Methods for genotyping selected polymorphism

• US 7,459,273 B2
• Filed: 08/05/2004
• Issued: 12/02/2008
• Est. Priority Date: 10/04/2002
• Status: Active Grant

• Current Assignee: Affymetrix, Inc. (Thermo Fisher Scientific Incorporated)
• Original Assignee: Affymetrix, Inc. (Thermo Fisher Scientific Incorporated)
• Inventors: Jones, Keith W., Shapero, Michael H., Fodor, Stephen P. A.
• Primary Examiner(s): Kim; Young J.
• Assistant Examiner(s): WOOLWINE, SAMUEL C
• Application Number:
  US10/912,445
• Publication Number:
  US 20050142577A1
• Time in Patent Office: 1,580 Days
• Field of Search: None
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6809 Methods for determination or identification of nucleic acids involving differential detection
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2600/156 Polymorphic or mutational markers

Abstract

Methods for genotyping polymorphisms using a locus specific primer that is complementary to a region near a selected polymorphism are described. Methods for synthesizing pools of locus specific primers that incorporate some degenerate positions are also disclosed. A plurality of different sequence capture probes are synthesized simultaneously using degenerate oligonucleotide synthesis. The sequence of the locus specific regions of the capture probes are related in that they have some bases that are identical in each sequence in the plurality of sequences and positions that vary from one locus specific region to another. The sequences are selected based on proximity to a polymorphism of interest and because they conform to a similar sequence pattern.

Claims

1. A method of genotyping a plurality of polymorphic positions in an organism comprising:

(a) identifying a plurality of target sequences each comprising one of said polymorphic positions, wherein each target sequence has the same common sequence within 1000 bases of the polymorphic position and wherein each target sequence has a degenerate priming site that is one species of a consensus sequence immediately adjacent to the common sequence, wherein the consensus sequence is 10-25 bases and at least 50% of the positions in the consensus sequence are the same in each target sequence and at least two of the bases in the consensus sequence vary between at least two of the target sequences, and wherein the common sequence and the consensus sequence are genomic sequences;

(b) obtaining a plurality of capture probes, comprising a first universal priming region, a region that is complementary to the common sequence and a degenerate region that is complementary to the consensus sequence, wherein said degenerate region comprises at least two degenerate positions that comprise a mixture of different nucleotides that vary between different capture probes in the plurality of capture probes;

(c) contacting a nucleic acid sample comprising genomic DNA from the organism with the plurality of capture probes;

(d) extending the capture probes through the polymorphic positions;

(e) amplifying the extended capture probes;

(f) hybridizing the amplified extended capture probes to an array of probes comprising allele specific probes for a plurality of the polymorphic positions; and

(g) analyzing the hybridization pattern to determine which alleles are present for at least two of the polymorphic positions.

2. The method of claim 1 wherein prior to step (c) the nucleic acid sample is fragmented and an adaptor comprising a second universal priming region is ligated to the fragments.

3. The method of claim 2 wherein the nucleic acid sample is fragmented with a first restriction enzyme, wherein each target sequence contains a recognition site for said first restriction enzyme and wherein the polymorphic position in each target sequence is between the recognition site for said first restriction enzyme and the common sequence.

4. The method of claim 2 wherein the amplifying of step (e) is by PCR using a first and a second primer for the first and the second universal priming regions.

5. The method of claim 1 wherein the common sequence is a recognition site for a restriction enzyme.

6. The method of claim 5 wherein the restriction enzyme is a Type IIS restriction enzyme.

7. The method of claim 1 wherein the amplified extended capture probes are labeled with a detectable label.

8. The method of claim 1 wherein there are at least 5 degenerate positions in the consensus sequence.

9. The method of claim 1 wherein there are at least 6 degenerate positions in the consensus sequence.

10. The method of claim 1 wherein there are at least 10 degenerate positions in the consensus sequence.

11. The method of claim 1 wherein the capture probes are synthesized as a single pool wherein a mixture of at least two different nucleotides are incorporated at each degenerate position.

12. A method for amplifying a collection of target sequences from a nucleic acid sample, wherein each target sequence comprises a polymorphic position, a common sequence of between 4 and 10 bases that is within 1000 bases of the polymorphic position and a consensus sequence immediately adjacent to the common sequence, wherein the consensus sequence is between 10 and 25 bases and comprises at least five degenerate positions, said method comprising:

fragmenting the nucleic acid sample with a selected restriction enzyme;

ligating an adaptor to the fragments to obtain adaptor-ligated fragments, wherein said adaptor comprises a first priming sequence;

contacting the adaptor-ligated fragments with a pool of at least 100 different species of capture probes in a single reaction, wherein each capture probe comprises a second priming sequence and a target specific sequence that comprises a region that is complementary to the common sequence and a region that is complementary to the consensus sequence and wherein the pool comprises degenerate bases corresponding to the at least five degenerate positions in the consensus sequence, wherein the pool comprises a mixture of the nucleotides A, G, C and T at each degenerate base;

extending at least some of the capture probes; and

amplifying the extended capture probes with primers to said first and second priming sequences.

13. The method of claim 12, wherein said plurality of different species of capture probes are synthesized on a solid support and the solid support is selected from the group consisting of arrays, beads, microparticles, microtitre dishes and gels;

wherein the step of extending at least some of the capture probes is done while the capture probes are attached to the solid support; and

further comprising releasing the extended capture probes from the solid support prior to amplifying the extended capture probes.

14. The method of claim 13, wherein, prior to releasing the extended capture probes from the solid support, nucleic acids that are not covalently attached to the solid support are removed.

15. The method of claim 12, wherein labeled nucleotides are incorporated into the extended capture probes and extended capture probes are isolated by affinity chromatography.

16. The method of claim 15, wherein said labeled nucleotides are labeled with biotin and, wherein avidin, streptavidin or an anti-biotin antibody is used to isolate extended capture probes.

17. The method of claim 12, wherein prior to amplification the extended capture probes are made double stranded and single stranded nucleic acid in the sample is digested with a nuclease.

18. The method of claim 12, wherein there are 1,000 to 5,000 different target sequences in the collection of target sequences.

19. The method of claim 12, wherein there are 2,000 to 10,000 different target sequences in the collection of target sequences.

20. The method of claim 12, wherein there are 10,000 to 1,000,000 different target sequences in the collection of target sequences.

21. A method of genotyping a plurality of polymorphisms in an individual comprising:

(a) selecting a plurality of polymorphisms to genotype wherein each polymorphism selected is within 1,000 base pairs of a recognition site for a first restriction enzyme;

(b) obtaining a plurality of at least 1000 capture probes wherein each capture probe comprises a common 5′

sequence and a different 3′

locus specific region that is complementary to a region that is within 1000 base pairs of one of the polymorphisms in the plurality of polymorphisms, and wherein the polymorphism is between said region and the recognition site for the first restriction enzyme, wherein said obtaining comprises synthesizing the capture probes in a pool, wherein at least one base is a degenerate base that is variable within the pool and wherein the pool comprises a mixture of the nucleotides A, G, C and T at that base;

(c) obtaining a biological sample comprising genomic DNA from the individual;

(d) contacting the biological sample with the plurality of at least 1000 capture probes;

(e) extending at least some of the plurality of at least 1000 capture probes;

(f) contacting the sample with the first restriction enzyme to produce fragments;

(g) ligating an adaptor to the fragments wherein the adaptor has an overhang that is complementary to the overhang generated by cleavage with the first restriction enzyme;

(h) amplifying fragments using a first adaptor primer and a second common primer;

(i) labeling the amplified fragments;

(j) hybridizing the amplified fragments to an array of probes comprising probes that are allele specific for each allele of each polymorphism in the plurality of polymorphisms; and

(k) analyzing the resulting hybridization pattern to determine which alleles of each of the polymorphisms in the plurality of polymorphisms is present.

22. The method of claim 21 wherein between 4 and 10 bases in the capture probes are degenerate.

23. The method of claim 21 wherein the capture probes are synthesized in a series of separate and pooled steps.

24. The method of claim 21 wherein said capture probes are synthesized on a solid support.

25. The method of claim 21 wherein said capture probes are attached to a solid support and the 3′

end of the capture probes is available for extension and wherein the extension step takes place while the capture probes are attached to the solid support.