Complexity management and analysis of genomic DNA

• US 7,267,966 B2
• Filed: 07/12/2001
• Issued: 09/11/2007
• Est. Priority Date: 10/27/1998
• Status: Expired due to Fees

• Current Assignee: Affymetrix, Inc. (Thermo Fisher Scientific Incorporated)
• Original Assignee: Affymetrix, Inc. (Thermo Fisher Scientific Incorporated)
• Inventors: Lipshutz, Robert J., Lockhart, David, Dong, Shoulian
• Primary Examiner(s): Kim; Young J.
• Application Number:
  US09/904,039
• Publication Number:
  US 20020142314A1
• Time in Patent Office: 2,252 Days
• Field of Search: 435/6, 435/91.2, 435/183, 435/4, 435/91.1, 536/23.1, 536/24.33, 536/24.3
• US Class Current: 435/91.2
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 1/6855 Ligating adaptors
• CPC Class Codes: C12Q 1/6858 Allele-specific amplification
• CPC Class Codes: C12Q 2521/313 Type II endonucleases, i.e. cutting outside recognition site
• CPC Class Codes: C12Q 2525/191 incorporating an adaptor
• CPC Class Codes: C12Q 2531/113 PCR
• CPC Class Codes: C12Q 2563/143 Magnetism, e.g. magnetic label
• CPC Class Codes: C12Q 2600/156 Polymorphic or mutational markers
• CPC Class Codes: Y10S 977/924 using nanostructure as support of dna analysis

Abstract

The present invention provides for novel methods of sample preparation and analysis involving reproducibly reducing the complexity of a nucleic sample. The invention further provides for analysis of the above sample by hybridization to an array which may be specifically designed to interrogate the desired fragments for particular characteristics, such as, for example, the presence or absence of a polymorphism. The invention further provides for novel methods of using a computer system to model enzymatic reactions in order to determine experimental conditions before conducting actual experiments.

Claims

1. A method of analyzing a first nucleic acid sample comprising:

(a) submitting a computer query to an electronic sequence database to identify the sequence and size of the fragments that are predicted to result from digestion of said first nucleic acid sample with at least one selected restriction enzyme;

(b) selecting a subset of said fragments that are within a selected size range from said computer query;

(c) identifying known polymorphisms present on said fragments in said subset of fragments;

(d) providing a nucleic acid array comprising a plurality of probes which are complementary to said polymorphisms identified in said subsets of fragments;

(e) providing said first nucleic acid sample;

(f) reproducibly reducing the complexity of said first nucleic acid sample to produce a second nucleic acid sample, wherein said reducing complexity step comprises;

(i) fragmenting said first nucleic acid sample with said at least one selected restriction enzyme of step (a); and

(ii) ligating adaptor sequences to said fragments of step (f)(i), and amplifying at least some of said fragments ligated with said adaptor sequences using a selected amplification method, thereby producing a second nucleic acid sample;

(g) hybridizing said second nucleic acid sample to the nucleic acid of array of (d); and

(h) analyzing a hybridization pattern resulting from said hybridizing step of (g).

2. The method of claim 1 wherein said second nucleic acid sample comprises at least 0.5% of the fragments in said first nucleic acid sample.

3. The method of claim 1 wherein said second nucleic acid sample comprises at least 3% of the fragments in said first nucleic acid sample.

4. The method of claim 1 wherein said second nucleic acid sample comprises at least 12% of the fragments in said first nucleic acid sample.

5. The method of claim 1 wherein said second nucleic acid sample comprises at least 50% of the fragments in said first nucleic acid sample.

6. The method of claim 1 wherein said first nucleic acid sample is DNA.

7. The method of claim 1 wherein said first nucleic acid sample is genomic DNA.

8. The method of claim 1 wherein said first nucleic acid sample is cDNA derived from RNA or mRNA.

9. The method of claim 1 wherein the steps of fragmenting said first nucleic acid sample to produce fragments, ligating adaptor sequences to said fragments, and amplifying at least some of said fragments ligated with said adapter sequences are performed in a single reaction vessel.

10. The method of claim 1 wherein said step of fragmenting said first nucleic acid sample comprises digestion with a type IIs endonuclease.

11. The method of claim 1 wherein said adaptor sequences comprise PCR primer template sequences.

12. The method of claim 1 wherein said adaptor sequences comprise tag sequences.

13. The method of claim 1 wherein said method for analyzing a first nucleic acid sample comprises determining whether the first nucleic acid sample contains sequence variations.

14. The method of claim 13 wherein said sequence variations are single nucleotide polymorphisms (SNPs).

15. A method of analyzing a first nucleic acid sample comprising:

providing a first nucleic acid sample;

obtaining a second nucleic acid sample by;

binding oligonucleotide probes containing a desired SNP sequence to magnetic beads to form probe-bead complexes;

hybridizing said probe-bead complexes to said first nucleic acid sample to form target-probe complexes comprising DNA targets hybridized to complementary oligonucleotide probes, wherein the target-probe complexes comprise a double stranded portion and single stranded DNA target regions;

exposing said target-probe complexes to a single strand DNA nuclease to remove said single stranded DNA target regions thereby obtaining double stranded DNA duplexes;

ligating a double stranded adaptor sequence comprising a restriction enzyme site to said double stranded DNA duplexes to obtain adaptor-ligated DNA duplexes;

digesting said adaptor-ligated DNA duplexes with a restriction enzyme to release the magnetic bead from the adaptor-ligated DNA duplex; and

generating said second nucleic acid sample by isolating the adaptor-ligated DNA duplexes released from the magnetic beads by digestion;

providing a nucleic acid array;

hybridizing said second nucleic acid sample to said array; and

analyzing a hybridization pattern resulting from said hybridization.

16. The method of claim 15 wherein said restriction enzyme is a type IIs endonuclease.

17. A method for genotyping a plurality of single nucleotide polymorphisms from a genomic DNA sample comprising:

(a) mixing said genomic DNA sample with a plurality of oligonucleotide probes, wherein each probe comprises a single nucleotide polymorphism and, wherein the probes are attached to beads, under conditions that allow formation of complexes comprising oligonucleotide probes bound to complementary genomic DNA target sequences;

(b) adding a single strand DNA nuclease to the complexes to remove single strand overhangs from the complexes, generating double stranded DNA duplexes attached to beads;

(c) ligating a first adaptor comprising a type uS restriction enzyme recognition site to the DNA duplexes;

(d) digesting the duplexes with a type IIs restriction enzyme to separate the beads from the portion of the duplex containing the single nucleotide polymorphism;

(e) ligating a second adaptor to the portion of the duplex containing the single nucleotide polymorphism;

(f) amplifying the portion of the duplex containing the single nucleotide polymorphism to generate amplified fragments;

(g) hybridizing the amplified fragments to an array of probes comprising allele specific probes complementary to said plurality of single nucleotide polymorphisms to generate a hybridization pattern; and

(h) analyzing said hybridization pattern to determine the genotype of each single nucleotide polymorphism in said plurality of single nucleotide polymorphisms.

18. The method of claim 17 wherein said beads are magnetic beads.

19. The method of claim 17 wherein said beads are glass beads.

20. The method of claim 17 wherein the genomic DNA sample is fractionated genomic DNA.