Compound probes and methods of increasing the effective probe densities of arrays

• US 20070259344A1
• Filed: 05/03/2006
• Published: 11/08/2007
• Est. Priority Date: 05/03/2006
• Status: Abandoned Application

• Current Assignee: Agilent Technologies, Inc.
• Original Assignee: Agilent Technologies, Inc.
• Inventors: Leproust, Eric M., Caren, Michael P., Gordon, David B., Amorese, Douglas A., Payne, Andrew
• Application Number:
  US11/417,313
• Publication Number:
  US 20070259344A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2525/197 incorporating a spacer/coupling moiety
• CPC Class Codes: C12Q 2565/507 characterised by the density of the capture oligonucleotide

Abstract

Methods and articles for analyzing nucleotide sequences of nucleic acid molecules, e.g., using multiple probes per spot of an array, are described. In some embodiments, the methods and articles can reduce the numbers of arrays necessary to probe regions of interest in a biological sample, and/or increase the resolution at which biological events are probed. In some cases, these methods exploit the vertical aspect of an array in order to decrease the number of arrays or spots required for an assay. These probes may be in the form of compound probes, which comprise at least first and second probes, including first and second nucleotide sequences capable of hybridizing to first and second target nucleotide sequences, respectively, in a nucleic acid molecule of interest.

Claims

1. An oligonucleotide probe comprising a plurality of hybridizing segments, wherein said hybridizing segments hybridize to non-contiguous regions in a target genome.

2. The oligonucleotide probe as in claim 1, wherein said oligonucleotide probe is at least 100 bases in length.

3. The oligonucleotide probe as in claim 1, wherein said hybridizing segments are each at least 40 bases in length.

4. The oligonucleotide probe as in claim 1, wherein said oligonucleotide probe comprises at least 3 hybridizing segments.

5. The oligonucleotide probe as in claim 1, wherein said hybridizing segments are contiguous.

6. The oligonucleotide probe as in claim 1, wherein said hybridizing segments are separated by a linker.

7. The oligonucleotide probe as in claim 1, wherein said linker comprises a nucleotide sequence that is optimized to minimize hybridization to the linker.

8. The oligonucleotide probe as in claim 1, wherein said non-contiguous regions are separated by at least 10 kb in a target mammalian genome.

9. The oligonucleotide probe as in claim 8, wherein said non-contiguous regions are present on different chromosomes of said mammalian genome.

10. An array comprising an oligonucleotide probe of claim 1.

11. A method of sample analysis:

a) contacting a sample comprising nucleic acids with an array of claim 10 under hybridizing conditions; and

b) assessing binding of said nucleic acids with said oligonucleotide.

12. A kit comprising the array of claim 10.

13. A compound probe, comprising:

at least a first oligonucleotide probe comprising a first nucleotide sequence capable of hybridizing to a first target nucleotide sequence in a nucleic acid molecule of interest; and

at least a second oligonucleotide probe comprising a second nucleotide sequence capable of hybridizing to a second target nucleotide sequence in the nucleic acid molecule of interest,

wherein the first and second nucleotide sequences of the first and second oligonucleotide probes, respectively, together are not genomically contiguous when hybridized to any single strand in the nucleic acid molecule of interest.

14. The compound probe as in claim 13, wherein the first and second nucleotide sequences of the first and second oligonucleotide probes, respectively, are contiguous with each other on the compound probe.

15. The compound probe as in claim 13, wherein the first and second nucleotide sequences of the first and second oligonucleotide probes, respectively, are separated from each other by a linker segment on the compound probe, and wherein the first and second nucleotide sequences including the linker segment, together are not genomically contiguous when hybridized to any single strand in the nucleic acid molecule of interest.

16. An array or array set for determining a location of a biological phenomenon in terms of chromosomal coordinates in a nucleic acid molecule of interest, comprising:

a plurality of spots, each spot comprising a homogenous composition of nucleotide sequences, each composition of a spot comprising;

at least a first oligonucleotide probe comprising a first nucleotide sequence capable of hybridizing to a first target nucleotide sequence in a nucleic acid molecule of interest; and

at least a second oligonucleotide probe comprising a second nucleotide sequence capable of hybridizing to a second target nucleotide sequence in the nucleic acid molecule of interest,

wherein the first and second nucleotide sequences of the first and second oligonucleotide probes, respectively, may be contiguous with each other on the compound probe or separated from each other by a linker segment on the compound probe, and wherein the first and second nucleotide sequences or first and second nucleotide sequences including the linker segment, together are not genomically contiguous when hybridized to any single strand in the nucleic acid molecule of interest.

17. A kit for determining a location of a biological phenomenon in terms of chromosomal coordinates in a nucleic acid molecule of interest, comprising:

an array or array set comprising a plurality of spots, each spot comprising a homogenous composition of nucleotide sequences, each composition of a spot comprising;

at least a first oligonucleotide probe comprising a first nucleotide sequence capable of hybridizing to a first target nucleotide sequence in a nucleic acid molecule of interest; and

at least a second oligonucleotide probe comprising a second nucleotide sequence capable of hybridizing to a second target nucleotide sequence in the nucleic acid molecule of interest,

wherein the first and second nucleotide sequences of the first and second oligonucleotide probes, respectively, may be contiguous with each other on the compound probe or separated from each other by a linker segment on the compound probe, and wherein the first and second nucleotide sequences or first and second nucleotide sequences including the linker segment, together are not genomically contiguous when hybridized to any single strand in the nucleic acid molecule of interest.

18. A method of determining a location of a biological phenomenon in terms of chromosomal coordinates in a nucleic acid molecule of interest, comprising:

contacting a sample comprising including target nucleotide sequences with an array comprising a plurality of oligonucleotide probes under conditions that permit hybridization between target nucleotide sequences of the sample and sequences of the oligonucleotide probes, and allowing hybridization of a target nucleotide sequence of the sample and a sequence of the oligonucleotide probe;

detecting a signal on the array or array set as a result of hybridization;

correlating the signal to at least two locations on the nucleic acid molecule of interest; and

determining a location of a biological phenomenon in the nucleic acid molecule of interest.

19. A method of determining a location of a biological phenomenon in terms of chromosomal coordinates in a nucleic acid molecule of interest, comprising:

contacting a sample comprising target nucleotide sequences with an array or array set comprising a plurality of oligonucleotide probes under conditions that permit hybridization between target nucleotide sequences of the sample and sequences of the oligonucleotide probes, and allowing hybridization of a target nucleotide sequence of the sample and a sequence of the oligonucleotide probe;

producing a signal on the array or array set as a result of hybridization, wherein the signal of a spot alone does not enable determination of the target nucleotide sequence hybridized on the spot;

detecting hybridization; and

determining a location of a biological phenomenon in the nucleic acid molecule of interest using a combination of signals produced after hybridization.

20. A method of assaying nucleotide sequences in a biological sample, comprising:

contacting a biological sample including target nucleotide sequences with the plurality of compound probes of the first array or array set comprising;

a plurality of compound probes, each compound probe comprising at least a first probe including a first nucleotide sequence complementary to a first nucleotide sequence in a biological sample and at least a second probe comprising a second nucleotide sequence complementary to a second nucleotide sequence in the biological sample;

under conditions that permit hybridization of complementary sequences between the target nucleotide sequences of the biological sample and nucleotide sequences of the first array or array set;

detecting hybridized compound probes of the first array or array set, wherein the hybridized compound probes can be hybridized partially or completely;

contacting the biological sample including target nucleotide sequences to the plurality of probes of the second array or array set comprising;

a plurality of probes including the first and second probes of the hybridized compound probes of the first array or array set

under conditions that permit hybridization of complementary sequences between the target nucleotide sequences of the biological sample and nucleotide sequences of the second array or array set; and

detecting hybridized probes of the second array or array set.