallopeptidase 3 (stromelysin 1,
progelatinase)), MAPK10 (mitogen-activated protein kinase 10), SP1
(Sp1 transcription factor), MYC (v-myc myelocytomatosis viral
oncogene homolog (avian)), CTSE (cathepsin E), PPARA (peroxisome
proliferator-activated receptor alpha), JUN (jun oncogene), TIMP1
(TIMP metallopeptidase inhibitor 1), IL5 (interleukin 5
(colony-stimulating factor, eosinophil)), IL1A (interleukin 1,
alpha), MMP9 (matrix metallopeptidase 9 (gelatinase B, 92 kDa
gelatinase, 92 kDa type IV collagenase)), HTR4 (5-hydroxytryptamine
(serotonin) receptor 4), HSPG2 (heparan sulfate proteoglycan 2),
KRAS (v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog). CYCS
(cytochrome c, somatic), SMG1 (SMG1 homolog, phosphatidylinositol
3-kinase-related kinase (C. elegans)), IL1R1 (interleukin 1
receptor, type I), PROK1 (prokineticin 1), MAPK3 (mitogen-activated
protein kinase 3), NTRK1 (neurotrophic tyrosine kinase, receptor,
type 1), IL13 (interleukin 13), MME (membrane
metallo-endopeptidase), TKT (transketolase), CXCR2 (chemokine
(C-X-C motif) receptor 2), IGF1R (insulin-like growth factor 1
receptor), RARA (retinoic acid receptor, alpha), CREBBP (CREB
binding protein), PTGS1 (prostaglandin-endoperoxide synthase 1
(prostaglandin G/H synthase and cyclooxygenase)), GALT
(galactose-1-phosphate uridylyltransferase), CHRM1 (cholinergic
receptor, muscarinic 1), ATXN1 (ataxin 1), PAWR (PRKC, apoptosis,
WT1, regulator). NOTCH2 (Notch homolog 2 (Drosophila)). M6PR
(mannose-6-phosphate receptor (cation dependent)), CYP46A1
(cytochrome P450, family 46, subfamily A, polypeptide 1), CSNK1 D
(casein kinase 1, delta). MAPK14 (mitogen-activated protein kinase
14), PRG2 (proteoglycan 2, bone marrow (natural killer cell
activator, eosinophil granule major basic protein)), PRKCA (protein
kinase C, alpha), L1 CAM (L1 cell adhesion molecule), CD40 (CD40
molecule, TNF receptor superfamily member 5), NR1I2 (nuclear
receptor subfamily 1, group I, member 2), JAG2 (jagged 2), CTNND1
(catenin (cadherin-associated protein), delta 1), CDH2 (cadherin 2,
type 1. N-cadherin (neuronal)), CMA1 (chymase 1, mast cell), SORT1
(sortilin 1), DLK1 (delta-like 1 homolog (Drosophila)), THEM4
(thioesterase superfamily member 4), JUP (junction plakoglobin),
CD46 (CD46 molecule, complement regulatory protein), CCL11
(chemokine (C-C motif) ligand 11), CAV3 (caveolin 3), RNASE3
(ribonuclease, RNase A family, 3 (eosinophil cationic protein)),
HSPA8 (heat shock 70 kDa protein 8), CASP9 (caspase 9,
apoptosis-related cysteine peptidase), CYP3A4 (cytochrome P450,
family 3, subfamily A, polypeptide 4), CCR3 (chemokine (C-C motif)
receptor 3), TFAP2A (transcription factor AP-2 alpha (activating
enhancer binding protein 2 alpha)), SCP2 (sterol carrier protein
2), CDK4 (cyclin-dependent kinase 4), HIF1A (hypoxia inducible
factor 1, alpha subunit (basic helix-loop-helix transcription
factor)), TCF7L2 (transcription factor 7-like 2 (T-cell specific,
HMG-box)), IL1R2 (interleukin 1 receptor, type II), B3GALTL (beta
1,3-galactosyltransferase-like), MDM2 (Mdm2 p53 binding protein
homolog (mouse)), RELA (v-rel reticuloendotheliosis viral oncogene
homolog A (avian)), CASP7 (caspase 7, apoptosis-related cysteine
peptidase), IDE (insulin-degrading enzyme), FABP4 (fatty acid
binding protein 4, adipocyte), CASK (calcium/calmodulin-dependent
serine protein kinase (MAGUK family)), ADCYAP1R1 (adenylate cyclase
activating polypeptide 1 (pituitary) receptor type I), ATF4
(activating transcription factor 4 (tax-responsive enhancer element
B67)), PDGFA (platelet-derived growth factor alpha polypeptide),
C21 or f33 (chromosome 21 open reading frame 33), SCG5
(secretogranin V (7B2 protein)), RNF123 (ring finger protein 123),
NFKB1 (nuclear factor of kappa light polypeptide gene enhancer in
B-cells 1), ERBB2 (v-erb-b2 erythroblastic leukemia viral oncogene
homolog 2, neuro/glioblastoma derived oncogene homolog (avian)),
CAV1 (caveolin 1, caveolae protein, 22 kDa), MMP7 (matrix
metallopeptidase 7 (matrilysin, uterine)), TGFA (transforming
growth factor, alpha), RXRA (retinoid X receptor, alpha), STX1A
(syntaxin 1A (brain)), PSMC4 (proteasome (prosome, macropain) 26S
subunit, ATPase, 4), P2RY2 (purinergic receptor P2Y, G-protein
coupled, 2), TNFRSF21 (tumor necrosis factor receptor superfamily,
member 21), DLG1 (discs, large homolog 1 (Drosophila)), NUMBL (numb
homolog (Drosophila)-like), SPN (sialophorin), PLSCR1 (phospholipid
scramblase 1), UBQLN2 (ubiquilin 2), UBQLN1 (ubiquilin 1), PCSK7
(proprotein convertase subtilisin/kexin type 7), SPON1 (spondin 1,
extracellular matrix protein), SILV (silver homolog (mouse)), QPCT
(glutaminyl-peptide cyclotransferase), HESS (hairy and enhancer of
split 5 (Drosophila)), GCC1 (GRIP and coiled-coil domain containing
1), and any combination thereof.
[0647] The genetically modified animal or cell may comprise 1, 2,
3, 4, 5, 6, 7, 8, 9, 10 or more disrupted chromosomal sequences
encoding a protein associated with a secretase disorder and zero,
1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more chromosomally integrated
sequences encoding a disrupted protein associated with a secretase
disorder.
[0648] Examples of proteins associated with Amyotrophic Lateral
Sclerosis may include SOD1 (superoxide dismutase 1), ALS2
(amyotrophic lateral sclerosis 2), FUS (fused in sarcoma), TARDBP
(TAR DNA binding protein), VAGFA (vascular endothelial growth
factor A), VAGFB (vascular endothelial growth factor B), and VAGFC
(vascular endothelial growth factor C), and any combination
thereof.
[0649] For example, US Patent Publication No. 20110023144,
describes use of zinc finger nucleases to genetically modify cells,
animals and proteins associated with amyotrophyic lateral sclerosis
(ALS) disease. ALS is characterized by the gradual steady
degeneration of certain nerve cells in the brain cortex, brain
stem, and spinal cord involved in voluntary movement.
[0650] Motor neuron disorders and the proteins associated with
these disorders are a diverse set of proteins that effect
susceptibility for developing a motor neuron disorder, the presence
of the motor neuron disorder, the severity of the motor neuron
disorder or any combination thereof. The present disclosure
comprises editing of any chromosomal sequences that encode proteins
associated with ALS disease, a specific motor neuron disorder. The
proteins associated with ALS are typically selected based on an
experimental association of ALS-related proteins to ALS. For
example, the production rate or circulating concentration of a
protein associated with ALS may be elevated or depressed in a
population with ALS relative to a population without ALS.
Differences in protein levels may be assessed using proteomic
techniques including but not limited to Western blot,
immunohistochemical staining, enzyme linked immunosorbent assay
(ELISA), and mass spectrometry. Alternatively, the proteins
associated with ALS may be identified by obtaining gene expression
profiles of the genes encoding the proteins using genomic
techniques including but not limited to DNA microarray analysis,
serial analysis of gene expression (SAGE), and quantitative
real-time polymerase chain reaction (Q-PCR).
[0651] By way of non-limiting example, proteins associated with ALS
include but are not limited to the following proteins: SOD1
superoxide dismutase 1, ALS3 amyotrophic lateral soluble sclerosis
3 SETX senataxin ALS5 amyotrophic lateral sclerosis 5 FUS fused in
sarcoma ALS7 amyotrophic lateral sclerosis 7 ALS2 amyotrophic
lateral DPP6 Dipeptidyl-peptidase 6 sclerosis 2 NEFH neurofilament,
heavy PTGS1 prostaglandin-polypeptide endoperoxide synthase 1
SLC1A2 solute carrier family 1 TNFRSF100B tumor necrosis factor
(glial high affinity receptor superfamily, glutamate transporter),
member 10b member 2 PRPH peripherin HSP90AA1 heat shock protein 90
kDa alpha (cytosolic), class A member 1 GRIA2 glutamate receptor,
IFNG interferon, gamma ionotropic, AMPA 2 S100B S100 calcium
binding FGF2 fibroblast growth factor 2 protein B AOX1 aldehyde
oxidase 1 CS citrate synthase TARDBP TAR DNA binding protein TXN
thioredoxin RAPH1 Ras association MAP3K5 mitogen-activated protein
(RaIGDS/AF-6) and kinase 5 pleckstrin homology domains 1 NBEAL1
neurobeachin-like 1 GPX1 glutathione peroxidase 1 ICA1L islet cell
autoantigen RAC1 ras-related C3 botulinum 1.69 kDa-like toxin
substrate 1 MAPT microtubule-associated ITPR2 inositol
1,4,5-protein tau triphosphate receptor, type 2 ALS2CR4 amyotrophic
lateral GLS glutaminase sclerosis 2 (juvenile) chromosome region,
candidate 4 ALS2CR8 amyotrophic lateral CNTFR ciliary neurotrophic
factor sclerosis 2 (juvenile) receptor chromosome region, candidate
8 ALS2CR11 amyotrophic lateral FOLH1 folate hydrolase 1 sclerosis 2
(juvenile) chromosome region, candidate 11 FAM117B family with
sequence P4HB prolyl 4-hydroxylase, similarity 117, member B beta
polypeptide CNTF ciliary neurotrophic factor SQSTM1 sequestosome 1
STRADB STE20-related kinase NAIP NLR family, apoptosis adaptor beta
inhibitory protein YWHAQ tyrosine 3-SLC33A1 solute carrier family
33 monooxygenase/tryptoph (acetyl-CoA transporter), an
5-monooxygenase member 1 activation protein, theta polypeptide
TRAK2 trafficking protein, FIG. 4 FIG. 4 homolog, SAC1 kinesin
binding 2 lipid phosphatase domain containing NIF3L1 NIF3 NGG1
interacting INA internexin neuronal factor 3-like 1 intermediate
filament protein, alpha PARD3B par-3 partitioning COXSA cytochrome
c oxidase defective 3 homolog B subunit VIIIA CDK15
cyclin-dependent kinase HECW1 HECT, C2 and WW 15 domain containing
E3 ubiquitin protein ligase 1 NOS1 nitric oxide synthase 1 MET met
proto-oncogene SOD2 superoxide dismutase 2, HSPB1 heat shock 27 kDa
mitochondrial protein 1 NEFL neurofilament, light CTSB cathepsin B
polypeptide ANG angiogenin, HSPA8 heat shock 70 kDa ribonuclease,
RNase A protein 8 family, 5 VAPB VAMP (vesicle-ESR1 estrogen
receptor 1 associated membrane protein)-associated protein B and C
SNCA synuclein, alpha HGF hepatocyte growth factor CAT catalase
ACTB actin, beta NEFM neurofilament, medium TH tyrosine hydroxylase
polypeptide BCL2 B-cell CLLlymphoma 2 FAS Fas (TNF receptor
superfamily, member 6) CASP3 caspase 3, apoptosis-CLU clusterin
related cysteine peptidase SMN1 survival of motor neuron G6PD
glucose-6-phosphate 1, telomeric dehydrogenase BAX BCL2-associated
X HSF1 heat shock transcription protein factor 1 RNF19A ring finger
protein 19A JUN jun oncogene ALS2CR12 amyotrophic lateral HSPA5
heat shock 70 kDa sclerosis 2 (juvenile) protein 5 chromosome
region, candidate 12 MAPK14 mitogen-activated protein IL10
interleukin 10 kinase 14 APEX1 APEX nuclease TXNRD1 thioredoxin
reductase 1 (multifunctional DNA repair enzyme) 1 NOS2 nitric oxide
synthase 2, TIMP1 TIMP metallopeptidase inducible inhibitor 1 CASP9
caspase 9, apoptosis-XIAP X-linked inhibitor of related cysteine
apoptosis peptidase GLG1 golgi glycoprotein 1 EPO erythropoietin
VEGFA vascular endothelial ELN elastin growth factor A GDNF glial
cell derived NFE2L2 nuclear factor (erythroid-neurotrophic factor
derived 2)-like 2 SLC6A3 solute carrier family 6 HSPA4 heat shock
70 kDa (neurotransmitter protein 4 transporter, dopamine), member 3
APOE apolipoprotein E PSMB8 proteasome (prosome, macropain)
subunit, beta type, 8 DCTN1 dynactin 1 TIMP3 TIMP metallopeptidase
inhibitor 3 KIFAP3 kinesin-associated SLC1A1 solute carrier family
1 protein 3 (neuronal/epithelial high affinity glutamate
transporter, system Xag), member 1 SMN2 survival of motor neuron
CCNC cyclin C 2, centromeric MPP4 membrane protein, STUB1 STIP1
homology and U-palmitoylated 4 box containing protein 1 ALS2
amyloid beta (A4) PRDX6 peroxiredoxin 6 precursor protein SYP
synaptophysin CABIN1 calcineurin binding protein 1 CASP1 caspase 1,
apoptosis-GART phosphoribosylglycinami related cysteine de
formyltransferase, peptidase phosphoribosylglycinami de synthetase,
phosphoribosylaminoimi dazole synthetase CDK5 cyclin-dependent
kinase 5 ATXN3 ataxin 3 RTN4 reticulon 4 C1QB complement component
1, q subcomponent, B chain VEGFC nerve growth factor HTT huntingtin
receptor PARK7 Parkinson disease 7 XDH xanthine dehydrogenase GFAP
glial fibrillary acidic MAP2 microtubule-associated protein protein
2 CYCS cytochrome c, somatic FCGR3B Fc fragment of IgG, low
affinity IIIb, CCS copper chaperone for UBL5 ubiquitin-like 5
superoxide dismutase MMP9 matrix metallopeptidase SLC18A3 solute
carrier family 18 9 ((vesicular acetylcholine), member 3 TRPM7
transient receptor HSPB2 heat shock 27 kDa potential cation
channel, protein 2 subfamily M, member 7 AKT1 v-akt murine thymoma
DERL1 Der1-like domain family, viral oncogene homolog 1 member 1
CCL2 chemokine (C-C motif) NGRN neugrin, neurite ligand 2 outgrowth
associated GSR glutathione reductase TPPP3 tubulin
polymerization-promoting protein family member 3 APAF1 apoptotic
peptidase BTBD10 BTB (POZ) domain activating factor 1 containing 10
GLUD1 glutamate CXCR4 chemokine (C-X-C motif) dehydrogenase 1
receptor 4 SLC1A3 solute carrier family 1 FLT1 fms-related tyrosine
(glial high affinity glutamate transporter), member 3 kinase 1 PON1
paraoxonase 1 AR androgen receptor LIF leukemia inhibitory factor
ERBB3 v-erb-b2 erythroblastic leukemia viral oncogene homolog 3
LGALS1 lectin, galactoside-CD44 CD44 molecule binding, soluble, 1
TP53 tumor protein p53 TLR3 toll-like receptor 3 GRIA1 glutamate
receptor, GAPDH glyceraldehyde-3-ionotropic, AMPA 1 phosphate
dehydrogenase GRIK1 glutamate receptor, DES desmin ionotropic,
kainate 1 CHAT choline acetyltransferase FLT4 fms-related tyrosine
kinase 4 CHMP2B chromatin modifying BAG1 BCL2-associated protein 2B
athanogene MT3 metallothionein 3 CHRNA4 cholinergic receptor,
nicotinic, alpha 4 GSS glutathione synthetase BAK1
BCL2-antagonist/killer 1 KDR kinase insert domain GSTP1 glutathione
S-transferase receptor (a type III pi 1 receptor tyrosine kinase)
OGG1 8-oxoguanine DNA IL6 interleukin 6 (interferon, glycosylase
beta 2).
[0652] The animal or cell may comprise 1, 2, 3, 4, 5, 6, 7, 8, 9,
10 or more disrupted chromosomal sequences encoding a protein
associated with ALS and zero, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more
chromosomally integrated sequences encoding the disrupted protein
associated with ALS. Preferred proteins associated with ALS include
SOD1 (superoxide dismutase 1), ALS2 (amyotrophic lateral sclerosis
2), FUS (fused in sarcoma), TARDBP (TAR DNA binding protein), VAGFA
(vascular endothelial growth factor A), VAGFB (vascular endothelial
growth factor B), and VAGFC (vascular endothelial growth factor C),
and any combination thereof.
[0653] Examples of proteins associated with prion diseases may
include SOD1 (superoxide dismutase 1), ALS2 (amyotrophic lateral
sclerosis 2), FUS (fused in sarcoma), TARDBP (TAR DNA binding
protein). VAGFA (vascular endothelial growth factor A), VAGFB
(vascular endothelial growth factor B), and VAGFC (vascular
endothelial growth factor C), and any combination thereof.
[0654] Examples of proteins related to neurodegenerative conditions
in prion disorders may include A2M (Alpha-2-Macroglobulin), AATF
(Apoptosis antagonizing transcription factor), ACPP (Acid
phosphatase prostate), ACTA2 (Actin alpha 2 smooth muscle aorta),
ADAM22 (ADAM metallopeptidase domain), ADORA3 (Adenosine A3
receptor), or ADRA1D (Alpha-1D adrenergic receptor for Alpha-1D
adrenoreceptor), for example.
[0655] Examples of proteins associated with Immunodeficiency may
include A2M [alpha-2-macroglobulin]; AANAT [arylalkylamine
N-acetyltransferase]; ABCA1 [ATP-binding cassette, sub-family A
(ABC1), member 1], ABCA2 [ATP-binding cassette, sub-family A
(ABC1), member 2]; or ABCA3 [ATP-binding cassette, sub-family A
(ABC1), member 3]; for example.
[0656] Examples of proteins associated with Trinucleotide Repeat
Disorders include AR (androgen receptor), FMR1 (fragile X mental
retardation 1), HTT (huntingtin), or DMPK (dystrophia
myotonica-protein kinase), FXN (frataxin), ATXN2 (ataxin 2), for
example.
[0657] Examples of proteins associated with Neurotransmission
Disorders include SST (somatostatin), NOS1 (nitric oxide synthase 1
(neuronal)). ADRA2A (adrenergic, alpha-2A-, receptor), ADRA2C
(adrenergic, alpha-2C-, receptor), TACR1 (tachykinin receptor 1),
or HTR2c (5-hydroxytryptamine (serotonin) receptor 2C), for
example.
[0658] Examples of neurodevelopmental-associated sequences include
A2BP1 [ataxin 2-binding protein 1], AADAT [aminoadipate
aminotransferase], AANAT [arylalkylamine N-acetyltransferase], ABAT
[4-aminobutyrate aminotransferase], ABCA1 [ATP-binding cassette,
sub-family A (ABC1), member 1], or ABCA13 [ATP-binding cassette,
sub-family A (ABC1), member 13], for example.
[0659] Further examples of preferred conditions treatable with the
present system include may be selected from: Aicardi-Goutieres
Syndrome; Alexander Disease; Allan-Herndon-Dudley Syndrome;
POLG-Related Disorders; Alpha-Mannosidosis (Type II and III);
Alstrom Syndrome; Angelman; Syndrome; Ataxia-Telangiectasia;
Neuronal Ceroid-Lipofuscinoses; Beta-Thalassemia; Bilateral Optic
Atrophy and (Infantile) Optic Atrophy Type 1; Retinoblastoma
(bilateral); Canavan Disease; Cerebrooculofacioskeletal Syndrome 1
[COFS1]; Cerebrotendinous Xanthomatosis; Cornelia de Lange
Syndrome; MAPT-Related Disorders; Genetic Prion Diseases; Dravet
Syndrome; Early-Onset Familial Alzheimer Disease; Friedreich Ataxia
[FRDA]; Fryns Syndrome; Fucosidosis; Fukuyama Congenital Muscular
Dystrophy; Galactosialidosis; Gaucher Disease; Organic Acidemias;
Hemophagocytic Lymphohistiocytosis; Hutchinson-Gilford Progeria
Syndrome; Mucolipidosis II; Infantile Free Sialic Acid Storage
Disease; PLA2G6-Associated Neurodegeneration; Jervell and
Lange-Nielsen Syndrome; Junctional Epidermolysis Bullosa;
Huntington Disease; Krabbe Disease (Infantile); Mitochondrial
DNA-Associated Leigh Syndrome and NARP; Lesch-Nyhan Syndrome;
LIS1-Associated Lissencephaly; Lowe Syndrome; Maple Syrup Urine
Disease; MECP2 Duplication Syndrome; ATP7A-Related Copper Transport
Disorders; LAMA2-Related Muscular Dystrophy; Arylsulfatase A
Deficiency; Mucopolysaccharidosis Types I, II or III; Peroxisome
Biogenesis Disorders, Zellweger Syndrome Spectrum;
Neurodegeneration with Brain Iron Accumulation Disorders; Acid
Sphingomyelinase Deficiency; Niemann-Pick Disease Type C; Glycine
Encephalopathy; ARX-Related Disorders; Urea Cycle Disorders;
COL1A1/2-Related Osteogenesis Imperfecta; Mitochondrial DNA
Deletion Syndromes; PLP1-Related Disorders; Perry Syndrome;
Phelan-McDermid Syndrome; Glycogen Storage Disease Type II (Pompe
Disease) (Infantile); MAPT-Related Disorders; MECP2-Related
Disorders; Rhizomelic Chondrodysplasia Punctata Type 1; Roberts
Syndrome; Sandhoff Disease; Schindler Disease-Type 1; Adenosine
Deaminase Deficiency; Smith-Lemli-Opitz Syndrome; Spinal Muscular
Atrophy; Infantile-Onset Spinocerebellar Ataxia; Hexosaminidase A
Deficiency; Thanatophoric Dysplasia Type 1; Collagen Type
VI-Related Disorders; Usher Syndrome Type I; Congenital Muscular
Dystrophy; Wolf-Hirschhorn Syndrome; Lysosomal Acid Lipase
Deficiency; and Xeroderma Pigmentosum.
[0660] As will be apparent, it is envisaged that the present system
can be used to target any polynucleotide sequence of interest. Some
examples of conditions or diseases that might be usefully treated
using the present system are included in the Tables above and
examples of genes currently associated with those conditions are
also provided there. However, the genes exemplified are not
exhaustive.
[0661] For example, "wild type StCas9" refers to wild type Cas9
from S thermophilus, the protein sequence of which is given in the
SwissProt database under accession number G3ECR1. Similarly, S
pyogenes Cas9 is included in SwissProt under accession number
Q99ZW2.
[0662] The ability to use CRISPR-Cas systems to perform efficient
and cost effective gene editing and manipulation will allow the
rapid selection and comparison of single and and multiplexed
genetic manipulations to transform such genomes for improved
production and enhanced traits. In this regard reference is made to
US patents and publications: U.S. Pat. No. 6,603,061
--Agrobacterium-Mediated Plant Transformation Method; U.S. Pat. No.
7,868,149--Plant Genome Sequences and Uses Thereof and US
2009/0100536--Transgenic Plants with Enhanced Agronomic Traits, all
the contents and disclosure of each of which are herein
incorporated by reference in their entirety. In the practice of the
invention, the contents and disclosure of Morrell et al "Crop
genomics:advances and applications" Nat Rev Genet. 2011 Dec. 29;
13(2):85-96 are also herein incorporated by reference in their
entirety.
EXAMPLES
[0663] The following examples are given for the purpose of
illustrating various embodiments of the invention and are not meant
to limit the present invention in any fashion. The present
examples, along with the methods described herein are presently
representative of preferred embodiments, are exemplary, and are not
intended as limitations on the scope of the invention. Changes
therein and other uses which are encompassed within the spirit of
the invention as defined by the scope of the claims will occur to
those skilled in the art.
Example 1: CRISPR Complex Activity in the Nucleus of a Eukaryotic
Cell
[0664] An example type II CRISPR system is the type II CRISPR locus
from Streptococcus pyogenes SF370, which contains a cluster of four
genes Cas9, Cas1, Cas2, and Csn1, as well as two non-coding RNA
elements, tracrRNA and a characteristic array of repetitive
sequences (direct repeats) interspaced by short stretches of
non-repetitive sequences (spacers, about 30 bp each). In this
system, targeted DNA double-strand break (DSB) is generated in four
sequential steps (FIG. 2A). First, two non-coding RNAs, the
pre-crRNA array and tracrRNA, are transcribed from the CRISPR
locus. Second, tracrRNA hybridizes to the direct repeats of
pre-crRNA, which is then processed into mature crRNAs containing
individual spacer sequences. Third, the mature crRNA:tracrRNA
complex directs Cas9 to the DNA target consisting of the
protospacer and the corresponding PAM via heteroduplex formation
between the spacer region of the crRNA and the protospacer DNA.
Finally, Cas9 mediates cleavage of target DNA upstream of PAM to
create a DSB within the protospacer (FIG. 2A). This example
describes an example process for adapting this RNA-programmable
nuclease system to direct CRISPR complex activity in the nuclei of
eukaryotic cells.
[0665] Cell Culture and Transfection
[0666] Human embryonic kidney (HEK) cell line HEK 293FT (Life
Technologies) was maintained in Dulbecco's modified Eagle's Medium
(DMEM) supplemented with 10% fetal bovine serum (HyClone), 2 mM
GlutaMAX (Life Technologies), 100 U/mL penicillin, and 100 g/mL
streptomycin at 37.degree. C. with 5% CO.sub.2 incubation. Mouse
neuro2A (N2A) cell line (ATCC) was maintained with DMEM
supplemented with 5% fetal bovine serum (HyClone), 2 mM GlutaMAX
(Life Technologies), 100 U/mL penicillin, and 100 .mu.g/mL
streptomycin at 37.degree. C. with 5% CO.sub.2.
[0667] HEK 293FT or N2A cells were seeded into 24-well plates
(Corning) one day prior to transfection at a density of 200,000
cells per well. Cells were transfected using Lipofectamine 2000
(Life Technologies) following the manufacturer's recommended
protocol. For each well of a 24-well plate a total of 800 ng of
plasmids were used.
[0668] Surveyor Assay and Sequencing Analysis for Genome
Modification
[0669] HEK 293FT or N2A cells were transfected with plasmid DNA as
described above. After transfection, the cells were incubated at
37.degree. C. for 72 hours before genomic DNA extraction. Genomic
DNA was extracted using the QuickExtract DNA extraction kit
(Epicentre) following the manufacturer's protocol. Briefly, cells
were resuspended in QuickExtract solution and incubated at
65.degree. C. for 15 minutes and 98.degree. C. for 10 minutes.
Extracted genomic DNA was immediately processed or stored at
-20.degree. C.
[0670] The genomic region surrounding a CRISPR target site for each
gene was PCR amplified, and products were purified using QiaQuick
Spin Column (Qiagen) following manufacturer's protocol. A total of
400 ng of the purified PCR products were mixed with 2 .mu.l
10.times. Taq polymerase PCR buffer (Enzymatics) and ultrapure
water to a final volume of 20 .mu.l, and subjected to a
re-annealing process to enable heteroduplex formation: 95.degree.
C. for 10 min, 95.degree. C. to 85.degree. C. ramping at -2.degree.
C./s, 85.degree. C. to 25.degree. C. at -0.25.degree. C./s, and
25.degree. C. hold for 1 minute. After re-annealing, products were
treated with Surveyor nuclease and Surveyor enhancer S
(Transgenomics) following the manufacturer's recommended protocol,
and analyzed on 4-20% Novex TBE poly-acrylamide gels (Life
Technologies). Gels were stained with SYBR Gold DNA stain (Life
Technologies) for 30 minutes and imaged with a Gel Doc gel imaging
system (Bio-rad). Quantification was based on relative band
intensities, as a measure of the fraction of cleaved DNA. FIG. 7
provides a schematic illustration of this Surveyor assay.
[0671] Restriction fragment length polymorphism assay for detection
of homologous recombination.
[0672] HEK 293FT and N2A cells were transfected with plasmid DNA,
and incubated at 37.degree. C. for 72 hours before genomic DNA
extraction as described above. The target genomic region was PCR
amplified using primers outside the homology arms of the homologous
recombination (HR) template. PCR products were separated on a 1%
agarose gel and extracted with MinElute GelExtraction Kit (Qiagen).
Purified products were digested with HindIII (Fermentas) and
analyzed on a 6% Novex TBE poly-acrylamide gel (Life
Technologies).
[0673] RNA Secondary Structure Prediction and Analysis
[0674] RNA secondary structure prediction was performed using the
online webserver RNAfold developed at Institute for Theoretical
Chemistry at the University of Vienna, using the centroid structure
prediction algorithm (see e.g. A. R. Gruber et al., 2008, Cell
106(1): 23-24; and PA Carr and GM Church, 2009, Nature
Biotechnology 27(12): 1151-62).
[0675] RNA Purification
[0676] HEK 293FT cells were maintained and transfected as stated
above. Cells were harvested by trypsinization followed by washing
in phosphate buffered saline (PBS). Total cell RNA was extracted
with TRI reagent (Sigma) following manufacturer's protocol.
Extracted total RNA was quantified using Naonodrop (Thermo
Scientific) and normalized to same concentration.
[0677] Northern Blot Analysis of crRNA and tracrRNA Expression in
Mammalian Cells
[0678] RNAs were mixed with equal volumes of 2.times. loading
buffer (Ambion), heated to 95.degree. C. for 5 min, chilled on ice
for 1 min, and then loaded onto 8% denaturing polyacrylamide gels
(SequaGel, National Diagnostics) after pre-running the gel for at
least 30 minutes. The samples were electrophoresed for 1.5 hours at
40 W limit. Afterwards, the RNA was transferred to Hybond N+
membrane (GE Healthcare) at 300 mA in a semi-dry transfer apparatus
(Bio-rad) at room temperature for 1.5 hours. The RNA was
crosslinked to the membrane using autocrosslink button on
Stratagene UV Crosslinker the Stratalinker (Stratagene). The
membrane was pre-hybridized in ULTRAhyb-Oligo Hybridization Buffer
(Ambion) for 30 min with rotation at 42.degree. C., and probes were
then added and hybridized overnight. Probes were ordered from IDT
and labeled with [gamma-.sup.32P] ATP (Perkin Elmer) with T4
polynucleotide kinase (New England Biolabs). The membrane was
washed once with pre-warmed (42.degree. C.) 2.times.SSC, 0.5% SDS
for 1 min followed by two 30 minute washes at 42.degree. C. The
membrane was exposed to a phosphor screen for one hour or overnight
at room temperature and then scanned with a phosphorimager
(Typhoon).
[0679] Bacterial CRISPR System Construction and Evaluation
[0680] CRISPR locus elements, including tracrRNA, Cas9, and leader
were PCR amplified from Streptococcus pyogenes SF370 genomic DNA
with flanking homology arms for Gibson Assembly. Two BsaI type IIS
sites were introduced in between two direct repeats to facilitate
easy insertion of spacers (FIG. 8). PCR products were cloned into
EcoRV-digested pACYC184 downstream of the tet promoter using Gibson
Assembly Master Mix (NEB). Other endogenous CRISPR system elements
were omitted, with the exception of the last 50 bp of Csn2. Oligos
(Integrated DNA Technology) encoding spacers with complimentary
overhangs were cloned into the BsaI-digested vector pDC000 (NEB)
and then ligated with T7 ligase (Enzymatics) to generate pCRISPR
plasmids. Challenge plasmids containing spacers with PAM
[0681] expression in mammalian cells (expression constructs
illustrated in FIG. 6A, with functionality as determined by results
of the Surveyor assay shown in FIG. 6B). Transcription start sites
are marked as +1, and transcription terminator and the sequence
probed by northern blot are also indicated. Expression of processed
tracrRNA was also confirmed by Northern blot. FIG. 6C shows results
of a Northern blot analysis of total RNA extracted from 293FT cells
transfected with U6 expression constructs carrying long or short
tracrRNA, as well as SpCas9 and DR-EMX1(1)-DR. Left and right
panels are from 293FT cells transfected without or with SpRNase
III, respectively. U6 indicate loading control blotted with a probe
targeting human U6 snRNA. Transfection of the short tracrRNA
expression construct led to abundant levels of the processed form
of tracrRNA (.about.75 bp). Very low amounts of long tracrRNA are
detected on the Northern blot.
[0682] To promote precise transcriptional initiation, the RNA
polymerase III-based U6 promoter was selected to drive the
expression of tracrRNA (FIG. 2C). Similarly, a U6 promoter-based
construct was developed to express a pre-crRNA array consisting of
a single spacer flanked by two direct repeats (DRs, also
encompassed by the term "tracr-mate sequences"; FIG. 2C). The
initial spacer was designed to target a 33-base-pair (bp) target
site (30-bp protospacer plus a 3-bp CRISPR motif (PAM) sequence
satisfying the NGG recognition motif of Cas9) in the human EMX1
locus (FIG. 2C), a key gene in the development of the cerebral
cortex.
[0683] To test whether heterologous expression of the CRISPR system
(SpCas9, SpRNase III, tracrRNA, and pre-crRNA) in mammalian cells
can achieve targeted cleavage of mammalian chromosomes, HEK 293FT
cells were transfected with combinations of CRISPR components.
Since DSBs in mammalian nuclei are partially repaired by the
non-homologous end joining (NHEJ) pathway, which leads to the
formation of indels, the Surveyor assay was used to detect
potential cleavage activity at the target EMX1 locus (FIG. 7) (see
e.g. Guschin et al., 2010, Methods Mol Biol 649: 247).
Co-transfection of all four CRISPR components was able to induce up
to 5.0% cleavage in the protospacer (see FIG. 2D). Co-transfection
of all CRISPR components minus SpRNase III also induced up to 4.7%
indel in the protospacer, suggesting that there may be endogenous
mammalian RNases that are capable of assisting with crRNA
maturation, such as for example the related Dicer and Drosha
enzymes. Removing any of the remaining three components abolished
the genome cleavage activity of the CRISPR system (FIG. 2D). Sanger
sequencing of amplicons containing the target locus verified the
cleavage activity: in 43 sequenced clones, 5 mutated alleles
(11.6%) were found. Similar experiments using a variety of guide
sequences produced indel percentages as high as 29% (see FIGS. 3-6,
10, and 11). These results define a three-component system for
efficient CRISPR-mediated genome modification in mammalian cells.
To optimize the cleavage efficiency, Applicants also tested whether
different isoforms of tracrRNA affected the cleavage efficiency and
found that, in this example system, only the short (89-bp)
transcript form was able to mediate cleavage of the human FAX1
genomic locus (FIG. 6B).
[0684] FIG. 12 provides an additional Northern blot analysis of
crRNA processing in mammalian cells. FIG. 12A illustrates a
schematic showing the expression vector for a single spacer flanked
by two direct repeats (DR-EMX1(1)-DR). The 30 bp spacer targeting
the human EMX1 locus protospacer 1 (see FIG. 6) and the direct
repeat sequences are shown in the sequence beneath FIG. 12A. The
line indicates the region whose reverse-complement sequence was
used to generate Northern blot probes for EMX1(1) crRNA detection.
FIG. 12B shows a Northern blot analysis of total RNA extracted from
293FT cells transfected with U6 expression constructs carrying
DR-EMX1(1)-DR. Left and right panels are from 293FT cells
transfected without or with SpRNase III respectively. DR-EMX1(1)-DR
was processed into mature crRNAs only in the presence of SpCas9 and
short tracrRNA and was not dependent on the presence of SpRNase
III. The mature crRNA detected from transfected 293FT total RNA is
.about.33 bp and is shorter than the 39-42 bp mature crRNA from S.
pyogenes. These results demonstrate that a CRISPR system can be
transplanted into eukaryotic cells and reprogrammed to facilitate
cleavage of endogenous mammalian target polynucleotides.
[0685] FIG. 2 illustrates the bacterial CRISPR system described in
this example. FIG. 2A illustrates a schematic showing the CRISPR
locus 1 from Streptococcus pyogenes SF370 and a proposed mechanism
of CRISPR-mediated DNA cleavage by this system. Mature crRNA
processed from the direct repeat-spacer array directs Cas9 to
genomic targets consisting of complimentary protospacers and a
protospacer-adjacent motif (PAM). Upon target-spacer base pairing,
Cas9 mediates a double-strand break in the target DNA. FIG. 2B
illustrates engineering of S. pyogenes Cas9 (SpCas9) and RNase III
(SpRNase III) with nuclear localization signals (NLSs) to enable
import into the mammalian nucleus. FIG. 2C illustrates mammalian
expression of SpCas9 and SpRNase III driven by the constitutive
EF1a promoter and tracrRNA and pre-crRNA array (DR-Spacer-DR)
driven by the RNA Po13 promoter U6 to promote precise transcription
initiation and termination. A protospacer from the human EMX1 locus
with a satisfactory PAM sequence is used as the spacer in the
pre-crRNA array. FIG. 2D illustrates surveyor nuclease assay for
SpCas9-mediated minor insertions and deletions. SpCas9 was
expressed with and without SpRNase III, tracrRNA, and a pre-crRNA
array carrying the EMX1-target spacer. FIG. 2E illustrates a
schematic representation of base pairing between target locus and
EMX1-targeting crRNA, as well as an example chromatogram showing a
micro deletion adjacent to the SpCas9 cleavage site. FIG. 2F
illustrates mutated alleles identified from sequencing analysis of
43 clonal amplicons showing a variety of micro insertions and
deletions. Dashes indicate deleted bases, and non-aligned or
mismatched bases indicate insertions or mutations. Scale bar=10
.mu.m.
[0686] To further simplify the three-component system, a chimeric
crRNA-tracrRNA hybrid design was adapted, where a mature crRNA
(comprising a guide sequence) may be fused to a partial tracrRNA
via a stem-loop to mimic the natural crRNA:tracrRNA duplex. To
increase co-delivery efficiency, a bicistronic expression vector
was created to drive co-expression of a chimeric RNA and SpCas9 in
transfected cells. In parallel, the bicistronic vectors were used
to express a pre-crRNA (DR-guide sequence-DR) with SpCas9, to
induce processing into crRNA with a separately expressed tracrRNA
(compare FIG. 11B top and bottom). FIG. 8 provides schematic
illustrations of bicistronic expression vectors for pre-crRNA array
(FIG. 8A) or chimeric crRNA (represented by the short line
downstream of the guide sequence insertion site and upstream of the
EF1.alpha. promoter in FIG. 8B) with hSpCas9, showing location of
various elements and the point of guide sequence insertion. The
expanded sequence around the location of the guide sequence
insertion site in FIG. 8B also shows a partial DR sequence
(GTTTTAGAGCTA (SEQ ID NO: 88)) and a partial tracrRNA sequence
(TAGCAAGTTAAAATAAGGCTAGTCCGTTTTT (SEQ ID NO: 89)). Guide sequences
can be inserted between BbsI sites using annealed oligonucleotides.
Sequence design for the oligonucleotides are shown below the
schematic illustrations in FIG. 8, with appropriate ligation
adapters indicated. WPRE represents the Woodchuck hepatitis virus
post-transcriptional regulatory element. The efficiency of chimeric
RNA-mediated cleavage was tested by targeting the same EMX1 locus
described above. Using both Surveyor assay and Sanger sequencing of
amplicons, Applicants confirmed that the chimeric RNA design
facilitates cleavage of human EMX1 locus with approximately a 4.7%
modification rate (FIG. 3).
[0687] Generalizability of CRISPR-mediated cleavage in eukaryotic
cells was tested by targeting additional genomic loci in both human
and mouse cells by designing chimeric RNA targeting multiple sites
in the human EMX1 and PVALB, as well as the mouse Th loci. FIG. 13
illustrates the selection of some additional targeted protospacers
in human PVALB (FIG. 13A) and mouse Th (FIG. 13B) loci. Schematics
of the gene loci and the location of three protospacers within the
last exon of each are provided. The underlined sequences include 30
bp of protospacer sequence and 3 bp at the 3' end corresponding to
the PAM sequences. Protospacers on the sense and anti-sense strands
are indicated above and below the DNA sequences, respectively. A
modification rate of 6.3% and 0.75% was achieved for the human
PVALB and mouse Th loci respectively, demonstrating the broad
applicability of the CRISPR system in modifying different loci
across multiple organisms (FIG. 5). While cleavage was only
detected with one out of three spacers for each locus using the
chimeric constructs, all target sequences were cleaved with
efficiency of indel production reaching 27% when using the
co-expressed pre-crRNA arrangement (FIGS. 6 and 13).
[0688] FIG. 11 provides a further illustration that SpCas9 can be
reprogrammed to target multiple genomic loci in mammalian cells.
FIG. 11A provides a schematic of the human FMX1 locus showing the
location of five protospacers, indicated by the underlined
sequences. FIG. 11B provides a schematic of the pre-crRNA/trcrRNA
complex showing hybridization between the direct repeat region of
the pre-crRNA and tracrRNA (top), and a schematic of a chimeric RNA
design comprising a 20 bp guide sequence, and tracr mate and tracr
sequences consisting of partial direct repeat and tracrRNA
sequences hybridized in a hairpin structure (bottom). Results of a
Surveyor assay comparing the efficacy of Cas9-mediated cleavage at
five protospacers in the human EMX1 locus is illustrated in FIG.
11C. Each protospacer is targeted using either processed
pre-crRNA/tracrRNA complex (crRNA) or chimeric RNA (chiRNA).
[0689] Since the secondary structure of RNA can be crucial for
intermolecular interactions, a structure prediction algorithm based
on minimum free energy and Boltzmann-weighted structure ensemble
was used to compare the putative secondary structure of all guide
sequences used in the genome targeting experiment (see e.g. Gruber
et al., 2008, Nucleic Acids Research, 36: W70). Analysis revealed
that in most cases, the effective guide sequences in the chimeric
crRNA context were substantially free of secondary structure
motifs, whereas the ineffective guide sequences were more likely to
form internal secondary structures that could prevent base pairing
with the target protospacer DNA. It is thus possible that
variability in the spacer secondary structure might impact the
efficiency of CRISPR-mediated interference when using a chimeric
crRNA.
[0690] Further vector designs for SpCas9 are shown in FIG. 22,
which illustrates single expression vectors incorporating a U6
promoter linked to an insertion site for a guide oligo, and a Cbh
promoter linked to SpCas9 coding sequence. The vector shown in FIG.
22b includes a tracrRNA coding sequence linked to an H1
promoter.
[0691] In the bacterial assay, all spacers facilitated efficient
CRISPR interference (FIG. 3C). These results suggest that there may
be additional factors affecting the efficiency of CRISPR activity
in mammalian cells.
[0692] To investigate the specificity of CRISPR-mediated cleavage,
the effect of single-nucleotide mutations in the guide sequence on
protospacer cleavage in the mammalian genome was analyzed using a
series of EMX1-targeting chimeric crRNAs with single point
mutations (FIG. 3A). FIG. 3B illustrates results of a Surveyor
nuclease assay comparing the cleavage efficiency of Cas9 when
paired with different mutant chimeric RNAs. Single-base mismatch up
to 12-bp 5' of the PAM substantially abrogated genomic cleavage by
SpCas9, whereas spacers with mutations at farther upstream
positions retained activity against the original protospacer target
(FIG. 3B). In addition to the PAM, SpCas9 has single-base
specificity within the last 12-bp of the spacer. Furthermore,
CRISPR is able to mediate genomic cleavage as efficiently as a pair
of TALE nucleases (TALEN) targeting the same EMX1 protospacer. FIG.
3C provides a schematic showing the design of TALENs targeting
EMX1, and FIG. 3D shows a Surveyor gel comparing the efficiency of
TALEN and Cas9 (n=3).
[0693] Having established a set of components for achieving
CRISPR-mediated gene editing in mammalian cells through the
error-prone NHEJ mechanism, the ability of CRISPR to stimulate
homologous recombination (HR), a high fidelity gene repair pathway
for making precise edits in the genome, was tested. The wild type
SpCas9 is able to mediate site-specific DSBs, which can be repaired
through both NHEJ and HR. In addition, an aspartate-to-alanine
substitution (D10A) in the RuvC I catalytic domain of SpCas9 was
engineered to convert the nuclease into a nickase (SpCas9n;
illustrated in FIG. 4A) (see e.g. Sapranausaks el al., 2011,
Nucleic Acids Resch, 39: 9275; Gasiunas et al., 2012, Proc. Natl.
Acad. Sci. USA, 109:E2579), such that nicked genomic DNA undergoes
the high-fidelity homology-directed repair (HDR). Surveyor assay
confirmed that SpCas9n does not generate indels at the EMX1
protospacer target. As illustrated in FIG. 4B, co-expression of
EMX1-targeting chimeric crRNA with SpCas9 produced indels in the
target site, whereas co-expression with SpCas9n did not (n=3).
Moreover, sequencing of 327 amplicons did not detect any indels
induced by SpCas9n. The same locus was selected to test
CRISPR-mediated HR by co-transfecting HEK 293FT cells with the
chimeric RNA targeting EMX1, hSpCas9 or hSpCas9n, as well as a HR
template to introduce a pair of restriction sites (HindIII and
NheI) near the protospacer. FIG. 4C provides a schematic
illustration of the HR strategy, with relative locations of
recombination points and primer annealing sequences (arrows).
SpCas9 and SpCas9n indeed catalyzed integration of the HR template
into the EMX1 locus. PCR amplification of the target region
followed by restriction digest with HindIII revealed cleavage
products corresponding to expected fragment sizes (arrows in
restriction fragment length polymorphism gel analysis shown in FIG.
4D), with SpCas9 and SpCas9n mediating similar levels of HR
efficiencies. Applicants further verified HR using Sanger
sequencing of genomic amplicons (FIG. 4E). These results
demonstrate the utility of CRISPR for facilitating targeted gene
insertion in the mammalian genome. Given the 14-bp (12-bp from the
spacer and 2-bp from the PAM) target specificity of the wild type
SpCas9, the availability of a nickase can significantly reduce the
likelihood of off-target modifications, since single strand breaks
are not substrates for the error-prone NHEJ pathway.
[0694] Expression constructs mimicking the natural architecture of
CRISPR loci with arrayed spacers (FIG. 2A) were constructed to test
the possibility of multiplexed sequence targeting. Using a single
CRISPR array encoding a pair of EMX1- and PVALB-targeting spacers,
efficient cleavage at both loci was detected (FIG. 4F, showing both
a schematic design of the crRNA array and a Surveyor blot showing
efficient mediation of cleavage). Targeted deletion of larger
genomic regions through concurrent DSBs using spacers against two
targets within EMX1 spaced by 119 bp was also tested, and a 1.6%
deletion efficacy (3 out of 182 amplicons; FIG. 4G) was detected.
This demonstrates that the CRISPR system can mediate multiplexed
editing within a single genome.
Example 2: CRISPR System Modifications and Alternatives
[0695] The ability to use RNA to program sequence-specific DNA
cleavage defines a new class of genome engineering tools for a
variety of research and industrial applications. Several aspects of
the CRISPR system can be further improved to increase the
efficiency and versatility of CRISPR targeting. Optimal Cas9
activity may depend on the availability of free Mg.sup.2+ at levels
higher than that present in the mammalian nucleus (see e.g. Jinek
et al., 2012, Science, 337:816), and the preference for an NGG
motif immediately downstream of the protospacer restricts the
ability to target on average every 12-bp in the human genome (FIG.
9, evaluating both plus and minus strands of human chromosomal
sequences). Some of these constraints can be overcome by exploring
the diversity of CRISPR loci across the microbial metagenome (see
e.g. Makarova et al., 2011, Nat Rev Microbiol, 9:467). Other CRISPR
loci may be transplanted into the mammalian cellular milieu by a
process similar to that described in Example 1. For example, FIG.
10 illustrates adaptation of the Type II CRISPR system from CRISPR
1 of Streptococcus thermophilus LMD-9 for heterologous expression
in mammalian cells to achieve CRISPR-mediated genome editing. FIG.
10A provides a Schematic illustration of CRISPR 1 from S.
thermophilus LMD-9. FIG. 10B illustrates the design of an
expression system for the S. thermophilus CRISPR system. Human
codon-optimized hStCas9 is expressed using a constitutive
EF1.alpha. promoter. Mature versions of tracrRNA and crRNA are
expressed using the U6 promoter to promote precise transcription
initiation. Sequences from the mature crRNA and tracrRNA are
illustrated. A single base indicated by the lower case "a" in the
crRNA sequence is used to remove the polyU sequence, which serves
as a RNA polIII transcriptional terminator. FIG. 10C provides a
schematic showing guide sequences targeting the human EMX1 locus.
FIG. 10D shows the results of hStCas9-mediated cleavage in the
target locus using the Surveyor assay. RNA guide spacers 1 and 2
induced 14% and 6.4%, respectively. Statistical analysis of
cleavage activity across biological replica at these two
protospacer sites is also provided in FIG. 5. FIG. 14 provides a
schematic of additional protospacer and corresponding PAM sequence
targets of the S. thermophilus CRISPR system in the human EMX1
locus. Two protospacer sequences are highlighted and their
corresponding PAM sequences satisfying NNAGAAW motif are indicated
by underlining 3' with respect to the corresponding highlighted
sequence. Both protospacers target the anti-sense strand.
Example 3: Sample Target Sequence Selection Algorithm
[0696] A software program is designed to identify candidate CRISPR
target sequences on both strands of an input DNA sequence based on
desired guide sequence length and a CRISPR motif sequence (PAM) for
a specified CRISPR enzyme. For example, target sites for Cas9 from
S. pyogenes, with PAM sequences NGG, may be identified by searching
for 5'-N.sub.x-NGG-3' both on the input sequence and on the
reverse-complement of the input. Likewise, target sites for Cas9 of
S. thermophilus CRISPR1, with PAM sequence NNAGAAW, may be
identified by searching for 5'-N.sub.x-NNAGAAW-3' (SEQ ID NO: 90)
both on the input sequence and on the reverse-complement of the
input. Likewise, target sites for Cas9 of S. thermophilus CRISPR3,
with PAM sequence NGGNG, may be identified by searching for
5'-N.sub.x-NGGNG-3' both on the input sequence and on the
reverse-complement of the input. The value "x" in N.sub.x may be
fixed by the program or specified by the user, such as 20.
[0697] Since multiple occurrences in the genome of the DNA target
site may lead to nonspecific genome editing, after identifying all
potential sites, the program filters out sequences based on the
number of times they appear in the relevant reference genome. For
those CRISPR enzymes for which sequence specificity is determined
by a `seed` sequence, such as the 11-12 bp 5' from the PAM
sequence, including the PAM sequence itself, the filtering step may
be based on the seed sequence. Thus, to avoid editing at additional
genomic loci, results are filtered based on the number of
occurrences of the seed:PAM sequence in the relevant genome. The
user may be allowed to choose the length of the seed sequence. The
user may also be allowed to specify the number of occurrences of
the seed:PAM sequence in a genome for purposes of passing the
filter. The default is to screen for unique sequences. Filtration
level is altered by changing both the length of the seed sequence
and the number of occurrences of the sequence in the genome. The
program may in addition or alternatively provide the sequence of a
guide sequence complementary to the reported target sequence(s) by
providing the reverse complement of the identified target
sequence(s). An example visualization of some target sites in the
human genome is provided in FIG. 18.
[0698] Further details of methods and algorithms to optimize
sequence selection can be found in U.S. application Ser. No.
61/064,798 (Attorney docket 44790.11.2022; Broad Reference
BI-2012/084); incorporated herein by reference.
Example 4: Evaluation of Multiple Chimeric crRNA-tracrRNA
Hybrids
[0699] This example describes results obtained for chimeric RNAs
(chiRNAs; comprising a guide sequence, a tracr mate sequence, and a
tracr sequence in a single transcript) having tracr sequences that
incorporate different lengths of wild-type tracrRNA sequence. FIG.
16a illustrates a schematic of a bicistronic expression vector for
chimeric RNA and Cas9. Cas9 is driven by the CBh promoter and the
chimeric RNA is driven by a U6 promoter. The chimeric guide RNA
consists of a 20 bp guide sequence (Ns) joined to the tracr
sequence (running from the first "U" of the lower strand to the end
of the transcript), which is truncated at various positions as
indicated. The guide and tracr sequences are separated by the
tracr-mate sequence GUUUUAGAGCUA (SEQ ID NO: 61) followed by the
loop sequence GAAA. Results of SURVEYOR assays for Cas9-mediated
indels at the human EMX1 and PVALB loci are illustrated in FIGS.
16b and 16c, respectively. Arrows indicate the expected SURVEYOR
fragments. ChiRNAs are indicated by their "+n" designation, and
crRNA refers to a hybrid RNA where guide and tracr sequences are
expressed as separate transcripts. Quantification of these results,
performed in triplicate, are illustrated by histogram in FIGS. 17a
and 17b, corresponding to FIGS. 16b and 16c, respectively ("N.D."
indicates no indels detected). Protospacer IDs and their
corresponding genomic target, protospacer sequence, PAM sequence,
and strand location are provided in Table D. Guide sequences were
designed to be complementary to the entire protospacer sequence in
the case of separate transcripts in the hybrid system, or only to
the underlined portion in the case of chimeric RNAs.
TABLE-US-00010 TABLE D SEQ protospacer genomic ID ID target
protospacer sequence (5' to 3') PAM NO: strand 1 EMX1
GGACATCGATGTCACCTCCAATGACTAGGG TGG 91 + 2 EMX1
CATTGGAGGTGACATCGATGTCCTCCCCAT TGG 92 - 3 EMX1
GGAAGGGCCTGAGTCCGAGCAGAAGAAGAA GGG 93 + 4 PVALB
GGTGGCGAGAGGGGCCGAGATTGGGTGTTC AGG 94 + 5 PVALB
ATGCAGGAGGGTGGCGAGAGGGGCCGAGAT TGG 95 +
[0700] Further details to optimize guide sequences can be found in
U.S. application Ser. No. 61/836,127 (Attorney docket
44790.08.2022; Broad Reference BI-2013/004G); incorporated herein
by reference.
[0701] Initially, three sites within the EMX1 locus in human HEK
293FT cells were targeted. Genome modification efficiency of each
chiRNA was assessed using the SURVEYOR nuclease assay, which
detects mutations resulting from DNA double-strand breaks (DSBs)
and their subsequent repair by the non-homologous end joining
(NHEJ) DNA damage repair pathway. Constructs designated chiRNA(+n)
indicate that up to the +n nucleotide of wild-type tracrRNA is
included in the chimeric RNA construct, with values of 48, 54, 67,
and 85 used for n. Chimeric RNAs containing longer fragments of
wild-type tracrRNA (chiRNA(+67) and chiRNA(+85)) mediated DNA
cleavage at all three EMX1 target sites, with chiRNA(+85) in
particular demonstrating significantly higher levels of DNA
cleavage than the corresponding crRNA/tracrRNA hybrids that
expressed guide and tracr sequences in separate transcripts (FIGS.
16b and 17a). Two sites in the PVALB locus that yielded no
detectable cleavage using the hybrid system (guide sequence and
tracr sequence expressed as separate transcripts) were also
targeted using chiRNAs. chiRNA(+67) and chiRNA(+85) were able to
mediate significant cleavage at the two PVALB protospacers (FIGS.
16c and 17b).
For all five targets in the EMX1 and PVALB loci, a consistent
increase in genome modification efficiency with increasing tracr
sequence length was observed. Without wishing to be bound by any
theory, the secondary structure formed by the 3' end of the
tracrRNA may play a role in enhancing the rate of CRISPR complex
formation.
Example 5: Cas9 Diversity
[0702] The CRISPR-Cas system is an adaptive immune mechanism
against invading exogenous DNA employed by diverse species across
bacteria and archaea. The type II CRISPR-Cas9 system consists of a
set of genes encoding proteins responsible for the "acquisition" of
foreign DNA into the CRISPR locus, as well as a set of genes
encoding the "execution" of the DNA cleavage mechanism; these
include the DNA nuclease (Cas9), a non-coding transactivating
cr-RNA (tracrRNA), and an array of foreign DNA-derived spacers
flanked by direct repeats (crRNAs). Upon maturation by Cas9, the
tracRNA and crRNA duplex guide the Cas9 nuclease to a target DNA
sequence specified by the spacer guide sequences, and mediates
double-stranded breaks in the DNA near a short sequence motif in
the target DNA that is required for cleavage and specific to each
CRISPR-Cas system. The type II CRISPR-Cas systems are found
throughout the bacterial kingdom and highly diverse in in Cas9
protein sequence and size, tracrRNA and crRNA direct repeat
sequence, genome organization of these elements, and the motif
requirement for target cleavage. One species may have multiple
distinct CRISPR-Cas systems.
[0703] Applicants evaluated 207 putative Cas9s from bacterial
species identified based on sequence homology to known Cas9s and
structures orthologous to known subdomains, including the HNH
endonuclease domain and the RuvC endonuclease domains [information
from the Eugene Koonin and Kira Makarova]. Phylogenetic analysis
based on the protein sequence conservation of this set revealed
five families of Cas9s, including three groups of large Cas9s
(.about.1400 amino acids) and two of small Cas9s (.about.1100 amino
acids) (see FIGS. 19 and 20A-F).
[0704] Further details of Cas9s and mutations of the Cas9 enzyme to
convert into a nickase or DNA binding protein and use of same with
altered functionality can be found in U.S. application Serial Nos.
61/836,101 and 61/835,936 (Attorney docket 44790.09.2022 and
4790.07.2022 and Broad Reference BI-2013/004E and BI-2013/004F
respectively) incorporated herein by reference.
Example 6: Cas9 Orthologs
[0705] Applicants analyzed Cas9 orthologs to identify the relevant
PAM sequences and the corresponding chimeric guide RNA. Having an
expanded set of PAMs provides broader targeting across the genome
and also significantly increases the number of unique target sites
and provides potential for identifying novel Cas9s with increased
levels of specificity in the genome.
[0706] The specificity of Cas9 orthologs can be evaluated by
testing the ability of each Cas9 to tolerate mismatches between the
guide RNA and its DNA target. For example, the specificity of
SpCas9 has been characterized by testing the effect of mutations in
the guide RNA on cleavage efficiency. Libraries of guide RNAs were
made with single or multiple mismatches between the guide sequence
and the target DNA. Based on these findings, target sites for
SpCas9 can be selected based on the following guidelines:
[0707] To maximize SpCas9 specificity for editing a particular
gene, one should choose a target site within the locus of interest
such that potential `off-target` genomic sequences abide by the
following four constraints: First and foremost, they should not be
followed by a PAM with either 5'-NGG or NAG sequences. Second,
their global sequence similarity to the target sequence should be
minimized. Third, a maximal number of mismatches should lie within
the PAM-proximal region of the off-target site. Finally, a maximal
number of mismatches should be consecutive or spaced less than four
bases apart.
[0708] Similar methods can be used to evaluate the specificity of
other Cas9 orthologs and to establish criteria for the selection of
specific target sites within the genomes of target species. As
mentioned previously phylogenetic analysis based on the protein
sequence conservation of this set revealed five families of Cas9s,
including three groups of large Cas9s (.about.1400 amino acids) and
two of small Cas9s (.about.1100 amino acids) (see FIGS. 19 and
20A-F). Further details on Cas orthologs can be found in U.S.
application Serial Nos 61/836,101 and 61/835,936 (Attorney docket
44790.09.2022 and 4790.07.2022 and Broad Reference BI-2013/004E and
BI-2013/004F respectively) incorporated herein by reference.
Example 7: Methodological Improvement to Simplify Cloning and
Delivery
[0709] Rather than encoding the U6-promoter and guide RNA on a
plasmid, Applicants amplified the U6 promoter with a DNA oligo to
add on the guide RNA. The resulting PCR product may be transfected
into cells to drive expression of the guide RNA.
[0710] Example primer pair that allows the generation a PCR product
consisting of U6-promoter::guideRNA targeting human Emx1 locus:
TABLE-US-00011 Forward Primer: (SEQ ID NO: 96)
AAACTCTAGAgagggcctatttcccatgattc Reverse Primer (carrying the guide
RNA, which is underlined): (SEQ ID NO: 97)
acctctagAAAAAAAGCACCGACTCGGTGCCACTTTTTCAAGTTGATAA
CGGACTAGCCTTATTTTAACTTGCTATGCTGTTTTGTTTCCAAAACAGC
ATAGCTCTAAAACCCCTAGTCATTGGAGGTGACGGTGTTTCGTCCTTTC CACaag
Example 8: Methodological Improvement to Improve Activity
[0711] Rather than use po13 promoters, in particular RNA polymerase
III (e.g. U6 or H1 promoters), to express guide RNAs in eukaryotic
cells, Applicants express the T7 polymerase in eukaryotic cells to
drive expression of guide RNAs using the T7 promoter.
[0712] One example of this system may involve introduction of three
pieces of DNA:
[0713] 1. expression vector for Cas9
[0714] 2. expression vector for T7 polymerase
[0715] 3. expression vector containing guideRNA fused to the T7
promoter
Example 9: Methodological Improvement to Reduce Toxicity of Cas9:
Delivery of Cas9 in the Form of mRNA
[0716] Delivery of Cas9 in the form of mRNA enables transient
expression of Cas9 in cells, to reduce toxicity. For example,
humanized SpCas9 may be amplified using the following primer
pair:
TABLE-US-00012 Forward Primer (to add on T7 promoter for in vitro
transcription): (SEQ ID NO: 98)
TAATACGACTCACTATAGGAAGTGCGCCACCATGGCCCCAAAGAAGAAG CGG Reverse
Primer (to add on polyA tail): (SEQ ID NO: 99)
GGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTttcttaCTTTTTCTTTT TTGCCTGGCCG
[0717] Applicants transfect the Cas9 mRNA into cells with either
guide RNA in the form of RNA or DNA cassettes to drive guide RNA
expression in eukaryotic cells.
Example 10: Methodological Improvement to Reduce Toxicity of Cas9:
Use of an Inducible Promoter
[0718] Applicants transiently turn on Cas9 expression only when it
is needed for carrying out genome modification. Examples of
inducible system include tetracycline inducible promoters (Tet-On
or Tet-Off), small molecule two-hybrid transcription activations
systems (FKBP, ABA, etc), or light inducible systems (Phytochrome,
LOV domains, or cryptochrome).
Example 11: Improvement of the Cas9 System for In Vivo
Application
[0719] Applicants conducted a Metagenomic search for a Cas9 with
small molecular weight. Most Cas9 homologs are fairly large. For
example the SpCas9 is around 1368 aa long, which is too large to be
easily packaged into viral vectors for delivery. A graph
representing the length distribution of Cas9 homologs is generated
from sequences deposited in GenBank (FIG. 23). Some of the
sequences may have been mis-annotated and therefore the exact
frequency for each length may not necessarily be accurate.
Nevertheless it provides a glimpse at distribution of Cas9 proteins
and suggest that there are shorter Cas9 homologs.
[0720] Through computational analysis, Applicants found that in the
bacterial strain Campylobacter, there are two Cas9 proteins with
less than 1000 amino acids. The sequence for one Cas9 from
Campylobacter jejuni is presented below. At this length, CjCas9 can
be easily packaged into AAV, lentiviruses, Adenoviruses, and other
viral vectors for robust delivery into primary cells and in vivo in
animal models. In a preferred embodiment of the invention, the Cas9
protein from S. aureus is used.
[0721] >Campylobacter jejuni Cas9 (CjCas9)
TABLE-US-00013 (SEQ ID NO: 100)
MARILAFDIGISSIGWAFSENDILKGCGVRIFTKVENPKTGESLALPRR
LARSARKRLARRKARLNHLKHLIANEFKLNYEDYQSFDESLAKAYKGSL
ISPYELRFRALNELLSKQDFARVILHIAKRRGYDDIKNSDDKEKGAILK
AIKQNEEKLANYQSVGEYLYKEYFQKFKENSKEFTNVRNKKESYERCIA
QSFLKDELKLIFKKQREFGFSFSKKFEEEVLSVAFYKRALKDFSHLVGN
CSFFTDEKRAPKNSPLAFMFVALTRIINLLNNLKNTEGILYTKDDLNAL
LNEVLKNGTLTYKQTKKLLGLSDDYEFKGEKGTYFIEFKKYKEFIKALG
EHNLSQDDLNEIAKDITLIKDEIKLKKALAKYDLNQNQIDSLSKLEFKD
HLNISFKALKLVTPLMLEGKKYDEACNELNLKVAINEDKKDFLPAFNET
YYKDEVTNPVVLRAIKEYRKVLNALLKKYGKVHKINIELAREVGHNHSQ
RAKIEKEQNENYKAKKDAELECEKLGLKINSKNILKLRLFKEQKEFCAY
SGEKIKISDLQDEKMLEIDHIYPYSRSFDDSYMNKVLVFTKQNQEKLNQ
TPFEAFGNDSAKWQKIEVLAKNLPTKKQKRILDKNYKDKEQKNFKDRNL
NDTRYIARLVLNYTKDYLDFLPLSDDENTKLNDTQKGSKVHVEAKSGML
TSALRHTWGFSAKDRNNHLHHAIDAVIIAYANNSIVKAFSDFKKEQESN
SAELYAKKISELDYKNKRKFFEPFSGFRQKVLDKIDEIFVSKPERKKPS
GALHEETFRKEEEFYQSYGGKEGVLKALELGKIRKVNGKIVKNGDMFRV
DIFKHKKTNKFYAVPIYTMDFALKVLPNKAVARSKKGEIKDWILMDENY
EFCFSLYKDSLILIQTKDMQEPEFVYYNAFTSSTVSLIVSKHDNKFETL
SKNQKILFKNANEKEVIAKSIGIQNLKVFEKYIVSALGEVTKAEFRQRE DFKK.
[0722] The putative tracrRNA element for this CjCas9 is:
TABLE-US-00014 (SEQ ID NO: 101)
TATAATCTCATAAGAAATTTAAAAAGGGACTAAAATAAAGAGTTTGCGG
GACTCTGCGGGGTTACAATCCCCTAAAACCGCTTTTAAAATT
[0723] The Direct Repeat sequence is:
TABLE-US-00015 (SEQ ID NO: 102)
ATTTTACCATAAAGAAATTTAAAAAGGGACTAAAAC
[0724] An example of a chimeric guideRNA for CjCas9 is:
TABLE-US-00016 (SEQ ID NO: 103)
NNNNNNNNNNNNNNNNNNNNGUUUUAGUCCCGAAAGGGACUAAAAUAAA
GAGUUUGCGGGACUCUGCGGGGUUACAAUCCCCUAAAACCGCUUUU
Example 12: Cas9 Optimization
[0725] For enhanced function or to develop new functions,
Applicants generate chimeric Cas9 proteins by combining fragments
from different Cas9 homologs. For example, two example chimeric
Cas9 proteins:
[0726] For example, Applicants fused the N-term of StlCas9
(fragment from this protein is in bold) with C-term of SpCas9
(fragment from this protein is underlined).
[0727] >St1(N)Sp(C)Cas9
TABLE-US-00017 (SEQ ID NO: 104)
MSDLVVLGLDIGIGSVGVGILNKVTGEIIHKNSRIFPAAQAENNLVRRTN
RQGRRLARRKKHRRVRLNRLFEESGLITDFTKISINLNPYQLRVKGLTDE
LSNEELFIALKNMVKHRGISYLDDASDDGNSSVGDYAQIVKENSKQLETK
TPGQIQLERYQTYGQLRGDFTVEKDGKKHRLINVFPTSAYRSEALRILQT
QQEFNPQITDEFINRYLEILTGKRKYYHGPGNEKSRTDYGRYRTSGETLD
NIFGILIGKCTFYPDEFRAAKASYTAQEFNLLNDLNNLTVPTETKKLSKE
QKNQIINYVKNEKAMGPAKLFKYIAKLLSCDVADIKGYRIDKSGKAEIHT
FEAYRKMKTLETLDIEQMDRETLDKLAYVLTLNTEREGIQEALEHEFADG
SFSQKQVDELVQFRKANSSIFGKGWHNFSVKLMMELIPELYETSEEQMTI
LTRLGKQKTTSSSNKTKYIDEKLLTEEIYNPVVAKSVRQAIKIVNAAIKE
YGDFDNIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVE
NTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSI
DNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTK
AERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIRE
VKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYP
KLESEFVYGDYKVYDVRKMIAKSEQEIGKATAFYFFYSNIMNFFKTEITL
ANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQT
GGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEKG
KSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYS
LFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDN
EQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPI
REQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSI
TGLYETRIDLSQLGGD
[0728] >Sp(N)St1(C)Cas9
TABLE-US-00018 (SEQ ID NO: 105)
MDKKYSIGLDIGTNSVGWAVITDEYKVPSKKEFKVLGNTDRHSIKKNLI
GALLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSF
FHRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDST
DKADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQL
FEENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIAL
SLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAA
KNLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQ
LPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLV
KLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKI
EKILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQ
SFIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPA
FLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRF
NASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFEDREMIEERL
KTYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKS
DGFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIK
KGILQTVKVVDELVKVMGRHKPENIVIEMARETNEDDEKKAIQKIQKAN
KDEKDAAMLKAANQYNGKAELPHSVFHGHKQLATKIRLWHQQGERCLYT
GKTISIHDLINNSNQFEVDHILPLSITFDDSLANKVLVYATANQEKGQR
TPYQALDSMDDAWSFRELKAFVRESKTLSNKKKEYLLTEEDISKFDVRK
KFIERNLVDTRYASRVVLNALQEHFRAHKIDTKVSVVRGQFTSQLRRHW
GIEKTRDTYHHHAVDALIIAASSQLNLWKKQKNTLVSYSEDQLLDIETG
ELISDDEYKESVFKAPYQHFVDTLKSKEFEDSILFSYQVDSKFNRKISD
ATIYATRQAKVGKDKADETYVLGKIKDIYTQDGYDAFMKIYKKDKSKFL
MYRHDPQTFEKVIEPILENYPNKQINEKGKEVPCNPFLKYKEEHGYIRK
YSKKGNGPEIKSLKYYDSKLGNHIDITPKDSNNKVVLQSVSPWARADVY
FNKTTGKYEILGLKYADLQFEKGTGTYKISQEKYNDIKKKEGVDSDSEF
KFTLYKNDLLLVKDTETKEQQLFRFLSRTMPKQKHYVELKPYDKQKFEG
GEALIKVLGNVANSGQCKKGLGKSNISIYKVRTDVLGNQHIIKNEGDKP KLDF
[0729] The benefit of making chimeric Cas9 include:
[0730] reduce toxicity
[0731] improve expression in eukaryotic cells
[0732] enhance specificity
[0733] reduce molecular weight of protein, make protein smaller by
combining the smallest domains from different Cas9 homologs.
[0734] Altering the PAM sequence requirement
Example 13: Utilization of Cas9 as a Generic DNA Binding
Protein
[0735] Applicants used Cas9 as a generic DNA binding protein by
mutating the two catalytic domains (D10 and H840) responsible for
cleaving both strands of the DNA target. In order to upregulate
gene transcription at a target locus Applicants fused the
transcriptional activation domain (VP64) to Cas9. Applicants
hypothesized that it would be important to see strong nuclear
localization of the Cas9-VP64 fusion protein because transcription
factor activation strength is a function of time spent at the
target. Therefore, Applicants cloned a set of Cas9-VP64-GFP
constructs, transfected them into 293 cells and assessed their
localization under a fluorescent microscope 12 hours
post-transfection.
[0736] The same constructs were cloned as a 2A-GFP rather than a
direct fusion in order to functionally test the constructs without
a bulky GFP present to interfere. Applicants elected to target the
Sox2 locus with the Cas9 transactivator because it could be useful
for cellular reprogram and the locus has already been validated as
a target for TALE-TF mediated transcriptional activation. For the
Sox2 locus Applicants chose eight targets near the transcriptional
start site (TSS). Each target was 20 bp long with a neighboring NGG
protospacer adjacent motif (PAM). Each Cas9-VP64 construct was
co-transfected with each PCR generated chimeric crispr RNA (chiRNA)
in 293 cells. 72 hours post transfection the transcriptional
activation was assessed using RT-qPCR.
[0737] To further optimize the transcriptional activator,
Applicants titrated the ratio of chiRNA (Sox2.1 and Sox2.5) to Cas9
(NLS-VP64-NLS-hSpCas9-NLS-VP64-NLS), transfected into 293 cells,
and quantified using RT-qPCR. These results indicate that Cas9 can
be used as a generic DNA binding domain to upregulate gene
transcription at a target locus.
[0738] Applicants designed a second generation of constructs.
(Table below).
TABLE-US-00019 pLenti-EF1a-GFP-2A-6xHis-NLS-VP64-NLS-hSpCsn(D10A,
H840A)-NLS ("6xHis" disclosed as SEQ ID NO: 370)
pLenti-EF1a-GFP-2A-6xHis-NLS-VP64-NLS-hSpCsn1(D10A, H840A) ("6xHis"
disclosed as SEQ ID NO: 370)
pLenti-EF1a-GFP-2A-6xHis-NLS-VP64-NLS-NLS-hSpCsn1 (D10A, H840A)
("6xHis" disclosed as SEQ ID NO: 370)
pLenti-EF1a-GFP-2A-6xHis-NLS-hSpCsn1(D10A, H840A)- NLA ("6xHis"
disclosed as SEQ ID NO: 370)
pLenti-EF1a-GFP-2A-6xHis-NLS-hSpCsn1(D10A, H840A) ("6xHis"
disclosed as SEQ ID NO: 370)
pLenti-EF1a-GFP-2A-6xHis-NLS-NLS-hSpCsn1(D10A, H840A) ("6xHis"
disclosed as SEQ ID NO: 370)
[0739] Applicants use these constructs to assess transcriptional
activation (VP64 fused constructs) and repression (Cas9 only) by
RT-qPCR. Applicants assess the cellular localization of each
construct using anti-His antibody, nuclease activity using a
Surveyor nuclease assay, and DNA binding affinity using a gel shift
assay. In a preferred embodiment of the invention, the gel shift
assay is an EMSA gel shift assay.
Example 14: Cas9 Transgenic and Knock in Mice
[0740] To generate a mouse that expresses the Cas9 nuclease
Applicants submit two general strategies, transgenic and knock in.
These strategies may be applied to generate any other model
organism of interest, for e.g. Rat. For each of the general
strategies Applicants made a constitutively active Cas9 and a Cas9
that is conditionally expressed (Cre recombinase dependent). The
constitutively active Cas9 nuclease is expressed in the following
context: pCAG-NLS-Cas9-NLS-P2A-EGFP-WPRE-bGHpolyA. pCAG is the
promoter, NLS is a nuclear localization signal, P2A is the peptide
cleavage sequence, EGFP is enhanced green fluorescent protein, WPRE
is the woodchuck hepatitis virus posttranscriptional regulatory
element, and bGHpolyA is the bovine growth hormone poly-A signal
sequence (FIGS. 25A-B). The conditional version has one additional
stop cassette element, loxP-SV40 polyA x3-loxP, after the promoter
and before NLS-Cas9-NLS (i.e.
pCAG-loxP-SV40polyAx3-loxP-NLS-Cas9-NLS-P2A-EGFP-WPRE-bGHpolyA).
The important expression elements can be visualized as in FIG. 26.
The constitutive construct should be expressed in all cell types
throughout development, whereas, the conditional construct will
only allow Cas9 expression when the same cell is expressing the Cre
recombinase. This latter version will allow for tissue specific
expression of Cas9 when Cre is under the expression of a tissue
specific promoter. Moreover, Cas9 expression could be induced in
adult mice by putting Cre under the expression of an inducible
promoter such as the TET on or off system.
[0741] Validation of Cas9 constructs: Each plasmid was functionally
validated in three ways: 1) transient transfection in 293 cells
followed by confirmation of GFP expression; 2) transient
transfection in 293 cells followed by immunofluorescence using an
antibody recognizing the P2A sequence; and 3) transient
transfection followed by Surveyor nuclease assay. The 293 cells may
be 293FT or 293 T cells depending on the cells that are of
interest. In a preferred embodiment the cells are 293FT cells. The
results of the Surveyor were run out on the top and bottom row of
the gel for the conditional and constitutive constructs,
respectively. Each was tested in the presence and absence of
chimeric RNA targeted to the hEMX1 locus (chimeric RNA hEMX1.1).
The results indicate that the construct can successfully target the
hEMX1 locus only in the presence of chimeric RNA (and Cre in the
conditional case). The gel was quantified and the results are
presented as average cutting efficiency and standard deviation for
three samples.
[0742] Transgenic Cas9 mouse: To generate transgenic mice with
constructs, Applicants inject pure, linear DNA into the pronucleus
of a zygote from a pseudo pregnant CB56 female. Founders are
identified, genotyped, and backcrossed to CB57 mice. The constructs
were successfully cloned and verified by Sanger sequencing.
[0743] Knock in Cas9 mouse: To generate Cas9 knock in mice
Applicants target the same constitutive and conditional constructs
to the Rosa26 locus. Applicants did this by cloning each into a
Rosa26 targeting vector with the following elements: Rosa26 short
homology arm-constitutive/conditional Cas9 expression
cassette--pPGK-Neo-Rosa26 long homology arm--pPGK-DTA. pPGK is the
promoter for the positive selection marker Neo, which confers
resistance to neomycin, a 1 kb short arm, a 4.3 kb long arm, and a
negative selection diphtheria toxin (DTA) driven by PGK.
[0744] The two constructs were electroporated into R1 mESCs and
allowed to grow for 2 days before neomycin selection was applied.
Individual colonies that had survived by days 5-7 were picked and
grown in individual wells. 5-7 days later the colonies were
harvested, half were frozen and the other half were used for
genotyping. Genotyping was done by genomic PCR, where one primer
annealed within the donor plasmid (AttpF) and the other outside of
the short homology arm (Rosa26-R) Of the 22 colonies harvested for
the conditional case, 7 were positive (Left). Of the 27 colonies
harvested for the constitutive case, zero were positive (Right). It
is likely that Cas9 causes some level of toxicity in the mESC and
for this reason there were no positive clones. To test this
Applicants introduced a Cre expression plasmid into correctly
targeted conditional Cas9 cells and found very low toxicity after
many days in culture. The reduced copy number of Cas9 in correctly
targeted conditional Cas9 cells (1-2 copies per cell) is enough to
allow stable expression and relatively no cytotoxicity. Moreover,
this data indicates that the Cas9 copy number determines toxicity.
After electroporation each cell should get several copies of Cas9
and this is likely why no positive colonies were found in the case
of the constitutive Cas9 construct. This provides strong evidence
that utilizing a conditional, Cre-dependent strategy should show
reduced toxicity. Applicants inject correctly targeted cells into a
blastocyst and implant into a female mouse. Chimerics are
identified and backcrossed. Founders are identified and
genotyped.
[0745] Utility of the conditional Cas9 mouse: Applicants have shown
in 293 cells that the Cas9 conditional expression construct can be
activated by co-expression with Cre. Applicants also show that the
correctly targeted R1 mESCs can have active Cas9 when Cre is
expressed. Because Cas9 is followed by the P2A peptide cleavage
sequence and then EGFP Applicants identify successful expression by
observing EGFP. This same concept is what makes the conditional
Cas9 mouse so useful. Applicants may cross their conditional Cas9
mouse with a mouse that ubiquitously expresses Cre (ACTB-Cre line)
and may arrive at a mouse that expresses Cas9 in every cell. It
should only take the delivery of chimeric RNA to induce genome
editing in embryonic or adult mice. Interestingly, if the
conditional Cas9 mouse is crossed with a mouse expressing Cre under
a tissue specific promoter, there should only be Cas9 in the
tissues that also express Cre. This approach may be used to edit
the genome in only precise tissues by delivering chimeric RNA to
the same tissue.
Example 15: Cas9 Diversity and Chimeric RN4s
[0746] The CRISPR-Cas system is an adaptive immune mechanism
against invading exogenous DNA employed by diverse species across
bacteria and archaea. The type II CRISPR-Cas system consists of a
set of genes encoding proteins responsible for the "acquisition" of
foreign DNA into the CRISPR locus, as well as a set of genes
encoding the "execution" of the DNA cleavage mechanism; these
include the DNA nuclease (Cas9), a non-coding transactivating
cr-RNA (tracrRNA), and an array of foreign DNA-derived spacers
flanked by direct repeats (crRNAs). Upon maturation by Cas9, the
tracrRNA and crRNA duplex guide the Cas9 nuclease to a target DNA
sequence specified by the spacer guide sequences, and mediates
double-stranded breaks in the DNA near a short sequence motif in
the target DNA that is required for cleavage and specific to each
CRISPR-Cas system. The type II CRISPR-Cas systems are found
throughout the bacterial kingdom and highly diverse in in Cas9
protein sequence and size, tracrRNA and crRNA direct repeat
sequence, genome organization of these elements, and the motif
requirement for target cleavage. One species may have multiple
distinct CRISPR-Cas systems.
[0747] Applicants evaluated 207 putative Cas9s from bacterial
species identified based on sequence homology to known Cas9s and
structures orthologous to known subdomains, including the HNH
endonuclease domain and the RuvC endonuclease domains [information
from the Eugene Koonin and Kira Makarova]. Phylogenetic analysis
based on the protein sequence conservation of this set revealed
five families of Cas9s, including three groups of large Cas9s
(.about.1400 amino acids) and two of small Cas9s (.about.1100 amino
acids) (FIGS. 19A-D and 20A-F).
[0748] Applicants have also optimized Cas9 guide RNA using in vitro
methods.
Example 16: Cas9 Mutations
[0749] In this example, Applicants show that the following
mutations can convert SpCas9 into a nicking enzyme: D10A, E762A,
H840A, N854A, N863A, D986A.
[0750] Applicants provide sequences showing where the mutation
points are located within the SpCas9 gene (FIG. 24A-M). Applicants
also show that the nickases are still able to mediate homologous
recombination. Furthermore, Applicants show that SpCas9 with these
mutations (individually) do not induce double strand break.
[0751] Cas9 orthologs all share the general organization of 3-4
RuvC domains and a HNH domain. The 5' most RuvC domain cleaves the
non-complementary strand, and the HNH domain cleaves the
complementary strand. All notations are in reference to the guide
sequence.
[0752] The catalytic residue in the 5' RuvC domain is identified
through homology comparison of the Cas9 of interest with other Cas9
orthologs (from S. pyogenes type II CRISPR locus, S. thermophilus
CRISPR locus 1, S. thermophilus CRISPR locus 3, and Franciscilla
novicida type II CRISPR locus), and the conserved Asp residue is
mutated to alanine to convert Cas9 into a complementary-strand
nicking enzyme. Similarly, the conserved His and Asn residues in
the HNH domains are mutated to Alanine to convert Cas9 into a
non-complementary-strand nicking enzyme.
Example 17: Cas9 Transcriptional Activation and Cas9 Repressor
[0753] Cas9 Transcriptional Activation
[0754] A second generation of constructs were designed and tested
(Table 1). These constructs are used to assess transcriptional
activation (VP64 fused constructs) and repression (Cas9 only) by
RT-qPCR. Applicants assess the cellular localization of each
construct using anti-His antibody, nuclease activity using a
Surveyor nuclease assay, and DNA binding affinity using a gel shift
assay.
[0755] Cas Repressor
[0756] It has been shown previously that dCas9 can be used as a
generic DNA binding domain to repress gene expression. Applicants
report an improved dCas9 design as well as dCas9 fusions to the
repressor domains KRAB and SID4x. From the plasmid library created
for modulating transcription using Cas9 in Table 1, the following
repressor plasmids were functionally characterized by qPCR: pXRP27,
pXRP28, pXRP29, pXRP48, pXRP49, pXRP50, pXRP51, pXRP52, pXRP53,
pXRP56, pXRP58, pXRP59, pXRP61, and pXRP62.
[0757] Each dCas9 repressor plasmid was co-transfected with two
guide RNAs targeted to the coding strand of the beta-catenin gene.
RNA was isolated 72 hours after transfection and gene expression
was quantified by RT-qPCR. The endogenous control gene was GAPDH.
Two validated shRNAs were used as positive controls. Negative
controls were certain plasmids transfected without gRNA, these are
denoted as "pXRP## control". The plasmids pXRP28, pXRP29, pXRP48,
and pXRP49 could repress the beta-catenin gene when using the
specified targeting strategy. These plasmids correspond to dCas9
without a functional domain (pXRP28 and pXRP28) and dCas9 fused to
SID4x (pXRP48 and pXRP49).
[0758] Further work investigates: repeating the above experiment,
targeting different genes, utilizing other gRNAs to determine the
optimal targeting position, and multiplexed repression.
TABLE-US-00020 TABLE 1 (Table 1 discloses "GGGGS3" as SEQ ID NO:
106, "EAAAK3" as SEQ ID NO: 107 and "GGGGGS3" as SEQ ID NO: 108)
pXRP024-pLenti2-EF1a-VP64-NLS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP025-pLenti2-EF1a-VP64-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP026-pLenti2-EF1a-VP64-NLS-EAAAK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP027-pLenti2-EF1a-NLS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP028-pLenti2-EF1a-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP029-pLenti2-EF1a-NLS-EAAAK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP030-pLenti2-pSV40-VP64-NLS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP031-pLenti2-pPGK-VP64-NLS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP032-pLenti2-LTR-VP64-NLS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP033-pLenti2-pSV40-VP64-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPR-
E
pXRP034-pLenti2-pPGK-VP64-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP035-pLenti2-LTR-VP64-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP036-pLenti2-pSV40-VP64-NLS-EAAAK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPR-
E
pXRP037-pLenti2-pPGK-VP64-NLS-EAAAK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP038-pLenti2-LTR-VP64-NLS-EAANK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP048-pLenti2-EF1a-SID4x-NLS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP049-pLenti2-EF1a-SID4X-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPR-
E
pXRP050-pLenti2-EF1a-SID4X-NLS-EAAAK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPR-
E
pXRP051-pLenti2-EF1a-KRAB-NTS-FLAG-Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP052-pLenti2-EFTa-KRAB-NLS-GGGGS.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP053-pLenti2-EF1a-KRAB-NLS-EAAAK.sub.3Linker-dCas9-NLS-gLuc-2A-GFP-WPRE
pXRP054-pLenti2-EF1a-dCas9-Linker-FLAG-NLS-VP64-gLuc-2A-GFP-WPRE
pXRP055-pLenti2-EF1a-dCas9-Linker-FLAG-NLS-SID4X-gLuc-2A-GFP-WPRE
pXRP056-pLenti2-EF1a-dCas9-Linker-FLAG-NLS-KRAB-gLuc-2A-GFP-WPRE
pXRP057-pLenti2-EF1a-dCas9-GGGGGS.sub.3-NLS-VP64-gLuc-2A-GFP-WPRE
pXRP058-pLenti2-EF1a-dCas9-GGGGGS.sub.3-NLS-SID4X-gLuc-2A-GFP-WPRE
pXRP059-ptenti2-EF1a-dCas9-GGGGGS.sub.3-NLS-KRAB-gLuc-2A-GFP-WPRE
pXRP060-pLenti2-EF1a-dCas9-EAAAK.sub.3-NLS-VP64-gLuc-2A-GFP-WPRE
pXRP061-pLenti2-EF1a-dCas9-EAAAK.sub.3-NLS-SID4X-gLuc-2A-GFP-WPRE
pXRP062-pLenti2-EF1a-dCas9-EAAAK.sub.3-NLS-KRAB-gLuc-2A-GFP-WPRE
pXRP024-pLenti2-EF1a-VP64-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP025-pLenti2-EF1a-VP64-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP026-pLenti2-EF1a-VP64-NLS-EAAAK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP027-pLenti2-EF1a-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP028-pLenti2-EF1a-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP029-pLenti2-EF1a-NLS-EAAAK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP030-pLenti2-pSV40-VP64-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP031-pLenti2-pPGK-VP64-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP032-pLenti2-LTR-VP64-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP033-pLenti2-pSV40-VP64-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP034-pLenti2-pPGK-VP64-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP035-ptenti2-LTR-VP64-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP036-ptenti2-pSV40-VP64-NLS-EAAAK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP037-pLenti2-pPGK-VP64-NLS-EAAAK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP038-pLenti2-LTR-VP64-NLS-EAANK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP048-pLenti2-EF1a-SID4x-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP049-pLenti2-EF1a-SID4X-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP050-pLenti2-EF1a-SID4X-NLS-EAAAK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP051-pLenti2-EF1a-KRAB-NLS-FLAG-Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP052-pLenti2-EF1a-KRAB-NLS-GGGGS.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP053-pLenti2-EF1a-KRAB-NLS-EAAAK.sub.3Linker-Cas9-NLS-gLuc-2A-GFP-WPRE
pXRP054-pLenti2-EF1a-Cas9-Linker-FLAG-NLS-VP64-gLuc-2A-GFP-WPRE
pXRP055-pLenti2-EF1a-Cas9-Linker-FLAG-NLS-SID4X-gLuc-2A-GFP-WPRE
pXRP056-pLenti2-EF1a-Cas9-Linker-FLAG-NLS-KRAB-gLuc-2A-GFP-WPRE
pXRP057-pLenti2-EF1a-Cas9-GGGGGS.sub.3-NLS-VP64-gLuc-2A-GFP-WPRE
pXRP058-ptenti2-EF1a-Cas9-GGGGGS.sub.3-NLS-SID4X-gLuc-2A-GFP-WPRE
pXRP059-pLenti2-EF1a-Cas9-GGGGGS.sub.3-NLS-KRAB-OAK-2A-GFP-WPRE
pXRP060-pLenti2-EF1a-Cas9-EAAAK.sub.3-NLS-VP64-gLuc-2A-GFP-WPRE
pXRP061-pLenti2-EF1a-Cas9-EAAAK.sub.3-NLS-SID4X-gLuc-2A-GFP-WPRE
pXRP062-pLenti2-EF1a-Cas9-EAAAK.sub.3-NLS-KRAB-gLuc-2A-GFP-WPRE
Example 18: Targeted Deletion of Genies Involved in Cholesterol
Biosynthesis, Fatty Acid Biosynthesis, and Other Metabolic
Disorders, Genes Encoding Mis-Folded Proteins Involved in Amyloid
and Other Diseases, Oncogenes Leading to Cellular Transformation,
Latent Viral Genes, and Genes Leading to Dominant-Negative
Disorders, Amongst Other Disorders
[0759] Applicants demonstrate gene delivery of a CRISPR-Cas system
in the liver, brain, ocular, epithelial, hematopoetic, or another
tissue of a subject or a patient in need thereof, suffering from
metabolic disorders, amyloidosis and protein-aggregation related
diseases, cellular transformation arising from genetic mutations
and translocations, dominant negative effects of gene mutations,
latent viral infections, and other related symptoms, using either
viral or nanoparticle delivery system.
[0760] Study Design:
[0761] Subjects or patients in need thereof suffering from
metabolic disorders, amyloidosis and protein aggregation related
disease which include but are not limited to human, non-primate
human, canine, feline, bovine, equine, other domestic animals and
related mammals. The CRISPR-Cas system is guided by a chimeric
guide RNA and targets a specific site of the human genomic loci to
be cleaved. After cleavage and non-homologous end-joining mediated
repair, frame-shift mutation results in knock out of genes.
[0762] Applicants select guide-RNAs targeting genes involved in
above-mentioned disorders to be specific to endogenous loci with
minimal off-target activity. Two or more guide RNAs may be encoded
into a single CRISPR array to induce simultaneous double-stranded
breaks in DNA leading to micro-deletions of affected genes or
chromosomal regions.
[0763] Identification and Design of Gene Targets
[0764] For each candidate disease gene, Applicants select DNA
sequences of interest include protein-coding exons, sequences
including and flanking known dominant negative mutation sites,
sequences including and flanking pathological repetitive sequences.
For gene-knockout approaches, early coding exons closest to the
start codon offer best options for achieving complete knockout and
minimize possibility of truncated protein products retaining
partial function.
[0765] Applicants analyze sequences of interest for all possible
targetable 20-bp sequences immediately 5' to a NGG motif (for
SpCas9 system) or a NNAGAAW (for St1Cas9 system). Applicants choose
sequences for unique, single RNA-guided Cas9 recognition in the
genome to minimize off-target effects based on computational
algorithm to determine specificity.
[0766] Cloning of Guide Sequences into a Delivery System
[0767] Guide sequences are synthesized as double-stranded 20-24 bp
oligonucleotides. After 5'-phosphorylation treatment of oligos and
annealing to form duplexes, oligos are ligated into suitable vector
depending on the delivery method:
[0768] Virus-Based Delivery Methods
[0769] AAV-based vectors (PX260, 330, 334, 335) have been described
elsewhere
[0770] Lentiviral-based vectors use a similar cloning strategy of
directly ligating guide sequences into a single vector carrying a
U6 promoter-driven chimeric RNA scaffold and a EF1a promoter-driven
Cas9 or Cas9 nickase.
[0771] Virus production is described elsewhere.
[0772] Nanoparticle-Based RNA Delivery Methods
[0773] 1. Guide sequences are synthesized as an oligonucleotide
duplex encoding T7 promoter-guide sequence-chimeric RNA. A T7
promoter is added 5' of Cas9 by PCR method.
[0774] 2. T7-driven Cas9 and guide-chimeric RNAs are transcribed in
vitro, and Cas9 mRNA is further capped and A-tailed using
commercial kits. RNA products are purified per kit
instructions.
[0775] Hydrodynamic tail vein delivery methods (for mouse)
[0776] Guide sequences are cloned into AAV plasmids as described
above and elsewhere in this application.
[0777] In Vitro Validation on Cell Lines
[0778] Transfection
[0779] 1. DNA Plasmid Transfection
[0780] Plasmids carrying guide sequences are transfected into human
embryonic kidney (HEK293T) or human embryonic stem (hES) cells,
other relevant cell types using lipid-, chemical-, or
electroporation-based methods. For a 24-well transfection of
HEK293T cells (.about.260,000 cells), 500 ng of total DNA is
transfected into each single well using Lipofectamine 2000. For a
12-well transfection of hES cells, 1 ug of total DNA is transfected
into a single well using Fugene HD.
[0781] 2. RNA Transfection
[0782] Purified RNA described above is used for transfection into
HEK293T cells. 1-2 ug of RNA may be transfected into .about.260,000
using Lipofectamine 2000 per manufacturer's instruction. RNA
delivery of Cas9 and chimeric RNA is shown in FIG. 28.
[0783] Assay of Indel Formation In Vitro
[0784] Cells are harvested 72-hours post-transfection and assayed
for indel formation as an indication of double-stranded breaks.
[0785] Briefly, genomic region around target sequence is PCR
amplified (.about.400-600 bp amplicon size) using high-fidelity
polymerase. Products are purified, normalized to equal
concentration, and slowly annealed from 95.degree. C. to 4.degree.
C. to allow formation of DNA heteroduplexes. Post annealing, the
Cel-I enzyme is used to cleave heteroduplexes, and resulting
products are separated on a polyacrylamide gel and indel efficiency
calculated.
[0786] In Vivo Proof of Principle in Animal
[0787] Delivery Mechanisms
[0788] AAV or Lentivirus production is described elsewhere.
[0789] Nanoparticle formulation: RNA mixed into nanoparticle
formulation
[0790] Hydrodynamic tail vein injections with DNA plasmids in mice
are conducted using a commercial kit
[0791] Cas9 and guide sequences are delivered as virus,
nanoparticle-coated RNA mixture, or DNA plasmids, and injected into
subject animals. A parallel set of control animals is injected with
sterile saline, Cas9 and GFP, or guide sequence and GFP alone.
[0792] Three weeks after injection, animals are tested for
amelioration of symptoms and sacrificed. Relevant organ systems
analyzed for indel formation. Phenotypic assays include blood
levels of HDL, LDL, lipids,
[0793] Assay for Indel Formation
[0794] DNA is extracted from tissue using commercial kits; indel
assay will be performed as described for in vitro
demonstration.
[0795] Therapeutic applications of the CRISPR-Cas system are
amenable for achieving tissue-specific and temporally controlled
targeted deletion of candidate disease genes. Examples include
genes involved in cholesterol and fatty acid metabolism, amyloid
diseases, dominant negative diseases, latent viral infections,
among other disorders.
[0796] Examples of a single guide-RNA to introduce targeted indels
at a gene locus
TABLE-US-00021 SEQ Disease GENE SPACER PAM ID NO: Mechanism
References Hypercholesterolemia HMG- GCCAAATTG CGG 109 Knockout
Fluvastatin: a review of its CR GACGACCCT pharmacology and use in
the CG management of hypercholest- erolaemia. (Plosker GL et al.
Drugs 1996, 51(3): 433-459) Hypercholesterolemia SQLE CGAGGAGAC TGG
110 Knockout Potential role of nonstatin CCCCGTTTC cholesterol
lowering agents GG (Trapani et al. IUBMB Life, Volume 63, Issue 11,
pages 964-971, November 2011) Hyperlipidemia DGAT CCCGCCGCC AGG 111
Knockout DGAT1 inhibitors as anti-obesity 1 GCCGTGGCT and
anti-diabetic agents. (Birch CG AM et al. Current Opinion in Drug
Discovery & Development [2010, 13(4): 489-496) Leukemia BCR-
TGAGCTCTA AGG 112 Knockout Killing of leukemic cells with a ABL
CGAGATCCA BCR/ABL fusion gene by RNA CA interference (RNAi). (Fuchs
et al. Oncogene 2002, 21(37): 5716-5724)
[0797] Examples of a pair of guide-RNA to introduce chromosomal
microdeletion at a gene locus
TABLE-US-00022 SEQ Disease GENE SPACER PAM ID NO: Mechanism
References Hyperlipidemia PLIN2 CTCAAAATT TGG 113 Microdeletion
Perilipin-2 Null Mice are guide1 CATACCGGT Protected Against
Diet-Induced TG Obesity, Adipose Inflammation and Fatty Liver
Disease (McManaman JL et al. The Journal of Lipid Research,
jlr.M035063. First Published on Feb. 12, 2013) Hyperlipidemia PLIN2
CGTTAAACA TGG 114 Microdeletion guide2 ACAACCGGA CT Hyperlipidemia
SREBP TTCACCCCG ggg 115 Microdeletion Inhibition of SREBP by a
guide1 CGGCGCTGA Small Molecule, Betulin, AT Improves
Hyperlipidemia and Insulin Resistance and Reduces Atherosclerotic
Plaques (Tang J et al. Cell Metabolism, Volume 13, Issue 1, 44-56,
5 Jan. 2011) Hyperlipidemia SREBP ACCACTACC agg 116 Microdeletion
guide2 AGTCCGTCC AC
Example 19: Targeted Integration of Repair for Genes Carrying
Disease-Causing Mutations; Reconstitution of Enzyme Deficiencies
and Other Related Diseases
[0798] Study Design
[0799] I. Identification and design of gene targets [0800]
Described in Example 22
[0801] II. Cloning of guide sequences and repair templates into a
delivery system [0802] Described above in Example 22 [0803]
Applicants clone DNA repair templates to include homology arms with
diseased allele as well a wild-type repair template
[0804] III. In vitro validation on cell lines [0805] a.
Transfection is described above in Example 22; Cas9, guide RNAs,
and repair template are co-transfected into relevant cell types.
[0806] b. Assay for repair in vitro [0807] i. Applicants harvest
cells 72-hours post-transfection and assay for repair [0808] ii.
Briefly, Applicants amplify genomic region around repair template
PCR using high-fidelity polymerase. Applicants sequence products
for decreased incidence of mutant allele.
[0809] IV. In vivo proof of principle in animal [0810] a. Delivery
mechanisms are described above Examples 22 and 34. [0811] b. Assay
for repair in vivo [0812] i. Applicants perform the repair assay as
described in the in vitro demonstration.
[0813] V. Therapeutic applications [0814] The CRISPR-Cas system is
amenable for achieving tissue-specific and temporally controlled
targeted deletion of candidate disease genes. Examples include
genes involved in cholesterol and fatty acid metabolism, amyloid
diseases, dominant negative diseases, latent viral infections,
among other disorders.
[0815] Example of one single missense mutation with repair
template:
TABLE-US-00023 Disease GENE SPACER PAM Familial amyloid TTR
AGCCTTTCTGAACACATGCA CGG polyneuropathy (SEQ ID NO: 117) Mechanism
References V30M repair Transthyretin mutations in health and
disease (Joao et al. Human Mutation, Volume 5, Issue 3, pages
191-196, 1995) V30M allele CCTGCCATCAATGTGGCCATGCATGTGTTCA GAAAGGCT
(SEQ ID NO: 118) WT allele CCTGCCATCAATGTGGCCGTGCATGTGTTCA GAAAGGCT
(SEQ ID NO: 119)
Example 20: Therapeutic Application of the CRISPR-Cas System in
Glaucoma, Amyloidosis, and Huntington's Disease
[0816] Glaucoma: Applicants design guide RNAs to target the first
exon of the mycilin (MYOC) gene. Applicants use adenovirus vectors
(Ad5) to package both Cas9 as well as a guide RNA targeting the
MYOC gene. Applicants inject adenoviral vectors into the trabecular
meshwork where cells have been implicated in the pathophysiology of
glaucoma. Applicants initially test this out in mouse models
carrying the mutated MYOC gene to see whether they improve visual
acuity and decrease pressure in the eyes. Therapeutic application
in humans employ a similar strategy.
[0817] Amyloidosis: Applicants design guide RNAs to target the
first exon of the transthyretin (TTR) gene in the liver. Applicants
use AAV8 to package Cas9 as well as guide RNA targeting the first
exon of the TTR gene. AAV8 has been shown to have efficient
targeting of the liver and will be administered intravenously. Cas9
can be driven either using liver specific promoters such as the
albumin promoter, or using a constitutive promoter. A pol3 promoter
drives the guide RNA.
[0818] Alternatively, Applicants utilize hydrodynamic delivery of
plasmid DNA to knockout the TTR gene. Applicants deliver a plasmid
encoding Cas9 and the guideRNA targeting Exon1 of TTR.
[0819] As a further alternative approach, Applicants administer a
combination of RNA (mRNA for Cas9, and guide RNA). RNA can be
packaged using liposomes such as Invivofectamine from Life
Technologies and delivered intravenously. To reduce RNA-induced
immunogenicity, increase the level of Cas9 expression and guide RNA
stability, Applicants modify the Cas9 mRNA using 5' capping.
Applicants also incorporate modified RNA nucleotides into Cas9 mRNA
and guide RNA to increase their stability and reduce immunogenicity
(e.g. activation of TLR). To increase efficiency, Applicants
administer multiple doses of the virus, DNA, or RNA.
[0820] Huntington's Disease: Applicants design guide RNA based on
allele specific mutations in the HTT gene of patients. For example,
in a patient who is heterozygous for HTT with expanded CAG repeat,
Applicants identify nucleotide sequences unique to the mutant HTT
allele and use it to design guideRNA. Applicants ensure that the
mutant base is located within the last 9 bp of the guide RNA (which
Applicants have ascertained has the ability to discriminate between
single DNA base mismatches between the target size and the guide
RNA).
[0821] Applicants package the mutant HTT allele specific guide RNA
and Cas9 into AAV9 and deliver into the striatum of Huntington's
patients. Virus is injected into the striatum stereotactically via
a craniotomy. AAV9 is known to transduce neurons efficiently.
Applicants drive Cas9 using a neuron specific promoter such as
human Synapsin I.
Example 21: Therapeutic Application of the CRISPR-Cas System in
HIV
[0822] Chronic viral infection is a source of significant morbidity
and mortality. While there exists for many of these viruses
conventional antiviral therapies that effectively target various
aspects of viral replication, current therapeutic modalities are
usually non-curative in nature due to "viral latency." By its
nature, viral latency is characterized by a dormant phase in the
viral life cycle without active viral production. During this
period, the virus is largely able to evade both immune surveillance
and conventional therapeutics allowing for it to establish
long-standing viral reservoirs within the host from which
subsequent re-activation can permit continued propagation and
transmission of virus. Key to viral latency is the ability to
stably maintain the viral genome, accomplished either through
episomal or proviral latency, which stores the viral genome in the
cytoplasm or integrates it into the host genome, respectively. In
the absence of effective vaccinations which would prevent primary
infection, chronic viral infections characterized by latent
reservoirs and episodes of lytic activity can have significant
consequences: human papilloma virus (HPV) can result in cervical
cancer, hepatitis C virus (HCV) predisposes to hepatocellular
carcinoma, and human immunodeficiency virus eventually destroys the
host immune system resulting in susceptibility to opportunistic
infections. As such, these infections require life-long use of
currently available antiviral therapeutics. Further complicating
matters is the high mutability of many of these viral genomes which
lead to the evolution of resistant strains for which there exists
no effective therapy.
[0823] The CRISPR-Cas system is a bacterial adaptive immune system
able to induce double-stranded DNA breaks (DSB) in a
multiplex-able, sequence-specific manner and has been recently
re-constituted within mammalian cell systems. It has been shown
that targeting DNA with one or numerous guide-RNAs can result in
both indels and deletions of the intervening sequences,
respectively. As such, this new technology represents a means by
which targeted and multiplexed DNA mutagenesis can be accomplished
within a single cell with high efficiency and specificity.
Consequently, delivery of the CRISPR-Cas system directed against
viral DNA sequences could allow for targeted disruption and
deletion of latent viral genomes even in the absence of ongoing
viral production.
[0824] As an example, chronic infection by HIV-1 represents a
global health issue with 33 million individuals infected and an
annual incidence of 2.6 million infections. The use of the
multimodal highly active antiretroviral therapy (HAART), which
simultaneously targets multiple aspects of viral replication, has
allowed HIV infection to be largely managed as a chronic, not
terminal, illness. Without treatment, progression of HIV to AIDS
occurs usually within 9-10 years resulting in depletion of the host
immune system and occurrence of opportunistic infections usually
leading to death soon thereafter. Secondary to viral latency,
discontinuation of HAART invariably leads to viral rebound.
Moreover, even temporary disruptions in therapy can select for
resistant strains of HIV uncontrollable by available means.
Additionally, the costs of HAART therapy are significant: within
the US $10,000-15,0000 per person per year. As such, treatment
approaches directly targeting the HIV genome rather than the
process of viral replication represents a means by which
eradication of latent reservoirs could allow for a curative
therapeutic option.
[0825] Development and delivery of an HIV-1 targeted CRISPR-Cas
system represents a unique approach differentiable from existing
means of targeted DNA mutagenesis, i.e. ZFN and TALENs, with
numerous therapeutic implications. Targeted disruption and deletion
of the HIV-1 genome by CRISPR-mediated DSB and indels in
conjunction with HAART could allow for simultaneous prevention of
active viral production as well as depletion of latent viral
reservoirs within the host.
[0826] Once integrated within the host immune system, the
CRISPR-Cas system allows for generation of a HIV-1 resistant
sub-population that, even in the absence of complete viral
eradication, could allow for maintenance and re-constitution of
host immune activity. This could potentially prevent primary
infection by disruption of the viral genome preventing viral
production and integration, representing a means to "vaccination".
Multiplexed nature of the CRISPR-Cas system allows targeting of
multiple aspects of the genome simultaneously within individual
cells.
[0827] As in HAART, viral escape by mutagenesis is minimized by
requiring acquisition of multiple adaptive mutations concurrently.
Multiple strains of HIV-1 can be targeted simultaneously which
minimizes the chance of super-infection and prevents subsequent
creation of new recombinants strains. Nucleotide, rather than
protein, mediated sequence-specificity of the CRISPR-Cas system
allows for rapid generation of therapeutics without need for
significantly altering delivery mechanism.
[0828] In order to accomplish this, Applicants generate CRISPR-Cas
guide RNAs that target the vast majority of the HIV-1 genome while
taking into account HIV-1 strain variants for maximal coverage and
effectiveness. Sequence analyses of genomic conservation between
HIV-1 subtypes and variants should allow for targeting of flanking
conserved regions of the genome with the aims of deleting
intervening viral sequences or induction of frame-shift mutations
which would disrupt viral gene functions.
[0829] Applicants accomplish delivery of the CRISPR-Cas system by
conventional adenoviral or lentiviral-mediated infection of the
host immune system. Depending on approach, host immune cells could
be a) isolated, transduced with CRISPR-Cas, selected, and
re-introduced in to the host or b) transduced in vivo by systemic
delivery of the CRISPR-Cas system. The first approach allows for
generation of a resistant immune population whereas the second is
more likely to target latent viral reservoirs within the host.
TABLE-US-00024 Examples of potential HIV-1 targeted spacers adapted
from Mcintyre et al, which generated shRNAs against HIV-1 optimized
for maximal coverage of HIV-1 variants. CACTGCTTAAGCCTCGCTCGAGG
(SEQ ID NO: 120) TCACCAGCAATATTCGCTCGAGG (SEQ ID NO: 121)
CACCAGCAATATTCCGCTCGAGG (SEQ ID NO: 122) TAGCAACAGACATACGCTCGAGG
(SEQ ID NO: 123) GGGCAGTAGTAATACGCTCGAGG (SEQ ID NO: 124)
CCAATTCCCATACATTATTGTAC (SEQ ID NO: 125)
Example 22: Targeted Correction of DeltaF508 or Other Mutations in
Cystic Fibrosis
[0830] An aspect of the invention provides for a pharmaceutical
composition that may comprise an CRISPR-Cas gene therapy particle
and a biocompatible pharmaceutical carrier. According to another
aspect, a method of gene therapy for the treatment of a subject
having a mutation in the CFTR gene comprises administering a
therapeutically effective amount of a CRISPR-Cas gene therapy
particle to the cells of a subject.
[0831] This Example demonstrates gene transfer or gene delivery of
a CRISPR-Cas system in airways of subject or a patient in need
thereof, suffering from cystic fibrosis or from cystic fibrosis
related symptoms, using adeno-associated virus (AAV) particles.
[0832] Study Design: Subjects or patients in need there of: Human,
non-primate human, canine, feline, bovine, equine and other
domestic animals, related. This study tests efficacy of gene
transfer of a CRISPR-Cas system by a AAV vector. Applicants
determine transgene levels sufficient for gene expression and
utilize a CRISPR-Cas system comprising a Cas9 enzyme to target
deltaF508 or other CFTR-inducing mutations.
[0833] The treated subjects receive pharmaceutically effective
amount of aerosolized AAV vector system per lung endobronchially
delivered while spontaneously breathing. The control subjects
receive equivalent amount of a pseudotyped AAV vector system with
an internal control gene. The vector system may be delivered along
with a pharmaceutically acceptable or biocompatible pharmaceutical
carrier. Three weeks or an appropriate time interval following
vector administration, treated subjects are tested for amelioration
of cystic fibrosis related symptoms.
[0834] Applicants Use an Adenovirus or an AAV Particle.
[0835] Applicants clone the following gene constructs, each
operably linked to one or more regulatory sequences (Cbh or EF1a
promoter for Cas9, U6 or H1 promoter for chimeric guide RNA), into
one or more adenovirus or AAV vectors or any other compatible
vector: A CFTRdelta508 targeting chimeric guide RNA (FIG. 31B), a
repair template for deltaF508 mutation (FIG. 31C) and a codon
optimized Cas9 enzyme with optionally one or more nuclear
localization signal or sequence(s) (NLS(s)). e.g., two (2)
NLSs.
[0836] Identification of Cas9 Target Site
[0837] Applicants analyzed the human CFTR genomic locus and
identified the Cas9 target site (FIG. 31A). (PAM may contain a NGG
or a NNAGAAW motif).
[0838] Gene Repair Strategy
[0839] Applicants introduce an adenovirus/AAV vector system
comprising a Cas9 (or Cas9 nickase) and the guide RNA along with a
adenovirus/AAV vector system comprising the homology repair
template containing the F508 residue into the subject via one of
the methods of delivery discussed earlier. The CRISPR-Cas system is
guided by the CFTRdelta 508 chimeric guide RNA and targets a
specific site of the CFTR genomic locus to be nicked or cleaved.
After cleavage, the repair template is inserted into the cleavage
site via homologous recombination correcting the deletion that
results in cystic fibrosis or causes cystic fibrosis related
symptoms. This strategy to direct delivery and provide systemic
introduction of CRISPR systems with appropriate guide RNAs can be
employed to target genetic mutations to edit or otherwise
manipulate genes that cause metabolic, liver, kidney and protein
diseases and disorders such as those in Table B.
Example 23: Generation of Gene Knockout Cell Library
[0840] This example demonstrates how to generate a library of cells
where each cell has a single gene knocked out:
[0841] Applicants make a library of ES cells where each cell has a
single gene knocked out, and the entire library of ES cells will
have every single gene knocked out. This library is useful for the
screening of gene function in cellular processes as well as
diseases.
[0842] To make this cell library, Applicants integrate Cas9 driven
by an inducible promoter (e.g. doxycycline inducible promoter) into
the ES cell. In addition, Applicants integrate a single guide RNA
targeting a specific gene in the ES cell. To make the ES cell
library, Applicants simply mix ES cells with a library of genes
encoding guide RNAs targeting each gene in the human genome.
Applicants first introduce a single BxB1 attB site into the AAVS1
locus of the human ES cell. Then Applicants use the BxB1 integrase
to facilitate the integration of individual guide RNA genes into
the BxB1 attB site in AAVS1 locus. To facilitate integration, each
guide RNA gene is contained on a plasmid that carries of a single
attP site. This way BxB1 will recombine the attB site in the genome
with the attP site on the guide RNA containing plasmid.
[0843] To generate the cell library, Applicants take the library of
cells that have single guide RNAs integrated and induce Cas9
expression. After induction, Cas9 mediates double strand break at
sites specified by the guide RNA. To verify the diversity of this
cell library, Applicants carry out whole exome sequencing to ensure
that Applicants are able to observe mutations in every single
targeted gene. This cell library can be used for a variety of
applications, including who library-based screens, or can be sorted
into individual cell clones to facilitate rapid generation of
clonal cell lines with individual human genes knocked out.
Example 24: Engineering of Microalgae Using Cas9
[0844] Methods of Delivering Cas9
[0845] Method 1: Applicants deliver Cas9 and guide RNA using a
vector that expresses Cas9 under the control of a constitutive
promoter such as Hsp70A-Rbc S2 or Beta2-tubulin.
[0846] Method 2: Applicants deliver Cas9 and T7 polymerase using
vectors that expresses Cas9 and T7 polymerase under the control of
a constitutive promoter such as Hsp70A-Rbc S2 or Beta2-tubulin.
Guide RNA will be delivered using a vector containing T7 promoter
driving the guide RNA.
[0847] Method 3: Applicants deliver Cas9 mRNA and in vitro
transcribed guide RNA to algae cells. RNA can be in vitro
transcribed. Cas9 mRNA will consist of the coding region for Cas9
as well as 3'UTR from Cop1 to ensure stabilization of the Cas9
mRNA.
[0848] For Homologous recombination, Applicants provide an
additional homology directed repair template.
[0849] Sequence for a cassette driving the expression of Cas9 under
the control of beta-2 tubulin promoter, followed by the 3' UTR of
Cop1.
TABLE-US-00025 (SEQ ID NO: 126)
TCTTTCTTGCGCTATGACACTTCCAGCAAAAGGTAGGGCGGGCTGCGAGACGGCTTCCCGGCGCTGCATGCAAC-
ACCG
ATGATGCTTCGACCCCCCGAAGCTCCTTCGGGGCTGCATGGGCGCTCCGATGCCGCTCCAGGGCGAGCGCTGTT-
TAAA
TAGCCAGGCCCCCGATTGCAAAGACATTATAGCGAGCTACCAAAGCCATATTCAAACACCTAGATCACTACCAC-
TTCT
ACACAGGCCACTCGAGCTTGTGATCGCACTCCGCTAAGGGGGCGCCTCTTCCTCTTCGTTTCAGTCACAACCCG-
CAAA
CATGTACCCATACGATGTTCCAGATTACGCTTCGCCGAAGAAAAAGCGCAAGGTCGAAGCGTCCGACAAGAAGT-
ACAG
CATCGGCCTGGACATCGGCACCAACTCTGTGGGCTGGGCCGTGATCACCGACGAGTACAAGGTGCCCAGCAAGA-
AATT
CAAGGTGCTGGGCAACACCGACCGGCACAGCATCAAGAAGAACCTGATCGGAGCCCTGCTGTTCGACAGCGGCG-
AAAC
AGCCGAGGCCACCCGGCTGAAGAGAACCGCCAGAAGAAGATACACCAGACGGAAGAACCGGATCTGCTATCTGC-
AAGA
GATCTTCAGCAACGAGATGGCCAAGGTGGACGACAGCTTCTTCCACAGACTGGAAGAGTCCTTCCTGGTGGAAG-
AGGA
TAAGAAGCACGAGCGGCACCCCATCTTCGGCAACATCGTGGACGAGGTGGCCTACCACGAGAAGTACCCCACCA-
TCTA
CCACCTGAGAAAGAAACTGGTGGACAGCACCGACAAGGCCGACCTGCGGCTGATCTATCTGGCCCTGGCCCACA-
TGAT
CAAGTTCCGGGGCCACTTCCTGATCGAGGGCGACCTGAACCCCGACAACAGCGACGTGGACAAGCTGTTCATCC-
AGCT
GGTGCAGACCTACAACCAGCTGTTCGAGGAAAACCCCATCAACGCCAGCGGCGTGGACGCCAAGGCCATCCTGT-
CTGC
CAGACTGAGCAAGAGCAGACGGCTGGAAAATCTGATCGCCCAGCTGCCCGGCGAGAAGAAGAATGGCCTGTTCG-
GCAA
CCTGATTGCCCTGAGCCTGGGCCTGACCCCCAACTTCAAGAGCAACTTCGACCTGGCCGAGGATGCCAAACTGC-
AGCT
GAGCAAGGACACCTACGACGACGACCTGGACAACCTGCTGGCCCAGATCGGCGACCAGTACGCCGACCTGTTTC-
TGGC
CGCCAAGAACCTGTCCGACGCCATCCTGCTGAGCGACATCCTGAGAGTGAACACCGAGATCACCAAGGCCCCCC-
TGAG
CGCCTCTATGATCAAGAGATACGACGAGCACCACCAGGACCTGACCCTGCTGAAAGCTCTCGTGCGGCAGCAGC-
TGCC
TGAGAAGTACAAAGAGATTTTCTTCGACCAGAGCAAGAACGGCTACGCCGGCTACATTGACGGCGGAGCCAGCC-
AGGA
AGAGTTCTACAAGTTCATCAAGCCCATCCTGGAAAAGATGGACGGCACCGAGGAACTGCTCGTGAAGCTGAACA-
GAGA
GGACCTGCTGCGGAAGCAGCGGACCTTCGACAACGGCAGCATCCCCCACCAGATCCACCTGGGAGAGCTGCACG-
CCAT
TCTGCGGCGGCAGGAAGATTTTTACCCATTCCTGAAGGACAACCGGGAAAAGATCGAGAAGATCCTGACCTTCC-
GCAT
CCCCTACTACGTGGGCCCTCTGGCCAGGGGAAACAGCAGATTCGCCTGGATGACCAGAAAGAGCGAGGAAACCA-
TCAC
CCCCTGGAACTTCGAGGAAGTGGTGGACAAGGGCGCTTCCGCCCAGAGCTTCATCGAGCGGATGACCAACTTCG-
ATAA
GAACCTGCCCAACGAGAAGGTGCTGCCCAAGCACAGCCTGCTGTACGAGTACTTCACCGTGTATAACGAGCTGA-
CCAA
AGTGAAATACGTGACCGAGGGAATGAGAAAGCCCGCCTTCCTGAGCGGCGAGCAGAAAAAGGCCATCGTGGACC-
TGCT
GTTCAAGACCAACCGGAAAGTGACCGTGAAGCAGCTGAAAGAGGACTACTTCAAGAAAATCGAGTGCTTCGACT-
CCGT
GGAAATCTCCGGCGTGGAAGATCGGTTCAACGCCTCCCTGGGCACATACCACGATCTGCTGAAAATTATCAAGG-
ACAA
GGACTTCCTGGACAATGAGGAAAACGAGGACATTCTGGAAGATATCGTGCTGACCCTGACACTGTTTGAGGACA-
GAGA
GATGATCGAGGAACGGCTGAAAACCTATGCCCACCTGTTCGACGACAAAGTGATGAAGCAGCTGAAGCGGCGGA-
GATA
CACCGGCTGGGGCAGGCTGAGCCGGAAGCTGATCAACGGCATCCGGGACAAGCAGTCCGGCAAGACAATCCTGG-
ATTT
CCTGAAGTCCGACGGCTTCGCCAACAGAAACTTCATGCAGCTGATCCACGACGACAGCCTGACCTTTAAAGAGG-
ACAT
CCAGAAAGCCCAGGTGTCCGGCCAGGGCGATAGCCTGCACGAGCACATTGCCAATCTGGCCGGCAGCCCCGCCA-
TTAA
GAAGGGCATCCTGCAGACAGTGAAGGTGGTGGACGAGCTCGTGAAAGTGATGGGCCGGCACAAGCCCGAGAACA-
TCGT
GATCGAAATGGCCAGAGAGAACCAGACCACCCAGAAGGGACAGAAGAACAGCCGCGAGAGAATGAAGCGGATCG-
AAGA
GGGCATCAAAGAGCTGGGCAGCCAGATCCTGAAAGAACACCCCGTGGAAAACACCCAGCTGCAGAACGAGAAGC-
TGTA
CCTGTACTACCTGCAGAATGGGCGGGATATGTACGTGGACCAGGAACTGGACATCAACCGGCTGTCCGACTACG-
ATGT
GGACCATATCGTGCCTCAGAGCTTTCTGAAGGACGACTCCATCGACAACAAGGTGCTGACCAGAAGCGACAAGA-
ACCG
GGGCAAGAGCGACAACGTGCCCTCCGAAGAGGTCGTGAAGAAGATGAAGAACTACTGGCGGCAGCTGCTGAACG-
CCAA
GCTGATTACCCAGAGAAAGTTCGACAATCTGACCAAGGCCGAGAGAGGCGGCCTGAGCGAACTGGATAAGGCCG-
GCTT
CATCAAGAGACAGCTGGTGGAAACCCGGCAGATCACAAAGCACGTGGCACAGATCCTGGACTCCCGGATGAACA-
CTAA
GTACGACGAGAATGACAAGCTGATCCGGGAAGTGAAAGTGATCACCCTGAAGTCCAAGCTGGTGTCCGATTTCC-
GGAA
GGATTTCCAGTTTTACAAAGTGCGCGAGATCAACAACTACCACCACGCCCACGACGCCTACCTGAACGCCGTCG-
TGGG
AACCGCCCTGATCAAAAAGTACCCTAAGCTGGAAAGCGAGTTCGTGTACGGCGACTACAAGGTGTACGACGTGC-
GGAA
GATGATCGCCAAGAGCGAGCAGGAAATCGGCAAGGCTACCGCCAAGTACTTCTTCTACAGCAACATCATGAACT-
TTTT
CAAGACCGAGATTACCCTGGCCAACGGCGAGATCCGGAAGCGGCCTCTGATCGAGACAAACGGCGAAACCGGGG-
AGAT
CGTGTGGGATAAGGGCCGGGATTTTGCCACCGTGCGGAAAGTGCTGAGCATGCCCCAAGTGAATATCGTGAAAA-
AGAC
CGAGGTGCAGACAGGCGGCTTCAGCAAAGAGTCTATCCTGCCCAAGAGGAACAGCGATAAGCTGATCGCCAGAA-
AGAA
GGACTGGGACCCTAAGAAGTACGGCGGCCTTCGACAGCCCCACCGTGGCCTATTCTGTGCTGGTGGTGGCCAAA-
GTGG
AAAAGGGCAAGTCCAAGAAACTGAAGAGTGTGAAAGAGCTGCTGGGGATCACCATCATGGAAAGAAGCAGCTTC-
GAGA
AGAATCCCATCGACTTTCTGGAAGCCAAGGGCTACAAAGAAGTGAAAAAGGACCTGATCATCAAGCTGCCTAAG-
TACT
CCCTGTTCGAGCTGGAAAACGGCCGGAAGAGAATGCTGGCCTCTGCCGGCGAACTGCAGAAGGGAAACGAACTG-
GCCC
TGCCCTCCAAATATGTGAACTTCCTGTACCTGGCCAGCCACTATGAGAAGCTGAAGGGCTCCCCCGAGGATAAT-
GAGC
AGAAACAGCTGTTTGTGGAACAGCACAAGCACTACCTGGACGAGATCATCGAGCAGATCAGCGAGTTCTCCAAG-
AGAG
TGATCCTGGCCGACGCTAATCTGGACAAAGTGCTGTCCGCCTACAACAAGCACCGGGATAAGCCCATCAGAGAG-
CAGG
CCGAGAATATCATCCACCTGTTTACCCTGACCAATCTGGGAGCCCCTGCCGCCTTCAAGTACTTTGACACCACC-
ATCG
ACCGGAAGAGGTACACCAGCACCAAAGAGGTGCTGGACGCCACCCTGATCCACCAGAGCATCACCGGCCTGTAC-
GAGA
CACGGATCGACCTGTCTCAGCTGGGAGGCGACAGCCCCAAGAAGAAGAGAAAGGTGGAGGCCAGCTAAGGATCC-
GGCA
AGACTGGCCCCGCTTGGCAACGCAACAGTGAGCCCCTCCCTAGTGTGTTTGGGGATGTGACTATGTATTCGTGT-
GTTG
GCCAACGGGTCAACCCGAACAGATTGATACCCGCCTTGGCATTTCCTGTCAGAATGTAACGTCAGTTGATGGTA-
CT
[0850] Sequence for a cassette driving the expression of T7
polymerase under the control of beta-2 tubulin promoter, followed
by the 3' UTR of Cop1:
TABLE-US-00026 (SEQ ID NO: 127)
TCTTTCTTGCGCTATGACACTTCCAGCAAAAGGTAGGGCGGGCTGCGAGACGGCTTCCCGGCGTGCATGCAA
CACCGATGATGCTTCGACCCCCCGAAGCTCCTTCGGGGCTGCATGGGCGCTCCGATGCCGCTCCAGGGCGAG
CGCTGTTTAAATAGCCAGGCCCCCGATTGCAAAGACATTATAGCGAGCTACCAAAGCCATATTCAAACACCT
AGATCACTACCACTTCTACACAGGCCACTCGAGCTTGTGATCGCACTCCGCTAAGGGGGCGCCTCTTCCTCT
TCGTTTCAGTCACAACCCGCAAACatgcctaagaagaagaggaaggttaacacgattaacatcgctaagaac
gacttctctgacatcgaactggctgctatcccgttcaacactctggctgaccattacggtgagcgtttagct
cgcgaacagttggcccttgagcatgagtcttacgagatgggtgaagcacgcttccgcaagatgtttgagcgt
caacttaaagctggtgaggttgcggataacgctgccgccaagcctctcatcactaccctactccctaagatg
attgcacgcatcaacgactggtttgaggaagtgaaagctaagcgcggcaagcgcccgacagccttccagttc
ctgcaagaaatcaagccggaagccgtagcgtacatcaccattaagaccactctggcttgcctaaccagtgct
gacaatacaaccgttcaggctgtagcaagcgcaatcggtcgggccattgaggacgaggctcgcttcggtcgt
atccgtgaccttgaagctaagcacttcaagaaaaacgttgaggaacaactcaacaagcgcgtagggcacgtc
tacaagaaagcatttatgcaagttgtcgaggctgacatgctctctaagggtctactcggtggcgaggcgtgg
tcttcgtggcataaggaagactctattcatgtaggagtacgctgcatcgagatgctcattgagtcaaccgga
atggttagcttacaccgccaaaatgctggcgtagtaggtcaagactctgagactatcgaactcgcacctgaa
tacgctgaggctatcgcaacccgtgcaggtgcgctggctggcatctctccgatgttccaaccttgcgtagtt
cctcctaagccgtggactggcattactggtggtggctattgggctaacggtcgtcgtcctctggcgctggtg
cgtactcacagtaagaaagcactgatgcgctacgaagacgtttacatgcctgaggtgtacaaagcgattaac
attgcgcaaaacaccgcatggaaaatcaacaagaaagtcctagcggtcgccaacgtaatcaccaagtggaag
cattgtccggtcgaggacatccctgcgattgagcgtgaagaactcccgatgaaaccggaagacatcgacatg
aatcctgaggctctcaccgcgtggaaacgtgctgccgctgctgtgtaccgcaaggacaaggctcgcaagtct
cgccgtatcagccttgagttcatgcttgagcaagccaataagtttgctaaccataaggccatctggttccct
tacaacatggactggcgcggtcgtgtttacgctgtgtcaatgttcaacccgcaaggtaacgatatgaccaaa
ggactgcttacgctggcgaaaggtaaaccaatcggtaaggaaggttactactggctgaaaatccacggtgca
aactgtgcgggtgtcgacaaggttccgttccctgagcgcatcaagttcattgaggaaaaccacgagaacatc
atggcttgcgctaagtctccactggagaacacttggtgggctgagcaagattctccgttctgcttccttgcg
ttctgctttgagtacgctggggtacagcaccacggcctgagctataactgctcccttccgctggcgtttgac
gggtcttgctctggcatccagcacttctccgcgatgctccgagatgaggtaggtggtcgcgcggttaacttg
cttcctagtgaaaccgttcaggacatctacgggattgttgctaagaaagtcaacgagattctacaagcagac
gcaatcaatgggaccgataacgaagtagttaccgtgaccgatgagaacactggtgaaatctctgagaaagtc
aagctgggcactaaggcactggctggtcaatggctggcttacggtgttactcgcagtgtgactaagcgttca
gtcatgacgctggcttacgggtccaaagagttcggcttccgtcaacaagtgctggaagataccattcagcca
gctattgattccggcaagggtctgatgttcactcagccgaatcaggctgctggatacatggctaagctgatt
tgggaatctgtgagcgtgacggtggtagctgcggttgaagcaatgaactggcttaagtctgctgctaagctg
ctggctgctgaggtcaaagataagaagactggagagattcttcgcaagcgttgcgctgtgcattgggtaact
cctgatggtttccctgtgtggcaggaatacaagaagcctattcagacgcgcttgaacctgatgttcctcggt
cagttccgcttacagcctaccattaacaccaacaaagatagcgagattgatgcacacaaacaggagtctggt
atcgctcctaactttgtacacagccaagacggtagccaccttcgtaagactgtagtgtgggcacacgagaag
tacggaatcgaatcttttgcactgattcacgactccttcggtacgattccggctgacgctgcgaacctgttc
aaagcagtgcgcgaaactatggttgacacatatgagtcttgtgatgtactggctgatttctacgaccagttc
gctgaccagttgcacgagtctcaattggacaaaatgccagcacttccggctaaaggtaacttgaacctccgt
gacattcttagagtcggacttcgcgttcgcgtaaGGATCCGGCAAGACTGGCCCCGCTTGGCAACGCAACAG
TGAGCCCCTCCCTAGTGTGTTTGGGGATGTGACTATGTATTCGTGTGTTGGCCAACGGGTCAACCCGAACAG
ATTGATACCCGCCTTGGCATTTCCTGTCAGAATGTAACGTCAGTTGATGGTACT
[0851] Sequence of guide RNA driven by the T7 promoter (T7
promoter, Ns represent targeting sequence):
TABLE-US-00027 (SEQ ID NO: 128)
gaaatTAATACGACTCACTATANNNNNNNNNNNNNNNNNNNNgttttag
agctaGAAAtagcaagttaaaataaggctagtccgttatcaacttgaaa
aagtggcaccgagtcggtgcttttttt
[0852] Gene Delivery:
[0853] Chlamydomonas reinhardtii strain CC-124 and CC-125 from the
Chlamydomonas Resource Center will be used for electroporation.
Electroporation protocol follows standard recommended protocol from
the GeneArt Chlamydomonas Engineering kit.
[0854] Also, Applicants generate a line of Chlamydomonas
reinhardtii that expresses Cas9 constitutively. This can be done by
using pChlamy1 (linearized using PvuI) and selecting for hygromycin
resistant colonies. Sequence for pChlamy1 containing Cas9 is below.
In this way to achieve gene knockout one simply needs to deliver
RNA for the guideRNA. For homologous recombination Applicants
deliver guideRNA as well as a linearized homologous recombination
template.
[0855] pChlamy1-Cas9:
TABLE-US-00028 (SEQ ID NO: 129)
TGCGGTATTTCACACCGCATCAGGTGGCACTTTTCGGGGAAATGTGCGCGGAACCCCTATTTGTTTATTTTTCT-
AAAT
ACATTCAAATATGTATCCGCTCATGAGATTATCAAAAAGGATCTTCACCTAGATCCTTTTAAATTAAAAATGAA-
GTTT
TAAATCAATCTAAAGTATATATGAGTAAACTTGGTCTGACAGTTACCAATGCTTAATCAGTGAGGCACCTATCT-
CAGC
GATCTGTCTATTTCGTTCATCCATAGTTGCCTGACTCCCCGTCGTGTAGATAACTACGATACGGGAGGGCTTAC-
CATC
TGGCCCCAGTGCTGCAATGATACCGCGAGACCCACGCTCACCGGCTCCAGATTTATCAGCAATAAACCAGCCAG-
CCGG
AAGGGCCGAGCGCAGAAGTGGTCCTGCAACTTTATCCGCCTCCATCCAGTCTATTAATTGTTGCCGGGAAGCTA-
GAGT
AAGTAGTTCGCCAGTTAATAGTTTGCGCAACGTTGTTGCCATTGCTACAGGCATCGTGGTGTCACGCTCGTCGT-
TTGG
TATGGCTTCATTCAGCTCCGGTTCCCAACGATCAAGGCGAGTTACATGATCCCCCATGTTGTGCAAAAAAGCGG-
TTAG
CTCCTTCGGTCCTCCGATCGTTGTCAGAAGTAAGTTGGCCGCAGTGTTATCACTCATGGTTATGGCAGCACTGC-
ATAA
TTCTCTTACTGTCATGCCATCCGTAAGATGCTTTTCTGTGACTGGTGAGTACTCAACCAAGTCATTCTGAGAAT-
AGTG
TATGCGGCGACCGAGTTGCTCTTGCCCGGCGTCAATACGGGATAATACCGCGCCACATAGCAGAACTTTAAAAG-
TGCT
CATCATTGGAAAACGTTCTTCGGGGCGAAAACTCTCAAGGATCTTACCGCTGTTGAGATCCAGTTCGATGTAAC-
CCAC
TCGTGCACCCAACTGATCTTCAGCATCTTTTACTTTCACCAGCGTTTCTGGGTGAGCAAAAACAGGAAGGCAAA-
ATGC
CGCAAAAAAGGGAATAAGGGCGACACGGAAATGTTGAATACTCATACTCTTCCTTTTTCAATATTATTGAAGCA-
TTTA
TCAGGGTTATTGTCTCATGACCAAAATCCCTTAACGTGAGTTTTCGTTCCACTGAGCGTCAGACCCCGTAGAAA-
AGAT
CAAAGGATCTTCTTGAGATCCTTTTTTTCTGCGCGTAATCTGCTGCTTGCAAACAAAAAAACCACCGCTACCAG-
CGGT
GGTTTGTTTGCCGGATCAAGAGCTACCAACTCTTTTTCCGAAGGTAACTGGCTTCAGCAGAGCGCAGATACCAA-
ATAC
TGTTCTTCTAGTGTAGCCGTAGTTAGGCCACCACTTCAAGAACTCTGTAGCACCGCCTACATACCTCGCTCTGC-
TAAT
CCTGTTACCAGTGGCTGTTGCCAGTGGCGATAAGTCGTGTCTTACCGGGTTGGACTCAAGACGATAGTTACCGG-
ATAA
GGCGCAGCGGTCGGGCTGAACGGGGGGTTCGTGCACACAGCCCAGCTTGGAGCGAACGACCTACACCGAACTGA-
GATA
CCTACAGCGTGAGCTATGAGAAAGCGCCACGCTTCCCGAAGGGAGAAAGGCGGACAGGTATCCGGTAAGCGGCA-
GGGT
CGGAACAGGAGAGCGCACGAGGGAGCTTCCAGGGGGAAACGCCTGGTATCTTTATAGTCCTGTCGGGTTTCGCC-
ACCT
CTGACTTGAGCGTCGATTTTTGTGATGCTCGTCAGGGGGGCGGAGCCTATGGAAAAACGCCAGCAACGCGGCCT-
TTTT
ACGGTTCCTGGCCTTTTGCTGGCCTTTTGCTCACATGTTCTTTCCTGCGTTATCCCCTGATTCTGTGGATAACC-
GTAT
TACCGCCTTTGAGTGAGCTGATACCGCTCGCCGCAGCCGAACGACCGAGCGCAGCGAGTCAGTGAGCGAGGAAG-
CGGT
CGCTGAGGCTTGACATGATTGGTGCGTATGTTTGTATGAAGCTACAGGACTGATTTGGCGGGCTATGAGGGCGG-
GGGA
AGCTCTGGAAGGGCCGCGATGGGGCGCGCGGCGTCCAGAAGGCGCCATACGGCCCGCTGGCGGCACCCATCCGG-
TATA
AAAGCCCGCGACCCCGAACGGTGACCTCCACTTTCAGCGACAAACGAGCACTTATACATACGCGACTATTCTGC-
CGCT
ATACATAACCACTCAGCTAGCTTAAGATCCCATCAAGCTTGCATGCCGGGCGCGCCAGAAGGAGCGCAGCCAAA-
CCAG
GATGATGTTTGATGGGGTATTTGAGCACTTGCAACCCTTATCCGGAAGCCCCCTGGCCCACAAAGGCTAGGCGC-
CAAT
GCAAGCAGTTCGCATGCAGCCCCTGGAGCGGTGCCCTCCTGATAAACCGGCCAGGGGGCCTATGTTCTTTACTT-
TTTT
ACAAGAGAAGTCACTCAACATCTTAAAATGGCCAGGTGAGTCGACGAGCAAGCCCGGCGGATCAGGCAGCGTGC-
TTGC
AGATTTGACTTGCAACGCCCGCATTGTGTCGACGAAGGCTTTTGGCTCCTCTGTCGCTGTCTCAAGCAGCATCT-
AACC
CTGCGTCGCCGTTTCCATTTGCAGGAGATTCGAGGTACCATGTACCCATACGATGTTCCAGATTACGCTTCGCC-
GAAG
AAAAAGCGCAAGGTCGAAGCGTCCGACAAGAAGTACAGCATCGGCCTGGACATCGGCACCAACTCTGTGGGCTG-
GGCC
GTGATCACCGACGAGTACAAGGTGCCCAGCAAGAAATTCAAGGTGCTGGGCAACACCGACCGGCACAGCATCAA-
GAAG
AACCTGATCGGAGCCCTGCTGTTCGACAGCGGCGAAACAGCCGAGGCCACCCGGCTGAAGAGAACCGCCAGAAG-
AAGA
TACACCAGACGGAAGAACCGGATCTGCTATCTGCAAGAGATCTTCAGCAACGAGATGGCCAAGGTGGACGACAG-
CTTC
TTCCACAGACTGGAAGAGTCCTTCCTGGTGGAAGAGGATAAGAAGCACGAGCGGCACCCCATCTTCGGCAACAT-
CGTG
GACGAGGTGGCCTACCACGAGAAGTACCCCACCATCTACCACCTGAGAAAGAAACTGGTGGACAGCACCGACAA-
GGCC
GACCTGCGGCTGATCTATCTGGCCCTGGCCCACATGATCAAGTTCCGGGGCCACTTCCTGATCGAGGGCGACCT-
GAAC
CCCGACAACAGCGACGTGGACAAGCTGTTCATCCAGCTGGTGCAGACCTACAACCAGCTGTTCGAGGAAAACCC-
CATC
AACGCCAGCGGCGTGGACGCCAAGGCCATCCTGTCTGCCAGACTGAGCAAGAGCAGACGGCTGGAAAATCTGAT-
CGCC
CAGCTGCCCGGCGAGAAGAAGAATGGCCTGTTCGGCAACCTGATTGCCCTGAGCCTGGGCCTGACCCCCAACTT-
CAAG
AGCAACTTCGACCTGGCCGAGGATGCCAAACTGCAGCTGAGCAAGGACACCTACGACGACGACCTGGACAACCT-
GCTG
GCCCAGATCGGCGACCAGTACGCCGACCTGTTTCTGGCCGCCAAGAACCTGTCCGACGCCATCCTGCTGAGCGA-
CATC
CTGAGAGTGAACACCGAGATCACCAAGGCCCCCCTGAGCGCCTCTATGATCAAGAGATACGACGAGCACCACCA-
GGAC
CTGACCCTGCTGAAAGCTCTCGTGCGGCAGCAGCTGCCTGAGAAGTACAAAGAGATTTTCTTCGACCAGAGCAA-
GAAC
GGCTACGCCGGCTACATTGACGGCGGAGCCAGCCAGGAAGAGTTCTACAAGTTCATCAAGCCCATCCTGGAAAA-
GATG
GACGGCACCGAGGAACTGCTCGTGAAGCTGAACAGAGAGGACCTGCTGCGGAAGCAGCGGACCTTCGACAACGG-
CAGC
ATCCCCCACCAGATCCACCTGGGAGAGCTGCACGCCATTCTGCGGCGGCAGGAAGATTTTTACCCATTCCTGAA-
GGAC
AACCGGGAAAAGATCGAGAAGATCCTGACCTTCCGCATCCCCTACTACGTGGGCCCTCTGGCCAGGGGAAACAG-
CAGA
TTCGCCTGGATGACCAGAAAGAGCGAGGAAACCATCACCCCCTGGAACTTCGAGGAAGTGGTGGACAAGGGCGC-
TTCC
GCCCAGAGCTTCATCGAGCGGATGACCAACTTCGATAAGAACCTGCCCAACGAGAAGGTGCTGCCCAAGCACAG-
CCTG
CTGTACGAGTACTTCACCGTGTATAACGAGCTGACCAAAGTGAAATACGTGACCGAGGGAATGAGAAAGCCCGC-
CTTC
CTGAGCGGCGAGCAGAAAAAGGCCATCGTGGACCTGCTGTTCAAGACCAACCGGAAAGTGACCGTGAAGCAGCT-
GAAA
GAGGACTACTTCAAGAAAATCGAGTGCTTCGACTCCGTGGAAATCTCCGGCGTGGAAGATCGGTTCAACGCCTC-
CCTG
GGCACATACCACGATCTGCTGAAAATTATCAAGGACAAGGACTTCCTGGACAATGAGGAAAACGAGGACATTCT-
GGAA
GATATCGTGCTGACCCTGACACTGTTTGAGGACAGAGAGATGATCGAGGAACGGCTGAAAACCTATGCCCACCT-
GTTC
GACGACAAAGTGATGAAGCAGCTGAAGCGGCGGAGATACACCGGCTGGGGCAGGCTGAGCCGGAAGCTGATCAA-
CGGC
ATCCGGGACAAGCAGTCCGGCAAGACAATCCTGGATTTCCTGAAGTCCGACGGCTTCGCCAACAGAAACTTCAT-
GCAG
CTCTGATCCACGACGACAGCCTGACCTTTAAAGAGGACATCCAGAAAGCCCAGGTGTCCGGCCAGGGCGATAGC-
CTGC
ACGAGCACATTGCCAATCTGGCCGGCAGCCCCGCCATTAAGAAGGGCATCCTGCAGACAGTGAAGGTGGTGGAC-
GAGC
TCGTGAAAGTGATGGGCCGGCACAAGCCCGAGAACATCGTGATCGAAATGGCCAGAGAGAACCAGACCACCCAG-
AAGG
GACAGAAGAACAGCCGCGAGAGAATGAAGCGGATCGAAGAGGGCATCAAAGAGCTGGGCAGCCAGATCCTGAAA-
GAAC
ACCCCGTGGAAAACACCCAGCTGCAGAACGAGAAGCTGTACCTGTACTACCTGCAGAATGGGCGGGATATGTAC-
GTGG
ACCAGGAACTGGACATCAACCGGCTGTCCGACTACGATGTGGACCATATCGTGCCTCAGAGCTTTCTGAAGGAC-
GACT
CCATCGACAACAAGGTGCTGACCAGAAGCGACAAGAACCGGGGCAAGAGCGACAACGTGCCCTCCGAAGAGGTC-
GTGA
AGAAGATGAAGAACTACTGGCGGCAGCTGCTGAACGCCAAGCTGATTACCCAGAGAAAGTTCGACAATCTGACC-
AAGG
CCGAGAGAGGCGGCCTGAGCGAACTGGATAAGGCCGGCTTCATCAAGAGACAGCTGGTGGAAACCCGGCAGATC-
ACAA
AGCACGTGGCACAGATCCTGGACTCCCGGATGAACACTAAGTACGACGAGAATGACAAGCTGATCCGGGAAGTG-
AAAG
TGATCACCCTGAAGTCCAAGCTGGTGTCCGATTTCCGGAAGGATTTCCAGTTTTACAAAGTGCGCGAGATCAAC-
AACT
ACCACCACGCCCACGACGCCTACCTGAACGCCGTCGTGGGAACCGCCCTGATCAAAAAGTACCCTAAGCTGGAA-
AGCG
AGTTCGTGTACGGCGACTACAAGGTGTACGACGTGCGGAAGATGATCGCCAAGAGCGAGCAGGAAATCGGCAAG-
GCTA
CCGCCAAGTACTTCTTCTACAGCAACATCATGAACTTTTTCAAGACCGAGATTACCCTGGCCAACGGCGAGATC-
CGGA
AGCGGCCTCTGATCGAGACAAACGGCGAAACCGGGGAGATCGTGTGGGATAAGGGCCGGGATTTTGCCACCGTG-
CGGA
AAGTGCTGAGCATGCCCCAAGTGAATATCGTGAAAAAGACCGAGGTGCAGACAGGCGGCTTCAGCAAGAGTCTA-
TCCT
GCCCAAGAGGAACAGCGATAAGCTGATCGCCAGAAAGAAGGACTGGGACCCTAAGAAGTACGGCGGCTTCGACA-
GCCC
CACCGTGGCCTATTCTGTGCTGGTGGTGGCCAAAGTGGAAAAGGGCAAGTCCAAGAAACTGAAGAGTGTGAAAG-
AGCT
GCTGGGGATCACCATCATGGAAAGAAGCAGCTTCGAGAAGAATCCCATCGACTTTCTGGAAGCCAAGGGCTACA-
AAGA
AGTGAAAAAGGACCTGATCATCAAGCTGCCTAAGTACTCCCTGTTCGAGCTGGAAAACGGCCGGAAGAGAATGC-
TGGC
CTCTGCCGGCGAACTGCAGAAGGGAAACGAACTGGCCCTGCCCTCCAAATATGTGAACTTCCTGTACCTGGCCA-
GCCA
CTATGAGAAGCTGAAGGGCTCCCCCGAGGATAATGAGCAGAAACAGCTGTTTGTGGAACAGCACAAGCACTACC-
TGGA
CGAGATCATCGAGCAGATCAGCGAGTTCTCCAAGAGAGTGATCCTGGCCGACGCTAATCTGGACAAAGTGCTGT-
CCGC
CTACAACAAGCACCGGGATAAGCCCATCAGAGAGCAGGCCGAGAATATCATCCACCTGTTTACCCTGACCAATC-
TGGG
AGCCCCTGCCGCCTTCAAGTACTTTGACACCACCATCGACCGGAAGAGGTACACCAGCACCAAAGAGGTGCTGG-
ACGC
CACCCTGATCCACCAGAGCATCACCGGCCTGTACGAGACACGGATCGACCTGTCTCAGCTGGGAGGCGACAGCC-
CCAA
GAAGAAGAGAAAGGTGGAGGCCAGCTAACATATGATTCGAATGTCTTTCTTGCGCTATGACACTTCCAGCAAAA-
GGTA
GGGCGGGCTGCGAGACGGCTTCCCGGCGCTGCATGCAACACCGATGATGCTTCGACCCCCCGAAGCTCCTTCGG-
GGCT
GCATGGGCGCTCCGATGCCGCTCCAGGGCGAGCGCTGTTTAAATAGCCAGGCCCCCGATTGCAAAGACATTATA-
GCGA
GCTACCAAAGCCATATTCAAACACCTAGATCACTACCACTTCTACACAGGCCACTCGAGCTTGTGATCGCACTC-
CGCT
AAGGGGGCGCCTCTTCCTCTTCGTTTCAGTCACAACCCGCAAACATGACACAAGAATCCCTGTTACTTCTCGAC-
CGTA
TTGATTCGGATGATTCCTACGCGAGCCTGCGGAACGACCAGGAATTCTGGGAGGTGAGTCGACGAGCAAGCCCG-
GCGG
ATCAGGCAGCGTGCTTGCAGATTTGACTTGCAACGCCCGCATTGTGTCGACGAAGGCTTTTGGCTCCTCTGTCG-
CTGT
CTCAAGCAGCATCTAACCCTGCGTCGCCGTTTCCATTTGCAGCCGCTGGCCCGCCGAGCCCTGGAGGAGCTCGG-
GCTG
CCGGTGCCGCCGGTGCTGCGGGTGCCCGGCGAGAGCACCAACCCCGTACTGGTCGGCGAGCCCGGCCCGGTGAT-
CAAG
CTGTTCGGCGAGCACTGGTGCGGTCCGGAGAGCCTCGCGTCGGAGTCGGAGGCGTACGCGGTCCTGGCGGACGC-
CCCG
GTGCCGGTGCCCCGCCTCCTCGGCCGCGGCGAGCTGCGGCCCGGCACCGGAGCCTGGCCGTGGCCCTACCTGGT-
GATG
AGCCGGATGACCGGCACCACCTGGCGGTCCGCGATGGACGGCACGACCGACCGGAACGCGCTGCTCGCCCTGGC-
CCGC
GAACTCGGCCGGGTGCTCGGCCGGCTGCACAGGGTGCCGCTGACCGGGAACACCGTGCTCACCCCCCATTCCGA-
GGTC
TTCCCGGAACTGCTGCGGGAACGCCGCGCGGCGACCGTCGAGGACCACCGCGGGTGGGGCTACCTCTCGCCCCG-
GCTG
CTGGACCGCCTGGAGGACTGGCTGCCGGACGTGGACACGCTGCTGGCCGGCCGCGAACCCCGGTTCGTCCACGG-
CGAC
CTGCACGGGACCAACATCTTCGTGGACCTGGCCGCGACCGAGGTCACCGGGATCGTCGACTTCACCGACGTCTA-
TGCG
GGAGATCTCCCGCTACAGCCTGGTGCAACTGCATCTCAACGCCTTCCGGGGCGACCGCGAGATCCTGGCCGCGC-
TGCT
CGACGGGGCGCAGTGGAAGCGGACCGAGGACTTCGCCCGCGAACTGCTCGCCTTCACCTTCCTGCACGACTTCG-
AGGT
GTTCGAGGAGACCCCGCTGGATCTCTCCGGCTTCACCGATCCGGAGGAACTGGCGCAGTTCCTCTGGGGGCCGC-
CGGA
CACCGCCCCCGGCGCCTGATAAGGATCCGGCAAGACTGGCCCCGCTTGGCAACGCAACAGTGAGCCCCTCCCTA-
GTGT
GTTTGGGGATGTGACTATGTATTCGTGTGTTGGCCAACGGGTCAACCCGAACAGATTGATACCCGCCTTGGCAT-
TTCC TGTCAGAATGTAACGTCAGTTGATGGTACT
[0856] For all modified Chlamydomonas reinhardtii cells, Applicants
use PCR1 SURVEYOR nuclease assay, and DNA sequencing to verify
successful modification.
Example 25: Use of Cas9 to Target a Variety of Disease Types
[0857] Diseases that involve mutations in protein coding
sequence:
[0858] Dominant disorders may be targeted by inactivating the
dominant negative allele. Applicants use Cas9 to target a unique
sequence in the dominant negative allele and introduce a mutation
via NHEJ. The NHEJ-induced indel may be able to introduce a
frame-shift mutation in the dominant negative allele and eliminate
the dominant negative protein. This may work if the gene is
haplo-sufficient (e.g. MYOC mutation induced glaucoma and
Huntington's disease).
[0859] Recessive disorders may be targeted by repairing the disease
mutation in both alleles. For dividing cells, Applicants use Cas9
to introduce double strand breaks near the mutation site and
increase the rate of homologous recombination using an exogenous
recombination template. For dividing cells, this may be achieved
using multiplexed nickase activity to catalyze the replacement of
the mutant sequence in both alleles via NHEJ-mediated ligation of
an exogenous DNA fragment carrying complementary overhangs.
[0860] Applicants also use Cas9 to introduce protective mutations
(e.g. inactivation of CCR5 to prevent HIV infection, inactivation
of PCSK9 for cholesterol reduction, or introduction of the A673T
into APP to reduce the likelihood of Alzheimer's disease).
[0861] Diseases that Involve Non-Coding Sequences
[0862] Applicants use Cas9 to disrupt non-coding sequences in the
promoter region, to alter transcription factor binding sites and
alter enhancer or repressor elements. For example, Cas9 may be used
to excise out the Klf1 enhancer EHS1 in hematopoietic stem cells to
reduce BCL11a levels and reactivate fetal globin gene expression in
differentiated erythrocytes
[0863] Applicants also use Cas9 to disrupt functional motifs in the
5' or 3' untranslated regions. For example, for the treatment of
myotonic dystrophy, Cas9 may be used to remove CTG repeat
expansions in the DMPK gene.
Example 26: Multiplexed Nickase
[0864] Aspects of optimization and the teachings of Cas9 detailed
in this application may also be used to generate Cas9 nickases.
Applicants use Cas9 nickases in combination with pairs of guide
RNAs to generate DNA double strand breaks with defined overhangs.
When two pairs of guide RNAs are used, it is possible to excise an
intervening DNA fragment. If an exogenous piece of DNA is cleaved
by the two pairs of guide RNAs to generate compatible overhangs
with the genomic DNA, then the exogenous DNA fragment may be
ligated into the genomic DNA to replace the excised fragment. For
example, this may be used to remove trinucleotide repeat expansion
in the huntintin (HTT) gene to treat Huntington's Disease.
[0865] If an exogenous DNA that bears fewer number of CAG repeats
is provided, then it may be able to generate a fragment of DNA that
bears the same overhangs and can be ligated into the HTT genomic
locus and replace the excised fragment (fragments below disclosed
as SEQ ID NOS 130-137, respectively, in order of appearance).
TABLE-US-00029 HTT locus with fragment excised by Cas9 nickase . .
. CCGTGCCGGGCGGGAGACCGCCATGG GGCCCGGCTGTGGCTGAGGAGC . . . and two
pairs of . . GGCACGGCCCGCCCTCTGCC TGGGCCGGGCCGACACCGACTCCTCG . . .
guide RNAs + exogenous DNA fragment with fewer number of CAG
repeats CGACCCTGGAAA . . . reduced number of CAG repeats . . .
CCCCGCCGCCACCC also cleaved by Cas9 GGTACCGCTGGGACCTTT . . . . . .
GGGGCGGCGG nickse and the two pairs of guide RNAs
[0866] The ligation of the exogenous DNA fragment into the genome
does not require homologous recombination machineries and therefore
this method may be used in post-mitotic cells such as neurons.
Example 27: Delivery of CRISPR System
[0867] Cas9 and its chimeric guide RNA, or combination of tracrRNA
and crRNA, can be delivered either as DNA or RNA. Delivery of Cas9
and guide RNA both as RNA (normal or containing base or backbone
modifications) molecules can be used to reduce the amount of time
that Cas9 protein persist in the cell. This may reduce the level of
off-target cleavage activity in the target cell. Since delivery of
Cas9 as mRNA takes time to be translated into protein, it might be
advantageous to deliver the guide RNA several hours following the
delivery of Cas9 mRNA, to maximize the level of guide RNA available
for interaction with Cas9 protein.
[0868] In situations where guide RNA amount is limiting, it may be
desirable to introduce Cas9 as mRNA and guide RNA in the form of a
DNA expression cassette with a promoter driving the expression of
the guide RNA. This way the amount of guide RNA available will be
amplified via transcription.
[0869] A variety of delivery systems can be introduced to introduce
Cas9 (DNA or RNA) and guide RNA (DNA or RNA) into the host cell.
These include the use of liposomes, viral vectors, electroporation,
nanoparticles, nanowires (Shalek et al., Nano Letters, 2012),
exosomes. Molecular trojan horses liposomes (Pardridge et al., Cold
Spring Harb Protoc; 2010; doi:10.1101/pdb.prot5407) may be used to
deliver Cas9 and guide RNA across the blood brain barrier.
Example 28: Therapeutic Strategies for Trirncleotide Repeat
Disorders
[0870] As previously mentioned in the application, the target
polynucleotide of a CRISPR complex may include a number of
disease-associated genes and polynucleotides and some of these
disease associated gene may belong to a set of genetic disorders
referred to as Trinucleotide repeat disorders (referred to as also
trinucleotide repeat expansion disorders, triplet repeat expansion
disorders or codon reiteration disorders).
[0871] These diseases are caused by mutations in which the
trinucleotide repeats of certain genes exceed the normal, stable
threshold which may usually differ in a gene. The discovery of more
repeat expansion disorders has allowed for the classification of
these disorders into a number of categories based on underlying
similar characteristics. Huntington's disease (HD) and the
spinocerebellar ataxias that are caused by a CAG repeat expansion
in protein-coding portions of specific genes are included in
Category I. Diseases or disorders with expansions that tend to make
them phenotypically diverse and include expansions are usually
small in magnitude and also found in exons of genes are included in
Category II. Category III includes disorders or diseases which are
characterized by much larger repeat expansions than either Category
I or II and are generally located outside protein coding regions.
Examples of Category III diseases or disorders include but are not
limited to Fragile X syndrome, myotonic dystrophy, two of the
spinocerebellar ataxias, juvenile myoclonic epilepsy, and
Friedreich's ataxia.
[0872] Similar therapeutic strategies, like the one mentioned for
Friedreich's ataxia below may be adopted to address other
trinucleotide repeat or expansion disorders as well. For example,
another triple repeat disease that can be treated using almost
identical strategy is dystrophia myotonica 1 (DM1), where there is
an expanded CTG motif in the 3' UTR In Friedreich's ataxia, the
disease results from expansion of GAA trinucleotides in the first
intron of frataxin (FXN). One therapeutic strategy using CRISPR is
to excise the GAA repeat from the first intron. The expanded GAA
repeat is thought to affect the DNA structure and leads to recruit
the formation of heterochromatin which turn off the frataxin gene
(FIG. 32A).
[0873] Competitive Advantage over other therapeutic strategies are
listed below:
[0874] siRNA knockdown is not applicable in this case, as disease
is due to reduced expression of frataxin Viral gene therapy is
currently being explored. HSV-1 based vectors were used to deliver
the frataxin gene in animal models and have shown therapeutic
effect. However, long term efficacy of virus-based frataxin
delivery suffer from several problems: First, it is difficult to
regulate the expression of frataxin to match natural levels in
health individuals, and second, long term over expression of
frataxin leads to cell death.
[0875] Nucleases may be used to excise the GAA repeat to restore
healthy genotype, but Zinc Finger Nuclease and TALEN strategies
require delivery of two pairs of high efficacy nucleases, which is
difficult for both delivery as well as nuclease engineering
(efficient excision of genomic DNA by ZFN or TALEN is difficult to
achieve).
[0876] In contrast to above strategies, the CRISPR-Cas system has
clear advantages. The Cas9 enzyme is more efficient and more
multiplexible, by which it is meant that one or more targets can be
set at the same time. So far, efficient excision of genomic
DNA>30% by Cas9 in human cells and may be as high as 30%, and
may be improved in the future. Furthermore, with regard to certain
trinucleotide repeat disorders like Huntington's disease (HD),
trinucleotide repeats in the coding region may be addressed if
there are differences between the two alleles. Specifically, if a
HD patient is heterozygous for mutant HTT and there are nucleotide
differences such as SNPs between the wt and mutant I-ITT alleles,
then Cas9 may be used to specifically target the mutant HTT allele
ZFN or TALENs will not have the ability to distinguish two alleles
based on single base differences.
[0877] In adopting a strategy using the CRISPR-Cas 9 enzyme to
address Friedreich's ataxia, Applicants design a number of guide
RNAs targeting sites flanking the GAA expansion and the most
efficient and specific ones are chosen (FIG. 32B).
[0878] Applicants deliver a combination of guide RNAs targeting the
intron 1 of FXN along with Cas9 to mediate excision of the GAA
expansion region. AAV9 may be used to mediate efficient delivery of
Cas9 and in the spinal cord.
[0879] If the Alu element adjacent to the GAA expansion is
considered important, there may be constraints to the number of
sites that can be targeted but Applicants may adopt strategies to
avoid disrupting it.
[0880] Alternative Strategies:
[0881] Rather than modifying the genome using Cas9, Applicants may
also directly activate the FXN gene using Cas9 (nuclease activity
deficient)-based DNA binding domain to target a transcription
activation domain to the FXN gene. Applicants may have to address
the robustness of the Cas9-mediated artificial transcription
activation to ensure that it is robust enough as compared to other
methods (Tremblay et al., Transcription Activator-Like Effector
Proteins Induce the Expression of the Frataxin Gene; Human Gene
Therapy. August 2012, 23(8): 883-890.)
Example 29: Strategies for Minimizing Off-Target Cleavage Using Ca9
Nickase
[0882] As previously mentioned in the application, Cas9 may be
mutated to mediate single strand cleavage via one or more of the
following mutations: D10A, E762A, and H840A.
[0883] To mediate gene knockout via NHEJ, Applicants use a nickase
version of Cas9 along with two guide RNAs. Off-target nicking by
each individual guide RNA may be primarily repaired without
mutation, double strand breaks (which can lead to mutations via
NHEJ) only occur when the target sites are adjacent to each other.
Since double strand breaks introduced by double nicking are not
blunt, co-expression of end-processing enzymes such as TREX1 will
increase the level of NHEJ activity.
[0884] The following list of targets in tabular form are for genes
involved in the following diseases:
[0885] Lafora's Disease--target GSY1 or PPPIR3C (PTG) to reduce
glycogen in neurons.
[0886] Hypercholesterolemia--Target PCSK9
[0887] Target sequences are listed in pairs (L and R) with
different number of nucleotides in the spacer (0 to 3 bp). Each
spacer may also be used by itself with the wild type Cas9 to
introduce double strand break at the target locus.
TABLE-US-00030 GYS1 (human) GGCC-L ACCCTTGTTAGCCACCTCCC (SEQ ID NO:
138) GGCC-R GAACGCAGTGCTCTTCGAAG (SEQ ID NO: 139) GGNCC-L
CTCACGCCCTGCTCCGTGTA (SEQ ID NO: 140) GGNCC-R GGCGACAACTACTTCCTGGT
(SEQ ID NO: 141) GGNNCC-L CTCACGCCCTGCTCCGTGTA (SEQ ID NO: 142)
GGNNCC-R GGGCGACAACTACTTCCTGG (SEQ ID NO: 143) GGNNNCC-L
CCTCTTCAGGGCCGGGGTGG (SEQ ID NO: 144) GGNNNCC-R
GAGGACCCAGGTGGAACTGC (SEQ ID NO: 145) PCSK9 (human) GGCC-L
TCAGCTCCAGGCGGTCCTGG (SEQ ID NO: 146) GGCC-R AGCAGCAGCAGCAGTGGCAG
(SEQ ID NO: 147) GGNCC-L TGGGCACCGTCAGCTCCAGG (SEQ ID NO: 148)
GGNCC-R CAGCAGTGGCAGCGGCCACC (SEQ ID NO: 149) GGNNCC-L
ACCTCTCCCCTGGCCCTCAT (SEQ ID NO: 150) GGNNCC-R CCAGGACCGCCTGGAGCTGA
(SEQ ID NO: 151) GGNNNCC-L CCGTCAGCTCCAGGCGGTCC (SEQ ID NO: 152)
GGNNNCC-R AGCAGCAGCAGCAGTGGCAG (SEQ ID NO: 153) PPP1R3C GGCC-L
ATGTGCCAAGCAAAGCCTCA (SEQ ID NO: 154) (PTG) (human) GGCC-R
TTCGGTCATGCCCGTGGATG (SEQ ID NO: 155) GGNCC-L GTCGTTGAAATTCATCGTAC
(SEQ ID NO: 156) GGNCC-R ACCACCTGTGAAGAGTTTCC (SEQ ID NO: 157)
GGNNCC-L CGTCGTTGAAATTCATCGTA (SEQ ID NO: 158) GGNNCC-R
ACCACCTGTGAAGAGTTTCC (SEQ ID NO: 159) Gys1 (mouse) GGCC-L
GAACGCAGTGCTTTTCGAGG (SEQ ID NO: 160) GGCC-R ACCCTTGTTGGCCACCTCCC
(SEQ ID NO: 161) GGNCC-L GGTGACAACTACTATCTGGT (SEQ ID NO: 162)
GGNCC-R CTCACACCCTGCTCCGTGTA (SEQ ID NO: 163) GGNNCC-L
GGGTGACAACTACTATCTGG (SEQ ID NO: 164) GGNNCC-R CTCACACCCTGCTCCGTGTA
(SEQ ID NO: 165) GGNNNCC-L CGAGAACGCAGTGCTTTTCG (SEQ ID NO: 166)
GGNNNCC-R ACCCTTGTTGGCCACCTCCC (SEQ ID NO: 167) PPP1R3C GGCC-L
ATGAGCCAAGCAAATCCTCA (SEQ ID NO: 168) (PTG) (mouse) GGCC-R
TTCCGTCATGCCCGTGGACA (SEQ ID NO: 169) GGNCC-L CTTCGTTGAAAACCATTGTA
(SEQ ID NO: 170) GGNCC-R CCACCTCTGAAGAGTTTCCT (SEQ ID NO: 171)
GGNNCC-L CTTCGTTGAAAACCATTGTA (SEQ ID NO: 172) GGNNCC-R
ACCACCTCTGAAGAGTTTCC (SEQ ID NO: 173) GGNNNCC-L
CTTCCACTCACTCTGCGATT (SEQ ID NO: 174) GGNNNCC-R
ACCATGTCTCAGTGTCAAGC (SEQ ID NO: 175) PCSK9 GGCC-L
GGCGGCAACAGCGGCAACAG (SEQ ID NO: 176) (mouse) GGCC-R
ACTGCTCTGCGTGGCTGCGG (SEQ ID NO: 177) GGNNCC-L CCGCAGCCACGCAGAGCAGT
(SEQ ID NO: 178) GGNNCC-R GCACCTCTCCTCGCCCCGAT (SEQ ID NO: 179)
[0888] Alternative Strategies for Improving Stability of Guide RNA
and Increasing Specificity
[0889] 1. Nucleotides in the 5' of the guide RNA may be linked via
thiolester linkages rather than phosphoester linkage like in
natural RNA. Thiolester linkage may prevent the guide RNA from
being digested by endogenous RNA degradation machinery.
[0890] 2. Nucleotides in the guide sequence (5' 20 bp) of the guide
RNA can use bridged nucleic acids (BNA) as the bases to improve the
binding specificity.
Example 30: CRISPR-Cas for Rapid, Multiplex Genome Editing
[0891] Aspects of the invention relate to protocols and methods by
which efficiency and specificity of gene modification may be tested
within 3-4 days after target design, and modified clonal cell lines
may be derived within 2-3 weeks.
[0892] Programmable nucleases are powerful technologies for
mediating genome alteration with high precision. The RNA-guided
Cas9 nuclease from the microbial CRISPR adaptive immune system can
be used to facilitate efficient genome editing in eukaryotic cells
by simply specifying a 20-nt targeting sequence in its guide RNA.
Applicants describe a set of protocols for applying Cas9 to
facilitate efficient genome editing in mammalian cells and generate
cell lines for downstream functional studies. Beginning with target
design, efficient and specific gene modification can be achieved
within 3-4 days, and modified clonal cell lines can be derived
within 2-3 weeks.
[0893] The ability to engineer biological systems and organisms
holds enormous potential for applications across basic science,
medicine, and biotechnology. Programmable sequence-specific
endonucleases that facilitate precise editing of endogenous genomic
loci are now enabling systematic interrogation of genetic elements
and causal genetic variations in a broad range of species,
including those that have not been genetically tractable
previously. A number of genome editing technologies have emerged in
recent years, including zinc finger nucleases (ZFNs), transcription
activator-like effector nucleases (TALENs), and the RNA-guided
CRISPR-Cas nuclease system. The first two technologies use a common
strategy of tethering endonuclease catalytic domains to modular
DNA-binding proteins for inducing targeted DNA double stranded
breaks (DSB) at specific genomic loci. By contrast, Cas9 is a
nuclease guided by small RNAs through Watson-Crick base-pairing
with target DNA, presenting a system that is easy to design,
efficient, and well-suited for high-throughput and multiplexed gene
editing for a variety of cell types and organisms. Here Applicants
describe a set of protocols for applying the recently developed
Cas9 nuclease to facilitate efficient genome editing in mammalian
cells and generate cell lines for downstream functional
studies.
[0894] Like ZFNs and TALENs, Cas9 promotes genome editing by
stimulating DSB at the target genomic loci. Upon cleavage by Cas9,
the target locus undergoes one of two major pathways for DNA damage
repair, the error-prone non-homologous end joining (NHEJ) or the
high-fidelity homology directed repair (HDR) pathway. Both pathways
may be utilized to achieve the desired editing outcome.
[0895] NHEJ: In the absence of a repair template, the NHEJ process
re-ligates DSBs, which may leave a scar in the form of indel
mutations. This process can be harnessed to achieve gene knockouts,
as indels occurring within a coding exon may lead to frameshift
mutations and a premature stop codon. Multiple DSBs may also be
exploited to mediate larger deletions in the genome.
[0896] HDR: Homology directed repair is an alternate major DNA
repair pathway to NHEJ. Although HDR typically occurs at lower
frequencies than NHEJ, it may be harnessed to generate precise,
defined modifications at a target locus in the presence of an
exogenously introduced repair template. The repair template may be
either in the form of double stranded DNA, designed similarly to
conventional DNA targeting constructs with homology arms flanking
the insertion sequence, or single-stranded DNA oligonucleotides
(ssODNs). The latter provides an effective and simple method for
making small edits in the genome, such as the introduction of
single nucleotide mutations for probing causal genetic variations.
Unlike NHEJ, HDR is generally active only in dividing cells and its
efficiency varies depending on the cell type and state.
[0897] Overview of CRISPR: The CRISPR-Cas system, by contrast, is
at minimum a two-component system consisting of the Cas9 nuclease
and a short guide RNA. Re-targeting of Cas9 to different loci or
simultaneous editing of multiple genes simply requires cloning a
different 20-bp oligonucleotide. Although specificity of the Cas9
nuclease has yet to be thoroughly elucidated, the simple
Watson-Crick base-pairing of the CRISPR-Cas system is likely more
predictable than that of ZFN or TALEN domains.
[0898] The type II CRISPR-Cas (clustered regularly interspaced
short palindromic repeats) is a bacterial adaptive immune system
that uses Cas9, to cleave foreign genetic elements. Cas9 is guided
by a pair of non-coding RNAs, a variable crRNA and a required
auxiliary tracrRNA. The crRNA contains a 20-nt guide sequence
determines specificity by locating the target DNA via Watson-Crick
base-pairing. In the native bacterial system, multiple crRNAs are
co-transcribed to direct Cas9 against various targets. In the
CRISPR-Cas system derived from Streptococcus pyogenes, the target
DNA must immediately precede a 5'-NGG/NRG protospacer adjacent
motif (PAM), which can vary for other CRISPR systems.
[0899] CRISPR-Cas is reconstituted in mammalian cells through the
heterologous expression of human codon-optimized Cas9 and the
requisite RNA components. Furthermore, the crRNA and tracrRNA can
be fused to create a chimeric, synthetic guide RNA (sgRNA). Cas9
can thus be re-directed toward any target of interest by altering
the 20-nt guide sequence within the sgRNA.
[0900] Given its ease of implementation and multiplex capability,
Cas9 has been used to generate engineered eukaryotic cells carrying
specific mutations via both NHEJ and HDR. In addition, direct
injection of sgRNA and mRNA encoding Cas9 into embryos has enabled
the rapid generation of transgenic mice with multiple modified
alleles; these results hold promise for editing organisms that are
otherwise genetically intractable.
[0901] A mutant Cas9 carrying a disruption in one of its catalytic
domains has been engineered to nick rather than cleave DNA,
allowing for single-stranded breaks and preferential repair through
HDR, potentially ameliorating unwanted indel mutations from
off-target DSBs. Additionally, a Cas9 mutant with both DNA-cleaving
catalytic residues mutated has been adapted to enable
transcriptional regulation in E. coli, demonstrating the potential
of functionalizing Cas9 for diverse applications. Certain aspects
of the invention relate to the construction and application of Cas9
for multiplexed editing of human cells.
[0902] Applicants have provided a human codon-optimized, nuclear
localization sequence-flanked Cas9 to facilitate eukaryotic gene
editing. Applicants describe considerations for designing the 20-nt
guide sequence, protocols for rapid construction and functional
validation of sgRNAs, and finally use of the Cas9 nuclease to
mediate both NHEJ- and HDR-based genome modifications in human
embryonic kidney (HEK-293FT) and human stem cell (HUES9) lines.
This protocol can likewise be applied to other cell types and
organisms.
[0903] Target selection for sgRNA: There are two main
considerations in the selection of the 20-nt guide sequence for
gene targeting: 1) the target sequence should precede the 5'-NGG
PAM for S. pyogenes Cas9, and 2) guide sequences should be chosen
to minimize off-target activity. Applicants provided an online Cas9
targeting design tool that takes an input sequence of interest and
identifies suitable target sites. To experimentally assess
off-target modifications for each sgRNA, Applicants also provide
computationally predicted off-target sites for each intended
target, ranked according to Applicants' quantitative specificity
analysis on the effects of base-pairing mismatch identity,
position, and distribution.
[0904] The detailed information on computationally predicted
off-target sites is as follows:
[0905] Considerations for Off-target Cleavage Activities: Similar
to other nucleases, Cas9 can cleave off-target DNA targets in the
genome at reduced frequencies. The extent to which a given guide
sequence exhibit off-target activity depends on a combination of
factors including enzyme concentration, thermodynamics of the
specific guide sequence employed, and the abundance of similar
sequences in the target genome. For routine application of Cas9, it
is important to consider ways to minimize the degree of off-target
cleavage and also to be able to detect the presence of off-target
cleavage.
[0906] Minimizing off-target activity: For application in cell
lines, Applicants recommend following two steps to reduce the
degree of off-target genome modification. First, using our online
CRISPR target selection tool, it is possible to computationally
assess the likelihood of a given guide sequence to have off-target
sites. These analyses are performed through an exhaustive search in
the genome for off-target sequences that are similar sequences as
the guide sequence. Comprehensive experimental investigation of the
effect of mismatching bases between the sgRNA and its target DNA
revealed that mismatch tolerance is 1) position dependent--the 8-14
bp on the 3' end of the guide sequence are less tolerant of
mismatches than the 5' bases, 2) quantity dependent--in general
more than 3 mismatches are not tolerated, 3) guide sequence
dependent--some guide sequences are less tolerant of mismatches
than others, and 4) concentration dependent--off-target cleavage is
highly sensitive to the amount of transfected DNA. The Applicants'
target site analysis web tool (available at the website
genome-engineering.org/tools) integrates these criteria to provide
predictions for likely off-target sites in the target genome.
Second, Applicants recommend titrating the amount of Cas9 and sgRNA
expression plasmid to minimize off-target activity.
[0907] Detection of off-target activities: Using Applicants' CRISPR
targeting web tool, it is possible to generate a list of most
likely off-target sites as well as primers performing SURVEYOR or
sequencing analysis of those sites. For isogenic clones generated
using Cas9, Applicants strongly recommend sequencing these
candidate off-target sites to check for any undesired mutations. It
is worth noting that there may be off target modifications in sites
that are not included in the predicted candidate list and full
genome sequence should be performed to completely verify the
absence of off-target sites. Furthermore, in multiplex assays where
several DSBs are induced within the same genome, there may be low
rates of translocation events and can be evaluated using a variety
of techniques such as deep sequencing.
[0908] The online tool provides the sequences for all oligos and
primers necessary for 1) preparing the sgRNA constructs, 2)
assaying target modification efficiency, and 3) assessing cleavage
at potential off-target sites. It is worth noting that because the
U6 RNA polymerase III promoter used to express the sgRNA prefers a
guanine (G) nucleotide as the first base of its transcript, an
extra G is appended at the 5' of the sgRNA where the 20-nt guide
sequence does not begin with G.
[0909] Approaches for sgRNA construction and delivery: Depending on
the desired application, sgRNAs may be delivered as either 1) PCR
amplicons containing an expression cassette or 2) sgRNA-expressing
plasmids. PCR-based sgRNA delivery appends the custom sgRNA
sequence onto the reverse PCR primer used to amplify a U6 promoter
template. The resulting amplicon may be co-transfected with a
plasmid containing Cas9 (PX165). This method is optimal for rapid
screening of multiple candidate sgRNAs, as cell transfections for
functional testing can be performed mere hours after obtaining the
sgRNA-encoding primers. Because this simple method obviates the
need for plasmid-based cloning and sequence verification, it is
well suited for testing or co-transfecting a large number of sgRNAs
for generating large knockout libraries or other scale-sensitive
applications. Note that the sgRNA-encoding primers are over 100-bp,
compared to the .about.20-bp oligos required for plasmid-based
sgRNA delivery.
[0910] Construction of an expression plasmid for sgRNA is also
simple and rapid, involving a single cloning step with a pair of
partially complementary oligonucleotides. After annealing the oligo
pairs, the resulting guide sequences may be inserted into a plasmid
bearing both Cas9 and an invariant scaffold bearing the remainder
of the sgRNA sequence (PX330). The transfection plasmids may also
be modified to enable virus production for in vivo delivery.
[0911] In addition to PCR and plasmid-based delivery methods, both
Cas9 and sgRNA can be introduced into cells as RNA.
[0912] Design of repair template: Traditionally, targeted DNA
modifications have required use of plasmid-based donor repair
templates that contain homology arms flanking the site of
alteration. The homology arms on each side can vary in length, but
are typically longer than 500 bp. This method can be used to
generate large modifications, including insertion of reporter genes
such as fluorescent proteins or antibiotic resistance markers. The
design and construction of targeting plasmids has been described
elsewhere.
[0913] More recently, single-stranded DNA oligonucleotides (ssODNs)
have been used in place of targeting plasmids for short
modifications within a defined locus without cloning. To achieve
high HDR efficiencies, ssODNs contain flanking sequences of at
least 40 bp on each side that are homologous to the target region,
and can be oriented in either the sense or antisense direction
relative to the target locus.
[0914] Functional Testing
[0915] SURVEYOR nuclease assay: Applicants detected indel mutations
either by the SURVEYOR nuclease assay (or PCR amplicon sequencing.
Applicants online CRISPR target design tool provides recommended
primers for both approaches. However, SURVEYOR or sequencing
primers may also be designed manually to amplify the region of
interest from genomic DNA and to avoid non-specific amplicons using
NCBI Primer-BLAST. SURVEYOR primers should be designed to amplify
300-400 bp (for a 600-800 bp total amplicon) on either side of the
Cas9 target for allowing clear visualization of cleavage bands by
gel electrophoresis. To prevent excessive primer dimer formation,
SURVEYOR primers should be designed to be typically under 25-nt
long with melting temperatures of .about.60.degree. C. Applicants
recommend testing each pair of candidate primers for specific PCR
amplicons as well as for the absence of non-specific cleavage
during the SURVEYOR nuclease digestion process.
[0916] Plasmid- or ssODN-mediated HDR: HDR can be detected via
PCR-amplification and sequencing of the modified region. PCR
primers for this purpose should anneal outside the region spanned
by the homology arms to avoid false detection of residual repair
template (HDR Fwd and Rev, FIG. 30). For ssODN-mediated HDR,
SURVEYOR PCR primers can be used.
[0917] Detection of indels or HDR by sequencing: Applicants
detected targeted genome modifications by either Sanger or
next-generation deep sequencing (NGS). For the former, genomic DNA
from modified region can be amplified using either SURVEYOR or HDR
primers. Amplicons should be subcloned into a plasmid such as pUC19
for transformation, individual colonies can be sequenced to reveal
clonal genotype.
[0918] Applicants designed next-generation sequencing (NGS) primers
for shorter amplicons, typically in the 100-200 bp size range. For
detecting NHEJ mutations, it is important to design primers with at
least 10-20 bp between the priming regions and the Cas9 target site
to allow detection of longer indels. Applicants provide guidelines
for a two-step PCR method to attach barcoded adapters for multiplex
deep sequencing. Applicants recommend the Illumina platform, due to
its generally low levels of false positive indels. Off-target
analysis (described previously) can then be performed through read
alignment programs such as ClustalW, Geneious, or simple sequence
analysis scripts.
[0919] Materials and Reagents
[0920] sgRNA Preparation:
[0921] UltraPure DNaseRNase-free distilled water (Life
Technologies, cat. no. 10977-023)
[0922] Herculase II fusion polymerase (Agilent Technologies, cat.
no. 600679)
[0923] CRITICAL. Standard Taq polymerase, which lacks 3'-5'
exonuclease proofreading activity, has lower fidelity and can lead
to amplification errors. Herculase II is a high-fidelity polymerase
(equivalent fidelity to Pfu) that produces high yields of PCR
product with minimal optimization. Other high-fidelity polymerases
may be substituted.
[0924] Herculase II reaction buffer (5.times.; Agilent
Technologies, included with polymerase)
[0925] dNTP solution mix (25 mM each; Enzymatics, cat. no.
N205L)
[0926] MgCl2 (25 mM; ThermoScientific, cat. no. R0971)
[0927] QIAquick gel extraction kit (Qiagen, cat. no. 28704)
[0928] QIAprep spin miniprep kit (Qiagen, cat. no. 27106)
[0929] UltraPure TBE buffer (10.times.; Life Technologies, cat. no.
15581-028)
[0930] SeaKem LE agarose (Lonza, cat. no. 50004)
[0931] SYBR Safe DNA stain (10,000.times.; Life Technologies, cat.
no. S33102)
[0932] 1-kb Plus DNA ladder (Life Technologies, cat. no.
10787-018)
[0933] TrackIt CyanOrange loading buffer (Life Technologies, cat.
no. 10482-028)
[0934] FastDigest BbsI (BpiI) (Fermentas/ThermoScientific, cat. no.
FD1014)
[0935] Fermentas Tango Buffer (Fermentas/ThermoScientific, cat. no.
BY5)
[0936] DL-dithiothreitol (DTT; Fermentas/ThermoScientific, cat. no.
R0862)
[0937] T7 DNA ligase (Enzymatics, cat. no. L602L)
[0938] Critical: Do not substitute the more commonly used T4
ligase. T7 ligase has 1,000-fold higher activity on the sticky ends
than on the blunt ends and higher overall activity than
commercially available concentrated T4 ligases.
[0939] T7 2.times. Rapid Ligation Buffer (included with T7 DNA
ligase, Enzymatics, cat. no. L602L)
[0940] T4 Polynucleotide Kinase (New England Biolabs, cat. no
M0201S)
[0941] T4 DNA Ligase Reaction Buffer (10.times.; New England
Biolabs, cat. no B0202S)
[0942] Adenosine 5'-triphosphate (10 mM; New England Biolabs, cat.
no. P0756S)
[0943] PlasmidSafe ATP-dependent DNase (Epicentre, cat. no.
E3101K)
[0944] One Shot Stb13 chemically competent Escherichia coli (E.
coli) (Life Technologies, cat. no. C7373-03)
[0945] SOC medium (New England Biolabs, cat. no. B9020S)
[0946] LB medium (Sigma, cat. no. L3022)
[0947] LB agar medium (Sigma, cat. no. L2897)
[0948] Ampicillin, sterile filtered (100 mg ml-1; Sigma, cat. no.
A5354)
[0949] Mammalian Cell Culture:
[0950] HEK293FT cells (Life Technologies, cat. no. R700-07)
[0951] Dulbecco's minimum Eagle's medium (DMEM, 1.times., high
glucose; Life Technologies, cat. no. 10313-039)
[0952] Dulbecco's minimum Eagle's medium (DMEM, 1.times., high
glucose, no phenol red; Life Technologies, cat. no. 31053-028)
[0953] Dulbecco's phosphate-buffered saline (DPBS, 1.times.; Life
Technologies, cat. no. 14190-250)
[0954] Fetal bovine serum, qualified and heat inactivated (Life
Technologies, cat. no. 10438-034)
[0955] Opti-MEM I reduced-serum medium (FBS; Life Technologies,
cat. no. 11058-021)
[0956] Penicillin-streptomycin (100.times.; Life Technologies, cat.
no. 15140-163)
[0957] TrypLE.TM. Express (1.times., no Phenol Red; Life
Technologies, cat. no. 12604-013)
[0958] Lipofectamine 2000 transfection reagent (Life Technologies,
cat. no. 11668027)
[0959] Amaxa SF Cell Line 4D-Nucleofector.RTM. X Kit S (32 RCT;
Lonza, cat. no V4XC-2032)
[0960] HUES 9 cell line (HARVARD STEM CELL SCIENCE)
[0961] Geltrex LDEV-Free Reduced Growth Factor Basement Membrane
Matrix (Life Technologies, cat. no. A1413201)
[0962] mTeSR1 medium (Stemcell Technologies, cat. no. 05850)
[0963] Accutase cell detachment solution (Stemcell Technologies,
cat. no. 07920)
[0964] ROCK Inhibitor (Y-27632; Millipore, cat. no. SCM075)
[0965] Amaxa P3 Primary Cell 4D-Nucleofector.RTM. X Kit S (32 RCT;
Lonza cat. no. V4XP-3032)
[0966] Genotyping Analysis:
[0967] QuickExtract DNA extraction solution (Epicentre, cat. no.
QE09050)
[0968] PCR primers for SURVEYOR, RFLP analysis, or sequencing (see
Primer table)
[0969] Herculase II fusion polymerase (Agilent Technologies, cat.
no. 600679)
[0970] CRITICAL. As Surveyor assay is sensitive to single-base
mismatches, it is particularly important to use a high-fidelity
polymerase. Other high-fidelity polymerases may be substituted.
[0971] Herculase II reaction buffer (5.times.; Agilent
Technologies, included with polymerase)
[0972] dNTP solution mix (25 mM each; Enzymatics, cat. no.
N205L)
[0973] QIAquick gel extraction kit (Qiagen, cat. no. 28704)
[0974] Taq Buffer (10.times.; Genscript, cat. no. B0005)
[0975] SURVEYOR mutation detection kit for standard gel
electrophoresis (Transgenomic, cat. no. 706025)
[0976] UltraPure TBE buffer (10.times.; Life Technologies, cat. no.
15581-028)
[0977] SeaKem LE agarose (Lonza, cat. no. 50004) 4-20% TBE Gels 1.0
mm, 15 Well (Life Technologies, cat. no. EC62255BOX)
[0978] Novex.RTM. Hi-Density TBE Sample Buffer (5.times.; Life
Technologies, cat. no. LC6678)
[0979] SYBR Gold Nucleic Acid Gel Stain (10,000.times.; Life
Technologies, cat. no. S-11494)
[0980] 1-kb Plus DNA ladder (Life Technologies, cat. no.
10787-018)
[0981] TrackIt CyanOrange loading buffer (Life Technologies, cat.
no. 10482-028)
[0982] FastDigest HindIII (Fermentas/ThermoScientific, cat. no.
FD0504)
[0983] Equipment
[0984] Filtered sterile pipette tips (Corning)
[0985] Standard 1.5 ml microcentrifuge tubes (Eppendorf, cat. no.
0030 125.150)
[0986] Axygen 96-well PCR plates (VWR, cat. no. PCR-96M2-HSC)
[0987] Axygen 8-Strip PCR tubes (Fischer Scientific, cat. no.
14-222-250)
[0988] Falcon tubes, polypropylene, 15 ml (BD Falcon, cat. no.
352097)
[0989] Falcon tubes, polypropylene, 50 ml (BD Falcon, cat. no.
352070)
[0990] Round-bottom Tube with cell strainer cap, 5 ml (BD Falcon,
cat. no. 352235)
[0991] Petri dishes (60 mm.times.15 mm; BD Biosciences, cat. no.
351007)
[0992] Tissue culture plate (24 well; BD Falcon, cat no.
353047)
[0993] Tissue culture plate (96 well, flat bottom; BD Falcon, cat.
no. 353075)
[0994] Tissue culture dish (100 mm; BD Falcon, 353003)
[0995] 96-well thermocycler with programmable temperature stepping
functionality (Applied Biosystems Veriti, cat. no. 4375786).
[0996] Desktop microcentrifuges 5424, 5804 (Eppendorf)
[0997] Gel electrophoresis system (PowerPac basic power supply,
Bio-Rad, cat. no. 164-5050, and Sub-Cell GT System gel tray,
Bio-Rad, cat. no. 170-4401)
[0998] Novex XCell SureLock Mini-Cell (Life Technologies, cat. no.
EI0001)
[0999] Digital gel imaging system (GelDoc EZ, Bio-Rad, cat. no.
170-8270, and blue sample tray, Bio-Rad, cat. no. 170-8273)
[1000] Blue light transilluminator and orange filter goggles
(SafeImager 2.0; Invitrogen, cat. no. G6600)
[1001] Gel quantification software (Bio-Rad, ImageLab, included
with GelDoc EZ, or open-source ImageJ from the National Institutes
of Health, available at the website rsbweb.nih.gov/ij/) UV
spectrophotometer (NanoDrop 2000c, Thermo Scientific)
[1002] Reagent Setup
[1003] Tris-borate EDTA (TBE) electrophoresis solution Dilute TBE
buffer in distilled water to 1.times. working solution for casting
agarose gels and for use as a buffer for gel electrophoresis.
Buffer may be stored at room temperature (18-22.degree. C.) for at
least 1 year. [1004] ATP, 10 mM Divide 10 mM ATP into 50-.mu.l
aliquots and store at -20.degree. C. for up to 1 year; avoid
repeated freeze-thaw cycles. [1005] DTT, 10 mM Prepare 10 mM DTT
solution in distilled water and store in 20-.mu.l aliquots at
-70.degree. C. for up to 2 years; for each reaction, use a new
aliquot, as DTT is easily oxidized. [1006] D10 culture medium For
culture of HEK293FT cells, prepare D10 culture medium by
supplementing DMEM with 1.times.GlutaMAX and 10% (vol/vol) fetal
bovine serum. As indicated in the protocol, this medium can also be
supplemented with 1.times. penicillin-streptomycin. D10 medium can
be made in advance and stored at 4.degree. C. for up to 1 month.
[1007] mTeSR1 culture medium For culture of human embryonic stem
cells, prepare mTeSR1 medium by supplementing the 5.times.
supplement (included with mTeSR1 basal medium), and 100 ug/ml
Normocin.
[1008] Procedure
[1009] Design of Targeting Components and Use of the Online
Tool.cndot.Timing 1 d
[1010] 1| Input target genomic DNA sequence. Applicants provide an
online Cas9 targeting design tool that takes an input sequence of
interest, identifies and ranks suitable target sites, and
computationally predicts off-target sites for each intended target.
Alternatively, one can manually select guide sequence by
identifying the 20-bp sequence directly upstream of any 5'-NGG.
[1011] 2| Order necessary oligos and primers as specified by the
online tool. If the site is chosen manually, the oligos and primers
should be designed.
[1012] Preparation of sgRNA expression construct
[1013] 3| To generate the sgRNA expression construct, either the
PCR- or plasmid-based protocol can be used.
[1014] (A) Via PCR Amplification.cndot.Timing 2 h
[1015] (i) Applicants prepare diluted U6 PCR template. Applicants
recommend using PX330 as a PCR template, but any U6-containing
plasmid may likewise be used as the PCR template. Applicants
diluted template with ddH.sub.2O to a concentration of 10 ng/ul.
Note that if a plasmid or cassette already containing an U6-driven
sgRNA is used as a template, a gel extraction needs to be performed
to ensure that the product contains only the intended sgRNA and no
trace sgRNA carryover from template.
[1016] (ii) Applicants prepared diluted PCR oligos. U6-Fwd and
U6-sgRNA-Rev primers are diluted to a final concentration of 10 uM
in ddH.sub.2O (add 10 ul of 100 uM primer to 90 ul ddH.sub.2O).
[1017] (iii) U6-sgRNA PCR reaction. Applicants set up the following
reaction for each U6-sgRNA-Rev primer and mastermix as needed:
TABLE-US-00031 Component: Amount (ul) Final concentration Herculase
II PCR buffer, 5X 10 1X dNTP, 100 mM (25 mM each) 0.5 1 mM U6
template (PX330) 1 0.2 ng/ul U6-Fwd primer 1 0.2 uM U6-sgRNA-Rev
primer (variable) 1 0.2 uM Herculase II Fusion polymerase 0.5
Distilled water 36 Total 50
[1018] (iv) Applicants performed PCR reaction on the reactions from
step (iii) using the following cycling conditions:
TABLE-US-00032 Cycle number Denature Anneal Extend 1 95.degree. C.,
2 m 2-31 95.degree. C., 20 s 60.degree. C., 20 s 72.degree. C., 20
s 32 72.degree. C., 3 m
[1019] (v) After the reaction is completed, Applicants ran the
product on a gel to verify successful, single-band amplification.
Cast a 2% (wt/vol) agarose gel in 1.times. TBE buffer with 1.times.
SYBR Safe dye. Run 5 ul of the PCR product in the gel at 15 V cm-1
for 20-30 min. Successful amplicons should yield one single 370-bp
product and the template should be invisible. It should not be
necessary to gel extract the PCR amplicon.
[1020] (vi) Applicants purified the PCR product using the QIAquick
PCR purification kit according to the manufacturer's directions.
Elute the DNA in 35 ul of Buffer EB or water. Purified PCR products
may be stored at 4.degree. C. or -20.degree. C.
[1021] (B) Cloning sgRNA into Cas9-Containing Bicistronic
Expression Vector.cndot.Timing 3 d
[1022] (i) Prepare the sgRNA oligo inserts. Applicants resuspended
the top and bottom strands of oligos for each sgRNA design to a
final concentration of 100 uM. Phosphorylate and anneal the oligo
as follows:
TABLE-US-00033 Oligo 1 (100 uM) 1 ul Oligo 2 (100 uM) 1 ul T4
Ligation Buffer, 10X 1 ul T4 PNK 1 ul ddH.sub.2O 6 ul Total 10
ul
[1023] (ii) Anneal in a thermocycler using the following
parameters: [1024] 37.degree. C. for 30 m [1025] 95.degree. C. for
5 m [1026] Ramp down to 25.degree. C. at 5.degree. C. per m
[1027] (iii) Applicants diluted phosphorylated and annealed oligos
1:200 by add 1 ul of oligo to 199 ul room temperature
ddH.sub.2O.
[1028] (iv) Clone sgRNA oligo into PX330. Applicants set up Golden
Gate reaction for each sgRNA. Applicants recommend also setting up
a no-insert, PX330 only negative control.
TABLE-US-00034 PX330 (100 ng) x ul Diluted oligo duplex 2 ul from
step (iii) Tango Buffer, 10X 2 ul DTT, 10 mM 1 ul ATP, 10 mM 1 ul
FastDigest BbsI 1 ul T7 Ligase 0.5 ul ddH.sub.2O x ul Total 20
ul
[1029] (v) Incubate the Golden Gate reaction for a total of 1
h:
TABLE-US-00035 Cycle number Condition 1-6 37.degree. C. for 5 m,
21.degree. C. for 5 m
[1030] (vi) Applicants treated Golden Gate reaction with
PlasmidSafe exonuclease to digest any residual linearized DNA. This
step is optional but highly recommended.
TABLE-US-00036 Golden Gate reaction from step 4 11 ul 10X
PlasmidSafe Buffer 1.5 ul ATP, 10 mM 1.5 ul PlasmidSafe exonuclease
1 ul Total 15 ul
[1031] (vii) Applicants incubated the PlasmidSafe reaction at
37.degree. C. for 30 min, followed by inactivation at 70.degree. C.
for 30 min. Pause point: after completion, the reaction may be
frozen and continued later. The circular DNA should be stable for
at least 1 week.
[1032] (viii) Transformation. Applicants transformed the
PlasmidSafe-treated plasmid into a competent E. coli strain,
according to the protocol supplied with the cells. Applicants
recommend Stb13 for quick transformation. Briefly, Applicants added
5 ul of the product from step (vii) into 20 ul of ice-cold
chemically competent Stb13 cells. This is then incubated on ice for
10 m, heat shocked at 42.degree. C. for 30 s, returned immediately
to ice for 2 m, 100 ul of SOC medium is added, and this is plated
onto an LB plate containing 100 ug/ml ampicillin with incubation
overnight at 37.degree. C.
[1033] (ix) Day 2: Applicants inspected plates for colony growth.
Typically, there are no colonies on the negative control plates
(ligation of BbsI-digested PX330 only, no annealed sgRNA oligo),
and tens to hundreds of colonies on the PX330-sgRNA cloning
plates.
[1034] (x) From each plate, Applicants picked 2-3 colonies to check
correct insertion of sgRNA. Applicants used a sterile pipette tip
to inoculate a single colony into a 3 ml culture of LB medium with
100 ug/ml ampicillin. Incubate and shake at 37.degree. C.
overnight.
[1035] (xi) Day 3: Applicants isolated plasmid DNA from overnight
cultures using a QiAprep Spin miniprep kit according to the
manufacturer's instructions.
[1036] (xii) Sequence validate CRISPR plasmid. Applicants verified
the sequence of each colony by sequencing from the U6 promoter
using the U6-Fwd primer. Optional: sequence the Cas9 gene using
primers listed in the following Primer table.
TABLE-US-00037 Primer Sequence (5' to 3') Purpose U6-For
GAGGGCCTATTTCCCATGATTCC (SEQ ID NO: 180) Amplify U6-sgRNA U6-Rev
AAAAAAAGCACCGACTCGGTGCCACTTTTTCAAGTTGATAACGGACTAGCCTTA Amplify
U6-sgRNA; N is
TTTTAACTTGCTATTTCTAGCTCTAAAACNNNNNNNNNNNNNNNNNNNGTCCTT reverse
complement of TCCACAAG (SEQ ID NO: 181) target sgRNA-
CACCGNNNNNNNNNNNNNNNNNNN (SEQ ID NO: 182) Clone sgRNA into PX330
top sgRNA- AAACNNNNNNNNNNNNNNNNNNNC (SEQ ID NO: 183) Clone sgRNA
into PX330 bottom U6-EMX1-
AAAAAAAGCACCGACTCGGTGCCACTTTTTCAAGTTGATAACGGACTAGCCTTA Amplify
U6-EMX1 sgRNA Rev
TTTTAACTTGCTATTTCTAGCTCTAAAACCCCTAGTCATTGGAGGTGACCGGTG
TTTCGTCCTTTCCACAAG (SEQ ID NO: 184) EMX1-top
CACCGTCACCTCCAATGACTAGGG (SEQ ID NO: 185) Clone EMX1 sgRNA into
PX330 EMX1- AAACCCCTAGTCATTGGAGGTGAC (SEQ ID NO: 186) Clone EMX1
sgRNA into bottom PX330 ssODN-
CAGAAGAAGAAGGGCTCCCATCACATCAACCGGTGGCGCATTGCCACGAAGCAG EMX1 HDR
(sense; sense
GCCAATGGGGAGGACATCGATGTCACCTCCAATGACAAGCTTGCTAGCGGTGGG insertion
underlined) CAACCACAAACCCACGAGGGCAGAGTGCTGCTTGCTGCTGGCCAGGCCCCTGCG
TGGGCCCAAGCTGGACTCTGGCCACTCCCT (SEQ ID NO: 187) ssODN-
AGGGAGTGGCCAGAGTCCAGCTTGGGCCCACGCAGGGGCCTGGCCAGCAGCAAG EMX1 HDR
(antisense; antisense
CAGCACTCTGCCCTCGTGGGTTTGTGGTTGCCCACCGCTAGCAAGCTTGTCATT insertion
underlined) GGAGGTGACATCGATGTCCTCCCCATTGGCCTGCTTCGTGGCAATGCGCCACCG
GTTGATGTGATGGGAGCCCTTCTTCTTCTG (SEQ ID NO: 188) EMX1-
CCATCCCCTTCTGTGAATGT (SEQ ID NO: 189) EMX1 SURVEYOR assay SURV-F
PCR, sequencing EMX1- GGAGATTGGAGACACGGAGA (SEQ ID NO: 190) EMX1
SURVEYOR assay SURV-R PCR, sequencing EMX1- GGCTCCCTGGGTTCAAAGTA
(SEQ ID NO: 191) EMX1 RFLP analysis HDR-F PCR, sequencing EMX1-
AGAGGGGTCTGGATGTCGTAA (SEQ ID NO: 192) EMX1 RFLP analysis HDR-R
PCR, sequencing pUC19-F CGCCAGGGTTTTCCCAGTCACGAC (SEQ ID NO: 193)
pUC19 multiple cloning site F primer, for Sanger sequencing
[1037] Applicants referenced the sequencing results against the
PX330 cloning vector sequence to check that the 20 bp guide
sequence was inserted between the U6 promoter and the remainder of
the sgRNA scaffold. Details and sequence of the PX330 map in
GenBank vector map format (*.gb file) can be found at the website
crispr.genome-engineering.org.
[1038] (Optional) Design of ssODN Template.cndot.Timing 3 d
Planning Ahead
[1039] 3| Design and order ssODN. Either the sense or antisense
ssODN can be purchased directly from supplier. Applicants recommend
designing homology arms of at least 40 bp on either side and 90 bp
for optimal HDR efficiency. In Applicants' experience, antisense
oligos have slightly higher modification efficiencies.
[1040] 4| Applicants resuspended and diluted ssODN ultramers to a
final concentration of 10 uM. Do not combine or anneal the sense
and antisense ssODNs. Store at -20.degree. C.
[1041] 5| Note for HDR applications, Applicants recommend cloning
sgRNA into the PX330 plasmid.
[1042] Functional Validation of sgRNAs: Cell Culture and
Transfections.cndot.Timing 3-4 d
[1043] The CRISPR-Cas system has been used in a number of mammalian
cell lines. Conditions may vary for each cell line. The protocols
below details transfection conditions for HEK239FT cells. Note for
ssODN-mediated HDR transfections, the Amaxa SF Cell Line
Nucleofector Kit is used for optimal delivery of ssODNs. This is
described in the next section.
[1044] 7| HEK293FT maintenance. Cells are maintained according to
the manufacturer's recommendations. Briefly, Applicants cultured
cells in D10 medium (GlutaMax DMEM supplemented with 10% Fetal
Bovine Serum), at 37.degree. C. and 5% CO2.
[1045] 8| To passage, Applicants removed medium and rinsed once by
gently adding DPBS to side of vessel, so as not to dislodge cells.
Applicants added 2 ml of TrypLE to a T75 flask and incubated for 5
m at 37.degree. C. 10 ml of warm D10 medium is added to inactivate
and transferred to a 50 ml Falcon tube. Applicants dissociated
cells by triturating gently, and re-seeded new flasks as necessary.
Applicants typically passage cells every 2-3 d at a split ratio of
1:4 or 1:8, never allowing cells to reach more than 70% confluency.
Cell lines are restarted upon reaching passage number 15.
[1046] 9| Prepare cells for transfection. Applicants plated
well-dissociated cells onto 24-well plates in D10 medium without
antibiotics 16-24 h before transfection at a seeding density of
1.3.times.10.sup.5 cells per well and a seeding volume of 500 ul.
Scale up or down according to the manufacturer's manual as needed.
It is suggested to not plate more cells than recommended density as
doing so may reduce transfection efficiency.
[1047] 10| On the day of transfection, cells are optimal at 70-90%
confluency. Cells may be transfected with Lipofectamine 2000 or
Amaxa SF Cell Line Nucleofector Kit according to the manufacturers'
protocols.
[1048] (A) For sgRNAs cloned into PX330, Applicants transfected 500
ng of sequence-verified CRISPR plasmid; if transfecting more than
one plasmid, mix at equimolar ratio and no more than 500 ng
total.
[1049] (B) For sgRNA amplified by PCR, Applicants mixed the
following:
TABLE-US-00038 PX165 (Cas9 only) 200 ng sgRNA amplicon (each) 40 ng
pUC19 fill up total DNA to 500 ng
[1050] Applicants recommend transfecting in technical triplicates
for reliable quantification and including transfection controls
(e.g. GFP plasmid) to monitor transfection efficiency. In addition,
PX330 cloning plasmid and/or sgRNA amplicon may be transfected
alone as a negative control for downstream functional assays.
[1051] 11| Applicants added Lipofectamine complex to cells gently
as HEK293FT cells may detach easily from plate easily and result in
lower transfection efficiency.
[1052] 12| Applicants checked cells 24 h after transfection for
efficiency by estimating the fraction of fluorescent cells in the
control (e.g., GFP) transfection using a fluorescence microscope.
Typically cells are more than 70% transfected.
[1053] 13| Applicants supplemented the culture medium with an
additional 500 ul of warm D10 medium. Add D10 very slowly to the
side of the well and do not use cold medium, as cells can detach
easily.
[1054] 14| Cells are incubated for a total of 48-72 h
post-transfection before harvested for indel analysis. Indel
efficiency does not increase noticeably after 48 h.
[1055] (Optional) Co-Transfection of CRISPR Plasmids and ssODNs or
Targeting Plasmids for HR.cndot.Timing 3-4 d
[1056] 15| Linearize targeting plasmid. Targeting vector is
linearized if possible by cutting once at a restriction site in the
vector backbone near one of the homology arms or at the distal end
of either homology arm.
[1057] 16| Applicants ran a small amount of the linearized plasmid
alongside uncut plasmid on a 0.8-1% agarose gel to check successful
linearization. Linearized plasmid should run above the supercoiled
plasmid.
[1058] 17| Applicants purified linearized plasmid with the QIAQuick
PCR Purification kit.
[1059] 18| Prepare cells for transfection. Applicants cultured
HEK293FT in T75 or T225 flasks. Sufficient cell count before day of
transfection is planned for. For the Amaxa strip-cuvette format,
2.times.10.sup.6 cells are used per transfection.
[1060] 19| Prepare plates for transfection. Applicants added 1 ml
of warm D10 medium into each well of a 12 well plate. Plates are
placed into the incubator to keep medium warm.
[1061] 20| Nucleofection. Applicants transfected HEK293FT cells
according to the Amaxa SF Cell Line Nucleofector 4D Kit
manufacturer's instructions, adapted in the steps below. [1062] a.
For ssODN and CRISPR cotransfection, pre-mix the following DNA in
PCR tubes:
TABLE-US-00039 [1062] pCRISPR plasmid (Cas9 + sgRNA) 500 ng ssODN
template (10 uM) 1 ul
[1063] b. For HDR targeting plasmid and CRISPR cotransfection,
pre-mix the following DNA in PCR tubes:
TABLE-US-00040 [1063] CRISPR plasmid (Cas9 + sgRNA) 500 ng
Linearized targeting plasmid 500 ng
[1064] For transfection controls, see previous section. In
addition, Applicants recommend transfecting ssODN or targeting
plasmid alone as a negative control.
[1065] 21| Dissociate to single cells. Applicants removed medium
and rinsed once gently with DPBS, taking care not to dislodge
cells. 2 ml of TrypLE is added to a T75 flask and incubated for 5 m
at 37.degree. C. 10 ml of warm D10 medium is added to inactivate
and triturated gently in a 50 ml Falcon tube. It is recommended
that cells are triturated gently and dissociated to single cells.
Large clumps will reduce transfection efficiency. Applicants took a
10 ul aliquot from the suspension and diluted into 90 ul of D10
medium for counting. Applicants counted cells and calculated the
number of cells and volume of suspension needed for transfection.
Applicants typically transfected 2.times.10.sup.5 cells per
condition using the Amaxa Nucleocuvette strips, and recommend
calculating for 20% more cells than required to adjust for volume
loss in subsequent pipetting steps. The volume needed is
transferred into a new Falcon tube.
[1066] 23| Applicants spun down the new tube at 200.times.g for 5
m.
[1067] Applicants prepared the transfection solution by mixing the
SF solution and S1 supplement as recommended by Amaxa. For Amaxa
strip-cuvettes, a total of 20 ul of supplemented SF solution is
needed per transfection. Likewise, Applicants recommend calculating
for 20% more volume than required.
[1068] 25| Applicants removed medium completely from pelleted cells
from step 23 and gently resuspended in appropriate volume (20 ul
per 2.times.10.sup.5 cells) of S1-supplemented SF solution. Do not
leave cells in SF solution for extended period of time.
[1069] 26| 20 ul of resuspended cells is pipetted into each DNA
pre-mix from step 20. Pipette gently to mix and transfer to
Nucleocuvette strip chamber. This is repeated for each transfection
condition.
[1070] Electroporate cells using the Nucleofector 4D program
recommended by Amaxa, CM-130.
[1071] 28| Applicants gently and slowly pipetted 100 ul of warm D10
medium into each Nucleocuvette strip chamber, and transferred all
volume into the pre-warmed plate from step 19. CRITICAL. Cells are
very fragile at this stage and harsh pipetting can cause cell
death. Incubate for 24 h. At this point, transfection efficiency
can be estimated from fraction of fluorescent cells in positive
transfection control. Nucleofection typically results in greater
than 70-80% transfection efficiency. Applicants slowly added 1 ml
warm D10 medium to each well without dislodging the cells. Incubate
cells for a total of 72 h.
[1072] Human Embryonic Stem Cell (HUES9) Culture and
Transfection.cndot.Timing 3-4 d
[1073] Maintaining hESC (HUES9) line. Applicants routinely maintain
HUES9 cell line in feeder-free conditions with mTesR1 medium.
Applicants prepared mTeSR1 medium by adding the 5.times. supplement
included with basal medium and 100 ug/ml Normocin. Applicants
prepared a 10 ml aliquot of mTeSR1 medium supplemented further with
10 uM Rock Inhibitor. Coat tissue culture plate. Dilute cold
GelTrex 1:100 in cold DMEM and coat the entire surface of a 100 mm
tissue culture plate.
[1074] Place plate in incubator for at least 30 m at 37.degree. C.
Thaw out a vial of cells at 37.degree. C. in a 15 ml Falcon tube,
add 5 ml of mTeSR1 medium, and pellet at 200.times.g for 5 m.
Aspirate off GelTrex coating and seed .about.1.times.106 cells with
10 ml mTeSR1 medium containing Rock Inhibitor. Change to normal
mTeSR1 medium 24 h after transfection and re-feed daily. Passaging
cells. Re-feed cells with fresh mTeSR1 medium daily and passage
before reaching 70% confluency. Aspirate off mTeSR1 medium and wash
cells once with DPBS. Dissociate cells by adding 2 ml Accutase and
incubating at 37.degree. C. for 3-5 m. Add 10 ml mTeSR1 medium to
detached cells, transfer to 15 ml Falcon tube and resuspend gently.
Re-plate onto GelTrex-coated plates in mTeSR1 medium with 10 uM
Rock Inhibitor. Change to normal mTeSR1 medium 24 h after
plating.
[1075] Transfection. Applicants recommend culturing cells for at
least 1 week post-thaw before transfecting using the Amaxa P3
Primary Cell 4-D Nucleofector Kit (Lonza). Re-feed log-phase
growing cells with fresh medium 2 h before transfection. Dissociate
to single cells or small clusters of no more than 10 cells with
accutase and gentle resuspension. Count the number of cells needed
for nucleofection and spin down at 200.times.g for 5 m. Remove
medium completely and resuspend in recommended volume of
S1-supplemented P3 nucleofection solution. Gently plate
electroporated cells into coated plates in presence of 1.times.
Rock Inhibitor.
[1076] Check transfection success and re-feed daily with regular
mTeSR1 medium beginning 24 h after nucleofection. Typically,
Applicants observe greater than 70% transfection efficiency with
Amaxa Nucleofection. Harvest DNA. 48-72 h post transfection,
dissociate cells using accutase and inactivate by adding 5.times.
volume of mTeSR1. Spin cells down at 200.times.g for 5 m. Pelleted
cells can be directed processed for DNA extraction with
QuickExtract solution. It is recommended to not mechanically
dissociate cells without accutase. It is recommended to not spin
cells down without inactivating accutase or above the recommended
speed; doing so may cause cells to lyse.
[1077] Isolation of Clonal Cell Lines by FACS. Timing.cndot.2-3 h
Hands-on; 2-3 Weeks Expansion
[1078] Clonal isolation may be performed 24 h post-transfection by
FACS or by serial dilution.
[1079] 54| Prepare FACS buffer. Cells that do not need sorting
using colored fluorescence may be sorted in regular D10 medium
supplemented with 1.times. penicillin/streptinomycin. If colored
fluorescence sorting is also required, a phenol-free DMEM or DPBS
is substituted for normal DMEM. Supplement with 1.times.
penicillin/streptinomycin and filter through a 0.22 um Steriflip
filter.
[1080] 55| Prepare 96 well plates. Applicants added 100 ul of D10
media supplemented with 1.times. penicillin/streptinomycin per well
and prepared the number of plates as needed for the desired number
of clones.
[1081] 56| Prepare cells for FACS. Applicants dissociated cells by
aspirating the medium completely and adding 100 ul TrypLE per well
of a 24-well plate. Incubate for 5 m and add 400 ul warm D10
media.
[1082] 57| Resuspended cells are transferred into a 15 ml Falcon
tube and gently triturated 20 times. Recommended to check under the
microscope to ensure dissociation to single cells.
[1083] 58| Spin down cells at 200.times.g for 5 minutes.
[1084] 59| Applicants aspirated the media, and resuspended the
cells in 200 ul of FACS media.
[1085] 60| Cells are filtered through a 35 um mesh filter into
labeled FACS tubes. Applicants recommend using the BD Falcon
12.times.75 mm Tube with Cell Strainer cap. Place cells on ice
until sorting.
[1086] 61| Applicants sorted single cells into 96-well plates
prepared from step 55. Applicants recommend that in one single
designated well on each plate, sort 100 cells as a positive
control.
[1087] NOTE. The remainder of the cells may be kept and used for
genotyping at the population level to gauge overall modification
efficiency.
[1088] 62| Applicants returned cells into the incubator and allowed
them to expand for 2-3 weeks. 100 ul of warm D10 medium is added 5
d post sorting. Change 100 ul of medium every 3-5 d as
necessary.
[1089] 63| Colonies are inspected for "clonal" appearance 1 week
post sorting: rounded colonies radiating from a central point. Mark
off wells that are empty or may have been seeded with doublets or
multiplets.
[1090] 64| When cells are more than 60% confluent, Applicants
prepared a set of replica plates for passaging. 100 ul of D10
medium is added to each well in the replica plates. Applicants
dissociated cells directly by pipetting up and down vigorously 20
times. 20% of the resuspended volume was plated into the prepared
replica plates to keep the clonal lines. Change the medium every
2-3 d thereafter and passage accordingly.
[1091] 65| Use the remainder 80% of cells for DNA isolation and
genotyping.
[1092] Optional: Isolation of Clonal Cell Lines by Dilution.
Timing.cndot.2-3 h Hands-on; 2-3 Weeks Expansion
[1093] 66| Applicants dissociated cells from 24-well plates as
described above. Make sure to dissociate to single cells. A cell
strainer can be used to prevent clumping of cells.
[1094] 67| The number of cells are counted in each condition.
Serially dilute each condition in D10 medium to a final
concentration of 0.5 cells per 100 ul. For each 96 well plate,
Applicants recommend diluting to a final count of 60 cells in 12 ml
of D10. Accurate count of cell number is recommended for
appropriate clonal dilution. Cells may be recounted at an
intermediate serial dilution stage to ensure accuracy.
[1095] 68| Multichannel pipette was used to pipette 100 ul of
diluted cells to each well of a 96 well plate.
[1096] NOTE. The remainder of the cells may be kept and used for
genotyping at the population level to gauge overall modification
efficiency.
[1097] 69| Applicants inspected colonies for "clonal" appearance
.about.1 week post plating: rounded colonies radiating from a
central point. Mark off wells that may have seeded with doublets or
multiplets.
[1098] 70| Applicants returned cells to the incubator and allowed
them to expand for 2-3 weeks. Re-feed cells as needed as detailed
in previous section.
[1099] SURVEYOR Assay for CRISPR Cleavage Efficiency.
Timing.cndot.5-6 h
[1100] Before assaying cleavage efficiency of transfected cells,
Applicants recommend testing each new SURVEYOR primer on negative
(untransfected) control samples through the step of SURVEYOR
nuclease digestion using the protocol described below.
Occasionally, even single-band clean SURVEYOR PCR products can
yield non-specific SURVEYOR nuclease cleavage bands and potentially
interfere with accurate indel analysis.
[1101] 71| Harvest cells for DNA. Dissociate cells and spin down at
200.times.g for 5 m. NOTE. Replica plate at this stage as needed to
keep transfected cell lines.
[1102] 72| Aspirate the supernatant completely.
[1103] 73| Applicants used QuickExtract DNA extraction solution
according to the manufacturer's instructions. Applicants typically
used 50 ul of the solution for each well of a 24 well plate and 10
ul for a 96 well plate.
[1104] 74| Applicants normalized extracted DNA to a final
concentration of 100-200 ng/ul with ddH2O. Pause point: Extracted
DNA may be stored at -20.degree. C. for several months.
[1105] 75| Set up the SURVEYOR PCR. Master mix the following using
SURVEYOR primers provided by Applicants online/computer algorithm
tool:
TABLE-US-00041 Amount Final Component: (ul) concentration Herculase
II PCR buffer, 5X 10 1X dNTP, 100 mM (25 mM each) 1 1 mM SURVEYOR
Fwd primer (10 uM) 1 0.2 uM SURVEYOR Rev primer (10 uM) 1 0.2 uM
Herculase II Fusion polymerase 1 MgCl.sub.2 (25 mM) 2 1 mM
Distilled water 33 Total 49 (for each reaction)
[1106] 76| Applicants added 100-200 ng of normalized genomic DNA
template from step 74 for each reaction.
[1107] 77| PCR reaction was performed using the following cycling
conditions, for no more than 30 amplification cycles:
TABLE-US-00042 Cycle number Denature Anneal Extend 1 95.degree. C.,
2 min 2-31 95.degree. C., 20 s 60.degree. C., 20 s 72.degree. C.,
30 s 32 72.degree. C., 3 min
[1108] 78| Applicants ran 2-5 ul of PCR product on a 1% gel to
check for single-band product. Although these PCR conditions are
designed to work with most pairs of SURVEYOR primers, some primers
may need additional optimization by adjusting the template
concentration, MgCl.sub.2 concentration, and/or the annealing
temperature.
[1109] 79| Applicants purified the PCR reactions using the QIAQuick
PCR purification kit and normalized eluant to 20 ng/ul. Pause
point: Purified PCR product may be stored at -20.degree. C.
[1110] 80| DNA heteroduplex formation. The annealing reaction was
set up as follows:
TABLE-US-00043 Taq PCR buffer, 10X 2 ul Normalized DNA 18 ul (20
ng/ul) Total volume 20 ul
[1111] 81| Anneal the reaction using the following conditions:
TABLE-US-00044 Cycle number Condition 1 95.degree. C. 10 mn 2
95.degree. C.-85.degree. C., -2.degree. C./s 3 85.degree. C., 1 min
4 85.degree. C.-75.degree. C., -0.3.degree. C./s 5 75.degree. C., 1
min 6 75.degree. C.-65.degree. C., -0.3.degree. C./s 7 65.degree.
C., 1 min 8 65.degree. C.-55.degree. C., -0.3.degree. C./s 9
55.degree. C., 1 min 10 55.degree. C.-45.degree. C., -0.3.degree.
C./s 11 45.degree. C., 1 min 12 45.degree. C.-35.degree. C.,
-0.3.degree. C./s 13 35.degree. C., 1 min 14 35.degree.
C.-25.degree. C.,-0.3.degree. C./s 15 25.degree. C., 1 min
[1112] 82| SURVEYOR nuclease S digestion. Applicants prepared
master-mix and added the following components on ice to annealed
heteroduplexes from step 81 for a total final volume of 25 ul:
TABLE-US-00045 Amount Final Component (ul) Concentration MgCl.sub.2
solution, 0.15M 2.5 15 mM ddH.sub.2O 0.5 SURVEYOR nuclease S 1 1X
SURVEYOR enhancer S 1 1X Total 5
[1113] 83| Vortex well and spin down. Incubate the reaction at
42.degree. C. for 1 h.
[1114] 84| Optional: 2 ul of the Stop Solution from the SURVEYOR
kit may be added. Pause point. The digested product may be stored
at -20.degree. C. for analysis at a later time.
[1115] 85| Visualize the SURVEYOR reaction. SURVEYOR nuclease
digestion products may be visualized on a 2% agarose gel. For
better resolution, products may be run on a 4-20% gradient
Polyacrylamide TBE gel. Applicants loaded 10 ul of product with the
recommended loading buffer and ran the gel according to
manufacturer's instructions. Typically, Applicants run until the
bromophenol blue dye has migrated to the bottom of the gel. Include
DNA ladder and negative controls on the same gel.
[1116] 86| Applicants stained the gel with 1.times.SYBR Gold dye
diluted in TBE. The gel was gently rocked for 15 m.
[1117] 87| Applicants imaged the gel using a quantitative imaging
system without overexposing the bands. The negative controls should
have only one band corresponding to the size of the PCR product,
but may have occasionally non-specific cleavage bands of other
sizes. These will not interfere with analysis if they are different
in size from target cleavage bands. The sum of target cleavage band
sizes, provided by Applicants online/computer algorithm tool,
should be equal to the size of the PCR product.
[1118] 88| Estimate the cleavage intensity Applicants quantified
the integrated intensity of each band using ImageJ or other gel
quantification software.
[1119] 89| For each lane, Applicants calculated the fraction of the
PCR product cleaved (f.sub.cut) using the following formula:
f.sub.cut=(b+c)/(a+b+c), where a is the integrated intensity of the
undigested PCR product and b and c are the integrated intensities
of each cleavage product. 90| Cleavage efficiency may be estimated
using the following formula, based on the binomial probability
distribution of duplex formation:
91|indel (%)=100.times. {square root over ((1-(1-f.sub.cut)))}
[1120] Sanger Sequencing for Assessing CRISPR Cleavage Efficiency.
Timing.cndot.3 d
[1121] Initial steps are identical to Steps 71-79 of the SURVEYOR
assay. Note: SURVEYOR primers may be used for Sanger sequencing if
appropriate restriction sites are appended to the Forward and
Reverse primers. For cloning into the recommended pUC19 backbone,
EcoRI may be used for the Fwd primer and HindIII for the Rev
primer.
[1122] 92| Amplicon digestion. Set up the digestion reaction as
follows:
TABLE-US-00046 Amount Component (ul) Fast Digest buffer, 10X 3
FastDigest EcoRI 1 FastDigest HindIII 1 Normalized DNA 10 (20
ng/ul) ddH.sub.2O 15 Total volume 30
[1123] 93| pUC19 backbone digestion. Set up the digestion reaction
as follows:
TABLE-US-00047 Component Amount (ul) Fast Digest buffer, 10X 3
FastDigest EcoRI 1 FastDigest HindIII 1 FastAP Alkaline Phosphatase
1 pUC19 vector (200 ng/ul) 5 ddH.sub.2O 20 Total volume 30
[1124] 94| Applicants purified the digestion reactions using the
QIAQuick PCR purification kit. Pause point: Purified PCR product
may be stored at -20.degree. C.
[1125] 95| Applicants ligated the digested pUC19 backbone and
Sanger amplicons at a 1:3 vector:insert ratio as follows:
TABLE-US-00048 Component Amount (ul) Digested pUC19 x (50 ng)
Digested insert x (1:3 vector: insert molar ratio) T7 ligase 1 2X
Rapid 10 Ligation Buffer ddH.sub.2O x Total volume 20
[1126] 96| Transformation. Applicants transformed the
PlasmidSafe-treated plasmid into a competent E. coli strain,
according to the protocol supplied with the cells. Applicants
recommend Stb13 for quick transformation. Briefly, 5 ul of the
product from step 95 is added into 20 ul of ice-cold chemically
competent Stb13 cells, incubated on ice for 10 m, heat shocked at
42.degree. C. for 30 s, returned immediately to ice for 2 m, 100 ul
of SOC medium is added, and plated onto an LB plate containing 100
ug/ml ampicillin. This is incubated overnight at 37.degree. C.
[1127] 97| Day 2: Applicants inspected plates for colony growth.
Typically, there are no colonies on the negative control plates
(ligation of EcoRI-HindIII digested pUC19 only, no Sanger amplicon
insert), and tens to hundreds of colonies on the pUC19-Sanger
amplicon cloning plates.
[1128] 98| Day 3: Applicants isolated plasmid DNA from overnight
cultures using a QIAprep Spin miniprep kit according to the
manufacturer's instructions.
[1129] 99| Sanger sequencing. Applicants verified the sequence of
each colony by sequencing from the pUC19 backbone using the
pUC19--For primer. Applicants referenced the sequencing results
against the expected genomic DNA sequence to check for the presence
of Cas9-induced NHEJ mutations. % editing efficiency=(# modified
clones)/(# total clones). It is important to pick a reasonable
number of clones (>24) to generate accurate modification
efficiencies.
[1130] Genotyping for Microdeletion. Timing.cndot.2-3 d Hands on:
2-3 Weeks Expansion
[1131] 100| Cells were transfected as described above with a pair
of sgRNAs targeting the region to be deleted.
[1132] 10| 24 h post-transfection, clonal lines are isolated by
FACS or serial dilution as described above.
[1133] 102| Cells are expanded for 2-3 weeks.
[1134] 103| Applicants harvested DNA from clonal lines as described
above using 10 ul QuickExtract solution and normalized genomic DNA
with ddH.sub.2O to a final concentration of 50-100 ng/ul.
[1135] 104| PCR Amplify the modified region. The PCR reaction is
set up as follows:
TABLE-US-00049 Amount Final Component: (ul) concentration Herculase
II PCR buffer, 5X 10 1X dNTP, 100 mM (25 mM each) 1 1 mM Out Fwd
primer (10 uM) 1 0.2 uM Out Rev primer (10 uM) 1 0.2 uM Herculase
II Fusion polymerase 1 MgCl2 (25 mM) 2 1 mM ddH.sub.2O 32 Total 48
(for each reaction)
[1136] Note: if deletion size is more than 1 kb, set up a parallel
set of PCR reactions with In-Fwd and In-Rev primers to screen for
the presence of the wt allele.
[1137] 105| To screen for inversions, a PCR reaction is set up as
follows:
TABLE-US-00050 Amount Final Component: (ul) concentration Herculase
II PGR buffer, 5X 10 1X dNTP, 100 mM (25 mM each) 1 1 mM Out Fwd or
Out-Rev 1 0.2 uM primer (10 uM) In Fwd or In-Rev 1 0.2 uM primer
(10 uM) Herculase II Fusion 1 polymerase MgCl.sub.2 (25 mM) 2 1 mM
ddH.sub.2O 32 Total 48 (for each reaction)
[1138] Note: primers are paired either as Out-Fwd+In Fwd, or
Out-Rev+In-Rev.
[1139] 106| Applicants added 100-200 ng of normalized genomic DNA
template from step 103 for each reaction.
[1140] 107| PCR reaction was performed using the following cycling
conditions:
TABLE-US-00051 Cycle number Denature Anneal Extend 1 95.degree. C.,
2 min 2-31 95.degree. C., 20 s 60.degree. C., 20 s 72.degree. C.,
30 s 32 72.degree. C., 3 m
[1141] 108| Applicants run 2-5 ul of PCR product on a 1-2% gel to
check for product. Although these PCR conditions are designed to
work with most primers, some primers may need additional
optimization by adjusting the template concentration, MgCl.sub.2
concentration, and/or the annealing temperature.
[1142] Genotyping for Targeted Modifications Via HDR.
Timing.cndot.2-3 d, 2-3 h Hands on
[1143] 109| Applicants harvested DNA as described above using
QuickExtract solution and normalized genomic DNA with TE to a final
concentration of 100-200 ng/ul.
[1144] 110| PCR Amplify the modifiedregion. The PCR reaction is set
up as follows:
TABLE-US-00052 Amount Final Component: (ul) concentration Herculase
II PCR buffer, 5X 10 1X dNTP, 100 mM (25 mM each) 1 1 mM HDR Fwd
primer (10 uM) 1 0.2 uM HDR Rev primer (10 uM) 1 0.2 uM Herculase
II Fusion polymerase 1 MgCl.sub.2 (25 mM) 2 1 mM ddH.sub.2O 33
Total 49 (for each reaction)
[1145] 111| Applicants added 100-200 ng of genomic DNA template
from step 109 for each reaction and run the following program.
TABLE-US-00053 Cycle number Denature Anneal Extend 1 95.degree. C.,
2 min 2-31 95.degree. C., 20 s 60.degree. C., 20 s 72.degree. C.,
30-60 s per kb 32 72.degree. C., 3 min
[1146] 112| Applicants ran 5 ul of PCR product on a 0.8-1% gel to
check for single-band product. Primers may need additional
optimization by adjusting the template concentration, MgCl.sub.2
concentration, and/or the annealing temperature.
[1147] 113| Applicants purified the PCR reactions using the
QIAQuick PCR purification kit.
[1148] 114| In the HDR example, a HindIII restriction site is
inserted into the EMX1 gene. These are detected by a restriction
digest of the PCR amplicon:
TABLE-US-00054 Amount Component (ul) Purified PCR amplicon x
(200-300 ng) F.D. buffer, Green 1 HindIII 0.5 ddH2O x Total 10
[1149] i. The DNA is digested for 10 m at 37.degree. C.:
[1150] ii. Applicants ran 10 ul of the digested product with
loading dye on a 4-20% gradient polyacrylamide TBE gel until the
xylene cyanol band had migrated to the bottom of the gel.
[1151] iii. Applicants stained the gel with 1.times.SYBR Gold dye
while rocking for 15 m.
[1152] iv. The cleavage products are imaged and quantified as
described above in the SURVEYOR assay section. HDR efficiency is
estimated by the formula: (b+c)/(a+b+c), where a is the integrated
intensity for the undigested HDR PCR product, and b and c are the
integrated intensities for the HindIII-cut fragments.
[1153] 115| Alternatively, purified PCR amplicons from step 113 may
be cloned and genotyped using Sanger sequencing or NGS.
[1154] Deep Sequencing and Off-Target Analysis.cndot.Timing 1-2
d
[1155] The online CRISPR target design tool generates candidate
genomic off-target sites for each identified target site.
Off-target analysis at these sites can be performed by SURVEYOR
nuclease assay, Sanger sequencing, or next-generation deep
sequencing. Given the likelihood of low or undetectable
modification rates at many of these sites, Applicants recommend
deep sequencing with the Illumina Miseq platform for high
sensitivity and accuracy. Protocols will vary with sequencing
platform; here, Applicants briefly describe a fusion PCR method for
attaching sequencing adapters.
[1156] 116| Design deep sequencing primers. Next-generation
sequencing (NGS) primers are designed for shorter amplicons,
typically in the 100-200 bp size range. Primers may be manually
designed using NCBI Primer-Blast or generated with online CRISPR
target design tools (website at genome-engineering.org/tools).
[1157] 117| Harvest genomic DNA from Cas9-targeted cells. Normalize
QuickExtract genomic DNA to 100-200 ng/ul with ddH2O.
[1158] 118| Initial library preparation PCR. Using the NGS primers
from step 116, prepare the initial library preparation PCR
TABLE-US-00055 Amount Final Component: (ul) concentration Herculase
II PCR buffer, 5X 10 1X dNTP, 100 mM (25 mM each) 1 1 mM NGS Fwd
primer (10 uM) 1 0.2 uM NGS Rev primer (10 uM) 1 0.2 uM Herculase
III 1 Fusion polymerase MgCl2 (25 mM) 2 1 mM ddH2O 33 Total 49 (for
each reaction)
[1159] 119| Add 100-200 ng of normalized genomic DNA template for
each reaction.
[1160] 120| Perform PCR reaction using the following cycling
conditions, for no more than 20 amplification cycles:
TABLE-US-00056 Cycle number Denature Anneal Extend 1 95.degree. C.,
2 min 2-21 95.degree. C., 20 s 60.degree. C., 20 72.degree. C., 15
s 22 72.degree. C., 3 min
[1161] 121| Run 2-5 ul of PCR product on a 1% gel to check for
single-band product. As with all genomic DNA PCRs, NGS primers may
require additional optimization by adjusting the template
concentration, MgCl.sub.2 concentration, and/or the annealing
temperature.
[1162] 122| Purify the PCR reactions using the QIAQuick PCR
purification kit and normalize eluant to 20 ng/ul. Pause point:
Purified PCR product may be stored at -20.degree. C.
[1163] 123| Nextera XT DNA Sample Preparation Kit. Following the
manufacturer's protocol, generate Miseq sequencing-ready libraries
with unique barcodes for each sample.
[1164] 124| Analyze sequencing data. Off-target analysis may be
performed through read alignment programs such as ClustalW,
Geneious, or simple sequence analysis scripts.
[1165] Timing
[1166] Steps 1-2 Design and synthesis of sgRNA oligos and ssODNs:
1-5 d, variable depending on supplier
[1167] Steps 3-5 Construction of CRISPR plasmid or PCR expression
cassette: 2 h to 3 d
[1168] Steps 6-53 Transfection into cell lines: 3 d (1 h hands-on
time)
[1169] Steps 54-70 Optional derivation of clonal lines: 1-3 weeks,
variable depending on cell type
[1170] Steps 71-91 Functional validation of NHEJ via SURVEYOR: 5-6
h
[1171] Steps 92-124 Genotyping via Sanger or next-gen deep
sequencing: 2-3 d (3-4 h hands on time)
[1172] Addressing Situations Concerning Herein Examples
TABLE-US-00057 Situation Solution No amplification Titrate
U6-template of sgRNA concentration SURVEYOR or Titrate MgCl2;
normalize and HDR PCR titrate template dirty or no concentration;
annealing temp amplification gradient; redesign primers Unequal
amplification Set up separate PCRs to of alleles in detect wildtype
and deletion microdeletion alleles; Redesign primers with PCRs
similar sized amplicons Colonies on negative Increase BbsI;
increase Golden control plate Gate reaction cycle number; cut PX330
separately with Antarctic Phosphate treatment No sgRNA sequences
Screen additional colonies or wrong sequences Low lipofectamine
Check cell health and density; transfection titrate DNA; add GFP
efficiency transfection control Low nucleofection Check cell health
and density; transfection titrate DNA; suspend to efficiency single
cell Clumps or no cells Filter cells before FACS; after FACS
dissociate to single cells; resuspend in appropriate density Clumps
or no cells Recount cells; dissociate to single in serial dilution
cells and filter through strainer; check serial dilution High
SURVEYOR Redesign primers to prime background on from different
locations negative sample Dirty SURVEYOR Purify PCR product; reduce
result on gel input DNA; reduce 42.degree. C. incubation to 30 m No
SURVEYOR Purify and normalize PCR cleavage product; re-anneal with
TaqB buffer; Redesign sgRNAs; sequence verify Cas9 on px330
backbone Samples do not Supplement with MgCl2 to a sink in TBE
final concentration of 15 mM acrylamide gel or add loading buffer
containing glycerol
DISCUSSION
[1173] CRISPR-Cas may be easily multiplexed to facilitate
simultaneous modification of several genes and mediate chromosomal
microdeletions at high efficiencies. Applicants used two sgRNAs to
demonstrate simultaneous targeting of the human GRIN2B and DYRK1A
loci at efficiencies of up to 68% in HEK293FT cells. Likewise, a
pair of sgRNAs may be used to mediate microdeletions, such as
excision of an exon, which can be genotyped by PCR on a clonal
level. Note that the precise location of exon junctions can vary.
Applicants also demonstrated the use of ssODNs and targeting vector
to mediate HDR with both wildtype and nickase mutant of Cas9 in HEK
293FT and HUES9 cells (FIG. 30). Note that Applicants have not been
able to detect HDR in HUES9 cells using the Cas9 nickase, which may
be due to low efficiency or a potential difference in repair
activities in HUES9 cells. Although these values are typical, there
is some variability in the cleavage efficiency of a given sgRNA,
and on rare occasions certain sgRNAs may not work for reasons yet
unknown. Applicants recommend designing two sgRNAs for each locus,
and testing their efficiencies in the intended cell type.
Example 31: NLSs
[1174] Cas9 Transcriptional Modulator: Applicants set out to turn
the Cas9/gRNA CRISPR system into a generalized DNA binding system
in which functions beyond DNA cleavage can be executed. For
instance, by fusing functional domain(s) onto a catalytically
inactive Cas9 Applicants have imparted novel functions, such as
transcriptional activation/repression, methylation/demethylation,
or chromatin modifications. To accomplish this goal Applicants made
a catalytically inactive Cas9 mutant by changing two residues
essential for nuclease activity, D10 and H840, to alanine. By
mutating these two residues the nuclease activity of Cas9 is
abolished while maintaining the ability to bind target DNA. The
functional domains Applicants decided to focus on to test
Applicants' hypothesis are the transcriptional activator VP64 and
the transcriptional repressors SID and KRAB.
[1175] Cas9 Nuclear localization: Applicants hypothesized that the
most effective Cas9 transcriptional modulator would be strongly
localized to the nucleus where it would have its greatest influence
on transcription. Moreover, any residual Cas9 in the cytoplasm
could have unwanted effects. Applicants determined that wild-type
Cas9 does not localize into the nucleus without including multiple
nuclear localization signals (NLSs) (although a CRISPR system need
not have one or more NLSs but advantageously has at least one or
more NLS(s)). Because multiple NLS sequences were required it was
reasoned that it is difficult to get Cas9 into the nucleus and any
additional domain that is fused to Cas9 could disrupt the nuclear
localization. Therefore, Applicants made four Cas9-VP64-GFP fusion
constructs with different NLS sequences
(pXRP02-pLenti2-EF1a-NLS-hSpCsn1(10A,840A)-NLS-VP64-EGFP,
pXRP04-pLenti2-EF1a-NLS-hSpCsn1(10A,840A)-NLS-VP64-2A-EGFP-NLS,
pXRP06-pLenti2-EF1a-NLS-EGFP-VP64-NLS-hSpCsn1(10A,840A)-NLS,
pXRP08-pLenti2-EF1a-NLS-VP64-NLS-hSpCsn1(10A,840A)-NLS-VP64-EGFP-NLS).
These constructs were cloned into a lenti backbone under the
expression of the human EF1a promoter. The WPRE element was also
added for more robust protein expression. Each construct was
transfected into HEK 293FT cells using Lipofectame 2000 and imaged
24 hours post-transfection. The best nuclear localization is
obtained when the fusion proteins have NLS sequences on both the N-
and C-term of the fusion protein. The highest observed nuclear
localization occurred in the construct with four NLS elements.
[1176] To more robustly understand the influence of NLS elements on
Cas9 Applicants made 16 Cas9-GFP fusions by adding the same alpha
importin NLS sequence on either the N- or C-term looking at zero to
three tandem repeats. Each construct was transfected into HEK 293FT
cells using Lipofectame 2000 and imaged 24 hours post-transfection.
Notably, the number of NLS elements does not directly correlate
with the extent of nuclear localization. Adding an NLS on the
C-term has a greater influence on nuclear localization than adding
on the N-term.
[1177] Cas9 Transcriptional Activator: Applicants functionally
tested the Cas9-VP64 protein by targeting the Sox2 locus and
quantifying transcriptional activation by RT-qPCR. Eight DNA target
sites were chosen to span the promoter of Sox2. Each construct was
transfected into HEK 293FT cells using Lipofectame 2000 and 72
hours post-transfection total RNA was extracted from the cells. 1
ug of RNA was reverse transcribed into cDNA (qScript Supermix) in a
40 ul reaction. 2 ul of reaction product was added into a single 20
ul TaqMan assay qPCR reaction. Each experiment was performed in
biological and technical triplicates. No RT control and no template
control reactions showed no amplification. Constructs that do not
show strong nuclear localization, pXRP02 and pXRP04, result in no
activation. For the construct that did show strong nuclear
localization, pXRP08, moderate activation was observed.
Statistically significant activation was observed in the case of
guide RNAs Sox2.4 and Sox2.5.
Example 32: In Vivo Mouse Data
[1178] Material and Reagents
Herculase II fusion polymerase (Agilent Technologies, cat. no.
600679) 10.times. NEBuffer 4 (NEB, cat. No. B7004S) BsaI HF (NEB,
cat. No. R3535S) T7 DNA ligase (Enzymatics, cat. no. L602L) Fast
Digest buffer, 10.times. (ThermoScientific, cat. No. B64)
FastDigest NotI (ThermoScientific, cat. No. FD0594) FastAP Alkaline
Phosphatase (ThermoScientific, cat. No. EF0651) Lipofectamine2000
(Life Technologies, cat. No. 11668-019) Trypsin (Life Technologies,
cat. No. 15400054) Forceps #4 (Sigma, cat. No. Z168777-1EA) Forceps
#5 (Sigma, cat. No. F6521-1EA) 10.times. Hank's Balanced Salt
Solution (Sigma, cat. No. H4641-500 ML) Penicillin/Streptomycin
solution (Life Technologies, cat. No. P4333) Neurobasal (Life
Technologies, cat. No. 21103049) B27 Supplement (Life Technologies,
cat. No. 17504044) L-glutamine (Life Technologies, cat. No.
25030081) Glutamate (Sigma, cat. No. RES5063G-A7)
.beta.-mercaptoethanol (Sigma, cat. No. M6250-100 ML) HA rabbit
antibody (Cell Signaling, cat. No. 3724S) LIVE/DEAD.RTM. Cell
Imaging Kit (Life Technologies, cat. No. R37601) 30G World
Precision Instrument syringe (World Precision Instruments, cat. No.
NANOFIL) Stereotaxic apparatus (Kopf Instruments) UltraMicroPump3
(World Precision Instruments, cat. No. UMP3-4) Sucrose (Sigma, cat.
No. S7903) Calcium chloride (Sigma, cat. No. C1016) Magnesium
acetate (Sigma, cat. No. M0631)
Tris-HCl (Sigma, cat. no T5941)
[1179] EDTA (Sigma, cat. No. E6758) NP-40 (Sigma, cat. No. NP40)
Phenylmethanesulfonyl fluoride (Sigma, cat. No. 78830) Magnesium
chloride (Sigma, cat. No. M8266) Potassium chloride (Sigma, cat.
No. P9333) .beta.-glycerophosphate (Sigma, cat. No. G9422) Glycerol
(Sigma, cat. No. G9012) Vybrant.RTM. DyeCycle.TM. Ruby Stain (Life
technologies, cat. No. S4942) FACS Aria Flu-act-cell sorter (Koch
Institute of MIT, Cambridge US) DNAeasy Blood & Tissue Kit
(Qiagen, cat. No. 69504)
[1180] Procedure
[1181] Constructing gRNA Multiplexes for Using In Vivo in the
Brain
Applicants designed and PCR amplified single gRNAs targeting mouse
TET and DNMT family members (as described herein) Targeting
efficiency was assessed in N2a cell line (FIG. 33). To obtain
simultaneous modification of several genes in vivo, efficient gRNA
was multiplexed in AAV-packaging vector (FIG. 34). To facilitate
further analysis of system efficiency applicants added to the
system expression cassette consistent of GFP-KASH domain fusion
protein under control of human Synapsin I promoter (FIG. 34). This
modification allows for further analysis of system efficiency in
neuronal population (more detail procedure in section Sorting
nuclei and in vivo results).
[1182] All 4 parts of the system were PCR amplified using Herculase
II Fusion polymerase using following primers:
TABLE-US-00058 1st U6 Fw: (SEQ ID NO: 194)
gagggtctcgtccttgcggccgcgctagcgagggcctatttcccatgat tc 1st gRNA Rv:
(SEQ ID NO: 195) ctcggtctcggtAAAAAAgcaccgactcggtgccactttttcaagttga
taacggactagccttattttaacttgctaTTTCtagctctaaaacNNNN
NNNNNNNNNNNNNNNNGGTGTTTCGTCCTTTCCAC 2nd U6 Fw: (SEQ ID NO: 196)
gagggtctcTTTaccggtgagggcctatttcccatgattcc 2nd gRNA Rv: (SEQ ID NO:
197) ctcggtctccctcAAAAAAgcaccgactcggtgccactttttcaagttg
ataacggactagc cttattttaacttgctaTTTCtagctctaaaacNN
NNNNNNNNNNNNNNNNNNGGTGTTTCGTCCTTTCCAC 3rd U6 Fw: (SEQ ID NO: 198)
gagggtctcTTTgagctcgagggcctatttcccatgattc 3rd gRNA Rv: (SEQ ID NO:
199) ctcggtctcgcgtAAAAAAgcaccgactcggtgccactttttcaagttg ataacggactag
ccttattttaacttgctaTTTCtagctctaaaacNN
NNNNNNNNNNNNNNNNNNGGTGTTTCGTCCTTTCCA hSyn_GFP-kash Fw: (SEQ ID NO:
200) gagggtctcTTacgcgtgtgtctagac hSyn_GFP-kash Rev: (SEQ ID NO:
201) ctcggtctcAaggaCAGGGAAGGGAGCAGTGGTTCACGCCTGTAATCCC AGCAATTTGGGA
GGCCAAGGTGGGTAGATCACCTGAGATTAGGAGTTG C (NNNNNNNNNNNNNNNNNNNN is a
reverse compliment targeted genomic sequence)
[1183] Applicants used Golden Gate strategy to assemble all parts
(1:1 molecular ratio) of the system in a single step reaction:
TABLE-US-00059 1.sup.st U6_gRNA 18 ng 2.sup.nd U6_gRNA 18 ng
3.sup.rd U6_gRNA 18 ng Syn_GFP-kash 100 ng 10x NEBuffer 4 1.0 .mu.l
10x BSA 1.0 .mu.l 10 mM ATP 1.0 .mu.l BsaI HF 0.75 .mu.l T7 ligase
0.25 .mu.l ddH.sub.2O 10 .mu.l Cycle number Condition 1-50
37.degree. C. for 5 m, 21.degree. C. for 5 m
[1184] Golden Gate reaction product was PCR amplified using
Herculase II fusion polymerase and following primers:
TABLE-US-00060 (SEQ ID NO: 202) Fw 5'
cctgtccttgcggccgcgctagcgagggcc (SEQ ID NO: 203) Rv 5'
cacgcggccgcaaggacagggaagggagcag
[1185] PCR product was cloned into AAV backbone, between ITR
sequences using NotI restriction sites:
PCR product digestion:
TABLE-US-00061 Fast Digest buffer, 10X 3 .mu.l FastDigest NotI 1
.mu.l DNA 1 .mu.g ddH.sub.2O up to 30 .mu.l
[1186] AAV backbone digestion:
TABLE-US-00062 Fast Digest buffer, 10X 3 .mu.l FastDigest NotI 1
.mu.l FastAP Alkaline Phosphatase 1 .mu.l AAV backbone 1 .mu.g
ddH.sub.2O up to 30 .mu.l
[1187] After 20 min incubation in 37.degree. C. samples were
purified using QIAQuick PCR purification kit. Standardized samples
were ligated at a 1:3 vector:insert ratio as follows:
TABLE-US-00063 Digested pUC19 50 ng Digested insert 1:3 vector:
insert molar ratio T7 ligase 1 .mu.l 2X Rapid 5 .mu.l Ligation
Buffer ddH.sub.2O up to 10 .mu.l
[1188] After transformation of bacteria with ligation reaction
product, applicants confirmed obtained clones with Sanger
sequencing.
[1189] Positive DNA clones were tested in N2a cells after
co-transfection with Cas9 construct (FIGS. 35 and 36).
[1190] Design of New Cas9 Constructs for AAV Delivery
[1191] AAV delivery system despite its unique features has packing
limitation--to successfully deliver expressing cassette in vivo it
has to be in size <then 4.7 kb. To decrease the size of SpCas9
expressing cassette and facilitate delivery applicants tested
several alteration: different promoters, shorter polyA signal and
finally a smaller version of Cas9 from Staphylococcus aureus
(SaCas9) (FIGS. 37 and 38). All tested promoters were previously
tested and published to be active in neurons, including mouse Mecp2
(Gray et al., 2011), rat Map1b and truncated rat Map1b (Liu and
Fischer, 1996). Alternative synthetic polyA sequence was previously
shown to be functional as well (Levitt et al., 1989; Gray et al.,
2011). All cloned constructs were expressed in N2a cells after
transfection with Lipofectamine 2000, and tested with Western
blotting method (FIG. 39).
[1192] Testing AAV Multiplex System in Primary Neurons
[1193] To confirm functionality of developed system in neurons,
Applicants use primary neuronal cultures in vitro. Mouse cortical
neurons was prepared according to the protocol published previously
by Banker and Goslin (Banker and Goslin, 1988).
[1194] Neuronal cells are obtained from embryonic day 16. Embryos
are extracted from the euthanized pregnant female and decapitated,
and the heads are placed in ice-cold HBSS. The brains are then
extracted from the skulls with forceps (#4 and #5) and transferred
to another change of ice-cold HBSS. Further steps are performed
with the aid of a stereoscopic microscope in a Petri dish filled
with ice-cold HBSS and #5 forceps. The hemispheres are separated
from each other and the brainstem and cleared of meninges. The
hippocampi are then very carefully dissected and placed in a 15 ml
conical tube filled with ice-cold HBSS. Cortices that remain after
hippocampal dissection can be used for further cell isolation using
an analogous protocol after removing the brain steam residuals and
olfactory bulbs. Isolated hippocampi are washed three times with 10
ml ice-cold HBSS and dissociated by 15 min incubation with trypsin
in HBSS (4 ml HBSS with the addition of 10 .mu.l 2.5% trypsin per
hippocampus) at 37.degree. C. After trypsinization, the hippocampi
are very carefully washed three times to remove any traces of
trypsin with HBSS preheated to 37.degree. C. and dissociated in
warm HBSS. Applicants usually dissociate cells obtained from 10-12
embryos in 1 ml HBSS using 1 ml pipette tips and dilute dissociated
cells up to 4 ml. Cells are plated at a density of 250 cells/mm2
and cultured at 37.degree. C. and 5% CO2 for up to 3 week
[1195] HBSS
435 ml H2O
50 ml 10.times. Hank's Balanced Salt Solution
16.5 ml 0.3M HEPES pH 7.3
[1196] 5 ml penicillin-streptomycin solution Filter (0.2 .mu.m) and
store 4.degree. C.
[1197] Neuron Plating Medium (100 ml)
97 ml Neurobasal
2 ml B27 Supplement
[1198] 1 ml penicillin-streptomycin solution 250 .mu.l glutamine
125 .mu.l glutamate
[1199] Neurons are transduced with concentrated AAV1/2 virus or
AAV1 virus from filtered medium of HEK293FT cells, between 4-7 days
in culture and keep for at least one week in culture after
transduction to allow for delivered gene expression.
[1200] AAV-Driven Expression of the System
[1201] Applicants confirmed expression of SpCas9 and SaCas9 in
neuronal cultures after AAV delivery using Western blot method
(FIG. 42). One week after transduction neurons were collected in
NuPage SDS loading buffer with 3-mercaptoethanol to denaturate
proteins in 95.degree. C. for 5 min. Samples were separated on SDS
PAGE gel and transferred on PVDF membrane for WB protein detection.
Cas9 proteins were detected with HA antibody.
[1202] Expression of Syn-GFP-kash from gRNA multiplex AAV was
confirmed with fluorescent microscopy (FIG. 50).
[1203] Toxicity
[1204] To assess the toxicity of AAV with CRISPR system Applicants
tested overall morphology of neurons one week after virus
transduction (FIG. 45). Additionally, Applicants tested potential
toxicity of designed system with the LIVE/DEAD.RTM. Cell Imaging
Kit, which allows to distinguish live and dead cells in culture. It
is based on the presence of intracellular esterase activity (as
determined by the enzymatic conversion of the non-fluorescent
calcein AM to the intensely green fluorescent calcein). On the
other hand, the red, cell-impermeant component of the Kit enters
cells with damaged membranes only and bind to DNA generating
fluorescence in dead cells. Both flourophores can be easily
visualized in living cells with fluorescent microscopy. AAV-driven
expression of Cas9 proteins and multiplex gRNA constructs in the
primary cortical neurons was well tolerated and not toxic (FIGS. 43
and 44), what indicates that designed AAV system is suitable for in
vivo tests.
[1205] Virus Production
[1206] Concentrated virus was produced according to the methods
described in McClure et al., 2011. Supernatant virus production
occurred in HEK293FT cells.
[1207] Brain Surgeries
[1208] For viral vector injections 10-15 week old male C57BL/6N
mice were anesthetized with a Ketamine/Xylazine cocktail (Ketamine
dose of 100 mg/kg and Xylazine dose of 10 mg/kg) by intraperitoneal
injection. Intraperitonial administration of Buprenex was used as a
pre-emptive analgesic (1 mg/kg). Animals were immobilized in a Kopf
stereotaxic apparatus using intra-aural positioning studs and tooth
bar to maintain an immobile skull. Using a hand-held drill, a hole
(1-2 mm) at -3.0 mm posterior to Bregma and 3.5 mm lateral for
injection in the CAl region of the hippocampus was made. Using 30G
World Precision Instrument syringe at a depth of 2.5 mm, the
solution of AAV viral particles in a total volume of 1 ul was
injected. The injection was monitored by a `World Precision
Instruments UltraMicroPump3` injection pump at a flow rate of 0.5
ul/min to prevent tissue damage. When the injection was complete,
the injection needle was removed slowly, at a rate of 0.5 mm/min.
After injection, the skin was sealed with 6-0 Ethilon sutures.
Animals were postoperatively hydrated with 1 mL lactated Ringer's
(subcutaneous) and housed in a temperature controlled (37.degree.
C.) environment until achieving an ambulatory recovery. 3 weeks
after surgery animals were euthanized by deep anesthesia followed
by tissue removal for nuclei sorting or with 4% paraformaldehyde
perfusion for immunochemistry.
[1209] Sorting Nuclei and In Vivo Results
[1210] Applicants designed a method to specifically genetically tag
the gRNA targeted neuronal cell nuclei with GFP for Fluorescent
Activated Cell Sorting (FACS) of the labeled cell nuclei and
downstream processing of DNA, RNA and nuclear proteins. To that
purpose the applicants' multiplex targeting vector was designed to
express both a fusion protein between GFP and the mouse nuclear
membrane protein domain KASH (Starr D A, 2011, Current biology) and
the 3 gRNAs to target specific gene loci of interest (FIG. 34).
GFP-KASH was expressed under the control of the human Synapsin
promoter to specifically label neurons. The amino acid of the
fusion protein GFP-KASH was:
TABLE-US-00064 (SEQ ID NO: 204)
MVSKGEELFTGVVPILVELDGDVNGHKFSVSGEGEGDATYGKLTLKFICT
TGKLPVPWPTLVTTLTYGVQCFSRYPDHMKQHDFFKSAMPEGYVQERTIF
FKDDGNYKTRAEVKFEGDTLVNRIELKGIDFKEDGNILGHKLEYNYNSHN
VYIMADKQKNGIKVNFKIRHNIEDGSVQLADHYQQNTPIGDGPVLLPDNH
YLSTQSALSKDPNEKRDHMVLLEFVTAAGITLGMDELYKSGLRSREEEEE
TDSRMPHLDSPGSSQPRRSFLSRVIRAALPLQLLLLLLLLLACLLPASED
DYSCTQANNFARSFYPMLRYTNGPPPT
[1211] One week after AAV1/2 mediated delivery into the brain a
robust expression of GFP-KASH was observed. For FACS and downstream
processing of labeled nuclei, the hippocampi were dissected 3 weeks
after surgery and processed for cell nuclei purification using a
gradient centrifugation step. For that purpose the tissue was
homogenized in 320 mM Sucrose, 5 mM CaCl, 3 mM Mg(Ac)2, 10 mM Tris
pH 7.8, 0.1 mM EDTA, 0.1% NP40, 0.1 mM Phenylmethanesulfonyl
fluoride (PMSF), 1 mM .beta.-mercaptoethanol using 2 ml Dounce
homogenizer (Sigma) The homogenisate was centrifuged on a 25% to
29% Optiprep.RTM. gradient according to the manufacture's protocol
for 30 min at 3.500 rpm at 4.degree. C. The nuclear pellet was
resuspended in 340 mM Sucrose, 2 mM MgCl2, 25 mM KCl, 65 mM
glycerophosphate, 5% glycerol, 0.1 mM PMSF, 1 mM
.beta.-mercaptoethanol and Vybrant.RTM. DyeCycle.TM. Ruby Stain
(Life technologies) was added to label cell nuclei (offers
near-infrared emission for DNA). The labeled and purified nuclei
were sorted by FACS using an Aria Flu-act-cell sorter and BDFACS
Diva software. The sorted GFP+ and GFP- nuclei were finally used to
purify genomic DNA using DNAeasy Blood & Tissue Kit (Qiagen)
for Surveyor assay analysis of the targeted genomic regions. The
same approach can be easily used to purify nuclear RNA or protein
from targeted cells for downstream processing. Due to the 2-vector
system (FIG. 34) the applicants using in this approach efficient
Cas9 mediated DNA cleavage was expected to occur only in a small
subset of cells in the brain (cells which were co-infected with
both the multiplex targeting vector and the Cas9 encoding vector).
The method described here enables the applicants to specifically
purify DNA, RNA and nuclear proteins from the cell population
expressing the 3 gRNAs of interest and therefore are supposed to
undergo Cas9 mediated DNA cleavage. By using this method the
applicants were able to visualize efficient DNA cleavage in vivo
occurring only in a small subset of cells.
[1212] Essentially, what Applicants have shown here is targeted in
vivo cleavage. Furthermore, Applicants used a multiple approach,
with several different sequences targeted at the same time, but
independently. Presented system can be applied for studying brain
pathologic conditions (gene knock out, e.g. Parkinson disease) and
also open a field for further development of genome editing tools
in the brain. By replacing nuclease activity with gene
transcription regulators or epigenetic regulators it will be
possible to answer whole spectrum of scientific question about role
of gene regulation and epigenetic changes in the brain in not only
in the pathologic conditions but also in physiological process as
learning and memory formation. Finally, presented technology can be
applied in more complex mammalian system as primates, what allows
to overcome current technology limitations.
Example 33: Model Data
[1213] Several disease models have been specifically investigated.
These include de novo autism risk genes CHD8, KATNAL2, and SCN2A;
and the syndromic autism (Angelman Syndrome) gene UBE3A. These
genes and resulting autism models are of course preferred, but show
that the invention may be applied to any gene and therefore any
model is possible.
[1214] Applicants have made these cells lines using Cas9 nuclease
in human embryonic stem cells (hESCs). The lines were created by
transient transfection of hESCs with Cbh-Cas9-2A-EGFP and
pU6-sgRNA. Two sgRNAs are designed for each gene targeting most
often the same exons in which patient nonsense (knock-out)
mutations have been recently described from whole exome sequencing
studies of autistic patients. The Cas9-2A-EGFP and pU6 plasmids
were created specifically for this project.
Example 34: AAV Production System or Protocol
[1215] An AAV production system or protocol that was developed for,
and works particularly well with, high through put screening uses
is provided herein, but it has broader applicability in the present
invention as well. Manipulating endogenous gene expression presents
various challenges, as the rate of expression depends on many
factors, including regulatory elements, mRNA processing, and
transcript stability. To overcome this challenge, Applicants
developed an adeno-associated virus (AAV)-based vector for the
delivery. AAV has an ssDNA-based genome and is therefore less
susceptible to recombination.
[1216] AAV1/2 (serotype AAV1/2, i.e., hybrid or mosaic AAV1/AAV2
capsid AAV) heparin purified concentrated virus protocol
[1217] Media: D10+HEPES
500 ml bottle DMEM high glucose+Glutamax (GIBCO) 50 ml Hyclone FBS
(heat-inactivated) (Thermo Fischer) 5.5 ml HEPES solution (1M,
GIBCO) Cells: low passage HEK293FT (passage <10 at time of virus
production, thaw new cells of passage 2-4 for virus production,
grow up for 3-5 passages)
[1218] Transfection Reagent: Polvethylenimine (PEI) "Max"
Dissolve 50 mg PEI "Max" in 50 ml sterile Ultrapure H20
Adjust pH to 7.1
[1219] Filter with 0.22 um fliptop filter Seal tube and wrap with
parafilm Freeze aliquots at -20.degree. C. (for storage, can also
be used immediately)
[1220] Cell Culture
Culture low passage HEK293FT in D10+HEPES Passage everyday between
1:2 and 1:2.5 Advantageously do not allow cells to reach more than
85% confluency
[1221] For T75
[1222] Warm 10 ml HBSS (--Mg2+, --Ca2+, GIBCO)+1 ml TrypLE Express
(GIBCO) per flask to 37.degree. C.
(Waterbath)
[1223] Aspirate media fully [1224] Add 10 ml warm HBSS gently (to
wash out media completely) [1225] Add 1 ml TrypLE per Flask [1226]
Place flask in incubator (37.degree. C.) for Imin [1227] Rock flask
to detach cells [1228] Add 9 ml D10+HEPES media (37.degree. C.)
[1229] Pipette up and down 5 times to generate single cell
suspension [1230] Split at 1:2-1:2.5 (12 ml media for T75) ratio
(if cells are growing more slowly, discard and thaw a new batch,
they are not in optimal growth) [1231] transfer to T225 as soon as
enough cells are present (for ease of handling large amounts of
cells)
[1232] AAV Production (5*15 cm Dish Scale Per Construct):
Plate 10 million cells in 21.5 ml media into a 15 cm dish Incubate
for 18-22 hours at 37.degree. C. Transfection is ideal at 80%
confluence
[1233] Per Plate
Prewarm 22 ml media (D10+HEPES)
[1234] Prepare Tube with DNA Mixture (Use Endofree Maxiprep
DNA):
5.2 ug vector of interest plasmid 4.35 ug AAV 1 serotype plasmid
4.35 ug AAV 2 serotype plasmid 10.4 ug pDF6 plasmid (adenovirus
helper genes) .quadrature. Vortex to mix Add 434 uL DMEM (no
serum!) Add 130 ul PEI solution Vortex 5-10 seconds Add
DNA/DMEM/PEI mixture to prewarmed media Vortex briefly to mix
Replace media in 15 cm dish with DNA/DMEM/PEI mixture Return to
37.degree. C. incubator Incubate 48 h before harvesting (make sure
medium isn't turning too acidic)
[1235] Virus Harvest:
1. aspirate media carefully from 15 cm dish dishes (advantageously
do not dislodge cells) 2. Add 25 ml RT DPBS (Invitrogen) to each
plate and gently remove cells with a cell scraper. Collect
suspension in 50 ml tubes. 3. Pellet cells at 800.times.g for 10
minutes. 4. Discard supernatant
[1236] Pause Point: Freeze Cell Pellet at -80 C if Desired
5. resuspend pellet in 150 mM NaCl, 20 mM Tris pH 8.0, use 10 ml
per tissue culture plate. 6. Prepare a fresh solution of 10% sodium
deoxycholate in dH2O. Add 1.25 ml of this per tissue culture plate
for a final concentration of 0.5%. Add benzonase nuclease to a
final concentration of 50 units per ml. Mix tube thoroughly. 7.
Incubate at 37.degree. C. for 1 hour (Waterbath). 8. Remove
cellular debris by centrifuging at 3000.times.g for 15 mins.
Transfer to fresh 50 ml tube and ensure all cell debris has been
removed to prevent blocking of heparin columns.
[1237] Heparin Column Purification of AAV1/2:
[1238] 1. Set up HiTrap heparin columns using a peristaltic pump so
that solutions flow through the column at 1 ml per minute. It is
important to ensure no air bubbles are introduced into the heparin
column.
[1239] 2. Equilibrate the column with 10 ml 150 mM NaCl, 20 mM
Tris, pH 8.0 using the peristaltic pump.
[1240] 3. Binding of virus: Apply 50 ml virus solution to column
and allow to flow through.
[1241] 4. Wash step 1: column with 20 ml 100 mM NaCl, 20 mM Tris,
pH 8.0. (using the peristaltic pump)
[1242] 5. Wash step 2: Using a 3 ml or 5 ml syringe continue to
wash the column with 1 ml 200 mM NaCl, 20 mM Tris, pH 8.0, followed
by 1 ml 300 mM NaCl, 20 mM Tris, pH 8.0.
[1243] Discard the flow-through.
[1244] (prepare the syringes with different buffers during the 50
min flow through of virus solution above)
[1245] 6. Elution Using 5 ml syringes and gentle pressure (flow
rate of <1 ml/min) elute the virus from the column by
applying:
[1246] 1.5 ml 400 mM NaCl, 20 mM Tris, pH 8.0
[1247] 3.0 ml 450 mM NaCl, 20 mM Tris, pH 8.0
[1248] 1.5 ml 500 mM NaCl, 20 mM Tris, pH 8.0
[1249] Collect these in a 15 ml centrifuge tube.
[1250] Concentration of AAV1/2:
[1251] 1. Concentration step 1: Concentrate the eluted virus using
Amicon ultra 15 ml centrifugal filter units with a 100,000
molecular weight cutoff. Load column eluate into the concentrator
and centrifuge at 2000.times.g for 2 minutes (at room temperature.
Check concentrated volume--it should be approximately 500 .mu.l. If
necessary, centrifuge in 1 min intervals until correct volume is
reached.
[1252] 2. buffer exchange: Add 1 ml sterile DPBS to filter unit,
centrifuge in 1 min intervals until correct volume (500 ul) is
reached.
[1253] 3. Concentration step 2: Add 500 ul concentrate to an Amicon
Ultra 0.5 ml 100K filter unit. Centrifuge at 6000 g for 2 min.
Check concentrated volume--it should be approximately 100 .mu.l. If
necessary, centrifuge in 1 min intervals until correct volume is
reached.
[1254] 4. Recovery: Invert filter insert and insert into fresh
collection tube. Centrifuge at 1000 g for 2 min.
Aliquot and freeze at -80.degree. C. 1 ul is typically required per
injection site, small aliquots (e.g. 5 ul) are therefore
recommended (avoid freeze-thaw of virus). determine
DNaseI-resistant GC particle titer using qPCR (see separate
protocol)
[1255] Materials
Amicon Ultra, 0.5 ml, 100K; MILLIPORE; UFC510024
Amicon Ultra, 15 ml, 100K; MILLIPORE; UFC910024
[1256] Benzonase nuclease; Sigma-Aldrich, E1014 HiTrap Heparin
cartridge; Sigma-Aldrich; 54836 Sodium deoxycholate; Sigma-Aldrich;
D5670
[1257] AAV1 Supernatant Production Protocol
Media: D10+HEPES
[1258] 500 m bottle DMEM high glucose+Glutamax (Invitrogen) 50 ml
Hyclone FBS (heat-inactivated) (Thermo Fischer) 5.5 ml HEPES
solution (1M, GIBCO) Cells: low passage HEK293FT (passage <10 at
time of virus production) Thaw new cells of passage 2-4 for virus
production, grow up for 2-5 passages Transfection reagent:
Polyethylenimine (PEI) "Max" Dissolve 50 mg PEI "Max" in 50 ml
sterile Ultrapure H20
Adjust pH to 7.1
[1259] Filter with 0.22 um fliptop filter Seal tube and wrap with
parafilm Freeze aliquots at -20.degree. C. (for storage, can also
be used immediately)
Cell Culture
[1260] Culture low passage HEK293FT in D10+HEPES Passage everyday
between 1:2 and 1:2.5 Advantageously do let cells reach more than
85% confluency
For T75
[1261] Warm 10 ml HBSS (--Mg2+, --Ca2+, GIBCO)+1 ml TrypLE Express
(GIBCO) per flask to 37.degree. C. (Waterbath) [1262] Aspirate
media fully [1263] Add 10 ml warm HBSS gently (to wash out media
completely) [1264] Add 1 ml TrypLE per Flask [1265] Place flask in
incubator (37.degree. C.) for Imin [1266] Rock flask to detach
cells [1267] Add 9 ml D10+HEPES media (37.degree. C.) [1268]
Pipette up and down 5 times to generate single cell suspension
[1269] Split at 1:2-1:2.5 (12 ml media for T75) ratio (if cells are
growing more slowly, discard and thaw a new batch, they are not in
optimal growth) [1270] transfer to T225 as soon as enough cells are
present (for ease of handling large amounts of cells) AAV
production (single 15 cm dish scale) Plate 10 million cells in 21.5
ml media into a 15 cm dish Incubate for 18-22 hours at 37.degree.
C. Transfection is ideal at 80% confluence per plate Prewarm 22 ml
media (D10+HEPES) Prepare tube with DNA mixture (use endofree
maxiprep DNA): 5.2 ug vector of interest plasmid 8.7 ug AAV 1
serotype plasmid 10.4 ug DF6 plasmid (adenovirus helper genes)
Vortex to mix
[1271] Add 434 uL DMEM (no serum!) Add 130 ul PEI solution Vortex
5-10 seconds Add DNA/DMEM/PEI mixture to prewarmed media Vortex
briefly to mix Replace media in 15 cm dish with DNA/DMEM/PEI
mixture Return to 37.degree. C. incubator Incubate 48 h before
harvesting (advantageously monitor to ensure medium is not turning
too acidic)
[1272] Virus Harvest:
Remove supernatant from 15 cm dish Filter with 0.45 um filter (low
protein binding) Aliquot and freeze at -80.degree. C. Transduction
(primary neuron cultures in 24-well format, 5 DIV) Replace complete
neurobasal media in each well of neurons to be transduced with
fresh neurobasal (usually 400 ul out of 500 ul per well is
replaced) Thaw AAV supernatant in 37.degree. C. waterbath Let
equilibrate in incubator for 30 min Add 250 ul AAV supernatant to
each well
Incubate 24 h at 37.degree. C.
[1273] Remove media/supernatant and replace with fresh complete
neurobasal Expression starts to be visible after 48 h, saturates
around 6-7 Days Post Infection Constructs for pAAV plasmid with GOI
should not exceed 4.8 kb including both ITRS.
[1274] Example of a human codon optimized sequence (i.e. being
optimized for expression in humans) sequence: SaCas9 is provided
below:
TABLE-US-00065 (SEQ ID NO: 205)
ACCGGTGCCACCATGTACCCATACGATGTTCCAGATTAGCGCTTCGCCGAAGAAAAAGCGCAAGGTCGAAGCGT-
CCATG
AAAAGGAACTACATTCTGGGGCTGGACATCGGGATTACAAGCGTGGGGTATGGGATTATTGACTATGAAACAAG-
GGACG
TGATCGACGCAGGCGTCAGACTGTTCAAGGAGGCCAACGTGGAAAACAATGAGGGACGGAGAAGCAAGAGGGGA-
GCCAG
GCGCCTGAAACGACGGAGAAGGCACAGAATCCAGAGGGTGAAGAAACTGCTGTTCGATTACAACCTGCTGACCG-
ACCAT
TCTGAGCTGAGTGGAATTAATCCTTATGAAGCCAGGGTGAAAGGCCTGAGTCAGAAGCTGTCAGAGGAAGAGTT-
TTCCG
CAGCTCTGCTGCACCTGGCTAAGCGCCGAGGAGTGCATAACGTCAATGAGGTGGAAGAGGACACCGGCAACGAG-
CTGTC
TACAAAGGAACAGATCTCACGCAATAGCAAAGCTCTGGAAGAGAAGTATGTCGCAGAGCTGCAGCTGGAACGGC-
TGAAG
AAAGATGGCGAGGTGAGAGGGTCAATTAATAGGTTCAAGACAAGCGACTACGTCAAAGAAGCCAAGCAGCTGCT-
GAAAG
TGCAGAAGGCTTACCACCAGCTGGATCAGAGCTTCATCGATACTTATATCGACCTGCTGGAGACTCGGAGAACC-
TACTA
TGAGGGACCAGGAGAAGGGAGCCCCTTCGGATGGAAAGACATCAAGGAATGGTACGAGATGCTGATGGGACATT-
GCACC
TATTTTCCAGAAGAGCTGAGAAGCGTCAAGTACGCTTATAACGCAGATCTGTACAACGCCCTGAATGACCTGAA-
CAACC
TGGTCATCACCAGGGATGAAAACGAGAAACTGGAATACTATGAGAAGTTCCAGATCATCGAAAACGTGTTTAAG-
CAGAA
GAAAAAGCCTACACTGAAACAGATTGCTAAGGAGATCCTGGTCAACGAAGAGGACATCAAGGGCTACCGGGTGA-
CAAGC
ACTGGAAAACCAGAGTTCACCAATCTGAAAGTGTATCACGATATTAAGGACATCACAGCACGGAAAGAAATCAT-
TGAGA
ACGCCGAACTGCTGGATCAGATTGCTAAGATCCTGACTATCTACCAGAGCTCCGAGGACATCCAGGAAGAGCTG-
ACTAA
CCTGAACAGCGAGCTGACCCAGGAAGAGATCGAACAGATTAGTAATCTGAAGGGGTACACCGGAACACACAACC-
TGTCC
CTGAAAGCTATCAATCTGATTCTGGATGAGCTGTGGCATACAAACGACAATCAGATTGCAATCTTTAACCGGCT-
GAAGC
TGGTCCCAAAAAAGGTGGACCTGAGTCAGCAGAAAGAGATCCCAACCACACTGGTGGACGATTTCATTCTGTCA-
CCCGT
GGTCAAGCGGAGCTTCATCCAGAGCATCAAAGTGATCAACGCCATCATCAAGAAGTACGGCCTGCCCAATGATA-
TCATT
ATCGAGCTGGCTAGGGAGAAGAACAGCAAGGACGCACAGAAGATGATCAATGAGATGCAGAAACGAAACCGGCA-
GACCA
ATGAACGCATTGAAGAGATTATCCGAACTACCGGGAAAGAGAACGCAAAGTACCTGATTGAAAAAATCAAGCTG-
CACGA
TATGCAGGAGGGAAAGTGTCTGTATTCTCTGGAGGCCATCCCCCTGGAGGACCTGCTGAACAATCCATTCAACT-
ACGAG
GTCGATCATATTATCCCCAGAAGCGTGTCCTTCGACAATTCCTTTAACAACAAGGTGCTGGTCAAGCAGGAAGA-
GAACT
CTAAAAAGGGCAATAGGACTCCTTTCCAGTACCTGTCTAGTTCAGATTCCAAGATCTCTTACGAAACCTTTAAA-
AAGCA
CATTCTGAATCTGGCCAAAGGAAAGGGCCGCATCAGCAAGACCAAAAAGGAGTACCTGCTGGAAGAGCGGGACA-
TCAAC
AGATTCTCCGTCCAGAAGGATTTTATTAACCGGAATCTGGTGGACACAAGATACGCTACTCGCGGCCTGATGAA-
TCTGC
TGCGATCCTATTTCCGGGTGAACAATCTGGATGTGAAAGTCAAGTCCATCAACGGCGGGTTCACATCTTTTCTG-
AGGCG
CAAATGGAAGTTTAAAAAGGAGCGCAACAAAGGGTACAAGCACCATGCCGAAGATGCTCTGATTATCGCAAATG-
CCGAC
TTCATCTTTAAGGAGTGGAAAAAGCTGGACAAAGCCAAGAAAGTGATGGAGAACCAGATGTTCGAAGAGAAGCA-
GGCCG
AATCTATGCCCGAAATCGAGACAGAACAGGAGTACAAGGAGATTTTCATCACTCCTCACCAGATCAAGCATATC-
AAGGA
TTTCAAGGACTACAAGTACTCTCACCGGGTGGATAAAAAGCCCAACAGAGAGCTGATCAATGACACCCTGTATA-
GTACA
AGAAAAGACGATAAGGGGAATACCCTGATTGTGAACAATCTGAACGGACTGTACGACAAAGATAATGACAAGCT-
GAAAA
AGCTGATCAACAAAAGTCCCGAGAAGCTGCTGATGTACCACCATGATCCTCAGACATATCAGAAACTGAAGCTG-
ATTAT
GGAGCAGTACGGCGACGAGAAGAACCCACTGTATAAGTACTATGAAGAGACTGGGAACTACCTGACCAAGTATA-
GCAAA
AAGGATAATGGCCCCGTGATCAAGAAGATCAAGTACTATGGGAACAAGCTGAATGCCCATCTGGACATCACAGA-
CGATT
ACCCTAACAGTCGCAACAAGGTGGTCAAGCTGTCACTGAAGCCATACAGATTCGATGTCTATCTGGACAACGGC-
GTGTA
TAAATTTGTGACTGTCAAGAATCTGGATGTCATCAAAAAGGAGAACTACTATGAAGTGAATAGCAAGTGCTACG-
AAGAG
GCTAAAAAGCTGAAAAAGATTAGCAACCAGGCAGAGTTCATCGCCTCCTTTTACAACAACGACCTGATTAAGAT-
CAATG
GCGAACTGTATAGGGTCATCGGGGTGAACAATGATCTGCTGAACCGCATTGAAGTGAATATGATTGACATCACT-
TACCG
AGAGTATCTGGAAAACATGAATGATAAGCGCCCCCCTCGAATTATCAAAACAATTGCCTCTAAGACTCAGAGTA-
TCAAA
AAGTACTCAACCGACATTCTGGGAAACCTGTATGAGGTGAAGAGCAAAAAGCACCCTCAGATTATCAAAAAGGG-
CTAAG AATTC
Example 35: Minimizing Off-Target Cleavage Using Cas9 Nickase and
Two Guide RNAs
[1275] Cas9 is a RNA-guided DNA nuclease that may be targeted to
specific locations in the genome with the help of a 20 bp RNA
guide. However the guide sequence may tolerate some mismatches
between the guide sequence and the DNA-target sequence. The
flexibility is undesirable due to the potential for off-target
cleavage, when the guide RNA targets Cas9 to a an off-target
sequence that has a few bases different from the guide sequence.
For all experimental applications (gene targeting, crop
engineering, therapeutic applications, etc) it is important to be
able to improve the specificity of Cas9 mediated gene targeting and
reduce the likelihood of off-target modification by Cas9.
[1276] Applicants developed a method of using a Cas9 nickase mutant
in combination with two guide RNAs to facilitate targeted double
strand breaks in the genome without off-target modifications. The
Cas9 nickase mutant may be generated from a Cas9 nuclease by
disabling its cleavage activity so that instead of both strands of
the DNA duplex being cleaved only one strand is cleaved. The Cas9
nickase may be generated by inducing mutations in one ore more
domains of the Cas9 nuclease, e.g. Ruvc1 or HNH. These mutations
may include but are not limited to mutations in a Cas9 catalytic
domain, e.g in SpCas9 these mutations may be at positions D10 or
H840. These mutations may include but are not limited to D10A,
E762A, H840A, N854A, N863A or D986A in SpCas9 but nickases may be
generated by inducing mutations at corresponding positions in other
CRISPR enzymes or Cas9 orthologs. In a most preferred embodiment of
the invention the Cas9 nickase mutant is a SpCas9 nickase with a
D10A mutation.
[1277] The way this works is that each guide RNA in combination
with Cas9 nickase would induce the targeted single strand break of
a duplex DNA target. Since each guide RNA nicks one strand, the net
result is a double strand break. The reason this method eliminates
off-target mutations is because it is very unlikely to have an
off-target site that has high degrees of similarity for both guide
sequences (20 bp+2 bp(PAM)=22 bp specificity for each guide, and
two guides means any off-target site will have to have close to 44
bp of homologous sequence). Although it is still likely that
individual guides may have off-targets, but those off-targets will
only be nicked, which is unlikely to be repaired by the mutagenic
NHEJ process. Therefore the multiplexing of DNA double strand
nicking provides a powerful way of introducing targeted DNA double
strand breaks without off-target mutagenic effects.
[1278] Applicants carried out experiments involving the
co-transfection of HEK293FT cells with a plasmid encoding
Cas9(D10A) nickase as well as DNA expression cassettes for one or
more guides. Applicants transfected cells using Lipofectamine 2000,
and transfected cells were harvested 48 or 72 hours after
transfections. Double nicking-induced NHEJ were detected using the
SURVEYOR nuclease assay as described previously herein (FIGS. 51,
52 and 53).
[1279] Applicants have further identified parameters that relate to
efficient cleavage by the Cas9 nickase mutant when combined with
two guide RNAs and these parameters include but are not limited to
the length of the 5' overhang. Efficient cleavage is reported for
5' overhang of at least 26 base pairs. In a preferred embodiment of
the invention, the 5' overhang is at least 30 base pairs and more
preferably at least 34 base pairs. Overhangs of up to 200 base
pairs may be acceptable for cleavage, while 5' overhangs less than
100 base pairs are preferred and 5' overhangs less than 50 base
pairs are most preferred (FIGS. 54 and 55).
Example 36: Behavior Protocols
[1280] Elevated Plus Maze.
[1281] The Elevated Plus-Maze is used to assess anxiety-like
behavior, exploiting the conflict between the innate fear that
rodents have of open areas versus their desire to explore novel
environments.
[1282] The apparatus used for the elevated plus maze test is made
of stainless steel and consists of four arms (two open without
walls and two enclosed by 15 cm high walls) 35 cm long and 5 cm
wide. Each arm of the maze is attached to sturdy metal legs such
that it is elevated 40 cm off of the floor:
[1283] Mice are housed up to three per cage in a room with a 12 hr
light/dark cycle with ad libitum access to food and water.
[1284] Behavioral testing is performed between 9:00 A.M. and 6:00
P.M in the brightly lighted room. All the cages containing mice are
transferred to the behavior testing room 30 min before the first
trial begins.
[1285] A mouse is taken out of its cage and place at the junction
of the open and closed arms, facing the open arm opposite to where
the experimenter is and let for freely explore the maze for 5 min.
During that time animal is recorded and behavior is tracked. The
total distance traveled in the open arms, time spent in open arms,
the total number of transitions between arms, and the latency to
enter the open arm are measured automatically with the Noldus
software. At the end of the 5-min test, remove the rodent from the
plus maze and place into a transport cage. Place back inside its
homecage. The elevated plus maze is cleaned carefully and dry with
paper towels before testing with another mouse.
[1286] Fear Conditioning
[1287] Animals: 4-weeks old male mice (BL6J/57); 10 per group
[1288] Foot shock: 2 s; 0.5 mA
[1289] Protocol involved three phases:
[1290] 1. Exposure, which allowed the mice to acclimate and become
familiar with the training chamber. For unpaired group: 2 min of
acclimation, followed by presentation of the 20-sec tone cue,
followed by an 80-sec interval, repeated six times. For paired
group the acclimation period was 12 min.
[1291] 2. Training; mice were presented with the CS and or US
stimuli. Acclimation period -4 min. Six conditioning trials
involving a tone (CS) and a shock (US) were run in trial epochs
that lasted 100 sec (including the intertrial interval). For the
paired group, each trial consisted of a 20-sec "baseline" interval,
a 20-sec tone presentation, an 18-sec trace interval, a 2-sec
shock, and a 40-sec post-shock interval. Trials were the same for
the unpaired groups of mice except that the tone was omitted.
[1292] 3. Testing; mice were observed for freezing in response to
each context and to the tone and trace-CS. Each phase occurred at
24-h intervals. Mice were allowed to move freely in the training
(familiar) and test (altered; flat floor with a grid, bw patterns
on the walls; vanillin scent) contexts for 3 min. All mice received
four 100-sec testing trials. For all mice, each trial began with a
20-sec interval and the 20-sec tone presentation was followed by a
60-sec interval.
[1293] Scoring: All scoring was done based on video. The % of
freezing was observed in 5-sec increments throughout each context
test exposure and each 100-sec trial epoch. Freezing was scored as
1 or 0 in each time bin, if animal froze for at least 2s.
[1294] The data presented on the column charts is the average for
the group of 7 animals, error bars represent SEM. The data on the
line charts representing training/testing process in time, and each
point is the average of 7 animals, from 6 or 4 trials (training and
testing protocol, respectively). Error bars represent SEM.
[1295] Open Field.
[1296] The Open Field apparatus is broadly used to assess
exploratory behaviour and is validated for use in the measurement
of anxiety related behaviours. Animals are placed in the square
arena (40.times.40 cm) for 10 min while their behavior is recorded.
The total distance moved, velocity and time spent in the center of
arena are scored.
[1297] Novel Object Recognition.
[1298] The Novel Object Recognition test (NOR) is a popular test to
study learning and memory in rodents. It is based on their tendency
to interact more with a novel object than with a familiar object.
In general, animals are first placed in an apparatus and allowed to
explore an object. After a prescribed interval, the animal is
returned to the apparatus, which now contains the familiar object
and a novel object. Object recognition is distinguished by more
time spent interacting with the novel object. The NOR task is
particularly attractive because it requires no external motivation,
reward, or punishment but a little training or habituation is
required, and it can be completed in a relatively short time.
[1299] I Pretraining: [1300] 1. Following arrival in the colony,
the animals are allowed to acclimatize for at least 3-7 d. [1301]
2. At least 3 days before starting experiment animals are handled
daily for at least 3 min per day and exposed to the transport
routine. [1302] 3. Familiarization with the testing environment -24
h before experiment animals are exposed to testing arena
(40.times.40.times.35 cm, clear walls) in the behavior room for 10
min.
[1303] II Object recognition training: [1304] 1. Two `identical`
to-be-familiarized (sample) objects are placed in the back left and
right corners of the apparatus [1305] 2. Animal is placed at the
mid-point of the wall opposite the sample objects, what prevents
any unintentional bias in placing the animal such that it is
oriented more towards a particular side/object [1306] 3. The
experimenter is recording the animal behavior using camera, staying
behind the curtain so as not to serve as a cue for the animal or to
introduce unintentional bias into the study. [1307] 4. After the
planned sample-object exposure time (5-10 min), the animal is
removed from the apparatus and return to the colony for planned
training-to-testing interval. The apparatus is cleaned with 70%
ethanol between animals.
[1308] III Delay phase. Commonly used training-to-testing intervals
vary from 1 h (for robust object recognition) to 24 h.
[1309] IV Object recognition test: [1310] 1. To test for object
recognition after the training-to-testing interval, one of the
familiar sample objects is placed in one back corner of the
apparatus; the novel object is placed in the other back corner.
[1311] 2. Animal is placed in the apparatus as in step II.2. The
experimenter is recording animal behavior, staying behind the
curtain. [1312] 3. After the planned objects exposure time (3-5
min) animals is removed from apparatus and returned to colony. The
apparatus is cleaned with 70% ethanol between animals.
[1313] Data analysis: Recorded videos are used for later data
analysis: a) directed contact scoring (total duration of animal
contact with an object); b) within area scoring (an animal as
"interacting" with the object when its nose is in contact with the
object or directed at the object within minimal distance of 2 cm).
Commonly used measures include time with familiar object versus
novel object, a difference score (novel object interaction-familiar
object interaction), a discrimination ratio (novel object
interaction/total interaction with both objects). Object
recognition in these measures is reflected by more time interacting
with the novel than familiar object, a positive difference score or
a discrimination ratio above 0.5, respectively.
[1314] Barnes Maze.
[1315] Carol Barnes developed a dry-land maze test for spatial
learning and memory in 1979 where animals escaped from a brightly
lit, exposed circular open platform surface to a small dark
recessed chamber located under one of the 18 holes around the
perimeter of the platform. Although it was initially invented for
rats, the Barnes maze (BM) has become more popular to assess
spatial memory in mice, taking advantage of their superior
abilities to find and escape through small holes.
[1316] Procedure:
[1317] 1. Adaptation. Mouse is placed in a cylindrical black start
chamber in the middle of the maze. After 10 s have elapsed chamber
is removed and the buzzer is turned on together with strong light.
Mouse is gently guided to the escape box. Once the mouse is inside
the box, buzzer and light are turned off. The mouse should stay in
the escape box for 2 min.
[1318] 2. Spatial acquisition. Mouse is placed in the cylindrical
black start chamber in the middle of the maze. After 10 s have the
chamber is lifted and the buzzer and light are on. Mouse is allowed
to explore the maze for 3 minutes. The trial ends when the mouse
enters the goal tunnel or after 3 min have elapsed. Immediately
after the mouse enters the tunnel, the buzzer and the light are
turned off and the mouse is allowed to stay in the tunnel for 1
min. If the mouse does not reach the goal within 3 minutes the
experimenter is guiding it gently to the escape box and leave the
mouse inside for 1 min. Mouse stays in the home cage until next
trial. Whole trial is repeated 4 times in 15 minutes intervals
during next 3-4 days.
[1319] 3. Reference memory trial. 24 h after the last training day,
the probe trial is conducted. The target hole must be closed.
Animal is placed in the middle of the maze under the cylindrical
black start chamber and after 10 s the chamber is removed, the
buzzer and the light are turned on. Mouse is removed from the maze
after 90 s. The probe trial is done in order to determine if the
animal remembers where the target goal was located. Number of pokes
(errors) in each hole and latency and path length to reach the
virtually target hole are measured.
Example 37: SaCas9 Update
[1320] FIG. 69 shows an AAV-Sa-Cas9 vector, a liver-specific
AAV-Sa-Cas9 vector and an alternate AAV-Sa-Cas9 vector.
[1321] FIG. 70 shows data on optimized CMV-SaCas9-NLS-U6-sgRNA
vector (submitted vector design last time); new data compares
N'-term vs C'-term tagged SaCas9 and shows enhanced cleavage
efficiency using C'-term NLS tagging.
[1322] New targets were chosen in exons 4 and 5 of the mouse Pcsk9
gene (sequences and locations below). Exons 4-5 lie downstream of a
Pcsk9 N-terminal pro-domain region that is proteolytically cleaved
upon protein maturation, and indels in this downstream region are
expected to lead to protein degradation. Pcsk9 is involved in
cycling and negative regulation of the LDL-receptor, and loss of
Pcsk9 should indirectly lead to lowered plasma cholesterol
levels.
[1323] SgRNAs were cloned into AAV vector and tested for indel
activity in Hepa1-6 mouse hepatocyte cell line in single vector
transfection. 500 ng of vector was transfected into 200,000 Hepa1-6
cells by Lipofectamine 2000 and DNA collected for SURVEYOR assay,
showing cleavage of Pcsk9.
TABLE-US-00066 pAAV- CMV-SaCas9-NLS-U6-sgRNA(231:
atctcttagataccagcatc (SEQ ID NO: 206))
pAAV-CMV-SaCas9-NLS-U6-sgRNA(232: tcaatctcccgatgggcacc (SEQ ID NO:
207)) pAAV- CMV-SaCas9-NLS-U6-sgRNA(233: gcccatcgggagattgaggg (SEQ
ID NO: 208)) pAAV- CMV-SaCas9-NLS-U6-sgRNA(234:
acttcaacagcgtgccggag (SEQ ID NO: 209)) pAAV-
CMV-SaCas9-NLS-U6-sgRNA(235: ccgctgaccacacctgccag (SEQ ID NO: 210))
pAAV- CMV-SaCas9-NLS-U6-sgRNA(236: tggcaggtgtggtcagcggc (SEQ ID NO:
211))
[1324] FIG. 71 shows SURVEYOR image showing indels generated by new
Pcsk9 targets.
[1325] FIG. 72 shows SaCas9 specificity: genome-wide off target
sites (GWOTs) are predicted based on 2 criteria: they contain 4 or
fewer mismatched bases to intended SaCas9 target and bear the least
restrictive PAM for SaCas9, NNGRR. HEK 293FT cells are transfected
with either SpCas9 or SaCas9 with their corresponding sgRNAs at a
target site (EMX1: TAGGGTTAGGGGCCCCAGGC (SEQ ID NO: 2)) that has
CGGGGT as a PAM (sequence including PAM disclosed as SEQ ID NO:
369) so that it can be cut by either SpCas9 (CGG) or SaCas9
(CGGGGT). DNAs from cells are harvested and analyzed for indels by
Illumina sequencing at on-target and 41 predicted off-target loci
(following protocols from Hsu et al. Nature Biotech 2013 and data
analysis pipeline developed by David Scott and Josh Weinstein).
[1326] FIG. 73 shows that that SaCas9 may have a higher level of
off-target activity than SpCas9 at certain loci.
[1327] While preferred embodiments of the present invention have
been shown and described herein, it will be obvious to those
skilled in the art that such embodiments are provided by way of
example only. Numerous variations, changes, and substitutions will
now occur to those skilled in the art without departing from the
invention. It should be understood that various alternatives to the
embodiments of the invention described herein may be employed in
practicing the invention.
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Sequence CWU 1
1
443127DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 1gcactgaggg cctatttccc atgattc 27220DNAHomo
sapiens 2tagggttagg ggccccaggc 20320DNAHomo sapiens 3gagtccgagc
agaagaagaa 20420DNAHomo sapiens 4gagtcctagc aggagaagaa 20520DNAHomo
sapiens 5gagtctaagc agaagaagaa 20660RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 6nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn nnnnnnnnnn
nnnnggnnnn nnnnnnnnnn 60760RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 7nnnnnnnnnn
nnnnccnnnn nnnnnnnnnn nnnnnnnngg nnnnnnnnnn nnnnnnnnnn
60860RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 8nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn
nnnnnnnnnn nnnggnnnnn nnnnnnnnnn 60960RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 9nnnnnnnnnn nnnnnccnnn nnnnnnnnnn nnnnnnnngg
nnnnnnnnnn nnnnnnnnnn 601060RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 10nnnnnnnnnn
nnnnnnnnnn ccnnnnnnnn nnnnnnnnnn nnggnnnnnn nnnnnnnnnn
601160RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 11nnnnnnnnnn nnnnnccnnn nnnnnnnnnn
nnnnnnnngg nnnnnnnnnn nnnnnnnnnn 601260RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 12nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn nnnnnnnnnn
nggnnnnnnn nnnnnnnnnn 601360RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 13nnnnnnnnnn
nnnnnnnccn nnnnnnnnnn nnnnnnnngg nnnnnnnnnn nnnnnnnnnn
601460RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 14nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn
nnnnnnnnnn ggnnnnnnnn nnnnnnnnnn 601560RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 15nnnnnnnnnn nnnnnnnncc nnnnnnnnnn nnnnnnnngg
nnnnnnnnnn nnnnnnnnnn 601660RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 16nnnnnnnnnn
nnnnnnnnnn ccnnnnnnnn nnnnnnnnng gnnnnnnnnn nnnnnnnnnn
601760RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 17nnnnnnnnnn nnnnnnnnnc cnnnnnnnnn
nnnnnnnngg nnnnnnnnnn nnnnnnnnnn 601860RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 18nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn nnnnnnnngg
nnnnnnnnnn nnnnnnnnnn 601960RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 19nnnnnnnnnn
nnnnnnnnnn ccnnnnnnnn nnnnnnnngg nnnnnnnnnn nnnnnnnnnn
602060RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 20nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn
nnnnnnnggn nnnnnnnnnn nnnnnnnnnn 602160RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 21nnnnnnnnnn nnnnnnnnnn nccnnnnnnn nnnnnnnngg
nnnnnnnnnn nnnnnnnnnn 602260RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 22nnnnnnnnnn
nnnnnnnnnn ccnnnnnnnn nnnnnnggnn nnnnnnnnnn nnnnnnnnnn
602360RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 23nnnnnnnnnn nnnnnnnnnn nnccnnnnnn
nnnnnnnngg nnnnnnnnnn nnnnnnnnnn 602460RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 24nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn nnnnnggnnn
nnnnnnnnnn nnnnnnnnnn 602560RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 25nnnnnnnnnn
nnnnnnnnnn nnnccnnnnn nnnnnnnngg nnnnnnnnnn nnnnnnnnnn
602660RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 26nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn
nnnnggnnnn nnnnnnnnnn nnnnnnnnnn 602760RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 27nnnnnnnnnn nnnnnnnnnn nnnnccnnnn nnnnnnnngg
nnnnnnnnnn nnnnnnnnnn 602860RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 28nnnnnnnnnn
nnnnnnnnnn ccnnnnnnnn nnnggnnnnn nnnnnnnnnn nnnnnnnnnn
602960RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 29nnnnnnnnnn nnnnnnnnnn nnnnnccnnn
nnnnnnnngg nnnnnnnnnn nnnnnnnnnn 603060RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 30nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn nnggnnnnnn
nnnnnnnnnn nnnnnnnnnn 603160RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 31nnnnnnnnnn
nnnnnnnnnn nnnnnnccnn nnnnnnnngg nnnnnnnnnn nnnnnnnnnn
603260RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 32nnnnnnnnnn nnnnnnnnnn ccnnnnnnnn
nggnnnnnnn nnnnnnnnnn nnnnnnnnnn 603360RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 33nnnnnnnnnn nnnnnnnnnn nnnnnnnccn nnnnnnnngg
nnnnnnnnnn nnnnnnnnnn 603460RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 34nnnnnnnnnn
nnnnnnnnnn ccnnnnnnnn ggnnnnnnnn nnnnnnnnnn nnnnnnnnnn
603560RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 35nnnnnnnnnn nnnnnnnnnn nnnnnnnncc
nnnnnnnngg nnnnnnnnnn nnnnnnnnnn 603660RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 36nnnnnnnnnn nnnnnnnnnn ccnnnnnnng gnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn 603760RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 37nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnc cnnnnnnngg nnnnnnnnnn nnnnnnnnnn
603860RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 38nnnnnnnnnn nnnnnnnnnn ccnnnnnngg
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 603960RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 39nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ccnnnnnngg
nnnnnnnnnn nnnnnnnnnn 604060RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 40nnnnnnnnnn
nnnnnnnnnn ccnnnnnggn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
604160RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 41nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
nccnnnnngg nnnnnnnnnn nnnnnnnnnn 604260RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 42nnnnnnnnnn nnnnnnnnnn ccnnnnggnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn 604360RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 43nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnccnnnngg nnnnnnnnnn nnnnnnnnnn
604460RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 44nnnnnnnnnn nnnnnnnnnn ccnnnggnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 604560RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 45nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnccnnngg
nnnnnnnnnn nnnnnnnnnn 604660RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 46nnnnnnnnnn
nnnnnnnnnn ccnnggnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
604760RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 47nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
nnnnccnngg nnnnnnnnnn nnnnnnnnnn 604860RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 48nnnnnnnnnn nnnnnnnnnn ccnggnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn 604960RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 49nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnccngg nnnnnnnnnn nnnnnnnnnn
605060RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 50nnnnnnnnnn nnnnnnnnnn nccggnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 605160RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 51nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnccggn
nnnnnnnnnn nnnnnnnnnn 605260RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 52nnnnnnnnnn
nnnnnnnnnn nnnggnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
605360RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 53nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
nnnggccnnn nnnnnnnnnn nnnnnnnnnn 605460RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 54nnnnnnnnnn nnnnnnnnnn nncggnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn 605560RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 55nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnggnccnnn nnnnnnnnnn nnnnnnnnnn
605660RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 56nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn
nggnnccnnn nnnnnnnnnn nnnnnnnnnn 605760RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 57nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ggnnnccnnn
nnnnnnnnnn nnnnnnnnnn 605860RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 58nnnnnnnnnn
nnnnnnnnnn nnnnnnnnng gnnnnccnnn nnnnnnnnnn nnnnnnnnnn
605960RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 59nnnnnnnnnn nnnnnnnnnn nnnnnnnngg
nnnnnccnnn nnnnnnnnnn nnnnnnnnnn 60609PRTUnknownDescription of
Unknown 'LAGLIDADG' family motif peptide 60Leu Ala Gly Leu Ile Asp
Ala Asp Gly 1 5 6112RNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 61guuuuagagc ua 12627PRTSimian
virus 40 62Pro Lys Lys Lys Arg Lys Val 1 5
6316PRTUnknownDescription of Unknown Nucleoplasmin bipartite NLS
sequence 63Lys Arg Pro Ala Ala Thr Lys Lys Ala Gly Gln Ala Lys Lys
Lys Lys 1 5 10 15 649PRTUnknownDescription of Unknown C-myc NLS
sequence 64Pro Ala Ala Lys Arg Val Lys Leu Asp 1 5
6511PRTUnknownDescription of Unknown C-myc NLS sequence 65Arg Gln
Arg Arg Asn Glu Leu Lys Arg Ser Pro 1 5 10 6638PRTHomo sapiens
66Asn Gln Ser Ser Asn Phe Gly Pro Met Lys Gly Gly Asn Phe Gly Gly 1
5 10 15 Arg Ser Ser Gly Pro Tyr Gly Gly Gly Gly Gln Tyr Phe Ala Lys
Pro 20 25 30 Arg Asn Gln Gly Gly Tyr 35 6742PRTUnknownDescription
of Unknown IBB domain from importin-alpha sequence 67Arg Met Arg
Ile Glx Phe Lys Asn Lys Gly Lys Asp Thr Ala Glu Leu 1 5 10 15 Arg
Arg Arg Arg Val Glu Val Ser Val Glu Leu Arg Lys Ala Lys Lys 20 25
30 Asp Glu Gln Ile Leu Lys Arg Arg Asn Val 35 40
688PRTUnknownDescription of Unknown Myoma T protein sequence 68Val
Ser Arg Lys Arg Pro Arg Pro 1 5 698PRTUnknownDescription of Unknown
Myoma T protein sequence 69Pro Pro Lys Lys Ala Arg Glu Asp 1 5
708PRTHomo sapiens 70Pro Gln Pro Lys Lys Lys Pro Leu 1 5 7112PRTMus
musculus 71Ser Ala Leu Ile Lys Lys Lys Lys Lys Met Ala Pro 1 5 10
725PRTInfluenza virus 72Asp Arg Leu Arg Arg 1 5 737PRTInfluenza
virus 73Pro Lys Gln Lys Lys Arg Lys 1 5 7410PRTHepatitus delta
virus 74Arg Lys Leu Lys Lys Lys Ile Lys Lys Leu 1 5 10 7510PRTMus
musculus 75Arg Glu Lys Lys Lys Phe Leu Lys Arg Arg 1 5 10
7620PRTHomo sapiens 76Lys Arg Lys Gly Asp Glu Val Asp Gly Val Asp
Glu Val Ala Lys Lys 1 5 10 15 Lys Ser Lys Lys 20 7717PRTHomo
sapiens 77Arg Lys Cys Leu Gln Ala Gly Met Asn Leu Glu Ala Arg Lys
Thr Lys 1 5 10 15 Lys 7827DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 78nnnnnnnnnn
nnnnnnnnnn nnagaaw 277919DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 79nnnnnnnnnn
nnnnagaaw 198027DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 80nnnnnnnnnn nnnnnnnnnn nnagaaw
278118DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 81nnnnnnnnnn nnnagaaw
1882137DNAArtificial SequenceDescription of Artificial Sequence
Synthetic polynucleotide 82nnnnnnnnnn nnnnnnnnnn gtttttgtac
tctcaagatt tagaaataaa tcttgcagaa 60gctacaaaga taaggcttca tgccgaaatc
aacaccctgt cattttatgg cagggtgttt 120tcgttattta atttttt
13783123DNAArtificial SequenceDescription of Artificial Sequence
Synthetic polynucleotide 83nnnnnnnnnn nnnnnnnnnn gtttttgtac
tctcagaaat gcagaagcta caaagataag 60gcttcatgcc gaaatcaaca ccctgtcatt
ttatggcagg gtgttttcgt tatttaattt 120ttt 12384110DNAArtificial
SequenceDescription of Artificial Sequence Synthetic polynucleotide
84nnnnnnnnnn nnnnnnnnnn gtttttgtac tctcagaaat gcagaagcta caaagataag
60gcttcatgcc gaaatcaaca ccctgtcatt ttatggcagg gtgttttttt
11085102DNAArtificial SequenceDescription of Artificial Sequence
Synthetic polynucleotide 85nnnnnnnnnn nnnnnnnnnn gttttagagc
tagaaatagc aagttaaaat aaggctagtc 60cgttatcaac ttgaaaaagt ggcaccgagt
cggtgctttt tt 1028688DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 86nnnnnnnnnn
nnnnnnnnnn gttttagagc tagaaatagc aagttaaaat aaggctagtc 60cgttatcaac
ttgaaaaagt gttttttt 888776DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 87nnnnnnnnnn
nnnnnnnnnn gttttagagc tagaaatagc aagttaaaat aaggctagtc 60cgttatcatt
tttttt 768812DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 88gttttagagc ta
128931DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 89tagcaagtta aaataaggct agtccgtttt t
319027DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 90nnnnnnnnnn nnnnnnnnnn nnagaaw
279133DNAHomo sapiens 91ggacatcgat gtcacctcca atgactaggg tgg
339233DNAHomo sapiens 92cattggaggt gacatcgatg tcctccccat tgg
339333DNAHomo sapiens 93ggaagggcct gagtccgagc agaagaagaa ggg
339433DNAHomo sapiens 94ggtggcgaga ggggccgaga ttgggtgttc agg
339533DNAHomo sapiens 95atgcaggagg gtggcgagag gggccgagat tgg
339632DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 96aaactctaga gagggcctat ttcccatgat tc
3297153DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 97acctctagaa aaaaagcacc gactcggtgc cactttttca
agttgataac ggactagcct 60tattttaact tgctatgctg ttttgtttcc aaaacagcat
agctctaaaa cccctagtca 120ttggaggtga cggtgtttcg tcctttccac aag
1539852DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 98taatacgact cactatagga agtgcgccac catggcccca
aagaagaagc gg 529960DNAArtificial SequenceDescription of Artificial
Sequence Synthetic primer 99ggtttttttt tttttttttt tttttttttt
ttttcttact ttttcttttt tgcctggccg 60100984PRTCampylobacter jejuni
100Met Ala Arg Ile Leu Ala Phe Asp Ile Gly Ile Ser Ser Ile Gly Trp
1 5 10 15 Ala Phe Ser Glu Asn Asp Glu Leu Lys Asp Cys Gly Val Arg
Ile Phe 20 25 30 Thr Lys Val Glu Asn Pro Lys Thr Gly Glu Ser Leu
Ala Leu Pro Arg 35 40 45 Arg Leu Ala Arg Ser Ala Arg Lys Arg Leu
Ala Arg Arg Lys Ala Arg 50 55 60 Leu Asn His Leu Lys His Leu Ile
Ala Asn Glu Phe Lys Leu Asn Tyr 65 70 75 80 Glu Asp Tyr Gln Ser Phe
Asp Glu Ser Leu Ala Lys Ala Tyr Lys Gly 85 90 95 Ser Leu Ile Ser
Pro Tyr Glu Leu Arg Phe Arg Ala Leu Asn Glu Leu 100 105 110 Leu Ser
Lys Gln Asp Phe Ala Arg Val Ile Leu His Ile Ala Lys Arg 115
120 125 Arg Gly Tyr Asp Asp Ile Lys Asn Ser Asp Asp Lys Glu Lys Gly
Ala 130 135 140 Ile Leu Lys Ala Ile Lys Gln Asn Glu Glu Lys Leu Ala
Asn Tyr Gln 145 150 155 160 Ser Val Gly Glu Tyr Leu Tyr Lys Glu Tyr
Phe Gln Lys Phe Lys Glu 165 170 175 Asn Ser Lys Glu Phe Thr Asn Val
Arg Asn Lys Lys Glu Ser Tyr Glu 180 185 190 Arg Cys Ile Ala Gln Ser
Phe Leu Lys Asp Glu Leu Lys Leu Ile Phe 195 200 205 Lys Lys Gln Arg
Glu Phe Gly Phe Ser Phe Ser Lys Lys Phe Glu Glu 210 215 220 Glu Val
Leu Ser Val Ala Phe Tyr Lys Arg Ala Leu Lys Asp Phe Ser 225 230 235
240 His Leu Val Gly Asn Cys Ser Phe Phe Thr Asp Glu Lys Arg Ala Pro
245 250 255 Lys Asn Ser Pro Leu Ala Phe Met Phe Val Ala Leu Thr Arg
Ile Ile 260 265 270 Asn Leu Leu Asn Asn Leu Lys Asn Thr Glu Gly Ile
Leu Tyr Thr Lys 275 280 285 Asp Asp Leu Asn Ala Leu Leu Asn Glu Val
Leu Lys Asn Gly Thr Leu 290 295 300 Thr Tyr Lys Gln Thr Lys Lys Leu
Leu Gly Leu Ser Asp Asp Tyr Glu 305 310 315 320 Phe Lys Gly Glu Lys
Gly Thr Tyr Phe Ile Glu Phe Lys Lys Tyr Lys 325 330 335 Glu Phe Ile
Lys Ala Leu Gly Glu His Asn Leu Ser Gln Asp Asp Leu 340 345 350 Asn
Glu Ile Ala Lys Asp Ile Thr Leu Ile Lys Asp Glu Ile Lys Leu 355 360
365 Lys Lys Ala Leu Ala Lys Tyr Asp Leu Asn Gln Asn Gln Ile Asp Ser
370 375 380 Leu Ser Lys Leu Glu Phe Lys Asp His Leu Asn Ile Ser Phe
Lys Ala 385 390 395 400 Leu Lys Leu Val Thr Pro Leu Met Leu Glu Gly
Lys Lys Tyr Asp Glu 405 410 415 Ala Cys Asn Glu Leu Asn Leu Lys Val
Ala Ile Asn Glu Asp Lys Lys 420 425 430 Asp Phe Leu Pro Ala Phe Asn
Glu Thr Tyr Tyr Lys Asp Glu Val Thr 435 440 445 Asn Pro Val Val Leu
Arg Ala Ile Lys Glu Tyr Arg Lys Val Leu Asn 450 455 460 Ala Leu Leu
Lys Lys Tyr Gly Lys Val His Lys Ile Asn Ile Glu Leu 465 470 475 480
Ala Arg Glu Val Gly Lys Asn His Ser Gln Arg Ala Lys Ile Glu Lys 485
490 495 Glu Gln Asn Glu Asn Tyr Lys Ala Lys Lys Asp Ala Glu Leu Glu
Cys 500 505 510 Glu Lys Leu Gly Leu Lys Ile Asn Ser Lys Asn Ile Leu
Lys Leu Arg 515 520 525 Leu Phe Lys Glu Gln Lys Glu Phe Cys Ala Tyr
Ser Gly Glu Lys Ile 530 535 540 Lys Ile Ser Asp Leu Gln Asp Glu Lys
Met Leu Glu Ile Asp His Ile 545 550 555 560 Tyr Pro Tyr Ser Arg Ser
Phe Asp Asp Ser Tyr Met Asn Lys Val Leu 565 570 575 Val Phe Thr Lys
Gln Asn Gln Glu Lys Leu Asn Gln Thr Pro Phe Glu 580 585 590 Ala Phe
Gly Asn Asp Ser Ala Lys Trp Gln Lys Ile Glu Val Leu Ala 595 600 605
Lys Asn Leu Pro Thr Lys Lys Gln Lys Arg Ile Leu Asp Lys Asn Tyr 610
615 620 Lys Asp Lys Glu Gln Lys Asn Phe Lys Asp Arg Asn Leu Asn Asp
Thr 625 630 635 640 Arg Tyr Ile Ala Arg Leu Val Leu Asn Tyr Thr Lys
Asp Tyr Leu Asp 645 650 655 Phe Leu Pro Leu Ser Asp Asp Glu Asn Thr
Lys Leu Asn Asp Thr Gln 660 665 670 Lys Gly Ser Lys Val His Val Glu
Ala Lys Ser Gly Met Leu Thr Ser 675 680 685 Ala Leu Arg His Thr Trp
Gly Phe Ser Ala Lys Asp Arg Asn Asn His 690 695 700 Leu His His Ala
Ile Asp Ala Val Ile Ile Ala Tyr Ala Asn Asn Ser 705 710 715 720 Ile
Val Lys Ala Phe Ser Asp Phe Lys Lys Glu Gln Glu Ser Asn Ser 725 730
735 Ala Glu Leu Tyr Ala Lys Lys Ile Ser Glu Leu Asp Tyr Lys Asn Lys
740 745 750 Arg Lys Phe Phe Glu Pro Phe Ser Gly Phe Arg Gln Lys Val
Leu Asp 755 760 765 Lys Ile Asp Glu Ile Phe Val Ser Lys Pro Glu Arg
Lys Lys Pro Ser 770 775 780 Gly Ala Leu His Glu Glu Thr Phe Arg Lys
Glu Glu Glu Phe Tyr Gln 785 790 795 800 Ser Tyr Gly Gly Lys Glu Gly
Val Leu Lys Ala Leu Glu Leu Gly Lys 805 810 815 Ile Arg Lys Val Asn
Gly Lys Ile Val Lys Asn Gly Asp Met Phe Arg 820 825 830 Val Asp Ile
Phe Lys His Lys Lys Thr Asn Lys Phe Tyr Ala Val Pro 835 840 845 Ile
Tyr Thr Met Asp Phe Ala Leu Lys Val Leu Pro Asn Lys Ala Val 850 855
860 Ala Arg Ser Lys Lys Gly Glu Ile Lys Asp Trp Ile Leu Met Asp Glu
865 870 875 880 Asn Tyr Glu Phe Cys Phe Ser Leu Tyr Lys Asp Ser Leu
Ile Leu Ile 885 890 895 Gln Thr Lys Asp Met Gln Glu Pro Glu Phe Val
Tyr Tyr Asn Ala Phe 900 905 910 Thr Ser Ser Thr Val Ser Leu Ile Val
Ser Lys His Asp Asn Lys Phe 915 920 925 Glu Thr Leu Ser Lys Asn Gln
Lys Ile Leu Phe Lys Asn Ala Asn Glu 930 935 940 Lys Glu Val Ile Ala
Lys Ser Ile Gly Ile Gln Asn Leu Lys Val Phe 945 950 955 960 Glu Lys
Tyr Ile Val Ser Ala Leu Gly Glu Val Thr Lys Ala Glu Phe 965 970 975
Arg Gln Arg Glu Asp Phe Lys Lys 980 10191DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 101tataatctca taagaaattt aaaaagggac taaaataaag
agtttgcggg actctgcggg 60gttacaatcc cctaaaaccg cttttaaaat t
9110236DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 102attttaccat aaagaaattt aaaaagggac
taaaac 3610395RNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 103nnnnnnnnnn nnnnnnnnnn
guuuuagucc cgaaagggac uaaaauaaag aguuugcggg 60acucugcggg guuacaaucc
ccuaaaaccg cuuuu 951041115PRTArtificial SequenceDescription of
Artificial Sequence Synthetic polypeptide 104Met Ser Asp Leu Val
Leu Gly Leu Asp Ile Gly Ile Gly Ser Val Gly 1 5 10 15 Val Gly Ile
Leu Asn Lys Val Thr Gly Glu Ile Ile His Lys Asn Ser 20 25 30 Arg
Ile Phe Pro Ala Ala Gln Ala Glu Asn Asn Leu Val Arg Arg Thr 35 40
45 Asn Arg Gln Gly Arg Arg Leu Ala Arg Arg Lys Lys His Arg Arg Val
50 55 60 Arg Leu Asn Arg Leu Phe Glu Glu Ser Gly Leu Ile Thr Asp
Phe Thr 65 70 75 80 Lys Ile Ser Ile Asn Leu Asn Pro Tyr Gln Leu Arg
Val Lys Gly Leu 85 90 95 Thr Asp Glu Leu Ser Asn Glu Glu Leu Phe
Ile Ala Leu Lys Asn Met 100 105 110 Val Lys His Arg Gly Ile Ser Tyr
Leu Asp Asp Ala Ser Asp Asp Gly 115 120 125 Asn Ser Ser Val Gly Asp
Tyr Ala Gln Ile Val Lys Glu Asn Ser Lys 130 135 140 Gln Leu Glu Thr
Lys Thr Pro Gly Gln Ile Gln Leu Glu Arg Tyr Gln 145 150 155 160 Thr
Tyr Gly Gln Leu Arg Gly Asp Phe Thr Val Glu Lys Asp Gly Lys 165 170
175 Lys His Arg Leu Ile Asn Val Phe Pro Thr Ser Ala Tyr Arg Ser Glu
180 185 190 Ala Leu Arg Ile Leu Gln Thr Gln Gln Glu Phe Asn Pro Gln
Ile Thr 195 200 205 Asp Glu Phe Ile Asn Arg Tyr Leu Glu Ile Leu Thr
Gly Lys Arg Lys 210 215 220 Tyr Tyr His Gly Pro Gly Asn Glu Lys Ser
Arg Thr Asp Tyr Gly Arg 225 230 235 240 Tyr Arg Thr Ser Gly Glu Thr
Leu Asp Asn Ile Phe Gly Ile Leu Ile 245 250 255 Gly Lys Cys Thr Phe
Tyr Pro Asp Glu Phe Arg Ala Ala Lys Ala Ser 260 265 270 Tyr Thr Ala
Gln Glu Phe Asn Leu Leu Asn Asp Leu Asn Asn Leu Thr 275 280 285 Val
Pro Thr Glu Thr Lys Lys Leu Ser Lys Glu Gln Lys Asn Gln Ile 290 295
300 Ile Asn Tyr Val Lys Asn Glu Lys Ala Met Gly Pro Ala Lys Leu Phe
305 310 315 320 Lys Tyr Ile Ala Lys Leu Leu Ser Cys Asp Val Ala Asp
Ile Lys Gly 325 330 335 Tyr Arg Ile Asp Lys Ser Gly Lys Ala Glu Ile
His Thr Phe Glu Ala 340 345 350 Tyr Arg Lys Met Lys Thr Leu Glu Thr
Leu Asp Ile Glu Gln Met Asp 355 360 365 Arg Glu Thr Leu Asp Lys Leu
Ala Tyr Val Leu Thr Leu Asn Thr Glu 370 375 380 Arg Glu Gly Ile Gln
Glu Ala Leu Glu His Glu Phe Ala Asp Gly Ser 385 390 395 400 Phe Ser
Gln Lys Gln Val Asp Glu Leu Val Gln Phe Arg Lys Ala Asn 405 410 415
Ser Ser Ile Phe Gly Lys Gly Trp His Asn Phe Ser Val Lys Leu Met 420
425 430 Met Glu Leu Ile Pro Glu Leu Tyr Glu Thr Ser Glu Glu Gln Met
Thr 435 440 445 Ile Leu Thr Arg Leu Gly Lys Gln Lys Thr Thr Ser Ser
Ser Asn Lys 450 455 460 Thr Lys Tyr Ile Asp Glu Lys Leu Leu Thr Glu
Glu Ile Tyr Asn Pro 465 470 475 480 Val Val Ala Lys Ser Val Arg Gln
Ala Ile Lys Ile Val Asn Ala Ala 485 490 495 Ile Lys Glu Tyr Gly Asp
Phe Asp Asn Ile Val Ile Glu Met Ala Arg 500 505 510 Glu Asn Gln Thr
Thr Gln Lys Gly Gln Lys Asn Ser Arg Glu Arg Met 515 520 525 Lys Arg
Ile Glu Glu Gly Ile Lys Glu Leu Gly Ser Gln Ile Leu Lys 530 535 540
Glu His Pro Val Glu Asn Thr Gln Leu Gln Asn Glu Lys Leu Tyr Leu 545
550 555 560 Tyr Tyr Leu Gln Asn Gly Arg Asp Met Tyr Val Asp Gln Glu
Leu Asp 565 570 575 Ile Asn Arg Leu Ser Asp Tyr Asp Val Asp His Ile
Val Pro Gln Ser 580 585 590 Phe Leu Lys Asp Asp Ser Ile Asp Asn Lys
Val Leu Thr Arg Ser Asp 595 600 605 Lys Asn Arg Gly Lys Ser Asp Asn
Val Pro Ser Glu Glu Val Val Lys 610 615 620 Lys Met Lys Asn Tyr Trp
Arg Gln Leu Leu Asn Ala Lys Leu Ile Thr 625 630 635 640 Gln Arg Lys
Phe Asp Asn Leu Thr Lys Ala Glu Arg Gly Gly Leu Ser 645 650 655 Glu
Leu Asp Lys Ala Gly Phe Ile Lys Arg Gln Leu Val Glu Thr Arg 660 665
670 Gln Ile Thr Lys His Val Ala Gln Ile Leu Asp Ser Arg Met Asn Thr
675 680 685 Lys Tyr Asp Glu Asn Asp Lys Leu Ile Arg Glu Val Lys Val
Ile Thr 690 695 700 Leu Lys Ser Lys Leu Val Ser Asp Phe Arg Lys Asp
Phe Gln Phe Tyr 705 710 715 720 Lys Val Arg Glu Ile Asn Asn Tyr His
His Ala His Asp Ala Tyr Leu 725 730 735 Asn Ala Val Val Gly Thr Ala
Leu Ile Lys Lys Tyr Pro Lys Leu Glu 740 745 750 Ser Glu Phe Val Tyr
Gly Asp Tyr Lys Val Tyr Asp Val Arg Lys Met 755 760 765 Ile Ala Lys
Ser Glu Gln Glu Ile Gly Lys Ala Thr Ala Lys Tyr Phe 770 775 780 Phe
Tyr Ser Asn Ile Met Asn Phe Phe Lys Thr Glu Ile Thr Leu Ala 785 790
795 800 Asn Gly Glu Ile Arg Lys Arg Pro Leu Ile Glu Thr Asn Gly Glu
Thr 805 810 815 Gly Glu Ile Val Trp Asp Lys Gly Arg Asp Phe Ala Thr
Val Arg Lys 820 825 830 Val Leu Ser Met Pro Gln Val Asn Ile Val Lys
Lys Thr Glu Val Gln 835 840 845 Thr Gly Gly Phe Ser Lys Glu Ser Ile
Leu Pro Lys Arg Asn Ser Asp 850 855 860 Lys Leu Ile Ala Arg Lys Lys
Asp Trp Asp Pro Lys Lys Tyr Gly Gly 865 870 875 880 Phe Asp Ser Pro
Thr Val Ala Tyr Ser Val Leu Val Val Ala Lys Val 885 890 895 Glu Lys
Gly Lys Ser Lys Lys Leu Lys Ser Val Lys Glu Leu Leu Gly 900 905 910
Ile Thr Ile Met Glu Arg Ser Ser Phe Glu Lys Asn Pro Ile Asp Phe 915
920 925 Leu Glu Ala Lys Gly Tyr Lys Glu Val Lys Lys Asp Leu Ile Ile
Lys 930 935 940 Leu Pro Lys Tyr Ser Leu Phe Glu Leu Glu Asn Gly Arg
Lys Arg Met 945 950 955 960 Leu Ala Ser Ala Gly Glu Leu Gln Lys Gly
Asn Glu Leu Ala Leu Pro 965 970 975 Ser Lys Tyr Val Asn Phe Leu Tyr
Leu Ala Ser His Tyr Glu Lys Leu 980 985 990 Lys Gly Ser Pro Glu Asp
Asn Glu Gln Lys Gln Leu Phe Val Glu Gln 995 1000 1005 His Lys His
Tyr Leu Asp Glu Ile Ile Glu Gln Ile Ser Glu Phe 1010 1015 1020 Ser
Lys Arg Val Ile Leu Ala Asp Ala Asn Leu Asp Lys Val Leu 1025 1030
1035 Ser Ala Tyr Asn Lys His Arg Asp Lys Pro Ile Arg Glu Gln Ala
1040 1045 1050 Glu Asn Ile Ile His Leu Phe Thr Leu Thr Asn Leu Gly
Ala Pro 1055 1060 1065 Ala Ala Phe Lys Tyr Phe Asp Thr Thr Ile Asp
Arg Lys Arg Tyr 1070 1075 1080 Thr Ser Thr Lys Glu Val Leu Asp Ala
Thr Leu Ile His Gln Ser 1085 1090 1095 Ile Thr Gly Leu Tyr Glu Thr
Arg Ile Asp Leu Ser Gln Leu Gly 1100 1105 1110 Gly Asp 1115
1051374PRTArtificial SequenceDescription of Artificial Sequence
Synthetic polypeptide 105Met Asp Lys Lys Tyr Ser Ile Gly Leu Asp
Ile Gly Thr Asn Ser Val 1 5 10 15 Gly Trp Ala Val Ile Thr Asp Glu
Tyr Lys Val Pro Ser Lys Lys Phe 20 25 30 Lys Val Leu Gly Asn Thr
Asp Arg His Ser Ile Lys Lys Asn Leu Ile 35 40 45 Gly Ala Leu Leu
Phe Asp Ser Gly Glu Thr Ala Glu Ala Thr Arg Leu 50 55 60 Lys Arg
Thr Ala Arg Arg Arg Tyr Thr Arg Arg Lys Asn Arg Ile Cys 65 70 75 80
Tyr Leu Gln Glu Ile Phe Ser Asn Glu Met Ala Lys Val Asp Asp Ser 85
90 95 Phe Phe His Arg Leu Glu Glu Ser Phe Leu Val Glu Glu Asp Lys
Lys 100 105 110 His Glu Arg His Pro Ile Phe Gly Asn Ile Val Asp Glu
Val Ala Tyr 115 120 125 His Glu Lys Tyr Pro Thr Ile Tyr His Leu Arg
Lys Lys Leu Val Asp 130 135 140 Ser Thr Asp Lys Ala Asp Leu Arg Leu
Ile Tyr Leu Ala Leu Ala His 145 150 155 160 Met Ile Lys Phe Arg Gly
His Phe Leu Ile Glu Gly Asp Leu Asn Pro 165 170 175 Asp Asn Ser Asp
Val Asp Lys Leu Phe Ile Gln Leu Val Gln Thr Tyr 180 185 190 Asn Gln
Leu Phe Glu Glu Asn Pro Ile Asn Ala Ser Gly Val Asp Ala 195 200 205
Lys Ala Ile Leu Ser Ala Arg Leu Ser Lys Ser Arg Arg
Leu Glu Asn 210 215 220 Leu Ile Ala Gln Leu Pro Gly Glu Lys Lys Asn
Gly Leu Phe Gly Asn 225 230 235 240 Leu Ile Ala Leu Ser Leu Gly Leu
Thr Pro Asn Phe Lys Ser Asn Phe 245 250 255 Asp Leu Ala Glu Asp Ala
Lys Leu Gln Leu Ser Lys Asp Thr Tyr Asp 260 265 270 Asp Asp Leu Asp
Asn Leu Leu Ala Gln Ile Gly Asp Gln Tyr Ala Asp 275 280 285 Leu Phe
Leu Ala Ala Lys Asn Leu Ser Asp Ala Ile Leu Leu Ser Asp 290 295 300
Ile Leu Arg Val Asn Thr Glu Ile Thr Lys Ala Pro Leu Ser Ala Ser 305
310 315 320 Met Ile Lys Arg Tyr Asp Glu His His Gln Asp Leu Thr Leu
Leu Lys 325 330 335 Ala Leu Val Arg Gln Gln Leu Pro Glu Lys Tyr Lys
Glu Ile Phe Phe 340 345 350 Asp Gln Ser Lys Asn Gly Tyr Ala Gly Tyr
Ile Asp Gly Gly Ala Ser 355 360 365 Gln Glu Glu Phe Tyr Lys Phe Ile
Lys Pro Ile Leu Glu Lys Met Asp 370 375 380 Gly Thr Glu Glu Leu Leu
Val Lys Leu Asn Arg Glu Asp Leu Leu Arg 385 390 395 400 Lys Gln Arg
Thr Phe Asp Asn Gly Ser Ile Pro His Gln Ile His Leu 405 410 415 Gly
Glu Leu His Ala Ile Leu Arg Arg Gln Glu Asp Phe Tyr Pro Phe 420 425
430 Leu Lys Asp Asn Arg Glu Lys Ile Glu Lys Ile Leu Thr Phe Arg Ile
435 440 445 Pro Tyr Tyr Val Gly Pro Leu Ala Arg Gly Asn Ser Arg Phe
Ala Trp 450 455 460 Met Thr Arg Lys Ser Glu Glu Thr Ile Thr Pro Trp
Asn Phe Glu Glu 465 470 475 480 Val Val Asp Lys Gly Ala Ser Ala Gln
Ser Phe Ile Glu Arg Met Thr 485 490 495 Asn Phe Asp Lys Asn Leu Pro
Asn Glu Lys Val Leu Pro Lys His Ser 500 505 510 Leu Leu Tyr Glu Tyr
Phe Thr Val Tyr Asn Glu Leu Thr Lys Val Lys 515 520 525 Tyr Val Thr
Glu Gly Met Arg Lys Pro Ala Phe Leu Ser Gly Glu Gln 530 535 540 Lys
Lys Ala Ile Val Asp Leu Leu Phe Lys Thr Asn Arg Lys Val Thr 545 550
555 560 Val Lys Gln Leu Lys Glu Asp Tyr Phe Lys Lys Ile Glu Cys Phe
Asp 565 570 575 Ser Val Glu Ile Ser Gly Val Glu Asp Arg Phe Asn Ala
Ser Leu Gly 580 585 590 Thr Tyr His Asp Leu Leu Lys Ile Ile Lys Asp
Lys Asp Phe Leu Asp 595 600 605 Asn Glu Glu Asn Glu Asp Ile Leu Glu
Asp Ile Val Leu Thr Leu Thr 610 615 620 Leu Phe Glu Asp Arg Glu Met
Ile Glu Glu Arg Leu Lys Thr Tyr Ala 625 630 635 640 His Leu Phe Asp
Asp Lys Val Met Lys Gln Leu Lys Arg Arg Arg Tyr 645 650 655 Thr Gly
Trp Gly Arg Leu Ser Arg Lys Leu Ile Asn Gly Ile Arg Asp 660 665 670
Lys Gln Ser Gly Lys Thr Ile Leu Asp Phe Leu Lys Ser Asp Gly Phe 675
680 685 Ala Asn Arg Asn Phe Met Gln Leu Ile His Asp Asp Ser Leu Thr
Phe 690 695 700 Lys Glu Asp Ile Gln Lys Ala Gln Val Ser Gly Gln Gly
Asp Ser Leu 705 710 715 720 His Glu His Ile Ala Asn Leu Ala Gly Ser
Pro Ala Ile Lys Lys Gly 725 730 735 Ile Leu Gln Thr Val Lys Val Val
Asp Glu Leu Val Lys Val Met Gly 740 745 750 Arg His Lys Pro Glu Asn
Ile Val Ile Glu Met Ala Arg Glu Thr Asn 755 760 765 Glu Asp Asp Glu
Lys Lys Ala Ile Gln Lys Ile Gln Lys Ala Asn Lys 770 775 780 Asp Glu
Lys Asp Ala Ala Met Leu Lys Ala Ala Asn Gln Tyr Asn Gly 785 790 795
800 Lys Ala Glu Leu Pro His Ser Val Phe His Gly His Lys Gln Leu Ala
805 810 815 Thr Lys Ile Arg Leu Trp His Gln Gln Gly Glu Arg Cys Leu
Tyr Thr 820 825 830 Gly Lys Thr Ile Ser Ile His Asp Leu Ile Asn Asn
Ser Asn Gln Phe 835 840 845 Glu Val Asp His Ile Leu Pro Leu Ser Ile
Thr Phe Asp Asp Ser Leu 850 855 860 Ala Asn Lys Val Leu Val Tyr Ala
Thr Ala Asn Gln Glu Lys Gly Gln 865 870 875 880 Arg Thr Pro Tyr Gln
Ala Leu Asp Ser Met Asp Asp Ala Trp Ser Phe 885 890 895 Arg Glu Leu
Lys Ala Phe Val Arg Glu Ser Lys Thr Leu Ser Asn Lys 900 905 910 Lys
Lys Glu Tyr Leu Leu Thr Glu Glu Asp Ile Ser Lys Phe Asp Val 915 920
925 Arg Lys Lys Phe Ile Glu Arg Asn Leu Val Asp Thr Arg Tyr Ala Ser
930 935 940 Arg Val Val Leu Asn Ala Leu Gln Glu His Phe Arg Ala His
Lys Ile 945 950 955 960 Asp Thr Lys Val Ser Val Val Arg Gly Gln Phe
Thr Ser Gln Leu Arg 965 970 975 Arg His Trp Gly Ile Glu Lys Thr Arg
Asp Thr Tyr His His His Ala 980 985 990 Val Asp Ala Leu Ile Ile Ala
Ala Ser Ser Gln Leu Asn Leu Trp Lys 995 1000 1005 Lys Gln Lys Asn
Thr Leu Val Ser Tyr Ser Glu Asp Gln Leu Leu 1010 1015 1020 Asp Ile
Glu Thr Gly Glu Leu Ile Ser Asp Asp Glu Tyr Lys Glu 1025 1030 1035
Ser Val Phe Lys Ala Pro Tyr Gln His Phe Val Asp Thr Leu Lys 1040
1045 1050 Ser Lys Glu Phe Glu Asp Ser Ile Leu Phe Ser Tyr Gln Val
Asp 1055 1060 1065 Ser Lys Phe Asn Arg Lys Ile Ser Asp Ala Thr Ile
Tyr Ala Thr 1070 1075 1080 Arg Gln Ala Lys Val Gly Lys Asp Lys Ala
Asp Glu Thr Tyr Val 1085 1090 1095 Leu Gly Lys Ile Lys Asp Ile Tyr
Thr Gln Asp Gly Tyr Asp Ala 1100 1105 1110 Phe Met Lys Ile Tyr Lys
Lys Asp Lys Ser Lys Phe Leu Met Tyr 1115 1120 1125 Arg His Asp Pro
Gln Thr Phe Glu Lys Val Ile Glu Pro Ile Leu 1130 1135 1140 Glu Asn
Tyr Pro Asn Lys Gln Ile Asn Glu Lys Gly Lys Glu Val 1145 1150 1155
Pro Cys Asn Pro Phe Leu Lys Tyr Lys Glu Glu His Gly Tyr Ile 1160
1165 1170 Arg Lys Tyr Ser Lys Lys Gly Asn Gly Pro Glu Ile Lys Ser
Leu 1175 1180 1185 Lys Tyr Tyr Asp Ser Lys Leu Gly Asn His Ile Asp
Ile Thr Pro 1190 1195 1200 Lys Asp Ser Asn Asn Lys Val Val Leu Gln
Ser Val Ser Pro Trp 1205 1210 1215 Arg Ala Asp Val Tyr Phe Asn Lys
Thr Thr Gly Lys Tyr Glu Ile 1220 1225 1230 Leu Gly Leu Lys Tyr Ala
Asp Leu Gln Phe Glu Lys Gly Thr Gly 1235 1240 1245 Thr Tyr Lys Ile
Ser Gln Glu Lys Tyr Asn Asp Ile Lys Lys Lys 1250 1255 1260 Glu Gly
Val Asp Ser Asp Ser Glu Phe Lys Phe Thr Leu Tyr Lys 1265 1270 1275
Asn Asp Leu Leu Leu Val Lys Asp Thr Glu Thr Lys Glu Gln Gln 1280
1285 1290 Leu Phe Arg Phe Leu Ser Arg Thr Met Pro Lys Gln Lys His
Tyr 1295 1300 1305 Val Glu Leu Lys Pro Tyr Asp Lys Gln Lys Phe Glu
Gly Gly Glu 1310 1315 1320 Ala Leu Ile Lys Val Leu Gly Asn Val Ala
Asn Ser Gly Gln Cys 1325 1330 1335 Lys Lys Gly Leu Gly Lys Ser Asn
Ile Ser Ile Tyr Lys Val Arg 1340 1345 1350 Thr Asp Val Leu Gly Asn
Gln His Ile Ile Lys Asn Glu Gly Asp 1355 1360 1365 Lys Pro Lys Leu
Asp Phe 1370 10615PRTArtificial SequenceDescription of Artificial
Sequence Synthetic peptide 106Gly Gly Gly Gly Ser Gly Gly Gly Gly
Ser Gly Gly Gly Gly Ser 1 5 10 15 10715PRTArtificial
SequenceDescription of Artificial Sequence Synthetic peptide 107Glu
Ala Ala Ala Lys Glu Ala Ala Ala Lys Glu Ala Ala Ala Lys 1 5 10 15
10818PRTArtificial SequenceDescription of Artificial Sequence
Synthetic peptide 108Gly Gly Gly Gly Gly Ser Gly Gly Gly Gly Gly
Ser Gly Gly Gly Gly1 5 10 15 Gly Ser 10923DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 109gccaaattgg acgaccctcg cgg 2311023DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 110cgaggagacc cccgtttcgg tgg 2311123DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 111cccgccgccg ccgtggctcg agg 2311223DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 112tgagctctac gagatccaca agg 2311323DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 113ctcaaaattc ataccggttg tgg 2311423DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 114cgttaaacaa caaccggact tgg 2311523DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 115ttcaccccgc ggcgctgaat ggg 2311623DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 116accactacca gtccgtccac agg 2311723DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 117agcctttctg aacacatgca cgg 2311839DNAHomo sapiens
118cctgccatca atgtggccat gcatgtgttc agaaaggct 3911939DNAHomo
sapiens 119cctgccatca atgtggccgt gcatgtgttc agaaaggct
3912023DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 120cactgcttaa gcctcgctcg agg
2312123DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 121tcaccagcaa tattcgctcg agg
2312223DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 122caccagcaat attccgctcg agg
2312323DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 123tagcaacaga catacgctcg agg
2312423DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 124gggcagtagt aatacgctcg agg
2312523DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 125ccaattccca tacattattg tac
231264677DNAArtificial SequenceDescription of Artificial Sequence
Synthetic polynucleotide 126tctttcttgc gctatgacac ttccagcaaa
aggtagggcg ggctgcgaga cggcttcccg 60gcgctgcatg caacaccgat gatgcttcga
ccccccgaag ctccttcggg gctgcatggg 120cgctccgatg ccgctccagg
gcgagcgctg tttaaatagc caggcccccg attgcaaaga 180cattatagcg
agctaccaaa gccatattca aacacctaga tcactaccac ttctacacag
240gccactcgag cttgtgatcg cactccgcta agggggcgcc tcttcctctt
cgtttcagtc 300acaacccgca aacatgtacc catacgatgt tccagattac
gcttcgccga agaaaaagcg 360caaggtcgaa gcgtccgaca agaagtacag
catcggcctg gacatcggca ccaactctgt 420gggctgggcc gtgatcaccg
acgagtacaa ggtgcccagc aagaaattca aggtgctggg 480caacaccgac
cggcacagca tcaagaagaa cctgatcgga gccctgctgt tcgacagcgg
540cgaaacagcc gaggccaccc ggctgaagag aaccgccaga agaagataca
ccagacggaa 600gaaccggatc tgctatctgc aagagatctt cagcaacgag
atggccaagg tggacgacag 660cttcttccac agactggaag agtccttcct
ggtggaagag gataagaagc acgagcggca 720ccccatcttc ggcaacatcg
tggacgaggt ggcctaccac gagaagtacc ccaccatcta 780ccacctgaga
aagaaactgg tggacagcac cgacaaggcc gacctgcggc tgatctatct
840ggccctggcc cacatgatca agttccgggg ccacttcctg atcgagggcg
acctgaaccc 900cgacaacagc gacgtggaca agctgttcat ccagctggtg
cagacctaca accagctgtt 960cgaggaaaac cccatcaacg ccagcggcgt
ggacgccaag gccatcctgt ctgccagact 1020gagcaagagc agacggctgg
aaaatctgat cgcccagctg cccggcgaga agaagaatgg 1080cctgttcggc
aacctgattg ccctgagcct gggcctgacc cccaacttca agagcaactt
1140cgacctggcc gaggatgcca aactgcagct gagcaaggac acctacgacg
acgacctgga 1200caacctgctg gcccagatcg gcgaccagta cgccgacctg
tttctggccg ccaagaacct 1260gtccgacgcc atcctgctga gcgacatcct
gagagtgaac accgagatca ccaaggcccc 1320cctgagcgcc tctatgatca
agagatacga cgagcaccac caggacctga ccctgctgaa 1380agctctcgtg
cggcagcagc tgcctgagaa gtacaaagag attttcttcg accagagcaa
1440gaacggctac gccggctaca ttgacggcgg agccagccag gaagagttct
acaagttcat 1500caagcccatc ctggaaaaga tggacggcac cgaggaactg
ctcgtgaagc tgaacagaga 1560ggacctgctg cggaagcagc ggaccttcga
caacggcagc atcccccacc agatccacct 1620gggagagctg cacgccattc
tgcggcggca ggaagatttt tacccattcc tgaaggacaa 1680ccgggaaaag
atcgagaaga tcctgacctt ccgcatcccc tactacgtgg gccctctggc
1740caggggaaac agcagattcg cctggatgac cagaaagagc gaggaaacca
tcaccccctg 1800gaacttcgag gaagtggtgg acaagggcgc ttccgcccag
agcttcatcg agcggatgac 1860caacttcgat aagaacctgc ccaacgagaa
ggtgctgccc aagcacagcc tgctgtacga 1920gtacttcacc gtgtataacg
agctgaccaa agtgaaatac gtgaccgagg gaatgagaaa 1980gcccgccttc
ctgagcggcg agcagaaaaa ggccatcgtg gacctgctgt tcaagaccaa
2040ccggaaagtg accgtgaagc agctgaaaga ggactacttc aagaaaatcg
agtgcttcga 2100ctccgtggaa atctccggcg tggaagatcg gttcaacgcc
tccctgggca cataccacga 2160tctgctgaaa attatcaagg acaaggactt
cctggacaat gaggaaaacg aggacattct 2220ggaagatatc gtgctgaccc
tgacactgtt tgaggacaga gagatgatcg aggaacggct 2280gaaaacctat
gcccacctgt tcgacgacaa agtgatgaag cagctgaagc ggcggagata
2340caccggctgg ggcaggctga gccggaagct gatcaacggc atccgggaca
agcagtccgg 2400caagacaatc ctggatttcc tgaagtccga cggcttcgcc
aacagaaact tcatgcagct 2460gatccacgac gacagcctga cctttaaaga
ggacatccag aaagcccagg tgtccggcca 2520gggcgatagc ctgcacgagc
acattgccaa tctggccggc agccccgcca ttaagaaggg 2580catcctgcag
acagtgaagg tggtggacga gctcgtgaaa gtgatgggcc ggcacaagcc
2640cgagaacatc gtgatcgaaa tggccagaga gaaccagacc acccagaagg
gacagaagaa 2700cagccgcgag agaatgaagc ggatcgaaga gggcatcaaa
gagctgggca gccagatcct 2760gaaagaacac cccgtggaaa acacccagct
gcagaacgag aagctgtacc tgtactacct 2820gcagaatggg cgggatatgt
acgtggacca ggaactggac atcaaccggc tgtccgacta 2880cgatgtggac
catatcgtgc ctcagagctt tctgaaggac gactccatcg acaacaaggt
2940gctgaccaga agcgacaaga accggggcaa gagcgacaac gtgccctccg
aagaggtcgt 3000gaagaagatg aagaactact ggcggcagct gctgaacgcc
aagctgatta cccagagaaa 3060gttcgacaat ctgaccaagg ccgagagagg
cggcctgagc gaactggata aggccggctt 3120catcaagaga cagctggtgg
aaacccggca gatcacaaag cacgtggcac agatcctgga 3180ctcccggatg
aacactaagt acgacgagaa tgacaagctg atccgggaag tgaaagtgat
3240caccctgaag tccaagctgg tgtccgattt ccggaaggat ttccagtttt
acaaagtgcg 3300cgagatcaac aactaccacc acgcccacga cgcctacctg
aacgccgtcg tgggaaccgc 3360cctgatcaaa aagtacccta agctggaaag
cgagttcgtg tacggcgact acaaggtgta 3420cgacgtgcgg aagatgatcg
ccaagagcga gcaggaaatc ggcaaggcta ccgccaagta 3480cttcttctac
agcaacatca tgaacttttt caagaccgag attaccctgg ccaacggcga
3540gatccggaag cggcctctga tcgagacaaa cggcgaaacc ggggagatcg
tgtgggataa 3600gggccgggat tttgccaccg tgcggaaagt gctgagcatg
ccccaagtga atatcgtgaa 3660aaagaccgag gtgcagacag gcggcttcag
caaagagtct atcctgccca agaggaacag 3720cgataagctg atcgccagaa
agaaggactg ggaccctaag aagtacggcg gcttcgacag 3780ccccaccgtg
gcctattctg tgctggtggt ggccaaagtg gaaaagggca agtccaagaa
3840actgaagagt gtgaaagagc tgctggggat caccatcatg gaaagaagca
gcttcgagaa 3900gaatcccatc gactttctgg aagccaaggg ctacaaagaa
gtgaaaaagg acctgatcat 3960caagctgcct aagtactccc tgttcgagct
ggaaaacggc cggaagagaa tgctggcctc 4020tgccggcgaa ctgcagaagg
gaaacgaact ggccctgccc tccaaatatg tgaacttcct 4080gtacctggcc
agccactatg agaagctgaa gggctccccc gaggataatg agcagaaaca
4140gctgtttgtg gaacagcaca agcactacct ggacgagatc atcgagcaga
tcagcgagtt 4200ctccaagaga gtgatcctgg ccgacgctaa tctggacaaa
gtgctgtccg cctacaacaa 4260gcaccgggat aagcccatca gagagcaggc
cgagaatatc atccacctgt ttaccctgac 4320caatctggga gcccctgccg
ccttcaagta
ctttgacacc accatcgacc ggaagaggta 4380caccagcacc aaagaggtgc
tggacgccac cctgatccac cagagcatca ccggcctgta 4440cgagacacgg
atcgacctgt ctcagctggg aggcgacagc cccaagaaga agagaaaggt
4500ggaggccagc taaggatccg gcaagactgg ccccgcttgg caacgcaaca
gtgagcccct 4560ccctagtgtg tttggggatg tgactatgta ttcgtgtgtt
ggccaacggg tcaacccgaa 4620cagattgata cccgccttgg catttcctgt
cagaatgtaa cgtcagttga tggtact 46771273150DNAArtificial
SequenceDescription of Artificial Sequence Synthetic polynucleotide
127tctttcttgc gctatgacac ttccagcaaa aggtagggcg ggctgcgaga
cggcttcccg 60gcgctgcatg caacaccgat gatgcttcga ccccccgaag ctccttcggg
gctgcatggg 120cgctccgatg ccgctccagg gcgagcgctg tttaaatagc
caggcccccg attgcaaaga 180cattatagcg agctaccaaa gccatattca
aacacctaga tcactaccac ttctacacag 240gccactcgag cttgtgatcg
cactccgcta agggggcgcc tcttcctctt cgtttcagtc 300acaacccgca
aacatgccta agaagaagag gaaggttaac acgattaaca tcgctaagaa
360cgacttctct gacatcgaac tggctgctat cccgttcaac actctggctg
accattacgg 420tgagcgttta gctcgcgaac agttggccct tgagcatgag
tcttacgaga tgggtgaagc 480acgcttccgc aagatgtttg agcgtcaact
taaagctggt gaggttgcgg ataacgctgc 540cgccaagcct ctcatcacta
ccctactccc taagatgatt gcacgcatca acgactggtt 600tgaggaagtg
aaagctaagc gcggcaagcg cccgacagcc ttccagttcc tgcaagaaat
660caagccggaa gccgtagcgt acatcaccat taagaccact ctggcttgcc
taaccagtgc 720tgacaataca accgttcagg ctgtagcaag cgcaatcggt
cgggccattg aggacgaggc 780tcgcttcggt cgtatccgtg accttgaagc
taagcacttc aagaaaaacg ttgaggaaca 840actcaacaag cgcgtagggc
acgtctacaa gaaagcattt atgcaagttg tcgaggctga 900catgctctct
aagggtctac tcggtggcga ggcgtggtct tcgtggcata aggaagactc
960tattcatgta ggagtacgct gcatcgagat gctcattgag tcaaccggaa
tggttagctt 1020acaccgccaa aatgctggcg tagtaggtca agactctgag
actatcgaac tcgcacctga 1080atacgctgag gctatcgcaa cccgtgcagg
tgcgctggct ggcatctctc cgatgttcca 1140accttgcgta gttcctccta
agccgtggac tggcattact ggtggtggct attgggctaa 1200cggtcgtcgt
cctctggcgc tggtgcgtac tcacagtaag aaagcactga tgcgctacga
1260agacgtttac atgcctgagg tgtacaaagc gattaacatt gcgcaaaaca
ccgcatggaa 1320aatcaacaag aaagtcctag cggtcgccaa cgtaatcacc
aagtggaagc attgtccggt 1380cgaggacatc cctgcgattg agcgtgaaga
actcccgatg aaaccggaag acatcgacat 1440gaatcctgag gctctcaccg
cgtggaaacg tgctgccgct gctgtgtacc gcaaggacaa 1500ggctcgcaag
tctcgccgta tcagccttga gttcatgctt gagcaagcca ataagtttgc
1560taaccataag gccatctggt tcccttacaa catggactgg cgcggtcgtg
tttacgctgt 1620gtcaatgttc aacccgcaag gtaacgatat gaccaaagga
ctgcttacgc tggcgaaagg 1680taaaccaatc ggtaaggaag gttactactg
gctgaaaatc cacggtgcaa actgtgcggg 1740tgtcgacaag gttccgttcc
ctgagcgcat caagttcatt gaggaaaacc acgagaacat 1800catggcttgc
gctaagtctc cactggagaa cacttggtgg gctgagcaag attctccgtt
1860ctgcttcctt gcgttctgct ttgagtacgc tggggtacag caccacggcc
tgagctataa 1920ctgctccctt ccgctggcgt ttgacgggtc ttgctctggc
atccagcact tctccgcgat 1980gctccgagat gaggtaggtg gtcgcgcggt
taacttgctt cctagtgaaa ccgttcagga 2040catctacggg attgttgcta
agaaagtcaa cgagattcta caagcagacg caatcaatgg 2100gaccgataac
gaagtagtta ccgtgaccga tgagaacact ggtgaaatct ctgagaaagt
2160caagctgggc actaaggcac tggctggtca atggctggct tacggtgtta
ctcgcagtgt 2220gactaagcgt tcagtcatga cgctggctta cgggtccaaa
gagttcggct tccgtcaaca 2280agtgctggaa gataccattc agccagctat
tgattccggc aagggtctga tgttcactca 2340gccgaatcag gctgctggat
acatggctaa gctgatttgg gaatctgtga gcgtgacggt 2400ggtagctgcg
gttgaagcaa tgaactggct taagtctgct gctaagctgc tggctgctga
2460ggtcaaagat aagaagactg gagagattct tcgcaagcgt tgcgctgtgc
attgggtaac 2520tcctgatggt ttccctgtgt ggcaggaata caagaagcct
attcagacgc gcttgaacct 2580gatgttcctc ggtcagttcc gcttacagcc
taccattaac accaacaaag atagcgagat 2640tgatgcacac aaacaggagt
ctggtatcgc tcctaacttt gtacacagcc aagacggtag 2700ccaccttcgt
aagactgtag tgtgggcaca cgagaagtac ggaatcgaat cttttgcact
2760gattcacgac tccttcggta cgattccggc tgacgctgcg aacctgttca
aagcagtgcg 2820cgaaactatg gttgacacat atgagtcttg tgatgtactg
gctgatttct acgaccagtt 2880cgctgaccag ttgcacgagt ctcaattgga
caaaatgcca gcacttccgg ctaaaggtaa 2940cttgaacctc cgtgacatct
tagagtcgga cttcgcgttc gcgtaaggat ccggcaagac 3000tggccccgct
tggcaacgca acagtgagcc cctccctagt gtgtttgggg atgtgactat
3060gtattcgtgt gttggccaac gggtcaaccc gaacagattg atacccgcct
tggcatttcc 3120tgtcagaatg taacgtcagt tgatggtact
3150128125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic polynucleotide 128gaaattaata cgactcacta tannnnnnnn
nnnnnnnnnn nngttttaga gctagaaata 60gcaagttaaa ataaggctag tccgttatca
acttgaaaaa gtggcaccga gtcggtgctt 120ttttt 1251298452DNAArtificial
SequenceDescription of Artificial Sequence Synthetic polynucleotide
129tgcggtattt cacaccgcat caggtggcac ttttcgggga aatgtgcgcg
gaacccctat 60ttgtttattt ttctaaatac attcaaatat gtatccgctc atgagattat
caaaaaggat 120cttcacctag atccttttaa attaaaaatg aagttttaaa
tcaatctaaa gtatatatga 180gtaaacttgg tctgacagtt accaatgctt
aatcagtgag gcacctatct cagcgatctg 240tctatttcgt tcatccatag
ttgcctgact ccccgtcgtg tagataacta cgatacggga 300gggcttacca
tctggcccca gtgctgcaat gataccgcga gacccacgct caccggctcc
360agatttatca gcaataaacc agccagccgg aagggccgag cgcagaagtg
gtcctgcaac 420tttatccgcc tccatccagt ctattaattg ttgccgggaa
gctagagtaa gtagttcgcc 480agttaatagt ttgcgcaacg ttgttgccat
tgctacaggc atcgtggtgt cacgctcgtc 540gtttggtatg gcttcattca
gctccggttc ccaacgatca aggcgagtta catgatcccc 600catgttgtgc
aaaaaagcgg ttagctcctt cggtcctccg atcgttgtca gaagtaagtt
660ggccgcagtg ttatcactca tggttatggc agcactgcat aattctctta
ctgtcatgcc 720atccgtaaga tgcttttctg tgactggtga gtactcaacc
aagtcattct gagaatagtg 780tatgcggcga ccgagttgct cttgcccggc
gtcaatacgg gataataccg cgccacatag 840cagaacttta aaagtgctca
tcattggaaa acgttcttcg gggcgaaaac tctcaaggat 900cttaccgctg
ttgagatcca gttcgatgta acccactcgt gcacccaact gatcttcagc
960atcttttact ttcaccagcg tttctgggtg agcaaaaaca ggaaggcaaa
atgccgcaaa 1020aaagggaata agggcgacac ggaaatgttg aatactcata
ctcttccttt ttcaatatta 1080ttgaagcatt tatcagggtt attgtctcat
gaccaaaatc ccttaacgtg agttttcgtt 1140ccactgagcg tcagaccccg
tagaaaagat caaaggatct tcttgagatc ctttttttct 1200gcgcgtaatc
tgctgcttgc aaacaaaaaa accaccgcta ccagcggtgg tttgtttgcc
1260ggatcaagag ctaccaactc tttttccgaa ggtaactggc ttcagcagag
cgcagatacc 1320aaatactgtt cttctagtgt agccgtagtt aggccaccac
ttcaagaact ctgtagcacc 1380gcctacatac ctcgctctgc taatcctgtt
accagtggct gttgccagtg gcgataagtc 1440gtgtcttacc gggttggact
caagacgata gttaccggat aaggcgcagc ggtcgggctg 1500aacggggggt
tcgtgcacac agcccagctt ggagcgaacg acctacaccg aactgagata
1560cctacagcgt gagctatgag aaagcgccac gcttcccgaa gggagaaagg
cggacaggta 1620tccggtaagc ggcagggtcg gaacaggaga gcgcacgagg
gagcttccag ggggaaacgc 1680ctggtatctt tatagtcctg tcgggtttcg
ccacctctga cttgagcgtc gatttttgtg 1740atgctcgtca ggggggcgga
gcctatggaa aaacgccagc aacgcggcct ttttacggtt 1800cctggccttt
tgctggcctt ttgctcacat gttctttcct gcgttatccc ctgattctgt
1860ggataaccgt attaccgcct ttgagtgagc tgataccgct cgccgcagcc
gaacgaccga 1920gcgcagcgag tcagtgagcg aggaagcggt cgctgaggct
tgacatgatt ggtgcgtatg 1980tttgtatgaa gctacaggac tgatttggcg
ggctatgagg gcgggggaag ctctggaagg 2040gccgcgatgg ggcgcgcggc
gtccagaagg cgccatacgg cccgctggcg gcacccatcc 2100ggtataaaag
cccgcgaccc cgaacggtga cctccacttt cagcgacaaa cgagcactta
2160tacatacgcg actattctgc cgctatacat aaccactcag ctagcttaag
atcccatcaa 2220gcttgcatgc cgggcgcgcc agaaggagcg cagccaaacc
aggatgatgt ttgatggggt 2280atttgagcac ttgcaaccct tatccggaag
ccccctggcc cacaaaggct aggcgccaat 2340gcaagcagtt cgcatgcagc
ccctggagcg gtgccctcct gataaaccgg ccagggggcc 2400tatgttcttt
acttttttac aagagaagtc actcaacatc ttaaaatggc caggtgagtc
2460gacgagcaag cccggcggat caggcagcgt gcttgcagat ttgacttgca
acgcccgcat 2520tgtgtcgacg aaggcttttg gctcctctgt cgctgtctca
agcagcatct aaccctgcgt 2580cgccgtttcc atttgcagga gattcgaggt
accatgtacc catacgatgt tccagattac 2640gcttcgccga agaaaaagcg
caaggtcgaa gcgtccgaca agaagtacag catcggcctg 2700gacatcggca
ccaactctgt gggctgggcc gtgatcaccg acgagtacaa ggtgcccagc
2760aagaaattca aggtgctggg caacaccgac cggcacagca tcaagaagaa
cctgatcgga 2820gccctgctgt tcgacagcgg cgaaacagcc gaggccaccc
ggctgaagag aaccgccaga 2880agaagataca ccagacggaa gaaccggatc
tgctatctgc aagagatctt cagcaacgag 2940atggccaagg tggacgacag
cttcttccac agactggaag agtccttcct ggtggaagag 3000gataagaagc
acgagcggca ccccatcttc ggcaacatcg tggacgaggt ggcctaccac
3060gagaagtacc ccaccatcta ccacctgaga aagaaactgg tggacagcac
cgacaaggcc 3120gacctgcggc tgatctatct ggccctggcc cacatgatca
agttccgggg ccacttcctg 3180atcgagggcg acctgaaccc cgacaacagc
gacgtggaca agctgttcat ccagctggtg 3240cagacctaca accagctgtt
cgaggaaaac cccatcaacg ccagcggcgt ggacgccaag 3300gccatcctgt
ctgccagact gagcaagagc agacggctgg aaaatctgat cgcccagctg
3360cccggcgaga agaagaatgg cctgttcggc aacctgattg ccctgagcct
gggcctgacc 3420cccaacttca agagcaactt cgacctggcc gaggatgcca
aactgcagct gagcaaggac 3480acctacgacg acgacctgga caacctgctg
gcccagatcg gcgaccagta cgccgacctg 3540tttctggccg ccaagaacct
gtccgacgcc atcctgctga gcgacatcct gagagtgaac 3600accgagatca
ccaaggcccc cctgagcgcc tctatgatca agagatacga cgagcaccac
3660caggacctga ccctgctgaa agctctcgtg cggcagcagc tgcctgagaa
gtacaaagag 3720attttcttcg accagagcaa gaacggctac gccggctaca
ttgacggcgg agccagccag 3780gaagagttct acaagttcat caagcccatc
ctggaaaaga tggacggcac cgaggaactg 3840ctcgtgaagc tgaacagaga
ggacctgctg cggaagcagc ggaccttcga caacggcagc 3900atcccccacc
agatccacct gggagagctg cacgccattc tgcggcggca ggaagatttt
3960tacccattcc tgaaggacaa ccgggaaaag atcgagaaga tcctgacctt
ccgcatcccc 4020tactacgtgg gccctctggc caggggaaac agcagattcg
cctggatgac cagaaagagc 4080gaggaaacca tcaccccctg gaacttcgag
gaagtggtgg acaagggcgc ttccgcccag 4140agcttcatcg agcggatgac
caacttcgat aagaacctgc ccaacgagaa ggtgctgccc 4200aagcacagcc
tgctgtacga gtacttcacc gtgtataacg agctgaccaa agtgaaatac
4260gtgaccgagg gaatgagaaa gcccgccttc ctgagcggcg agcagaaaaa
ggccatcgtg 4320gacctgctgt tcaagaccaa ccggaaagtg accgtgaagc
agctgaaaga ggactacttc 4380aagaaaatcg agtgcttcga ctccgtggaa
atctccggcg tggaagatcg gttcaacgcc 4440tccctgggca cataccacga
tctgctgaaa attatcaagg acaaggactt cctggacaat 4500gaggaaaacg
aggacattct ggaagatatc gtgctgaccc tgacactgtt tgaggacaga
4560gagatgatcg aggaacggct gaaaacctat gcccacctgt tcgacgacaa
agtgatgaag 4620cagctgaagc ggcggagata caccggctgg ggcaggctga
gccggaagct gatcaacggc 4680atccgggaca agcagtccgg caagacaatc
ctggatttcc tgaagtccga cggcttcgcc 4740aacagaaact tcatgcagct
gatccacgac gacagcctga cctttaaaga ggacatccag 4800aaagcccagg
tgtccggcca gggcgatagc ctgcacgagc acattgccaa tctggccggc
4860agccccgcca ttaagaaggg catcctgcag acagtgaagg tggtggacga
gctcgtgaaa 4920gtgatgggcc ggcacaagcc cgagaacatc gtgatcgaaa
tggccagaga gaaccagacc 4980acccagaagg gacagaagaa cagccgcgag
agaatgaagc ggatcgaaga gggcatcaaa 5040gagctgggca gccagatcct
gaaagaacac cccgtggaaa acacccagct gcagaacgag 5100aagctgtacc
tgtactacct gcagaatggg cgggatatgt acgtggacca ggaactggac
5160atcaaccggc tgtccgacta cgatgtggac catatcgtgc ctcagagctt
tctgaaggac 5220gactccatcg acaacaaggt gctgaccaga agcgacaaga
accggggcaa gagcgacaac 5280gtgccctccg aagaggtcgt gaagaagatg
aagaactact ggcggcagct gctgaacgcc 5340aagctgatta cccagagaaa
gttcgacaat ctgaccaagg ccgagagagg cggcctgagc 5400gaactggata
aggccggctt catcaagaga cagctggtgg aaacccggca gatcacaaag
5460cacgtggcac agatcctgga ctcccggatg aacactaagt acgacgagaa
tgacaagctg 5520atccgggaag tgaaagtgat caccctgaag tccaagctgg
tgtccgattt ccggaaggat 5580ttccagtttt acaaagtgcg cgagatcaac
aactaccacc acgcccacga cgcctacctg 5640aacgccgtcg tgggaaccgc
cctgatcaaa aagtacccta agctggaaag cgagttcgtg 5700tacggcgact
acaaggtgta cgacgtgcgg aagatgatcg ccaagagcga gcaggaaatc
5760ggcaaggcta ccgccaagta cttcttctac agcaacatca tgaacttttt
caagaccgag 5820attaccctgg ccaacggcga gatccggaag cggcctctga
tcgagacaaa cggcgaaacc 5880ggggagatcg tgtgggataa gggccgggat
tttgccaccg tgcggaaagt gctgagcatg 5940ccccaagtga atatcgtgaa
aaagaccgag gtgcagacag gcggcttcag caaagagtct 6000atcctgccca
agaggaacag cgataagctg atcgccagaa agaaggactg ggaccctaag
6060aagtacggcg gcttcgacag ccccaccgtg gcctattctg tgctggtggt
ggccaaagtg 6120gaaaagggca agtccaagaa actgaagagt gtgaaagagc
tgctggggat caccatcatg 6180gaaagaagca gcttcgagaa gaatcccatc
gactttctgg aagccaaggg ctacaaagaa 6240gtgaaaaagg acctgatcat
caagctgcct aagtactccc tgttcgagct ggaaaacggc 6300cggaagagaa
tgctggcctc tgccggcgaa ctgcagaagg gaaacgaact ggccctgccc
6360tccaaatatg tgaacttcct gtacctggcc agccactatg agaagctgaa
gggctccccc 6420gaggataatg agcagaaaca gctgtttgtg gaacagcaca
agcactacct ggacgagatc 6480atcgagcaga tcagcgagtt ctccaagaga
gtgatcctgg ccgacgctaa tctggacaaa 6540gtgctgtccg cctacaacaa
gcaccgggat aagcccatca gagagcaggc cgagaatatc 6600atccacctgt
ttaccctgac caatctggga gcccctgccg ccttcaagta ctttgacacc
6660accatcgacc ggaagaggta caccagcacc aaagaggtgc tggacgccac
cctgatccac 6720cagagcatca ccggcctgta cgagacacgg atcgacctgt
ctcagctggg aggcgacagc 6780cccaagaaga agagaaaggt ggaggccagc
taacatatga ttcgaatgtc tttcttgcgc 6840tatgacactt ccagcaaaag
gtagggcggg ctgcgagacg gcttcccggc gctgcatgca 6900acaccgatga
tgcttcgacc ccccgaagct ccttcggggc tgcatgggcg ctccgatgcc
6960gctccagggc gagcgctgtt taaatagcca ggcccccgat tgcaaagaca
ttatagcgag 7020ctaccaaagc catattcaaa cacctagatc actaccactt
ctacacaggc cactcgagct 7080tgtgatcgca ctccgctaag ggggcgcctc
ttcctcttcg tttcagtcac aacccgcaaa 7140catgacacaa gaatccctgt
tacttctcga ccgtattgat tcggatgatt cctacgcgag 7200cctgcggaac
gaccaggaat tctgggaggt gagtcgacga gcaagcccgg cggatcaggc
7260agcgtgcttg cagatttgac ttgcaacgcc cgcattgtgt cgacgaaggc
ttttggctcc 7320tctgtcgctg tctcaagcag catctaaccc tgcgtcgccg
tttccatttg cagccgctgg 7380cccgccgagc cctggaggag ctcgggctgc
cggtgccgcc ggtgctgcgg gtgcccggcg 7440agagcaccaa ccccgtactg
gtcggcgagc ccggcccggt gatcaagctg ttcggcgagc 7500actggtgcgg
tccggagagc ctcgcgtcgg agtcggaggc gtacgcggtc ctggcggacg
7560ccccggtgcc ggtgccccgc ctcctcggcc gcggcgagct gcggcccggc
accggagcct 7620ggccgtggcc ctacctggtg atgagccgga tgaccggcac
cacctggcgg tccgcgatgg 7680acggcacgac cgaccggaac gcgctgctcg
ccctggcccg cgaactcggc cgggtgctcg 7740gccggctgca cagggtgccg
ctgaccggga acaccgtgct caccccccat tccgaggtct 7800tcccggaact
gctgcgggaa cgccgcgcgg cgaccgtcga ggaccaccgc gggtggggct
7860acctctcgcc ccggctgctg gaccgcctgg aggactggct gccggacgtg
gacacgctgc 7920tggccggccg cgaaccccgg ttcgtccacg gcgacctgca
cgggaccaac atcttcgtgg 7980acctggccgc gaccgaggtc accgggatcg
tcgacttcac cgacgtctat gcgggagact 8040cccgctacag cctggtgcaa
ctgcatctca acgccttccg gggcgaccgc gagatcctgg 8100ccgcgctgct
cgacggggcg cagtggaagc ggaccgagga cttcgcccgc gaactgctcg
8160ccttcacctt cctgcacgac ttcgaggtgt tcgaggagac cccgctggat
ctctccggct 8220tcaccgatcc ggaggaactg gcgcagttcc tctgggggcc
gccggacacc gcccccggcg 8280cctgataagg atccggcaag actggccccg
cttggcaacg caacagtgag cccctcccta 8340gtgtgtttgg ggatgtgact
atgtattcgt gtgttggcca acgggtcaac ccgaacagat 8400tgatacccgc
cttggcattt cctgtcagaa tgtaacgtca gttgatggta ct 845213027DNAHomo
sapiens 130ccgtgccggg cggggagacc gccatgg 2713122DNAHomo sapiens
131ggcccggctg tggctgagga gc 2213220DNAHomo sapiens 132cggtctcccg
cccggcacgg 2013326DNAHomo sapiens 133gctcctcagc cacagccggg ccgggt
2613412DNAHomo sapiens 134cgaccctgga aa 1213514DNAHomo sapiens
135ccccgccgcc accc 1413618DNAHomo sapiens 136tttccagggt cgccatgg
1813710DNAHomo sapiens 137ggcggcgggg 1013820DNAHomo sapiens
138acccttgtta gccacctccc 2013920DNAHomo sapiens 139gaacgcagtg
ctcttcgaag 2014020DNAHomo sapiens 140ctcacgccct gctccgtgta
2014120DNAHomo sapiens 141ggcgacaact acttcctggt 2014220DNAHomo
sapiens 142ctcacgccct gctccgtgta 2014320DNAHomo sapiens
143gggcgacaac tacttcctgg 2014420DNAHomo sapiens 144cctcttcagg
gccggggtgg 2014520DNAHomo sapiens 145gaggacccag gtggaactgc
2014620DNAHomo sapiens 146tcagctccag gcggtcctgg 2014720DNAHomo
sapiens 147agcagcagca gcagtggcag 2014820DNAHomo sapiens
148tgggcaccgt cagctccagg 2014920DNAHomo sapiens 149cagcagtggc
agcggccacc 2015020DNAHomo sapiens 150acctctcccc tggccctcat
2015120DNAHomo sapiens 151ccaggaccgc ctggagctga 2015220DNAHomo
sapiens 152ccgtcagctc caggcggtcc 2015320DNAHomo sapiens
153agcagcagca gcagtggcag 2015420DNAHomo sapiens 154atgtgccaag
caaagcctca 2015520DNAHomo sapiens 155ttcggtcatg cccgtggatg
2015620DNAHomo sapiens 156gtcgttgaaa ttcatcgtac 2015720DNAHomo
sapiens 157accacctgtg aagagtttcc 2015820DNAHomo sapiens
158cgtcgttgaa attcatcgta 2015920DNAHomo sapiens 159accacctgtg
aagagtttcc 2016020DNAMus musculus 160gaacgcagtg cttttcgagg
2016120DNAMus musculus 161acccttgttg gccacctccc 2016220DNAMus
musculus 162ggtgacaact actatctggt
2016320DNAMus musculus 163ctcacaccct gctccgtgta 2016420DNAMus
musculus 164gggtgacaac tactatctgg 2016520DNAMus musculus
165ctcacaccct gctccgtgta 2016620DNAMus musculus 166cgagaacgca
gtgcttttcg 2016720DNAMus musculus 167acccttgttg gccacctccc
2016820DNAMus musculus 168atgagccaag caaatcctca 2016920DNAMus
musculus 169ttccgtcatg cccgtggaca 2017020DNAMus musculus
170cttcgttgaa aaccattgta 2017120DNAMus musculus 171ccacctctga
agagtttcct 2017220DNAMus musculus 172cttcgttgaa aaccattgta
2017320DNAMus musculus 173accacctctg aagagtttcc 2017420DNAMus
musculus 174cttccactca ctctgcgatt 2017520DNAMus musculus
175accatgtctc agtgtcaagc 2017620DNAMus musculus 176ggcggcaaca
gcggcaacag 2017720DNAMus musculus 177actgctctgc gtggctgcgg
2017820DNAMus musculus 178ccgcagccac gcagagcagt 2017920DNAMus
musculus 179gcacctctcc tcgccccgat 2018023DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
180gagggcctat ttcccatgat tcc 23181126DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
181aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacnnnnnnn nnnnnnnnnn nnccggtgtt
tcgtcctttc 120cacaag 12618224DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 182caccgnnnnn nnnnnnnnnn nnnn
2418324DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 183aaacnnnnnn nnnnnnnnnn nnnc
24184126DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 184aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacccctagt cattggaggt
gaccggtgtt tcgtcctttc 120cacaag 12618524DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
185caccgtcacc tccaatgact aggg 2418624DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
186aaacccctag tcattggagg tgac 24187192DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
187cagaagaaga agggctccca tcacatcaac cggtggcgca ttgccacgaa
gcaggccaat 60ggggaggaca tcgatgtcac ctccaatgac aagcttgcta gcggtgggca
accacaaacc 120cacgagggca gagtgctgct tgctgctggc caggcccctg
cgtgggccca agctggactc 180tggccactcc ct 192188192DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
188agggagtggc cagagtccag cttgggccca cgcaggggcc tggccagcag
caagcagcac 60tctgccctcg tgggtttgtg gttgcccacc gctagcaagc ttgtcattgg
aggtgacatc 120gatgtcctcc ccattggcct gcttcgtggc aatgcgccac
cggttgatgt gatgggagcc 180cttcttcttc tg 19218920DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
189ccatcccctt ctgtgaatgt 2019020DNAArtificial SequenceDescription
of Artificial Sequence Synthetic primer 190ggagattgga gacacggaga
2019120DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 191ggctccctgg gttcaaagta 2019221DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
192agaggggtct ggatgtcgta a 2119324DNAArtificial SequenceDescription
of Artificial Sequence Synthetic primer 193cgccagggtt ttcccagtca
cgac 2419451DNAArtificial SequenceDescription of Artificial
Sequence Synthetic primer 194gagggtctcg tccttgcggc cgcgctagcg
agggcctatt tcccatgatt c 51195133DNAArtificial SequenceDescription
of Artificial Sequence Synthetic primer 195ctcggtctcg gtaaaaaagc
accgactcgg tgccactttt tcaagttgat aacggactag 60ccttatttta acttgctatt
tctagctcta aaacnnnnnn nnnnnnnnnn nnnnggtgtt 120tcgtcctttc cac
13319641DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 196gagggtctct ttaccggtga gggcctattt cccatgattc c
41197133DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 197ctcggtctcc tcaaaaaagc accgactcgg tgccactttt
tcaagttgat aacggactag 60ccttatttta acttgctatt tctagctcta aaacnnnnnn
nnnnnnnnnn nnnnggtgtt 120tcgtcctttc cac 13319840DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
198gagggtctct ttgagctcga gggcctattt cccatgattc
40199133DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 199ctcggtctcg cgtaaaaaag caccgactcg gtgccacttt
ttcaagttga taacggacta 60gccttatttt aacttgctat ttctagctct aaaacnnnnn
nnnnnnnnnn nnnnnggtgt 120ttcgtccttt cca 13320027DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
200gagggtctct tacgcgtgtg tctagac 2720198DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
201ctcggtctca aggacaggga agggagcagt ggttcacgcc tgtaatccca
gcaatttggg 60aggccaaggt gggtagatca cctgagatta ggagttgc
9820230DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 202cctgtccttg cggccgcgct agcgagggcc
3020331DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 203cacgcggccg caaggacagg gaagggagca g
31204327PRTArtificial SequenceDescription of Artificial Sequence
Synthetic polypeptide 204Met Val Ser Lys Gly Glu Glu Leu Phe Thr
Gly Val Val Pro Ile Leu 1 5 10 15 Val Glu Leu Asp Gly Asp Val Asn
Gly His Lys Phe Ser Val Ser Gly 20 25 30 Glu Gly Glu Gly Asp Ala
Thr Tyr Gly Lys Leu Thr Leu Lys Phe Ile 35 40 45 Cys Thr Thr Gly
Lys Leu Pro Val Pro Trp Pro Thr Leu Val Thr Thr 50 55 60 Leu Thr
Tyr Gly Val Gln Cys Phe Ser Arg Tyr Pro Asp His Met Lys 65 70 75 80
Gln His Asp Phe Phe Lys Ser Ala Met Pro Glu Gly Tyr Val Gln Glu 85
90 95 Arg Thr Ile Phe Phe Lys Asp Asp Gly Asn Tyr Lys Thr Arg Ala
Glu 100 105 110 Val Lys Phe Glu Gly Asp Thr Leu Val Asn Arg Ile Glu
Leu Lys Gly 115 120 125 Ile Asp Phe Lys Glu Asp Gly Asn Ile Leu Gly
His Lys Leu Glu Tyr 130 135 140 Asn Tyr Asn Ser His Asn Val Tyr Ile
Met Ala Asp Lys Gln Lys Asn 145 150 155 160 Gly Ile Lys Val Asn Phe
Lys Ile Arg His Asn Ile Glu Asp Gly Ser 165 170 175 Val Gln Leu Ala
Asp His Tyr Gln Gln Asn Thr Pro Ile Gly Asp Gly 180 185 190 Pro Val
Leu Leu Pro Asp Asn His Tyr Leu Ser Thr Gln Ser Ala Leu 195 200 205
Ser Lys Asp Pro Asn Glu Lys Arg Asp His Met Val Leu Leu Glu Phe 210
215 220 Val Thr Ala Ala Gly Ile Thr Leu Gly Met Asp Glu Leu Tyr Lys
Ser 225 230 235 240 Gly Leu Arg Ser Arg Glu Glu Glu Glu Glu Thr Asp
Ser Arg Met Pro 245 250 255 His Leu Asp Ser Pro Gly Ser Ser Gln Pro
Arg Arg Ser Phe Leu Ser 260 265 270 Arg Val Ile Arg Ala Ala Leu Pro
Leu Gln Leu Leu Leu Leu Leu Leu 275 280 285 Leu Leu Leu Ala Cys Leu
Leu Pro Ala Ser Glu Asp Asp Tyr Ser Cys 290 295 300 Thr Gln Ala Asn
Asn Phe Ala Arg Ser Phe Tyr Pro Met Leu Arg Tyr 305 310 315 320 Thr
Asn Gly Pro Pro Pro Thr 325 2053243DNAArtificial
SequenceDescription of Artificial Sequence Synthetic polynucleotide
205accggtgcca ccatgtaccc atacgatgtt ccagattacg cttcgccgaa
gaaaaagcgc 60aaggtcgaag cgtccatgaa aaggaactac attctggggc tggacatcgg
gattacaagc 120gtggggtatg ggattattga ctatgaaaca agggacgtga
tcgacgcagg cgtcagactg 180ttcaaggagg ccaacgtgga aaacaatgag
ggacggagaa gcaagagggg agccaggcgc 240ctgaaacgac ggagaaggca
cagaatccag agggtgaaga aactgctgtt cgattacaac 300ctgctgaccg
accattctga gctgagtgga attaatcctt atgaagccag ggtgaaaggc
360ctgagtcaga agctgtcaga ggaagagttt tccgcagctc tgctgcacct
ggctaagcgc 420cgaggagtgc ataacgtcaa tgaggtggaa gaggacaccg
gcaacgagct gtctacaaag 480gaacagatct cacgcaatag caaagctctg
gaagagaagt atgtcgcaga gctgcagctg 540gaacggctga agaaagatgg
cgaggtgaga gggtcaatta ataggttcaa gacaagcgac 600tacgtcaaag
aagccaagca gctgctgaaa gtgcagaagg cttaccacca gctggatcag
660agcttcatcg atacttatat cgacctgctg gagactcgga gaacctacta
tgagggacca 720ggagaaggga gccccttcgg atggaaagac atcaaggaat
ggtacgagat gctgatggga 780cattgcacct attttccaga agagctgaga
agcgtcaagt acgcttataa cgcagatctg 840tacaacgccc tgaatgacct
gaacaacctg gtcatcacca gggatgaaaa cgagaaactg 900gaatactatg
agaagttcca gatcatcgaa aacgtgttta agcagaagaa aaagcctaca
960ctgaaacaga ttgctaagga gatcctggtc aacgaagagg acatcaaggg
ctaccgggtg 1020acaagcactg gaaaaccaga gttcaccaat ctgaaagtgt
atcacgatat taaggacatc 1080acagcacgga aagaaatcat tgagaacgcc
gaactgctgg atcagattgc taagatcctg 1140actatctacc agagctccga
ggacatccag gaagagctga ctaacctgaa cagcgagctg 1200acccaggaag
agatcgaaca gattagtaat ctgaaggggt acaccggaac acacaacctg
1260tccctgaaag ctatcaatct gattctggat gagctgtggc atacaaacga
caatcagatt 1320gcaatcttta accggctgaa gctggtccca aaaaaggtgg
acctgagtca gcagaaagag 1380atcccaacca cactggtgga cgatttcatt
ctgtcacccg tggtcaagcg gagcttcatc 1440cagagcatca aagtgatcaa
cgccatcatc aagaagtacg gcctgcccaa tgatatcatt 1500atcgagctgg
ctagggagaa gaacagcaag gacgcacaga agatgatcaa tgagatgcag
1560aaacgaaacc ggcagaccaa tgaacgcatt gaagagatta tccgaactac
cgggaaagag 1620aacgcaaagt acctgattga aaaaatcaag ctgcacgata
tgcaggaggg aaagtgtctg 1680tattctctgg aggccatccc cctggaggac
ctgctgaaca atccattcaa ctacgaggtc 1740gatcatatta tccccagaag
cgtgtccttc gacaattcct ttaacaacaa ggtgctggtc 1800aagcaggaag
agaactctaa aaagggcaat aggactcctt tccagtacct gtctagttca
1860gattccaaga tctcttacga aacctttaaa aagcacattc tgaatctggc
caaaggaaag 1920ggccgcatca gcaagaccaa aaaggagtac ctgctggaag
agcgggacat caacagattc 1980tccgtccaga aggattttat taaccggaat
ctggtggaca caagatacgc tactcgcggc 2040ctgatgaatc tgctgcgatc
ctatttccgg gtgaacaatc tggatgtgaa agtcaagtcc 2100atcaacggcg
ggttcacatc ttttctgagg cgcaaatgga agtttaaaaa ggagcgcaac
2160aaagggtaca agcaccatgc cgaagatgct ctgattatcg caaatgccga
cttcatcttt 2220aaggagtgga aaaagctgga caaagccaag aaagtgatgg
agaaccagat gttcgaagag 2280aagcaggccg aatctatgcc cgaaatcgag
acagaacagg agtacaagga gattttcatc 2340actcctcacc agatcaagca
tatcaaggat ttcaaggact acaagtactc tcaccgggtg 2400gataaaaagc
ccaacagaga gctgatcaat gacaccctgt atagtacaag aaaagacgat
2460aaggggaata ccctgattgt gaacaatctg aacggactgt acgacaaaga
taatgacaag 2520ctgaaaaagc tgatcaacaa aagtcccgag aagctgctga
tgtaccacca tgatcctcag 2580acatatcaga aactgaagct gattatggag
cagtacggcg acgagaagaa cccactgtat 2640aagtactatg aagagactgg
gaactacctg accaagtata gcaaaaagga taatggcccc 2700gtgatcaaga
agatcaagta ctatgggaac aagctgaatg cccatctgga catcacagac
2760gattacccta acagtcgcaa caaggtggtc aagctgtcac tgaagccata
cagattcgat 2820gtctatctgg acaacggcgt gtataaattt gtgactgtca
agaatctgga tgtcatcaaa 2880aaggagaact actatgaagt gaatagcaag
tgctacgaag aggctaaaaa gctgaaaaag 2940attagcaacc aggcagagtt
catcgcctcc ttttacaaca acgacctgat taagatcaat 3000ggcgaactgt
atagggtcat cggggtgaac aatgatctgc tgaaccgcat tgaagtgaat
3060atgattgaca tcacttaccg agagtatctg gaaaacatga atgataagcg
cccccctcga 3120attatcaaaa caattgcctc taagactcag agtatcaaaa
agtactcaac cgacattctg 3180ggaaacctgt atgaggtgaa gagcaaaaag
caccctcaga ttatcaaaaa gggctaagaa 3240ttc 324320620DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 206atctcttaga taccagcatc 2020720DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 207tcaatctccc gatgggcacc 2020820DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 208gcccatcggg agattgaggg 2020920DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 209acttcaacag cgtgccggag 2021020DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 210ccgctgacca cacctgccag 2021120DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 211tggcaggtgt ggtcagcggc 20212102DNAArtificial
SequenceDescription of Artificial Sequence Synthetic polynucleotide
212gttttagagc tatgctgttt tgaatggtcc caaaacggaa gggcctgagt
ccgagcagaa 60gaagaagttt tagagctatg ctgttttgaa tggtcccaaa ac
102213100DNAHomo sapiens 213cggaggacaa agtacaaacg gcagaagctg
gaggaggaag ggcctgagtc cgagcagaag 60aagaagggct cccatcacat caaccggtgg
cgcattgcca 10021450DNAHomo sapiens 214agctggagga ggaagggcct
gagtccgagc agaagaagaa gggctcccac 5021530RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 215gaguccgagc agaagaagaa guuuuagagc
3021649DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 216agctggagga ggaagggcct gagtccgagc
agaagagaag ggctcccac 4921753DNAHomo sapiens 217ctggaggagg
aagggcctga gtccgagcag aagaagaagg gctcccatca cat 5321852DNAHomo
sapiens 218ctggaggagg aagggcctga gtccgagcag aagagaaggg ctcccatcac
at 5221954DNAHomo sapiens 219ctggaggagg aagggcctga gtccgagcag
aagaaagaag ggctcccatc acat 5422050DNAHomo sapiens 220ctggaggagg
aagggcctga gtccgagcag aagaagggct cccatcacat 5022147DNAHomo sapiens
221ctggaggagg aagggcctga gcccgagcag aagggctccc atcacat
4722248DNAHomo sapiens 222ctggaggagg aagggcctga gtccgagcag
aagaagaagg gctcccat 4822320RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 223gaguccgagc
agaagaagau 2022420RNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 224gaguccgagc agaagaagua
2022520RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 225gaguccgagc agaagaacaa
2022620RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 226gaguccgagc agaagaugaa
2022720RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 227gaguccgagc agaaguagaa
2022820RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 228gaguccgagc agaugaagaa
2022920RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 229gaguccgagc acaagaagaa
2023020RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 230gaguccgagg agaagaagaa
2023120RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 231gaguccgugc agaagaagaa
2023220RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 232gagucggagc agaagaagaa
2023320RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 233gagaccgagc agaagaagaa
2023424DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 234aatgacaagc ttgctagcgg tggg
2423539DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 235aaaacggaag ggcctgagtc cgagcagaag
aagaagttt 3923639DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 236aaacaggggc cgagattggg
tgttcagggc agaggtttt 3923738DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 237aaaacggaag
ggcctgagtc cgagcagaag aagaagtt 3823840DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 238aacggaggga ggggcacaga tgagaaactc agggttttag
4023938DNAHomo sapiens 239agcccttctt cttctgctcg gactcaggcc cttcctcc
3824040DNAHomo sapiens 240cagggaggga ggggcacaga tgagaaactc
aggaggcccc 4024180DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 241ggcaatgcgc caccggttga
tgtgatggga gcccttctag gaggccccca gagcagccac 60tggggcctca acactcaggc
8024233DNAHomo sapiens 242catcgatgtc ctccccattg gcctgcttcg tgg
3324333DNAHomo sapiens 243ttcgtggcaa tgcgccaccg gttgatgtga tgg
3324433DNAHomo sapiens 244tcgtggcaat gcgccaccgg ttgatgtgat ggg
3324533DNAHomo sapiens 245tccagcttct gccgtttgta ctttgtcctc cgg
3324633DNAHomo sapiens 246ggagggaggg gcacagatga gaaactcagg agg
3324733DNAHomo sapiens 247aggggccgag attgggtgtt cagggcagag agg
3324833DNAMus musculus 248caagcactga gtgccattag ctaaatgcat agg
3324933DNAMus musculus 249aatgcatagg gtaccaccca caggtgccag ggg
3325033DNAMus musculus 250acacacatgg gaaagcctct gggccaggaa agg
3325137DNAHomo sapiens 251ggaggaggta gtatacagaa acacagagaa gtagaat
3725237DNAHomo sapiens 252agaatgtaga ggagtcacag aaactcagca ctagaaa
3725398DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 253ggacgaaaca ccggaaccat tcaaaacagc
atagcaagtt aaaataaggc tagtccgtta 60tcaacttgaa aaagtggcac cgagtcggtg
cttttttt 98254186DNAArtificial SequenceDescription of Artificial
Sequence Synthetic polynucleotide 254ggacgaaaca ccggtagtat
taagtattgt tttatggctg ataaatttct ttgaatttct 60ccttgattat ttgttataaa
agttataaaa taatcttgtt ggaaccattc aaaacagcat 120agcaagttaa
aataaggcta gtccgttatc aacttgaaaa agtggcaccg agtcggtgct 180tttttt
18625595DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 255gggttttaga gctatgctgt tttgaatggt
cccaaaacgg gtcttcgaga agacgtttta 60gagctatgct gttttgaatg gtcccaaaac
ttttt 9525636DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 256aaacnnnnnn nnnnnnnnnn
nnnnnnnnnn nnnngt 3625736DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 257taaaacnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnn 3625884DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 258gtggaaagga cgaaacaccg ggtcttcgag aagacctgtt
ttagagctag aaatagcaag 60ttaaaataag gctagtccgt tttt
8425946RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 259nnnnnnnnnn nnnnnnnnng uuauuguacu
cucaagauuu auuuuu 4626091RNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 260guuacuuaaa
ucuugcagaa gcuacaaaga uaaggcuuca ugccgaaauc aacacccugu 60cauuuuaugg
caggguguuu ucguuauuua a 9126170DNAHomo sapiens 261ttttctagtg
ctgagtttct gtgactcctc tacattctac ttctctgtgt ttctgtatac 60tacctcctcc
70262122DNAHomo sapiens 262ggaggaaggg cctgagtccg agcagaagaa
gaagggctcc catcacatca accggtggcg 60cattgccacg aagcaggcca atggggagga
catcgatgtc acctccaatg actagggtgg 120gc 12226348RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 263acnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnguuuuaga
gcuaugcu 4826467DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 264agcauagcaa guuaaaauaa
ggctaguccg uuaucaacuu gaaaaagugg caccgagucg 60gugcuuu
6726562RNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 265nnnnnnnnnn nnnnnnnnnn guuuuagagc
uagaaauagc aaguuaaaau aaggcuaguc 60cg 6226673DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 266tgaatggtcc caaaacggaa gggcctgagt ccgagcagaa
gaagaagttt tagagctatg 60ctgttttgaa tgg 7326769DNAHomo sapiens
267ctggtcttcc acctctctgc cctgaacacc caatctcggc ccctctcgcc
accctcctgc 60atttctgtt 69268138DNAMus musculus 268acccaagcac
tgagtgccat tagctaaatg catagggtac cacccacagg tgccaggggc 60ctttcccaaa
gttcccagcc ccttctccaa cctttcctgg cccagaggct ttcccatgtg
120tgtggctgga ccctttga 13826921DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 269aaaaccaccc ttctctctgg c
2127021DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 270ggagattgga gacacggaga g 2127120DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
271ctggaaagcc aatgcctgac 2027220DNAArtificial SequenceDescription
of Artificial Sequence Synthetic primer 272ggcagcaaac tccttgtcct
2027320DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 273gtgctttgca gaggcctacc 2027420DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
274cctggagcgc atgcagtagt 2027522DNAArtificial SequenceDescription
of Artificial Sequence Synthetic primer 275accttctgtg tttccaccat tc
2227620DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 276ttggggagtg cacagacttc 2027730DNAArtificial
SequenceDescription of Artificial Sequence Synthetic probe
277tagctctaaa acttcttctt ctgctcggac 3027830DNAArtificial
SequenceDescription of Artificial Sequence Synthetic probe
278ctagccttat tttaacttgc tatgctgttt 3027999RNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 279nnnnnnnnnn nnnnnnnnnn guuuuagagc uagaaauagc
aaguuaaaau aaggcuaguc 60cguuaucaac uugaaaaagu ggcaccgagu cggugcuuu
9928012DNAHomo sapiens 280tagcgggtaa gc 1228112DNAHomo sapiens
281tcggtgacat gt 1228212DNAHomo sapiens 282actccccgta gg
1228312DNAHomo sapiens 283actgcgtgtt aa 1228412DNAHomo sapiens
284acgtcgcctg at 1228512DNAHomo sapiens 285taggtcgacc ag
1228612DNAHomo sapiens 286ggcgttaatg at 1228712DNAHomo sapiens
287tgtcgcatgt ta 1228812DNAHomo sapiens 288atggaaacgc at
1228912DNAHomo sapiens 289gccgaattcc tc 1229012DNAHomo sapiens
290gcatggtacg ga 1229112DNAHomo sapiens 291cggtactctt ac
1229212DNAHomo sapiens 292gcctgtgccg ta 1229312DNAHomo sapiens
293tacggtaagt cg 1229412DNAHomo sapiens 294cacgaaatta cc
1229512DNAHomo sapiens 295aaccaagata cg 1229612DNAHomo sapiens
296gagtcgatac gc 1229712DNAHomo sapiens 297gtctcacgat cg
1229812DNAHomo sapiens 298tcgtcgggtg ca 1229912DNAHomo sapiens
299actccgtagt ga 1230012DNAHomo sapiens 300caggacgtcc gt
1230112DNAHomo sapiens 301tcgtatccct ac 1230212DNAHomo sapiens
302tttcaaggcc gg 1230312DNAHomo sapiens 303cgccggtgga at
1230412DNAHomo sapiens 304gaacccgtcc ta 1230512DNAHomo sapiens
305gattcatcag cg 1230612DNAHomo sapiens 306acaccggtct tc
1230712DNAHomo sapiens 307atcgtgccct aa 1230812DNAHomo sapiens
308gcgtcaatgt tc 1230912DNAHomo sapiens 309ctccgtatct cg
1231012DNAHomo sapiens 310ccgattcctt cg 1231112DNAHomo sapiens
311tgcgcctcca gt 1231212DNAHomo sapiens 312taacgtcgga gc
1231312DNAHomo sapiens 313aaggtcgccc at 1231412DNAHomo sapiens
314gtcggggact at 1231512DNAHomo sapiens 315ttcgagcgat tt
1231612DNAHomo sapiens 316tgagtcgtcg ag 1231712DNAHomo sapiens
317tttacgcaga gg 1231812DNAHomo sapiens 318aggaagtatc gc
1231912DNAHomo sapiens 319actcgatacc at 1232012DNAHomo sapiens
320cgctacatag ca 1232112DNAHomo sapiens 321ttcataaccg gc
1232212DNAHomo sapiens 322ccaaacggtt aa 1232312DNAHomo sapiens
323cgattccttc gt 1232412DNAHomo sapiens 324cgtcatgaat aa
1232512DNAHomo sapiens 325agtggcgatg ac 1232612DNAHomo sapiens
326cccctacggc ac 1232712DNAHomo sapiens 327gccaacccgc ac
1232812DNAHomo sapiens 328tgggacaccg gt 1232912DNAHomo sapiens
329ttgactgcgg cg 1233012DNAHomo sapiens 330actatgcgta gg
1233112DNAHomo sapiens 331tcacccaaag cg 1233212DNAHomo sapiens
332gcaggacgtc cg 1233312DNAHomo sapiens 333acaccgaaaa cg
1233412DNAHomo sapiens 334cggtgtattg ag 1233512DNAHomo sapiens
335cacgaggtat gc 1233612DNAHomo sapiens 336taaagcgacc cg
1233712DNAHomo sapiens 337cttagtcggc ca 1233812DNAHomo sapiens
338cgaaaacgtg gc 1233912DNAHomo sapiens 339cgtgccctga ac
1234012DNAHomo sapiens 340tttaccatcg aa 1234112DNAHomo sapiens
341cgtagccatg tt 1234212DNAHomo sapiens 342cccaaacggt ta
1234312DNAHomo sapiens 343gcgttatcag aa 1234412DNAHomo sapiens
344tcgatggtaa ac 1234512DNAHomo sapiens 345cgactttttg ca
1234612DNAHomo sapiens 346tcgacgactc ac 1234712DNAHomo sapiens
347acgcgtcaga ta 1234812DNAHomo sapiens 348cgtacggcac ag
1234912DNAHomo sapiens 349ctatgccgtg ca 1235012DNAHomo sapiens
350cgcgtcagat at 1235112DNAHomo sapiens 351aagatcggta gc
1235212DNAHomo sapiens 352cttcgcaagg ag 1235312DNAHomo sapiens
353gtcgtggact ac 1235412DNAHomo sapiens 354ggtcgtcatc aa
1235512DNAHomo sapiens 355gttaacagcg tg 1235612DNAHomo sapiens
356tagctaaccg tt 1235712DNAHomo sapiens 357agtaaaggcg ct
1235812DNAHomo sapiens 358ggtaatttcg tg 1235915DNAHomo sapiens
359cagaagaaga agggc 1536051DNAHomo sapiens 360ccaatgggga ggacatcgat
gtcacctcca atgactaggg tggtgggcaa c 5136115DNAHomo sapiens
361ctctggccac tccct 1536252DNAHomo sapiens 362acatcgatgt cacctccaat
gacaagcttg ctagcggtgg gcaaccacaa ac 5236325DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 363caccgnnnnn nnnnnnnnnn nnnnn 2536425DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 364aaacnnnnnn nnnnnnnnnn nnnnc 2536554DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 365aacaccgggt cttcgagaag acctgtttta gagctagaaa
tagcaagtta aaat 5436654DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 366caaaacgggt
cttcgagaag acgttttaga gctatgctgt tttgaatggt ccca 543674104DNAHomo
sapiensCDS(1)..(4104) 367atg gac aag aag tac agc atc ggc ctg gac
atc ggc acc aac tct gtg 48Met Asp Lys Lys Tyr Ser Ile Gly Leu Asp
Ile Gly Thr Asn Ser Val 1 5 10 15 ggc tgg gcc gtg atc acc gac gag
tac aag gtg ccc agc aag aaa ttc 96Gly Trp Ala Val Ile Thr Asp Glu
Tyr Lys Val Pro Ser Lys Lys Phe 20 25 30 aag gtg ctg ggc aac acc
gac cgg cac agc atc aag aag aac ctg atc 144Lys Val Leu Gly Asn Thr
Asp Arg His Ser Ile Lys Lys Asn Leu Ile 35 40 45 gga gcc ctg ctg
ttc gac agc ggc gaa aca gcc gag gcc acc cgg ctg 192Gly Ala Leu Leu
Phe Asp Ser Gly Glu Thr Ala Glu Ala Thr Arg Leu 50 55 60 aag aga
acc gcc aga aga aga tac acc aga cgg aag aac cgg atc tgc 240Lys Arg
Thr Ala Arg Arg Arg Tyr Thr Arg Arg Lys Asn Arg Ile Cys 65 70 75 80
tat ctg caa gag atc ttc agc aac gag atg gcc aag gtg gac gac agc
288Tyr Leu Gln Glu Ile Phe Ser Asn Glu Met Ala Lys Val Asp Asp Ser
85 90 95 ttc ttc cac aga ctg gaa gag tcc ttc ctg gtg gaa gag gat
aag aag 336Phe Phe His Arg Leu Glu Glu Ser Phe Leu Val Glu Glu Asp
Lys Lys
100 105 110 cac gag cgg cac ccc atc ttc ggc aac atc gtg gac gag gtg
gcc tac 384His Glu Arg His Pro Ile Phe Gly Asn Ile Val Asp Glu Val
Ala Tyr 115 120 125 cac gag aag tac ccc acc atc tac cac ctg aga aag
aaa ctg gtg gac 432His Glu Lys Tyr Pro Thr Ile Tyr His Leu Arg Lys
Lys Leu Val Asp 130 135 140 agc acc gac aag gcc gac ctg cgg ctg atc
tat ctg gcc ctg gcc cac 480Ser Thr Asp Lys Ala Asp Leu Arg Leu Ile
Tyr Leu Ala Leu Ala His 145 150 155 160 atg atc aag ttc cgg ggc cac
ttc ctg atc gag ggc gac ctg aac ccc 528Met Ile Lys Phe Arg Gly His
Phe Leu Ile Glu Gly Asp Leu Asn Pro 165 170 175 gac aac agc gac gtg
gac aag ctg ttc atc cag ctg gtg cag acc tac 576Asp Asn Ser Asp Val
Asp Lys Leu Phe Ile Gln Leu Val Gln Thr Tyr 180 185 190 aac cag ctg
ttc gag gaa aac ccc atc aac gcc agc ggc gtg gac gcc 624Asn Gln Leu
Phe Glu Glu Asn Pro Ile Asn Ala Ser Gly Val Asp Ala 195 200 205 aag
gcc atc ctg tct gcc aga ctg agc aag agc aga cgg ctg gaa aat 672Lys
Ala Ile Leu Ser Ala Arg Leu Ser Lys Ser Arg Arg Leu Glu Asn 210 215
220 ctg atc gcc cag ctg ccc ggc gag aag aag aat ggc ctg ttc ggc aac
720Leu Ile Ala Gln Leu Pro Gly Glu Lys Lys Asn Gly Leu Phe Gly Asn
225 230 235 240 ctg att gcc ctg agc ctg ggc ctg acc ccc aac ttc aag
agc aac ttc 768Leu Ile Ala Leu Ser Leu Gly Leu Thr Pro Asn Phe Lys
Ser Asn Phe 245 250 255 gac ctg gcc gag gat gcc aaa ctg cag ctg agc
aag gac acc tac gac 816Asp Leu Ala Glu Asp Ala Lys Leu Gln Leu Ser
Lys Asp Thr Tyr Asp 260 265 270 gac gac ctg gac aac ctg ctg gcc cag
atc ggc gac cag tac gcc gac 864Asp Asp Leu Asp Asn Leu Leu Ala Gln
Ile Gly Asp Gln Tyr Ala Asp 275 280 285 ctg ttt ctg gcc gcc aag aac
ctg tcc gac gcc atc ctg ctg agc gac 912Leu Phe Leu Ala Ala Lys Asn
Leu Ser Asp Ala Ile Leu Leu Ser Asp 290 295 300 atc ctg aga gtg aac
acc gag atc acc aag gcc ccc ctg agc gcc tct 960Ile Leu Arg Val Asn
Thr Glu Ile Thr Lys Ala Pro Leu Ser Ala Ser 305 310 315 320 atg atc
aag aga tac gac gag cac cac cag gac ctg acc ctg ctg aaa 1008Met Ile
Lys Arg Tyr Asp Glu His His Gln Asp Leu Thr Leu Leu Lys 325 330 335
gct ctc gtg cgg cag cag ctg cct gag aag tac aaa gag att ttc ttc
1056Ala Leu Val Arg Gln Gln Leu Pro Glu Lys Tyr Lys Glu Ile Phe Phe
340 345 350 gac cag agc aag aac ggc tac gcc ggc tac att gac ggc gga
gcc agc 1104Asp Gln Ser Lys Asn Gly Tyr Ala Gly Tyr Ile Asp Gly Gly
Ala Ser 355 360 365 cag gaa gag ttc tac aag ttc atc aag ccc atc ctg
gaa aag atg gac 1152Gln Glu Glu Phe Tyr Lys Phe Ile Lys Pro Ile Leu
Glu Lys Met Asp 370 375 380 ggc acc gag gaa ctg ctc gtg aag ctg aac
aga gag gac ctg ctg cgg 1200Gly Thr Glu Glu Leu Leu Val Lys Leu Asn
Arg Glu Asp Leu Leu Arg 385 390 395 400 aag cag cgg acc ttc gac aac
ggc agc atc ccc cac cag atc cac ctg 1248Lys Gln Arg Thr Phe Asp Asn
Gly Ser Ile Pro His Gln Ile His Leu 405 410 415 gga gag ctg cac gcc
att ctg cgg cgg cag gaa gat ttt tac cca ttc 1296Gly Glu Leu His Ala
Ile Leu Arg Arg Gln Glu Asp Phe Tyr Pro Phe 420 425 430 ctg aag gac
aac cgg gaa aag atc gag aag atc ctg acc ttc cgc atc 1344Leu Lys Asp
Asn Arg Glu Lys Ile Glu Lys Ile Leu Thr Phe Arg Ile 435 440 445 ccc
tac tac gtg ggc cct ctg gcc agg gga aac agc aga ttc gcc tgg 1392Pro
Tyr Tyr Val Gly Pro Leu Ala Arg Gly Asn Ser Arg Phe Ala Trp 450 455
460 atg acc aga aag agc gag gaa acc atc acc ccc tgg aac ttc gag gaa
1440Met Thr Arg Lys Ser Glu Glu Thr Ile Thr Pro Trp Asn Phe Glu Glu
465 470 475 480 gtg gtg gac aag ggc gct tcc gcc cag agc ttc atc gag
cgg atg acc 1488Val Val Asp Lys Gly Ala Ser Ala Gln Ser Phe Ile Glu
Arg Met Thr 485 490 495 aac ttc gat aag aac ctg ccc aac gag aag gtg
ctg ccc aag cac agc 1536Asn Phe Asp Lys Asn Leu Pro Asn Glu Lys Val
Leu Pro Lys His Ser 500 505 510 ctg ctg tac gag tac ttc acc gtg tat
aac gag ctg acc aaa gtg aaa 1584Leu Leu Tyr Glu Tyr Phe Thr Val Tyr
Asn Glu Leu Thr Lys Val Lys 515 520 525 tac gtg acc gag gga atg aga
aag ccc gcc ttc ctg agc ggc gag cag 1632Tyr Val Thr Glu Gly Met Arg
Lys Pro Ala Phe Leu Ser Gly Glu Gln 530 535 540 aaa aag gcc atc gtg
gac ctg ctg ttc aag acc aac cgg aaa gtg acc 1680Lys Lys Ala Ile Val
Asp Leu Leu Phe Lys Thr Asn Arg Lys Val Thr 545 550 555 560 gtg aag
cag ctg aaa gag gac tac ttc aag aaa atc gag tgc ttc gac 1728Val Lys
Gln Leu Lys Glu Asp Tyr Phe Lys Lys Ile Glu Cys Phe Asp 565 570 575
tcc gtg gaa atc tcc ggc gtg gaa gat cgg ttc aac gcc tcc ctg ggc
1776Ser Val Glu Ile Ser Gly Val Glu Asp Arg Phe Asn Ala Ser Leu Gly
580 585 590 aca tac cac gat ctg ctg aaa att atc aag gac aag gac ttc
ctg gac 1824Thr Tyr His Asp Leu Leu Lys Ile Ile Lys Asp Lys Asp Phe
Leu Asp 595 600 605 aat gag gaa aac gag gac att ctg gaa gat atc gtg
ctg acc ctg aca 1872Asn Glu Glu Asn Glu Asp Ile Leu Glu Asp Ile Val
Leu Thr Leu Thr 610 615 620 ctg ttt gag gac aga gag atg atc gag gaa
cgg ctg aaa acc tat gcc 1920Leu Phe Glu Asp Arg Glu Met Ile Glu Glu
Arg Leu Lys Thr Tyr Ala 625 630 635 640 cac ctg ttc gac gac aaa gtg
atg aag cag ctg aag cgg cgg aga tac 1968His Leu Phe Asp Asp Lys Val
Met Lys Gln Leu Lys Arg Arg Arg Tyr 645 650 655 acc ggc tgg ggc agg
ctg agc cgg aag ctg atc aac ggc atc cgg gac 2016Thr Gly Trp Gly Arg
Leu Ser Arg Lys Leu Ile Asn Gly Ile Arg Asp 660 665 670 aag cag tcc
ggc aag aca atc ctg gat ttc ctg aag tcc gac ggc ttc 2064Lys Gln Ser
Gly Lys Thr Ile Leu Asp Phe Leu Lys Ser Asp Gly Phe 675 680 685 gcc
aac aga aac ttc atg cag ctg atc cac gac gac agc ctg acc ttt 2112Ala
Asn Arg Asn Phe Met Gln Leu Ile His Asp Asp Ser Leu Thr Phe 690 695
700 aaa gag gac atc cag aaa gcc cag gtg tcc ggc cag ggc gat agc ctg
2160Lys Glu Asp Ile Gln Lys Ala Gln Val Ser Gly Gln Gly Asp Ser Leu
705 710 715 720 cac gag cac att gcc aat ctg gcc ggc agc ccc gcc att
aag aag ggc 2208His Glu His Ile Ala Asn Leu Ala Gly Ser Pro Ala Ile
Lys Lys Gly 725 730 735 atc ctg cag aca gtg aag gtg gtg gac gag ctc
gtg aaa gtg atg ggc 2256Ile Leu Gln Thr Val Lys Val Val Asp Glu Leu
Val Lys Val Met Gly 740 745 750 cgg cac aag ccc gag aac atc gtg atc
gcc atg gcc aga gag aac cag 2304Arg His Lys Pro Glu Asn Ile Val Ile
Ala Met Ala Arg Glu Asn Gln 755 760 765 acc acc cag aag gga cag aag
aac agc cgc gag aga atg aag cgg atc 2352Thr Thr Gln Lys Gly Gln Lys
Asn Ser Arg Glu Arg Met Lys Arg Ile 770 775 780 gaa gag ggc atc aaa
gag ctg ggc agc cag atc ctg aaa gaa cac ccc 2400Glu Glu Gly Ile Lys
Glu Leu Gly Ser Gln Ile Leu Lys Glu His Pro 785 790 795 800 gtg gaa
aac acc cag ctg cag aac gag aag ctg tac ctg tac tac ctg 2448Val Glu
Asn Thr Gln Leu Gln Asn Glu Lys Leu Tyr Leu Tyr Tyr Leu 805 810 815
cag aat ggg cgg gat atg tac gtg gac cag gaa ctg gac atc aac cgg
2496Gln Asn Gly Arg Asp Met Tyr Val Asp Gln Glu Leu Asp Ile Asn Arg
820 825 830 ctg tcc gac tac gat gtg gac gcc atc gtg cct cag agc ttt
ctg aag 2544Leu Ser Asp Tyr Asp Val Asp Ala Ile Val Pro Gln Ser Phe
Leu Lys 835 840 845 gac gac tcc atc gac gcc aag gtg ctg acc aga agc
gac aag gcc cgg 2592Asp Asp Ser Ile Asp Ala Lys Val Leu Thr Arg Ser
Asp Lys Ala Arg 850 855 860 ggc aag agc gac aac gtg ccc tcc gaa gag
gtc gtg aag aag atg aag 2640Gly Lys Ser Asp Asn Val Pro Ser Glu Glu
Val Val Lys Lys Met Lys 865 870 875 880 aac tac tgg cgg cag ctg ctg
aac gcc aag ctg att acc cag aga aag 2688Asn Tyr Trp Arg Gln Leu Leu
Asn Ala Lys Leu Ile Thr Gln Arg Lys 885 890 895 ttc gac aat ctg acc
aag gcc gag aga ggc ggc ctg agc gaa ctg gat 2736Phe Asp Asn Leu Thr
Lys Ala Glu Arg Gly Gly Leu Ser Glu Leu Asp 900 905 910 aag gcc ggc
ttc atc aag aga cag ctg gtg gaa acc cgg cag atc aca 2784Lys Ala Gly
Phe Ile Lys Arg Gln Leu Val Glu Thr Arg Gln Ile Thr 915 920 925 aag
cac gtg gca cag atc ctg gac tcc cgg atg aac act aag tac gac 2832Lys
His Val Ala Gln Ile Leu Asp Ser Arg Met Asn Thr Lys Tyr Asp 930 935
940 gag aat gac aag ctg atc cgg gaa gtg aaa gtg atc acc ctg aag tcc
2880Glu Asn Asp Lys Leu Ile Arg Glu Val Lys Val Ile Thr Leu Lys Ser
945 950 955 960 aag ctg gtg tcc gat ttc cgg aag gat ttc cag ttt tac
aaa gtg cgc 2928Lys Leu Val Ser Asp Phe Arg Lys Asp Phe Gln Phe Tyr
Lys Val Arg 965 970 975 gag atc aac aac tac cac cac gcc cac gcc gcc
tac ctg aac gcc gtc 2976Glu Ile Asn Asn Tyr His His Ala His Ala Ala
Tyr Leu Asn Ala Val 980 985 990 gtg gga acc gcc ctg atc aaa aag tac
cct aag ctg gaa agc gag ttc 3024Val Gly Thr Ala Leu Ile Lys Lys Tyr
Pro Lys Leu Glu Ser Glu Phe 995 1000 1005 gtg tac ggc gac tac aag
gtg tac gac gtg cgg aag atg atc gcc 3069Val Tyr Gly Asp Tyr Lys Val
Tyr Asp Val Arg Lys Met Ile Ala 1010 1015 1020 aag agc gag cag gaa
atc ggc aag gct acc gcc aag tac ttc ttc 3114Lys Ser Glu Gln Glu Ile
Gly Lys Ala Thr Ala Lys Tyr Phe Phe 1025 1030 1035 tac agc aac atc
atg aac ttt ttc aag acc gag att acc ctg gcc 3159Tyr Ser Asn Ile Met
Asn Phe Phe Lys Thr Glu Ile Thr Leu Ala 1040 1045 1050 aac ggc gag
atc cgg aag cgg cct ctg atc gag aca aac ggc gaa 3204Asn Gly Glu Ile
Arg Lys Arg Pro Leu Ile Glu Thr Asn Gly Glu 1055 1060 1065 acc ggg
gag atc gtg tgg gat aag ggc cgg gat ttt gcc acc gtg 3249Thr Gly Glu
Ile Val Trp Asp Lys Gly Arg Asp Phe Ala Thr Val 1070 1075 1080 cgg
aaa gtg ctg agc atg ccc caa gtg aat atc gtg aaa aag acc 3294Arg Lys
Val Leu Ser Met Pro Gln Val Asn Ile Val Lys Lys Thr 1085 1090 1095
gag gtg cag aca ggc ggc ttc agc aaa gag tct atc ctg ccc aag 3339Glu
Val Gln Thr Gly Gly Phe Ser Lys Glu Ser Ile Leu Pro Lys 1100 1105
1110 agg aac agc gat aag ctg atc gcc aga aag aag gac tgg gac cct
3384Arg Asn Ser Asp Lys Leu Ile Ala Arg Lys Lys Asp Trp Asp Pro
1115 1120 1125 aag aag tac ggc ggc ttc gac agc ccc acc gtg gcc tat
tct gtg 3429Lys Lys Tyr Gly Gly Phe Asp Ser Pro Thr Val Ala Tyr Ser
Val 1130 1135 1140 ctg gtg gtg gcc aaa gtg gaa aag ggc aag tcc aag
aaa ctg aag 3474Leu Val Val Ala Lys Val Glu Lys Gly Lys Ser Lys Lys
Leu Lys 1145 1150 1155 agt gtg aaa gag ctg ctg ggg atc acc atc atg
gaa aga agc agc 3519Ser Val Lys Glu Leu Leu Gly Ile Thr Ile Met Glu
Arg Ser Ser 1160 1165 1170 ttc gag aag aat ccc atc gac ttt ctg gaa
gcc aag ggc tac aaa 3564Phe Glu Lys Asn Pro Ile Asp Phe Leu Glu Ala
Lys Gly Tyr Lys 1175 1180 1185 gaa gtg aaa aag gac ctg atc atc aag
ctg cct aag tac tcc ctg 3609Glu Val Lys Lys Asp Leu Ile Ile Lys Leu
Pro Lys Tyr Ser Leu 1190 1195 1200 ttc gag ctg gaa aac ggc cgg aag
aga atg ctg gcc tct gcc ggc 3654Phe Glu Leu Glu Asn Gly Arg Lys Arg
Met Leu Ala Ser Ala Gly 1205 1210 1215 gaa ctg cag aag gga aac gaa
ctg gcc ctg ccc tcc aaa tat gtg 3699Glu Leu Gln Lys Gly Asn Glu Leu
Ala Leu Pro Ser Lys Tyr Val 1220 1225 1230 aac ttc ctg tac ctg gcc
agc cac tat gag aag ctg aag ggc tcc 3744Asn Phe Leu Tyr Leu Ala Ser
His Tyr Glu Lys Leu Lys Gly Ser 1235 1240 1245 ccc gag gat aat gag
cag aaa cag ctg ttt gtg gaa cag cac aag 3789Pro Glu Asp Asn Glu Gln
Lys Gln Leu Phe Val Glu Gln His Lys 1250 1255 1260 cac tac ctg gac
gag atc atc gag cag atc agc gag ttc tcc aag 3834His Tyr Leu Asp Glu
Ile Ile Glu Gln Ile Ser Glu Phe Ser Lys 1265 1270 1275 aga gtg atc
ctg gcc gac gct aat ctg gac aaa gtg ctg tcc gcc 3879Arg Val Ile Leu
Ala Asp Ala Asn Leu Asp Lys Val Leu Ser Ala 1280 1285 1290 tac aac
aag cac cgg gat aag ccc atc aga gag cag gcc gag aat 3924Tyr Asn Lys
His Arg Asp Lys Pro Ile Arg Glu Gln Ala Glu Asn 1295 1300 1305 atc
atc cac ctg ttt acc ctg acc aat ctg gga gcc cct gcc gcc 3969Ile Ile
His Leu Phe Thr Leu Thr Asn Leu Gly Ala Pro Ala Ala 1310 1315 1320
ttc aag tac ttt gac acc acc atc gac cgg aag agg tac acc agc 4014Phe
Lys Tyr Phe Asp Thr Thr Ile Asp Arg Lys Arg Tyr Thr Ser 1325 1330
1335 acc aaa gag gtg ctg gac gcc acc ctg atc cac cag agc atc acc
4059Thr Lys Glu Val Leu Asp Ala Thr Leu Ile His Gln Ser Ile Thr
1340 1345 1350 ggc ctg tac gag aca cgg atc gac ctg tct cag ctg gga
ggc gac 4104Gly Leu Tyr Glu Thr Arg Ile Asp Leu Ser Gln Leu Gly Gly
Asp 1355 1360 1365 3681368PRTHomo sapiens 368Met Asp Lys Lys Tyr
Ser Ile Gly Leu Asp Ile Gly Thr Asn Ser Val 1 5 10 15 Gly Trp Ala
Val Ile Thr Asp Glu Tyr Lys Val Pro Ser Lys Lys Phe 20 25 30 Lys
Val Leu Gly Asn Thr Asp Arg His Ser Ile Lys Lys Asn Leu Ile 35 40
45 Gly Ala Leu Leu Phe Asp Ser Gly Glu Thr Ala Glu Ala Thr Arg Leu
50 55 60 Lys Arg Thr Ala Arg Arg Arg Tyr Thr Arg Arg Lys Asn Arg
Ile Cys 65 70 75 80 Tyr Leu Gln Glu Ile Phe Ser Asn Glu Met Ala Lys
Val Asp Asp Ser
85 90 95 Phe Phe His Arg Leu Glu Glu Ser Phe Leu Val Glu Glu Asp
Lys Lys 100 105 110 His Glu Arg His Pro Ile Phe Gly Asn Ile Val Asp
Glu Val Ala Tyr 115 120 125 His Glu Lys Tyr Pro Thr Ile Tyr His Leu
Arg Lys Lys Leu Val Asp 130 135 140 Ser Thr Asp Lys Ala Asp Leu Arg
Leu Ile Tyr Leu Ala Leu Ala His 145 150 155 160 Met Ile Lys Phe Arg
Gly His Phe Leu Ile Glu Gly Asp Leu Asn Pro 165 170 175 Asp Asn Ser
Asp Val Asp Lys Leu Phe Ile Gln Leu Val Gln Thr Tyr 180 185 190 Asn
Gln Leu Phe Glu Glu Asn Pro Ile Asn Ala Ser Gly Val Asp Ala 195 200
205 Lys Ala Ile Leu Ser Ala Arg Leu Ser Lys Ser Arg Arg Leu Glu Asn
210 215 220 Leu Ile Ala Gln Leu Pro Gly Glu Lys Lys Asn Gly Leu Phe
Gly Asn 225 230 235 240 Leu Ile Ala Leu Ser Leu Gly Leu Thr Pro Asn
Phe Lys Ser Asn Phe 245 250 255 Asp Leu Ala Glu Asp Ala Lys Leu Gln
Leu Ser Lys Asp Thr Tyr Asp 260 265 270 Asp Asp Leu Asp Asn Leu Leu
Ala Gln Ile Gly Asp Gln Tyr Ala Asp 275 280 285 Leu Phe Leu Ala Ala
Lys Asn Leu Ser Asp Ala Ile Leu Leu Ser Asp 290 295 300 Ile Leu Arg
Val Asn Thr Glu Ile Thr Lys Ala Pro Leu Ser Ala Ser 305 310 315 320
Met Ile Lys Arg Tyr Asp Glu His His Gln Asp Leu Thr Leu Leu Lys 325
330 335 Ala Leu Val Arg Gln Gln Leu Pro Glu Lys Tyr Lys Glu Ile Phe
Phe 340 345 350 Asp Gln Ser Lys Asn Gly Tyr Ala Gly Tyr Ile Asp Gly
Gly Ala Ser 355 360 365 Gln Glu Glu Phe Tyr Lys Phe Ile Lys Pro Ile
Leu Glu Lys Met Asp 370 375 380 Gly Thr Glu Glu Leu Leu Val Lys Leu
Asn Arg Glu Asp Leu Leu Arg 385 390 395 400 Lys Gln Arg Thr Phe Asp
Asn Gly Ser Ile Pro His Gln Ile His Leu 405 410 415 Gly Glu Leu His
Ala Ile Leu Arg Arg Gln Glu Asp Phe Tyr Pro Phe 420 425 430 Leu Lys
Asp Asn Arg Glu Lys Ile Glu Lys Ile Leu Thr Phe Arg Ile 435 440 445
Pro Tyr Tyr Val Gly Pro Leu Ala Arg Gly Asn Ser Arg Phe Ala Trp 450
455 460 Met Thr Arg Lys Ser Glu Glu Thr Ile Thr Pro Trp Asn Phe Glu
Glu 465 470 475 480 Val Val Asp Lys Gly Ala Ser Ala Gln Ser Phe Ile
Glu Arg Met Thr 485 490 495 Asn Phe Asp Lys Asn Leu Pro Asn Glu Lys
Val Leu Pro Lys His Ser 500 505 510 Leu Leu Tyr Glu Tyr Phe Thr Val
Tyr Asn Glu Leu Thr Lys Val Lys 515 520 525 Tyr Val Thr Glu Gly Met
Arg Lys Pro Ala Phe Leu Ser Gly Glu Gln 530 535 540 Lys Lys Ala Ile
Val Asp Leu Leu Phe Lys Thr Asn Arg Lys Val Thr 545 550 555 560 Val
Lys Gln Leu Lys Glu Asp Tyr Phe Lys Lys Ile Glu Cys Phe Asp 565 570
575 Ser Val Glu Ile Ser Gly Val Glu Asp Arg Phe Asn Ala Ser Leu Gly
580 585 590 Thr Tyr His Asp Leu Leu Lys Ile Ile Lys Asp Lys Asp Phe
Leu Asp 595 600 605 Asn Glu Glu Asn Glu Asp Ile Leu Glu Asp Ile Val
Leu Thr Leu Thr 610 615 620 Leu Phe Glu Asp Arg Glu Met Ile Glu Glu
Arg Leu Lys Thr Tyr Ala 625 630 635 640 His Leu Phe Asp Asp Lys Val
Met Lys Gln Leu Lys Arg Arg Arg Tyr 645 650 655 Thr Gly Trp Gly Arg
Leu Ser Arg Lys Leu Ile Asn Gly Ile Arg Asp 660 665 670 Lys Gln Ser
Gly Lys Thr Ile Leu Asp Phe Leu Lys Ser Asp Gly Phe 675 680 685 Ala
Asn Arg Asn Phe Met Gln Leu Ile His Asp Asp Ser Leu Thr Phe 690 695
700 Lys Glu Asp Ile Gln Lys Ala Gln Val Ser Gly Gln Gly Asp Ser Leu
705 710 715 720 His Glu His Ile Ala Asn Leu Ala Gly Ser Pro Ala Ile
Lys Lys Gly 725 730 735 Ile Leu Gln Thr Val Lys Val Val Asp Glu Leu
Val Lys Val Met Gly 740 745 750 Arg His Lys Pro Glu Asn Ile Val Ile
Ala Met Ala Arg Glu Asn Gln 755 760 765 Thr Thr Gln Lys Gly Gln Lys
Asn Ser Arg Glu Arg Met Lys Arg Ile 770 775 780 Glu Glu Gly Ile Lys
Glu Leu Gly Ser Gln Ile Leu Lys Glu His Pro 785 790 795 800 Val Glu
Asn Thr Gln Leu Gln Asn Glu Lys Leu Tyr Leu Tyr Tyr Leu 805 810 815
Gln Asn Gly Arg Asp Met Tyr Val Asp Gln Glu Leu Asp Ile Asn Arg 820
825 830 Leu Ser Asp Tyr Asp Val Asp Ala Ile Val Pro Gln Ser Phe Leu
Lys 835 840 845 Asp Asp Ser Ile Asp Ala Lys Val Leu Thr Arg Ser Asp
Lys Ala Arg 850 855 860 Gly Lys Ser Asp Asn Val Pro Ser Glu Glu Val
Val Lys Lys Met Lys 865 870 875 880 Asn Tyr Trp Arg Gln Leu Leu Asn
Ala Lys Leu Ile Thr Gln Arg Lys 885 890 895 Phe Asp Asn Leu Thr Lys
Ala Glu Arg Gly Gly Leu Ser Glu Leu Asp 900 905 910 Lys Ala Gly Phe
Ile Lys Arg Gln Leu Val Glu Thr Arg Gln Ile Thr 915 920 925 Lys His
Val Ala Gln Ile Leu Asp Ser Arg Met Asn Thr Lys Tyr Asp 930 935 940
Glu Asn Asp Lys Leu Ile Arg Glu Val Lys Val Ile Thr Leu Lys Ser 945
950 955 960 Lys Leu Val Ser Asp Phe Arg Lys Asp Phe Gln Phe Tyr Lys
Val Arg 965 970 975 Glu Ile Asn Asn Tyr His His Ala His Ala Ala Tyr
Leu Asn Ala Val 980 985 990 Val Gly Thr Ala Leu Ile Lys Lys Tyr Pro
Lys Leu Glu Ser Glu Phe 995 1000 1005 Val Tyr Gly Asp Tyr Lys Val
Tyr Asp Val Arg Lys Met Ile Ala 1010 1015 1020 Lys Ser Glu Gln Glu
Ile Gly Lys Ala Thr Ala Lys Tyr Phe Phe 1025 1030 1035 Tyr Ser Asn
Ile Met Asn Phe Phe Lys Thr Glu Ile Thr Leu Ala 1040 1045 1050 Asn
Gly Glu Ile Arg Lys Arg Pro Leu Ile Glu Thr Asn Gly Glu 1055 1060
1065 Thr Gly Glu Ile Val Trp Asp Lys Gly Arg Asp Phe Ala Thr Val
1070 1075 1080 Arg Lys Val Leu Ser Met Pro Gln Val Asn Ile Val Lys
Lys Thr 1085 1090 1095 Glu Val Gln Thr Gly Gly Phe Ser Lys Glu Ser
Ile Leu Pro Lys 1100 1105 1110 Arg Asn Ser Asp Lys Leu Ile Ala Arg
Lys Lys Asp Trp Asp Pro 1115 1120 1125 Lys Lys Tyr Gly Gly Phe Asp
Ser Pro Thr Val Ala Tyr Ser Val 1130 1135 1140 Leu Val Val Ala Lys
Val Glu Lys Gly Lys Ser Lys Lys Leu Lys 1145 1150 1155 Ser Val Lys
Glu Leu Leu Gly Ile Thr Ile Met Glu Arg Ser Ser 1160 1165 1170 Phe
Glu Lys Asn Pro Ile Asp Phe Leu Glu Ala Lys Gly Tyr Lys 1175 1180
1185 Glu Val Lys Lys Asp Leu Ile Ile Lys Leu Pro Lys Tyr Ser Leu
1190 1195 1200 Phe Glu Leu Glu Asn Gly Arg Lys Arg Met Leu Ala Ser
Ala Gly 1205 1210 1215 Glu Leu Gln Lys Gly Asn Glu Leu Ala Leu Pro
Ser Lys Tyr Val 1220 1225 1230 Asn Phe Leu Tyr Leu Ala Ser His Tyr
Glu Lys Leu Lys Gly Ser 1235 1240 1245 Pro Glu Asp Asn Glu Gln Lys
Gln Leu Phe Val Glu Gln His Lys 1250 1255 1260 His Tyr Leu Asp Glu
Ile Ile Glu Gln Ile Ser Glu Phe Ser Lys 1265 1270 1275 Arg Val Ile
Leu Ala Asp Ala Asn Leu Asp Lys Val Leu Ser Ala 1280 1285 1290 Tyr
Asn Lys His Arg Asp Lys Pro Ile Arg Glu Gln Ala Glu Asn 1295 1300
1305 Ile Ile His Leu Phe Thr Leu Thr Asn Leu Gly Ala Pro Ala Ala
1310 1315 1320 Phe Lys Tyr Phe Asp Thr Thr Ile Asp Arg Lys Arg Tyr
Thr Ser 1325 1330 1335 Thr Lys Glu Val Leu Asp Ala Thr Leu Ile His
Gln Ser Ile Thr 1340 1345 1350 Gly Leu Tyr Glu Thr Arg Ile Asp Leu
Ser Gln Leu Gly Gly Asp 1355 1360 1365 36926DNAHomo sapiens
369tagggttagg ggccccaggc cggggt 263706PRTArtificial
SequenceDescription of Artificial Sequence Synthetic 6xHis tag
370His His His His His His 1 5 37157DNAHomo sapiensCDS(1)..(57)
371ggc acc att aaa gaa aat atc att ggt gtt tcc tat gat gaa tat aga
48Gly Thr Ile Lys Glu Asn Ile Ile Gly Val Ser Tyr Asp Glu Tyr Arg 1
5 10 15 tac aga agc 57Tyr Arg Ser 37219PRTHomo sapiens 372Gly Thr
Ile Lys Glu Asn Ile Ile Gly Val Ser Tyr Asp Glu Tyr Arg 1 5 10 15
Tyr Arg Ser 37348DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 373att aaa gaa aat atc att ggc
ttt gtt tcc tat gat gaa tat aga tac 48Ile Lys Glu Asn Ile Ile Gly
Phe Val Ser Tyr Asp Glu Tyr Arg Tyr 1 5 10 15 37416PRTArtificial
SequenceDescription of Artificial Sequence Synthetic peptide 374Ile
Lys Glu Asn Ile Ile Gly Phe Val Ser Tyr Asp Glu Tyr Arg Tyr 1 5 10
15 37550DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 375ccnnnnnnnn nnnnnnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnngg 5037646DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 376ccnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnngg 4637742DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 377ccnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn gg
4237838DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 378ccnnnnnnnn nnnnnnnnnn nnnnnnnnnn
nnnnnngg 3837934DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 379ccnnnnnnnn nnnnnnnnnn
nnnnnnnnnn nngg 3438030DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 380ccnnnnnnnn
nnnnnnnnnn nnnnnnnngg 3038126DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 381ccnnnnnnnn
nnnnnnnnnn nnnngg 2638222DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 382ccnnnnnnnn
nnnnnnnnnn gg 2238318DNAArtificial SequenceDescription of
Artificial Sequence Synthetic oligonucleotide 383ccnnnnnnnn
nnnnnngg 1838416DNAArtificial SequenceDescription of Artificial
Sequence Synthetic oligonucleotide 384ccnnnnnnnn nnnngg
1638515DNAArtificial SequenceDescription of Artificial Sequence
Synthetic oligonucleotide 385ccnnnnnnnn nnngg 1538614DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 386ccnnnnnnnn nngg 1438713DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 387ccnnnnnnnn ngg 1338812DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 388ccnnnnnnnn gg 1238911DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 389ccnnnnnnng g 1139010DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 390ccnnnnnngg 1039112DNAArtificial
SequenceDescription of Artificial Sequence Synthetic
oligonucleotide 391ggnnnnnnnn cc 12392125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
392aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aactcacatc aaccggtggc gcaggtgttt
cgtcctttcc 120acaag 125393125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 393aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aactcacatc aaccggtggc gcaggtgttt cgtcctttcc 120acaag
125394125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 394aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacgaggaca aagtacaaac
ggcggtgttt cgtcctttcc 120acaag 125395125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
395aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgaggaca aagtacaaac ggcggtgttt
cgtcctttcc 120acaag 125396125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 396aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacgtggcgc attgccacga agcggtgttt cgtcctttcc 120acaag
125397125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 397aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aaccgagggc agagtgctgc
ttgggtgttt cgtcctttcc 120acaag 125398125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
398aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgagtccg agcagaagaa gaaggtgttt
cgtcctttcc 120acaag 125399125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 399aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacgaggaca aagtacaaac ggcggtgttt cgtcctttcc 120acaag
125400125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 400aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacagcagaa gaagaagggc
tccggtgttt cgtcctttcc 120acaag 125401125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
401aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aactcacatc aaccggtggc gcaggtgttt
cgtcctttcc 120acaag 125402125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 402aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacccctggc ccaggtgaag gtgggtgttt cgtcctttcc 120acaag
125403125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 403aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aactccctcc
ctggcccagg
tgaggtgttt cgtcctttcc 120acaag 125404125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
404aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgaaccgg aggacaaagt acaggtgttt
cgtcctttcc 120acaag 125405125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 405aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacaggtgaa ggtgtggttc cagggtgttt cgtcctttcc 120acaag
125406125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 406aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacggtgaag gtgtggttcc
agaggtgttt cgtcctttcc 120acaag 125407125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
407aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgaaccgg aggacaaagt acaggtgttt
cgtcctttcc 120acaag 125408125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 408aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacccctggc ccaggtgaag gtgggtgttt cgtcctttcc 120acaag
125409125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 409aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacaggtgaa ggtgtggttc
cagggtgttt cgtcctttcc 120acaag 125410125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
410aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgaggaca aagtacaaac ggcggtgttt
cgtcctttcc 120acaag 125411125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 411aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacgggaggg aggggcacag atgggtgttt cgtcctttcc 120acaag
125412125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 412aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aaccaccttc acctgggcca
gggggtgttt cgtcctttcc 120acaag 125413125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
413aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacaccctag tcattggagg tgaggtgttt
cgtcctttcc 120acaag 125414125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 414aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aaccagagca gccactgggg cctggtgttt cgtcctttcc 120acaag
125415125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 415aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aaccaccttc acctgggcca
gggggtgttt cgtcctttcc 120acaag 125416125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
416aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacccccatt ggcctgcttc gtgggtgttt
cgtcctttcc 120acaag 125417125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 417aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacattggcc tgcttcgtgg caaggtgttt cgtcctttcc 120acaag
125418125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 418aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aactcctcct ccagcttctg
ccgggtgttt cgtcctttcc 120acaag 125419125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
419aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aaccctccag cttctgccgt ttgggtgttt
cgtcctttcc 120acaag 125420125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 420aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacattggcc tgcttcgtgg caaggtgttt cgtcctttcc 120acaag
125421125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 421aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacgcagcaa gcagcactct
gccggtgttt cgtcctttcc 120acaag 125422125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
422aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacttcttct tctgctcgga ctcggtgttt
cgtcctttcc 120acaag 125423125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 423aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacaccggag gacaaagtac aaaggtgttt cgtcctttcc 120acaag
125424125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 424aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aactcttctt ctgctcggac
tcaggtgttt cgtcctttcc 120acaag 125425125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
425aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgttgatg tgatgggagc cctggtgttt
cgtcctttcc 120acaag 125426125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 426aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacgggccag ggagggaggg gcaggtgttt cgtcctttcc 120acaag
125427125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 427aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacgggaggg aggggcacag
atgggtgttt cgtcctttcc 120acaag 125428125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
428aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacccggttc tggaaccaca cctggtgttt
cgtcctttcc 120acaag 125429125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 429aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aactcacctg ggccagggag ggaggtgttt cgtcctttcc 120acaag
125430125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 430aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aactcacctg ggccagggag
ggaggtgttt cgtcctttcc 120acaag 125431125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
431aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgttctgg aaccacacct tcaggtgttt
cgtcctttcc 120acaag 125432125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 432aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacgggaggg aggggcacag atgggtgttt cgtcctttcc 120acaag
125433125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 433aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacgggccag ggagggaggg
gcaggtgttt cgtcctttcc 120acaag 125434125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
434aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aacgttctgg aaccacacct tcaggtgttt
cgtcctttcc 120acaag 125435125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 435aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacaggtgaa ggtgtggttc cagggtgttt cgtcctttcc 120acaag
125436125DNAArtificial SequenceDescription of Artificial Sequence
Synthetic primer 436aaaaaaagca ccgactcggt gccacttttt caagttgata
acggactagc cttattttaa 60cttgctattt ctagctctaa aacgaaccgg aggacaaagt
acaggtgttt cgtcctttcc 120acaag 125437125DNAArtificial
SequenceDescription of Artificial Sequence Synthetic primer
437aaaaaaagca ccgactcggt gccacttttt caagttgata acggactagc
cttattttaa 60cttgctattt ctagctctaa aaccaaaccc acgagggcag agtggtgttt
cgtcctttcc 120acaag 125438125DNAArtificial SequenceDescription of
Artificial Sequence Synthetic primer 438aaaaaaagca ccgactcggt
gccacttttt caagttgata acggactagc cttattttaa 60cttgctattt ctagctctaa
aacgagtttc tcatctgtgc cccggtgttt cgtcctttcc 120acaag
125439684DNAHomo
sapiensCDS(1)..(123)CDS(127)..(159)CDS(163)..(399)CDS(403)..(684)
439aaa acc acc ctt ctc tct ggc cca ctg tgt cct ctt cct gcc ctg cca
48Lys Thr Thr Leu Leu Ser Gly Pro Leu Cys Pro Leu Pro Ala Leu Pro 1
5 10 15 tcc cct tct gtg aat gtt aga ccc atg gga gca gct ggt cag agg
gga 96Ser Pro Ser Val Asn Val Arg Pro Met Gly Ala Ala Gly Gln Arg
Gly 20 25 30 ccc cgg cct ggg gcc cct aac cct atg tag cct cag tct
tcc cat cag 144Pro Arg Pro Gly Ala Pro Asn Pro Met Pro Gln Ser Ser
His Gln 35 40 45 gct ctc agc tca gcc tga gtg ttg agg ccc cag tgg
ctg ctc tgg ggg 192Ala Leu Ser Ser Ala Val Leu Arg Pro Gln Trp Leu
Leu Trp Gly 50 55 60 cct cct gag ttt ctc atc tgt gcc cct ccc tcc
ctg gcc cag gtg aag 240Pro Pro Glu Phe Leu Ile Cys Ala Pro Pro Ser
Leu Ala Gln Val Lys 65 70 75 gtg tgg ttc cag aac cgg agg aca aag
tac aaa cgg cag aag ctg gag 288Val Trp Phe Gln Asn Arg Arg Thr Lys
Tyr Lys Arg Gln Lys Leu Glu 80 85 90 gag gaa ggg cct gag tcc gag
cag aag aag aag ggc tcc cat cac atc 336Glu Glu Gly Pro Glu Ser Glu
Gln Lys Lys Lys Gly Ser His His Ile 95 100 105 110 aac cgg tgg cgc
att gcc acg aag cag gcc aat ggg gag gac atc gat 384Asn Arg Trp Arg
Ile Ala Thr Lys Gln Ala Asn Gly Glu Asp Ile Asp 115 120 125 gtc acc
tcc aat gac tag ggt ggg caa cca caa acc cac gag ggc aga 432Val Thr
Ser Asn Asp Gly Gly Gln Pro Gln Thr His Glu Gly Arg 130 135 140 gtg
ctg ctt gct gct ggc cag gcc cct gcg tgg gcc caa gct gga ctc 480Val
Leu Leu Ala Ala Gly Gln Ala Pro Ala Trp Ala Gln Ala Gly Leu 145 150
155 tgg cca ctc cct ggc cag gct ttg ggg agg cct gga gtc atg gcc cca
528Trp Pro Leu Pro Gly Gln Ala Leu Gly Arg Pro Gly Val Met Ala Pro
160 165 170 cag ggc ttg aag ccc ggg gcc gcc att gac aga ggg aca agc
aat ggg 576Gln Gly Leu Lys Pro Gly Ala Ala Ile Asp Arg Gly Thr Ser
Asn Gly 175 180 185 ctg gct gag gcc tgg gac cac ttg gcc ttc tcc tcg
gag agc ctg cct 624Leu Ala Glu Ala Trp Asp His Leu Ala Phe Ser Ser
Glu Ser Leu Pro 190 195 200 205 gcc tgg gcg ggc ccg ccc gcc acc gca
gcc tcc cag ctg ctc tcc gtg 672Ala Trp Ala Gly Pro Pro Ala Thr Ala
Ala Ser Gln Leu Leu Ser Val 210 215 220 tct cca atc tcc 684Ser Pro
Ile Ser 225 44041PRTHomo sapiens 440Lys Thr Thr Leu Leu Ser Gly Pro
Leu Cys Pro Leu Pro Ala Leu Pro 1 5 10 15 Ser Pro Ser Val Asn Val
Arg Pro Met Gly Ala Ala Gly Gln Arg Gly 20 25 30 Pro Arg Pro Gly
Ala Pro Asn Pro Met 35 40 44111PRTHomo sapiens 441Pro Gln Ser Ser
His Gln Ala Leu Ser Ser Ala 1 5 10 44279PRTHomo sapiens 442Val Leu
Arg Pro Gln Trp Leu Leu Trp Gly Pro Pro Glu Phe Leu Ile 1 5 10 15
Cys Ala Pro Pro Ser Leu Ala Gln Val Lys Val Trp Phe Gln Asn Arg 20
25 30 Arg Thr Lys Tyr Lys Arg Gln Lys Leu Glu Glu Glu Gly Pro Glu
Ser 35 40 45 Glu Gln Lys Lys Lys Gly Ser His His Ile Asn Arg Trp
Arg Ile Ala 50 55 60 Thr Lys Gln Ala Asn Gly Glu Asp Ile Asp Val
Thr Ser Asn Asp 65 70 75 44394PRTHomo sapiens 443Gly Gly Gln Pro
Gln Thr His Glu Gly Arg Val Leu Leu Ala Ala Gly 1 5 10 15 Gln Ala
Pro Ala Trp Ala Gln Ala Gly Leu Trp Pro Leu Pro Gly Gln 20 25 30
Ala Leu Gly Arg Pro Gly Val Met Ala Pro Gln Gly Leu Lys Pro Gly 35
40 45 Ala Ala Ile Asp Arg Gly Thr Ser Asn Gly Leu Ala Glu Ala Trp
Asp 50 55 60 His Leu Ala Phe Ser Ser Glu Ser Leu Pro Ala Trp Ala
Gly Pro Pro 65 70 75 80 Ala Thr Ala Ala Ser Gln Leu Leu Ser Val Ser
Pro Ile Ser 85 90
* * * * *
References