U.S. patent application number 11/471278 was filed with the patent office on 2008-02-14 for methods of detecting nucleic acids in individual cells and of identifying rare cells from large heterogeneous cell populations.
Invention is credited to Shiping Chen, Yuling Luo.
Application Number | 20080038725 11/471278 |
Document ID | / |
Family ID | 37595717 |
Filed Date | 2008-02-14 |
United States Patent
Application |
20080038725 |
Kind Code |
A1 |
Luo; Yuling ; et
al. |
February 14, 2008 |
Methods of detecting nucleic acids in individual cells and of
identifying rare cells from large heterogeneous cell
populations
Abstract
Methods of detecting multiple nucleic acid targets in single
cells through indirect capture of labels to the nucleic acids are
provided. Methods of assaying the relative levels of nucleic acid
targets through normalization to levels of reference nucleic acids
are also provided. Methods of detecting individual cells,
particularly rare cells from large heterogeneous cell populations,
through detection of nucleic acids are described. Related
compositions, systems, and kits are also provided.
Inventors: |
Luo; Yuling; (San Ramon,
CA) ; Chen; Shiping; (Fremont, CA) |
Correspondence
Address: |
QUINE INTELLECTUAL PROPERTY LAW GROUP, P.C.
P O BOX 458
ALAMEDA
CA
94501
US
|
Family ID: |
37595717 |
Appl. No.: |
11/471278 |
Filed: |
June 19, 2006 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
60691834 |
Jun 20, 2005 |
|
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|
Current U.S.
Class: |
435/6.16 |
Current CPC
Class: |
C12Q 1/6837 20130101;
C12Q 1/6841 20130101; C12Q 1/682 20130101; C12Q 1/6841 20130101;
C12Q 2537/143 20130101; C12Q 2537/125 20130101; C12Q 1/682
20130101; C12Q 2565/543 20130101; C12Q 2537/125 20130101; C12Q
2525/313 20130101; C12Q 1/6837 20130101; C12Q 2565/543 20130101;
C12Q 2537/125 20130101; C12Q 2525/313 20130101 |
Class at
Publication: |
435/6 |
International
Class: |
C12Q 1/68 20060101
C12Q001/68 |
Claims
1. A method of detecting two or more nucleic acid targets in an
individual cell, the method comprising: providing a sample
comprising the cell, which cell comprises or is suspected of
comprising a first nucleic acid target and a second nucleic acid
target; providing a first label probe comprising a first label and
providing a second label probe comprising a second label, wherein a
first signal from the first label is distinguishable from a second
signal from the second label; providing at least a first capture
probe and at least a second capture probe; hybridizing, in the
cell, the first capture probe to the first nucleic acid target,
when present in the cell, and the second capture probe to the
second nucleic acid target, when present in the cell; capturing the
first label probe to the first capture probe and the second label
probe to the second capture probe, thereby capturing the first
label probe to the first nucleic acid target and the second label
probe to the second nucleic acid target; and detecting the first
signal from the first label and the second signal from the second
label.
2-4. (canceled)
5. The method of claim 1, wherein providing at least a first
capture probe comprises providing two or more first capture probes;
wherein providing at least a second capture probe comprises
providing two or more second capture probes; wherein providing a
first label probe and a second label probe comprises providing a
plurality of the first label probes and a plurality of the second
label probes; wherein hybridizing the first capture probe to the
first nucleic acid target and the second capture probe to the
second nucleic acid target comprises hybridizing the two or more
first capture probes to the first nucleic acid target and the two
or more second capture probes to the second nucleic acid target;
wherein capturing the first label probe to the first capture probe
comprises hybridizing a first amplifier to each of the first
capture probes and hybridizing the plurality of first label probes
to the first amplifiers; and wherein capturing the second label
probe to the second capture probe comprises hybridizing a second
amplifier to each of the second capture probes and hybridizing the
plurality of second label probes to the second amplifiers.
6. (canceled)
7. The method of claim 1, wherein providing at least a first
capture probe comprises providing two or more first capture probes;
wherein providing at least a second capture probe comprises
providing two or more second capture probes; wherein providing a
first label probe and a second label probe comprises providing a
plurality of the first label probes and a plurality of the second
label probes; wherein hybridizing the first capture probe to the
first nucleic acid target and the second capture probe to the
second nucleic acid target comprises hybridizing the two or more
first capture probes to the first nucleic acid target and the two
or more second capture probes to the second nucleic acid target;
wherein capturing the first label probe to the first capture probe
comprises hybridizing a first preamplifier to each of the first
capture probes, hybridizing a plurality of first amplifiers to each
of the first preamplifiers, and hybridizing the plurality of first
label probes to the first amplifiers; and wherein capturing the
second label probe to the second capture probe comprises
hybridizing a second preamplifier to each of the second capture
probes, hybridizing a plurality of second amplifiers to each of the
second preamplifiers, and hybridizing the plurality of second label
probes to the second amplifiers.
8-9. (canceled)
10. The method of claim 1, wherein the cell comprises or is
suspected of comprising a third nucleic acid target; the method
comprising: providing a third label probe comprising a third label,
wherein a third signal from the third label is distinguishable from
the first and second signals, providing at least a third capture
probe, hybridizing in the cell the third capture probe to the third
nucleic acid target, when present in the cell, capturing the third
label probe to the third capture probe, and detecting the third
signal from the third label.
11. The method of claim 1, wherein each hybridization or capture
step is accomplished for all of the nucleic acid targets at the
same time.
12. The method of claim 1, wherein the first nucleic acid target
and the second nucleic acid target are independently selected from
the group consisting of: a DNA, an RNA, a chromosomal DNA, an mRNA,
a nucleic acid endogenous to the cell, and a nucleic acid
introduced to or expressed in the cell by infection of the cell
with a pathogen.
13. The method of claim 1, wherein the first nucleic acid target is
a first mRNA and wherein the second nucleic acid target is a second
mRNA.
14. The method of claim 1, wherein the first nucleic acid target
comprises a first chromosomal DNA polynucleotide sequence and
wherein the second nucleic acid target comprises a second
chromosomal DNA polynucleotide sequence.
15. The method of claim 1, wherein the first nucleic acid target
comprises a first region of an mRNA and wherein the second nucleic
acid target comprises a second region of the same mRNA.
16. The method of claim 1, wherein the second nucleic acid target
comprises a reference nucleic acid; the method comprising
normalizing the first signal to the second signal.
17. (canceled)
18. The method of claim 1, wherein detecting the first signal and
the second signal comprises measuring an intensity of the first
signal and an intensity of the second signal; the method comprising
correlating the intensity of the first signal and the second signal
with a quantity of the corresponding nucleic acid target present in
the cell.
19. The method of claim 1, wherein the cell is a circulating tumor
cell.
20. The method of claim 1, wherein the sample comprising the cell
is derived from a bodily fluid or from blood.
21. The method of claim 1, the method comprising identifying the
cell as a desired target cell based on detection of the first and
second signals from within the cell.
22-24. (canceled)
25. The method of claim 1, wherein the cell is in suspension in the
sample comprising the cell, and/or wherein the cell is in
suspension during the hybridizing, capturing, and/or detecting
steps.
26-27. (canceled)
28. A method of assaying a relative level of one or more target
nucleic acids in an individual cell, the method comprising:
providing a sample comprising the cell, which cell comprises or is
suspected of comprising a first, target nucleic acid, and which
cell comprises a second, reference nucleic acid; providing a first
label probe comprising a first label and providing a second label
probe comprising a second label, wherein a first signal from the
first label is distinguishable from a second signal from the second
label; capturing, in the cell, the first label probe to the first,
target nucleic acid, when present in the cell, and the second label
probe to the second, reference nucleic acid; detecting the first
signal from the first label and the second signal from the second
label in the individual cell, wherein detecting the first signal
and the second signal comprises measuring an intensity of the first
signal and an intensity of the second signal; and normalizing the
intensity of the first signal to the intensity of the second
signal.
29-46. (canceled)
47. A method of detecting an individual cell of a specified type,
the method comprising: providing a sample comprising a mixture of
cell types, which mixture comprises at least one cell of the
specified type; providing a first label probe comprising a first
label and providing a second label probe comprising a second label,
wherein a first signal from the first label is distinguishable from
a second signal from the second label; capturing, in the cell, the
first label probe to a first nucleic acid target, when present in
the cell, and the second label probe to a second nucleic acid
target, when present in the cell; detecting the first signal from
the first label and the second signal from the second label;
correlating the first and second signals detected from the cell
with the presence, absence, or amount of the first and second
nucleic acid targets in the cell; and identifying the cell as being
of the specified type based on detection of the presence, absence,
or amount of both the first and second nucleic acid targets within
the cell, wherein the specified type of cell is distinguishable
from the other cell type(s) in the mixture on the basis of either
the presence, absence, or amount of the first nucleic acid target
or the presence, absence, or amount of the second nucleic acid
target in the cell.
48-69. (canceled)
70. A composition, comprising: a fixed and permeabilized cell,
which cell comprises or is suspected of comprising a first nucleic
acid target and a second nucleic acid target; at least a first
capture probe capable of hybridizing to the first nucleic acid
target; at least a second capture probe capable of hybridizing to
the second nucleic acid target; and a first label probe comprising
a first label and a second label probe comprising a second label,
wherein a first signal from the first label is distinguishable from
a second signal from the second label.
71-89. (canceled)
90. A kit for detecting a first nucleic acid target and a second
nucleic acid target in an individual cell, comprising: at least one
reagent for fixing and/or permeabilizing the cell; at least a first
capture probe capable of hybridizing to the first nucleic acid
target; at least a second capture probe capable of hybridizing to
the second nucleic acid target; and a first label probe comprising
a first label and a second label probe comprising a second label,
wherein a first signal from the first label is distinguishable from
a second signal from the second label; packaged in one or more
containers.
91. A kit for detecting an individual cell of a specified type from
a mixture of cell types by detecting a first nucleic acid target
and a second nucleic acid target, the kit comprising: at least one
reagent for fixing and/or permeabilizing the cell; a first label
probe comprising a first label and a second label probe comprising
a second label, wherein a first signal from the first label is
distinguishable from a second signal from the second label; wherein
the specified type of cell is distinguishable from the other cell
type(s) in the mixture by presence, absence, or amount of the first
nucleic acid target in the cell or by presence, absence, or amount
of the second nucleic acid target in the cell; packaged in one or
more containers.
92. A method of detecting two or more nucleic acid targets in an
individual cell, the method comprising: providing a sample
comprising the cell, which cell comprises or is suspected of
comprising a first nucleic acid target and a second nucleic acid
target; capturing, in the cell, a first label to the first nucleic
acid target, when present in the cell, and a second label to the
second nucleic acid target, when present in the cell, wherein a
first signal from the first label is distinguishable from a second
signal from the second label, wherein an average of at least one
copy of the first label per nucleotide of the first nucleic acid
target is captured to the first nucleic acid target over a region
that spans at least 20 contiguous nucleotides of the first nucleic
acid target, and wherein an average of at least one copy of the
second label per nucleotide of the second nucleic acid target is
captured to the second nucleic acid target over a region that spans
at least 20 contiguous nucleotides of the second nucleic acid
target; and detecting the first signal from the first label and the
second signal from the second label.
93-94. (canceled)
95. A composition comprising: a cell, which cell comprises: a first
nucleic acid target; a second nucleic acid target; a first label
whose presence in the cell is indicative of the presence of the
first nucleic acid target in the cell, wherein an average of at
least one copy of the first label is present in the cell per
nucleotide of the first nucleic acid target over a region that
spans at least 20 contiguous nucleotides of the first nucleic acid
target; and a second label whose presence in the cell is indicative
of the presence of the second nucleic acid target in the cell,
wherein an average of at least one copy of the second label is
present in the cell per nucleotide of the second nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the second nucleic acid target; wherein a first signal from the
first label is distinguishable from a second signal from the second
label.
96. (canceled)
97. A method of performing comparative gene expression analysis in
single cells, the method comprising: providing a first mixed cell
population comprising one or more cells of a specified type;
providing a second mixed cell population comprising one or more
cells of the specified type; measuring an expression level of one
or more target nucleic acids relative to a reference nucleic acid
in the cells of the specified type of the first population, to
provide a first expression profile; measuring an expression level
of the one or more target nucleic acids relative to the reference
nucleic acid in the cells of the specified type of the second
population, to provide a second expression profile; and comparing
the first and second expression profiles.
98. A method of detecting one or more nucleic acid targets in an
individual cell, the method comprising: providing a sample
comprising the cell, which cell comprises or is suspected of
comprising a first nucleic acid target; providing a first label
probe comprising a first label; providing at least a first capture
probe; hybridizing, in the cell, the first capture probe to the
first nucleic acid target, when present in the cell; capturing the
first label probe to the first capture probe, thereby capturing the
first label probe to the first nucleic acid target; and detecting,
while the cell is in suspension, a first signal from the first
label.
99. A method as taught in the specification or figures.
100. A composition as taught in the specification or figures.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a non-provisional utility patent
application claiming priority to and benefit of the following prior
provisional patent application: U.S. Ser. No. 60/691,834, filed
Jun. 20, 2005, entitled "Method of Detecting and Enumerating Rare
Cells from Large Heterogeneous Cell Populations" by Luo and Chen,
which is incorporated herein by reference in its entirety for all
purposes.
FIELD OF THE INVENTION
[0002] The invention relates generally to nucleic acid chemistry
and biochemical assays. More particularly, the invention relates to
methods for in situ detection of nucleic acid analytes in single
cells. The invention also relates to detection and identification
of single cells, particularly rare cells.
BACKGROUND OF THE INVENTION
[0003] Ample evidence has demonstrated that cancer cells can
dissociate from the primary tumor and circulate in the lymph node,
bone marrow, peripheral blood or other body fluids. These
circulating tumor cells (CTC) have been shown to reflect the
biological characteristics of the primary tumors, including the
potential for metastasis development and tumor recurrence.
Therefore, the detection of CTC may indicate disease recurrence,
tumor cell spreading, and a high potential for distant metastasis.
All of these are significant informative clinical factors in
identifying high-risk cancer patients' disease status (e.g. Vogel
et al., 2002; Gilbey et al., 2004; Molnar et al., 2003; Vlems et
al., 2003; Ma et al., 2003).
[0004] Validation of the clinical utility of CTC detection as a
prognostic indicator has not been progressing as fast as expected,
in large part due to lack of suitable detection technologies. One
key difficulty in detecting CTC in peripheral blood or other body
fluids is that CTC are present in the circulation in extremely low
concentrations, estimated to be in the range of one tumor cell
among 10.sup.6-10.sup.7 normal white blood cells. As a result, any
detection technology for this application has to exhibit
exceptional sensitivity and specificity in order to limit both
false negative and false positive rate to an acceptable level.
[0005] One existing approach incorporates immunomagnetic separation
technology in detection of intact CTC (U.S. Pat. No. 6,365,362;
U.S. Pat. No. 6,645,731). Using this technology, a blood sample
from a cancer patient is incubated with magnetic beads coated with
antibodies directed against an epithelial surface antigen as for
example EpCAM (Cristofanilli et al., 2004). The magnetically
labeled cells are then isolated using a magnetic separator. The
immunomagnetically-enriched fraction is further processed for
downstream analysis for CTC identification. Using this technology,
it was shown in a prospective study that the number of CTC after
treatment is an independent predictor of progression-free survival
and overall survival in patients with metastatic breast cancer
(Cristofanilli et al., 2004). Although this technology has reported
high sensitivity, its applicability is limited by the availability
of detection antibodies that are highly sensitive and specific to
particular types of CTC. The antibodies can exhibit non-specific
binding to other cellular components which can lead to low signal
to noise ratio and impair later detection. The antibodies binding
to CTC may also bind to antigen present in other types of cells at
low level, resulting in a high level of false positives.
[0006] Another approach for determining the presence of CTC has
been to test for the tumor cell specific expression of messenger
RNA in blood. Real time reverse transcription-polymerase chain
reaction (QPCR) has been used to correlate the detection of CTC
with patient prognosis. Real-time RT-PCR has been used for
detecting CEA mRNA in peripheral blood of colorectal cancer
patients (Ito et al., 2002). Disease free survival of patients with
positive CEA mRNA in post-operative blood was significantly shorter
than in cases that were negative for CEA mRNA. These results
suggest that tumor cells were shed into the bloodstream and
resulted in poor patient outcomes in patients with colorectal
cancer. Another report demonstrated the clinical utility of
molecular detection of CTC in high-risk AJCC stage IIBC and IIIAB
melanoma patients using multiple mRNA markers by QPCR (Mocellin et
al., 2004). The advantage of detecting tumor specific mRNA
expression is that any tumor-specific gene can be used to serve as
a diagnostic/prognostic marker. However, the QPCR approach requires
the laborious procedure of mRNA isolation from the blood sample and
reverse transcription before the PCR reaction. False positives are
often observed using this technique due to sample contamination by
chromosomal DNA or low-level expression of the chosen marker gene
in normal blood cells (Fava et al. 2001). In addition, the limit of
detection sensitivity of this technique is at most about one tumor
cell per 1 ml of blood, and the technology cannot provide an
accurate count of CTC numbers.
[0007] It is highly desirable to detect and quantitate tumor cell
specific mRNA expression at a single cell level in blood or other
body fluids. A technology that can detect expression of multiple
specific mRNAs in individual cells in suspension would allow both
sensitive and specific detection and enumeration of CTC in blood or
other body fluids. In addition, such technology could enable the
collection of CTC cells for downstream cytological and molecular
analysis. Currently available techniques do not fulfill these
needs.
[0008] In situ hybridization (ISH) technology is an established
method of localizing and detecting specific mRNA sequences in
morphologically preserved tissue sections or cell preparations
(Hicks et al., 2004). The most common specimens used are frozen
sections, paraffin embedded sections or suspension cells that were
cytospun onto glass slides and fixed with methanol. Detection is
carried out using nucleic acid probes that are complementary to and
hybridize with specific nucleotide sequences within cells and
tissues. The sensitivity of the technique is such that threshold
levels of detection are in the range of 10-20 copies of mRNA per
cell.
[0009] However, ISH technology faces a number of technical
challenges that limit its wide use. First of all, cells immobilized
on solid surface exhibit poor hybridization kinetics. Secondly,
assay optimization is generally required for a target mRNA in probe
selection, labeling, and detection, for each tissue section in
fixation and permeabilization, and in hybridization and washing. In
addition, various experiments need to be performed to control for
the specificity of the probe, for tissue mRNA quality, and for the
hybridization efficacy of the experimental procedure. In addition
to technical issues, current ISH technology has relatively low
performance standards in term of its detection sensitivity and
reproducibility. The false positive rate is still high unless the
relevant cells are re-examined manually using their morphology,
which is time and labor-intensive. Current ISH technology also does
not have the capability to quantitatively determine the mRNA
expression level or to simultaneously measure the expression of
multiple target mRNA within cells, which may provide clinical
valuable information such as increased detection sensitivity and
specificity, and the identification of primary tumor type, source
and stage.
[0010] There are four main types of probes that are typically used
in performing in situ hybridization within cells: oligonucleotide
probes (usually 20-40 bases in length), single-stranded DNA probes
(200-500 bases in length), double stranded DNA probes, or RNA
probes (200-5000 bases in length). RNA probes are currently the
most widely used probes for in situ hybridization as they have the
advantage that RNA-RNA hybrids are very thermostable and are
resistant to digestion by RNases. RNA probe is a direct labeling
method that suffers a number of difficulties. First, separate
labeled probes have to be prepared for detecting each mRNA of
interest. Second, it is technically difficult to detect the
expression of multiple mRNA of interest in situ at the same time.
As a result, only sequential detection of multiple mRNAs using
different labeling methods has recently been reported (Schrock et
al, 1996; Kosman et al, 2004). Furthermore, with direct labeling
methods, there is no good way to control for potential
cross-hybridization with non-specific sequences in cells. Branched
DNA (bDNA) in situ hybridization is an indirect labeling method for
detecting mRNA in single cells (Player et al, 2001). This method
uses a series of oligonucleotide probes that have one portion
hybridizing to the specific mRNA of interest and another portion
hybridizing to the bDNA for signal amplification and detection.
bDNA ISH has the advantage of using unlabeled oligonucleotide
probes for detecting every mRNA of interest and the signal
amplification and detection are generic components in the assay.
However, the gene specific probes in the bDNA ISH need to be
theoretically screened against possible non-specific hybridization
interactions with other mRNA sequences in the cells. The
nonspecific hybridization of the oligonucleotide probes in bDNA ISH
can become a serious problem when multiple of those probes have to
be used for the detection of low abundance mRNAs. Similarly,
although use of bDNA ISH to detect or quantitate multiple mRNAs is
desirable, such nonspecific hybridization of the oligonucleotide
probes is a potential problem.
[0011] The present invention overcomes the above noted difficulties
and provides methods for detecting nucleic acids in and for
identifying individual cells. A complete understanding of the
invention will be obtained upon review of the following.
SUMMARY OF THE INVENTION
[0012] Methods of detecting nucleic acid targets in single cells,
including methods of detecting multiple targets in a single cell,
are provided. Methods of detecting individual cells, particularly
rare cells from large heterogeneous cell populations, through
detection of nucleic acids are described. Related compositions,
systems, and kits are also described.
[0013] A first general class of embodiments includes methods of
detecting two or more nucleic acid targets in an individual cell.
In the methods, a sample comprising the cell is provided. The cell
comprises, or is suspected of comprising, a first nucleic acid
target and a second nucleic acid target. A first label probe
comprising a first label and a second label probe comprising a
second label, wherein a first signal from the first label is
distinguishable from a second signal from the second label, are
provided. At least a first capture probe and at least a second
capture probe are also provided.
[0014] The first capture probe is hybridized, in the cell, to the
first nucleic acid target (when the first nucleic acid target is
present in the cell), and the second capture probe is hybridized,
in the cell, to the second nucleic acid target (when the second
nucleic acid target is present in the cell). The first label probe
is captured to the first capture probe and the second label probe
is captured to the second capture probe, thereby capturing the
first label probe to the first nucleic acid target and the second
label probe to the second nucleic acid target. The first signal
from the first label and the second signal from the second label
are then detected. Since the first and second labels are associated
with their respective nucleic acid targets through the capture
probes, presence of the label(s) in the cell indicates the presence
of the corresponding nucleic acid target(s) in the cell. The
methods are optionally quantitative. Thus, an intensity of the
first signal and an intensity of the second signal can be measured,
and the intensity of the first signal can be correlated with a
quantity of the first nucleic acid target in the cell while the
intensity of the second signal is correlated with a quantity of the
second nucleic acid target in the cell.
[0015] In one aspect, the label probes bind directly to the capture
probes. For example, in one class of embodiments, a single first
capture probe and a single second capture probe are provided, the
first label probe is hybridized to the first capture probe, and the
second label probe is hybridized to the second capture probe. In a
related class of embodiments, two or more first capture probes and
two or more second capture probes are provided, as are a plurality
of the first label probes (e.g., two or more identical first label
probes) and a plurality of the second label probes (e.g., two or
more identical second label probes). The two or more first capture
probes are hybridized to the first nucleic acid target, and the two
or more second capture probes are hybridized to the second nucleic
acid target. A single first label probe is hybridized to each of
the first capture probes, and a single second label probe is
hybridized to each of the second capture probes.
[0016] In another aspect, the label probes are captured to the
capture probes indirectly, for example, through binding of
preamplifiers and/or amplifiers. In one class of embodiments in
which amplifiers are employed, a single first capture probe, a
single second capture probe, a plurality of the first label probes,
and a plurality of the second label probes are provided. A first
amplifier is hybridized to the first capture probe and to the
plurality of first label probes, and a second amplifier is
hybridized to the second capture probe and to the plurality of
second label probes. In another class of embodiments, two or more
first capture probes, two or more second capture probes, a
plurality of the first label probes, and a plurality of the second
label probes are provided. The two or more first capture probes are
hybridized to the first nucleic acid target, and the two or more
second capture probes are hybridized to the second nucleic acid
target. A first amplifier is hybridized to each of the first
capture probes, and the plurality of first label probes is
hybridized to the first amplifiers. A second amplifier is
hybridized to each of the second capture probes, and the plurality
of second label probes is hybridized to the second amplifiers.
[0017] In one class of embodiments in which preamplifiers are
employed, a single first capture probe, a single second capture
probe, a plurality of the first label probes, and a plurality of
the second label probes are provided. A first preamplifier is
hybridized to the first capture probe, a plurality of first
amplifiers is hybridized to the first preamplifier, and the
plurality of first label probes is hybridized to the first
amplifiers. A second preamplifier is hybridized to the second
capture probe, a plurality of second amplifiers is hybridized to
the second preamplifier, and the plurality of second label probes
is hybridized to the second amplifiers. In another class of
embodiments, two or more first capture probes, two or more second
capture probes, a plurality of the first label probes, and a
plurality of the second label probes are provided. The two or more
first capture probes are hybridized to the first nucleic acid
target, and the two or more second capture probes are hybridized to
the second nucleic acid target. A first preamplifier is hybridized
to each of the first capture probes, a plurality of first
amplifiers is hybridized to each of the first preamplifiers, and
the plurality of first label probes is hybridized to the first
amplifiers. A second preamplifier is hybridized to each of the
second capture probes, a plurality of second amplifiers is
hybridized to each of the second preamplifiers, and the plurality
of second label probes is hybridized to the second amplifiers.
[0018] In embodiments in which two or more first capture probes
and/or two or more second capture probes are employed, the capture
probes preferably hybridize to nonoverlapping polynucleotide
sequences in their respective nucleic acid target.
[0019] In one class of embodiments, a plurality of the first label
probes and a plurality of the second label probes are provided. A
first amplified polynucleotide is produced by rolling circle
amplification of a first circular polynucleotide hybridized to the
first capture probe. The first circular polynucleotide comprises at
least one copy of a polynucleotide sequence identical to a
polynucleotide sequence in the first label probe, and the first
amplified polynucleotide thus comprises a plurality of copies of a
polynucleotide sequence complementary to the polynucleotide
sequence in the first label probe. The plurality of first label
probes is then hybridized to the first amplified polynucleotide.
Similarly, a second amplified polynucleotide is produced by rolling
circle amplification of a second circular polynucleotide hybridized
to the second capture probe. The second circular polynucleotide
comprises at least one copy of a polynucleotide sequence identical
to a polynucleotide sequence in the second label probe, and the
second amplified polynucleotide thus comprises a plurality of
copies of a polynucleotide sequence complementary to the
polynucleotide sequence in the second label probe. The plurality of
second label probes is then hybridized to the second amplified
polynucleotide. The amplified polynucleotides remain associated
with the capture probe(s), and the label probes are thus captured
to the nucleic acid targets.
[0020] The methods are useful for multiplex detection of nucleic
acids, including simultaneous detection of more than two nucleic
acid targets. Thus, the cell optionally comprises or is suspected
of comprising a third nucleic acid target, and the methods
optionally include: providing a third label probe comprising a
third label, wherein a third signal from the third label is
distinguishable from the first and second signals, providing at
least a third capture probe, hybridizing in the cell the third
capture probe to the third nucleic acid target (when present in the
cell), capturing the third label probe to the third capture probe,
and detecting the third signal from the third label. Fourth, fifth,
sixth, etc. nucleic acid targets are similarly simultaneously
detected in the cell if desired. Each hybridization or capture step
is preferably accomplished for all of the nucleic acid targets at
the same time.
[0021] A nucleic acid target can be essentially any nucleic acid
that is desirably detected in the cell. For example, a nucleic acid
target can be a DNA, a chromosomal DNA, an RNA, an mRNA, a
microRNA, a ribosomal RNA, or the like. The nucleic acid target can
be a nucleic acid endogenous to the cell. As another example, the
target can be a nucleic acid introduced to or expressed in the cell
by infection of the cell with a pathogen, for example, a viral or
bacterial genomic RNA or DNA, a plasmid, a viral or bacterial mRNA,
or the like.
[0022] The first and second (and/or optional third, fourth, etc.)
nucleic acid targets can be part of a single nucleic acid molecule,
or they can be separate molecules. In one class of embodiments, the
first nucleic acid target is a first mRNA and the second nucleic
acid target is a second mRNA. In another class of embodiments, the
first nucleic acid target comprises a first region of an mRNA and
the second nucleic acid target comprises a second region of the
same mRNA. In another class of embodiments, the first nucleic acid
target comprises a first chromosomal DNA polynucleotide sequence
and the second nucleic acid target comprises a second chromosomal
DNA polynucleotide sequence. The first and second chromosomal DNA
polynucleotide sequences are optionally located on the same
chromosome, e.g., within the same gene, or on different
chromosomes.
[0023] In one aspect, the signal(s) from nucleic acid target(s) are
normalized. In one class of embodiments, the second nucleic acid
target comprises a reference nucleic acid, and the method includes
normalizing the first signal to the second signal. The label
(first, second, third, etc.) can be essentially any convenient
label that directly or indirectly provides a detectable signal. In
one aspect, the first label is a first fluorescent label and the
second label is a second fluorescent label.
[0024] The methods can be used to detect the presence of the
nucleic acid targets in cells from essentially any type of sample.
For example, the sample can be derived from a bodily fluid such as
blood. The methods for detecting nucleic acid targets in cells can
be used to identify the cells. For example, a cell can be
identified as being of a desired type based on which nucleic acids,
and in what levels, it contains. Thus, in one class of embodiments,
the methods include identifying the cell as a desired target cell
based on detection of the first and second signals (and optional
third, fourth, etc. signals) from within the cell. As just a few
examples, the cell can be a circulating tumor cell, a virally
infected cell, a fetal cell in maternal blood, a bacterial cell or
other microorganism in a biological sample, or an endothelial cell,
precursor endothelial cell, or myocardial cell in blood.
[0025] The cell is typically fixed and permeabilized before
hybridization of the capture probes, to retain the nucleic acid
targets in the cell and to permit the capture probes, label probes,
etc. to enter the cell. The cell is optionally washed to remove
materials not captured to one of the nucleic acid targets. The cell
can be washed after any of various steps, for example, after
hybridization of the capture probes to the nucleic acid targets to
remove unbound capture probes, after hybridization of the
preamplifiers, amplifiers, and/or label probes to the capture
probes, and/or the like. It will be evident that double-stranded
nucleic acid target(s) are preferably denatured, e.g., by heat,
prior to hybridization of the corresponding capture probe(s) to the
target(s).
[0026] Preferably, the cell is in suspension for all or most of the
steps of the method. Thus, in one class of embodiments, the cell is
in suspension in the sample comprising the cell, and/or the cell is
in suspension during the hybridizing, capturing, and/or detecting
steps. In other embodiments, the cell is in suspension in the
sample comprising the cell, and the cell is fixed on a substrate
during the hybridizing, capturing, and/or detecting steps. For
example, the cell can be in suspension during the hybridization,
capturing, and optional washing steps and immobilized on a
substrate during the detection step. In embodiments in which the
cell is in suspension, the first and second (and optional third,
etc.) signals can be conveniently detected by flow cytometry.
Signals from the labels are typically detected in a single
operation.
[0027] One general class of embodiments provides methods of
assaying a relative level of one or more target nucleic acids in an
individual cell. In the methods, a sample comprising the cell is
provided. The cell comprises or is suspected of comprising a first,
target nucleic acid, and it comprises a second, reference nucleic
acid. A first label probe comprising a first label and a second
label probe comprising a second label, wherein a first signal from
the first label is distinguishable from a second signal from the
second label, are also provided. In the cell, the first label probe
is captured to the first, target nucleic acid (when present in the
cell) and the second label probe is captured to the second,
reference nucleic acid. The first signal from the first label and
the second signal from the second label are then detected in the
individual cell, and the intensity of each signal is measured. The
intensity of the first signal is normalized to the intensity of the
second (reference) signal. The level of the first, target nucleic
acid relative to the level of the second, reference nucleic acid in
the cell is thereby assayed, since the first and second labels are
associated with their respective nucleic acids. The methods are
optionally quantitative, permitting measurement of the amount of
the first, target nucleic acid relative to the amount of the
second, reference nucleic acid in the cell. Thus, the intensity of
the first signal normalized to that of the second signal can be
correlated with a quantity of the first, target nucleic acid
present in the cell.
[0028] The label probes can bind directly to the nucleic acids. For
example, the first label probe can hybridize to the first, target
nucleic acid and/or the second label probe can hybridize to the
second, reference nucleic acid. Alternatively, the label probes can
be bound indirectly to the nucleic acids, e.g., via capture probes.
In one class of embodiments, at least a first capture probe and at
least a second capture probe are provided. In the cell, the first
capture probe is hybridized to the first, target nucleic acid and
the second capture probe is hybridized to the second, reference
nucleic acid. The first label probe is captured to the first
capture probe and the second label probe is captured to the second
capture probe, thereby capturing the first label probe to the
first, target nucleic acid and the second label probe to the
second, reference nucleic acid. The features described for the
methods above apply to these embodiments as well, with respect to
configuration and number of the label and capture probes, optional
use of preamplifiers and/or amplifiers, rolling circle
amplification of circular polynucleotides, and the like.
[0029] The methods can be used for multiplex detection of nucleic
acids, including simultaneous detection of two or more target
nucleic acids. Thus, the cell optionally comprises or is suspected
of comprising a third, target nucleic acid, and the methods
optionally include: providing a third label probe comprising a
third label, wherein a third signal from the third label is
distinguishable from the first and second signals; capturing, in
the cell, the third label probe to the third, target nucleic acid
(when present in the cell); detecting the third signal from the
third label, which detecting comprises measuring an intensity of
the third signal; and normalizing the intensity of the third signal
to the intensity of the second signal. Fourth, fifth, sixth, etc.
nucleic acids are similarly simultaneously detected in the cell if
desired.
[0030] The methods for assaying relative levels of target nucleic
acids in cells can be used to identify the cells. For example, a
cell can be identified as being of a desired type based on which
nucleic acids, and in what levels, it contains. Thus, in one class
of embodiments, the methods include identifying the cell as a
desired target cell based on the normalized first signal (and
optional normalized third, fourth, etc. signals).
[0031] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to type of target and reference nucleic acids, cell type,
source of sample, fixation and permeabilization of the cell,
washing the cell, denaturation of double-stranded target and
reference nucleic acids, type of labels, use of optional blocking
probes, detection of signals, detection (and intensity measurement)
by flow cytometry or microscopy, presence of the cell in suspension
or immobilized on a substrate, and/or the like.
[0032] Another general class of embodiments provides methods of
performing comparative gene expression analysis in single cells. In
the methods, a first mixed cell population comprising one or more
cells of a specified type is provided. An expression level of one
or more target nucleic acids relative to a reference nucleic acid
is measured in the cells of the specified type of the first
population, to provide a first expression profile. A second mixed
cell population comprising one or more cells of the specified type
is also provided, and an expression level of the one or more target
nucleic acids relative to the reference nucleic acid is measured in
the cells of the specified type of the second population, to
provide a second expression profile. The first and second
expression profiles are then compared.
[0033] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to type of target and reference nucleic acids, cell type,
source of sample, fixation and permeabilization of the cell,
washing the cell, denaturation of double-stranded target and
reference nucleic acids, type of labels, use and configuration of
label probes, capture probes, preamplifiers and/or amplifiers, use
of optional blocking probes, detection of signals, detection (and
intensity measurement) by flow cytometry or microscopy, presence of
the cell in suspension or immobilized on a substrate, and/or the
like.
[0034] In one aspect, the invention provides methods that
facilitate association of a high density of labels to target
nucleic acids in cells. One general class of embodiments provides
methods of detecting two or more nucleic acid targets in an
individual cell. In the methods, a sample comprising the cell is
provided. The cell comprises or is suspected of comprising a first
nucleic acid target and a second nucleic acid target. In the cell,
a first label is captured to the first nucleic acid target (when
present in the cell) and a second label is captured to the second
nucleic acid target (when present in the cell). A first signal from
the first label is distinguishable from a second signal from the
second label. As noted, the labels are captured at high density.
Thus, an average of at least one copy of the first label per
nucleotide of the first nucleic acid target is captured to the
first nucleic acid target over a region that spans at least 20
contiguous nucleotides of the first nucleic acid target, and an
average of at least one copy of the second label per nucleotide of
the second nucleic acid target is captured to the second nucleic
acid target over a region that spans at least 20 contiguous
nucleotides of the second nucleic acid target. The first signal
from the first label and the second signal from the second label
are detected.
[0035] In one class of embodiments, an average of at least four,
eight, or twelve copies of the first label per nucleotide of the
first nucleic acid target are captured to the first nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the first nucleic acid target, and an average of at least four,
eight, or twelve copies of the second label per nucleotide of the
second nucleic acid target are captured to the second nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the second nucleic acid target. In one embodiment, an average of
at least sixteen copies of the first label per nucleotide of the
first nucleic acid target are captured to the first nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the first nucleic acid target, and an average of at least
sixteen copies of the second label per nucleotide of the second
nucleic acid target are captured to the second nucleic acid target
over a region that spans at least 20 contiguous nucleotides of the
second nucleic acid target.
[0036] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant, for example, with
respect to type of labels, detection of signals, type, treatment,
and suspension of the cell, and/or the like. A like density of
third, fourth, fifth, sixth, etc. labels is optionally captured to
third, fourth, fifth, sixth, etc. nucleic acid targets.
[0037] Another general class of embodiments provides methods of
detecting an individual cell of a specified type. In the methods, a
sample comprising a mixture of cell types including at least one
cell of the specified type is provided. A first label probe
comprising a first label and a second label probe comprising a
second label, wherein a first signal from the first label is
distinguishable from a second signal from the second label, are
provided. In the cell, the first label probe is captured to a first
nucleic acid target (when the first nucleic acid target is present
in the cell) and the second label probe is captured to a second
nucleic acid target (when the second nucleic acid target is present
in the cell). The first signal from the first label and the second
signal from the second label are detected and correlated with the
presence, absence, or amount of the corresponding, first and second
nucleic acid targets in the cell. The cell is identified as being
of the specified type based on detection of the presence, absence,
or amount of both the first and second nucleic acid targets within
the cell, where the specified type of cell is distinguishable from
the other cell type(s) in the mixture on the basis of either the
presence, absence, or amount of the first nucleic acid target or
the presence, absence, or amount of the second nucleic acid target
in the cell (that is, the nucleic acid targets are redundant
markers for the specified cell type). An intensity of the first
signal and an intensity of the second signal are optionally
measured and correlated with a quantity of the corresponding
nucleic acid present in the cell. In one class of embodiments, the
cell comprises a first nucleic acid target and a second nucleic
acid target, and the cell is identified as being of the specified
type based on detection of the presence or amount of both the first
and second nucleic acid targets within the cell, where the
specified type of cell is distinguishable from the other cell
type(s) in the mixture on the basis of either the presence or
amount of the first nucleic acid target or the presence or amount
of the second nucleic acid target in the cell.
[0038] The label probes can bind directly to the nucleic acid
targets. For example, the first label probe can hybridize to the
first nucleic acid target and/or the second label probe can
hybridize to the second nucleic acid target. The label probes are
optionally captured to the nucleic acid targets via capture probes.
In one class of embodiments, at least a first capture probe and at
least a second capture probe are provided. In the cell, the first
capture probe is hybridized to the first nucleic acid target and
the second capture probe is hybridized to the second nucleic acid
target. The first label probe is captured to the first capture
probe and the second label probe is captured to the second capture
probe, thereby capturing the first label probe to the first nucleic
acid target and the second label probe to the second nucleic acid
target. The features described for the methods above apply to these
embodiments as well, with respect to configuration and number of
the label and capture probes, optional use of preamplifiers and/or
amplifiers, rolling circle amplification of circular
polynucleotides, and the like.
[0039] Third, fourth, fifth, etc. nucleic acid targets are
optionally detected in the cell. For example, the method optionally
includes: providing a third label probe comprising a third label,
wherein a third signal from the third label is distinguishable from
the first and second signals, capturing in the cell the third label
probe to a third nucleic acid target (when the third target is
present in the cell), and detecting the third signal from the third
label. The third, fourth, fifth, etc. label probes are optionally
hybridized directly to their corresponding nucleic acid, or they
can be captured indirectly via capture probes as described for the
first and second label probes.
[0040] The first and/or second signal can be normalized to the
third signal. Thus, in some embodiments, the cell comprises the
third nucleic acid target, and the methods include identifying the
cell as being of the specified type based on the normalized first
and/or second signal, e.g., in embodiments in which the target cell
type is distinguishable from the other cell type(s) in the mixture
based on the copy number of the first and/or second nucleic acid
targets, rather than purely on their presence in the target cell
type and not in the other cell type(s).
[0041] As another example, the third nucleic acid target can serve
as a third redundant marker for the target cell type, e.g., to
improve specificity of the assay for the desired cell type. Thus,
in one class of embodiments, the methods include correlating the
third signal detected from the cell with the presence, absence, or
amount of the third nucleic acid target in the cell, and
identifying the cell as being of the specified type based on
detection of the presence, absence, or amount of the first, second,
and third nucleic acid targets within the cell, wherein the
specified type of cell is distinguishable from the other cell
type(s) in the mixture on the basis of either presence, absence, or
amount of the first nucleic acid target, presence, absence, or
amount of the second nucleic acid target, or presence, absence, or
amount of the third nucleic acid target in the cell.
[0042] The methods can be applied to detection and identification
of even rare cell types. For example, the ratio of cells of the
specified type to cells of all other type(s) in the mixture is
optionally less than 1:1.times.10.sup.4, less than
1:1.times.10.sup.5, less than 1:1.times.10.sup.6, less than
1:1.times.10.sup.7, less than 1:1.times.10.sup.8, or even less than
1:1.times.10.sup.9.
[0043] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to type of nucleic acid targets, cell type, source of
sample, fixation and permeabilization of the cell, washing the
cell, denaturation of double-stranded nucleic acids, type of
labels, use of optional blocking probes, detection of signals,
detection (and intensity measurement) of signals from the
individual cell by flow cytometry or microscopy, presence of the
cell in suspension or immobilized on a substrate, and/or the
like.
[0044] The invention also provides compositions useful in
practicing or produced by the methods. One exemplary class of
embodiments provides a composition that includes a fixed and
permeabilized cell, which cell comprises or is suspected of
comprising a first nucleic acid target and a second nucleic acid
target, at least a first capture probe capable of hybridizing to
the first nucleic acid target, at least a second capture probe
capable of hybridizing to the second nucleic acid target, a first
label probe comprising a first label, and a second label probe
comprising a second label. A first signal from the first label is
distinguishable from a second signal from the second label. The
cell optionally comprises the first and second capture probes and
label probes. The first and second capture probes are optionally
hybridized to their respective nucleic acid targets in the
cell.
[0045] The features described for the methods above for indirect
capture of the label probes to the nucleic acid targets apply to
these embodiments as well, for example, with respect to
configuration and number of the label and capture probes, optional
use of preamplifiers and/or amplifiers, and the like.
[0046] In one class of embodiments, the composition comprises a
plurality of the first label probes, a plurality of the second
label probes, a first amplified polynucleotide produced by rolling
circle amplification of a first circular polynucleotide hybridized
to the first capture probe, and a second amplified polynucleotide
produced by rolling circle amplification of a second circular
polynucleotide hybridized to the second capture probe. The first
circular polynucleotide comprises at least one copy of a
polynucleotide sequence identical to a polynucleotide sequence in
the first label probe, and the first amplified polynucleotide
comprises a plurality of copies of a polynucleotide sequence
complementary to the polynucleotide sequence in the first label
probe. The second circular polynucleotide comprises at least one
copy of a polynucleotide sequence identical to a polynucleotide
sequence in the second label probe, and the second amplified
polynucleotide comprises a plurality of copies of a polynucleotide
sequence complementary to the polynucleotide sequence in the second
label probe. The composition can also include reagents necessary
for producing the amplified polynucleotides, for example, an
exogenously supplied nucleic acid polymerase, an exogenously
supplied nucleic acid ligase, and/or exogenously supplied
nucleoside triphosphates (e.g., dNTPs).
[0047] The cell optionally includes additional nucleic acid
targets, and the composition (and cell) can include reagents for
detecting these targets. For example, the cell can comprise or be
suspected of comprising a third nucleic acid target, and the
composition can include at least a third capture probe capable of
hybridizing to the third nucleic acid target and a third label
probe comprising a third label. A third signal from the third label
is distinguishable from the first and second signals. The cell
optionally includes fourth, fifth, sixth, etc. nucleic acid
targets, and the composition optionally includes fourth, fifth,
sixth, etc. label probes and capture probes.
[0048] The cell can be present in a mixture of cells, for example,
a complex heterogeneous mixture. In one class of embodiments, the
cell is of a specified type, and the composition comprises one or
more other types of cells. These other cells can be present in
excess, even large excess, of the cell. For example, the ratio of
cells of the specified type to cells of all other type(s) in the
composition is optionally less than 1:1.times.10.sup.4, less than
1:1.times.10.sup.5, less than 1:1.times.10.sup.6, less than
1:1.times.10.sup.7, less than 1:1.times.10.sup.8, or even less than
1:1.times.10.sup.9.
[0049] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to type of nucleic acid target, type and source of cell,
location of various targets on a single molecule or on different
molecules, type of labels, inclusion of optional blocking probes,
and/or the like. The cell is optionally in suspension in the
composition.
[0050] One general class of embodiments provides a composition
comprising a cell, which cell includes a first nucleic acid target,
a second nucleic acid target, a first label whose presence in the
cell is indicative of the presence of the first nucleic acid target
in the cell, and a second label whose presence in the cell is
indicative of the presence of the second nucleic acid target in the
cell, wherein a first signal from the first label is
distinguishable from a second signal from the second label. An
average of at least one copy of the first label is present in the
cell per nucleotide of the first nucleic acid target over a region
that spans at least 20 contiguous nucleotides of the first nucleic
acid target, and an average of at least one copy of the second
label is present in the cell per nucleotide of the second nucleic
acid target over a region that spans at least 20 contiguous
nucleotides of the second nucleic acid target.
[0051] In one class of embodiments, the copies of the first label
are physically associated with the first nucleic acid target, and
the copies of the second label are physically associated with the
second nucleic acid target. For example, the first label can be
part of a first label probe and the second label part of a second
label probe, where the label probes are captured to the target
nucleic acids.
[0052] Essentially all of the features noted for the embodiments
above apply to these embodiments as well, as relevant, for example,
with respect to type and number of labels, suspension of the cell,
and/or the like. A like density of labels is optionally present for
third, fourth, fifth, sixth, etc. nucleic acid targets.
[0053] Another aspect of the invention provides kits useful for
practicing the methods. One general class of embodiments provides a
kit for detecting a first nucleic acid target and a second nucleic
acid target in an individual cell. The kit includes at least one
reagent for fixing and/or permeabilizing the cell, at least a first
capture probe capable of hybridizing to the first nucleic acid
target, at least a second capture probe capable of hybridizing to
the second nucleic acid target, a first label probe comprising a
first label, and a second label probe comprising a second label,
wherein a first signal from the first label is distinguishable from
a second signal from the second label, packaged in one or more
containers.
[0054] Essentially all of the features noted for the embodiments
above apply to these embodiments as well, as relevant; for example,
with respect to number of nucleic acid targets, configuration and
number of the label and capture probes, inclusion of preamplifiers
and/or amplifiers, inclusion of blocking probes, inclusion of
amplification reagents, type of nucleic acid target, location of
various targets on a single molecule or on different molecules,
type of labels, inclusion of optional blocking probes, and/or the
like.
[0055] Another general class of embodiments provides a kit for
detecting an individual cell of a specified type from a mixture of
cell types by detecting a first nucleic acid target and a second
nucleic acid target. The kit includes at least one reagent for
fixing and/or permeabilizing the cell, a first label probe
comprising a first label, and a second label probe comprising a
second label, wherein a first signal from the first label is
distinguishable from a second signal from the second label,
packaged in one or more containers. The specified type of cell is
distinguishable from the other cell type(s) in the mixture by
presence, absence, or amount of the first nucleic acid target in
the cell or by presence, absence, or amount of the second nucleic
acid target in the cell.
[0056] Essentially all of the features noted for the embodiments
above apply to these embodiments as well, as relevant; for example,
with respect to number of nucleic acid targets, inclusion of
capture probes, configuration and number of the label and/or
capture probes, inclusion of preamplifiers and/or amplifiers,
inclusion of blocking probes, inclusion of amplification reagents,
type of nucleic acid target, location of various targets on a
single molecule or on different molecules, type of labels,
inclusion of optional blocking probes, and/or the like.
BRIEF DESCRIPTION OF THE DRAWINGS
[0057] FIG. 1 schematically illustrates QMAGEX technology workflow
for an exemplary embodiment.
[0058] FIG. 2 schematically illustrates a direct labeling approach
in which label probes are hybridized to the target nucleic
acid.
[0059] FIG. 3 schematically illustrates an indirect labeling
approach in which label probes are hybridized to capture probes
hybridized to the target nucleic acid.
[0060] FIG. 4 schematically illustrates an indirect labeling
capture probe design approach that utilizes a pair of independent
capture probes to enhance the specificity of the label probe
capture to the target nucleic acid.
[0061] FIG. 5 schematically illustrates an indirect labeling
capture probe design approach that utilizes three or more
independent capture probes to enhance the specificity of the label
probe capture to the target nucleic acid.
[0062] FIG. 6 schematically illustrates probe design approaches to
detect multiple target molecules in parallel using either direct
labeling (Panel A) or indirect labeling with two independent
capture probes (Panel B).
[0063] FIG. 7 schematically illustrates probe design approaches to
reducing false positive rates in rare cell identification by
attaching multiple types of signal-generating particles (labels) to
the same target molecule. Panel A shows multiple types of
signal-generating particles (labels) on one target. Panel B shows
multiple types of signal-generating particles (labels) on more than
one target, where the relative signal strengths of the particle set
are maintained across all targets. Panel C shows a set of
signal-generating particles (labels) on a target molecule, where
different targets have distinctively different sets.
[0064] FIG. 8 Panels A-D schematically illustrate different
structures of exemplary amplifiers.
[0065] FIG. 9 schematically illustrates utilizing rolling circle
amplification to amplify signal. As shown in Panel A, a circular
nucleotide molecule is attached to capture probe(s). As shown in
Panel B, a long chain molecule with many repeated sequences appears
as a result of rolling circle amplification. As shown in Panel C,
many signal probes can be hybridized to the repeated sequences to
achieve signal amplification.
[0066] FIG. 10 schematically illustrates one embodiment of the
assay instrument configuration.
[0067] Schematic figures are not necessarily to scale.
DEFINITIONS
[0068] Unless defined otherwise, all technical and scientific terms
used herein have the same meaning as commonly understood by one of
ordinary skill in the art to which the invention pertains. The
following definitions supplement those in the art and are directed
to the current application and are not to be imputed to any related
or unrelated case, e.g., to any commonly owned patent or
application. Although any methods and materials similar or
equivalent to those described herein can be used in the practice
for testing of the present invention, the preferred materials and
methods are described herein. Accordingly, the terminology used
herein is for the purpose of describing particular embodiments
only, and is not intended to be limiting.
[0069] As used in this specification and the appended claims, the
singular forms "a," "an" and "the" include plural referents unless
the context clearly dictates otherwise. Thus, for example,
reference to "a molecule" includes a plurality of such molecules,
and the like.
[0070] The term "about" as used herein indicates the value of a
given quantity varies by +/-10% of the value, or optionally +/-5%
of the value, or in some embodiments, by +/-1% of the value so
described.
[0071] The term "polynucleotide" (and the equivalent term "nucleic
acid") encompasses any physical string of monomer units that can be
corresponded to a string of nucleotides, including a polymer of
nucleotides (e.g., a typical DNA or RNA polymer), peptide nucleic
acids (PNAs), modified oligonucleotides (e.g., oligonucleotides
comprising nucleotides that are not typical to biological RNA or
DNA, such as 2'-O-methylated oligonucleotides), and the like. The
nucleotides of the polynucleotide can be deoxyribonucleotides,
ribonucleotides or nucleotide analogs, can be natural or
non-natural, and can be unsubstituted, unmodified, substituted or
modified. The nucleotides can be linked by phosphodiester bonds, or
by phosphorothioate linkages, methylphosphonate linkages,
boranophosphate linkages, or the like. The polynucleotide can
additionally comprise non-nucleotide elements such as labels,
quenchers, blocking groups, or the like. The polynucleotide can be,
e.g., single-stranded or double-stranded.
[0072] A "nucleic acid target" or "target nucleic acid" refers to a
nucleic acid, or optionally a region thereof, that is to be
detected.
[0073] A "polynucleotide sequence" or "nucleotide sequence" is a
polymer of nucleotides (an oligonucleotide, a DNA, a nucleic acid,
etc.) or a character string representing a nucleotide polymer,
depending on context. From any specified polynucleotide sequence,
either the given nucleic acid or the complementary polynucleotide
sequence (e.g., the complementary nucleic acid) can be
determined.
[0074] The term "gene" is used broadly to refer to any nucleic acid
associated with a biological function. Genes typically include
coding sequences and/or the regulatory sequences required for
expression of such coding sequences. The term gene can apply to a
specific genomic sequence, as well as to a cDNA or an mRNA encoded
by that genomic sequence. Genes also include non-expressed nucleic
acid segments that, for example, form recognition sequences for
other proteins. Non-expressed regulatory sequences include
promoters and enhancers, to which regulatory proteins such as
transcription factors bind, resulting in transcription of adjacent
or nearby sequences.
[0075] Two polynucleotides "hybridize" when they associate to form
a stable duplex, e.g., under relevant assay conditions. Nucleic
acids hybridize due to a variety of well characterized
physico-chemical forces, such as hydrogen bonding, solvent
exclusion, base stacking and the like. An extensive guide to the
hybridization of nucleic acids is found in Tijssen (1993)
Laboratory Techniques in Biochemistry and Molecular
Biology-Hybridization with Nucleic Acid Probes, part I chapter 2,
"Overview of principles of hybridization and the strategy of
nucleic acid probe assays" (Elsevier, New York), as well as in
Ausubel, infra.
[0076] A first polynucleotide "capable of hybridizing" to a second
polynucleotide contains a first polynucleotide sequence that is
complementary to a second polynucleotide sequence in the second
polynucleotide. The first and second polynucleotides are able to
form a stable duplex, e.g., under relevant assay conditions.
[0077] The "T.sub.m" (melting temperature) of a nucleic acid duplex
under specified conditions (e.g., relevant assay conditions) is the
temperature at which half of the base pairs in a population of the
duplex are disassociated and half are associated. The T.sub.m for a
particular duplex can be calculated and/or measured, e.g., by
obtaining a thermal denaturation curve for the duplex (where the
T.sub.m is the temperature corresponding to the midpoint in the
observed transition from double-stranded to single-stranded
form).
[0078] The term "complementary" refers to a polynucleotide that
forms a stable duplex with its "complement," e.g., under relevant
assay conditions. Typically, two polynucleotide sequences that are
complementary to each other have mismatches at less than about 20%
of the bases, at less than about 10% of the bases, preferably at
less than about 5% of the bases, and more preferably have no
mismatches.
[0079] A "label" is a moiety that facilitates detection of a
molecule. Common labels in the context of the present invention
include fluorescent, luminescent, light-scattering, and/or
calorimetric labels. Suitable labels include enzymes and
fluorescent moieties, as well as radionuclides, substrates,
cofactors, inhibitors, chemiluminescent moieties, magnetic
particles, and the like. Patents teaching the use of such labels
include U.S. Pat. Nos. 3,817,837; 3,850,752; 3,939,350; 3,996,345;
4,277,437; 4,275,149; and 4,366,241. Many labels are commercially
available and can be used in the context of the invention.
[0080] The term "label probe" refers to an entity that binds to a
target molecule, directly or indirectly, and enables the target to
be detected, e.g., by a readout instrument. A label probe (or "LP")
is typically a single-stranded polynucleotide that comprises at
least one label which directly or indirectly provides a detectable
signal. The label can be covalently attached to the polynucleotide,
or the polynucleotide can be configured to bind to the label (e.g.,
a biotinylated polynucleotide can bind a streptavidin-associated
label). The label probe can, for example, hybridize directly to a
target nucleic acid, or it can hybridize to a nucleic acid that is
in turn hybridized to the target nucleic acid or to one or more
other nucleic acids that are hybridized to the nucleic acid. Thus,
the label probe can comprise a polynucleotide sequence that is
complementary to a polynucleotide sequence of the target nucleic
acid, or it can comprise at least one polynucleotide sequence that
is complementary to a polynucleotide sequence in a capture probe,
amplifier, or the like.
[0081] A "capture probe" is a polynucleotide that is capable of
hybridizing to a target nucleic acid and capturing a label probe to
that target nucleic acid. The capture probe can hybridize directly
to the label probe, or it can hybridize to one or more nucleic
acids that in turn hybridize to the label probe; for example, the
capture probe can hybridize to an amplifier or a preamplifier. The
capture probe thus includes a first polynucleotide sequence that is
complementary to a polynucleotide sequence of the target nucleic
acid and a second polynucleotide sequence that is complementary to
a polynucleotide sequence of the label probe, amplifier,
preamplifier, or the like. The capture probe is preferably
single-stranded.
[0082] An "amplifier" is a molecule, typically a polynucleotide,
that is capable of hybridizing to multiple label probes. Typically,
the amplifier hybridizes to multiple identical label probes. The
amplifier also hybridizes to at least one capture probe or nucleic
acid bound to a capture probe. For example, the amplifier can
hybridize to at least one capture probe and to a plurality of label
probes, or to a preamplifier and a plurality of label probes. The
amplifier can be, e.g., a linear, forked, comb-like, or branched
nucleic acid. As noted for all polynucleotides, the amplifier can
include modified nucleotides and/or nonstandard internucleotide
linkages as well as standard deoxyribonucleotides, ribonucleotides,
and/or phosphodiester bonds. Suitable amplifiers are described, for
example, in U.S. Pat. No. 5,635,352, U.S. Pat. No. 5,124,246, U.S.
Pat. No. 5,710,264, and U.S. Pat. No. 5,849,481.
[0083] A "preamplifier" is a molecule, typically a polynucleotide,
that serves as an intermediate between one or more capture probes
and amplifiers. Typically, the preamplifier hybridizes
simultaneously to one or more capture probes and to a plurality of
amplifiers. Exemplary preamplifiers are described, for example, in
U.S. Pat. No. 5,635,352 and U.S. Pat. No. 5,681,697.
[0084] A "pathogen" is a biological agent, typically a
microorganism, that causes disease or illness to its host.
[0085] A "microorganism" is an organism of microscopic or
submicroscopic size. Examples include, but are not limited to,
bacteria, fungi, yeast, protozoans, microscopic algae (e.g.,
unicellular algae), viruses (which are typically included in this
category although they are incapable of growth and reproduction
outside of host cells), subviral agents, viroids, and
mycoplasma.
[0086] A variety of additional terms are defined or otherwise
characterized herein.
DETAILED DESCRIPTION
[0087] Among other aspects, the present invention provides
multiplex assays that can be used for simultaneous detection, and
optionally quantitation, of two or more nucleic acid targets in a
single cell. A related aspect of the invention provides methods for
detecting the level of one or more target nucleic acids relative to
that of a reference nucleic acid in an individual cell.
[0088] In general, in the assays of the invention, a label probe is
captured to each target nucleic acid. The label probe can be
captured to the target through direct binding of the label probe to
the target. Preferably, however, the label probe is captured
indirectly through binding to capture probes, amplifiers, and/or
preamplifiers that bind to the target. Use of the optional
amplifiers and preamplifiers facilitates capture of multiple copies
of the label probe to the target, thus amplifying signal from the
target without requiring enzymatic amplification of the target
itself. Binding of the capture probes is optionally cooperative,
reducing background caused by undesired cross hybridization of
capture probes to non-target nucleic acids (a greater problem in
multiplex assays than singleplex assays since more probes must be
used in multiplex assays, increasing the likelihood of cross
hybridization).
[0089] One aspect of the invention relates to detection of single
cells, including detection of rare cells from a heterogeneous
mixture of cells. Individual cells are detected through detection
of nucleic acids whose presence, absence, copy number, or the like
are characteristic of the cell.
[0090] Compositions, kits, and systems related to the methods are
also provided.
Methods of Detecting Nucleic Acids and Cells
[0091] Multiplex Detection of Nucleic Acids
[0092] As noted, one aspect of the invention provides multiplex
nucleic acid assays in single cells. Thus, one general class of
embodiments includes methods of detecting two or more nucleic acid
targets in an individual cell. In the methods, a sample comprising
the cell is provided. The cell comprises, or is suspected of
comprising, a first nucleic acid target and a second nucleic acid
target. A first label probe comprising a first label and a second
label probe comprising a second label, wherein a first signal from
the first label is distinguishable from a second signal from the
second label, are provided. At least a first capture probe and at
least a second capture probe are also provided.
[0093] The first capture probe is hybridized, in the cell, to the
first nucleic acid target (when the first nucleic acid target is
present in the cell), and the second capture probe is hybridized,
in the cell, to the second nucleic acid target (when the second
nucleic acid target is present in the cell). The first label probe
is captured to the first capture probe and the second label probe
is captured to the second capture probe, thereby capturing the
first label probe to the first nucleic acid target and the second
label probe to the second nucleic acid target. The first signal
from the first label and the second signal from the second label
are then detected. Since the first and second labels are associated
with their respective nucleic acid targets through the capture
probes, presence of the label(s) in the cell indicates the presence
of the corresponding nucleic acid target(s) in the cell. The
methods are optionally quantitative. Thus, an intensity of the
first signal and an intensity of the second signal can be measured,
and the intensity of the first signal can be correlated with a
quantity of the first nucleic acid target in the cell while the
intensity of the second signal is correlated with a quantity of the
second nucleic acid target in the cell.
[0094] In one aspect, the label probes bind directly to the capture
probes. For example, in one class of embodiments, a single first
capture probe and a single second capture probe are provided, the
first label probe is hybridized to the first capture probe, and the
second label probe is hybridized to the second capture probe. In a
related class of embodiments, two or more first capture probes and
two or more second capture probes are provided, as are a plurality
of the first label probes (e.g., two or more identical first label
probes) and a plurality of the second label probes (e.g., two or
more identical second label probes). The two or more first capture
probes are hybridized to the first nucleic acid target, and the two
or more second capture probes are hybridized to the second nucleic
acid target. A single first label probe is hybridized to each of
the first capture probes, and a single second label probe is
hybridized to each of the second capture probes.
[0095] In another aspect, the label probes are captured to the
capture probes indirectly, for example, through binding of
preamplifiers and/or amplifiers. Use of amplifiers and
preamplifiers can be advantageous in increasing signal strength,
since they can facilitate binding of large numbers of label probes
to each nucleic acid target.
[0096] In one class of embodiments in which amplifiers are
employed, a single first capture probe, a single second capture
probe, a plurality of the first label probes, and a plurality of
the second label probes are provided. A first amplifier is
hybridized to the first capture probe and to the plurality of first
label probes, and a second amplifier is hybridized to the second
capture probe and to the plurality of second label probes. In
another class of embodiments, two or more first capture probes, two
or more second capture probes, a plurality of the first label
probes, and a plurality of the second label probes are provided.
The two or more first capture probes are hybridized to the first
nucleic acid target, and the two or more second capture probes are
hybridized to the second nucleic acid target. A first amplifier is
hybridized to each of the first capture probes, and the plurality
of first label probes is hybridized to the first amplifiers. A
second amplifier is hybridized to each of the second capture
probes, and the plurality of second label probes is hybridized to
the second amplifiers.
[0097] In one class of embodiments in which preamplifiers are
employed, a single first capture probe, a single second capture
probe, a plurality of the first label probes, and a plurality of
the second label probes are provided. A first preamplifier is
hybridized to the first capture probe, a plurality of first
amplifiers is hybridized to the first preamplifier, and the
plurality of first label probes is hybridized to the first
amplifiers. A second preamplifier is hybridized to the second
capture probe, a plurality of second amplifiers is hybridized to
the second preamplifier, and the plurality of second label probes
is hybridized to the second amplifiers. In another class of
embodiments, two or more first capture probes, two or more second
capture probes, a plurality of the first label probes, and a
plurality of the second label probes are provided. The two or more
first capture probes are hybridized to the first nucleic acid
target, and the two or more second capture probes are hybridized to
the second nucleic acid target. A first preamplifier is hybridized
to each of the first capture probes, a plurality of first
amplifiers is hybridized to each of the first preamplifiers, and
the plurality of first label probes is hybridized to the first
amplifiers. A second preamplifier is hybridized to each of the
second capture probes, a plurality of second amplifiers is
hybridized to each of the second preamplifiers, and the plurality
of second label probes is hybridized to the second amplifiers.
Optionally, additional preamplifiers can be used as intermediates
between a preamplifier hybridized to the capture probe(s) and the
amplifiers.
[0098] In the above classes of embodiments, one capture probe
hybridizes to each label probe, amplifier, or preamplifier. In
alternative classes of related embodiments, two or more capture
probes hybridize to the label probe, amplifier, or preamplifier.
See, e.g., the section below entitled "Implementation,
applications, and advantages."
[0099] In embodiments in which two or more first capture probes
and/or two or more second capture probes are employed, the capture
probes preferably hybridize to nonoverlapping polynucleotide
sequences in their respective nucleic acid target. The capture
probes can, but need not, cover a contiguous region of the nucleic
acid target. Blocking probes, polynucleotides which hybridize to
regions of the nucleic acid target not occupied by capture probes,
are optionally provided and hybridized to the target. For a given
nucleic acid target, the corresponding capture probes and blocking
probes are preferably complementary to physically distinct,
nonoverlapping sequences in the nucleic acid target, which
nonoverlapping sequences are preferably, but not necessarily,
contiguous. Having the capture probes and optional blocking probes
be contiguous with each other can in some embodiments enhance
hybridization strength, remove secondary structure, and ensure more
consistent and reproducible signal.
[0100] In many embodiments, such as those above, enzymatic
manipulation is not required to capture the label probes to the
capture probes. In other embodiments, however, enzymatic
manipulation, particularly amplification of nucleic acids
intermediate between the capture probes and the label probes,
facilitates detection of the nucleic acid targets. For example, in
one class of embodiments, a plurality of the first label probes and
a plurality of the second label probes are provided. A first
amplified polynucleotide is produced by rolling circle
amplification of a first circular polynucleotide hybridized to the
first capture probe. The first circular polynucleotide comprises at
least one copy of a polynucleotide sequence identical to a
polynucleotide sequence in the first label probe, and the first
amplified polynucleotide thus comprises a plurality of copies of a
polynucleotide sequence complementary to the polynucleotide
sequence in the first label probe. The plurality of first label
probes is then hybridized to the first amplified polynucleotide.
Similarly, a second amplified polynucleotide is produced by rolling
circle amplification of a second circular polynucleotide hybridized
to the second capture probe (preferably, at the same time the first
amplified polynucleotide is produced). The second circular
polynucleotide comprises at least one copy of a polynucleotide
sequence identical to a polynucleotide sequence in the second label
probe, and the second amplified polynucleotide thus comprises a
plurality of copies of a polynucleotide sequence complementary to
the polynucleotide sequence in the second label probe. The
plurality of second label probes is then hybridized to the second
amplified polynucleotide. The amplified polynucleotides remain
associated (e.g., covalently) with the capture probe(s), and the
label probes are thus captured to the nucleic acid targets. A
circular polynucleotide can be provided and hybridized to the
capture probe, or a linear polynucleotide that is circularized by
ligation after it binds to the capture probe (e.g., a padlock
probe) can be employed. Techniques for rolling circle
amplification, including use of padlock probes, are well known in
the art. See, e.g., Larsson et al. (2004) "In situ genotyping
individual DNA molecules by target-primed rolling-circle
amplification of padlock probes" Nat Methods. 1(3):227-32, Nilsson
et al. (1994) Science 265:2085-2088, and Antson et al. (2000)
"PCR-generated padlock probes detect single nucleotide variation in
genomic DNA" Nucl Acids Res 28(12):E58.
[0101] Potential capture probe sequences are optionally examined
for possible interactions with non-corresponding nucleic acid
targets, the preamplifiers, the amplifiers, the label probes,
and/or any relevant genomic sequences, for example. Sequences
expected to cross-hybridize with undesired nucleic acids are
typically not selected for use in the capture probes. Examination
can be, e.g., visual (e.g., visual examination for
complementarity), computational (e.g., a BLAST search of the
relevant genomic database, or computation and comparison of binding
free energies), and/or experimental (e.g., cross-hybridization
experiments). Label probe sequences are preferably similarly
examined, to help minimize potential undesirable
cross-hybridization.
[0102] A capture probe, preamplifier, amplifier, and/or label probe
optionally comprises at least one non-natural nucleotide. For
example, a capture probe and a preamplifier (or amplifier or label
probe) that hybridizes to it optionally comprise, at complementary
positions, at least one pair of non-natural nucleotides that base
pair with each other but that do not Watson-Crick base pair with
the bases typical to biological DNA or RNA (i.e., A, C, G, T, or
U). Examples of nonnatural nucleotides include, but are not limited
to, Locked NucleicAcid.TM. nucleotides (available from Exiqon A/S,
(www.) exiqon.com; see, e.g., SantaLucia Jr. (1998) Proc Natl Acad
Sci 95:1460-1465) and isoG, isoC, and other nucleotides used in the
AEGIS system (Artificially Expanded Genetic Information System,
available from EraGen Biosciences, (www.) eragen.com; see, e.g.,
U.S. Pat. No. 6,001,983, U.S. Pat. No. 6,037,120, and U.S. Pat. No.
6,140,496). Use of such non-natural base pairs (e.g., isoG-isoC
base pairs) in the probes can, for example, reduce background
and/or simplify probe design by decreasing cross hybridization, or
it can permit use of shorter probes when the non-natural base pairs
have higher binding affinities than do natural base pairs.
[0103] As noted, the methods are useful for multiplex detection of
nucleic acids, including simultaneous detection of more than two
nucleic acid targets. Thus, the cell optionally comprises or is
suspected of comprising a third nucleic acid target, and the
methods optionally include: providing a third label probe
comprising a third label, wherein a third signal from the third
label is distinguishable from the first and second signals,
providing at least a third capture probe, hybridizing in the cell
the third capture probe to the third nucleic acid target (when the
third target is present in the cell), capturing the third label
probe to the third capture probe, and detecting the third signal
from the third label. Fourth, fifth, sixth, etc. nucleic acid
targets are similarly simultaneously detected in the cell if
desired.
[0104] A nucleic acid target can be essentially any nucleic acid
that is desirably detected in the cell. For example, a nucleic acid
target can be a DNA, a chromosomal DNA, an RNA, an mRNA, a
microRNA, a ribosomal RNA, or the like. The nucleic acid target can
be a nucleic acid endogenous to the cell. As another example, the
target can be a nucleic acid introduced to or expressed in the cell
by infection of the cell with a pathogen, for example, a viral or
bacterial genomic RNA or DNA, a plasmid, a viral or bacterial mRNA,
or the like.
[0105] The first and second (and/or optional third, fourth, etc.)
nucleic acid targets can be part of a single nucleic acid molecule,
or they can be separate molecules. Various advantages and
applications of both approaches are discussed in greater detail
below and in the section entitled "Implementation, applications,
and advantages." In one class of embodiments, the first nucleic
acid target is a first mRNA and the second nucleic acid target is a
second mRNA. In another class of embodiments, the first nucleic
acid target comprises a first region of an mRNA and the second
nucleic acid target comprises a second region of the same mRNA;
this approach can increase specificity of detection of the mRNA. In
another class of embodiments, the first nucleic acid target
comprises a first chromosomal DNA polynucleotide sequence and the
second nucleic acid target comprises a second chromosomal DNA
polynucleotide sequence. The first and second chromosomal DNA
polynucleotide sequences are optionally located on the same
chromosome, e.g., within the same gene, or on different
chromosomes.
[0106] In one aspect, the signal(s) from nucleic acid target(s) are
normalized. In one class of embodiments, the second nucleic acid
target comprises a reference nucleic acid, and the method includes
normalizing the first signal to the second signal. The reference
nucleic acid is a nucleic acid selected as a standard of
comparison. It will be evident that choice of the reference nucleic
acid can depend on the desired application. For example, for gene
expression analysis, where the first and optional third, fourth,
etc. nucleic acid targets are mRNAs whose expression levels are to
be determined, the reference nucleic acid can be an mRNA
transcribed from a housekeeping gene. As another example, the first
nucleic acid target can be an mRNA whose expression is altered in a
pathological state, e.g., an mRNA expressed in a tumor cell and not
a normal cell or expressed at a higher level in a tumor cell than
in a normal cell, while the second nucleic acid target is an mRNA
expressed from a housekeeping gene or similar gene whose expression
is not altered in the pathological state. As yet another example,
the first nucleic acid target can be a chromosomal DNA sequence
that is amplified or deleted in a tumor cell, while the second
nucleic acid target is another chromosomal DNA sequence that is
maintained at its normal copy number in the tumor cell. Exemplary
reference nucleic acids are described herein, and many more are
well known in the art.
[0107] Optionally, results from the cell are compared with results
from a reference cell. That is, the first and second targets are
also detected in a reference cell, for example, a non-tumor,
uninfected, or other healthy normal cell, chosen as a standard of
comparison depending on the desired application. The signals can be
normalized to a reference nucleic acid as noted above. As just one
example, the first nucleic acid target can be the Her-2 gene, with
the goal of measuring Her-2 gene amplification. Signal from Her-2
can be normalized to that from a reference gene, whose copy number
is stably maintained in the genomic DNA. The normalized signal for
the Her-2 gene from a target cell (e.g., a tumor cell or suspected
tumor cell) can be compared to the normalized signal from a
reference cell (e.g., a normal cell), to determine copy number in
the cancer cell in comparison to normal cells.
[0108] The label (first, second, third, etc.) can be essentially
any convenient label that directly or indirectly provides a
detectable signal. In one aspect, the first label is a first
fluorescent label and the second label is a second fluorescent
label. Detecting the signal from the labels thus comprises
detecting fluorescent signals from the labels. A variety of
fluorescent labels whose signals can be distinguished from each
other are known, including, e.g., fluorophores and quantum dots. As
other examples, the label can be a luminescent label, a
light-scattering label (e.g., colloidal gold particles), or an
enzyme (e.g., alkaline phosphatase or horseradish peroxidase).
[0109] The methods can be used to detect the presence of the
nucleic acid targets in cells from essentially any type of sample.
For example, the sample can be derived from a bodily fluid, a
bodily waste, blood, bone marrow, sputum, urine, lymph node, stool,
vaginal secretions, cervical pap smear, oral swab or other swab or
smear, spinal fluid, saliva, sputum, ejaculatory fluid, semen,
lymph fluid, an intercellular fluid, a tissue (e.g., a tissue
homogenate), a biopsy, and/or a tumor. The sample and/or the cell
can be derived from one or more of a human, an animal, a plant, and
a cultured cell. Samples derived from even relatively large volumes
of materials such as bodily fluid or bodily waste can be screened
in the methods of the invention, and removal of such materials is
relatively non-invasive. Samples are optionally taken from a
patient, following standard laboratory methods after informed
consent.
[0110] The methods for detecting nucleic acid targets in cells can
be used to identify the cells. For example, a cell can be
identified as being of a desired type based on which nucleic acids,
and in what levels, it contains. Thus, in one class of embodiments,
the methods include identifying the cell as a desired target cell
based on detection of the first and second signals (and optional
third, fourth, etc. signals) from within the cell. The cell can be
identified on the basis of the presence or absence of one or more
of the nucleic acid targets. Similarly, the cell can be identified
on the basis of the relative signal strength from or expression
level of one or more of the nucleic acid targets. Signals are
optionally normalized as noted above and/or compared to those from
a reference cell.
[0111] The methods can be applied to detection and identification
of even rare cell types. Thus, the sample including the cell can be
a mixture of desired target cells and other, nontarget cells, which
can be present in excess of the target cells. For example, the
ratio of target cells to cells of all other type(s) in the sample
is optionally less than 1:1.times.10.sup.4, less than
1:1.times.10.sup.5, less than 1:1.times.10.sup.6, less than
1:1.times.10.sup.7, less than 1:1.times.10.sup.8, or even less than
1:1.times.10.sup.9.
[0112] Essentially any type of cell that can be differentiated
based on its nucleic acid content (presence, absence, expression
level or copy number of one or more nucleic acids) can be detected
and identified using the methods and a suitable choice of nucleic
acid targets. As just a few examples, the cell can be a circulating
tumor cell, a virally infected cell, a fetal cell in maternal
blood, a bacterial cell or other microorganism in a biological
sample (e.g., blood or other body fluid), an endothelial cell,
precursor endothelial cell, or myocardial cell in blood, a stem
cell, or a T-cell. Rare cell types can be enriched prior to
performing the methods, if necessary, by methods known in the art
(e.g., lysis of red blood cells, isolation of peripheral blood
mononuclear cells, further enrichment of rare target cells through
magnetic-activated cell separation (MACS), etc.). The methods are
optionally combined with other techniques, such as DAPI staining
for nuclear DNA. It will be evident that a variety of different
types of nucleic acid markers are optionally detected
simultaneously by the methods and used to identify the cell. For
example, a cell can be identified based on the presence or relative
expression level of one nucleic acid target in the cell and the
absence of another nucleic acid target from the cell; e.g., a
circulating tumor cell can be identified by the presence or level
of one or more markers found in the tumor cell and not found (or
found at different levels) in blood cells, and its identity can be
confirmed by the absence of one or more markers present in blood
cells and not circulating tumor cells. The principle may be
extended to using any other type of markers such as protein based
markers in single cells.
[0113] The cell is typically fixed and permeabilized before
hybridization of the capture probes, to retain the nucleic acid
targets in the cell and to permit the capture probes, label probes,
etc. to enter the cell. The cell is optionally washed to remove
materials not captured to one of the nucleic acid targets. The cell
can be washed after any of various steps, for example, after
hybridization of the capture probes to the nucleic acid targets to
remove unbound capture probes, after hybridization of the
preamplifiers, amplifiers, and/or label probes to the capture
probes, and/or the like.
[0114] The various capture and hybridization steps can be performed
simultaneously or sequentially, in essentially any convenient
order. Preferably, a given hybridization step is accomplished for
all of the nucleic acid targets at the same time. For example, all
the capture probes (first, second, etc.) can be added to the cell
at once and permitted to hybridize to their corresponding targets,
the cell can be washed, amplifiers (first, second, etc.) can be
hybridized to the corresponding capture probes, the cell can be
washed, the label probes (first, second, etc.) can be hybridized to
the corresponding amplifiers, and the cell can then be washed again
prior to detection of the labels. As another example, the capture
probes can be hybridized to the targets, the cell can be washed,
amplifiers and label probes can be added together and hybridized,
and the cell can then be washed prior to detection. It will be
evident that double-stranded nucleic acid target(s) are preferably
denatured, e.g., by heat, prior to hybridization of the
corresponding capture probe(s) to the target(s).
[0115] Preferably, the cell is in suspension for all or most of the
steps of the method, for ease of handling. However, the methods are
also applicable to cells in solid tissue samples (e.g., tissue
sections) and/or cells immobilized on a substrate (e.g., a slide or
other surface). Thus, in one class of embodiments, the cell is in
suspension in the sample comprising the cell, and/or the cell is in
suspension during the hybridizing, capturing, and/or detecting
steps. For example, the cell can be in suspension in the sample and
during the hybridization, capture, optional washing, and detection
steps. In other embodiments, the cell is in suspension in the
sample comprising the cell, and the cell is fixed on a substrate
during the hybridizing, capturing, and/or detecting steps. For
example, the cell can be in suspension during the hybridization,
capture, and optional washing steps and immobilized on a substrate
during the detection step.
[0116] Signals from the labels can be detected, and their
intensities optionally measured, by any of a variety of techniques
well known in the art. For example, in embodiments in which the
cell is in suspension, the first and second (and optional third,
etc.) signals can be conveniently detected by flow cytometry. In
embodiments in which cells are immobilized on a substrate, the
first and second (and optional third etc.) signals can be detected,
for example, by laser scanner or microscope, e.g., a fluorescent or
automated scanning microscope. As noted, detection is at the level
of individual, single cells. Signals from the labels are typically
detected in a single operation (e.g., a single flow cytometry run
or a single microscopy or scanning session), rather than
sequentially in separate operations for each label. Such a single
detection operation can, for example, involve changing optical
filters between detection of the different labels, but it does not
involve detection of the first label followed by capture of the
second label and then detection of the second label. In some
embodiments, the first and second (and optional third etc.) labels
are captured to their respective targets simultaneously but are
detected in separate detection steps or operations.
[0117] Additional features described herein, e.g., in the section
below entitled "Implementation, applications, and advantages," can
be applied to the methods, as relevant. For example, as described
in greater detail below, a label probe can include more than one
label, identical or distinct. Signal strength is optionally
adjusted between targets depending on their expected copy numbers,
if desired; for example, the signal for an mRNA expressed at low
levels can be amplified to a greater degree (e.g., by use of more
labels per label probe and/or use of preamplifiers and amplifiers
to capture more label probes per copy of the target) than the
signal for a highly expressed mRNA.
[0118] In another aspect of the invention, two or more nucleic
acids are detected by PCR amplification of the nucleic acids in
situ in individual cells. To prevent leakage of the resulting
amplicons out of the cells, a water-oil emulsion can be made as
mentioned in Li et al. (2006) "BEAMing up for detection and
quantification of rare sequence variants" Nature Methods 3(2):95-7
that separates single cells into different compartments.
[0119] Detection of Relative Levels by Normalization to Reference
Nucleic Acids
[0120] As discussed briefly above, the signal detected for a
nucleic acid of interest can be normalized to that of a standard,
reference nucleic acid. One general class of embodiments thus
provides methods of assaying a relative level of one or more target
nucleic acids in an individual cell. In the methods, a sample
comprising the cell is provided. The cell comprises or is suspected
of comprising a first, target nucleic acid, and it comprises a
second, reference nucleic acid. A first label probe comprising a
first label and a second label probe comprising a second label,
wherein a first signal from the first label is distinguishable from
a second signal from the second label, are also provided. In the
cell, the first label probe is captured to the first, target
nucleic acid (when the first, target nucleic acid is present in the
cell) and the second label probe is captured to the second,
reference nucleic acid. The first signal from the first label and
the second signal from the second label are then detected in the
individual cell, and the intensity of each signal is measured. The
intensity of the first signal is normalized to the intensity of the
second (reference) signal. The level of the first, target nucleic
acid relative to the level of the second, reference nucleic acid in
the cell is thereby assayed, since the first and second labels are
associated with their respective nucleic acids. The methods are
optionally quantitative, permitting measurement of the amount of
the first, target nucleic acid relative to the amount of the
second, reference nucleic acid in the cell. Thus, the intensity of
the first signal normalized to that of the second signal can be
correlated with a quantity of the first, target nucleic acid
present in the cell.
[0121] The label probes can bind directly to the nucleic acids. For
example, the first label probe can hybridize to the first, target
nucleic acid and/or the second label probe can hybridize to the
second, reference nucleic acid. Alternatively, some or all of the
label probes can be indirectly bound to their corresponding nucleic
acids, e.g., through capture probes. For example, the first and
second label probes can bind directly to the nucleic acids, or one
can bind directly while the other binds indirectly, or both can
bind indirectly.
[0122] The label probes are optionally captured to the nucleic
acids via capture probes. In one class of embodiments, at least a
first capture probe and at least a second capture probe are
provided. In the cell, the first capture probe is hybridized to the
first, target nucleic acid and the second capture probe is
hybridized to the second, reference nucleic acid. The first label
probe is captured to the first capture probe and the second label
probe is captured to the second capture probe, thereby capturing
the first label probe to the first, target nucleic acid and the
second label probe to the second, reference nucleic acid. The
features described for the methods above apply to these embodiments
as well, with respect to configuration and number of the label and
capture probes, optional use of preamplifiers and/or amplifiers,
rolling circle amplification of circular polynucleotides, and the
like.
[0123] The methods can be used for multiplex detection of nucleic
acids, including simultaneous detection of two or more target
nucleic acids. Thus, the cell optionally comprises or is suspected
of comprising a third, target nucleic acid, and the methods
optionally include: providing a third label probe comprising a
third label, wherein a third signal from the third label is
distinguishable from the first and second signals; capturing, in
the cell, the third label probe to the third, target nucleic acid
(when present in the cell); detecting the third signal from the
third label, which detecting comprises measuring an intensity of
the third signal; and normalizing the intensity of the third signal
to the intensity of the second signal. Alternatively, the third
signal can be normalized to that from a different reference nucleic
acid. Fourth, fifth, sixth, etc. nucleic acids are similarly
simultaneously detected in the cell if desired. The third, fourth,
fifth, etc. label probes are optionally hybridized directly to
their corresponding nucleic acid, or they can be captured
indirectly via capture probes as described for the first and second
label probes.
[0124] The methods can be used for gene expression analysis,
detection of gene amplification or deletion, or detection or
diagnosis of disease, as just a few examples. A target nucleic acid
can be essentially any nucleic acid that is desirably detected in
the cell. For example, a target nucleic acid can be a DNA, a
chromosomal DNA, an RNA, an mRNA, a microRNA, a ribosomal RNA, or
the like. The target nucleic acid can be a nucleic acid endogenous
to the cell, or as another example, the target can be a nucleic
acid introduced to or expressed in the cell by infection of the
cell with a pathogen, for example, a viral or bacterial genomic RNA
or DNA, a plasmid, a viral or bacterial mRNA, or the like. The
reference nucleic acid can similarly be a DNA, an mRNA, a
chromosomal DNA, an mRNA, an RNA endogenous to the cell, or the
like.
[0125] As described above, choice of the reference nucleic acid can
depend on the desired application. For example, for gene expression
analysis, where the first and optional third, fourth, etc. target
nucleic acids are mRNAs whose expression levels are to be
determined, the reference nucleic acid can be an mRNA transcribed
from a housekeeping gene. As another example, the first, target
nucleic acid can be an mRNA whose expression is altered in a
pathological state, e.g., an mRNA expressed in a tumor cell and not
a normal cell or expressed at a higher level in a tumor cell than
in a normal cell, while the reference nucleic acid is an mRNA
expressed from a housekeeping gene or similar gene whose expression
is not altered in the pathological state. In a similar example, the
target nucleic acid can be a viral or bacterial nucleic acid while
the reference nucleic acid is endogenous to the cell. As yet
another example, the first, target nucleic acid can be a
chromosomal DNA sequence that is amplified or deleted in a tumor
cell, while the reference nucleic acid is another chromosomal DNA
sequence that is maintained at its normal copy number in the tumor
cell. Exemplary reference nucleic acids are described herein, and
many more are well known in the art.
[0126] In one class of embodiments, the first, target nucleic acid
is a first mRNA and the second, reference nucleic acid is a second
mRNA. In another class of embodiments, the first, target nucleic
acid comprises a first chromosomal DNA polynucleotide sequence and
the second, reference nucleic acid comprises a second chromosomal
DNA polynucleotide sequence. The first and second chromosomal DNA
polynucleotide sequences are optionally located on the same
chromosome or on different chromosomes.
[0127] Optionally, normalized results from the cell are compared
with normalized results from a reference cell. That is, the target
and reference nucleic acids are also detected in a reference cell,
for example, a non-tumor, uninfected, or other healthy normal cell,
chosen as a standard of comparison depending on the desired
application. As just one example, the first, target nucleic acid
can be the Her-2 gene, with the goal of measuring Her-2 gene
amplification. Signal from Her-2 can be normalized to that from a
reference gene whose copy number is stably maintained in the
genomic DNA. The normalized signal for the Her-2 gene from a target
cell (e.g., a tumor cell or suspected tumor cell) can be compared
to the normalized signal from a reference cell (e.g., a normal
cell), to determine copy number in the cancer cell in comparison to
normal cells.
[0128] Signal strength is optionally adjusted between the target
and reference nucleic acids depending on their expected copy
numbers, if desired. For example, the signal for a target mRNA
expressed at low levels can be amplified to a greater degree (e.g.,
by use of more labels per label probe and/or use of capture probes,
preamplifiers and amplifiers to capture more label probes per copy
of the target) than the signal for a highly expressed mRNA (which
can, e.g., be detected by direct binding of the label probe to the
reference nucleic acid, by use of capture probes and amplifier
without a preamplifier, or the like).
[0129] The methods for assaying relative levels of target nucleic
acids in cells can be used to identify the cells. For example, a
cell can be identified as being of a desired type based on which
nucleic acids, and in what levels, it contains. Thus, in one class
of embodiments, the methods include identifying the cell as a
desired target cell based on the normalized first signal (and
optional normalized third, fourth, etc. signals). As described
herein, the cell can be identified on the basis of the presence or
absence of one or more of the target nucleic acids. Similarly, the
cell can be identified on the basis of the relative signal strength
from or expression level of one or more target nucleic acids.
Signals are optionally compared to those from a reference cell.
[0130] The methods can be applied to detection and identification
of even rare cell types. Thus, the sample including the cell can be
a mixture of desired target cells and other, nontarget cells, which
can be present in excess of the target cells. For example, the
ratio of target cells to cells of all other type(s) in the sample
is optionally less than 1:1.times.10.sup.4, less than
1:1.times.10.sup.5, less than 1:1.times.10.sup.6, less than
1:1.times.10.sup.7, less than 1:1.times.10.sup.8, or even less than
1:1.times.10.sup.9.
[0131] Essentially any type of cell that can be differentiated
based on its nucleic acid content (presence, absence, or copy
number of one or more nucleic acids) can be detected and identified
using the methods and a suitable choice of target and reference
nucleic acids. As just a few examples, the cell can be a
circulating tumor cell, a virally infected cell, a fetal cell in
maternal blood, a bacterial cell or other microorganism in a
biological sample (e.g., blood or other body fluid), or an
endothelial cell, precursor endothelial cell, or myocardial cell in
blood. Rare cell types can be enriched prior to performing the
methods, if necessary, by methods known in the art (e.g., lysis of
red blood cells, isolation of peripheral blood mononuclear cells,
etc.). The methods are optionally combined with other techniques,
such as DAPI staining for nuclear DNA. It will be evident that a
variety of different types of nucleic acid markers are optionally
detected simultaneously by the methods and used to identify the
cell. For example, a cell can be identified based on the presence
or relative expression level of one target nucleic acid in the cell
and the absence of another target nucleic acid from the cell; e.g.,
a circulating tumor cell can be identified by the presence or level
of one or more markers found in the tumor cell and not found (or
found at different levels) in blood cells, and by the absence of
one or more markers present in blood cells and not circulating
tumor cells. The principle may be extended to using any other type
of markers such as protein based markers in single cells.
[0132] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to source of sample, fixation and permeabilization of the
cell, washing the cell, denaturation of double-stranded target and
reference nucleic acids, type of labels, use of optional blocking
probes, detection of signals, detection (and intensity measurement)
by flow cytometry or microscopy, presence of the cell in suspension
or immobilized on a substrate, and/or the like. Also, additional
features described herein, e.g., in the section entitled
"Implementation, applications, and advantages," can be applied to
the methods, as relevant.
[0133] The methods of the invention can be used for gene expression
analysis in single cells. Currently, gene expression analysis deals
with heterogeneous cell populations such as blood or tumor
specimens. Blood contains various subtypes of leukocytes, and when
changes in gene expression of whole blood or RNA isolated from
blood are measured, it is not known what subtype of blood cells
actually changed their gene expression. It is possible that gene
expression of only a certain subtype of blood cells is affected in
a disease state or by drug treatment, for example. Technology that
can measure gene expression in single cells, so changes of gene
expression in single cells can be examined, is thus desirable.
Similarly, a tumor specimen contains a heterogeneous cell
population including tumor cells, normal cells, stromal cells,
immune cells, etc. Current technology looks at the sum of the
expression of all those cells through total RNA or cell lysate.
However, the overall expression change may not be representative of
that in target tumor cells. So again, it would be useful to look at
the expression changes in single cells so that the target tumor
cells can be examined specifically, to see how the target cells
change in gene expression and how they respond to drug treatment,
for example.
[0134] In one aspect, the present invention provides methods for
gene expression analysis in single cells. Single cell gene
expression analysis can be accomplished by measuring expression of
a target gene and normalizing against the expression of a
housekeeping gene, as described above. As just a couple of
examples, the normalized expression in a disease state can be
compared to that in the normal state, or the expression in a drug
treated state can be compared to that in the normal state. The
change of expression level in single cells may have biological
significance indicating disease progression, drug therapeutic
efficacy and/or toxicity, tumor staging and classification,
etc.
[0135] Accordingly, one general class of embodiments provides
methods of performing comparative gene expression analysis in
single cells. In the methods, a first mixed cell population
comprising one or more cells of a specified type is provided. A
second mixed cell population comprising one or more cells of the
specified type is also provided. An expression level of one or more
target nucleic acids relative to a reference nucleic acid is
measured in the cells of the specified type of the first
population, to provide a first expression profile. An expression
level of the one or more target nucleic acids relative to the
reference nucleic acid is measured in the cells of the specified
type of the second population, to provide a second expression
profile. The first and second expression profiles are compared.
[0136] In one class of embodiments, the one or more target nucleic
acids are one or more mRNAs, e.g., two or more, three or more, four
or more, etc. mRNAs. The expression level of each mRNA can be
determined relative to that of a housekeeping gene whose mRNA
serves as the reference nucleic acid.
[0137] The first and/or second mixed cell population contains at
least one other type of cell in addition to the specified type,
more typically at least two or more other types of cells, and
optionally several to many other types of cells (e.g., as is found
in whole blood, a tumor, or other complex biological sample). The
ratio of cells of the specified type to cells of all other type(s)
in the first or second mixed cell population is optionally less
than 1:1.times.10.sup.4, less than 1:1.times.10.sup.5, less than
1:1.times.10.sup.6, less than 1:1.times.10.sup.7, less than
1:1.times.10.sup.8, or even less than 1:1.times.10.sup.9.
[0138] As will be evident, a change in gene expression profile
between the two populations may indicate a disease state or
progression, a drug response, a therapeutic efficacy, etc. Thus,
for example, the first mixed cell population can be from a patient
who has been diagnosed or who is to be diagnosed with a particular
disease or disorder, while the second mixed population is from a
healthy individual. Similarly, the first and second mixed
populations can be from a single individual but taken at different
time points, for example, to follow disease progression or to
assess response to drug treatment. Accordingly, the first mixed
cell population can be taken from an individual (e.g., a human)
before treatment is initiated with a drug or other compound, while
the second population is taken at a specified time after treatment
is initiated. As another example, the first mixed population can be
from a treated individual while the second mixed population is from
an untreated individual.
[0139] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to type of target and reference nucleic acids, cell type,
source of sample, fixation and permeabilization of the cell,
washing the cell, denaturation of double-stranded target and
reference nucleic acids, type of labels, use and configuration of
label probes, capture probes, preamplifiers and/or amplifiers, use
of optional blocking probes, detection of signals, detection (and
intensity measurement) by flow cytometry or microscopy, presence of
the cell in suspension or immobilized on a substrate, and/or the
like. Exemplary target and reference nucleic acids are described
herein.
[0140] In another aspect, the methods can be used to compare copy
number in single cells from a first population (e.g., tumor cells)
with copy number in single cells from a second population (e.g.,
normal cells used as a reference). The nucleic acid target(s) can
be transcripts or genomic DNA, where, for example, the degree of
amplification or deletion of genes such as her-2 can correlate with
tumor progression. In another aspect, the methods can be applied to
gene expression analysis in single cells in even a single
population, including, for example, cells of the same type but at
different stages of the cell cycle.
[0141] Label Density
[0142] The methods of the invention permit far more labels to be
captured to small regions of target nucleic acids than do currently
existing techniques. For example, standard FISH techniques
typically use probes that cover 20 kb or more, and a probe
typically has fluorophores chemically conjugated at a density of
approximately one fluorescent molecule per seven nucleotides of the
probe. When molecular beacon target detection is employed, one
label pair is captured to the target in the region covered by the
beacon, typically about 40 nucleotides. For additional discussion
of exemplary current techniques, see, e.g., U.S. patent application
publications 2004/0091880 and 2005/0181463, U.S. Pat. No.
6,645,731, and international patent application publications WO
95/09245 and 03/019141.
[0143] Methods described herein, in comparison, readily permit
capture of hundreds of labels (e.g., 400 or more) to the region of
the target covered by a single capture probe, e.g., 20-25
nucleotides or more. The theoretical degree of amplification
achieved from a single capture probe is readily calculated for any
given configuration of capture probes, amplifiers, etc; for
example, the theoretical degree of amplification achieved from a
single capture probe, and thus the number of labels per length in
nucleotides of the capture probe, can be equal to the number of
preamplifiers bound to the capture probe times the number of
amplifiers that bind each preamplifier times the number of label
probes that bind each preamplifier times the number of labels per
label probe.
[0144] Thus, in one aspect, the invention provides methods that
facilitate association of a high density of labels to target
nucleic acids in cells. One general class of embodiments provides
methods of detecting two or more nucleic acid targets in an
individual cell. In the methods, a sample comprising the cell is
provided. The cell comprises or is suspected of comprising a first
nucleic acid target and a second nucleic acid target. In the cell,
a first label is captured to the first nucleic acid target (when
present in the cell) and a second label is captured to the second
nucleic acid target (when present in the cell). A first signal from
the first label is distinguishable from a second signal from the
second label. As noted, the labels are captured at high density.
Thus, an average of at least one copy of the first label per
nucleotide of the first nucleic acid target is captured to the
first nucleic acid target over a region that spans at least 20
contiguous nucleotides of the first nucleic acid target, and an
average of at least one copy of the second label per nucleotide of
the second nucleic acid target is captured to the second nucleic
acid target over a region that spans at least 20 contiguous
nucleotides of the second nucleic acid target. The first signal
from the first label and the second signal from the second label
are detected.
[0145] In one class of embodiments, an average of at least four,
eight, or twelve copies of the first label per nucleotide of the
first nucleic acid target are captured to the first nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the first nucleic acid target, and an average of at least four,
eight, or twelve copies of the second label per nucleotide of the
second nucleic acid target are captured to the second nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the second nucleic acid target. In one embodiment, an average of
at least sixteen copies of the first label per nucleotide of the
first nucleic acid target are captured to the first nucleic acid
target over a region that spans at least 20 contiguous nucleotides
of the first nucleic acid target, and an average of at least
sixteen copies of the second label per nucleotide of the second
nucleic acid target are captured to the second nucleic acid target
over a region that spans at least 20 contiguous nucleotides of the
second nucleic acid target.
[0146] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant, for example, with
respect to type of labels, detection of signals, type, treatment,
and suspension of the cell, and/or the like. The regions of the
first and second nucleic acid targets optionally span at least 25,
50, 100, 200, or more contiguous nucleotides and/or at most 2000,
1000, 500, 200, 100, 50, or fewer nucleotides. A like density of
third, fourth, fifth, sixth, etc. labels is optionally present for
(e.g., captured to) third, fourth, fifth, sixth, etc. nucleic acid
targets.
[0147] Detection of Target Cells
[0148] As described above, cells can be detected and identified by
detecting their constituent nucleic acids. For certain
applications, for example, detection of rare cells from large
heterogeneous mixtures of cells, detection of multiple, redundant
nucleic acid markers in order to detect the rare cell is
advantageous. The following hypothetical example illustrates one
advantage of detecting redundant markers.
[0149] Say that circulating tumor cells (CTC) are to be detected
from a blood sample in which the CTC concentration is one in
10.sup.6 normal white blood cells. If a single nucleic acid marker
for the CTC (e.g., a nucleic acid whose presence or copy number can
uniquely and sufficiently distinguish the cell from the rest of the
cell population) has a detection specificity of 1 in 10.sup.3, 1000
cells will be mistakenly identified as "CTC" when 10.sup.6 cells
are counted. (Such false positives can result from random
background signal generated by nonspecific binding of the relevant
probe(s) or from similar factors.) If an additional independent
marker is included which, on its own, also has a detection
specificity of 1 in 10.sup.3, and if a cell is identified as a CTC
only if both markers are positive, the combined detection
specificity is now theoretically dramatically increased, to 1 in
10.sup.3.times.10.sup.3=10.sup.6. This specificity is sufficient
for direct CTC detection in normal white blood cells under these
assumptions. Similarly, if three independent redundant markers are
used for identification of CTC, the detection specificity can be
boosted to 1 in 10.sup.9. Use of two or more redundant markers thus
reduces the number of false positives and facilitates detection of
even rare cells from complex samples.
[0150] Accordingly, one general class of embodiments provides
methods of detecting an individual cell of a specified type. In the
methods, a sample comprising a mixture of cell types including at
least one cell of the specified type is provided. A first label
probe comprising a first label and a second label probe comprising
a second label, wherein a first signal from the first label is
distinguishable from a second signal from the second label, are
provided. In the cell, the first label probe is captured to a first
nucleic acid target (when the first nucleic acid target is present
in the cell) and the second label probe is captured to a second
nucleic acid target (when the second nucleic acid target is present
in the cell). The first signal from the first label and the second
signal from the second label are detected and correlated with the
presence, absence, or amount of the corresponding, first and second
nucleic acid targets in the cell. The cell is identified as being
of the specified type based on detection of the presence, absence,
or amount (e.g., a non-zero amount) of both the first and second
nucleic acid targets within the cell, where the specified type of
cell is distinguishable from the other cell type(s) in the mixture
on the basis of either the presence, absence, or amount of the
first nucleic acid target or the presence, absence, or amount of
the second nucleic acid target in the cell (that is, the nucleic
acid targets are redundant markers for the specified cell type). An
intensity of the first signal and an intensity of the second signal
are optionally measured and correlated with a quantity of the
corresponding nucleic acid present in the cell.
[0151] Each nucleic acid target that serves as a marker for the
specified cell type can distinguish the cell type by its presence
in the cell, by its amount (copy number, e.g., its genomic copy
number or its transcript expression level), or by its absence from
the cell (a negative marker). A set of nucleic acid targets can
include different types of such markers; that is, one nucleic acid
target can serve as a positive marker, distinguishing the cell by
its presence or non-zero amount in the cell, while another serves
as a negative marker, distinguishing the cell by its absence from
the cell. For example, in one class of embodiments, the cell
comprises a first nucleic acid target and a second nucleic acid
target, and the cell is identified as being of the specified type
based on detection of the presence or amount of both the first and
second nucleic acid targets within the cell, where the specified
type of cell is distinguishable from the other cell type(s) in the
mixture on the basis of either the presence or amount of the first
nucleic acid target or the presence or amount of the second nucleic
acid target in the cell.
[0152] The label probes can bind directly to the nucleic acid
targets. For example, the first label probe can hybridize to the
first nucleic acid target and/or the second label probe can
hybridize to the second nucleic acid target. Alternatively, some or
all of the label probes can be indirectly bound to their
corresponding nucleic acid targets, e.g., through capture probes.
For example, the first and second label probes can bind directly to
the nucleic acid targets, or one can bind directly while the other
binds indirectly, or both can bind indirectly.
[0153] The label probes are optionally captured to the nucleic acid
targets via capture probes. In one class of embodiments, at least a
first capture probe and at least a second capture probe are
provided. In the cell, the first capture probe is hybridized to the
first nucleic acid target and the second capture probe is
hybridized to the second nucleic acid target. The first label probe
is captured to the first capture probe and the second label probe
is captured to the second capture probe, thereby capturing the
first label probe to the first nucleic acid target and the second
label probe to the second nucleic acid target. The features
described for the methods above apply to these embodiments as well,
with respect to configuration and number of the label and capture
probes, optional use of preamplifiers and/or amplifiers, rolling
circle amplification of circular polynucleotides, and the like.
[0154] Third, fourth, fifth, etc. nucleic acid targets are
optionally detected in the cell. For example, the method optionally
includes: providing a third label probe comprising a third label,
wherein a third signal from the third label is distinguishable from
the first and second signals, capturing in the cell the third label
probe to a third nucleic acid target (when present in the cell),
and detecting the third signal from the third label. The third,
fourth, fifth, etc. label probes are optionally hybridized directly
to their corresponding nucleic acid, or they can be captured
indirectly via capture probes as described for the first and second
label probes.
[0155] The additional markers can be used in any of a variety of
ways. For example, the cell can comprise the third nucleic acid
target, and the first and/or second signal can be normalized to the
third signal. The methods can include identifying the cell as being
of the specified type based on the normalized first and/or second
signal, e.g., in embodiments in which the target cell type is
distinguishable from the other cell type(s) in the mixture based on
the copy number of the first and/or second nucleic acid targets,
rather than purely on their presence in the target cell type and
not in the other cell type(s). Examples include cells detectable
based on a pattern of differential gene expression, CTC or other
tumor cells detectable by overexpression of one or more specific
mRNAs, and CTC or other tumor cells detectable by amplification or
deletion of one or more specific chromosomal regions.
[0156] As another example, the third nucleic acid target can serve
as a third redundant marker for the target cell type, e.g., to
improve specificity of the assay for the desired cell type. Thus,
in one class of embodiments, the methods include correlating the
third signal detected from the cell with the presence, absence, or
amount of the third nucleic acid target in the cell, and
identifying the cell as being of the specified type based on
detection of the presence, absence, or amount of the first, second,
and third nucleic acid targets within the cell, wherein the
specified type of cell is distinguishable from the other cell
type(s) in the mixture on the basis of either presence, absence, or
amount of the first nucleic acid target, presence, absence, or
amount of the second nucleic acid target, or presence, absence, or
amount of the third nucleic acid target in the cell.
[0157] As yet another example, the additional markers can assist in
identifying the cell type. For example, the presence, absence, or
amount of the first and third markers may suffice to identify the
cell type, as could the presence, absence, or amount of the second
and fourth markers; all four markers could be detected to provide
two redundant sets of markers and therefore increased specificity
of detection. As another example, one or more additional markers
can be used in negative selection against undesired cell types; for
example, identity of a cell as a CTC can be further verified by the
absence from the cell of one or more markers present in blood cells
and not circulating tumor cells.
[0158] Detection of additional nucleic acid targets can also
provide further information useful in diagnosis, outcome prediction
or the like, regardless of whether the targets serve as markers for
the particular cell type. For example, additional nucleic acid
targets can include markers for proliferating potential, apoptosis,
or other metastatic, genetic, or epigenetic changes.
[0159] Signals from the additional targets are optionally
normalized to a reference nucleic acid as described above. Signal
strength is optionally adjusted between targets depending on their
expected copy numbers, if desired. Signals from the target nucleic
acids in the cell are optionally compared to those from a reference
cell, as noted above.
[0160] A nucleic acid target can be essentially any nucleic acid
that is desirably detected in the cell. For example, a nucleic acid
target can be a DNA, a chromosomal DNA, an RNA, an mRNA, a
microRNA, a ribosomal RNA, or the like. The nucleic acid target can
be a nucleic acid endogenous to the cell. As another example, the
target can be a nucleic acid introduced to or expressed in the cell
by infection of the cell with a pathogen, for example, a viral or
bacterial genomic RNA or DNA, a plasmid, a viral or bacterial mRNA,
or the like.
[0161] The first and second (and/or optional third, fourth, etc.)
nucleic acid targets can be part of a single nucleic acid molecule,
or they can be separate molecules. Various advantages and
applications of both approaches are discussed in greater detail
below, e.g., in the section entitled "Implementation, applications,
and advantages." In one class of embodiments, the first nucleic
acid target is a first mRNA and the second nucleic acid target is a
second mRNA. In another class of embodiments, the first nucleic
acid target comprises a first region of an mRNA and the second
nucleic acid target comprises a second region of the same mRNA. In
another class of embodiments, the first nucleic acid target
comprises a first chromosomal DNA polynucleotide sequence and the
second nucleic acid target comprises a second chromosomal DNA
polynucleotide sequence. The first and second chromosomal DNA
polynucleotide sequences are optionally located on the same
chromosome, e.g., within the same gene, or on different
chromosomes.
[0162] The methods can be applied to detection and identification
of even rare cell types. For example, the ratio of cells of the
specified type to cells of all other type(s) in the mixture is
optionally less than 1:1.times.10.sup.4, less than
1:1.times.10.sup.5, less than 1:1.times.10.sup.6, less than
1:1.times.10.sup.7, less than 1:1.times.10.sup.8, or even less than
1:1.times.10.sup.9.
[0163] Essentially any type of cell that can be differentiated
based on suitable markers (or redundant regions of a single marker,
e.g., a single mRNA or amplified/deleted chromosomal region) can be
detected and identified using the methods. As just a few examples,
the cell can be a circulating tumor cell, a virally infected cell,
a fetal cell in maternal blood, a bacterial cell or other
microorganism in a biological sample (e.g., blood or other body
fluid), an endothelial cell, precursor endothelial cell, or
myocardial cell in blood, stem cell, or T-cell. Rare cell types can
be enriched prior to performing the methods, if necessary, by
methods known in the art (e.g., lysis of red blood cells, isolation
of peripheral blood mononuclear cells, etc.).
[0164] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to source of sample, fixation and permeabilization of the
cell, washing the cell, denaturation of double-stranded nucleic
acids, type of labels, use of optional blocking probes, detection
of signals, detection (and intensity measurement) of signals from
the individual cell by flow cytometry or microscopy, presence of
the cell in suspension or immobilized on a substrate, and/or the
like. Also, additional features described herein, e.g., in the
section entitled "Implementation, applications, and advantages,"
can be applied to the methods, as relevant.
[0165] In another aspect, detection of individual cells of a
specified type is performed as described above, but the first and
second nucleic acid targets need not be redundant markers for that
cell type. The nucleic acid targets can be essentially any desired
nucleic acids, including, for example, redundant and/or
non-redundant markers for the cell type.
Compositions and Kits
[0166] The invention also provides compositions useful in
practicing or produced by the methods. One exemplary class of
embodiments provides a composition that includes a fixed and
permeabilized cell, which cell comprises or is suspected of
comprising a first nucleic acid target and a second nucleic acid
target, at least a first capture probe capable of hybridizing to
the first nucleic acid target, at least a second capture probe
capable of hybridizing to the second nucleic acid target, a first
label probe comprising a first label, and a second label probe
comprising a second label. A first signal from the first label is
distinguishable from a second signal from the second label. The
cell optionally comprises the first and second capture probes and
label probes. The first and second capture probes are optionally
hybridized to their respective nucleic acid targets in the
cell.
[0167] The features described for the methods above for indirect
capture of the label probes to the nucleic acid targets apply to
these embodiments as well. For example, the label probes can
hybridize to the capture probes. In one class of embodiments, the
composition includes a single first capture probe and a single
second capture probe, where the first label probe is capable of
hybridizing to the first capture probe and the second label probe
is capable of hybridizing to the second capture probe. In another
class of embodiments, the composition includes two or more first
capture probes, two or more second capture probes, a plurality of
the first label probes, and a plurality of the second label probes.
A single first label probe is capable of hybridizing to each of the
first capture probes, and a single second label probe is capable of
hybridizing to each of the second capture probes.
[0168] In another aspect, amplifiers can be employed to increase
the number of label probes captured to each target. For example, in
one class of embodiments, the composition includes a single first
capture probe, a single second capture probe, a plurality of the
first label probes, a plurality of the second label probes, a first
amplifier, and a second amplifier. The first amplifier is capable
of hybridizing to the first capture probe and to the plurality of
first label probes, and the second amplifier is capable of
hybridizing to the second capture probe and to the plurality of
second label probes. In another class of embodiments, the
composition includes two or more first capture probes, two or more
second capture probes, a multiplicity of the first label probes, a
multiplicity of the second label probes, a first amplifier, and a
second amplifier. The first amplifier is capable of hybridizing to
one of the first capture probes and to a plurality of first label
probes, and the second amplifier is capable of hybridizing to one
of the second capture probes and to a plurality of second label
probes.
[0169] In another aspect, preamplifiers and amplifiers are employed
to capture the label probes to the targets. In one class of
embodiments, the composition includes a single first capture probe,
a single second capture probe, a multiplicity of the first label
probes, a multiplicity of the second label probes, a plurality of
first amplifiers, a plurality of second amplifiers, a first
preamplifier, and a second preamplifier. The first preamplifier is
capable of hybridizing to the first capture probe and to the
plurality of first amplifiers, and the second preamplifier is
capable of hybridizing to the second capture probe and to the
plurality of second amplifiers. The first amplifier is capable of
hybridizing to the first preamplifier and to a plurality of first
label probes, and the second amplifier is capable of hybridizing to
the second preamplifier and to a plurality of second label probes.
In a related class of embodiments, the composition includes two or
more first capture probes, two or more second capture probes, a
multiplicity of the first label probes, a multiplicity of the
second label probes, a multiplicity of first amplifiers, a
multiplicity of second amplifiers, a plurality of first
preamplifiers, and a plurality of second preamplifiers. The first
preamplifier is capable of hybridizing to one of the first capture
probes and to a plurality of first amplifiers, the second
preamplifier is capable of hybridizing to one of the second capture
probes and to a plurality of second amplifiers, the first amplifier
is capable of hybridizing to the first preamplifier and to a
plurality of first label probes, and the second amplifier is
capable of hybridizing to the second preamplifier and to a
plurality of second label probes. Optionally, additional
preamplifiers can be used as intermediates between a preamplifier
hybridized to the capture probe(s) and the amplifiers.
[0170] In the above classes of embodiments, one capture probe
hybridizes to each label probe, amplifier, or preamplifier. In
alternative classes of related embodiments, two or more capture
probes hybridize to the label probe, amplifier, or
preamplifier.
[0171] In one class of embodiments, the composition comprises a
plurality of the first label probes, a plurality of the second
label probes, a first amplified polynucleotide produced by rolling
circle amplification of a first circular polynucleotide hybridized
to the first capture probe, and a second amplified polynucleotide
produced by rolling circle amplification of a second circular
polynucleotide hybridized to the second capture probe. The first
circular polynucleotide comprises at least one copy of a
polynucleotide sequence identical to a polynucleotide sequence in
the first label probe, and the first amplified polynucleotide
comprises a plurality of copies of a polynucleotide sequence
complementary to the polynucleotide sequence in the first label
probe (and can thus hybridize to a plurality of the label probes).
The second circular polynucleotide comprises at least one copy of a
polynucleotide sequence identical to a polynucleotide sequence in
the second label probe, and the second amplified polynucleotide
comprises a plurality of copies of a polynucleotide sequence
complementary to the polynucleotide sequence in the second label
probe. The composition can also include reagents necessary for
producing the amplified polynucleotides, for example, an
exogenously supplied nucleic acid polymerase, an exogenously
supplied nucleic acid ligase, and/or exogenously supplied
nucleoside triphosphates (e.g., dNTPs).
[0172] The cell optionally includes additional nucleic acid
targets, and the composition (and cell) can include reagents for
detecting these targets. For example, the cell can comprise or be
suspected of comprising a third nucleic acid target, and the
composition can include at least a third capture probe capable of
hybridizing to the third nucleic acid target and a third label
probe comprising a third label. A third signal from the third label
is distinguishable from the first and second signals. The cell
optionally includes fourth, fifth, sixth, etc. nucleic acid
targets, and the composition optionally includes fourth, fifth,
sixth, etc. label probes and capture probes.
[0173] Essentially all of the features noted for the methods above
apply to these embodiments as well, as relevant; for example, with
respect to type of nucleic acid target, location of various targets
on a single molecule or on different molecules, type of labels,
inclusion of optional blocking probes, and/or the like. For
example, it is worth noting that the second nucleic acid target
optionally comprises a reference nucleic acid. In other
embodiments, the first and second nucleic acid targets serve as
markers for a specified cell type, e.g., redundant markers.
[0174] The cell can be essentially any type of cell from any
source, particularly a cell that can be differentiated based on its
nucleic acid content (presence, absence, or copy number of one or
more nucleic acids). As just a few examples, the cell can be a
circulating tumor cell, a virally infected cell, a fetal cell in
maternal blood, a bacterial cell or other microorganism in a
biological sample (e.g., blood or other body fluid), or an
endothelial cell, precursor endothelial cell, or myocardial cell in
blood. For example, the cell can be derived from a bodily fluid,
blood, bone marrow, sputum, urine, lymph node, stool, cervical pap
smear, oral swab or other swab or smear, spinal fluid, saliva,
sputum, semen, lymph fluid, an intercellular fluid, a tissue (e.g.,
a tissue homogenate), a biopsy, and/or a tumor. The cell can be
derived from one or more of a human, an animal, a plant, and a
cultured cell.
[0175] The cell can be present in a mixture of cells, for example,
a complex heterogeneous mixture. In one class of embodiments, the
cell is of a specified type, and the composition comprises one or
more other types of cells. These other cells can be present in
excess, even large excess, of the cell. For example, the ratio of
cells of the specified type to cells of all other type(s) in the
composition is optionally less than 1:1.times.10.sup.4, less than
1:1.times.10.sup.5, less than 1:1.times.10.sup.6, less than
1:1.times.10.sup.7, less than 1:1.times.10.sup.8, or even less than
1:1.times.10.sup.9.
[0176] The cell is optionally immobilized on a substrate, present
in a tissue section, or the like. Preferably, however, the cell is
in suspension in the composition. The composition can be contained
in a flow cytometer or similar instrument. Additional features
described herein, e.g., in the section entitled "Implementation,
applications, and advantages," can be applied to the compositions,
as relevant.
[0177] Another aspect of the invention provides compositions in
which a large number of labels are correlated with each target
nucleic acid. One general class of embodiments thus provides a
composition comprising a cell, which cell includes a first nucleic
acid target, a second nucleic acid target, a first label whose
presence in the cell is indicative of the presence of the first
nucleic acid target in the cell, and a second label whose presence
in the cell is indicative of the presence of the second nucleic
acid target in the cell, wherein a first signal from the first
label is distinguishable from a second signal from the second
label. An average of at least one copy of the first label is
present in the cell per nucleotide of the first nucleic acid target
over a region that spans at least 20 contiguous nucleotides of the
first nucleic acid target, and an average of at least one copy of
the second label is present in the cell per nucleotide of the
second nucleic acid target over a region that spans at least 20
contiguous nucleotides of the second nucleic acid target.
[0178] In one class of embodiments, the copies of the first label
are physically associated with the first nucleic acid target, and
the copies of the second label are physically associated with the
second nucleic acid target. For example, the first label can be
part of a first label probe and the second label part of a second
label probe, where the label probes are captured to the target
nucleic acids.
[0179] In one class of embodiments, an average of at least four,
eight, or twelve copies of the first label are present in the cell
per nucleotide of the first nucleic acid target over a region that
spans at least 20 contiguous nucleotides of the first nucleic acid
target, and an average of at least four, eight, or twelve copies of
the second label are present in the cell per nucleotide of the
second nucleic acid target over a region that spans at least 20
contiguous nucleotides of the second nucleic acid target. In one
embodiment, an average of at least sixteen copies of the first
label are present in the cell per nucleotide of the first nucleic
acid target over a region that spans at least 20 contiguous
nucleotides of the first nucleic acid target, and an average of at
least sixteen copies of the second label are present in the cell
per nucleotide of the second nucleic acid target over a region that
spans at least 20 contiguous nucleotides of the second nucleic acid
target.
[0180] Essentially all of the features noted for the embodiments
above apply to these embodiments as well, as relevant, for example,
with respect to type of labels, suspension of the cell, and/or the
like. The regions of the first and second nucleic acid targets are
typically regions covered by a probe, primer, or similar
polynucleotide employed to detect the respective target. The
regions of the first and second nucleic acid targets optionally
span at least 25, 50, 100, 200, or more contiguous nucleotides
and/or at most 2000, 1000, 500, 200, 100, 50, or fewer nucleotides.
A like density of labels is optionally captured to third, fourth,
fifth, sixth, etc. nucleic acid targets. The composition optionally
includes PCR primers, a thermostable polymerase, and/or the like,
in embodiments in which the targets are detected by multiplex in
situ PCR.
[0181] Another aspect of the invention provides kits useful for
practicing the methods. One general class of embodiments provides a
kit for detecting a first nucleic acid target and a second nucleic
acid target in an individual cell. The kit includes at least one
reagent for fixing and/or permeabilizing the cell, at least a first
capture probe capable of hybridizing to the first nucleic acid
target, at least a second capture probe capable of hybridizing to
the second nucleic acid target, a first label probe comprising a
first label, and a second label probe comprising a second label,
wherein a first signal from the first label is distinguishable from
a second signal from the second label, packaged in one or more
containers.
[0182] Essentially all of the features noted for the embodiments
above apply to these embodiments as well, as relevant; for example,
with respect to number of nucleic acid targets, configuration and
number of the label and capture probes, inclusion of preamplifiers
and/or amplifiers, inclusion of blocking probes, inclusion of
amplification reagents, type of nucleic acid target, location of
various targets on a single molecule or on different molecules,
type of labels, inclusion of optional blocking probes, and/or the
like. The kit optionally also includes instructions for detecting
the nucleic acid targets in the cell and/or identifying the cell as
being of a specified type, one or more buffered solutions (e.g.,
diluent, hybridization buffer, and/or wash buffer), reference
cell(s) comprising one or more of the nucleic acid targets, and/or
the like.
[0183] Another general class of embodiments provides a kit for
detecting an individual cell of a specified type from a mixture of
cell types by detecting a first nucleic acid target and a second
nucleic acid target. The kit includes at least one reagent for
fixing and/or permeabilizing the cell, a first label probe
comprising a first label (for detection of the first nucleic acid
target), and a second label probe comprising a second label (for
detection of the second nucleic acid target), wherein a first
signal from the first label is distinguishable from a second signal
from the second label, packaged in one or more containers. The
specified type of cell is distinguishable from the other cell
type(s) in the mixture by presence, absence, or amount of the first
nucleic acid target in the cell or by presence, absence, or amount
of the second nucleic acid target in the cell (that is, the two
targets are redundant markers for the specified cell type).
[0184] Essentially all of the features noted for the embodiments
above apply to these embodiments as well, as relevant; for example,
with respect to number of nucleic acid targets, inclusion of
capture probes, configuration and number of the label and/or
capture probes, inclusion of preamplifiers and/or amplifiers,
inclusion of blocking probes, inclusion of amplification reagents,
type of nucleic acid target, location of various targets on a
single molecule or on different molecules, type of labels,
inclusion of optional blocking probes, and/or the like. The kit
optionally also includes instructions for identifying the cell as
being of the specified type, one or more buffered solutions (e.g.,
diluent, hybridization buffer, and/or wash buffer), reference
cell(s) comprising one or more of the nucleic acid targets, and/or
the like.
Implementation, Applications and Advantages
[0185] Various aspects of the invention are described in additional
detail below. Exemplary embodiments and applications are also
described.
[0186] The new technology (methods, compositions, systems, and
kits), QMAGEX (Quantitative Multiplex Analysis of Gene Expression
in Single Cell), disclosed herein is capable of detection and
quantification of multiple nucleic acids within individual cells.
The technology is significantly different from existing ISH
technology in several aspects, although they both can measure mRNA
expression in individual cells. First, cells preferably remain in
suspension status during all or at least most of the assay steps in
the assays of the present invention, which greatly improves assay
hybridization kinetics, resulting in better reproducibility and
shorter assay time. Second, the instant technology has the
capability for analyzing the expression of multiple mRNA
transcripts within cells simultaneously and quantitatively. This is
highly desirable, since, for example, detection of multiple tumor
marker genes could greatly improve the accuracy of CTC
identification (Mocellin et al., 2004) and greatly reduce the false
positive rate. Quantitative analysis of gene expression level could
not only further aid in discriminating the CTC from other types of
cells but also could help in distinguishing the type and source of
primary tumors as well as the stages of tumor progression. Third,
the instant technology enables the use of a flow cytometer as the
base for detection, which, compared with microscope-based detection
instruments, offers higher throughput. In addition, the flow
cytometer is capable of sorting out cells, e.g., tumor cells, for
further study. Subsequent to the detection and quantification of
mRNA expression, isolation of the CTC or other cells may be
advantageous for further identity confirmation or for additional
cytological and molecular analysis. Fourth, the instant technology
has vastly improved detection sensitivity and reproducibility, and
is capable of single copy gene detection and quantification. In
addition, the instant technology uses a standard, generic set of
probe labeling and detection technology (e.g., the same set of
preamplifiers, amplifiers, and label probes can be used to detect
multiple different sets of nucleic acid targets, requiring only
synthesis of a new set of capture probes for each new set of
nucleic acid targets), and optionally uses standardized procedures
for cell fixation and permeation and for hybridization and washing.
Furthermore, the technology can include built-in internal controls
for assay specificity and efficiency.
[0187] The instant technology can be used not only for the
detection and enumeration of rare CTC in blood samples or other
body fluids, but also for any type of rare cell identification and
enumeration events. Applications include, but are not limited to:
detection of minimal residual disease in leukemia and lymphoma;
recurrence monitoring after chemotherapy treatment (Hess et al.);
detection of other pre-cancerous cells, such as the detection of
HPV-containing cervical cells in body fluids; detection of viral or
bacterial nucleic acid in an infected cell; detection of fetal
cells in maternal blood; detection of micro-tumor lesions during
early stage of tumor growth; or detection of residual tumor cells
after surgery for margin management. In all of these cases, target
cell specific gene expression is likely to be buried in the
background of large numbers of heterogeneous cell populations. As a
result, microarray or RT-PCR based expression analysis, which
require the isolation of mRNA from a large population of cells,
will have difficulty detecting the presence of those rare cell
events accurately or reliably, whereas the invented technology can
readily be applied.
[0188] It should also be noted that although single cell detection
and quantification of multiple mRNA transcripts is illustrated here
as the main application, such technology is equally applicable to
detection of other rare cell events that include changes in
chromosomal DNA or cellular nucleic acid content. Examples include,
but are not limited to, detection of her-2/neu gene amplification,
detection of Rb gene deletion, detection of somatic mutations,
detection of chromosome translocation such as in chronic
myelogenous leukemia (BCR-ABL), or detection of HPV insertion to
chromosomal DNA of cervical cancer cells.
[0189] Finally, the probe design, multiplexing and amplification
aspects of the instant technology can be applied in quantitative,
multiplex gene expression analysis and in measuring chromosomal DNA
changes at a single cell level in solid tissue sections, such as
formalin-fixed, paraffin embedded (FFPE) tissue samples.
[0190] The QMAGEX technology comprises an assay and optional
associated apparatus to implement the assay in an automated
fashion. FIG. 1 illustrates major elements of the QMAGEX assay work
flow, which, for one exemplary embodiment in which amplifiers are
employed, include:
[0191] Fixation and Permeation: Cells in the sample are fixed and
permeated (permeabilized) in suspension. The fixation step
immobilizes nucleic acids (e.g., mRNA or chromosomal DNA) and
cross-links them to the cellular structure. Then the cell membrane
is permeabilized so that target-specific nucleic acid probes and
signal-generating particles, such as fluorescently labeled nucleic
acid probes, can enter the cell and bind to the target.
[0192] Denaturation: If the detection target is double-stranded
chromosomal DNA, a denaturation step is added to convert the
double-stranded target into single-stranded DNA, ready to be bound
with the target-specific probes.
[0193] Capture Probe Hybridization: Carefully selected
target-specific capture probes or probe sets are hybridized to the
target nucleic acids. The capture probes serve to link the target
molecules specifically to signal-generating particles. The
technology enables multiple target genes in the cell to be
recognized by different probe sets simultaneously and with a high
degree of specificity.
[0194] Signal Amplification: Signals from target molecules are
amplified by binding a large scaffold molecule, an amplifier, to
the capture probes or probe sets. Each scaffold has multiple
locations to accept label probes and signal-generating particles.
In a multiplex assay, multiple distinct amplifiers are used.
[0195] Labeling: Label probes, to which signal generating particles
(labels) are attached, hybridize to the amplifier in this step. In
a multiplex assay, multiple distinct label probes are used.
[0196] Washing: The excess probes or signal generating particles
that are not bound or that are nonspecifically bound to the cells
are removed through a washing step, which reduces background noise
and improves the detection signal to noise ratio. Additional
washing steps may be added during the capture probe hybridization
or signal amplification steps to further enhance the assay
performance.
[0197] Detection: The labeled suspension cells are detected using
Fluorescent Activated Cell Sorting (FACS) or a flow cytometer, or
are immobilized on a solid surface and detected using a microscope
or scanner based instrument.
[0198] In the following section, major elements of the QMAGEX
technology will be described in detail. In the following, the term
label probe refers to an entity that binds to the target molecule,
directly or indirectly, and enables the target to be detected by a
readout instrument. The label probe, in general, comprises a
nucleic acid or modified nucleic acid molecule that binds to the
target, directly or indirectly, and one or more "signal generating
particle" (i.e., label) that produces the signal recognizable by
the readout instrument. In indirect mode, the label probe can
either be attached to the target molecule through binding to a
capture probe directly or through binding to an amplifier that is
in turn linked to a capture probe. Exemplary signal-generating
particles (labels) include, but are not limited to, fluorescent
molecules, nano-particles, radioactive isotopes, chemiluminescent
molecules (e.g., digoxigenin, dinitrophenyl). Fluorescent molecules
include, but are not limited to, fluorescein (FITC), cy3, cy5,
alexa dyes, phycoerythrin, etc. Nano-particles include, but are not
limited to, fluorescent quantum dots, scattering particles, etc.
The term capture probe refers to a nucleic acid or a modified
nucleic acid that links the target to a specific type of label
probe, directly or indirectly. The term "capture probe set" refers
to multiple nucleic acids or modified nucleic acids that link a
target to a specific type of label probe, directly or indirectly,
for increased assay sensitivity. The term amplifier refers to a
large scaffold molecule(s) that binds to one or more capture probes
or to a preamplifier on one side and to multiple label probes on
another side.
Fixation
[0199] In this step, the nucleic acids are immobilized within cells
by cross-linking them within the cellular structure. There are a
variety of well known methods to fix cells in suspension with a
fixative reagent and to block the endogenous RNase activities,
which can be adapted for use in the present invention. Fixative
reagents include formalin (formaldehyde), paraformaldehyde,
gluteraldehyde, ethanol, methanol, etc. One common fixative
solution for tissue sections includes 0.25% gluteraldehyde and 4%
paraformaldehyde in phosphate buffer. Another common fixative
solution for tissue sections includes 50% ethanol, 10% formalin
(containing 37% formaldehyde), and 5% acetic acid. Different
combinations of the fixative reagents at various concentrations are
optionally tested to find the optimal composition for fixing cells
in suspension, using techniques well known in the art. Duration of
the fixing treatment can also be optimized. A number of different
RNase inhibitors can be included in the fixative solution, such as
RNAlater (Ambion), citric acid or LiCl, etc.
Permeation
[0200] Fixation results in cross-linking of the target nucleic
acids with proteins or other cellular components within cells,
which may hinder or prevent infiltration of the capture probes into
the cells and mask the target molecules for hybridization. The
assays of the invention thus typically include a follow-on
permeation step to enable in-cell hybridization. One technique
involves the application of heat for varying lengths of time to
break the cross-linking. This has been demonstrated to increase the
accessibility of the mRNA in the cells for hybridization.
Detergents (e.g., Triton X-100 or SDS) and Proteinase K can also be
used to increase the permeability of the fixed cells. Detergent
treatment, usually with Triton X-100 or SDS, is frequently used to
permeate the membranes by extracting the lipids. Proteinase K is a
nonspecific protease that is active over a wide pH range and is not
easily inactivated. It is used to digest proteins that surround the
target mRNA. Again, optimal concentrations and duration of
treatment can be experimentally determined as is well known in the
art. A cell washing step can follow, to remove the dissolved
materials produced in the permeation step.
[0201] Optionally, prior to fixation and permeation, cells in
suspension are collected and treated to inactivate RNase and/or to
reduce autofluorescence. DEPC treatment (e.g. Braissant and Wahli
(1988) "A simplified in situ hybridization protocol using
non-radioactively labeled probes to detect abundant and rare mRNAs
on tissue sections" Biochemica 1:10-16) and RNAlater (Ambion, Inc.)
have been demonstrated to be effective in stabilizing and
protecting cellular RNA. Sodium borohydride and high heat have also
been shown to preserve the integrity of RNA and to reduce
autofluorescence, facilitating the detection of genes expressed at
a low level (Capodieci et al. (2005) "Gene expression profiling in
single cells within tissue" Nat Methods 2(9):663-5). Other methods
of reducing cellular autofluorescence such as trypan blue (Mosiman
et al. (1997) "Reducing cellular autofluorescence in flow
cytometry: an in situ method" Cytometry 30(3):151-6) or singly
labeled quencher oligonucleotide probe (Nolan et al. (2003) "A
simple quenching method for fluorescence background reduction and
its application to the direct, quantitative detection of specific
mRNA" Anal Chem. 2003 75(22):6236-43) are optionally employed.
Capture Probe Hybridization
[0202] In this assay step, the capture probe or capture probe set
binds to the intended target molecule by hybridization. One
indicator for a successful target hybridization is specificity,
i.e. the capture probes or probe sets should substantially only
link the label probes to the specific target molecule of interest,
not to any other molecules. Probe selection and design are
important in achieving specific hybridization.
[0203] Probe Selection and Design
[0204] The assays of the invention employ two types of approaches
in probe design to link the target nucleic acids in cells to signal
generating particles: "direct labeling" and "indirect labeling". In
the direct labeling approach, the target molecule hybridizes to or
captures one or more label probes (LP) directly. The LPs contain
the signal-generating particles (SGP), as shown in FIG. 2. A
different LP needs to be used to attach additional SGP at different
positions on the target molecule. In order to ensure hybridization
specificity, the label probe is preferably stringently selected to
ensure that it does not cross-hybridize with nonspecific nucleic
acid sequences.
[0205] In the indirect labeling approach, an additional capture
probe (CP) is employed. An example is shown in FIG. 3. The target
molecule captures the label probe through the capture probe. In
each capture probe, there is at least one section, T, complementary
to a section on the target molecule, and another section, L,
complementary to a section on the label probe. The T and L sections
are connected by a section C. To attach more SGPs to different
positions on the same target molecule, different capture probes are
needed, but the label probe can remain the same. The sequence of L
is carefully selected to ensure that it does not cross-hybridize
substantially with any sequences in the nucleic acids in cells. In
a further embodiment, the L portion of the capture probe and the
label probe contain chemically modified or nonnatural nucleotides
that do not hybridize with natural nucleotides in cells. In another
embodiment, L and the label probe (or a portion thereof) are not
even nucleic acid sequences. For example, L can be a weak affinity
binding antibody that recognizes the signal-generating probe, which
in this case is or includes an antigen; L can be covalently
conjugated to an oligonucleotide that comprises the T section of
the capture probe. Optionally, for two adjacent capture probes, the
T sections hybridize to the target and two of the low affinity
binding antibody binds to the antigen on the label probe at the
same time, which results in strong affinity binding of the antigen.
The capture and label probes are specific for a target gene of
interest. Multiple capture probes (probe set) can be bound to the
same target gene of interest in order to attach more
signal-generating particles for higher detection sensitivity. In
this situation, the probe set for the same target gene can share
the same label probe.
[0206] Although both approaches can be used in the instant
technology, the indirect capture approach is preferred because it
enables the label probe to be target independent and further
disclosure will show that it can offer better specificity and
sensitivity.
[0207] In a further indirect capture embodiment shown in FIG. 4,
two adjacent capture probes are incorporated in a probe set
targeting a gene of interest. T.sub.1 and T.sub.2 are designed to
be complementary to two unique and adjacent sections on the target
nucleic acid. L.sub.1 and L.sub.2, which can be different or the
same, are complementary to two adjacent sections on the label
probe. Their binding sections, T, L or both, are designed so that
the linkage between the label probe and the target is unstable and
tends to fall off at hybridization temperature when only one of the
capture probes is in place. Such a design should enable exceptional
specificity because the signal-generating label probe can only be
attached to the target gene of interest when two independent
capture probes both recognize the target and bind to the adjacent
sequences or in very close proximity of the target gene. In a
further embodiment, the melting temperature, T.sub.m, of the T
sections of the two capture probes are designed to be significantly
above the hybridization temperature while the T.sub.m of the L
sections is below the hybridization temperature. As a result, T
sections bind to the target molecule strongly and stably during
hybridization, while L sections bind to the label probe weakly and
unstably if only one of the capture probes is present. However, if
both capture probes are present, the combination of L.sub.1 and
L.sub.2 holds the label probe strongly and stably during
hybridization. In another embodiment, T.sub.m of the T sections is
below hybridization temperature while T.sub.m of the L sections is
substantially above. In the same way, the linkage between the label
probe and the target can only survive the hybridization when both
capture probes are hybridized to the target in a cooperative
fashion.
[0208] In another embodiment, three or more of the target nucleic
acid specific, neighboring capture probes are used for the stable
capture of one label probe within cells (FIG. 5). The basic design
of the probes is the same as discussed above, but the capture of
one signal-generating probe should have even higher specificity
than when two neighboring probes are used since now three
independent probes have to bind to the same target molecule of
interest in neighboring positions in order to generate signal.
[0209] Multiplexing
[0210] To perform multiplexed detection for more than one target
gene, e.g., as shown in FIG. 6, each target gene has to be
specifically bound by different capture and label probes. In
addition, the signal generating particle (the label) attached to
the label probe should provide distinctively different signals for
each target that can be read by the detection instrument. In the
direct labeling approach (e.g., FIG. 6 Panel A), suitable label
probes with minimal cross-hybridization can be harder to find
because each label probe has to be able to bind to the target
strongly but not cross-hybridize to any other nucleic acid
molecules in the system. For this approach to provide optimal
results, the target binding portion of the label probe should be
judiciously designed so that it does not substantially
cross-hybridize with nonspecific sequences. In the indirect
labeling approach (e.g., FIG. 6 Panel B), because of the unique
multiple capture probe design approach, even when one capture probe
binds to a nonspecific target, it will not result in the binding of
the label probe to the nonspecific target. The assay specificity
can be greatly improved. Thus the capture probe design illustrated
in FIG. 4 and FIG. 5 is typically preferred in some multiplex assay
applications. In one class of embodiments, the signal-generating
particles attached to different target genes are different
fluorescent molecules with distinctive emission spectra.
[0211] The capacity of the instant technology to measure more than
one parameter simultaneously can enable detection of rare cells in
a large heterogeneous cell population. As noted above, the
concentration of CTC is estimated to be in the range of one tumor
cell among every 10.sup.6-10.sup.7 normal blood cells. In existing
FACS based immunoassays, on the other hand, random dye aggregation
in cells may produce one false positive cell count in every ten
thousand cells. Such an assay can thus not be used for CTC
detection due to the unacceptably high false positive rates. This
problem can be solved elegantly using the instant technology. In
one particular embodiment, expression of more than one tumor genes
are used as the targets for multiplex detection. Only cells that
express all the target genes are counted as tumor cells. In this
way, the false positive rate of the CTC detection can be
dramatically reduced. For example, since dye aggregation in cells
is a random event, if the false positive rate of a single color
detection is 10.sup.-4, the false positive rate for two color or
three color detection can be as low as 10.sup.-8 or 10.sup.-12,
respectively. In situations where the relative levels of expression
of the target genes are known, these relative levels can be
measured using the multiplex detection methods disclosed herein and
the information can be used to further reduce the false positive
rate of the detection.
[0212] In another embodiment, schematically illustrated in FIG. 7
Panel A, more than one signal-generating particles are linked to
the same target nucleic acid. These particles generate distinct
signals in the detection instrument. The relative strengths of
these signals can be predetermined by designing the number of each
type of particles attached to the target. The number of
signal-generating particles on a target can be controlled in probe
design by changing the number of probe sets or employing different
signal amplification methods, e.g., as described in the following
section. The rare cells are identified only when the relative
signal strengths of these particles measured by the detection
instrument equal the pre-determined values. This embodiment is
useful when there are not enough suitable markers or when their
expression levels are unknown in a particular type of rare cells.
In yet another embodiment, shown in FIG. 7 Panel B, the same set of
signal-generating particles are attached to more than one target.
The relative signal strengths of the particle set are controlled to
be the same on all selected targets. This embodiment is useful in
situations in which the rare cell is identified when any of the
target molecules are present. In yet another embodiment, depicted
in FIG. 7 Panel C, each target molecule has a set of signal
generating particles attached to it, but the particle sets are
distinctively different from target to target.
[0213] The detection of multiple target nucleic acid species of
interest can be applied to quantitative measurement of one target.
Due to different sample and experimental conditions, the abundance
of a particular target molecule in a cell normally cannot be
determined precisely through the detection of the signal level
associated with the target. However, more precise measurement can
be accomplished by normalizing the signal of a gene of interest to
that of a reference/housekeeping gene. A reference/housekeeping
gene is defined as a gene that is generally always present or
expressed in cells. The expression of the reference/housekeeping
gene is generally constitutive and tends not to change under
different biological conditions. 18S, 28S, GAPD, ACTB, PPIB etc.
have generally been considered as reference or housekeeping genes,
and they have been used in normalizing gene expression data
generated from different samples and/or under varying assay
conditions.
[0214] In another embodiment, a special label probe set can be
designed that does not bind to any capture probe or target
specifically. The signal associated to this label probe can be used
to establish the background of hybridization signal in individual
cells. Thus the abundance of a particular target molecule can be
quantitatively determined by first subtracting the background
hybridization signal, then normalizing against the background
subtracted reference/housekeeping gene hybridization signal.
[0215] In yet another embodiment, two or more chromosomal DNA
sequences of interest can be detected simultaneously in cells. In
the detection of multiple DNA sequences in cells, the label probes
for the DNA sequences are distinct from each other and they do not
cross-hybridize with each other. In embodiments in which
cooperative indirect capture is employed, because of the design
scheme, even when one probe binds to a nonspecific DNA sequence, it
will not result in the capture of the signal-generating probe to
the nonspecific DNA sequences.
[0216] In yet another embodiment, the detection of multiple target
chromosomal DNA sequences of interest enables quantitative analysis
of gene amplification, gene deletion, or gene translocations in
single cells. This is accomplished by normalizing the signal of a
gene of interest to that of a reference gene. The signal ratio of
the gene of interest to the reference gene for a particular cell of
interest is compared with the ratio in reference cells. A reference
gene is defined as a gene that stably maintains its copy numbers in
the genomic DNA. A reference cell is defined as a cell that
contains the normal copy number of the gene of interest and the
reference gene. If the signal ratio is higher in the cells of
interest in comparison to the reference cells, gene amplification
is detected. If the ratio is lower in the cells of interest in
comparison to the reference cells, then gene deletion is
detected.
Signal Amplification & Labeling
[0217] The direct labeling approach depicted in FIG. 2 and FIG. 6
Panel A offers only limited sensitivity because only a relatively
small number of signal-generating particles (labels) can be
attached to each label probe. One way to increase sensitivity is to
use in vitro transcribed RNA that incorporates signal-generating
particles, but specificity will suffer as a result.
[0218] The "indirect labeling" approach not only can improve
specificity as described above but also can be used to improve the
detection sensitivity. In this approach, the label probe is
hybridized or connected to an amplifier molecule, which provides
many more attachment locations for label probes. The structure and
attachment method of the amplifier can take many forms. FIG. 8
Panels A-D show a number of amplification schemes as illustrative
examples. In Panel A, multiple singly-labeled label probes bind to
the amplifier. In Panel B, multiple multiply-labeled label probes
bind to the amplifier. In Panel C, multiple singly-labeled label
probes bind to the amplifier, and multiple copies of the amplifier
are bound to a preamplifier. In one particular embodiment, the
amplifier is one or multiple branched DNA molecules (Panel D). The
sequence of the label probe is preferably selected carefully so
that it does not substantially cross-hybridize with any endogenous
nucleic acids in the cell. In fact, the label probe does not have
to be a natural polynucleotide molecule. Chemical modification of
the molecule, for example, inclusion of nonnatural nucleotides, can
ensure that the label probe only hybridizes to the amplifier and
not to nucleic acid molecules naturally occurring in the cells. In
multiplex assays, distinct amplifiers and label probes will be
designed and used for the different targets.
[0219] In one embodiment, as schematically illustrated in FIG. 9, a
circular polynucleotide molecule is captured by the capture probe
set. Along the circle, there can be one sequence or more than one
repeat of the same sequence that binds to label probe (FIG. 9 Panel
A). In the signal amplification step of the assay, a rolling circle
amplification procedure (Larsson et al, 2004) is carried out. As
the result of this procedure, a long chain polynucleotide molecule
attached to the capture probes is produced (FIG. 9 Panel B). There
are many repeating sequences along the chain, on which label probes
can be attached by hybridization (FIG. 9 Panel C). In multiplex
assays, distinct capture probes, rolling circles, and label probes
will be designed and used.
[0220] In one embodiment, a portion of the signal-generating probe
can be PCR-amplified. In another embodiment, each portion of
multiple signal-generating probes can be PCR-amplified
simultaneously.
[0221] Although a specific capture approach (indirect labeling with
capture probe pairs) has been used to illustrate the labeling and
amplification schemes in FIGS. 8 and 9, it is important to note
that any other probe capture approaches, direct or indirect,
described in previous sections can be used in combination with the
labeling and amplification schemes described in these sections. The
capture probe, labeling methods, and amplifier configurations
described above are independent of each other and can be used in
any combination in a particular assay design.
Hybridization Conditions
[0222] The composition of the hybridization solution can affect
efficiency of the hybridization process. Hybridization typically
depends on the ability of the oligonucleotide to anneal to a
complementary mRNA strand below its melting point (T.sub.m). The
value of the T.sub.m is the temperature at which half of the
oligonucleotide duplex is present in a single stranded form. The
factors that influence the hybridization of the oligonucleotide
probes to the target nucleic acids can include temperature, pH,
monovalent cation concentration, presence of organic solvents, etc.
A typical hybridization solution can contain some or all of the
following reagents, e.g., dextran sulfate, formamide, DTT
(dithiothreitol), SSC (NaCl plus sodium citrate), EDTA, etc. Other
components can also be added to decrease the chance of nonspecific
binding of the oligonucleotide probes, including, e.g.,
single-stranded DNA, tRNA acting as a carrier RNA, polyA,
Denhardt's solution, etc. Exemplary hybridization conditions can be
found in the art and/or determined empirically as well known in the
art. See, e.g., U.S. patent application publication 2002/0172950,
Player et al. (2001) J. Histochem. Cytochem. 49:603-611, and Kenny
et al. (2002) J. Histochem. Cytochem. 50:1219-1227, which also
describe fixation, permeabilization, and washing.
[0223] An additional prehybridization is optionally carried out to
reduce background staining. Prehybridization involves incubating
the fixed tissue or cells with a solution that is composed of all
the elements of the hybridization solution, minus the probe.
Washing
[0224] Following the labeling step, the cells are preferably washed
to remove unbound probes or probes which have loosely bound to
imperfectly matched sequences. Washing is generally started with a
low stringency wash buffer such as 2.times.SSC+1 mM EDTA
(1.times.SSC is 0.15M NaCl, 0.015M Na-citrate), then followed by
washing with higher stringency wash buffer such as 0.2.times.SSC+1
mM EDTA or 0.1.times.SSC+1 mM EDTA.
[0225] Washing is important in reducing background noise, improving
signal to noise ratio of and quantification with the assay.
Established washing procedures can be found, e.g., in Bauman and
Bentvelzen (1988) "Flow cytometric detection of ribosomal RNA in
suspended cells by fluorescent in situ hybridization" Cytometry
9(6):517-24 and Yu et al. (1992) "Sensitive detection of RNAs in
single cells by flow cytometry" Nucleic Acids Res. 20(1):83-8.
[0226] Washing can be accomplished by executing a suitable number
of washing cycles, i.e., one or more. Each cycle in general
includes the following steps: mixing the cells with a suitable
buffer solution, detaching non-specifically bound materials from
the cells, and removing the buffer together with the waste. Each
step is described in more detail below.
[0227] Mix the cells with wash buffer: In some assays, the cells
are immobilized on the surface of a substrate before being washed.
In such cases, the washing buffer is mixed together with the
substrate surface. In many other embodiments, the cells to be
washed are free-floating. The washing buffer is added to cell
pellets or to the solution in which the cells are floating.
[0228] Detach non-specifically bound materials from cells: Any of a
number of techniques can be employed here to reduce nonspecific
binding after cell permeability treatment and probe hybridization
to encourage non-specifically bound probes to detach from the cells
and dissolve into the wash buffer. These include raising the
temperature to somewhere just below the melting temperature of the
specifically bound probes and employing agitation using a magnetic
or mechanical stirrer or perturbation with sonic or ultrasonic
waves. Agitation of the mixture can also be achieved by shaking the
container with a rocking or vortex motion.
[0229] Remove buffer together with waste: Any convenient method can
be employed to separate and remove the washing buffer and waste
from the target cells in the sample. For example, the floating
cells or substrates that the cells bound to are separated from the
buffer and waste through centrifugation. After the spin, the cells
or substrates form a pellet at the bottom of the container. The
buffer and waste are decanted from the top.
[0230] As another example, the mixture is optionally transferred to
(or formed in) a container the bottom of which is made of a porous
membrane. The pore size of the membrane is chosen to be smaller
than the target cells or the substrates that the cells are bound to
but large enough to allow for debris and other waste materials to
pass through. To remove the waste, the air or liquid pressure is
optionally adjusted such that the pressure is higher inside the
container than outside, thus driving the buffer and waste out of
the container while the membrane retains the target cells inside.
The waste can also be removed, e.g., by filtering the buffer and
waste through the membrane driven by the force of gravity or by
centrifugal force.
[0231] As yet another example, the cells can be immobilized on the
surface of a large substrate, for example, a slide or the bottom of
a container, through cell fixing or affinity attachment utilizing
surface proteins. The buffer and waste can be removed directly by
either using a vacuum to decant from the top or by turning the
container upside down. As yet another example, the cells are
optionally immobilized on magnetic beads, e.g., by either chemical
fixing or surface protein affinity attachment. The beads can then
be immobilized on the container by attaching a magnetic field on
the container. The buffer and waste can then be removed directly
without the loss of cells the same way as described in the previous
example. As yet another example, the nonspecifically bound probes
within cells are induced to migrate out of the cells by
electrophoretic methods while the specifically bound probes
remain.
[0232] As stated before, a washing cycle is completed by conducting
each of the three steps above, and the washing procedure is
accomplished by executing one or more (e.g., several) such washing
cycles. Different washing buffers, detachment, or waste removal
techniques may be used in different washing cycles.
Detection
[0233] In the instant technology, the target cells that have
signal-generating particles (labels) specifically hybridized to
nucleic acid targets in them can be identified out of a large
heterogeneous population after non-specifically bound probes and
other wastes are removed through washing. Essentially any
convenient method for the detection and identification can be
employed.
[0234] In one embodiment, the suspension cells are immobilized onto
a solid substrate after the labeling or washing step described
above. The detection can be achieved using microscope based
instruments. Specifically, in cases where the signal generated by
the probes is chemiluminescent light, an imaging microscope with a
CCD camera or a scanning microscope can be used to convert the
light signal into digital information. In cases where the probe
carries a label emitting a fluorescent signal, a fluorescent
imaging or scanning microscope based instrument can be used for
detection. In addition, since the target cells are, in general,
rare among a large cell population, automatic event finding
algorithms can be used to automatically identify and count the
number of target cells in the population. Cells in suspension can
be immobilized onto solid surfaces by any of a number of
techniques. In one embodiment, a container with large flat bottom
surface is used to hold the solution with the suspended cells. The
container is then centrifuged to force the floating cells to settle
on the bottom. If the surface is sufficiently large in comparison
to the concentration of cells in the solution, cells are not likely
to overlap on the bottom surface. In most cases, even if the cells
overlap, the target cells will not because they are relatively rare
in a large population. In another embodiment, suspended cells are
cytospun onto a flat surface. After removal of fluids, the cells
are immobilized on the surface by surface tension.
[0235] In preferred embodiments of this invention, cells are
floating (in suspension) or are immobilized on floating substrates,
such as beads, so that pre-detection procedures, such as
hybridization and washing, can be carried out efficiently in
solution. There are several methods to detect rare target cells out
of a large floating cell population. The preferred method is to use
a detection system based on the concept of flow cytometry, where
the floating cells or substrates are streamlined and pass in front
of excitation and detection optics one by one. The target cells are
identified through the optical signal emitted by the probes
specifically bound to the nucleic acid targets in the cells. The
optical signal can, e.g., be luminescent light or fluorescent light
of a specific wavelength.
Advantages
[0236] In summary, the instant QMAGEX technology has a number of
unique elements that enable multiplex nucleic acid detection in
single cells and detection of target cells. These elements include
the following.
[0237] Nucleic acid molecules immobilized inside cells are used as
markers for the identification of CTC (or other cell types).
Compared with protein based markers, nucleic acids are more stable,
widely available, and provide better signal to noise ratio in
detection. In addition, the detection technique can be readily
applied to a wide range of tumors or even other applications
related to cell identification or classification. As another
advantage, nucleic acid molecules are quantifiably measured at an
individual cell level, instead of in a mixed cell population. This
feature ensures that the cell as a key functional unit in the
biological system is preserved for study. In many applications
involving a mixed population of cells, this feature can be very
useful in extracting real, useful information out of the assay.
(For example, a CTC can be identified based on detection of the
presence or expression level(s) of a set of nucleic acid marker(s)
in the cell; the presence or copy number of additional nucleic
acids in the cell can then provide additional information useful in
diagnosis, predicting outcome, or the like.)
[0238] Cells optionally remain in suspension or in pellets that can
be re-suspended in all steps of the assay before final detection.
This feature significantly improves assay kinetics, simplifies the
process, enhances the reproducibility, and keeps the cell in its
most functional relevant status. On the other hand, significant
aspects of the invention, including probe selection and design,
multiplexing, amplification and labeling, can be applied directly
to in situ hybridization technique for the detection and
enumeration of rare cells in tissue samples.
[0239] A unique indirect capture probe design approach is
optionally employed to achieve exceptional target hybridization
specificity, which results in better signal to noise ratio in
detection.
[0240] The assays enable the detection of multiple target genes or
multiple parameters on the same gene simultaneously. This feature
benefits the detection of rare cells such as CTC in a number of
ways. First, it can reduce the false positive rate, which is
essential in cancer diagnostics. Second, it can provide additional,
clinically important information related to the detected tumor
cell, which may include the progression stage and/or original type
and source of the primary tumor.
[0241] The invented technology incorporates a signal amplification
scheme, which boosts the detection sensitivity and enables the
detection of rare cells among a large number of normal cells with
high confidence.
[0242] Detection can be implemented on FACS or flow cytometer based
instruments or on microscope based platforms. The former can be
fully automated and provides fast detection and the additional
benefit of sorting out identified cells for further study, if
desired. The latter platform is more widely available and has the
benefit of allowing final manual identification through
morphology.
Systems
[0243] In one aspect, the invention provides systems and apparatus
configured to carry out the procedures of the novel assays. The
apparatus or system comprises one or more (and preferably all) of
at least the following elements.
[0244] Fluid handling: The apparatus optionally includes a
subsystem that can add reagents, and if required by the assay,
decant fluids from the sample container (e.g., a removable or
fixed, disposable or reusable container, for example a sample tube,
multiwell plate, or the like). The subsystem can be based on a
pipette style fluid transfer system where different fluids are
handled by one pump head with disposable tips. As an alternative
example, each reagent may have its own dedicated fluid channel.
[0245] Mixing and agitation: The apparatus optionally includes a
device to mix different reagents in the sample solution and
encourage any non-specifically bound material to detach from the
cells. The device may have a mechanism to introduce a vortex or
rocking motion to the holder of the sample container or to couple
sound or ultrasound to the container. Alternatively, a magnetic
stirrer can be put into the sample container and be driven by
rotating magnetic field produced by an element installed in a
holder for the container.
[0246] Temperature control: The temperature of the sample can be
controlled to a level above the room temperature by installing a
heater and a temperature probe to the chamber that holds the sample
container. A peltier device can be used to control the temperature
to a level above or below ambient. Temperature control is
important, e.g., for performance of the hybridization and washing
procedures in the assays.
[0247] Cell and waste fluid separation: The apparatus optionally
includes a device that can remove waste fluid from the sample
mixture while retaining cells for further analysis. The device may
comprise a sample container that has a porous membrane as its
bottom. The pore size of the membrane is smaller than the cells but
larger than the waste material in the mixed solution. The space
below the membrane can be sealed and connected to a vacuum pump. As
an alternative example, the space above the membrane can be sealed
and connected to a positive pressure source. In a different
embodiment, the device can comprise a centrifuge. The container
with the membrane bottom is loaded into the centrifuge, which spins
to force the waste solution to filter out through the membrane. In
another configuration of this device, the sample container has a
solid bottom. Cells deposit at the bottom after centrifugation, and
the waste solution is decanted from the top by the fluid handling
subsystem described above.
[0248] This device can also perform a function that prepares the
sample for final readout. In embodiments where the readout is by
microscopy, the cells are typically deposited and attached to a
flat surface. A centrifuge in the device can achieve this if the
bottom of the container is flat. In another approach, a flat plate
can spin within its plane, and the system can employ the fluid
handling device to drop the solution containing the cells at the
center of the spin. The cells will be evenly spun on the plate
surface.
[0249] Detection: The detection element of the invented apparatus
can be integrated with the rest of the system, or alternatively it
can be separate from the rest of the subsystems described above. In
one embodiment, the readout device is based on a microscope, which
may be an imaging or scanning microscope. In another embodiment,
the device is based on a fluorescent imaging or scanning microscope
with multiple excitation and readout wavelengths for different
probes. In a preferred embodiment, the readout device is based on
flow cytometry. The cytometry approach is preferred because it can
read floating cells directly out of fluid at multiple wavelengths
thus greatly improving the efficiency of the assay.
[0250] All of the above elements can be integrated into one
instrument. Alternatively, these elements may be included in a
number of instruments, which work together as a system to perform
the assay. FIG. 10 illustrates one particular exemplary embodiment
of the instrument configuration. In this particular configuration,
the sample is held in a container (sample test tube) with a
membrane bottom. Reagents are added from the top of the tube using
a pump through a multiport valve. Waste is removed from bottom by
vacuum. The holder for the sample container is fixed on an
agitation table and the space around the sample is temperature
controlled (temp controlled zone) by the temperature controller.
The fluid handling element can introduce reagents (fixation and
permeation reagents, hybridization buffer, probes sets, and wash
buffer) into the sample tube, remove waste into a waste container,
and feed cells to a flow cytometer for detection.
[0251] One class of embodiments provides a system comprising a
holder configured to accept a sample container; a temperature
controller configured to maintain the sample container at a
selected temperature (e.g., a temperature selected by a user of the
system or a preset temperature, different temperatures are
optionally selected for different steps in an assay procedure); a
fluid handling element fluidly connected to the sample container
and configured to add fluid to and/or remove fluid from the sample
container; a mixing element configured to mix (e.g., stir or
agitate) contents of the sample container; and a detector for
detecting one or more signals from within individual cells, wherein
the detector is optionally fluidly connected to the sample
container. One of more fluid reservoirs (e.g., for fixation or
permeabilization reagents, wash buffer, probe sets, and/or waste)
are optionally fluidly connected to the sample container.
[0252] A system of the invention optionally includes a computer.
The computer can include appropriate software for receiving user
instructions, either in the form of user input into a set of
parameter fields, e.g., in a GUI, or in the form of preprogrammed
instructions, e.g., preprogrammed for a variety of different
specific operations. The software optionally converts these
instructions to appropriate language for controlling the operation
of components of the system (e.g., for controlling a fluid handling
element and/or laser). The computer can also receive data from
other components of the system, e.g., from a detector, and can
interpret the data, provide it to a user in a human readable
format, or use that data to initiate further operations, in
accordance with any programming by the user.
Nucleic Acid Targets
[0253] As noted, a nucleic acid target can be essentially any
nucleic acid that is desirably detected in a cell. Choice of
targets will obviously depend on the desired application, e.g.,
expression analysis, disease diagnosis, staging, or prognosis,
target identification or validation, pathway analysis, drug
screening, drug efficacy studies, or any of many other
applications. Large numbers of suitable targets have been described
in the art, and many more can be identified using standard
techniques.
[0254] For detection of CTC, as just one example, a variety of
suitable nucleic acid targets are known. For example, a multiplex
panel of markers for CTC detection could include one or more of the
following markers: epithelial cell-specific (e.g. CK19, Mucl,
EpCAM), blood cell-specific as negative selection (e.g. CD45),
tumor origin-specific (e.g. PSA, PSMA, HPN for prostate cancer and
mam, mamB, her-2 for breast cancer), proliferating
potential-specific (e.g. Ki-67, CEA, CA15-3), apoptosis markers
(e.g. BCL-2, BCL-XL), and other markers for metastatic, genetic and
epigenetic changes. As another example, targets can include HOXB13
and IL17BR mRNAs, whose ratio in primary tumor has been shown to
predict clinical outcome of breast cancer patients treated with
tamoxifen (Ma et al. (2004) "A two-gene expression ratio predicts
clinical outcome in breast cancer patients treated with tamoxifen"
Cancer Cell 5(6):607-16 and Goetz et al. (2006) "A Two-Gene
Expression Ratio of Homeobox 13 and Interleukin-17B Receptor for
Prediction of Recurrence and Survival in Women Receiving Adjuvant
Tamoxifen" Clin Cancer Res 12:2080-2087). See also, e.g., Gewanter,
R. M., A. E. Katz, et al. (2003) "RT-PCR for PSA as a prognostic
factor for patients with clinically localized prostate cancer
treated with radiotherapy" Urology 61(5):967-71; Giatromanolaki et
al. (2004) "Assessment of highly angiogenic and disseminated in the
peripheral blood disease in breast cancer patients predicts for
resistance to adjuvant chemotherapy and early relapse" Int J Cancer
108(4):620-7; Halabi et al. (2003) "Prognostic significance of
reverse transcriptase polymerase chain reaction for
prostate-specific antigen in metastatic prostate cancer: a nested
study within CALGB 9583" J Clin Oncol 21(3):490-5; Hardingham et
al. (2000) "Molecular detection of blood-borne epithelial cells in
colorectal cancer patients and in patients with benign bowel
disease" Int J Cancer 89(1):8-13; Hayes et al. (2002) "Monitoring
expression of HER-2 on circulating epithelial cells in patients
with advanced breast cancer" Int J Oncol 21(5):1111-7; Jotsuka, et
al. (2004) "Persistent evidence of circulating tumor cells detected
by means of RT-PCR for CEA mRNA predicts early relapse: a
prospective study in node-negative breast cancer" Surgery
135(4):419-26; Allen-Mersh T et al. (2003) "Colorectal cancer
recurrence is predicted by RT-PCR detection of circulating cancer
cells at 24 hours after primary excision" ASCO meeting, Chicago,
May 2003; Shariat et al. (2003) "Early postoperative peripheral
blood reverse transcription PCR assay for prostate-specific antigen
is associated with prostate cancer progression in patients
undergoing radical prostatectomy" Cancer Res 63(18):5874-8; Smith
et al. (2000) "Response of circulating tumor cells to systemic
therapy in patients with metastatic breast cancer: comparison of
quantitative polymerase chain reaction and immunocytochemical
techniques" J Clin Oncol 18(7):1432-9; Stathopoulou et al. (2002)
"Molecular detection of cytokeratin-19-positive cells in the
peripheral blood of patients with operable breast cancer:
evaluation of their prognostic significance" J Clin Oncol
20(16):3404-12; and Xenidis et al. (2003) "Peripheral blood
circulating cytokeratin-19 mRNA-positive cells after the completion
of adjuvant chemotherapy in patients with operable breast cancer"
Ann Oncol 14(6):849-55.
[0255] One preferred class of nucleic acid targets to be detected
in the methods herein are those involved in cancer. Any nucleic
acid that is associated with cancer can be detected in the methods
of the invention, e.g., those that encode over expressed or mutated
polypeptide growth factors (e.g., sis), overexpressed or mutated
growth factor receptors (e.g., erb-B1), over expressed or mutated
signal transduction proteins such as G-proteins (e.g., Ras), or
non-receptor tyrosine kinases (e.g., abl), or over expressed or
mutated regulatory proteins (e.g., myc, myb, jun, fos, etc.) and/or
the like. In general, cancer can often be linked to signal
transduction molecules and corresponding oncogene products, e.g.,
nucleic acids encoding Mos, Ras, Raf, and Met; and transcriptional
activators and suppressors, e.g., p53, Tat, Fos, Myc, Jun, Myb,
Rel, and/or nuclear receptors. p53, colloquially referred to as the
"molecular policeman" of the cell, is of particular relevance, as
about 50% of all known cancers can be traced to one or more genetic
lesion in p53.
[0256] Taking one class of genes that are relevant to cancer as an
example for discussion, many nuclear hormone receptors have been
described in detail and the mechanisms by which these receptors can
be modified to confer oncogenic activity have been worked out. For
example, the physiological and molecular basis of thyroid hormone
action is reviewed in Yen (2001) "Physiological and Molecular Basis
of Thyroid Hormone Action" Physiological Reviews 81(3):1097-1142,
and the references cited therein. Known and well characterized
nuclear receptors include those for glucocorticoids (GRs),
androgens (ARs), mineralocorticoids (MRs), progestins (PRs),
estrogens (ERs), thyroid hormones (TRs), vitamin D (VDRs),
retinoids (RARs and RXRs), and the peroxisome proliferator
activated receptors (PPARs) that bind eicosanoids. The so called
"orphan nuclear receptors" are also part of the nuclear receptor
superfamily, and are structurally homologous to classic nuclear
receptors, such as steroid and thyroid receptors. Nucleic acids
that encode any of these receptors, or oncogenic forms thereof, can
be detected in the methods of the invention. About 40% of all
pharmaceutical treatments currently available are agonists or
antagonists of nuclear receptors and/or oncogenic forms thereof,
underscoring the relative importance of these receptors (and their
coding nucleic acids) as targets for analysis by the methods of the
invention.
[0257] One exemplary class of target nucleic acids are those that
are diagnostic of colon cancer, e.g., in samples derived from
stool. Colon cancer is a common disease that can be sporadic or
inherited. The molecular basis of various patterns of colon cancer
is known in some detail. In general, germline mutations are the
basis of inherited colon cancer syndromes, while an accumulation of
somatic mutations is the basis of sporadic colon cancer. In
Ashkenazi Jews, a mutation that was previously thought to be a
polymorphism may cause familial colon cancer. Mutations of at least
three different classes of genes have been described in colon
cancer etiology: oncogenes, suppressor genes, and mismatch repair
genes. One example nucleic acid encodes DCC (deleted in colon
cancer), a cell adhesion molecule with homology to fibronectin. An
additional form of colon cancer is an autosomal dominant gene,
hMSH2, that comprises a lesion. Familial adenomatous polyposis is
another form of colon cancer with a lesion in the MCC locus on
chromosome number 5. For additional details on colon cancer, see,
Calvert et al. (2002) "The Genetics of Colorectal Cancer" Annals of
Internal Medicine 137 (7): 603-612 and the references cited
therein. For a variety of colon cancers and colon cancer markers
that can be detected in stool, see, e.g., Boland (2002) "Advances
in Colorectal Cancer Screening: Molecular Basis for Stool-Based DNA
Tests for Colorectal Cancer: A Primer for Clinicans" Reviews In
Gastroenterological Disorders Volume 2, Supp. 1 and the references
cited therein. As with other cancers, mutations in a variety of
other genes that correlate with cancer, such as Ras and p53, are
useful diagnostic indicators for cancer.
[0258] Cervical cancer is another exemplary target for detection,
e.g., by detection of nucleic acids that are diagnostic of such
cancer in samples obtained from vaginal secretions. Cervical cancer
can be caused by the papova virus (e.g., human papilloma virus) and
has two oncogenes, E6 and E7. E6 binds to and removes p53 and E7
binds to and removes PRB. The loss of p53 and uncontrolled action
of E2F/DP growth factors without the regulation of pRB is one
mechanism that leads to cervical cancer.
[0259] Another exemplary target for detection by the methods of the
invention is retinoblastoma, e.g., in samples derived from tears.
Retinoblastoma is a tumor of the eyes which results from
inactivation of the pRB gene. It has been found to transmit
heritably when a parent has a mutated pRB gene (and, of course,
somatic mutation can cause non-heritable forms of the cancer).
[0260] Neurofibromatosis Type 1 can be detected in the methods of
the invention. The NF1 gene is inactivated, which activates the
GTPase activity of the ras oncogene. If NF1 is missing, ras is
overactive and causes neural tumors. The methods of the invention
can be used to detect Neurofibromatosis Type 1 in CSF or via tissue
sampling.
[0261] Many other forms of cancer are known and can be found by
detecting associated genetic lesions using the methods of the
invention. Cancers that can be detected by detecting appropriate
lesions include cancers of the lymph, blood, stomach, gut, colon,
testicles, pancreas, bladder, cervix, uterus, skin, and essentially
all others for which a known genetic lesion exists. For a review of
the topic, see, e.g., The Molecular Basis of Human Cancer Coleman
and Tsongalis (Eds) Humana Press; ISBN: 0896036340; 1st edition
(August 2001).
[0262] Similarly, nucleic acids from pathogenic or infectious
organisms can be detected by the methods of the invention, e.g.,
for infectious fungi, e.g., Aspergillus, or Candida species;
bacteria, particularly E. coli, which serves a model for pathogenic
bacteria (and, of course certain strains of which are pathogenic),
as well as medically important bacteria such as Staphylococci
(e.g., aureus), or Streptococci (e.g., pneumoniae); protozoa such
as sporozoa (e.g., Plasmodia), rhizopods (e.g., Entamoeba) and
flagellates (Trypanosoma, Leishmania, Trichomonas, Giardia, etc.);
viruses such as (+) RNA viruses (examples include Poxviruses e.g.,
vaccinia; Picornaviruses, e.g. polio; Togaviruses, e.g., rubella;
Flaviviruses, e.g., HCV; and Coronaviruses), (-) RNA viruses (e.g.,
Rhabdoviruses, e.g., VSV; Paramyxovimses, e.g., RSV;
Orthomyxovimses, e.g., influenza; Bunyaviruses; and Arenaviruses),
dsDNA viruses (Reoviruses, for example), RNA to DNA viruses, i.e.,
Retroviruses, e.g., HIV and HTLV, and certain DNA to RNA viruses
such as Hepatitis B.
[0263] As noted previously, gene amplification or deletion events
can be detected at a chromosomal level using the methods of the
invention, as can altered or abnormal expression levels. One
preferred class of nucleic acid targets to be detected in the
methods herein include oncogenes or tumor suppressor genes subject
to such amplification or deletion. Exemplary nucleic acid targets
include, but are not limited to, integrin (e.g., deletion),
receptor tyrosine kinases (RTKs; e.g., amplification, point
mutation, translocation, or increased expression), NF1 (e.g.,
deletion or point mutation), Akt (e.g., amplification, point
mutation, or increased expression), PTEN (e.g., deletion or point
mutation), MDM2 (e.g., amplification), SOX (e.g., amplification),
RAR (e.g., amplification), CDK2 (e.g., amplification or increased
expression), Cyclin D (e.g., amplification or translocation),
Cyclin E (e.g., amplification), Aurora A (e.g., amplification or
increased expression), P53 (e.g., deletion or point mutation), NBS1
(e.g., deletion or point mutation), Gli (e.g., amplification or
translocation), Myc (e.g., amplification or point mutation), HPV-E7
(e.g., viral infection), and HPV-E6 (e.g., viral infection).
[0264] For embodiments in which a nucleic acid target is used as a
reference, suitable reference nucleic acids have similarly been
described in the art or can be determined. For example, a variety
of genes whose copy number is stably maintained in various tumor
cells is known in the art. Housekeeping genes whose transcripts can
serve as references in gene expression analyses include, for
example, 18S rRNA, 28S rRNA, GAPD, ACTB, and PPIB. Additional
similar nucleic acids have been described in the art and can be
adapted to the practice of the present invention.
Labels
[0265] A wide variety of labels are well known in the art and can
be adapted to the practice of the present invention. For example,
luminescent labels and light-scattering labels (e.g., colloidal
gold particles) have been described. See, e.g., Csaki et al. (2002)
"Gold nanoparticles as novel label for DNA diagnostics" Expert Rev
Mol Diagn 2:187-93.
[0266] As another example, a number of fluorescent labels are well
known in the art, including but not limited to, hydrophobic
fluorophores (e.g., phycoerythrin, rhodamine, Alexa Fluor 488 and
fluorescein), green fluorescent protein (GFP) and variants thereof
(e.g., cyan fluorescent protein and yellow fluorescent protein),
and quantum dots. See e.g., The Handbook: A Guide to Fluorescent
Probes and Labeling Technologies, Tenth Edition or Web Edition
(2006) from Invitrogen (available on the world wide web at
probes.invitrogen.com/handbook), for descriptions of fluorophores
emitting at various different wavelengths (including tandem
conjugates of fluorophores that can facilitate simultaneous
excitation and detection of multiple labeled species). For use of
quantum dots as labels for biomolecules, see e.g., Dubertret et al.
(2002) Science 298:1759; Nature Biotechnology (2003) 21:41-46; and
Nature Biotechnology (2003) 21:47-51.
[0267] Labels can be introduced to molecules, e.g. polynucleotides,
during synthesis or by postsynthetic reactions by techniques
established in the art. For example, kits for fluorescently
labeling polynucleotides with various fluorophores are available
from Molecular Probes, Inc. ((www.) molecularprobes.com), and
fluorophore-containing phosphoramidites for use in nucleic acid
synthesis are commercially available. Similarly, signals from the
labels (e.g., absorption by and/or fluorescent emission from a
fluorescent label) can be detected by essentially any method known
in the art. For example, multicolor detection and the like are well
known in the art. Instruments for detection of labels are likewise
well known and widely available, e.g., scanners, microscopes, flow
cytometers, etc. For example, flow cytometers are widely available,
e.g., from Becton-Dickinson ((www.) bd.com) and Beckman Coulter
((www.) beckman.com).
Molecular Biological Techniques
[0268] In practicing the present invention, many conventional
techniques in molecular biology, microbiology, and recombinant DNA
technology are optionally used. These techniques are well known and
are explained in, for example, Berger and Kimmel, Guide to
Molecular Cloning Techniques, Methods in Enzymology volume 152
Academic Press, Inc., San Diego, Calif.; Sambrook et al., Molecular
Cloning--A Laboratory Manual (3rd Ed.), Vol. 1-3, Cold Spring
Harbor Laboratory, Cold Spring Harbor, N.Y., 2000 and Current
Protocols in Molecular Biology, F. M. Ausubel et al., eds., Current
Protocols, a joint venture between Greene Publishing Associates,
Inc. and John Wiley & Sons, Inc., (supplemented through 2006).
Other useful references, e.g. for cell isolation and culture (e.g.,
for subsequent nucleic acid isolation) include Freshney (1994)
Culture of Animal Cells, a Manual of Basic Technique, third
edition, Wiley-Liss, New York and the references cited therein;
Payne et al. (1992) Plant Cell and Tissue Culture in Liquid Systems
John Wiley & Sons, Inc. New York, N.Y.; Gamborg and Phillips
(Eds.) (1995) Plant Cell, Tissue and Organ Culture; Fundamental
Methods Springer Lab Manual, Springer-Verlag (Berlin Heidelberg New
York) and Atlas and Parks (Eds.) The Handbook of Microbiological
Media (1993) CRC Press, Boca Raton, Fla.
[0269] Making Polynucleotides
[0270] Methods of making nucleic acids (e.g., by in vitro
amplification, purification from cells, or chemical synthesis),
methods for manipulating nucleic acids (e.g., by restriction enzyme
digestion, ligation, etc.) and various vectors, cell lines and the
like useful in manipulating and making nucleic acids are described
in the above references. In addition, methods of making branched
polynucleotides (e.g., amplification multimers) are described in
U.S. Pat. No. 5,635,352, U.S. Pat. No. 5,124,246, U.S. Pat. No.
5,710,264, and U.S. Pat. No. 5,849,481, as well as in other
references mentioned above.
[0271] In addition, essentially any polynucleotide (including,
e.g., labeled or biotinylated polynucleotides) can be custom or
standard ordered from any of a variety of commercial sources, such
as The Midland Certified Reagent Company ((www.) mcrc.com), The
Great American Gene Company ((www.) genco.com), ExpressGen Inc.
((www.) expressgen.com), Qiagen (oligos.qiagen.com) and many
others.
[0272] A label, biotin, or other moiety can optionally be
introduced to a polynucleotide, either during or after synthesis.
For example, a biotin phosphoramidite can be incorporated during
chemical synthesis of a polynucleotide. Alternatively, any nucleic
acid can be biotinylated using techniques known in the art;
suitable reagents are commercially available, e.g., from Pierce
Biotechnology ((www.) piercenet.com). Similarly, any nucleic acid
can be fluorescently labeled, for example, by using commercially
available kits such as those from Molecular Probes, Inc. ((www.)
molecularprobes.com) or Pierce Biotechnology ((www.) piercenet.com)
or by incorporating a fluorescently labeled phosphoramidite during
chemical synthesis of a polynucleotide.
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[0296] It is understood that the examples and embodiments described
herein are for illustrative purposes only and that various
modifications or changes in light thereof will be suggested to
persons skilled in the art and are to be included within the spirit
and purview of this application and scope of the appended
claims.
[0297] While the foregoing invention has been described in some
detail for purposes of clarity and understanding, it will be clear
to one skilled in the art from a reading of this disclosure that
various changes in form and detail can be made without departing
from the true scope of the invention. For example, all the
techniques and apparatus described above can be used in various
combinations. All publications, patents, patent applications,
and/or other documents cited in this application are incorporated
by reference in their entirety for all purposes to the same extent
as if each individual publication, patent, patent application,
and/or other document were individually indicated to be
incorporated by reference for all purposes.
* * * * *