Allele-specific copy number measurement using single nucleotide polymorphism and DNA arrays

• US 8,685,642 B2
• Filed: 07/30/2007
• Issued: 04/01/2014
• Est. Priority Date: 07/30/2007
• Status: Active Grant

• Current Assignee: Agilent Technologies, Inc.
• Original Assignee: Agilent Technologies, Inc.
• Inventors: Sampas, Nicholas Michael
• Primary Examiner(s): POHNERT, STEVEN C
• Application Number:
  US11/881,932
• Publication Number:
  US 20090035762A1
• Time in Patent Office: 2,437 Days
• Field of Search: None
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2565/501 being an array of oligonucleotides

Abstract

Methods and systems for allelic detection and allele-specific copy number are provided herein. The described methods use identification of single nucleotide polymorphism using restriction enzymes and CGH analysis. Microarrays comprising probes designed by the described methods are provided. Also included are methods for identifying SNP sites and copy number in samples obtained from patient populations.

Claims

1. A method for sample analysis, comprising:

a) contacting a first DNA sample with a first restriction enzyme to provide a digested sample, wherein;

i) said DNA sample may comprise a target sequence comprising a SNP site; and

ii) said first restriction enzyme cleaves said target sequence at a cleavage site only if a first allele of a SNP is present at said SNP site;

b) hybridizing said digested sample to a surface-bound polynucleotide comprising a probe sequence that hybridizes to said target sequence wherein;

i. the surface-bound polynucleotide is up to 200 nucleotides in length,

ii. the probe sequence comprises said cleavage site, and

iii. the probe sequence is designed such that cleavage of the target sequence at said cleavage site by said first restriction enzyme results in less hybridization of the digested sample relative to a sample in which the target sequence is undigested by the first restriction enzyme;

c) comparing the hybridization signal between the digested sample and the probe sequence to a reference signal, and

d) determining whether the first allele of the SNP is present in the DNA sample, wherein the hybridization signal of the digested sample to the probe sequence as compared to the reference signal indicates whether the first allele of said SNP is present in the DNA sample.

2. The method of claim 1, wherein said reference signal is the hybridization signal between a reference sample and the probe sequence, wherein the reference sample comprises one or more known alleles of the SNP at said SNP site and has been contacted with said first restriction enzyme.

3. The method of claim 1, wherein said reference signal is the hybridization signal between a reference sample and the probe sequence, wherein the reference sample is a second portion of said first DNA sample that has not been contacted with said first restriction enzyme.

4. The method of claim 2, wherein said reference sample comprises a plurality of DNA samples from different subjects.

5. The method of claim 1, wherein said surface-bound polynucleotide is from 30 to 60 nucleotides in length.

6. The method of claim 5, wherein, in said probe sequence, the nucleotide immediately 5′

of said cleavage site is located within at least 10 nucleotides from the center of the probe sequence.

7. The method of claim 1, wherein said probe sequence is complementary to a second allele of said SNP.

8. The method of claim 1, wherein the probe sequence comprises a base deletion at a position that corresponds to the SNP site.

9. The method of claim 1, wherein the probe sequence has a generic base at the SNP site.

10. The method of claim 1, further comprising determining whether said DNA sample is homozygous or heterozygous for said first allele.

11. The method of claim 1, further comprising determining the copy number of said target sequence.

12. The method of claim 1, wherein the first DNA sample is fragmented genomic DNA.

13. The method of claim 1, wherein the first restriction enzyme is a four base cutter.

14. The method of claim 1, wherein the first restriction enzyme is a five base cutter.

15. The method of claim 1, wherein the first restriction enzyme is a six base cutter.

16. The method of claim 1, wherein the first restriction enzyme is RsaI.

17. The method of claim 1, wherein the first restriction enzyme is AluI.

18. The method of claim 2, wherein said digested sample and the reference sample are co-hybridized to the same array.

19. The method of claim 1, wherein the first DNA sample is a cDNA sample.

20. The method of claim 1, wherein the surface-bound polynucleotide is part of an array.

21. The method of claim 1, wherein said first DNA sample is not a PCR product.