U.S. patent application number 16/149420 was filed with the patent office on 2019-02-28 for neuronal viability factor and use thereof.
The applicant listed for this patent is Centre National De La Recherche Scientifique - CNRS, Institut National de la Sante et de la Recherche Medicale. Invention is credited to Celine Jaillard, Thierry Leveillard, Olivier Poch, Jose-Alain Sahel.
Application Number | 20190064189 16/149420 |
Document ID | / |
Family ID | 38573348 |
Filed Date | 2019-02-28 |
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United States Patent
Application |
20190064189 |
Kind Code |
A1 |
Leveillard; Thierry ; et
al. |
February 28, 2019 |
NEURONAL VIABILITY FACTOR AND USE THEREOF
Abstract
The present invention concerns a pharmaceutical composition
comprising a pharmaceutically acceptable carrier and a compound
selected in the group comprising (i) a polypeptide comprising an
amino acid sequence selected in the group comprising the amino acid
sequence of the long isoform in Homo sapiens of the RdCVF2 gene
(SEQ ID NO: 10), orthologs, derivatives and fragments thereof, (ii)
a polynucleotide coding for said polypeptide, (iii) a vector
comprising said polynucleotide, and (iv) a host cell genetically
engineered expressing said polypeptide; the use of such a
composition for the manufacture of a medicament for treating and/or
preventing a neurodegenerative disorder in a subject; and a method
of testing a subject thought to have or be predisposed to having a
neurodegenerative disorder.
Inventors: |
Leveillard; Thierry;
(Maisons-Alfort, FR) ; Sahel; Jose-Alain; (Paris,
FR) ; Jaillard; Celine; (Antony, FR) ; Poch;
Olivier; (Strasbourg, FR) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Institut National de la Sante et de la Recherche Medicale
Centre National De La Recherche Scientifique - CNRS |
Paris
Paris |
|
FR
FR |
|
|
Family ID: |
38573348 |
Appl. No.: |
16/149420 |
Filed: |
October 2, 2018 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15205797 |
Jul 8, 2016 |
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16149420 |
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12602736 |
Jun 1, 2010 |
9575075 |
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PCT/EP2008/057031 |
Jun 5, 2008 |
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15205797 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C12Q 2600/156 20130101;
A61P 25/00 20180101; A61P 25/28 20180101; A61P 25/14 20180101; A61P
27/00 20180101; G01N 2800/2835 20130101; G01N 33/6896 20130101;
C12Q 2600/158 20130101; A61K 38/44 20130101; C07K 14/435 20130101;
C12Q 2600/118 20130101; A61K 38/1709 20130101; C12Q 1/6883
20130101; C07K 14/00 20130101; G01N 2800/2821 20130101; A61P 25/16
20180101 |
International
Class: |
G01N 33/68 20060101
G01N033/68; C07K 14/435 20060101 C07K014/435; C07K 14/00 20060101
C07K014/00; A61K 38/44 20060101 A61K038/44; C12Q 1/6883 20060101
C12Q001/6883; A61K 38/17 20060101 A61K038/17 |
Foreign Application Data
Date |
Code |
Application Number |
Jun 5, 2007 |
EP |
07109652.3 |
Claims
1. A pharmaceutical composition comprising a pharmaceutically
acceptable carrier and a compound selected in the group consisting
of: (i) a polypeptide comprising an amino acid sequence selected in
the group consisting of the amino acid sequence of the long isoform
in Homo sapiens of the RdCVF2 gene (SEQ ID NO:10), orthologs,
derivatives and fragments thereof; (ii) a polynucleotide coding for
said polypeptide; (iii) a vector comprising said polynucleotide;
and (iv) a host cell genetically engineered expressing said
polypeptide.
2. The pharmaceutical composition according to claim 1, wherein the
derivatives are selected in the group consisting of polypeptides
having a percentage of identity of at least 75% with SEQ ID NO. 10
or orthologs thereof.
3. The pharmaceutical composition according to claim 1, wherein
said fragments refer to polypeptides having a length of at least 25
amino acids.
4. The pharmaceutical composition according to claim 1, wherein the
polynucleotide is selected in the group consisting of RNA and
DNA.
5. The pharmaceutical composition according to claim 4, wherein
said polynucleotide comprises a sequence which encodes the sequence
SEQ ID NO. 10.
6. The pharmaceutical composition according to claim 1, wherein the
vector is an expression vector selected in the group consisting of
plasmids, viral particles and phages.
7. The pharmaceutical composition according to claim 1, wherein the
host cell is selected in the group consisting of bacterial cells,
fungal cells, insect cells, animal cells, and plant cells.
8. A method, for treating and/or preventing a neurodegenerative
disorder, comprising the administration of an effective amount of a
compound selected in the group consisting of: (i) a polypeptide
comprising an amino acid sequence selected in the group consisting
of the amino acid sequence of long isoform in Homo sapiens of the
RdCVF2 gene (SEQ ID NO:10), orthologs, derivatives and fragments
thereof; (ii) a polynucleotide coding for said polypeptide; (iii) a
vector comprising said polynucleotide; and (iv) a host cell
genetically engineered expressing said polypeptide to a patient in
need thereof.
9. The method according to claim 8, wherein the neurodegenerative
disorder is a disease associated with the degeneration of neurons
selected in the group consisting of degenerative disorders of the
central nervous system, degenerative disorders of the
photoreceptors, and degenerative disorders of the olfactory
neurons.
10. The method according to claim 9, wherein the degenerative
disorder of the central nervous system, is selected in the group
consisting of Alzheimer's Disease, Parkinson's Disease, and
Huntington's Disease/Chorea.
11. The method according to claim 9, wherein the degenerative
disorders of the photoreceptors is cone dystrophy.
12. A method of testing a subject thought to have or be predisposed
to having neurodegenerative disorder, which comprises the step of
analyzing a biological sample for: (i) detecting the presence of
mutation in the RdCVF2 gene and/or its associated promoter, and/or
(ii) analyzing the expression of the RdCVF2 gene.
13. The pharmaceutical composition according to claim 2, wherein
the derivatives are selected in the group consisting of
polypeptides having a percentage of identity of at least 85% with
SEQ ID NO. 10 and orthologs thereof.
14. The pharmaceutical composition according to claim 3, wherein
said fragments refer to polypeptides having a length of at least 50
amino acids.
15. (Ne The pharmaceutical composition according to claim 4,
wherein the polynucleotide is DNA.
16. A method for treating Alzheimer's Disease comprising the
administration of an effective amount of: (i) a polynucleotide
coding for a polypeptide comprising an amino acid sequence of long
isoform in Homo sapiens of the RdCVF2 gene and having the sequence
forth in SEQ ID NO:10; or (ii) a vector comprising said
polynucleotide.
17. A method according to claim 16, wherein the vector is an
expression vector selected in the group consisting of plasmids,
viral particles and phages.
Description
[0001] This application claims the priority of the patent
application EP07109652.3 filed Jun. 5, 2007, which is incorporated
herein by reference.
FIELD OF THE INVENTION
[0002] The present invention relates to neurodegenerative
disorders, and more particularly to a pharmaceutical composition
for treating and/or preventing neurodegenerative disorders.
BACKGROUND OF THE INVENTION
[0003] Neurodegenerative disorders have provided a challenge for
many years, in both basic research and clinical contexts.
[0004] As an example of such a neurodegenerative disorder,
retinitis pigmentosa (RP) is a genetically heterogeneous retinal
degeneration characterized by the sequential degeneration of a
population of neurons corresponding to rod and cone photoreceptors.
The RP first clinical signs are night blindness and narrowing of
the peripheral field of vision which progressively worsens to
become "tunnel-like". Eventually, the central vision is reduced to
complete blindness in most cases. At a cellular level, the retinal
rod photoreceptors involved in night and side visions slowly
degenerate. Subsequently, the cone photoreceptors responsible for
both color and high-contrast vision, visual acuity, detail
perception and normal light vision are similarly affected. The
retinal degeneration 1 (rd1) mouse is the most studied animal model
for retinitis pigmentosa. It carries a recessive mutation in the
rod-specific cGMP phosphodiesterase beta subunit gene leading to
rod photoreceptor death through apoptosis (CARTER-DAWSON et al.,
Invest. Ophthalmol. Vis. Sci., vol. 17(6), p: 489-498, 1978;
PORTERA-CAILLIAU et al., Proc. Natl. Acad. Sci. USA, vol.91(3), p:
974-978, 1994) followed by cone death presumably through lack of
trophic support (MOHAND-SAID et al., Proc. Natl. Acad Sci. U.S.A,
vol. 95(14), p: 8357-8362, 1998).
[0005] Accordingly, the technical problem underlying the present
invention is to provide novel compounds having neurotrophic
activities, which compounds are suitable for the treatment of
neurodegenerative disorders such as retinitis pigmentosa for which
no treatment is actually available.
[0006] The RdCVF gene, also called thioredoxin-like 6 (Txn16) or
Nucleoredoxin-like 1 (Nxn11), encodes the Q8VC33 UniProt [6]
protein, which has limited similarity to the thioredoxin
superfamily and which exerts trophic activity on cone
photoreceptors (LEVEILLARD et al., Nat. Genet. vol. 36(7), p:
755-759, 2004). Thioredoxins (TXN) are usually small proteins which
can be involved with pleiotropic activities such as redox control,
regulation of apoptosis and cytokine activity (HOLMGREN, Annu. Rev.
Biochem., vol. 54, p: 237-271, 1985; HOLMGREN, J. Biol. Chem., vol.
264(24), p: 13963-13966, 1989; ARNER and HOLMGREN , Eur. J.
Biochem., vol. 267(20), p: 6102-6109, 2000). The TXN conserved
active site contains two distinct cysteines (CXXC) that contribute
to a thiol-oxydoreductase activity (ARNER and HOLMGREN, 2000,
abovementioned; POWIS and MONTFORT, Anna. Rev. Pharmacol. Toxicol.,
vol. 41, p: 261-295, 2001) catalyzes the reduction of disulfide
bonds in multiple substrate proteins (HOLMGREN, J. Biol. Chem.,
vol. 254(18) , p: 9113-9119, 1979; HOLMGREN, J. Biol. Chem., vol.
254(19), p: 9627-9632, 1979). The RdCVF gene encodes two products
via alternative splicing: a full length protein and a C-terminal
post-transcriptionally truncated protein sharing similarities with
TRX80. This latter form of human thioredoxin-1 (Txn) (PEKKARI et
al., J. Biol. Chem., vol. 275(48), p: 37474-37480, 2000; PEKKARI et
al., Blood, vol. 105(4),: 1598-1605, 2005; LIU et al., Blood, vol.
105(4): 1606-1613, 2005) has no thiol-reductase activity but is
involved in controlling growth of peripheral mononuclear blood
cells (PEKKARI et al., 2000, abovementioned; PEKKARI et al., FEBS
Lett., vol. 539(1-3): 143-148, 2003). Similar to Txn, RdCVF looks
like a bifunctional gene because it encodes both a long form
(RdCVF-L, 217 aa, Q8VC33) having a putative thiol-oxydoreductase
activity (JEFFERY, Trends Biochem. Sci., vol. 24(1): 8-11, 1999;
JEFFERY, Trends Genet., vol. 19(8): 415-417, 2003) and a short form
(RdCVF-S, 109 aa, Q91W38) with trophic activity for cones but no
redox activity.
SUMMARY OF THE INVENTION
[0007] The present invention relates to a pharmaceutical
composition comprising a pharmaceutically acceptable carrier and a
compound selected in the group comprising: [0008] (i) a polypeptide
comprising an amino acid sequence selected in the group comprising
the amino acid sequence of the short isoform in Homo sapiens of the
RdCVF2 gene (SEQ ID NO:1), orthologs, derivatives and fragments
thereof; [0009] (ii) a polynucleotide coding for said polypeptide;
[0010] (iii) a vector comprising said polynucleotide; and [0011]
(iv) a host cell genetically engineered expressing said
polypeptide.
[0012] In another embodiment, the present invention relates to a
use, for treating and/or preventing a neurodegenerative disorder,
of a compound selected in the group comprising: [0013] (i) a
polypeptide comprising an amino acid sequence selected in the group
comprising the amino acid sequence of the isoform in Homo sapiens
of the RdCVF2 gene (SEQ ID NO:1), orthologs, derivatives and
fragments thereof; [0014] (ii) a polynucleotide coding for said
polypeptide; [0015] (iii) a vector comprising said polynucleotide;
and [0016] (iv) a host cell genetically engineered expressing said
polypeptide.
[0017] In still another embodiment, the present invention relates
to a method of preventing and/or treating a neurodegenerative
disease comprising providing, to a subject displaying or predicted
to display a neurodegenerative disorder, an effective amount of a
composition comprising a compound selected in the group
comprising:
[0018] (i) a polypeptide comprising an amino acid sequence selected
in the group comprising the amino acid sequence of the short
isoform in Homo sapiens of the RdCVF2 gene (SEQ ID NO:1),
orthologs, derivatives and fragments thereof;
[0019] (ii) a polynucleotide coding for said polypeptide;
[0020] (iii) a vector comprising said polynucleotide; and
[0021] (iv) a host cell genetically engineered expressing said
polypeptide.
[0022] In still another embodiment, the present invention finally
relates a method of testing a subject thought to have or be
predisposed to having a neurodegenerative disorder, which comprises
detecting the presence of a mutation in the RdCVF2 gene and/or its
associated promoter in a biological sample from said subject
BRIEF DESCRIPTION OF THE DRAWINGS
[0023] FIG. 1A-B shows the RdCVF and RdCVF2 gene structure
conservation.
[0024] FIG. 2A-C shows the Sequence and structure similarities of
mouse RdCVF and RdCVF2 proteins with thioredoxin superfamily
members.
[0025] FIG. 3A-D shows the validation of the RdCVF2 expression in
retina.
[0026] FIG. 4 shows the cone viability assay in the presence of
RdCVF-S and RdCVF2-S.
DETAILED DESCRIPTION
[0027] The present invention is based on the discovery of a new
gene RdCVF2 as a gene paralogous to RdCVF, with the protein encoded
by said gene enhancing the viability of neurons such as cone
photoreceptors and olfactory neurons.
[0028] Thus, in a first aspect, the present invention provides a
pharmaceutical composition comprising a pharmaceutically acceptable
carrier and a compound selected in the group comprising:
[0029] (i) a polypeptide comprising an amino acid sequence selected
in the group comprising the amino acid sequence of the short
isoform in Homo sapiens of the RdCVF2 gene (SEQ ID NO:1),
orthologs, derivatives and fragments thereof;
[0030] (ii) a polynucleotide coding for said polypeptide;
[0031] (iii) a vector comprising said polynucleotide; and
[0032] (iv) a host cell genetically engineered expressing said
polypeptide.
[0033] As used herein, the term "polypeptide" refers to a molecular
chain of amino acids enhancing the viability of neurons such as
cone photoreceptors or olfactory neurons. This polypeptide, if
required, can be modified in vitro and/or in vivo, for example by
glycosylation, myristoylation, amidation, carboxylation or
phosphorylation, and may be obtained, for example, by synthetic or
recombinant techniques known in the art.
[0034] According to a preferred embodiment, the composition of the
invention comprises a pharmaceutically acceptable carrier and a
compound selected in the group comprising:
[0035] (i) a polypeptide comprising an amino acid sequence selected
in the group comprising the amino acid sequence of the long isoform
in Homo sapiens of the RdCVF2 gene (SEQ ID NO:10), orthologs,
derivatives and fragments thereof;
[0036] (ii) a polynucleotide coding for said polypeptide;
[0037] (iii) a vector comprising said polynucleotide; and
[0038] (iv) a host cell genetically engineered expressing said
polypeptide.
[0039] As used herein, the term "orthologs" refers to proteins in
different species than the proteins SEQ ID NO. 1 and SEQ ID NO. 10
in Homo sapiens that evolved from a common ancestral gene by
speciation. As an example of such orthologs, one can cite the
proteins corresponding to RdCVF2-S in Mus musculus (SEQ ID NO. 2),
Rattus norvegicus (SEQ ID NO. 3), Pan troglodytes (SEQ ID NO. 4),
Bos Taurus (SEQ ID NO. 5), Gallus gallus (SEQ ID NO. 6), Xenopus
laevis (SEQ ID NO. 7), Tetraodon nigroviridis (SEQ ID NO. 8), and
Danio rerio (SEQ ID NO. 9).
[0040] As used herein, the term "derivatives" refers to
polypeptides having a percentage of identity of at least 75% with
SEQ ID NO. 1, SEQ ID NO. 10 or ortholog thereof, preferably of at
least 85%, as an example of at least 90%, and more preferably of at
least 95%.
[0041] It has to be noted that the short isoform of RdCVF2 in Homo
sapiens has less than 40% of identity with the short isoform of
RdCVF in Homo sapiens.
[0042] As used herein "fragments" refers to polypeptides having a
length of at least 25 amino acids, preferably at least 50 amino
acids, as an example at least 75 or 85 amino acids, and more
preferably of at least 100 amino acids.
[0043] As used herein, "percentage of identity" between two amino
acids sequences, means the percentage of identical amino-acids,
between the two sequences to be compared, obtained with the best
alignment of said sequences, this percentage being purely
statistical and the differences between these two sequences being
randomly spread over the amino acids sequences. As used herein,
"best alignment" or "optimal alignment", means the alignment for
which the determined percentage of identity (see below) is the
highest. Sequences comparison between two amino acids sequences are
usually realized by comparing these sequences that have been
previously align according to the best alignment; this comparison
is realized on segments of comparison in order to identify and
compared the local regions of similarity. The best sequences
alignment to perform comparison can be realized, beside by a manual
way, by using the global homology algorithm developed by SMITH and
WATERMAN (Ad. App. Math., vol. 2, p: 482, 1981), by using the local
homology algorithm developed by NEDDLEMAN and WUNSCH (J. Mol.
Biol., vol. 48, p: 443, 1970), by using the method of similarities
developed by PEARSON and LIPMAN (Proc. Natl. Acd. Sci. USA, vol.
85, p: 2444, 1988), by using computer softwares using such
algorithms (GAP, BESTFIT, BLAST P, BLAST N, FASTA, TFASTA in the
Wisconsin Genetics software Package, Genetics Computer Group, 575
Science Dr., Madison, Wis. USA), by using the MUSCLE multiple
alignment algorithms (Edgar, Robert C., Nucleic Acids Research,
vol. 32, p: 1792, 2004). To get the best local alignment, one can
preferably used BLAST software, with the BLOSUM 62 matrix, or the
PAM 30 matrix. The identity percentage between two sequences of
amino acids is determined by comparing these two sequences
optimally aligned, the amino acids sequences being able to comprise
additions or deletions in respect to the reference sequence in
order to get the optimal alignment between these two sequences. The
percentage of identity is calculated by determining the number of
identical position between these two sequences, and dividing this
number by the total number of compared positions, and by
multiplying the result obtained by 100 to get the percentage of
identity between these two sequences.
[0044] The phrase "pharmaceutically acceptable" refers to molecular
entities and compositions that are physiologically tolerable and do
not typically produce an allergic or similar untoward reaction,
such as gastric upset, dizziness and the like, when administered to
a human. Preferably, as used herein, the term "pharmaceutically
acceptable" means approved by a regulatory agency of the Federal or
a state government or listed in the U.S. Pharmacopeia or other
generally recognized pharmacopeia for use in animals, and more
particularly in humans.
[0045] The term "carrier" refers to a diluent, adjuvant, excipient,
or vehicle with which the compound is administered. Such
pharmaceutical carriers can be sterile liquids, such as water and
oils, including those of petroleum, animal, vegetable or synthetic
origin, such as peanut oil, soybean oil, mineral oil, sesame oil
and the like. Water or aqueous solution saline solutions and
aqueous dextrose and glycerol solutions are preferably employed as
carriers, particularly for injectable solutions. Suitable
pharmaceutical carriers are described in "Remington's
Pharmaceutical Sciences" by E. W. Martin.
[0046] As used herein, the term "polynucleotide" refers to RNA or
DNA, preferably to DNA. Said DNA may be double-stranded or
single-stranded.
[0047] Preferably, the polynucleotide comprises the sequence SEQ ID
NO. 11.
[0048] Preferably, the polynucleotide comprises a sequence which
encodes the sequence SEQ ID NO:10.
[0049] The polynucleotide of the invention may also include the
coding sequence of the polypeptide defined previously, additional
coding sequence such as leader sequence or a proprotein sequence,
and/or additional non-coding sequence, such as introns or 5'and/or
3' UTR sequences.
[0050] As used herein, the term "vector" refers to an expression
vector, and may be for example in the form of a plasmid, a viral
particle, a phage, etc.
[0051] Such vectors may include bacterial plasmids, phage DNA,
baculovirus, yeast plasmids, vectors derived from combinations of
plasmids and phage DNA, viral DNA such as vaccinia, adenovirus,
fowl pox virus, and pseudorabies. Large numbers of suitable vectors
are known to those of skill in the art and are commercially
available. The following vectors are provided by way of example.
Bacterial: pQE70, pQE60, pQE-9 (QIAGEN), pbs, pD10, phagescript,
psiX174, pbluescript SK, pbsks, pNH8A, pNH16a, pNH18A, pNH46A
(STRATAGENE), ptrc99a, pKK223-3, pKK233-3, pDR540, pRIT5
(PHARMACIA). Eukaryotic: pWLNEO, pSV2CAT, pOG44, pXT1, pSG
(STRATAGENE), pSVK3, pBPV, pMSG, pSVL (PHARMACIA). However, any
other vector may be used as long as it is replicable and viable in
the host.
[0052] The polynucleotide sequence, preferably the DNA sequence in
the vector is operatively linked to an appropriate expression
control sequence(s) (promoter) to direct mRNA synthesis. As
representative examples of such promoters, one can mentioned
prokaryotic or eukaryotic promoters such as CMV immediate early,
HSV thymidine kinase, early and late SV40, LTRs from retrovirus,
and mouse metallothionein-I. The expression vector also contains a
ribosome binding site for translation initiation and a
transcription vector. The vector may also include appropriate
sequences for amplifying expression.
[0053] In addition, the vectors preferably contain one or more
selectable marker genes to provide a phenotypic trait for selection
of transformed host cells such as dihydrofolate reductase or
neomycin resistance for eukaryotic cell culture, or such as
tetracycline or ampicillin resistance in E. coli.
[0054] As used herein, the term "host cell genetically engineered"
relates to host cells which have been transduced, transformed or
transfected with the polynucleotide or with the vector described
previously.
[0055] As representative examples of appropriate host cells, one
can cites bacterial cells, such as E. coli, Streptomyces,
Salmonella typhimurium, fungal cells such as yeast, insect cells
such as Sf9, animal cells such as CHO or COS, plant cells, etc. The
selection of an appropriate host is deemed to be within the scope
of those skilled in the art from the teachings herein.
[0056] Preferably, said host cell is an animal cell, and most
preferably a human cell.
[0057] The introduction of the polynucleotide or of the vector
described previously into the host cell can be effected by method
well known from one of skill in the art such as calcium phosphate
transfection, DEAE-Dextran mediated transfection, or
electroporation.
[0058] The composition of the invention may comprise one or more
additives (e.g., stabilizers, preservatives). See, generally,
Ullmann's Encyclopedia of Industrial Chemistry, 6.sup.th Ed.
(various editors, 1989-1998, Marcel Dekker); and Pharmaceutical
Dosage Forms and Drug Delivery Systems (ANSEL et al., 1994,
WILLIAMS & WILKINS).
[0059] In a further aspect, the present invention provides a use,
for treating and/or preventing a neurodegenerative disorder, of a
compound selected in the group comprising:
[0060] (i) a polypeptide comprising an amino acid sequence selected
in the group comprising the amino acid sequence of the short
isoform in Homo sapiens of the RdCVF2 gene (SEQ ID NO:1),
orthologs, derivatives and fragments thereof;
[0061] (ii) a polynucleotide coding for said polypeptide;
[0062] (iii) a vector comprising said polynucleotide; and
[0063] (iv) a host cell genetically engineered expressing said
polypeptide.
[0064] In a further aspect, the present invention provides a use,
for treating and/or preventing a neurodegenerative disorder, of a
compound selected in the group comprising:
[0065] (v) a polypeptide comprising an amino acid sequence selected
in the group comprising the amino acid sequence of the long isoform
in Homo sapiens of the RdCVF2 gene (SEQ ID NO:10), orthologs,
derivatives and fragments thereof;
[0066] (vi) a polynucleotide coding for said polypeptide;
[0067] (vii) a vector comprising said polynucleotide; and
[0068] (viii) a host cell genetically engineered expressing said
polypeptide.
[0069] Typically, the medicament may be used for the therapeutic or
prophylactic treatment of a subject, said subject corresponding to
a mammal, in particular to a human.
[0070] As used herein, the expression "neurodegenerative disorder"
refers to a disease associated with the degeneration of neurons
such as degenerative disorders of the central nervous system,
preferably implying Purkinje cells degeneration, degenerative
disorders of the photoreceptors, or degenerative disorders of the
olfactory neurons.
[0071] As an example of degenerative disorders of the central
nervous system, one can cite Alzheimer's Disease, Parkinson's
Disease, and Huntington's Disease/Chorea.
[0072] As an example of degenerative disorders of the
photoreceptors, one can cite cone dystrophy (e.g., retinitis
pigmentosa).
[0073] As an example of degenerative disorders of olfactory
neurons, one can cite anosmia.
[0074] Said polypeptide, polynucleotide, vector, and host cell are
as described previously.
[0075] According to a preferred embodiment, said medicament may be
used for treating and/or preventing degenerative disorders of the
photoreceptors or degenerative disorders of the olfactory
neurons.
[0076] There is also provided a method of preventing and/or
treating a neurodegenerative disease comprising providing, to a
subject displaying or predicted to display a neurodegenerative
disorder, an effective amount of a composition comprising a
compound selected in the group comprising:
[0077] (i) a polypeptide comprising an amino acid sequence selected
in the group comprising the amino acid sequence of the short
isoform in Homo sapiens of the RdCVF2 gene (SEQ ID NO:1),
orthologs, derivatives and fragments thereof;
[0078] (ii) a polynucleotide coding for said polypeptide;
[0079] (iii) a vector comprising said polynucleotide; and
[0080] (iv) a host cell genetically engineered expressing said
polypeptide.
[0081] According to the present invention, an "effective amount" of
a composition is one which is sufficient to achieve a desired
biological effect, in this case increasing the neuron viability. It
is understood that the effective dosage will be dependent upon the
age, sex, health, and weight of the recipient, kind of concurrent
treatment, if any, frequency of treatment, and the nature of the
effect desired. The ranges of effective doses provided below are
not intended to limit the invention and represent preferred dose
ranges. However, the preferred dosage can be tailored to the
individual subject, as is understood and determinable by one of
skill in the art, without undue experimentation.
[0082] Said polypeptide, polynucleotide, vector, and host cell are
as described previously.
[0083] There is also provided a method of testing a subject thought
to have or be predisposed to having a neurodegenerative disorder,
which comprises the step of analyzing a biological sample from said
subject for:
[0084] (i) detecting the presence of a mutation in the RdCVF2 gene
and/or its associated promoter, and/or
[0085] (ii) analyzing the expression of the RdCVF2 gene.
[0086] As used herein, the term "biological sample" refers to any
sample from a subject such as blood or serum.
[0087] As used herein, the expression "neurodegenerative disorder"
refers to a disease associated with the degeneration of neurons
such as degenerative disorders of the central nervous system,
degenerative disorders of the photoreceptors, or degenerative
disorders of the olfactory neurons.
[0088] Preferably, neurodegenerative disorder is a degenerative
disorder of the photoreceptors such as cone dystrophy (e.g.,
retinitis pigmentosa).
[0089] Typical techniques for detecting a mutation in the RdCVF2
gene may include restriction fragment length polymorphism,
hybridisation techniques, DNA sequencing, exonuclease resistance,
microsequencing, solid phase extension using ddNTPs, extension in
solution using ddNTPs, oligonucleotide assays, methods for
detecting single nucleotide polymorphism such as dynamic
allele-specific hybridisation, ligation chain reaction,
mini-sequencing, DNA "chips", allele-specific oligonucleotide
hybridisation with single or dual-labelled probes merged with PCR
or with molecular beacons, and others.
[0090] Analyzing the expression of the RdCVF2 gene may be assessed
by any of a wide variety of well-known methods for detecting
expression of a transcribed nucleic acid or translated protein.
[0091] In a preferred embodiment, the expression of the RdCVF2 gene
is assessed by analyzing the expression of mRNA transcript or mRNA
precursors, such as nascent RNA, of said gene. Said analysis can be
assessed by preparing mRNA/cDNA from cells in a biological sample
from a subject, and hybridizing the mRNA/cDNA with a reference
polynucleotide. The prepared mRNA/cDNA can be used in hybridization
or amplification assays that include, but are not limited to,
Southern or Northern analyses, polymerase chain reaction analyses,
such as quantitative PCR (TaqMan), and probes arrays such as
GeneChip.TM. DNA Arrays (AFFYMETRIX).
[0092] Advantageously, the analysis of the expression level of mRNA
transcribed from the RdCVF2 gene involves the process of nucleic
acid amplification, e. g., by RT-PCR (the experimental embodiment
set forth in U.S. Pat. No. 4,683, 202), ligase chain reaction
(BARANY, Proc. Natl. Acad. Sci. USA, vol. 88, p: 189-193, 1991),
self sustained sequence replication (GUATELLI et al., Proc. Natl.
Acad. Sci. USA, vol. 87, p: 1874-1878, 1990), transcriptional
amplification system (KWOH et al., 1989, Proc. Natl. Acad. Sci.
USA, vol. 86, p: 1173-1177, 1989), Q-Beta Replicase (LIZARDI et
al., Biol. Technology, vol. 6, p: 1197, 1988), rolling circle
replication (U.S. Pat. No. 5,854,033) or any other nucleic acid
amplification method, followed by the detection of the amplified
molecules using techniques well known to those of skill in the art.
These detection schemes are especially useful for the detection of
nucleic acid molecules if such molecules are present in very low
numbers. As used herein, amplification primers are defined as being
a pair of nucleic acid molecules that can anneal to 5' or 3'
regions of a gene (plus and minus strands, respectively, or
vice-versa) and contain a short region in between. In general,
amplification primers are from about 10 to 30 nucleotides in length
and flank a region from about 50 to 200 nucleotides in length.
Under appropriate conditions and with appropriate reagents, such
primers permit the amplification of a nucleic acid molecule
comprising the nucleotide sequence flanked by the primers.
[0093] In view of the present application, one of skill in the art
can simply identify the sequence of the gene RdCVF2 in a
subject.
[0094] As an example, the sequence of the cDNA coding for the short
isoform of RdCVF2 in Homo sapiens has the sequence SEQ ID NO.
11.
[0095] In another preferred embodiment, the expression of the
RdCVF2 gene is assessed by analyzing the expression of the protein
translated from said gene. Said analysis can be assessed using an
antibody (e.g., a radio-labeled, chromophore-labeled,
fluorophore-labeled, or enzyme-labeled antibody), an antibody
derivative (e.g., an antibody conjugate with a substrate or with
the protein or ligand of a protein of a protein/ligand pair (e.g.,
biotin-streptavidin)), or an antibody fragment (e.g., a
single-chain antibody, an isolated antibody hypervariable domain,
etc.) which binds specifically to the protein translated from the
RdCVF2 gene.
[0096] Said analysis can be assessed by a variety of techniques
well known from one of skill in the art including, but not limited
to, enzyme immunoassay (EIA), radioimmunoassay (RIA), Western blot
analysis and enzyme linked immunoabsorbant assay (RIA).
[0097] Polyclonal antibodies can be prepared by immunizing a
suitable animal, such as mouse, rabbit or goat, with a protein
encoded by the RdCVF2 gene or a fragment thereof. The antibody
titer in the immunized animal can be monitored over time by
standard techniques, such as with an enzyme linked immunosorbent
assay (ELISA) using immobilized polypeptide. At an appropriate time
after immunization, e.g., when the specific antibody titers are
highest, antibody producing cells can be obtained from the animal
and used to prepare monoclonal antibodies (mAb) by standard
techniques, such as the hybridoma technique originally described by
KOHLER and MILSTEIN (Nature, vol. 256, p: 495-497, 1975), the human
B cell hybridoma technique (KOZBOR et al., Immunol., vol. 4, p: 72,
1983), the EBV- hybridoma technique (COLE et al., In Monoclonal
Antibodies and Cancer Therapy, Alan R. Liss, Inc., p: 77-96, 1985)
or trioma techniques. The technology for producing hybridomas is
well known (see generally Current Protocols in Immunology, COLIGAN
et al. ed. , John Wiley & Sons, New York, 1994). Hybridoma
cells producing the desired monoclonal antibody are detected by
screening the hybridoma culture supernatants for antibodies that
bind the polypeptide of interest, e.g., using a standard ELISA
assay.
[0098] The method of the invention may comprise comparing the level
of expression of the RdCVF2 gene in a biological sample from a
subject with the normal expression level of said gene in a control.
A significantly weaker level of expression of said gene in the
biological sample of a subject as compared to the normal expression
level is an indication that the patient has or is predisposed to
developing a neurodegenerative disorder.
[0099] The "normal" level of expression of the RdCVF2 gene is the
level of expression of said gene in a biological sample of a
subject not afflicted by any neurodegenerative disorder, preferably
not afflicted with retinis pigmentosa. Preferably, said normal
level of expression is assessed in a control sample (e.g., sample
from a healthy subject, which is not afflicted by any
neurodegenerative disorder) and preferably, the average expression
level of said gene in several control samples.
[0100] In the following, the invention is described in more detail
with reference to amino acid sequences, nucleic acid sequences and
the examples. Yet, no limitation of the invention is intended by
the details of the examples. Rather, the invention pertains to any
embodiment which comprises details which are not explicitly
mentioned in the examples herein, but which the skilled person
finds without undue effort.
EXAMPLES
1) Identification of RdCVF2, a Gene Paralogous to RdCVF
[0101] The mouse RdCVF gene is located on chromosome 8 and contains
three exons and can be transcribed in two distinct splice variants
corresponding to RdCVF-L (long) and RdCVF-S (short)
respectively.
[0102] The structure of both RdCVF splice variants is described in
FIG. 1, panel a. The RdCVF-L mRNA (NM_145598, mouse chromosome 8,
minus strand, from 70'033'763 to 70'027'717) is composed of three
exons (1-3) of 348, 687 and 1751 bp. The RdCVF-S mRNA (BC017153,
from 70'033'785 to 70'032'615) is composed of one exon (1172 bp).
Coding and non-coding regions are depicted in dark grey) and light
grey respectively. The genomic region surrounding the stop codon at
the end of the first coding exon and the corresponding orthologous
sequences in 12 other vertebrate genomes are aligned. The black
triangles indicate the end of the first RdCVF-L coding exon.
Conserved stop codons are colored in red. At bottom, lengths of the
coding (CDS) and terminal untranslated regions (UTR) are given.
[0103] The RdCVF-L splice variant is composed of three exons, which
variant codes for a protein wherein the last 109 amino acids are
called the "cap".
[0104] The RdCVF-S splice variant is composed of a single exon in
which the coding sequence is the same as the first exon of the long
form extended by one codon followed by a stop codon (TGA) and
finally a 3' untranslated region (UTR).
[0105] Consequently, the "cap" (i.e., the last 109 amino acids) of
RdCVF-L are missing in RdCVF-S.
[0106] A blast search on databases enabled the identification of a
paralogous gene called RdCVF2.
[0107] The structure of both RdCVF2 splice variants is described in
FIG. 1, panel b. The RdCVF2-L mRNA (AK015847, mouse chromosome 13,
plus strand, from 50'202'630 to 50'206'797) is composed of two
exons (1-2) of 603 and 564 bp. The RdCVF2-S mRNA (BC016199, from
50'202'667 to 50'205'571) is composed of one exon (2904 bp). Coding
and non-coding regions are depicted in dark grey) and light grey
respectively. The genomic region surrounding the stop codon at the
end of the first coding exon and the corresponding orthologous
sequences in 12 other vertebrate genomes are aligned. The black
triangles indicate the end of the first RdCVF2-L coding exon.
Conserved stop codons are colored in red. At bottom, lengths of the
coding (CDS) and terminal untranslated regions (UTR) are given.
[0108] This analysis enables to locate RdCVF2 gene on chromosome 13
and to demonstrate that RdCVF and RdCVF2 sequences and gene
structures are highly similar between both. In fact, it appears
that RdCVF2 also encodes both a thioredoxin-like protein (156 aa,
SEQ ID NO. 12) and a shorter form (101 aa, SEQ ID NO. 2) called
RdCVF2-L and RdCVF2-S respectively.
[0109] Finally, the sequence analysis has revealed that the degree
of homology between RdCVF and RdCVF2 is 58.0% for the long isoforms
and 53.5% for the short isoforms.
2) Conservation of RdCVF and RdCVF2 Gene Structure During
Evolution
[0110] Cone viability is related to the production of the RdCVF-S
form and, by extension, to the presence of the stop codon at the
end of the first exon required to obtain that isoform.
[0111] To evaluate conservation of that stop codon further, the
UCSC genome browser BLAT (HINRICHS et al., Nucleic Acids Res., vol.
34 (Database issue): D590-598, 2006; KENT, Genome Res., vol. 12(4):
656-664, 2002) server was used to map the mouse RdCVF and RdCVF2
genes to all the available vertebrate genomes and to extract the
corresponding genomic sequences.
[0112] The results have shown that both loci were found in 13
vertebrates. All these organisms exhibited both genes except
Takifiugu rubripes and Tetraodon nigroviridis, in which RdCVF was
duplicated at the same chromosomal location (RdCVF a and b) with an
additional intron inserted into the first coding exon of this loci.
It is noteworthy that the stop codon at the end of the first exon
is strictly conserved in the vast majority (FIG. 1, panel a and
b).
[0113] Finally, this observation implies the possible existence of
RdCVFs short isoforms in most vertebrates, excepting Gallus gallus
and Brachydanio rerio RdCVF; Tetraodon nigroviridis and Takifugu
rubripes RdCVFb.
3) Analysis of RdCVF and RdCVF2 Protein Sequences
[0114] In order to identify candidate RdCVF and RdCVF2 orthologous
proteins, homology searches in the UniProt (WU et al., Nucleic
Acids Res., vol. 34(Database issue), p: D187-191, 2006) and EMBL
(COCHRANE et al., Nucleic Acids Res., vol. 34(Database issue):
D10-15, 2006) public sequence databases were performed using the
BLAST programs (ALTSCHUL et al., J. Mol. Biol., vol. 215(3):
403-410, 1990; ALTSCHUL et al., Nucleic Acids Res., vol. 25(17):
3389-3402, 1997).
[0115] Proteins orthologous to RdCVF(-L/2-L) referring to the long
isoforms of both RdCVF genes, were identified or predicted in
vertebrates (Rattus norvegicus, Homo sapiens, Pan troglodytes, Bos
taunts, Canis familiaris, Gallus gallus, Xenopus laevis, Tetraodon
nigroviridis, Brachydanio rerio) according to protein or genome
database searches.
[0116] Then, TBA (BLANCHETTE et al., Genome Res., vol. 14(4):
708-715, 2004) and PipeAlign (PLEWNIAK et al., Nucleic Acids Res.,
vol. 31(13): 3829-3832, 2003) programs were used with default
parameters to generate the multiple alignments of genomic and
protein sequences respectively. Protein alignment occasionally
included manual adjustments in keeping with the protein secondary
structure conservation.
[0117] The FIG. 2 (panel a) show the sequences alignment of RdCVF,
RdCVF2, tryparedoxin (TRYX), nucleoredoxin (NXN) and thioredoxin
(TXN). The name, organism and accession number (in brackets) of
each protein sequence are given (left). Identical (white text on
black) small (A, D, G, P, S, T; white text on green) hydrophobic
(A, C, F, G, I, L, M, S, T, V, W, Y; black text on yellow) polar
(D, E, H, K, N, Q, R, S; blue text) and charged (D, E, K, R; white
text on red) conserved residues are shown according to a
conservation threshold of 85%. A consensus sequence is given below
the multiple alignments in which s, h, p and c correspond to small,
hydrophobic, polar and charged residues respectively. The secondary
structures (.beta. sheet and .alpha. helix) of the Crithidia
fasciculata tryparedoxin I structure (1EWX) are given below the
consensus sequence. The blue dashed rectangles indicate the three
RdCVF(2) specific insertions. The green dashed rectangle shows the
"cap" region absent in RdCVF(2)-S. The position of the human
thioredoxin cleavage product (TRX80) is indicated (red triangle).
Panel b displays the structure of the Crithidia fasciculata TRYX-I
(1EWX) (left) mouse RdCVF-L (center) and mouse RdCVF2-L (right)
models. Regions of TRYX-I backbone conserved in RdCVF(2)-L are
colored in red. The "cap" region and the three specific insertions
are depicted in green and blue respectively. The putative catalytic
site (C.sub.44XXC.sub.47) is shown in yellow with a space-filling
representation.
[0118] A phylogenetic analysis among the TXN superfamily
established that RdCVF and RdCVF2 proteins are closely related to
the TRYX and NXN members (MICOSSI et al., Acta Crystallogr. D.
Biol. Crystallogr., vol. 58(Pt 1): 21-28, 2002; KRUMME et al.,
Biochemistry, vol. 42(50): 14720-14728, 2003; ALPHEY et al., J.
Biol. Chem., vol. 274(36): 25613-25622, 1999; EKLUND et al.,
Proteins, vol. 11(1): 13-28, 1991; KUROOKA et al., Genomics, vol.
39(3): 331-339, 1997; LAUGHNER et al., Plant Physiol., vol. 118(3):
987-996, 1998). Even distant homologs such as Crithidia fasciculata
tryparedoxin I (O96438, TRYX-I) (ALPHEY et al., 1999,
abovementioned) exhibit 42.5% and 45.4% sequence similarity to
mouse RdCVF(-L/2-L) proteins. Three insertions in the multiple
alignment (called 1, 2 and 3) allow one to distinguish these
phylogenetic protein families (FIG. 2, panel a).
[0119] Insertion 3 (residues 87-110) contains the conserved motif
WLALP [W.sub.108(L,V)(A,F)(L,V,I)P.sub.112] and clearly
discriminates the TRYX family [TRYX, NXN, RdCVF and RdCVF2] from
TXN superfamily.
[0120] Insertion 2 (63-72) and two additional residues (96-97) of
insertion 3 allow one to differentiate the RdCVF and RdCVF2
proteins from the rest of the TRYX family.
[0121] Finally, insertion 1 (16-21) unambiguously separates RdCVF
from all the other TXN superfamily members including RdCVF2. It has
to be noted that the thioredoxin active site C.sub.44XXC.sub.47 is
only conserved in 44.4% (4/9) and 72.7% (8/11) of the RdCVF and
RdCVF2 vertebrate proteins respectively.
4) Structural Modeling of RdCVF and RdCVF2
[0122] The high sequence similarity of RdCVFs with TRYX proteins
prompted us to build the RdCVF(-L/2-L/-S/2-S) structural models
with Crithidia fasciculata TRYX-I crystal structure (PDB accession
number: 1EWX, 1.7 .ANG. resolution structure) (ALPHEY et al., 1999,
abovementioned) as a template. By analogy with human TXN and TRX80
models (PEKKARI et al., 2000, abovementioned) the RdCVF(-S/2-S)
structure models were assumed to maintain the same overall folding.
Structural models for mouse RdCVF and RdCVF2 (both S and L forms)
using the 155 and 147 first residues respectively were constructed
using the Builder homology modeling package (KOEHL and DELARUE, J.
Mol. Biol., vol. 239(2): 249-275, 1994; KOEHL and DELARUE, Nat.
Struct. Biol., vol. 2(2): 163-170, 1995; KOEHL and DELARUE, Curr.
Opin. Struct. Biol., vol. 6(2): 222-226, 1996). The final models
were further refined by energy minimization, using ENCAD (LEVITT et
al., Computer Physics Comm., vol. 91: 215-231, 1995). On each model
1000 steps of conjugate gradient minimization was applied. The
E.sub.146(1EWX).fwdarw.P.sub.146(RdCVF-L) mutation obliges the
local backbone conformation in the template structure to be adapted
to fit the proline. Builder samples simultaneously the conformation
of the loops in the five insertions/deletions and in the E.fwdarw.P
mutation region, and the conformation of the side-chains, using a
self consistent mean field approach. PyMOL (www.pymol.org) was used
to render the final structures.
[0123] The FIG. 2 (panel b) show the structures of TRYX-I (1EWX)
and RdCVF(-L/2-L).
[0124] FIG. 2 displays the 1EWX secondary structures (.beta.-sheet
and .alpha.-helix) below the multiple alignment (panel a) and in
the TRYX-I 3D-structure (panel b).
[0125] The structure modelization shows that insertions 1, 2 and 3
correspond respectively to: an increase in size of the
.beta..sub.1.1-.beta..sub.1.2 sheets, a one turn extension in the
.alpha..sub.2 helix, and a larger structural region containing the
TRYX-specific .alpha..sub.sup-.beta..sub.sup and .alpha..sub.3
extension. The two residues (96-97) belonging to insertion 3 in the
RdCVF proteins correspond to a larger constrained loop before
strand .beta..sub.sup and allow one to discriminate these proteins
from TRYX members. It is worth noting that the location on the
folded protein where the three insertions co-localize are on the
opposite side from the putative catalytic site (C.sub.44XXC.sub.47)
in RdCVFs (FIG. 2, panel b).
[0126] Finally, the C-terminal region absent in RdCVF(-S/2-S)
proteins (hereafter called "cap" and depicted in green in FIG. 2,
panel b) is positionally fixed relative to the catalytic site. The
"cap" region in TXN proteins interacts with the recycling enzyme
thioredoxin reductase [7, 13] and its absence might impair the
thioredoxin activity in TRX80 and RdCVF(-S/2-S) [4, 13].
[0127] A striking feature of these structural models is the clear
spatial proximity of residues from the three insertions. This
coincidence points to a possibly novel interaction site in
RdCVF(-L/2-L). As expected, the backbone conformation of the
refined model of RdCVF(-S/2-S) is the same as its counterpart in
the long forms, with minor modifications observed in the
side-chains at the interface between the non-"cap" and "cap"
regions. It should be emphasized that the absence of the "cap"
yields to the emergence of a major hydrophobic patch at the
RdCVF(-S/2-S) surface. As a consequence the hydrophobic part of the
accessible surface area of RdCVF proteins increases from 2394
.ANG..sup.2 in the long form to 3157 .ANG..sup.2 in the short
form.
4) RdCVF-S, RdCVF2-S and RdCVF2-L are Expressed in the Retina in a
Rod-Dependent Manner
[0128] Total RNA from neural retina of 8, 15 and 35-day-old wild
type (C57BL/6@N), and rd1 mutant, (C3H/He@N) mice and from
olfactory epithelium (Balb/c) was purified by cesium gradient
(CHIRGWIN et al., Biochemistry, vol.18(24): 5294-5299, 1979).
[0129] Double-stranded cDNA was synthesized from 5 .mu.g total RNA
using Superscript Choice System (INVITROGEN). cDNAs were produced
by random priming and normalized according to glucose-6-phosphate
dehydrogenase (GAPDH) mRNA. First strand cDNA (0.2 .mu.l) was
amplified in triplicate using 2 .mu.M of the specific primers.
Primers 5'-CATCACCAACAAAGGGCGGAAG-3' (SEQ ID NO. 13) and
5'-CATTCCTCAGCAGAGAAGGGAAC-3' (SEQ ID NO. 14) were used for
RdCVF2-S; primers 5'-CCGTGCTATTGTTTCAGAGCCCTTAACTTTCTATC-3' (SEQ ID
NO. 15) and 5'-CTGACACTCCAATCGTAAAAGGCAGAAAACGC-3' (SEQ ID NO. 16)
were used for RdCVF2-L. Primers 5'-AAGCCGATGAGCAACTTCC-3'(SEQ ID
NO. 17) and 5'-TCATCTCCCAGTGGATTCTT-3' (SEQ ID NO. 18) were used
for rhodopsin on a lightcycler (Roche, Basel, Switzerland).
[0130] For northern blotting analysis, 2 .mu.g of poly-A mRNA was
used and the membrane was hybridized to a probe corresponding to
exon 1 of the RdCVF2 gene using standard method.
[0131] The absence of DNA contamination was checked by omitting the
reverse transcriptase. Results are displayed as fold difference
compared to the lowest expression.
[0132] The FIG. 3, panel a show the results of RT-PCR on wild type
and rd1 mice retina at post-natal day 35 for the short (RdCVF2-S,
176 pb fragment) and long (RdCVF2-L, 170 pb fragment) isoforms of
RdCVF2.
[0133] The FIG. 3, panel b shows the expression of RdCVF2
transcripts in brain, testis, normal retina (wt), degenerated
retina (rd1) and in the whole mouse embryo at embryonic day 12.5
(ED12.5).
[0134] The results established that RdCVF2-S and -L are expressed
in the wild-type mouse retina (FIG. 3, panel a). Interestingly,
RdCVF2-S and -L expression was absent in the retina of the rd1
mouse after rod-photoreceptor degeneration. The results also show
that in addition to the expression in the retina, most likely by
rod photoreceptors since its expression is absent in the
degenerated retina (rd1), a weaker expression of RdCVF2 is observed
in the brain and testis. Moreover, the results have shown that an
expression of the two messengers RNA corresponding to the short
(RdCVF2-S) and the long (RdCVF2-L) isoforms is also detected in the
olfactory epithelium. Finally, no expression was detected in the
whole mouse embryo at embryonic day 12.5.
[0135] The expression of RdCVF2-S and -L mRNA in the retina and in
the olfactory epithelium was analyzed by in situ hybridization with
a digoxigenin (DIG)-labeled murine antisense riboprobe.
[0136] Mouse RdCVF2-S and RdCVF2-L was amplified by PCR using the
following primers: primers 5'-GTAGCTTTGTACTTTGCGGCG-3' (SEQ ID NO.
19) and 5'-GTCATCAGAAAATGTATCACCTCCATAGG-3' (SEQ ID NO. 20) for
RdCVF2-S; primers 5'-GCCATCTCTGCGACTTATTTTTACC-3' (SEQ ID NO. 21)
and 5'-AATTAGTGCCACCAGCACCATC-3' (SEQ ID NO. 22) for RdCVF2-L. The
PCR product was cloned into PGEM easy vector (PROMEGA). Sense and
antisense RdCVF2 mRNA probes generated from SP6 or T7 promoters and
labeled with digoxigenin-UTP (ROCHE) were generated according to
manufacturer's instruction.
[0137] After defrosting and drying at room temperature, retina and
olfactory epithelium sections were post-fixed on ice for 10 min in
4% paraformaldehyde washed in PBS at room temperature for 10 min.
retina sections were hybridized with sense and antisense RdCVF2
mRNA probes generated from SP6 or T7 promoters and labeled with
digoxigenin-UTP. In situ hybridization and digoxigenin-labeled
probe detection were performed as described previously (ROGER et
al., Dev. Biol., vol. 298(2): 527-539, 2006). The specificity of
the staining was demonstrated by the lack of hybridization signal
with the sense probe.
[0138] The FIG. 3, panel c shows the results of In situ
hybridization on sections of wild-type and rd1 mice retina with
digoxigenin-labeled RdCVF2-S and L riboprobes (AS: antisens, S:
sens). Original magnification: 40.times..
[0139] The results show that the transcripts for RdCVF2-S and -L
were detected in the photoreceptor layer. No staining was observed
with the sense control probes, supporting the specificity of the
RdCVF2-S and L probes. Finally, no expression was detected in the
rd1 retina after rod degeneration (result not shown). Moreover, the
results have shown that the localisation of labelled cells in
olfactory epithelium suggests that basal cells, immature and mature
neurons strongly express RdCVF2 mRNA, and that no expression of
RdCVF2 mRNA was observed at the apical position of the cytoplasm of
the supporting cells. It must be noted that a small expression of
RdCVF2 mRNA was also observed during development (E12.5)
specifically restrictive to the nasal development.
[0140] Finally, the expression of RdCVF2-S and of RdCVF2-L were
analysed during the process of rod degeneration.
[0141] The FIG. 3, panel d show the expression time-courses of both
RdCVF2 isoforms and rhodopsin transcripts in wild type (wt) and rd1
mice at post natal day 8, 15 and 31 (PN8, PN15 and PN35).
[0142] The results established that at post-natal day 8 (PN8)
before the onset of rod loss, RdCVF2-S is expressed at similar
level in the wild-type and in the rd1 retina similarly to the rod
photopigment gene rhodopsin. From PN15 to PN35, the degeneration of
rods (measured by the decrease in rhodopsin expression) is
correlated with a decrease in RdCVF2-S expression. Consequently,
these results indicate that RdCVF2-S is expressed in a
rod-dependent manner.
[0143] The same results have been observed with RdCVF2-L (data not
shown).
5) RdCVF2 mRNA is Not Only Expressed in the Retina and in Olfactive
Epithelium but Also in Other Tissues
[0144] Mouse mRNA and EST sequences associated with both RdCVF and
RdCVF2 isoforms (L and S) were used to estimate the tissue
specificity of each messenger. The results are presented in the
following table.
TABLE-US-00001 iso- mRNA and EST EMBL Expression Genes form
accession numbers location RdCVF L BC021911; BI738445; CB849876;
Retina, RPE, CK623520; BI731629; BI872244; choroid and/or BG294111;
BI734135; BU505070; eye BU840744; BQ929742; BQ938066; BI73223;
CK628091; BY742305; N539863; CO424399; BB277874; BB279867; CO426411
BF470336; BE983242; AW495183 None S BC017153; CB849876; BG299078;
Retina and/or BY742292 eye RdCVF-2 L CK621895; CK620198; BG288447;
Retina BB282056; BB279962; BB281743; BB277718; BB277574; BB277714;
BI732427 BC038905; BI108740 Mammary tumor, tumor and/or gross
tissue BY715393; AV266697 Testis DT906804 Hematopoietic stem cells
BY435086 amnion AI324093 Placenta BB552115 Oviduct AA261233 Foetus
BB241367 Thymus AI536471 Mammary gland BX632214; BF460609; BX514476
S BC016199; BG297304; BG297383 Retina BX514476 None
[0145] As reported before (LEVEILLARD et al., 2004,
abovementioned), the results confirmed that RdCVF-L and RdCVF-S
mRNAs are specifically expressed in eye and retina as 20/23 and 4/4
sequences were found in these tissues respectively. The results
show that mouse RdCVF2-L mRNA is also preferentially expressed in
retina (10/24) but is also present in other tissue types such as
tumor (2), testis (2), stem cells (2), amnion (1), placenta (1),
oviduct (1), foetus (1), thymus (1), and mammary gland (1). These
results confirmed the expression of RdCVF2 observed in the testis
and brain (FIG. 4, panel b). Finally, EST and mRNA sequences
corresponding to RdCVF2-S are exclusively expressed in retina
(3/4).
6) RdCVF2 Cone Viability Effects
[0146] The strong similarities between RdCVF and RdCVF2 loci in
terms of gene organization, conservation of sequence and
rod-dependent expression led us to hypothesize that RdCVF2 protein
might also be able to promote cone viability as previously reported
for RdCVF-S (LEVEILLARD et al., 2004, abovementioned).
[0147] RdCVF(-S/2-S/2-L) isoforms were cloned into the expression
plasmid pcDNA3 and transfected into COS-1 cells. 48 hours after
transfection, the conditioned media from the COS-transfected cells
was harvested and incubated with a cone-enriched primary cell
culture system from chicken embryo (60-80% of cones) (FINTZ et al.,
Invest. Ophthalmol. Vis. Sci., vol. 44(2): 818-825 2003).
[0148] After seven days of incubation, a period over which these
post-mitotic cells degenerate, the viability of the cells in the
culture was scored using the Live/Dead assay (MOLECULAR PROBES) and
a cell counting platform as previously described [4]. The viability
corresponding to three independent assays is represented as fold
over pcDNA3 used as negative control.
[0149] The FIG. 4 shows the rescue activity of RdCVF-S and RdCVF2-S
when compared to that of empty vector (pcDNA3). Statistical
analysis (Tuckey test) shows that the results are statistically
significant (p<0.001).
[0150] The results show that the number of live cells in the
presence of RdCVF-S is twice than the control (pcDNA3). A less
pronounced, but statistically significant, increase in cone
viability (1.6 fold) is observed for RdCVF2-S. These findings
confirm that RdCVF2-S is also a cone viability factor similar to
RdCVF-S (LEVEILLARD et al., 2004, abovementioned). Importantly, no
synergistic trophic effect on cones is observed when both RdCVF-S
and RdCVF2-S are co-tranfected in COS-1 cells pointing to use of
the same pathway by both factors (data not shown).
7) RdCVF2 OSN Viability Effects
[0151] Since RdCVF2 is also expressed in olfactory neurons, the
possible viability activity of RdCVF2 on culture of Olfactory
Sensitive Neurons (OSN) has been analysed.
[0152] Adult mice were killed by decapitation. The posterior part
of the nasal septum was dissected free of the nasal cavity and
immediately placed in ice-cold Dulbecco's modified Eagle's medium
(DMEM) containing 50 .mu.g/ml gentamicin (EUROBIO; GIBCO) and 10%
(v/v) fetal calf serum (EUROBIO). The cartilage of the septum was
removed and the olfactory mucosa was incubated for 30 min at
37.degree. C. in a 2.4 units/ml dispase II solution (ROCHE). The
olfactory epithelium was carefully separated from the underlying
lamina propria under the dissection microscope and was gently
triturated about 20 times to separate the cells. The resulting cell
suspension was transferred to a 50 ml conical tube and the dispase
was inactivated by adding 40 ml of HBSS without Calcium and
magnesium. The cell suspension was centrifuged at 700 rpm for 5
min. The supernatant was aspirated and the pellet containing the
cells was resuspended in a medium composed of DMEM containing
insulin (10 .mu.g/ml, SIGMA), transferin (10 .mu.g/ml, SIGMA),
selenium (10 .mu.g/ml, SIGMA), calf foetal serum (5%), ascorbic
acid (200 .mu.M,). Cells were plated at the density of cells/cm2 on
12 mm sterile glass coverslips coated with 5 .mu.g/cm2 human
collagen IV (SIGMA).
[0153] Expression vectors encoding for RdCVF(-S/2-S/2-L) isoforms
described previously were transfected into COS-1 cells. 48 hours
after transfection, the conditioned media from the COS-transfected
cells was harvested and incubated with the culture of OSN. After 4
days of culture, cells were fixed and labelled with tubulin III,
and counted.
[0154] The results shown in FIG. 5 have established that the OSN
cell viability was more important in the presence of the RdCVF2-S
isoform compared to control. Protective effects were observed with
RdCVF2-L.
8) RdCVF2 Purkinje Cells Viability Effects
[0155] After decapitation of mouse at postnatal day 1-3, brains
were dissected out into cold Gey's balanced salt solution
containing 5 mg/ml glucose, and meninges were removed. Cerebellar
parasagittal slices (350 or 250 .mu.m thick) were cut on a McIlwain
tissue chopper and transferred onto membranes of 30 mm MILLIPORE
culture inserts with 0.4 .mu.m pore size (MILLICELL; MILLIPORE,
Bedford, Mass.). Slices were maintained in culture in six-well
plates containing 1 ml or in 10 cm culture dishes containing 3 ml
of medium at 35.degree. C. in an atmosphere of humidified 5% CO2.
The medium was composed of 50% basal medium with Earle's salts
(INVITROGEN), 25% HBSS (INVITROGEN), 25% horse serum (INVITROGEN),
L-glutamine (1 mM), and 5 mg/ml glucose (Stoppini et al., J.
Neurosci. Methods., vol. 37(2), p: 173-82, 1991).
[0156] Expression vectors encoding for RdCVF(-S/2-S/2-L) isoforms
described previously were transfected into COS-1 cells. 48 hours
after transfection, the conditioned media from the COS-transfected
cells was harvested and incubated with the culture of purkinje
cells. After 4 days of culture, cells were fixed and counted.
9) RdCVF2 Cortical Neurons Viability Effects
[0157] Serum-free preparation of mouse cortical primary cultures
was performed with mouse at postnatal day 1. After removal of
meninges, entire cortices were mechanically dissociated in a
phosphate buffer saline glucose solution without added divalent
cations (100 mM NaCl, 3 mM KCl, 1.5 mM KH2PO4, 7.9 mM Na2HPO4, 33
mM glucose, 100 U/ml penicillin and 100 .mu.g/ml streptomycin) and
resuspended in Neurobasal-medium (GIBCO-INVITROGEN) containing 2%
B27 supplement (GIBCO), 0.5 mM glutamine, and 25 .mu.M glutamate.
Cells were then cultured onto poly-ornithine-coated coverslips to
produce cultures highly enriched in neurons.
[0158] Expression vectors encoding for RdCVF(-S/2-S/2-L) isoforms
described previously were transfected into COS-1 cells. 48 hours
after transfection, the conditioned media from the COS-transfected
cells was harvested and incubated with the culture of cortical
neurons. After 4 days of culture, cells were fixed and counted.
[0159] Finally, the results established that a novel trophic factor
for cone survival, and more generally for neuron survival has been
identified. This factor defines a novel family of bifunctional
proteins with potential involvement in neuroprotection and response
to oxidative stress.
Sequence CWU 1 SEQUENCE LISTING <160> NUMBER OF SEQ ID
NOS: 78 <210> SEQ ID NO 1 <211> LENGTH: 101 <212>
TYPE: PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE:
1 Met Val Asp Ile Leu Gly Glu Arg His Leu Val Thr Cys Lys Gly Ala 1
5 10 15 Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu
Tyr 20 25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr
Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala
Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp
Gly Ser Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His
Gly Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln
100 <210> SEQ ID NO 2 <211> LENGTH: 101 <212>
TYPE: PRT <213> ORGANISM: Mus musculus <400> SEQUENCE:
2 Met Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1
5 10 15 Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu
Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr
Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala
Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp
Gly Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His
Gly Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln
100 <210> SEQ ID NO 3 <211> LENGTH: 101 <212>
TYPE: PRT <213> ORGANISM: Rattus norvegicus <400>
SEQUENCE: 3 Met Val Asp Val Leu Gly Gly Arg Arg Leu Met Thr Arg Glu
Gly Thr 1 5 10 15 Leu Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val
Val Ala Leu Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ala Pro Ser Arg
Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val
Ser Glu Ala Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val
Ser Ala Asp Arg Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg
Glu Leu His Gly Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro
Tyr Arg Gln 100 <210> SEQ ID NO 4 <211> LENGTH: 101
<212> TYPE: PRT <213> ORGANISM: Pan troglodytes
<400> SEQUENCE: 4 Met Val Asp Ile Leu Gly Gly Arg His Leu Val
Thr Cys Lys Gly Ala 1 5 10 15 Thr Val Glu Ala Glu Ala Ala Leu Gln
Asn Lys Val Val Ala Leu Tyr 20 25 30 Phe Ala Ala Ala Arg Cys Ala
Pro Ser Arg Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr
Ala Leu Val Ala Glu Ala Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val
Val Phe Val Ser Ala Asp Gly Ser Ser Gln Glu Met Leu 65 70 75 80 Asp
Phe Met Arg Glu Leu His Gly Ala Trp Leu Ala Leu Pro Phe His 85 90
95 Asp Pro Tyr Arg Gln 100 <210> SEQ ID NO 5 <211>
LENGTH: 101 <212> TYPE: PRT <213> ORGANISM: Bos taurus
<400> SEQUENCE: 5 Met Val Asp Val Leu Gly Gly Arg Arg Leu Val
Thr Cys Asp Gly Ala 1 5 10 15 Trp Val Glu Ala Glu Ala Ala Leu Gln
Asn Lys Val Val Ala Leu Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ala
Pro Ser Arg Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Glu
Glu Leu Val Asp Asp Ala Arg Pro Pro Ala Pro 50 55 60 Phe Glu Val
Val Phe Val Ser Ala Asp Gly Ser Ala His Glu Met Leu 65 70 75 80 Glu
Phe Met Lys Glu Leu His Gly Ala Trp Leu Ala Leu Pro Phe His 85 90
95 Asp Pro Tyr Arg Gln 100 <210> SEQ ID NO 6 <211>
LENGTH: 101 <212> TYPE: PRT <213> ORGANISM: Gallus
gallus <400> SEQUENCE: 6 Met Val Asp Val Phe Ser Gly Arg Leu
Leu Val Ser Lys Asp Gly Arg 1 5 10 15 Ser Val Asp Pro Glu Glu Ala
Leu Gln Asn Lys Val Gly Gly Leu Tyr 20 25 30 Phe Ser Ala Gly Trp
Cys Ser Pro Cys Arg Asp Phe Thr Pro Val Leu 35 40 45 Cys Asp Phe
Tyr Thr Asp Leu Leu Glu Glu Cys Gln Pro Pro Ala Pro 50 55 60 Phe
Glu Val Val Phe Ile Ser Ser Asp His Ser Ala Glu Glu Met Val 65 70
75 80 Ser Tyr Met His Ser Met His Gly Asp Trp Leu Ala Leu Pro Phe
His 85 90 95 Asp Pro Tyr Lys Gln 100 <210> SEQ ID NO 7
<211> LENGTH: 100 <212> TYPE: PRT <213> ORGANISM:
Xenopus laevis <400> SEQUENCE: 7 Met Asp Ile Phe Ser Gly His
Ile Leu Leu Asn Lys Tyr Gly Glu Arg 1 5 10 15 Val Asp Pro Glu Glu
Ala Leu Gln Asn Lys Ile Val Gly Leu Tyr Phe 20 25 30 Ser Ala Ser
Trp Cys Ser Pro Cys Arg Asp Phe Thr Pro Ile Leu Cys 35 40 45 Asp
Phe Tyr Thr Glu Leu Val Glu Glu Ser Glu Pro Pro Ala Gln Phe 50 55
60 Glu Ile Val Phe Ile Ser Ser Asp Lys Ser Pro Glu Glu Met Val Asp
65 70 75 80 Tyr Met His Asp Met Gln Gly Asp Trp Leu Ala Leu Pro Phe
His Asp 85 90 95 Pro Tyr Lys Gln 100 <210> SEQ ID NO 8
<211> LENGTH: 101 <212> TYPE: PRT <213> ORGANISM:
Tetraodon nigroviridis <400> SEQUENCE: 8 Met Val Glu Val Phe
Thr Gly Arg Thr Leu Leu Asn Lys Asp Gly Asp 1 5 10 15 Leu Val Asp
Pro Glu Glu Ala Leu Arg Asn Lys Val Val Gly Ile Tyr 20 25 30 Phe
Ser Ala Gly Trp Cys Pro Pro Cys Arg Asp Phe Thr Pro Ile Leu 35 40
45 Cys Asp Phe Tyr Thr Glu Leu Val Glu Glu Ser Asp Pro Pro Ala Gln
50 55 60 Phe Glu Val Val Phe Val Ser Ser Asp Lys Thr Ser Glu Asp
Met Val 65 70 75 80 Glu Tyr Tyr His Asp Leu His Gly Asp Trp Leu Ala
Leu Pro Trp Ser 85 90 95 Asp Asp Tyr Lys Lys 100 <210> SEQ ID
NO 9 <211> LENGTH: 101 <212> TYPE: PRT <213>
ORGANISM: Danio rerio <400> SEQUENCE: 9 Met Val Glu Val Phe
Ser Gly Arg Thr Leu Val Asn Lys Glu Gly Asp 1 5 10 15 Leu Val Glu
Pro Glu Glu Ala Leu Arg Asn Lys Val Val Gly Leu Tyr 20 25 30 Phe
Ser Ala Gly Trp Cys Pro Pro Cys Arg Asp Phe Thr Pro Leu Leu 35 40
45 Cys Asp Phe Tyr Thr Glu Leu Val Glu Glu Thr Glu Pro Pro Ala Gln
50 55 60 Phe Glu Ile Val Phe Ile Ser Ser Asp Lys Ser Thr Glu Asp
Met Val 65 70 75 80 Glu Tyr Tyr His Asp Met His Gly Asp Trp Leu Ala
Leu Pro Trp Thr 85 90 95 Asp Pro Tyr Lys Gln 100 <210> SEQ ID
NO 10 <211> LENGTH: 156 <212> TYPE: PRT <213>
ORGANISM: Homo sapiens <400> SEQUENCE: 10 Met Val Asp Ile Leu
Gly Glu Arg His Leu Val Thr Cys Lys Gly Ala 1 5 10 15 Thr Val Glu
Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu Tyr 20 25 30 Phe
Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr Pro Leu Leu 35 40
45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala Arg Arg Pro Ala Pro
50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly Ser Ser Gln Glu
Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly Ala Trp Leu Ala
Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu Leu Arg Lys Arg
Tyr Asn Val Thr Ala Ile 100 105 110 Pro Lys Leu Val Ile Val Lys Gln
Asn Gly Glu Val Ile Thr Asn Lys 115 120 125 Gly Arg Lys Gln Ile Arg
Glu Arg Gly Leu Ala Cys Phe Gln Asp Trp 130 135 140 Val Glu Ala Ala
Asp Ile Phe Gln Asn Phe Ser Val 145 150 155 <210> SEQ ID NO
11 <211> LENGTH: 306 <212> TYPE: DNA <213>
ORGANISM: Homo sapiens <400> SEQUENCE: 11 atggttgaca
ttctgggcga gcggcacctg gtgacctgta agggcgcgac ggtggaggcc 60
gaggcggcgc tgcagaacaa ggtggtggca ctgtacttcg cggcggcccg gtgcgcgccg
120 agccgcgact tcacgccgct gctctgcgac ttctatacgg cgctggtggc
cgaggcgcgg 180 cggcccgcgc ccttcgaagt ggtcttcgtg tcagccgacg
gcagctccca ggagatgctg 240 gacttcatgc gcgagctgca tggcgcctgg
ctggcgctgc ccttccacga cccctaccgg 300 cagtga 306 <210> SEQ ID
NO 12 <211> LENGTH: 156 <212> TYPE: PRT <213>
ORGANISM: Mus musculus <400> SEQUENCE: 12 Met Val Asp Val Leu
Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10 15 Val Val Glu
Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr 20 25 30 Phe
Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro Leu Leu 35 40
45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg Arg Pro Ala Pro
50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly Ser Ala Glu Glu
Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly Ser Trp Leu Ala
Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu Leu Lys Lys Arg
Tyr Glu Ile Thr Ala Ile 100 105 110 Pro Lys Leu Val Val Ile Lys Gln
Asn Gly Ala Val Ile Thr Asn Lys 115 120 125 Gly Arg Lys Gln Ile Arg
Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130 135 140 Val Glu Ala Ala
Asp Val Phe Gln Asn Phe Ser Gly 145 150 155 <210> SEQ ID NO
13 <211> LENGTH: 22 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic-Primer <400> SEQUENCE: 13
catcaccaac aaagggcgga ag 22 <210> SEQ ID NO 14 <211>
LENGTH: 23 <212> TYPE: DNA <213> ORGANISM: Artificial
sequence <220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 14 cattcctcag cagagaaggg aac
23 <210> SEQ ID NO 15 <211> LENGTH: 35 <212>
TYPE: DNA <213> ORGANISM: Artificial sequence <220>
FEATURE: <223> OTHER INFORMATION: Synthetic-Primer
<400> SEQUENCE: 15 ccgtgctatt gtttcagagc ccttaacttt ctatc 35
<210> SEQ ID NO 16 <211> LENGTH: 31 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic-Primer <400>
SEQUENCE: 16 tgacactcca atcgtaaaag gcagaaaacg c 31 <210> SEQ
ID NO 17 <211> LENGTH: 19 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic-Primer <400> SEQUENCE: 17
aagccgatga gcaacttcc 19 <210> SEQ ID NO 18 <211>
LENGTH: 20 <212> TYPE: DNA <213> ORGANISM: Artificial
sequence <220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 18 tcatctccca gtggattctt 20
<210> SEQ ID NO 19 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic-Primer <400>
SEQUENCE: 19 gtagctttgt actttgcggc g 21 <210> SEQ ID NO 20
<211> LENGTH: 29 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic-Primer <400> SEQUENCE: 20 gtcatcagaa
aatgtatcac ctccatagg 29 <210> SEQ ID NO 21 <211>
LENGTH: 25 <212> TYPE: DNA <213> ORGANISM: Artificial
sequence <220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 21 gccatctctg cgacttattt
ttacc 25 <210> SEQ ID NO 22 <211> LENGTH: 22
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 22 aattagtgcc accagcacca tc
22 <210> SEQ ID NO 23 <211> LENGTH: 4 <212> TYPE:
PRT <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S
<400> SEQUENCE: 23 Glu Leu Arg Arg 1 <210> SEQ ID NO 24
<211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1 - RdCVF-S - M. musculus
<400> SEQUENCE: 24 gaactgagga ggtgaggccc c 21 <210> SEQ
ID NO 25 <211> LENGTH: 21 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - R. norvegicus
<400> SEQUENCE: 25 gacctgagga ggtgaggccc c 21 <210> SEQ
ID NO 26 <211> LENGTH: 21 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - M. domestica
<400> SEQUENCE: 26 gagctgaaaa ggtgagccta c 21 <210> SEQ
ID NO 27 <211> LENGTH: 21 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - H. sapiens
<400> SEQUENCE: 27 gatctgagga ggtgaggagg g 21 <210> SEQ
ID NO 28 <211> LENGTH: 21 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - P. troglodytes
<400> SEQUENCE: 28 gatctgagga ggtgaggagg g 21 <210> SEQ
ID NO 29 <211> LENGTH: 22 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Figure 1 - RdCVF-S - M. mulatta <400>
SEQUENCE: 29 gaactgagga ggtgasggag gg 22 <210> SEQ ID NO 30
<211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1 - RdCVF-S - B. taurus <400>
SEQUENCE: 30 gacctgagga ggtgagacaa g 21 <210> SEQ ID NO 31
<211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1 - RdCVF-S - C. familiaris
<400> SEQUENCE: 31 gacctgagga ggtgaggtgg g 21 <210> SEQ
ID NO 32 <211> LENGTH: 128 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Figure 1 - RdCVF-S - G. gallus <220>
FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION:
(16)..(115) <223> OTHER INFORMATION: N= A, T, G or C
<220> FEATURE: <221> NAME/KEY: misc_feature <222>
LOCATION: (116)..(125) <223> OTHER INFORMATION: n is a, c, g,
or t <400> SEQUENCE: 32 gacctgagga ggtggnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 60 nnnnnnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 120 nnnnntaa 128
<210> SEQ ID NO 33 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -X.
tropicalis <400> SEQUENCE: 33 gaattcagga ggtgagatag g 21
<210> SEQ ID NO 34 <211> LENGTH: 54 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -B.
rerio <220> FEATURE: <221> NAME/KEY: misc_feature
<222> LOCATION: (16)..(51) <223> OTHER INFORMATION: N=
A, T, G or C <400> SEQUENCE: 34 ccctataggc agtacnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ntga 54 <210> SEQ ID NO 35
<211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1 - RdCVF-S -T. rubripes
<400> SEQUENCE: 35 ccatacagac agtaggtgga t 21 <210> SEQ
ID NO 36 <211> LENGTH: 21 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -T. nigroviridis
<400> SEQUENCE: 36 ccatacagac agtaggtgga c 21 <210> SEQ
ID NO 37 <211> LENGTH: 24 <212> TYPE: DNA <213>
ORGANISM: Artificial sequence <220> FEATURE: <223>
OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -T. rubripes
<400> SEQUENCE: 37 cccttcagga ggtgtgtggt ttag 24 <210>
SEQ ID NO 38 <211> LENGTH: 58 <212> TYPE: DNA
<213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Figure 1 - RdCVF-S - T. nigroviridis
<220> FEATURE: <221> NAME/KEY: misc_feature <222>
LOCATION: (16)..(55) <223> OTHER INFORMATION: N= A, T, G or C
<400> SEQUENCE: 38 ccttttagga ggtgtnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnntga 58 <210> SEQ ID NO 39
<211> LENGTH: 4 <212> TYPE: PRT <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1- RdCVF2-L <400> SEQUENCE:
39 Pro Tyr Arg His 1 <210> SEQ ID NO 40 <211> LENGTH: 4
<212> TYPE: PRT <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION: Synthetic -
Figure 1- RdCVF2-S <400> SEQUENCE: 40 Pro Tyr Arg Gln 1
<210> SEQ ID NO 41 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - M.
musculus <400> SEQUENCE: 41 ccctaccggc agtgagtggg gac 23
<210> SEQ ID NO 42 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - R.
norvegicus <400> SEQUENCE: 42 ccctaccggc agtgagtggg gac 23
<210> SEQ ID NO 43 <400> SEQUENCE: 43 000 <210>
SEQ ID NO 44 <211> LENGTH: 23 <212> TYPE: DNA
<213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - H.
sapiens <400> SEQUENCE: 44 ccctaccggc agtgagtggg ggc 23
<210> SEQ ID NO 45 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - P.
troglodytes <400> SEQUENCE: 45 ccctaccggc agtgagtggg ggc 23
<210> SEQ ID NO 46 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - M.
mulatta <400> SEQUENCE: 46 ccctaccagc agtgagtggg ggc 23
<210> SEQ ID NO 47 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - B.
taurus <400> SEQUENCE: 47 ccctaccggc agtgagtgga ggc 23
<210> SEQ ID NO 48 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - G.
gallus <400> SEQUENCE: 48 ccctacaagc agtaagtacc gca 23
<210> SEQ ID NO 49 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -X.
tropicalis <400> SEQUENCE: 49 ccatacaagc agtaagttcc ttg 23
<210> SEQ ID NO 50 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -B.
rerio <400> SEQUENCE: 50 ccatacaaac agtgagttca cca 23
<210> SEQ ID NO 51 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -T.
rubripes <400> SEQUENCE: 51 gactacaaga agtgagtgag gtt 23
<210> SEQ ID NO 52 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -T.
nigroviridis <400> SEQUENCE: 52 gactacaaga agtgagtccg cct 23
<210> SEQ ID NO 53 <211> LENGTH: 109 <212> TYPE:
PRT <213> ORGANISM: Escherichia coli <400> SEQUENCE: 53
Met Ser Asp Lys Ile Ile His Leu Thr Asp Asp Ser Phe Asp Thr Asp 1 5
10 15 Val Leu Lys Ala Asp Gly Ala Ile Leu Val Asp Phe Trp Ala Glu
Trp 20 25 30 Cys Gly Pro Cys Lys Met Ile Ala Pro Ile Leu Asp Glu
Ile Ala Asp 35 40 45 Glu Tyr Gln Gly Lys Leu Thr Val Ala Lys Leu
Asn Ile Asp Gln Asn 50 55 60 Pro Gly Thr Ala Pro Lys Tyr Gly Ile
Arg Gly Ile Pro Thr Leu Leu 65 70 75 80 Leu Phe Lys Asn Gly Glu Val
Ala Ala Thr Lys Val Gly Ala Leu Ser 85 90 95 Lys Gly Gln Leu Lys
Glu Phe Leu Asp Ala Asn Leu Ala 100 105 <210> SEQ ID NO 54
<211> LENGTH: 105 <212> TYPE: PRT <213> ORGANISM:
Homo sapiens <400> SEQUENCE: 54 Met Val Lys Gln Ile Glu Ser
Lys Thr Ala Phe Gln Glu Ala Leu Asp 1 5 10 15 Ala Ala Gly Asp Lys
Leu Val Val Val Asp Phe Ser Ala Thr Trp Cys 20 25 30 Gly Pro Cys
Lys Met Ile Lys Pro Phe Phe His Ser Leu Ser Glu Lys 35 40 45 Tyr
Ser Asn Val Ile Phe Leu Glu Val Asp Val Asp Asp Cys Gln Asp 50 55
60 Val Ala Ser Glu Cys Glu Val Lys Cys Met Pro Thr Phe Gln Phe Phe
65 70 75 80 Lys Lys Gly Gln Lys Val Gly Glu Phe Ser Gly Ala Asn Lys
Glu Lys 85 90 95 Leu Glu Ala Thr Ile Asn Glu Leu Val 100 105
<210> SEQ ID NO 55 <211> LENGTH: 435 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 55 Met
Ser Gly Phe Leu Glu Glu Leu Leu Gly Asp Lys Leu Val Thr Gly 1 5 10
15 Gly Gly Glu Glu Val Asp Val His Ser Leu Gly Ala Arg Gly Ile Ala
20 25 30 Leu Leu Gly Leu Tyr Phe Gly Cys Ser Leu Ser Ala Pro Cys
Ala Gln 35 40 45 Leu Ser Ala Ser Leu Ala Ala Phe Tyr Gly Arg Leu
Arg Gly Asp Ala 50 55 60 Ala Ala Gly Pro Gly Ala Gly Ala Gly Ala
Gly Ala Ala Ala Glu Pro 65 70 75 80 Glu Pro Arg His Arg Leu Glu Ile
Val Phe Val Ser Ser Asp Gln Asp 85 90 95 Gln Arg Gln Trp Gln Asp
Phe Val Arg Asp Met Pro Trp Leu Ala Leu 100 105 110 Pro Tyr Lys Glu
Lys His Arg Lys Leu Lys Leu Trp Asn Lys Tyr Arg 115 120 125 Val Ser
Asn Ile Pro Ser Leu Ile Phe Leu Asp Ala Thr Thr Gly Lys 130 135 140
Val Val Cys Arg Asn Gly Leu Leu Val Ile Arg Asp Asp Pro Glu Gly 145
150 155 160 Leu Glu Phe Pro Trp Gly Pro Lys Pro Phe Arg Glu Val Ile
Ala Gly 165 170 175 Pro Leu Leu Arg Asn Asn Gly Gln Ser Leu Glu Ser
Ser Ser Leu Glu 180 185 190 Gly Ser His Val Gly Val Tyr Phe Ser Ala
His Trp Cys Pro Pro Cys 195 200 205 Arg Ser Leu Thr Arg Val Leu Val
Glu Ser Tyr Arg Lys Ile Lys Glu 210 215 220 Ala Gly Gln Glu Phe Glu
Ile Ile Phe Val Ser Ala Asp Arg Ser Glu 225 230 235 240 Glu Ser Phe
Lys Gln Tyr Phe Ser Glu Met Pro Trp Leu Ala Val Pro 245 250 255 Tyr
Thr Asp Glu Ala Arg Arg Ser Arg Leu Asn Arg Leu Tyr Gly Ile 260 265
270 Gln Gly Ile Pro Thr Leu Ile Val Leu Asp Pro Gln Gly Glu Val Ile
275 280 285 Thr Arg Gln Gly Arg Val Glu Val Leu Asn Asp Glu Asp Cys
Arg Glu 290 295 300 Phe Pro Trp His Pro Lys Pro Val Leu Glu Leu Ser
Asp Ser Asn Ala 305 310 315 320 Val Gln Leu Asn Glu Gly Pro Cys Leu
Val Leu Phe Val Asp Ser Glu 325 330 335 Asp Asp Gly Glu Ser Glu Ala
Ala Lys Gln Leu Ile Gln Pro Ile Ala 340 345 350 Glu Lys Ile Ile Ala
Lys Tyr Lys Ala Lys Glu Glu Glu Ala Pro Leu 355 360 365 Leu Phe Phe
Val Ala Gly Glu Asp Asp Met Thr Asp Ser Leu Arg Asp 370 375 380 Tyr
Thr Asn Leu Pro Glu Ala Ala Pro Leu Leu Thr Ile Leu Asp Met 385 390
395 400 Ser Ala Arg Ala Lys Tyr Val Met Asp Val Glu Glu Ile Thr Pro
Ala 405 410 415 Ile Val Glu Thr Phe Val Asn Asp Phe Leu Ala Glu Lys
Leu Lys Pro 420 425 430 Glu Pro Ile 435 <210> SEQ ID NO 56
<211> LENGTH: 146 <212> TYPE: PRT <213> ORGANISM:
Crithidia fasciculata <400> SEQUENCE: 56 Met Ser Gly Leu Asp
Lys Tyr Leu Pro Gly Ile Glu Lys Leu Arg Arg 1 5 10 15 Gly Asp Gly
Glu Val Glu Val Lys Ser Leu Ala Gly Lys Leu Val Phe 20 25 30 Phe
Tyr Phe Ser Ala Ser Trp Cys Pro Pro Cys Arg Gly Phe Thr Pro 35 40
45 Gln Leu Ile Glu Phe Tyr Asp Lys Phe His Glu Ser Lys Asn Phe Glu
50 55 60 Val Val Phe Cys Thr Trp Asp Glu Glu Glu Asp Gly Phe Ala
Gly Tyr 65 70 75 80 Phe Ala Lys Met Pro Trp Leu Ala Val Pro Phe Ala
Gln Ser Glu Ala 85 90 95 Val Gln Lys Leu Ser Lys His Phe Asn Val
Glu Ser Ile Pro Thr Leu 100 105 110 Ile Gly Val Asp Ala Asp Ser Gly
Asp Val Val Thr Thr Arg Ala Arg 115 120 125 Ala Thr Leu Val Lys Asp
Pro Glu Gly Glu Gln Phe Pro Trp Lys Asp 130 135 140 Ala Pro 145
<210> SEQ ID NO 57 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 57 Met
Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10
15 Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg
Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly
Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu
Leu Lys Lys Arg Tyr Glu Ile Thr Ala Ile 100 105 110 Pro Lys Leu Val
Val Ile Lys Gln Asn Gly Ala Val Ile Thr Asn Lys 115 120 125 Gly Arg
Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130 135 140
Val Glu Ala Ala Asp Val Phe Gln Asn Phe Ser Gly 145 150 155
<210> SEQ ID NO 58 <211> LENGTH: 101 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 58 Met
Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10
15 Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg
Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly
Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln 100
<210> SEQ ID NO 59 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Rattus norvegicus <400> SEQUENCE:
59 Met Val Asp Val Leu Gly Gly Arg Arg Leu Met Thr Arg Glu Gly Thr
1 5 10 15 Leu Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala
Leu Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ala Pro Ser Arg Asp Phe
Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu
Ala Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala
Asp Arg Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu
His Gly Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg
His Glu Leu Lys Lys Arg Tyr Asp Ile Thr Val Ile 100 105 110 Pro Lys
Val Val Val Ile Lys Gln Asn Gly Ala Val Ile Thr Asn Lys 115 120 125
Gly Arg Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130
135 140 Val Glu Ala Ala Asp Val Phe Gln Asn Phe Ser Gly 145 150 155
<210> SEQ ID NO 60 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 60 Met
Val Asp Ile Leu Gly Glu Arg His Leu Val Thr Cys Lys Gly Ala 1 5 10
15 Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala Arg
Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly
Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu
Leu Arg Lys Arg Tyr Asn Val Thr Ala Ile 100 105 110 Pro Lys Leu Val
Ile Val Lys Gln Asn Gly Glu Val Ile Thr Asn Lys 115 120 125 Gly Arg
Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asp Trp 130 135 140
Val Glu Ala Ala Asp Ile Phe Gln Asn Phe Ser Val 145 150 155
<210> SEQ ID NO 61 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Pan troglodytes <400> SEQUENCE: 61
Met Val Asp Ile Leu Gly Gly Arg His Leu Val Thr Cys Lys Gly Ala 1 5
10 15 Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu
Tyr 20 25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr
Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala
Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp
Gly Ser Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His
Gly Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His
Glu Leu Arg Lys Arg Tyr Asn Val Thr Ala Ile 100 105 110 Pro Lys Leu
Val Ile Val Lys Gln Asn Gly Glu Val Ile Thr Asn Lys 115 120 125 Gly
Arg Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asp Trp 130 135
140 Val Glu Ala Ala Asp Ile Phe Gln Asn Phe Ser Val 145 150 155
<210> SEQ ID NO 62 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Bos taurus <400> SEQUENCE: 62 Met
Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Cys Asp Gly Ala 1 5 10
15 Trp Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Gly Arg Cys Ala Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Glu Glu Leu Val Asp Asp Ala Arg
Pro Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ala His Glu Met Leu 65 70 75 80 Glu Phe Met Lys Glu Leu His Gly
Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu
Leu Arg Thr Arg Tyr His Ile Thr Ala Ile 100 105 110 Pro Arg Leu Val
Ile Leu Lys Pro Ser Gly Glu Val Ile Thr Asp Lys 115 120 125 Gly Arg
Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130 135 140
Val Glu Ala Ala Asp Ile Phe Gln Asn Phe Ser Ser 145 150 155
<210> SEQ ID NO 63 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Gallus gallus <400> SEQUENCE: 63
Met Val Asp Val Phe Ser Gly Arg Leu Leu Val Ser Lys Asp Gly Arg 1 5
10 15 Ser Val Asp Pro Glu Glu Ala Leu Gln Asn Lys Val Gly Gly Leu
Tyr 20 25 30 Phe Ser Ala Gly Trp Cys Ser Pro Cys Arg Asp Phe Thr
Pro Val Leu 35 40 45 Cys Asp Phe Tyr Thr Asp Leu Leu Glu Glu Cys
Gln Pro Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Ile Ser Ser Asp
His Ser Ala Glu Glu Met Val 65 70 75 80 Ser Tyr Met His Ser Met His
Gly Asp Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Lys His
Asp Leu Lys Lys Lys Tyr Asn Ile Thr Ala Ile 100 105 110 Pro Lys Leu
Val Ile Val Lys Gln Thr Gly Glu Val Ile Thr Asp Lys 115 120 125 Gly
Arg Lys Gln Ile Arg Asp Lys Gly Leu Ser Cys Phe Arg Asn Trp 130 135
140 Leu Glu Gly Ala Asp Ile Phe Gln Asn Phe Ser Ser 145 150 155
<210> SEQ ID NO 64 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Xenopus laevis <400> SEQUENCE: 64
Met Asp Ile Phe Ser Gly His Ile Leu Leu Asn Lys Tyr Gly Glu Arg 1 5
10 15 Val Asp Pro Glu Glu Ala Leu Gln Asn Lys Ile Val Gly Leu Tyr
Phe 20 25 30 Ser Ala Ser Trp Cys Ser Pro Cys Arg Asp Phe Thr Pro
Ile Leu Cys 35 40 45 Asp Phe Tyr Thr Glu Leu Val Glu Glu Ser Glu
Pro Pro Ala Gln Phe 50 55 60 Glu Ile Val Phe Ile Ser Ser Asp Lys
Ser Pro Glu Glu Met Val Asp 65 70 75 80 Tyr Met His Asp Met Gln Gly
Asp Trp Leu Ala Leu Pro Phe His Asp 85 90 95 Pro Tyr Lys His Glu
Leu Lys Asn Lys Tyr Lys Ile Thr Ala Ile Pro 100 105 110 Lys Leu Val
Ile Val Lys Gln Asn Gly Asp Val Ile Thr Asp Lys Gly 115 120 125 Arg
Lys Gln Ile Arg Glu Arg Gly Leu Ser Cys Phe Arg Thr Trp Leu 130 135
140 Glu Val Gly Asp Val Phe Gln Asn Phe Thr Gly Lys 145 150 155
<210> SEQ ID NO 65 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Tetraodon nigroviridis <400>
SEQUENCE: 65 Met Val Glu Val Phe Thr Gly Arg Thr Leu Leu Asn Lys
Asp Gly Asp 1 5 10 15 Leu Val Asp Pro Glu Glu Ala Leu Arg Asn Lys
Val Val Gly Ile Tyr 20 25 30 Phe Ser Ala Gly Trp Cys Pro Pro Cys
Arg Asp Phe Thr Pro Ile Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu
Val Glu Glu Ser Asp Pro Pro Ala Gln 50 55 60 Phe Glu Val Val Phe
Val Ser Ser Asp Lys Thr Ser Glu Asp Met Val 65 70 75 80 Glu Tyr Tyr
His Asp Leu His Gly Asp Trp Leu Ala Leu Pro Trp Ser 85 90 95 Asp
Asp Tyr Lys Asn Glu Leu Lys Gln Arg Tyr Lys Ile Thr Ala Val 100 105
110 Pro Lys Leu Val Ile Val Lys Glu Ser Gly Glu Val Ile Thr Asp Lys
115 120 125 Gly Arg Lys Gln Ile Arg Asp Arg Gly Leu Ala Cys Phe Arg
Ser Trp 130 135 140 Leu Asp Ala Ala Glu Val Phe Gln Asn Phe Glu Gly
145 150 155 <210> SEQ ID NO 66 <211> LENGTH: 156
<212> TYPE: PRT <213> ORGANISM: Danio rerio <400>
SEQUENCE: 66 Met Val Glu Val Phe Ser Gly Arg Thr Leu Val Asn Lys
Glu Gly Asp 1 5 10 15 Leu Val Glu Pro Glu Glu Ala Leu Arg Asn Lys
Val Val Gly Leu Tyr 20 25 30 Phe Ser Ala Gly Trp Cys Pro Pro Cys
Arg Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu
Val Glu Glu Thr Glu Pro Pro Ala Gln 50 55 60 Phe Glu Ile Val Phe
Ile Ser Ser Asp Lys Ser Thr Glu Asp Met Val 65 70 75 80 Glu Tyr Tyr
His Asp Met His Gly Asp Trp Leu Ala Leu Pro Trp Thr 85 90 95 Asp
Pro Tyr Lys His Glu Leu Lys Lys Arg Tyr Asn Ile Thr Ala Val 100 105
110 Pro Lys Leu Val Ile Val Lys Glu Asn Gly Gln Val Ile Thr Asp Lys
115 120 125 Gly Arg Lys Gln Ile Arg Asp Gln Gly Leu Ala Cys Phe Arg
Ser Trp 130 135 140 Ile Glu Val Ala Glu Ile Phe Gln Asn Phe Lys Gly
145 150 155 <210> SEQ ID NO 67 <211> LENGTH: 217
<212> TYPE: PRT <213> ORGANISM: Mus musculus
<400> SEQUENCE: 67 Met Ala Ser Leu Phe Ser Gly Arg Ile Leu
Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln Asp Glu Val Glu Thr Glu Ala
Glu Leu Ser Arg Arg Leu Glu Asn 20 25 30 Arg Leu Val Leu Leu Phe
Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln 35 40 45 Ala Phe Ala Pro
Val Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Leu Arg Ala Ala Gln Leu Ala Leu Val Tyr Val Ser Gln 65 70 75 80
Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg Asp Met Pro Glu 85
90 95 Lys Trp Leu Phe Leu Pro Phe His Asp Glu Leu Arg Arg Asp Leu
Gly 100 105 110 Arg Gln Phe Ser Val Arg Gln Leu Pro Ala Val Val Val
Leu Lys Pro 115 120 125 Gly Gly Asp Val Leu Thr Ser Asp Ala Thr Glu
Glu Ile Gln Arg Leu 130 135 140 Gly Pro Ala Cys Phe Ala Asn Trp Gln
Glu Ala Ala Glu Leu Leu Asp 145 150 155 160 Arg Ser Phe Leu Gln Pro
Glu Asp Leu Asp Glu Pro Ala Arg Arg Ser 165 170 175 Ile Thr Glu Pro
Leu Arg Arg Arg Lys Tyr Arg Val Asp Arg Asp Val 180 185 190 Gly Arg
Glu Arg Gly Arg Asn Gly Arg Asp Ser Gly Asp Pro Gln Gly 195 200 205
Asp Ala Gly Thr Arg Ala Glu Leu Trp 210 215 <210> SEQ ID NO
68 <211> LENGTH: 109 <212> TYPE: PRT <213>
ORGANISM: Mus musculus <400> SEQUENCE: 68 Met Ala Ser Leu Phe
Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln Asp Glu
Val Glu Thr Glu Ala Glu Leu Ser Arg Arg Leu Glu Asn 20 25 30 Arg
Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln 35 40
45 Ala Phe Ala Pro Val Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu
50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala Leu Val Tyr Val
Ser Gln 65 70 75 80 Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg
Asp Met Pro Glu 85 90 95 Lys Trp Leu Phe Leu Pro Phe His Asp Glu
Leu Arg Arg 100 105 <210> SEQ ID NO 69 <211> LENGTH:
576 <212> TYPE: PRT <213> ORGANISM: Rattus norvegicus
<400> SEQUENCE: 69 Met Val Ser Leu Phe Ser Gly Arg Ile Leu
Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln Asp Glu Val Glu Thr Glu Ala
Glu Leu Ser Arg Arg Leu Glu Asn 20 25 30 Arg Leu Val Leu Leu Phe
Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln 35 40 45 Ala Phe Ala Pro
Val Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Leu Arg Ala Ala Gln Leu Ala Leu Val Tyr Val Ser Gln 65 70 75 80
Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg Asp Met Pro Glu 85
90 95 Lys Trp Leu Phe Leu Pro Phe His Asp Asp Leu Arg Arg Asp Leu
Gly 100 105 110 Arg Gln Phe Ser Val Arg Gln Leu Pro Ala Val Val Val
Leu Lys Pro 115 120 125 Gly Gly Asp Val Leu Thr Ser Asp Ala Thr Asp
Glu Ile Gln Arg Leu 130 135 140 Gly Pro Ala Cys Phe Ala Asn Trp Gln
Glu Ala Ala Glu Leu Leu Asp 145 150 155 160 Arg Ser Phe Leu Gln Pro
Glu Asp Leu Asp Glu Pro Ala Arg Arg Ser 165 170 175 Ile Thr Glu Pro
Leu Arg Arg Arg Lys Tyr Arg Val Asp Arg Asp Ala 180 185 190 Gly Arg
Gly Arg Gly Arg Asn Glu Cys Asp Ser Arg Asn Pro Gln Gly 195 200 205
Gly Arg Gly Cys Arg Asp Gly Ala Leu Val Ile Pro Pro Ala Pro Gln 210
215 220 Gly Thr Arg Val His Trp Trp Asn Phe Gly Asp Leu Gln Gly Asn
Ser 225 230 235 240 Gly Leu Gly Ile Gly Val Gln Leu Arg Val Gln Pro
Val Gly Ala Tyr 245 250 255 Ala Pro Gln Leu Arg Ala Pro Cys Leu Glu
Leu Glu Gln Gln Leu Arg 260 265 270 Ser Gln Arg Asp Gln His Arg Gly
Arg Asp Ala Gln Lys Gly His Arg 275 280 285 Gly Gln Tyr Pro Ala Ser
Ala Cys Ala Met Gly Arg Ser Tyr Gly Gly 290 295 300 Arg Val Leu Ala
Ala Met Thr Leu Leu Gly Ile Pro Ala Ala Val Leu 305 310 315 320 Val
Ala Leu Ala Ala Gln Leu Leu Phe Gln Leu Gln Ala Gly Arg Ala 325 330
335 Glu Leu Arg Gly Ile Arg Thr Asp Gly Leu His Pro Glu Leu Asp Pro
340 345 350 Asp Ala Gly Leu Pro Glu Ala Ala Ala Gly Ala Leu Leu Pro
Leu Ala 355 360 365 Thr Ala Leu Ala Ala Leu Ala Gln Val Leu Gly Leu
Gly Cys Leu Leu 370 375 380 Leu Ala Ala Leu Cys Gly His Leu Gly Ala
Glu Leu Ala Arg Gly Pro 385 390 395 400 Gly Pro Gly Arg Leu Thr Leu
Asn Val Trp Ser Cys Phe Asn Leu Pro 405 410 415 Asn Leu Gly Arg Arg
Ala Leu Ala Ile Tyr Ala Leu Leu Leu Phe Glu 420 425 430 Ile Glu Ala
Gly Ala Ala Ala Ala Ser Ile Leu Gly Ser Gly Ala Leu 435 440 445 Ile
Leu Val Ala Ile Met Thr His Thr Leu Phe Arg Ala Val Gln Ala 450 455
460 Thr Arg Arg Gly Leu Arg Glu Leu Pro Pro Pro Ser Ser Glu Asp Glu
465 470 475 480 Pro Ala Arg Ser Ser Glu Asp Ser Lys Ala Gly Cys Arg
Ala Gln Pro 485 490 495 Gln Gln Gly Thr His Cys Gln Ile Phe Tyr Asn
Pro Ser Gln Glu Leu 500 505 510 Gly Asp Pro Pro Gly Ser Met Ala Thr
Cys Ile Thr Ser Ala Val Leu 515 520 525 Glu Arg Ala Ser Glu Ser Ser
Leu Leu Ala Ser His Leu Pro Gln Thr 530 535 540 Leu Arg Ser Met Gly
Pro Trp Asp Gly Val Thr Tyr Glu Met His Gly 545 550 555 560 Met Leu
Gly His Arg Pro Pro Asp Met Gly Lys Asp Ala Thr Leu Val 565 570 575
<210> SEQ ID NO 70 <211> LENGTH: 212 <212> TYPE:
PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 70 Met
Ala Ser Leu Phe Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10
15 Gln Asp Glu Leu Asp Thr Glu Ala Glu Val Ser Arg Arg Leu Glu Asn
20 25 30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln
Cys Gln 35 40 45 Ala Phe Val Pro Ile Leu Lys Asp Phe Phe Val Arg
Leu Thr Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala
Leu Val Tyr Val Ser Gln 65 70 75 80 Asp Ser Thr Glu Glu Gln Gln Asp
Leu Phe Leu Lys Asp Met Pro Lys 85 90 95 Lys Trp Leu Phe Leu Pro
Phe Glu Asp Asp Leu Arg Arg Asp Leu Gly 100 105 110 Arg Gln Phe Ser
Val Glu Arg Leu Pro Ala Val Val Val Leu Lys Pro 115 120 125 Asp Gly
Asp Val Leu Thr Arg Asp Gly Ala Asp Glu Ile Gln Arg Leu 130 135 140
Gly Thr Ala Cys Phe Ala Asn Trp Gln Glu Ala Ala Glu Val Leu Asp 145
150 155 160 Arg Asn Phe Gln Leu Pro Glu Asp Leu Glu Asp Gln Glu Pro
Arg Ser 165 170 175 Leu Thr Glu Cys Leu Arg Arg His Lys Tyr Arg Val
Glu Lys Ala Ala 180 185 190 Arg Gly Gly Arg Asp Pro Gly Gly Gly Gly
Gly Glu Glu Gly Gly Ala 195 200 205 Gly Gly Leu Phe 210 <210>
SEQ ID NO 71 <211> LENGTH: 202 <212> TYPE: PRT
<213> ORGANISM: Pan troglodytes <220> FEATURE:
<221> NAME/KEY: misc_feature <222> LOCATION:
(168)..(201) <223> OTHER INFORMATION: Xaa can be any
naturally occurring amino acid <400> SEQUENCE: 71 Met Ala Ser
Leu Phe Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln
Asp Glu Leu Asp Thr Glu Ala Glu Val Ser Arg Arg Leu Glu Asn 20 25
30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln
35 40 45 Ala Phe Val Pro Ile Leu Lys Asp Phe Phe Val Arg Leu Thr
Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala Leu Val
Tyr Val Ser Gln 65 70 75 80 Asp Ser Thr Glu Glu Gln Gln Asp Leu Phe
Leu Lys Asp Met Pro Lys 85 90 95 Lys Trp Leu Phe Leu Pro Phe Glu
Asp Asp Leu Arg Arg Asp Leu Gly 100 105 110 Arg Gln Phe Ser Val Glu
Arg Leu Pro Ala Val Val Val Leu Lys Pro 115 120 125 Asp Gly Asp Val
Leu Thr Arg Asp Gly Ala Asp Glu Ile Gln Arg Leu 130 135 140 Gly Thr
Ala Cys Phe Ala Asn Trp Gln Glu Ala Ala Glu Val Leu Asp 145 150 155
160 Arg Asn Phe Gln Leu Pro Glu Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa
165 170 175 Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa
Xaa Xaa 180 185 190 Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Ala 195 200
<210> SEQ ID NO 72 <211> LENGTH: 218 <212> TYPE:
PRT <213> ORGANISM: Canis familiaris <400> SEQUENCE: 72
Met Ala Ser Leu Phe Ser Gly Arg Val Leu Ile Arg Asn Asn Ser Asp 1 5
10 15 Gln Asp Glu Leu Asp Thr Glu Ala Glu Leu Ser Arg Arg Leu Glu
Asn 20 25 30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ser Cys Pro
Gln Cys Gln 35 40 45 Ala Phe Ala Pro Ile Leu Arg Asp Phe Phe Val
Arg Leu Thr Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu
Ala Leu Val Tyr Val Ser Gln 65 70 75 80 Asp Pro Thr Glu Glu Gln Gln
Asp Leu Phe Leu Arg Asp Met Pro Lys 85 90 95 Lys Trp Leu Phe Leu
Pro Phe Glu Asp Asp Leu Arg Arg Asp Leu Gly 100 105 110 Arg Arg Phe
Ser Val Glu Arg Leu Pro Ala Val Val Val Leu Lys Pro 115 120 125 Gly
Gly Asp Val Leu Ser Arg Asp Ala Thr Asp Glu Ile Arg Arg Leu 130 135
140 Gly Pro Ala Cys Phe Ala Asn Trp Gln Glu Ala Ala Glu Val Leu Asp
145 150 155 160 Arg Asn Phe Leu Gln Pro Glu Asp Leu Asp Asp Pro Ala
Pro Arg Ser 165 170 175 Leu Thr Glu Pro Leu Arg Arg Cys Lys Tyr Arg
Val Asp Arg Glu Ala 180 185 190 Arg Gly Lys Arg Gly Pro Gly Gly Gly
Ser Gln Pro Glu Gly Gly Arg 195 200 205 Gly Ala Glu Gly Gly Ala Gly
Asp Leu Phe 210 215 <210> SEQ ID NO 73 <211> LENGTH:
218 <212> TYPE: PRT <213> ORGANISM: Bos taurus
<400> SEQUENCE: 73 Met Ala Ser Leu Phe Ser Gly Arg Val Leu
Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln Asp Glu Leu Asp Thr Glu Ala
Glu Leu Ser Arg Arg Leu Glu Asn 20 25 30 Arg Leu Val Leu Leu Phe
Phe Gly Ala Gly Ser Cys Pro Glu Cys Gln 35 40 45 Ala Phe Ala Pro
Ile Leu Arg Asp Phe Phe Val Arg Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Leu Arg Ala Ala Gln Val Ala Leu Val Tyr Val Ser Gln 65 70 75 80
Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg Asp Met Pro Glu 85
90 95 Lys Trp Leu Phe Leu Pro Phe Glu Asp Asp Leu Arg Arg Asp Leu
Gly 100 105 110 Arg Gln Phe Ser Val Glu Arg Leu Pro Ala Val Val Val
Leu Lys Pro 115 120 125 Ser Gly Asp Val Leu Thr Leu Asp Ala Ala Asp
Glu Ile Arg Arg Leu 130 135 140 Gly Pro Ala Cys Phe Ala Asn Trp Gln
Glu Ala Ala Glu Val Leu Asp 145 150 155 160 Arg Ser Phe Leu Gln Pro
Glu Asp Leu Asp Asp Pro Ala Pro Arg Ser 165 170 175 Leu Thr Glu Pro
Leu Arg Arg Cys Lys Tyr Arg Val Asp Pro Ala Ala 180 185 190 Arg Arg
Ala Arg Gly Arg Gly Arg Ala Gly Gly Ser Gly Gln Glu Gly 195 200 205
Glu Ala Glu Gly Glu Ala Ala Gly Leu Phe 210 215 <210> SEQ ID
NO 74 <211> LENGTH: 207 <212> TYPE: PRT <213>
ORGANISM: Gallus gallus <400> SEQUENCE: 74 Met Ala Ser Leu
Phe Ala Gly Lys Val Leu Ile Val Asn Asn Arg Asp 1 5 10 15 Arg Asp
Glu Val Glu Thr Glu Arg Glu Arg Cys Ser Ala Leu Glu Asn 20 25 30
Arg Val Met Leu Leu Tyr Phe Gly Ala Ala Glu Cys Pro Arg Cys Gln 35
40 45 Ser Phe Ala Pro Arg Leu Lys Asp Phe Phe Val Arg Leu Thr Asp
Glu 50 55 60 Phe Tyr Val Glu Arg Ala Ser Gln Leu Cys Leu Val Tyr
Val Ser Arg 65 70 75 80 Asp Ala Thr Ala Gln Gln Glu Glu Ala Phe Leu
Arg Ser Met Pro Arg 85 90 95 Arg Trp Leu Ser Leu Pro Phe Arg Asp
Glu Phe Lys Arg Glu Leu Glu 100 105 110 Leu Arg Phe Val Val Ser Glu
Val Pro Arg Val Val Val Leu Lys Pro 115 120 125 Asn Gly Asp Val Ile
Val Gly Asn Ala Val Asp Glu Ile Thr Ser Met 130 135 140 Gly Pro Ala
Cys Phe Gln Asn Trp Gln Glu Ala Ala Glu Leu Val Asp 145 150 155 160
Arg Asn Phe Arg Leu Ala Glu Asp Phe Asp Glu Cys Ala Arg Arg Ser 165
170 175 Ile Thr Asp Pro Leu Arg Arg Leu Lys Tyr Lys Leu Gly Lys Gly
Glu 180 185 190 Glu Pro Arg Ser Glu Glu Gln Lys Glu Asp Gly Asp Glu
Ser Ser 195 200 205 <210> SEQ ID NO 75 <211> LENGTH:
215 <212> TYPE: PRT <213> ORGANISM: Xenopus laevis
<400> SEQUENCE: 75 Met Ala Asp Leu Phe Leu Asp Lys Ile Leu
Val Lys Asn Asn Arg Asp 1 5 10 15 Gln Asp Glu Leu Asp Thr Glu Arg
Glu Ile Trp Glu Arg Leu Glu Asn 20 25 30 Arg Val Ile Leu Leu Phe
Phe Ala Lys Ser Arg Ser Ser Gln Cys Gln 35 40 45 Glu Phe Ala Pro
Leu Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Asp Arg Ser Ser Gln Leu Ala Leu Val Tyr Val Ser Leu 65 70 75 80
Asp Gln Ser Glu Glu Glu Gln Glu Arg Phe Leu Lys Asp Met Pro Lys 85
90 95 Arg Trp Leu Phe Val Pro Phe Lys Asp Glu Glu Phe Arg Arg Asn
Leu 100 105 110 Glu Ala Gln Phe Ser Val Ser Arg Val Pro Val Leu Val
Val Leu Lys 115 120 125 Pro Ser Gly His Val Ile Ser Phe Asn Ala Val
Asp Glu Val Val Arg 130 135 140 Leu Gly Pro Pro Cys Phe Lys Asn Trp
Gln Glu Val Ser Glu Ile Ile 145 150 155 160 Asp Arg Ser Phe Leu Leu
Pro Glu Phe Thr Asp Asp Arg Ala Gly Arg 165 170 175 Ser Met Thr Asp
Pro Ile Arg Arg Ile Lys Tyr Lys Asp Glu Thr Thr 180 185 190 Asn Glu
Lys Lys Lys Arg Lys His Cys Asp Asp Glu Asp Glu Gly Gly 195 200 205
Gly Gly Gly Thr Glu Phe Phe 210 215 <210> SEQ ID NO 76
<211> LENGTH: 180 <212> TYPE: PRT <213> ORGANISM:
Tetraodon nigroviridis <400> SEQUENCE: 76 Met Val Asp Leu Phe
Leu Asn Arg Val Leu Val Glu Asn Asn Trp Asp 1 5 10 15 Gln Asp Gln
Leu Asn Thr Glu Arg Glu Ile Val Gly Ile Leu Glu Asn 20 25 30 Arg
Ile Leu Leu Leu Phe Phe Ala Ser Ala Ser Cys Gln Lys Cys Gln 35 40
45 Asp Phe Leu Pro Ile Leu Asn Asn Phe Phe Lys Arg Leu Lys Asp Pro
50 55 60 Ala His Ile Glu Tyr Pro Lys Leu Leu Ala Leu Ile Phe Ile
Ser Leu 65 70 75 80 Asp Gln Ser Glu Glu Gln Gln Glu Arg Phe Leu Lys
Glu Leu His Lys 85 90 95 Lys Val Leu Phe Leu Ala Phe Asp Asp Pro
Tyr Arg Gln Glu Leu Gln 100 105 110 Ala Met Phe Glu Val Lys Glu Leu
Pro Thr Val Val Val Leu Arg Pro 115 120 125 Asp Gly Ser Val Leu Ala
Ala Asn Ala Ala Gln Asp Ile Cys Ser Tyr 130 135 140 Gly Ser Glu Cys
Phe Arg Asp Trp Gln Glu Ser Ala Glu Leu Ile Glu 145 150 155 160 Arg
Thr Phe Met Leu Asn Glu Glu Phe Asp Asn Leu Asn Leu Arg Thr 165 170
175 Ser Ala Thr Pro 180 <210> SEQ ID NO 77 <211>
LENGTH: 169 <212> TYPE: PRT <213> ORGANISM: Tetraodon
nigroviridis <400> SEQUENCE: 77 Met Val Asp Leu Phe Ile Asp
Arg Val Leu Leu Lys Asn Asn Ser Glu 1 5 10 15 Arg Asp Glu Leu Asp
Thr Glu Arg Glu Ile Val Ala Arg Leu Gln Asn 20 25 30 Arg Ile Leu
Leu Leu Phe Phe Gly Cys Val Val Ser Arg Ser Cys Gln 35 40 45 Leu
Phe Ala Pro Lys Leu Ser Ser Phe Phe Lys Gln Leu Thr Asp Glu 50 55
60 Ala Tyr Val Asp Arg Ser Ala Gln Leu Val Leu Leu Tyr Ile Ser Met
65 70 75 80 Asp Gln Ser Glu Gln Gln Leu Ser Ser Phe Leu Gln Glu Leu
Pro Lys 85 90 95 Lys Cys Leu Phe Leu Ala Phe Glu Asp Pro Phe Arg
Arg Glu Leu Glu 100 105 110 Ala Met Phe Asn Val Glu Glu Leu Pro Thr
Val Val Val Leu Arg Pro 115 120 125 Asp Cys Ser Val Leu Ala Ala Asn
Ala Val Glu Glu Ile Leu Arg Leu 130 135 140 Gly Pro Asp Cys Tyr Arg
Asn Trp Gln Glu Ala Ala Glu Leu Tyr Arg 145 150 155 160 Gln Glu Leu
Pro Asp Gln Arg Arg Leu 165 <210> SEQ ID NO 78 <211>
LENGTH: 215 <212> TYPE: PRT <213> ORGANISM: Danio rerio
<400> SEQUENCE: 78 Met Val Asp Leu Phe Leu Gly Lys Val Leu
Val Lys Asn Asn Lys Asp 1 5 10 15 Arg Asp Glu Leu Asp Thr Glu Arg
Glu Ile Ile Leu Arg Leu Gln Asn 20 25 30 Arg Ile Leu Met Leu Phe
Phe Gly Ser Gly Asp Ser Glu Lys Cys Gln 35 40 45 Asp Phe Ala Pro
Thr Leu Lys Asp Phe Tyr Lys Lys Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Glu Arg Ser Ala Gln Leu Val Leu Leu Tyr Ile Ser Leu 65 70 75 80
Asp Ser Ser Glu Glu Gln Gln Glu Lys Phe Leu Lys Glu Leu Pro Lys 85
90 95 Arg Cys Leu Phe Leu Pro Tyr Glu Asp Pro Tyr Arg Gln Glu Leu
Gly 100 105 110 Val Met Phe Glu Val Arg Asp Leu Pro Arg Val Val Val
Leu Arg Pro 115 120 125 Asp Cys Ser Val Leu Ser Pro Asn Ala Val Ser
Glu Ile Cys Thr Leu 130 135 140 Gly Thr Asp Cys Phe Arg Asn Trp Gln
Glu Gly Ala Glu Leu Ile Asp 145 150 155 160 Arg Asn Phe Met Met Asn
Glu Glu Phe Asp Glu Gly Lys Met Arg Ser 165 170 175 Met Thr Asp Pro
Ile Arg Arg Ile Lys Tyr Lys Val Glu Asp Glu Lys 180 185 190 Lys Lys
Lys Lys Lys Arg Asp Asp Asp Asp Asp Asp Asp Asp Gly Gly 195 200 205
Gly Gly Gly Gly Pro Trp Gly 210 215
1 SEQUENCE LISTING <160> NUMBER OF SEQ ID NOS: 78 <210>
SEQ ID NO 1 <211> LENGTH: 101 <212> TYPE: PRT
<213> ORGANISM: Homo sapiens <400> SEQUENCE: 1 Met Val
Asp Ile Leu Gly Glu Arg His Leu Val Thr Cys Lys Gly Ala 1 5 10 15
Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu Tyr 20
25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr Pro Leu
Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala Arg Arg
Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly Ser
Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly Ala
Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln 100
<210> SEQ ID NO 2 <211> LENGTH: 101 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 2 Met
Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10
15 Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg
Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly
Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln 100
<210> SEQ ID NO 3 <211> LENGTH: 101 <212> TYPE:
PRT <213> ORGANISM: Rattus norvegicus <400> SEQUENCE: 3
Met Val Asp Val Leu Gly Gly Arg Arg Leu Met Thr Arg Glu Gly Thr 1 5
10 15 Leu Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu
Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ala Pro Ser Arg Asp Phe Thr
Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala
Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp
Arg Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His
Gly Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln
100 <210> SEQ ID NO 4 <211> LENGTH: 101 <212>
TYPE: PRT <213> ORGANISM: Pan troglodytes <400>
SEQUENCE: 4 Met Val Asp Ile Leu Gly Gly Arg His Leu Val Thr Cys Lys
Gly Ala 1 5 10 15 Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val
Val Ala Leu Tyr 20 25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg
Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val
Ala Glu Ala Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val
Ser Ala Asp Gly Ser Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg
Glu Leu His Gly Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro
Tyr Arg Gln 100 <210> SEQ ID NO 5 <211> LENGTH: 101
<212> TYPE: PRT <213> ORGANISM: Bos taurus <400>
SEQUENCE: 5 Met Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Cys Asp
Gly Ala 1 5 10 15 Trp Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val
Val Ala Leu Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ala Pro Ser Arg
Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Glu Glu Leu Val
Asp Asp Ala Arg Pro Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val
Ser Ala Asp Gly Ser Ala His Glu Met Leu 65 70 75 80 Glu Phe Met Lys
Glu Leu His Gly Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro
Tyr Arg Gln 100 <210> SEQ ID NO 6 <211> LENGTH: 101
<212> TYPE: PRT <213> ORGANISM: Gallus gallus
<400> SEQUENCE: 6 Met Val Asp Val Phe Ser Gly Arg Leu Leu Val
Ser Lys Asp Gly Arg 1 5 10 15 Ser Val Asp Pro Glu Glu Ala Leu Gln
Asn Lys Val Gly Gly Leu Tyr 20 25 30 Phe Ser Ala Gly Trp Cys Ser
Pro Cys Arg Asp Phe Thr Pro Val Leu 35 40 45 Cys Asp Phe Tyr Thr
Asp Leu Leu Glu Glu Cys Gln Pro Pro Ala Pro 50 55 60 Phe Glu Val
Val Phe Ile Ser Ser Asp His Ser Ala Glu Glu Met Val 65 70 75 80 Ser
Tyr Met His Ser Met His Gly Asp Trp Leu Ala Leu Pro Phe His 85 90
95 Asp Pro Tyr Lys Gln 100 <210> SEQ ID NO 7 <211>
LENGTH: 100 <212> TYPE: PRT <213> ORGANISM: Xenopus
laevis <400> SEQUENCE: 7 Met Asp Ile Phe Ser Gly His Ile Leu
Leu Asn Lys Tyr Gly Glu Arg 1 5 10 15 Val Asp Pro Glu Glu Ala Leu
Gln Asn Lys Ile Val Gly Leu Tyr Phe 20 25 30 Ser Ala Ser Trp Cys
Ser Pro Cys Arg Asp Phe Thr Pro Ile Leu Cys 35 40 45 Asp Phe Tyr
Thr Glu Leu Val Glu Glu Ser Glu Pro Pro Ala Gln Phe 50 55 60 Glu
Ile Val Phe Ile Ser Ser Asp Lys Ser Pro Glu Glu Met Val Asp 65 70
75 80 Tyr Met His Asp Met Gln Gly Asp Trp Leu Ala Leu Pro Phe His
Asp 85 90 95 Pro Tyr Lys Gln 100 <210> SEQ ID NO 8
<211> LENGTH: 101 <212> TYPE: PRT <213> ORGANISM:
Tetraodon nigroviridis <400> SEQUENCE: 8 Met Val Glu Val Phe
Thr Gly Arg Thr Leu Leu Asn Lys Asp Gly Asp 1 5 10 15 Leu Val Asp
Pro Glu Glu Ala Leu Arg Asn Lys Val Val Gly Ile Tyr 20 25 30 Phe
Ser Ala Gly Trp Cys Pro Pro Cys Arg Asp Phe Thr Pro Ile Leu 35 40
45 Cys Asp Phe Tyr Thr Glu Leu Val Glu Glu Ser Asp Pro Pro Ala Gln
50 55 60 Phe Glu Val Val Phe Val Ser Ser Asp Lys Thr Ser Glu Asp
Met Val 65 70 75 80 Glu Tyr Tyr His Asp Leu His Gly Asp Trp Leu Ala
Leu Pro Trp Ser 85 90 95 Asp Asp Tyr Lys Lys 100 <210> SEQ ID
NO 9 <211> LENGTH: 101 <212> TYPE: PRT <213>
ORGANISM: Danio rerio <400> SEQUENCE: 9 Met Val Glu Val Phe
Ser Gly Arg Thr Leu Val Asn Lys Glu Gly Asp 1 5 10 15 Leu Val Glu
Pro Glu Glu Ala Leu Arg Asn Lys Val Val Gly Leu Tyr 20 25 30
Phe Ser Ala Gly Trp Cys Pro Pro Cys Arg Asp Phe Thr Pro Leu Leu 35
40 45 Cys Asp Phe Tyr Thr Glu Leu Val Glu Glu Thr Glu Pro Pro Ala
Gln 50 55 60 Phe Glu Ile Val Phe Ile Ser Ser Asp Lys Ser Thr Glu
Asp Met Val 65 70 75 80 Glu Tyr Tyr His Asp Met His Gly Asp Trp Leu
Ala Leu Pro Trp Thr 85 90 95 Asp Pro Tyr Lys Gln 100 <210>
SEQ ID NO 10 <211> LENGTH: 156 <212> TYPE: PRT
<213> ORGANISM: Homo sapiens <400> SEQUENCE: 10 Met Val
Asp Ile Leu Gly Glu Arg His Leu Val Thr Cys Lys Gly Ala 1 5 10 15
Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu Tyr 20
25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr Pro Leu
Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala Arg Arg
Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly Ser
Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly Ala
Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu Leu
Arg Lys Arg Tyr Asn Val Thr Ala Ile 100 105 110 Pro Lys Leu Val Ile
Val Lys Gln Asn Gly Glu Val Ile Thr Asn Lys 115 120 125 Gly Arg Lys
Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asp Trp 130 135 140 Val
Glu Ala Ala Asp Ile Phe Gln Asn Phe Ser Val 145 150 155 <210>
SEQ ID NO 11 <211> LENGTH: 306 <212> TYPE: DNA
<213> ORGANISM: Homo sapiens <400> SEQUENCE: 11
atggttgaca ttctgggcga gcggcacctg gtgacctgta agggcgcgac ggtggaggcc
60 gaggcggcgc tgcagaacaa ggtggtggca ctgtacttcg cggcggcccg
gtgcgcgccg 120 agccgcgact tcacgccgct gctctgcgac ttctatacgg
cgctggtggc cgaggcgcgg 180 cggcccgcgc ccttcgaagt ggtcttcgtg
tcagccgacg gcagctccca ggagatgctg 240 gacttcatgc gcgagctgca
tggcgcctgg ctggcgctgc ccttccacga cccctaccgg 300 cagtga 306
<210> SEQ ID NO 12 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 12 Met
Val Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10
15 Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg
Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly
Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu
Leu Lys Lys Arg Tyr Glu Ile Thr Ala Ile 100 105 110 Pro Lys Leu Val
Val Ile Lys Gln Asn Gly Ala Val Ile Thr Asn Lys 115 120 125 Gly Arg
Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130 135 140
Val Glu Ala Ala Asp Val Phe Gln Asn Phe Ser Gly 145 150 155
<210> SEQ ID NO 13 <211> LENGTH: 22 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic-Primer <400>
SEQUENCE: 13 catcaccaac aaagggcgga ag 22 <210> SEQ ID NO 14
<211> LENGTH: 23 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic-Primer <400> SEQUENCE: 14 cattcctcag
cagagaaggg aac 23 <210> SEQ ID NO 15 <211> LENGTH: 35
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 15 ccgtgctatt gtttcagagc
ccttaacttt ctatc 35 <210> SEQ ID NO 16 <211> LENGTH: 31
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 16 tgacactcca atcgtaaaag
gcagaaaacg c 31 <210> SEQ ID NO 17 <211> LENGTH: 19
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 17 aagccgatga gcaacttcc 19
<210> SEQ ID NO 18 <211> LENGTH: 20 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic-Primer <400>
SEQUENCE: 18 tcatctccca gtggattctt 20 <210> SEQ ID NO 19
<211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic-Primer <400> SEQUENCE: 19 gtagctttgt
actttgcggc g 21 <210> SEQ ID NO 20 <211> LENGTH: 29
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 20 gtcatcagaa aatgtatcac
ctccatagg 29 <210> SEQ ID NO 21 <211> LENGTH: 25
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 21 gccatctctg cgacttattt
ttacc 25 <210> SEQ ID NO 22 <211> LENGTH: 22
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION:
Synthetic-Primer <400> SEQUENCE: 22 aattagtgcc accagcacca tc
22 <210> SEQ ID NO 23 <211> LENGTH: 4 <212> TYPE:
PRT <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S
<400> SEQUENCE: 23 Glu Leu Arg Arg 1 <210> SEQ ID NO 24
<211> LENGTH: 21 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - M.
musculus <400> SEQUENCE: 24 gaactgagga ggtgaggccc c 21
<210> SEQ ID NO 25 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - R.
norvegicus <400> SEQUENCE: 25 gacctgagga ggtgaggccc c 21
<210> SEQ ID NO 26 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - M.
domestica <400> SEQUENCE: 26 gagctgaaaa ggtgagccta c 21
<210> SEQ ID NO 27 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - H.
sapiens <400> SEQUENCE: 27 gatctgagga ggtgaggagg g 21
<210> SEQ ID NO 28 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - P.
troglodytes <400> SEQUENCE: 28 gatctgagga ggtgaggagg g 21
<210> SEQ ID NO 29 <211> LENGTH: 22 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Figure 1 - RdCVF-S - M. mulatta
<400> SEQUENCE: 29 gaactgagga ggtgasggag gg 22 <210>
SEQ ID NO 30 <211> LENGTH: 21 <212> TYPE: DNA
<213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - B.
taurus <400> SEQUENCE: 30 gacctgagga ggtgagacaa g 21
<210> SEQ ID NO 31 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S - C.
familiaris <400> SEQUENCE: 31 gacctgagga ggtgaggtgg g 21
<210> SEQ ID NO 32 <211> LENGTH: 128 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Figure 1 - RdCVF-S - G. gallus
<220> FEATURE: <221> NAME/KEY: misc_feature <222>
LOCATION: (16)..(115) <223> OTHER INFORMATION: N= A, T, G or
C <220> FEATURE: <221> NAME/KEY: misc_feature
<222> LOCATION: (116)..(125) <223> OTHER INFORMATION: n
is a, c, g, or t <400> SEQUENCE: 32 gacctgagga ggtggnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 60 nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn 120 nnnnntaa
128 <210> SEQ ID NO 33 <211> LENGTH: 21 <212>
TYPE: DNA <213> ORGANISM: Artificial sequence <220>
FEATURE: <223> OTHER INFORMATION: Synthetic - Figure 1 -
RdCVF-S -X. tropicalis <400> SEQUENCE: 33 gaattcagga
ggtgagatag g 21 <210> SEQ ID NO 34 <211> LENGTH: 54
<212> TYPE: DNA <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION: Synthetic -
Figure 1 - RdCVF-S -B. rerio <220> FEATURE: <221>
NAME/KEY: misc_feature <222> LOCATION: (16)..(51) <223>
OTHER INFORMATION: N= A, T, G or C <400> SEQUENCE: 34
ccctataggc agtacnnnnn nnnnnnnnnn nnnnnnnnnn nnnnnnnnnn ntga 54
<210> SEQ ID NO 35 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -T.
rubripes <400> SEQUENCE: 35 ccatacagac agtaggtgga t 21
<210> SEQ ID NO 36 <211> LENGTH: 21 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -T.
nigroviridis <400> SEQUENCE: 36 ccatacagac agtaggtgga c 21
<210> SEQ ID NO 37 <211> LENGTH: 24 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF-S -T.
rubripes <400> SEQUENCE: 37 cccttcagga ggtgtgtggt ttag 24
<210> SEQ ID NO 38 <211> LENGTH: 58 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Figure 1 - RdCVF-S - T. nigroviridis
<220> FEATURE: <221> NAME/KEY: misc_feature <222>
LOCATION: (16)..(55) <223> OTHER INFORMATION: N= A, T, G or C
<400> SEQUENCE: 38 ccttttagga ggtgtnnnnn nnnnnnnnnn
nnnnnnnnnn nnnnnnnnnn nnnnntga 58 <210> SEQ ID NO 39
<211> LENGTH: 4 <212> TYPE: PRT <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1- RdCVF2-L <400> SEQUENCE:
39 Pro Tyr Arg His 1 <210> SEQ ID NO 40 <211> LENGTH: 4
<212> TYPE: PRT <213> ORGANISM: Artificial sequence
<220> FEATURE: <223> OTHER INFORMATION: Synthetic -
Figure 1- RdCVF2-S <400> SEQUENCE: 40 Pro Tyr Arg Gln 1
<210> SEQ ID NO 41 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - M.
musculus <400> SEQUENCE: 41 ccctaccggc agtgagtggg gac 23
<210> SEQ ID NO 42 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - R.
norvegicus
<400> SEQUENCE: 42 ccctaccggc agtgagtggg gac 23 <210>
SEQ ID NO 43 <400> SEQUENCE: 43 000 <210> SEQ ID NO 44
<211> LENGTH: 23 <212> TYPE: DNA <213> ORGANISM:
Artificial sequence <220> FEATURE: <223> OTHER
INFORMATION: Synthetic - Figure 1 - RdCVF2-S - H. sapiens
<400> SEQUENCE: 44 ccctaccggc agtgagtggg ggc 23 <210>
SEQ ID NO 45 <211> LENGTH: 23 <212> TYPE: DNA
<213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - P.
troglodytes <400> SEQUENCE: 45 ccctaccggc agtgagtggg ggc 23
<210> SEQ ID NO 46 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - M.
mulatta <400> SEQUENCE: 46 ccctaccagc agtgagtggg ggc 23
<210> SEQ ID NO 47 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - B.
taurus <400> SEQUENCE: 47 ccctaccggc agtgagtgga ggc 23
<210> SEQ ID NO 48 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S - G.
gallus <400> SEQUENCE: 48 ccctacaagc agtaagtacc gca 23
<210> SEQ ID NO 49 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -X.
tropicalis <400> SEQUENCE: 49 ccatacaagc agtaagttcc ttg 23
<210> SEQ ID NO 50 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -B.
rerio <400> SEQUENCE: 50 ccatacaaac agtgagttca cca 23
<210> SEQ ID NO 51 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -T.
rubripes <400> SEQUENCE: 51 gactacaaga agtgagtgag gtt 23
<210> SEQ ID NO 52 <211> LENGTH: 23 <212> TYPE:
DNA <213> ORGANISM: Artificial sequence <220> FEATURE:
<223> OTHER INFORMATION: Synthetic - Figure 1 - RdCVF2-S -T.
nigroviridis <400> SEQUENCE: 52 gactacaaga agtgagtccg cct 23
<210> SEQ ID NO 53 <211> LENGTH: 109 <212> TYPE:
PRT <213> ORGANISM: Escherichia coli <400> SEQUENCE: 53
Met Ser Asp Lys Ile Ile His Leu Thr Asp Asp Ser Phe Asp Thr Asp 1 5
10 15 Val Leu Lys Ala Asp Gly Ala Ile Leu Val Asp Phe Trp Ala Glu
Trp 20 25 30 Cys Gly Pro Cys Lys Met Ile Ala Pro Ile Leu Asp Glu
Ile Ala Asp 35 40 45 Glu Tyr Gln Gly Lys Leu Thr Val Ala Lys Leu
Asn Ile Asp Gln Asn 50 55 60 Pro Gly Thr Ala Pro Lys Tyr Gly Ile
Arg Gly Ile Pro Thr Leu Leu 65 70 75 80 Leu Phe Lys Asn Gly Glu Val
Ala Ala Thr Lys Val Gly Ala Leu Ser 85 90 95 Lys Gly Gln Leu Lys
Glu Phe Leu Asp Ala Asn Leu Ala 100 105 <210> SEQ ID NO 54
<211> LENGTH: 105 <212> TYPE: PRT <213> ORGANISM:
Homo sapiens <400> SEQUENCE: 54 Met Val Lys Gln Ile Glu Ser
Lys Thr Ala Phe Gln Glu Ala Leu Asp 1 5 10 15 Ala Ala Gly Asp Lys
Leu Val Val Val Asp Phe Ser Ala Thr Trp Cys 20 25 30 Gly Pro Cys
Lys Met Ile Lys Pro Phe Phe His Ser Leu Ser Glu Lys 35 40 45 Tyr
Ser Asn Val Ile Phe Leu Glu Val Asp Val Asp Asp Cys Gln Asp 50 55
60 Val Ala Ser Glu Cys Glu Val Lys Cys Met Pro Thr Phe Gln Phe Phe
65 70 75 80 Lys Lys Gly Gln Lys Val Gly Glu Phe Ser Gly Ala Asn Lys
Glu Lys 85 90 95 Leu Glu Ala Thr Ile Asn Glu Leu Val 100 105
<210> SEQ ID NO 55 <211> LENGTH: 435 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 55 Met
Ser Gly Phe Leu Glu Glu Leu Leu Gly Asp Lys Leu Val Thr Gly 1 5 10
15 Gly Gly Glu Glu Val Asp Val His Ser Leu Gly Ala Arg Gly Ile Ala
20 25 30 Leu Leu Gly Leu Tyr Phe Gly Cys Ser Leu Ser Ala Pro Cys
Ala Gln 35 40 45 Leu Ser Ala Ser Leu Ala Ala Phe Tyr Gly Arg Leu
Arg Gly Asp Ala 50 55 60 Ala Ala Gly Pro Gly Ala Gly Ala Gly Ala
Gly Ala Ala Ala Glu Pro 65 70 75 80 Glu Pro Arg His Arg Leu Glu Ile
Val Phe Val Ser Ser Asp Gln Asp 85 90 95 Gln Arg Gln Trp Gln Asp
Phe Val Arg Asp Met Pro Trp Leu Ala Leu 100 105 110 Pro Tyr Lys Glu
Lys His Arg Lys Leu Lys Leu Trp Asn Lys Tyr Arg 115 120 125 Val Ser
Asn Ile Pro Ser Leu Ile Phe Leu Asp Ala Thr Thr Gly Lys 130 135 140
Val Val Cys Arg Asn Gly Leu Leu Val Ile Arg Asp Asp Pro Glu Gly 145
150 155 160 Leu Glu Phe Pro Trp Gly Pro Lys Pro Phe Arg Glu Val Ile
Ala Gly 165 170 175 Pro Leu Leu Arg Asn Asn Gly Gln Ser Leu Glu Ser
Ser Ser Leu Glu 180 185 190 Gly Ser His Val Gly Val Tyr Phe Ser Ala
His Trp Cys Pro Pro Cys 195 200 205 Arg Ser Leu Thr Arg Val Leu Val
Glu Ser Tyr Arg Lys Ile Lys Glu 210 215 220 Ala Gly Gln Glu Phe Glu
Ile Ile Phe Val Ser Ala Asp Arg Ser Glu 225 230 235 240 Glu Ser Phe
Lys Gln Tyr Phe Ser Glu Met Pro Trp Leu Ala Val Pro 245 250 255 Tyr
Thr Asp Glu Ala Arg Arg Ser Arg Leu Asn Arg Leu Tyr Gly Ile 260 265
270 Gln Gly Ile Pro Thr Leu Ile Val Leu Asp Pro Gln Gly Glu Val Ile
275 280 285 Thr Arg Gln Gly Arg Val Glu Val Leu Asn Asp Glu Asp Cys
Arg Glu 290 295 300
Phe Pro Trp His Pro Lys Pro Val Leu Glu Leu Ser Asp Ser Asn Ala 305
310 315 320 Val Gln Leu Asn Glu Gly Pro Cys Leu Val Leu Phe Val Asp
Ser Glu 325 330 335 Asp Asp Gly Glu Ser Glu Ala Ala Lys Gln Leu Ile
Gln Pro Ile Ala 340 345 350 Glu Lys Ile Ile Ala Lys Tyr Lys Ala Lys
Glu Glu Glu Ala Pro Leu 355 360 365 Leu Phe Phe Val Ala Gly Glu Asp
Asp Met Thr Asp Ser Leu Arg Asp 370 375 380 Tyr Thr Asn Leu Pro Glu
Ala Ala Pro Leu Leu Thr Ile Leu Asp Met 385 390 395 400 Ser Ala Arg
Ala Lys Tyr Val Met Asp Val Glu Glu Ile Thr Pro Ala 405 410 415 Ile
Val Glu Thr Phe Val Asn Asp Phe Leu Ala Glu Lys Leu Lys Pro 420 425
430 Glu Pro Ile 435 <210> SEQ ID NO 56 <211> LENGTH:
146 <212> TYPE: PRT <213> ORGANISM: Crithidia
fasciculata <400> SEQUENCE: 56 Met Ser Gly Leu Asp Lys Tyr
Leu Pro Gly Ile Glu Lys Leu Arg Arg 1 5 10 15 Gly Asp Gly Glu Val
Glu Val Lys Ser Leu Ala Gly Lys Leu Val Phe 20 25 30 Phe Tyr Phe
Ser Ala Ser Trp Cys Pro Pro Cys Arg Gly Phe Thr Pro 35 40 45 Gln
Leu Ile Glu Phe Tyr Asp Lys Phe His Glu Ser Lys Asn Phe Glu 50 55
60 Val Val Phe Cys Thr Trp Asp Glu Glu Glu Asp Gly Phe Ala Gly Tyr
65 70 75 80 Phe Ala Lys Met Pro Trp Leu Ala Val Pro Phe Ala Gln Ser
Glu Ala 85 90 95 Val Gln Lys Leu Ser Lys His Phe Asn Val Glu Ser
Ile Pro Thr Leu 100 105 110 Ile Gly Val Asp Ala Asp Ser Gly Asp Val
Val Thr Thr Arg Ala Arg 115 120 125 Ala Thr Leu Val Lys Asp Pro Glu
Gly Glu Gln Phe Pro Trp Lys Asp 130 135 140 Ala Pro 145 <210>
SEQ ID NO 57 <211> LENGTH: 156 <212> TYPE: PRT
<213> ORGANISM: Mus musculus <400> SEQUENCE: 57 Met Val
Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10 15
Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr 20
25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro Leu
Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg Arg
Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly Ser
Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly Ser
Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu Leu
Lys Lys Arg Tyr Glu Ile Thr Ala Ile 100 105 110 Pro Lys Leu Val Val
Ile Lys Gln Asn Gly Ala Val Ile Thr Asn Lys 115 120 125 Gly Arg Lys
Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130 135 140 Val
Glu Ala Ala Asp Val Phe Gln Asn Phe Ser Gly 145 150 155 <210>
SEQ ID NO 58 <211> LENGTH: 101 <212> TYPE: PRT
<213> ORGANISM: Mus musculus <400> SEQUENCE: 58 Met Val
Asp Val Leu Gly Gly Arg Arg Leu Val Thr Arg Glu Gly Thr 1 5 10 15
Val Val Glu Ala Glu Val Ala Leu Gln Asn Lys Val Val Ala Leu Tyr 20
25 30 Phe Ala Ala Gly Arg Cys Ser Pro Ser Arg Asp Phe Thr Pro Leu
Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu Ala Arg Arg
Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly Ser
Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly Ser
Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg Gln 100
<210> SEQ ID NO 59 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Rattus norvegicus <400> SEQUENCE:
59 Met Val Asp Val Leu Gly Gly Arg Arg Leu Met Thr Arg Glu Gly Thr
1 5 10 15 Leu Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala
Leu Tyr 20 25 30 Phe Ala Ala Gly Arg Cys Ala Pro Ser Arg Asp Phe
Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Glu Leu Val Ser Glu
Ala Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala
Asp Arg Ser Ala Glu Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu
His Gly Ser Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg
His Glu Leu Lys Lys Arg Tyr Asp Ile Thr Val Ile 100 105 110 Pro Lys
Val Val Val Ile Lys Gln Asn Gly Ala Val Ile Thr Asn Lys 115 120 125
Gly Arg Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asn Trp 130
135 140 Val Glu Ala Ala Asp Val Phe Gln Asn Phe Ser Gly 145 150 155
<210> SEQ ID NO 60 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 60 Met
Val Asp Ile Leu Gly Glu Arg His Leu Val Thr Cys Lys Gly Ala 1 5 10
15 Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu Tyr
20 25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr Pro
Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala Arg
Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp Gly
Ser Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His Gly
Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His Glu
Leu Arg Lys Arg Tyr Asn Val Thr Ala Ile 100 105 110 Pro Lys Leu Val
Ile Val Lys Gln Asn Gly Glu Val Ile Thr Asn Lys 115 120 125 Gly Arg
Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asp Trp 130 135 140
Val Glu Ala Ala Asp Ile Phe Gln Asn Phe Ser Val 145 150 155
<210> SEQ ID NO 61 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Pan troglodytes <400> SEQUENCE: 61
Met Val Asp Ile Leu Gly Gly Arg His Leu Val Thr Cys Lys Gly Ala 1 5
10 15 Thr Val Glu Ala Glu Ala Ala Leu Gln Asn Lys Val Val Ala Leu
Tyr 20 25 30 Phe Ala Ala Ala Arg Cys Ala Pro Ser Arg Asp Phe Thr
Pro Leu Leu 35 40 45 Cys Asp Phe Tyr Thr Ala Leu Val Ala Glu Ala
Arg Arg Pro Ala Pro 50 55 60 Phe Glu Val Val Phe Val Ser Ala Asp
Gly Ser Ser Gln Glu Met Leu 65 70 75 80 Asp Phe Met Arg Glu Leu His
Gly Ala Trp Leu Ala Leu Pro Phe His 85 90 95 Asp Pro Tyr Arg His
Glu Leu Arg Lys Arg Tyr Asn Val Thr Ala Ile 100 105 110 Pro Lys Leu
Val Ile Val Lys Gln Asn Gly Glu Val Ile Thr Asn Lys 115 120 125 Gly
Arg Lys Gln Ile Arg Glu Arg Gly Leu Ala Cys Phe Gln Asp Trp 130 135
140 Val Glu Ala Ala Asp Ile Phe Gln Asn Phe Ser Val 145 150 155
<210> SEQ ID NO 62 <211> LENGTH: 156 <212> TYPE:
PRT <213> ORGANISM: Bos taurus
<400> SEQUENCE: 62 Met Val Asp Val Leu Gly Gly Arg Arg Leu
Val Thr Cys Asp Gly Ala 1 5 10 15 Trp Val Glu Ala Glu Ala Ala Leu
Gln Asn Lys Val Val Ala Leu Tyr 20 25 30 Phe Ala Ala Gly Arg Cys
Ala Pro Ser Arg Asp Phe Thr Pro Leu Leu 35 40 45 Cys Asp Phe Tyr
Glu Glu Leu Val Asp Asp Ala Arg Pro Pro Ala Pro 50 55 60 Phe Glu
Val Val Phe Val Ser Ala Asp Gly Ser Ala His Glu Met Leu 65 70 75 80
Glu Phe Met Lys Glu Leu His Gly Ala Trp Leu Ala Leu Pro Phe His 85
90 95 Asp Pro Tyr Arg His Glu Leu Arg Thr Arg Tyr His Ile Thr Ala
Ile 100 105 110 Pro Arg Leu Val Ile Leu Lys Pro Ser Gly Glu Val Ile
Thr Asp Lys 115 120 125 Gly Arg Lys Gln Ile Arg Glu Arg Gly Leu Ala
Cys Phe Gln Asn Trp 130 135 140 Val Glu Ala Ala Asp Ile Phe Gln Asn
Phe Ser Ser 145 150 155 <210> SEQ ID NO 63 <211>
LENGTH: 156 <212> TYPE: PRT <213> ORGANISM: Gallus
gallus <400> SEQUENCE: 63 Met Val Asp Val Phe Ser Gly Arg Leu
Leu Val Ser Lys Asp Gly Arg 1 5 10 15 Ser Val Asp Pro Glu Glu Ala
Leu Gln Asn Lys Val Gly Gly Leu Tyr 20 25 30 Phe Ser Ala Gly Trp
Cys Ser Pro Cys Arg Asp Phe Thr Pro Val Leu 35 40 45 Cys Asp Phe
Tyr Thr Asp Leu Leu Glu Glu Cys Gln Pro Pro Ala Pro 50 55 60 Phe
Glu Val Val Phe Ile Ser Ser Asp His Ser Ala Glu Glu Met Val 65 70
75 80 Ser Tyr Met His Ser Met His Gly Asp Trp Leu Ala Leu Pro Phe
His 85 90 95 Asp Pro Tyr Lys His Asp Leu Lys Lys Lys Tyr Asn Ile
Thr Ala Ile 100 105 110 Pro Lys Leu Val Ile Val Lys Gln Thr Gly Glu
Val Ile Thr Asp Lys 115 120 125 Gly Arg Lys Gln Ile Arg Asp Lys Gly
Leu Ser Cys Phe Arg Asn Trp 130 135 140 Leu Glu Gly Ala Asp Ile Phe
Gln Asn Phe Ser Ser 145 150 155 <210> SEQ ID NO 64
<211> LENGTH: 156 <212> TYPE: PRT <213> ORGANISM:
Xenopus laevis <400> SEQUENCE: 64 Met Asp Ile Phe Ser Gly His
Ile Leu Leu Asn Lys Tyr Gly Glu Arg 1 5 10 15 Val Asp Pro Glu Glu
Ala Leu Gln Asn Lys Ile Val Gly Leu Tyr Phe 20 25 30 Ser Ala Ser
Trp Cys Ser Pro Cys Arg Asp Phe Thr Pro Ile Leu Cys 35 40 45 Asp
Phe Tyr Thr Glu Leu Val Glu Glu Ser Glu Pro Pro Ala Gln Phe 50 55
60 Glu Ile Val Phe Ile Ser Ser Asp Lys Ser Pro Glu Glu Met Val Asp
65 70 75 80 Tyr Met His Asp Met Gln Gly Asp Trp Leu Ala Leu Pro Phe
His Asp 85 90 95 Pro Tyr Lys His Glu Leu Lys Asn Lys Tyr Lys Ile
Thr Ala Ile Pro 100 105 110 Lys Leu Val Ile Val Lys Gln Asn Gly Asp
Val Ile Thr Asp Lys Gly 115 120 125 Arg Lys Gln Ile Arg Glu Arg Gly
Leu Ser Cys Phe Arg Thr Trp Leu 130 135 140 Glu Val Gly Asp Val Phe
Gln Asn Phe Thr Gly Lys 145 150 155 <210> SEQ ID NO 65
<211> LENGTH: 156 <212> TYPE: PRT <213> ORGANISM:
Tetraodon nigroviridis <400> SEQUENCE: 65 Met Val Glu Val Phe
Thr Gly Arg Thr Leu Leu Asn Lys Asp Gly Asp 1 5 10 15 Leu Val Asp
Pro Glu Glu Ala Leu Arg Asn Lys Val Val Gly Ile Tyr 20 25 30 Phe
Ser Ala Gly Trp Cys Pro Pro Cys Arg Asp Phe Thr Pro Ile Leu 35 40
45 Cys Asp Phe Tyr Thr Glu Leu Val Glu Glu Ser Asp Pro Pro Ala Gln
50 55 60 Phe Glu Val Val Phe Val Ser Ser Asp Lys Thr Ser Glu Asp
Met Val 65 70 75 80 Glu Tyr Tyr His Asp Leu His Gly Asp Trp Leu Ala
Leu Pro Trp Ser 85 90 95 Asp Asp Tyr Lys Asn Glu Leu Lys Gln Arg
Tyr Lys Ile Thr Ala Val 100 105 110 Pro Lys Leu Val Ile Val Lys Glu
Ser Gly Glu Val Ile Thr Asp Lys 115 120 125 Gly Arg Lys Gln Ile Arg
Asp Arg Gly Leu Ala Cys Phe Arg Ser Trp 130 135 140 Leu Asp Ala Ala
Glu Val Phe Gln Asn Phe Glu Gly 145 150 155 <210> SEQ ID NO
66 <211> LENGTH: 156 <212> TYPE: PRT <213>
ORGANISM: Danio rerio <400> SEQUENCE: 66 Met Val Glu Val Phe
Ser Gly Arg Thr Leu Val Asn Lys Glu Gly Asp 1 5 10 15 Leu Val Glu
Pro Glu Glu Ala Leu Arg Asn Lys Val Val Gly Leu Tyr 20 25 30 Phe
Ser Ala Gly Trp Cys Pro Pro Cys Arg Asp Phe Thr Pro Leu Leu 35 40
45 Cys Asp Phe Tyr Thr Glu Leu Val Glu Glu Thr Glu Pro Pro Ala Gln
50 55 60 Phe Glu Ile Val Phe Ile Ser Ser Asp Lys Ser Thr Glu Asp
Met Val 65 70 75 80 Glu Tyr Tyr His Asp Met His Gly Asp Trp Leu Ala
Leu Pro Trp Thr 85 90 95 Asp Pro Tyr Lys His Glu Leu Lys Lys Arg
Tyr Asn Ile Thr Ala Val 100 105 110 Pro Lys Leu Val Ile Val Lys Glu
Asn Gly Gln Val Ile Thr Asp Lys 115 120 125 Gly Arg Lys Gln Ile Arg
Asp Gln Gly Leu Ala Cys Phe Arg Ser Trp 130 135 140 Ile Glu Val Ala
Glu Ile Phe Gln Asn Phe Lys Gly 145 150 155 <210> SEQ ID NO
67 <211> LENGTH: 217 <212> TYPE: PRT <213>
ORGANISM: Mus musculus <400> SEQUENCE: 67 Met Ala Ser Leu Phe
Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln Asp Glu
Val Glu Thr Glu Ala Glu Leu Ser Arg Arg Leu Glu Asn 20 25 30 Arg
Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln 35 40
45 Ala Phe Ala Pro Val Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu
50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala Leu Val Tyr Val
Ser Gln 65 70 75 80 Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg
Asp Met Pro Glu 85 90 95 Lys Trp Leu Phe Leu Pro Phe His Asp Glu
Leu Arg Arg Asp Leu Gly 100 105 110 Arg Gln Phe Ser Val Arg Gln Leu
Pro Ala Val Val Val Leu Lys Pro 115 120 125 Gly Gly Asp Val Leu Thr
Ser Asp Ala Thr Glu Glu Ile Gln Arg Leu 130 135 140 Gly Pro Ala Cys
Phe Ala Asn Trp Gln Glu Ala Ala Glu Leu Leu Asp 145 150 155 160 Arg
Ser Phe Leu Gln Pro Glu Asp Leu Asp Glu Pro Ala Arg Arg Ser 165 170
175 Ile Thr Glu Pro Leu Arg Arg Arg Lys Tyr Arg Val Asp Arg Asp Val
180 185 190 Gly Arg Glu Arg Gly Arg Asn Gly Arg Asp Ser Gly Asp Pro
Gln Gly 195 200 205 Asp Ala Gly Thr Arg Ala Glu Leu Trp 210 215
<210> SEQ ID NO 68 <211> LENGTH: 109 <212> TYPE:
PRT <213> ORGANISM: Mus musculus <400> SEQUENCE: 68 Met
Ala Ser Leu Phe Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10
15 Gln Asp Glu Val Glu Thr Glu Ala Glu Leu Ser Arg Arg Leu Glu Asn
20 25 30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln
Cys Gln 35 40 45
Ala Phe Ala Pro Val Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu 50
55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala Leu Val Tyr Val Ser
Gln 65 70 75 80 Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg Asp
Met Pro Glu 85 90 95 Lys Trp Leu Phe Leu Pro Phe His Asp Glu Leu
Arg Arg 100 105 <210> SEQ ID NO 69 <211> LENGTH: 576
<212> TYPE: PRT <213> ORGANISM: Rattus norvegicus
<400> SEQUENCE: 69 Met Val Ser Leu Phe Ser Gly Arg Ile Leu
Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln Asp Glu Val Glu Thr Glu Ala
Glu Leu Ser Arg Arg Leu Glu Asn 20 25 30 Arg Leu Val Leu Leu Phe
Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln 35 40 45 Ala Phe Ala Pro
Val Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Leu Arg Ala Ala Gln Leu Ala Leu Val Tyr Val Ser Gln 65 70 75 80
Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg Asp Met Pro Glu 85
90 95 Lys Trp Leu Phe Leu Pro Phe His Asp Asp Leu Arg Arg Asp Leu
Gly 100 105 110 Arg Gln Phe Ser Val Arg Gln Leu Pro Ala Val Val Val
Leu Lys Pro 115 120 125 Gly Gly Asp Val Leu Thr Ser Asp Ala Thr Asp
Glu Ile Gln Arg Leu 130 135 140 Gly Pro Ala Cys Phe Ala Asn Trp Gln
Glu Ala Ala Glu Leu Leu Asp 145 150 155 160 Arg Ser Phe Leu Gln Pro
Glu Asp Leu Asp Glu Pro Ala Arg Arg Ser 165 170 175 Ile Thr Glu Pro
Leu Arg Arg Arg Lys Tyr Arg Val Asp Arg Asp Ala 180 185 190 Gly Arg
Gly Arg Gly Arg Asn Glu Cys Asp Ser Arg Asn Pro Gln Gly 195 200 205
Gly Arg Gly Cys Arg Asp Gly Ala Leu Val Ile Pro Pro Ala Pro Gln 210
215 220 Gly Thr Arg Val His Trp Trp Asn Phe Gly Asp Leu Gln Gly Asn
Ser 225 230 235 240 Gly Leu Gly Ile Gly Val Gln Leu Arg Val Gln Pro
Val Gly Ala Tyr 245 250 255 Ala Pro Gln Leu Arg Ala Pro Cys Leu Glu
Leu Glu Gln Gln Leu Arg 260 265 270 Ser Gln Arg Asp Gln His Arg Gly
Arg Asp Ala Gln Lys Gly His Arg 275 280 285 Gly Gln Tyr Pro Ala Ser
Ala Cys Ala Met Gly Arg Ser Tyr Gly Gly 290 295 300 Arg Val Leu Ala
Ala Met Thr Leu Leu Gly Ile Pro Ala Ala Val Leu 305 310 315 320 Val
Ala Leu Ala Ala Gln Leu Leu Phe Gln Leu Gln Ala Gly Arg Ala 325 330
335 Glu Leu Arg Gly Ile Arg Thr Asp Gly Leu His Pro Glu Leu Asp Pro
340 345 350 Asp Ala Gly Leu Pro Glu Ala Ala Ala Gly Ala Leu Leu Pro
Leu Ala 355 360 365 Thr Ala Leu Ala Ala Leu Ala Gln Val Leu Gly Leu
Gly Cys Leu Leu 370 375 380 Leu Ala Ala Leu Cys Gly His Leu Gly Ala
Glu Leu Ala Arg Gly Pro 385 390 395 400 Gly Pro Gly Arg Leu Thr Leu
Asn Val Trp Ser Cys Phe Asn Leu Pro 405 410 415 Asn Leu Gly Arg Arg
Ala Leu Ala Ile Tyr Ala Leu Leu Leu Phe Glu 420 425 430 Ile Glu Ala
Gly Ala Ala Ala Ala Ser Ile Leu Gly Ser Gly Ala Leu 435 440 445 Ile
Leu Val Ala Ile Met Thr His Thr Leu Phe Arg Ala Val Gln Ala 450 455
460 Thr Arg Arg Gly Leu Arg Glu Leu Pro Pro Pro Ser Ser Glu Asp Glu
465 470 475 480 Pro Ala Arg Ser Ser Glu Asp Ser Lys Ala Gly Cys Arg
Ala Gln Pro 485 490 495 Gln Gln Gly Thr His Cys Gln Ile Phe Tyr Asn
Pro Ser Gln Glu Leu 500 505 510 Gly Asp Pro Pro Gly Ser Met Ala Thr
Cys Ile Thr Ser Ala Val Leu 515 520 525 Glu Arg Ala Ser Glu Ser Ser
Leu Leu Ala Ser His Leu Pro Gln Thr 530 535 540 Leu Arg Ser Met Gly
Pro Trp Asp Gly Val Thr Tyr Glu Met His Gly 545 550 555 560 Met Leu
Gly His Arg Pro Pro Asp Met Gly Lys Asp Ala Thr Leu Val 565 570 575
<210> SEQ ID NO 70 <211> LENGTH: 212 <212> TYPE:
PRT <213> ORGANISM: Homo sapiens <400> SEQUENCE: 70 Met
Ala Ser Leu Phe Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10
15 Gln Asp Glu Leu Asp Thr Glu Ala Glu Val Ser Arg Arg Leu Glu Asn
20 25 30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln
Cys Gln 35 40 45 Ala Phe Val Pro Ile Leu Lys Asp Phe Phe Val Arg
Leu Thr Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala
Leu Val Tyr Val Ser Gln 65 70 75 80 Asp Ser Thr Glu Glu Gln Gln Asp
Leu Phe Leu Lys Asp Met Pro Lys 85 90 95 Lys Trp Leu Phe Leu Pro
Phe Glu Asp Asp Leu Arg Arg Asp Leu Gly 100 105 110 Arg Gln Phe Ser
Val Glu Arg Leu Pro Ala Val Val Val Leu Lys Pro 115 120 125 Asp Gly
Asp Val Leu Thr Arg Asp Gly Ala Asp Glu Ile Gln Arg Leu 130 135 140
Gly Thr Ala Cys Phe Ala Asn Trp Gln Glu Ala Ala Glu Val Leu Asp 145
150 155 160 Arg Asn Phe Gln Leu Pro Glu Asp Leu Glu Asp Gln Glu Pro
Arg Ser 165 170 175 Leu Thr Glu Cys Leu Arg Arg His Lys Tyr Arg Val
Glu Lys Ala Ala 180 185 190 Arg Gly Gly Arg Asp Pro Gly Gly Gly Gly
Gly Glu Glu Gly Gly Ala 195 200 205 Gly Gly Leu Phe 210 <210>
SEQ ID NO 71 <211> LENGTH: 202 <212> TYPE: PRT
<213> ORGANISM: Pan troglodytes <220> FEATURE:
<221> NAME/KEY: misc_feature <222> LOCATION:
(168)..(201) <223> OTHER INFORMATION: Xaa can be any
naturally occurring amino acid <400> SEQUENCE: 71 Met Ala Ser
Leu Phe Ser Gly Arg Ile Leu Ile Arg Asn Asn Ser Asp 1 5 10 15 Gln
Asp Glu Leu Asp Thr Glu Ala Glu Val Ser Arg Arg Leu Glu Asn 20 25
30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ala Cys Pro Gln Cys Gln
35 40 45 Ala Phe Val Pro Ile Leu Lys Asp Phe Phe Val Arg Leu Thr
Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu Ala Leu Val
Tyr Val Ser Gln 65 70 75 80 Asp Ser Thr Glu Glu Gln Gln Asp Leu Phe
Leu Lys Asp Met Pro Lys 85 90 95 Lys Trp Leu Phe Leu Pro Phe Glu
Asp Asp Leu Arg Arg Asp Leu Gly 100 105 110 Arg Gln Phe Ser Val Glu
Arg Leu Pro Ala Val Val Val Leu Lys Pro 115 120 125 Asp Gly Asp Val
Leu Thr Arg Asp Gly Ala Asp Glu Ile Gln Arg Leu 130 135 140 Gly Thr
Ala Cys Phe Ala Asn Trp Gln Glu Ala Ala Glu Val Leu Asp 145 150 155
160 Arg Asn Phe Gln Leu Pro Glu Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa
165 170 175 Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa
Xaa Xaa 180 185 190 Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Xaa Ala 195 200
<210> SEQ ID NO 72 <211> LENGTH: 218 <212> TYPE:
PRT <213> ORGANISM: Canis familiaris <400> SEQUENCE: 72
Met Ala Ser Leu Phe Ser Gly Arg Val Leu Ile Arg Asn Asn Ser Asp 1 5
10 15 Gln Asp Glu Leu Asp Thr Glu Ala Glu Leu Ser Arg Arg Leu Glu
Asn 20 25 30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ser Cys Pro
Gln Cys Gln 35 40 45 Ala Phe Ala Pro Ile Leu Arg Asp Phe Phe Val
Arg Leu Thr Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Leu
Ala Leu Val Tyr Val Ser Gln
65 70 75 80 Asp Pro Thr Glu Glu Gln Gln Asp Leu Phe Leu Arg Asp Met
Pro Lys 85 90 95 Lys Trp Leu Phe Leu Pro Phe Glu Asp Asp Leu Arg
Arg Asp Leu Gly 100 105 110 Arg Arg Phe Ser Val Glu Arg Leu Pro Ala
Val Val Val Leu Lys Pro 115 120 125 Gly Gly Asp Val Leu Ser Arg Asp
Ala Thr Asp Glu Ile Arg Arg Leu 130 135 140 Gly Pro Ala Cys Phe Ala
Asn Trp Gln Glu Ala Ala Glu Val Leu Asp 145 150 155 160 Arg Asn Phe
Leu Gln Pro Glu Asp Leu Asp Asp Pro Ala Pro Arg Ser 165 170 175 Leu
Thr Glu Pro Leu Arg Arg Cys Lys Tyr Arg Val Asp Arg Glu Ala 180 185
190 Arg Gly Lys Arg Gly Pro Gly Gly Gly Ser Gln Pro Glu Gly Gly Arg
195 200 205 Gly Ala Glu Gly Gly Ala Gly Asp Leu Phe 210 215
<210> SEQ ID NO 73 <211> LENGTH: 218 <212> TYPE:
PRT <213> ORGANISM: Bos taurus <400> SEQUENCE: 73 Met
Ala Ser Leu Phe Ser Gly Arg Val Leu Ile Arg Asn Asn Ser Asp 1 5 10
15 Gln Asp Glu Leu Asp Thr Glu Ala Glu Leu Ser Arg Arg Leu Glu Asn
20 25 30 Arg Leu Val Leu Leu Phe Phe Gly Ala Gly Ser Cys Pro Glu
Cys Gln 35 40 45 Ala Phe Ala Pro Ile Leu Arg Asp Phe Phe Val Arg
Leu Thr Asp Glu 50 55 60 Phe Tyr Val Leu Arg Ala Ala Gln Val Ala
Leu Val Tyr Val Ser Gln 65 70 75 80 Asp Pro Thr Glu Glu Gln Gln Asp
Leu Phe Leu Arg Asp Met Pro Glu 85 90 95 Lys Trp Leu Phe Leu Pro
Phe Glu Asp Asp Leu Arg Arg Asp Leu Gly 100 105 110 Arg Gln Phe Ser
Val Glu Arg Leu Pro Ala Val Val Val Leu Lys Pro 115 120 125 Ser Gly
Asp Val Leu Thr Leu Asp Ala Ala Asp Glu Ile Arg Arg Leu 130 135 140
Gly Pro Ala Cys Phe Ala Asn Trp Gln Glu Ala Ala Glu Val Leu Asp 145
150 155 160 Arg Ser Phe Leu Gln Pro Glu Asp Leu Asp Asp Pro Ala Pro
Arg Ser 165 170 175 Leu Thr Glu Pro Leu Arg Arg Cys Lys Tyr Arg Val
Asp Pro Ala Ala 180 185 190 Arg Arg Ala Arg Gly Arg Gly Arg Ala Gly
Gly Ser Gly Gln Glu Gly 195 200 205 Glu Ala Glu Gly Glu Ala Ala Gly
Leu Phe 210 215 <210> SEQ ID NO 74 <211> LENGTH: 207
<212> TYPE: PRT <213> ORGANISM: Gallus gallus
<400> SEQUENCE: 74 Met Ala Ser Leu Phe Ala Gly Lys Val Leu
Ile Val Asn Asn Arg Asp 1 5 10 15 Arg Asp Glu Val Glu Thr Glu Arg
Glu Arg Cys Ser Ala Leu Glu Asn 20 25 30 Arg Val Met Leu Leu Tyr
Phe Gly Ala Ala Glu Cys Pro Arg Cys Gln 35 40 45 Ser Phe Ala Pro
Arg Leu Lys Asp Phe Phe Val Arg Leu Thr Asp Glu 50 55 60 Phe Tyr
Val Glu Arg Ala Ser Gln Leu Cys Leu Val Tyr Val Ser Arg 65 70 75 80
Asp Ala Thr Ala Gln Gln Glu Glu Ala Phe Leu Arg Ser Met Pro Arg 85
90 95 Arg Trp Leu Ser Leu Pro Phe Arg Asp Glu Phe Lys Arg Glu Leu
Glu 100 105 110 Leu Arg Phe Val Val Ser Glu Val Pro Arg Val Val Val
Leu Lys Pro 115 120 125 Asn Gly Asp Val Ile Val Gly Asn Ala Val Asp
Glu Ile Thr Ser Met 130 135 140 Gly Pro Ala Cys Phe Gln Asn Trp Gln
Glu Ala Ala Glu Leu Val Asp 145 150 155 160 Arg Asn Phe Arg Leu Ala
Glu Asp Phe Asp Glu Cys Ala Arg Arg Ser 165 170 175 Ile Thr Asp Pro
Leu Arg Arg Leu Lys Tyr Lys Leu Gly Lys Gly Glu 180 185 190 Glu Pro
Arg Ser Glu Glu Gln Lys Glu Asp Gly Asp Glu Ser Ser 195 200 205
<210> SEQ ID NO 75 <211> LENGTH: 215 <212> TYPE:
PRT <213> ORGANISM: Xenopus laevis <400> SEQUENCE: 75
Met Ala Asp Leu Phe Leu Asp Lys Ile Leu Val Lys Asn Asn Arg Asp 1 5
10 15 Gln Asp Glu Leu Asp Thr Glu Arg Glu Ile Trp Glu Arg Leu Glu
Asn 20 25 30 Arg Val Ile Leu Leu Phe Phe Ala Lys Ser Arg Ser Ser
Gln Cys Gln 35 40 45 Glu Phe Ala Pro Leu Leu Lys Asp Phe Phe Val
Arg Leu Thr Asp Glu 50 55 60 Phe Tyr Val Asp Arg Ser Ser Gln Leu
Ala Leu Val Tyr Val Ser Leu 65 70 75 80 Asp Gln Ser Glu Glu Glu Gln
Glu Arg Phe Leu Lys Asp Met Pro Lys 85 90 95 Arg Trp Leu Phe Val
Pro Phe Lys Asp Glu Glu Phe Arg Arg Asn Leu 100 105 110 Glu Ala Gln
Phe Ser Val Ser Arg Val Pro Val Leu Val Val Leu Lys 115 120 125 Pro
Ser Gly His Val Ile Ser Phe Asn Ala Val Asp Glu Val Val Arg 130 135
140 Leu Gly Pro Pro Cys Phe Lys Asn Trp Gln Glu Val Ser Glu Ile Ile
145 150 155 160 Asp Arg Ser Phe Leu Leu Pro Glu Phe Thr Asp Asp Arg
Ala Gly Arg 165 170 175 Ser Met Thr Asp Pro Ile Arg Arg Ile Lys Tyr
Lys Asp Glu Thr Thr 180 185 190 Asn Glu Lys Lys Lys Arg Lys His Cys
Asp Asp Glu Asp Glu Gly Gly 195 200 205 Gly Gly Gly Thr Glu Phe Phe
210 215 <210> SEQ ID NO 76 <211> LENGTH: 180
<212> TYPE: PRT <213> ORGANISM: Tetraodon nigroviridis
<400> SEQUENCE: 76 Met Val Asp Leu Phe Leu Asn Arg Val Leu
Val Glu Asn Asn Trp Asp 1 5 10 15 Gln Asp Gln Leu Asn Thr Glu Arg
Glu Ile Val Gly Ile Leu Glu Asn 20 25 30 Arg Ile Leu Leu Leu Phe
Phe Ala Ser Ala Ser Cys Gln Lys Cys Gln 35 40 45 Asp Phe Leu Pro
Ile Leu Asn Asn Phe Phe Lys Arg Leu Lys Asp Pro 50 55 60 Ala His
Ile Glu Tyr Pro Lys Leu Leu Ala Leu Ile Phe Ile Ser Leu 65 70 75 80
Asp Gln Ser Glu Glu Gln Gln Glu Arg Phe Leu Lys Glu Leu His Lys 85
90 95 Lys Val Leu Phe Leu Ala Phe Asp Asp Pro Tyr Arg Gln Glu Leu
Gln 100 105 110 Ala Met Phe Glu Val Lys Glu Leu Pro Thr Val Val Val
Leu Arg Pro 115 120 125 Asp Gly Ser Val Leu Ala Ala Asn Ala Ala Gln
Asp Ile Cys Ser Tyr 130 135 140 Gly Ser Glu Cys Phe Arg Asp Trp Gln
Glu Ser Ala Glu Leu Ile Glu 145 150 155 160 Arg Thr Phe Met Leu Asn
Glu Glu Phe Asp Asn Leu Asn Leu Arg Thr 165 170 175 Ser Ala Thr Pro
180 <210> SEQ ID NO 77 <211> LENGTH: 169 <212>
TYPE: PRT <213> ORGANISM: Tetraodon nigroviridis <400>
SEQUENCE: 77 Met Val Asp Leu Phe Ile Asp Arg Val Leu Leu Lys Asn
Asn Ser Glu 1 5 10 15 Arg Asp Glu Leu Asp Thr Glu Arg Glu Ile Val
Ala Arg Leu Gln Asn 20 25 30 Arg Ile Leu Leu Leu Phe Phe Gly Cys
Val Val Ser Arg Ser Cys Gln 35 40 45 Leu Phe Ala Pro Lys Leu Ser
Ser Phe Phe Lys Gln Leu Thr Asp Glu 50 55 60 Ala Tyr Val Asp Arg
Ser Ala Gln Leu Val Leu Leu Tyr Ile Ser Met 65 70 75 80 Asp Gln Ser
Glu Gln Gln Leu Ser Ser Phe Leu Gln Glu Leu Pro Lys 85 90 95 Lys
Cys Leu Phe Leu Ala Phe Glu Asp Pro Phe Arg Arg Glu Leu Glu 100 105
110 Ala Met Phe Asn Val Glu Glu Leu Pro Thr Val Val Val Leu Arg Pro
115 120 125
Asp Cys Ser Val Leu Ala Ala Asn Ala Val Glu Glu Ile Leu Arg Leu 130
135 140 Gly Pro Asp Cys Tyr Arg Asn Trp Gln Glu Ala Ala Glu Leu Tyr
Arg 145 150 155 160 Gln Glu Leu Pro Asp Gln Arg Arg Leu 165
<210> SEQ ID NO 78 <211> LENGTH: 215 <212> TYPE:
PRT <213> ORGANISM: Danio rerio <400> SEQUENCE: 78 Met
Val Asp Leu Phe Leu Gly Lys Val Leu Val Lys Asn Asn Lys Asp 1 5 10
15 Arg Asp Glu Leu Asp Thr Glu Arg Glu Ile Ile Leu Arg Leu Gln Asn
20 25 30 Arg Ile Leu Met Leu Phe Phe Gly Ser Gly Asp Ser Glu Lys
Cys Gln 35 40 45 Asp Phe Ala Pro Thr Leu Lys Asp Phe Tyr Lys Lys
Leu Thr Asp Glu 50 55 60 Phe Tyr Val Glu Arg Ser Ala Gln Leu Val
Leu Leu Tyr Ile Ser Leu 65 70 75 80 Asp Ser Ser Glu Glu Gln Gln Glu
Lys Phe Leu Lys Glu Leu Pro Lys 85 90 95 Arg Cys Leu Phe Leu Pro
Tyr Glu Asp Pro Tyr Arg Gln Glu Leu Gly 100 105 110 Val Met Phe Glu
Val Arg Asp Leu Pro Arg Val Val Val Leu Arg Pro 115 120 125 Asp Cys
Ser Val Leu Ser Pro Asn Ala Val Ser Glu Ile Cys Thr Leu 130 135 140
Gly Thr Asp Cys Phe Arg Asn Trp Gln Glu Gly Ala Glu Leu Ile Asp 145
150 155 160 Arg Asn Phe Met Met Asn Glu Glu Phe Asp Glu Gly Lys Met
Arg Ser 165 170 175 Met Thr Asp Pro Ile Arg Arg Ile Lys Tyr Lys Val
Glu Asp Glu Lys 180 185 190 Lys Lys Lys Lys Lys Arg Asp Asp Asp Asp
Asp Asp Asp Asp Gly Gly 195 200 205 Gly Gly Gly Gly Pro Trp Gly 210
215
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