SNP detection

• US 6,410,231 B1
• Filed: 02/26/1999
• Issued: 06/25/2002
• Est. Priority Date: 02/26/1999
• Status: Expired due to Fees

• Current Assignee: Incyte Pharmaceuticals, Inc. (Incyte Corporation)
• Original Assignee: Incyte Genomics, Inc. (Incyte Corporation)
• Inventors: Theriault, Thomas, Arnold, Lyle, Bedilion, Tod
• Primary Examiner(s): Jones, W. Gary
• Assistant Examiner(s): SITTON, JEHANNE SOUAYA
• Application Number:
  US09/259,898
• Time in Patent Office: 1,215 Days
• Field of Search: 435/6, 435/91.1, 435/91.2, 536/23.1, 536/24.3, 514/44
• US Class Current: 435/6.1
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence

Abstract

The invention provides methods, compositions and systems for detecting multiple single nucleotide polymorphisms (SNPs) in a population of target polynucleotides in parallel in a sandwich assay employing SNP probes, capture polynucleotides and, optionally, auxiliary polynucleotides. The relative affinities of the SNP probes for the corresponding SNP regions can be increased with reagents which normalize the melting temperatures of the probes and/or by positionally facilitating interactions between the SNP probe, the SNP region, the capture polynucleotide and/or the auxiliary polynucleotides, such as through a minor groove binder. The probes may comprise a degenerate set of all possible same-sized polynucleotides and the capture polynucleotides are generally immobilized and arrayed at corresponding discrete elements in high density.

Claims

1. A method for detecting multiple SNPs in a population of target polynucleotides in parallel, the method comprising the steps of:

(a) combining sample polynucleotides;

capture polynucleotides and SNP probes under conditions wherein;

a subset of the sample polynucleotides are target polynucleotides, each comprising a different capture region and a different SNP region comprising a corresponding different SNP,

the capture polynucleotides are immobilized and arrayed at corresponding discrete elements on a substrate and each capture polynucleotide comprises a sequence which specifically hybridizes to a corresponding different capture region,

each SNP probe comprises a sequence complementary to a corresponding different SNP region,

the target polynucleotides are immmobilized by hybridizing to the capture polynucleotides whereby each target polynucleotide is immobilized at a corresponding discrete element of the substrate to provide a first discrimination of the sample polynucleotides, and

the relative affinity of each SNP probe for the corresponding SNP region is sufficient to provide selective hybridization of the SNP probe to the corresponding SNF region, whereby each SNP probe selectively hybridizes to the corresponding SNP region to provide a second discrimination of the sample polynucleotides; and

(b) detecting the presence of each SNP probe on the substrate, wherein the presence of a given SNP probe at a given element indicates the presence of the corresponding SNP in the corresponding target polynucleotide.

2. The method of claim 1, wherein the SNP probes are a subset of assay probes and the assay probes comprise a degenerate set of all possible same-sized polynucleotides.

3. The method of claim 1, wherein the sample polynucleotides comprise fragmented genomic DNA.

4. The method of claim 1, wherein the capture polynucleotides are a subset of immobilized polynucleotides and the immobilized polynucleotides are a segregated and arrayed cDNA library.

5. The method of claim 1, wherein the capture polynucleotides are immobilized and arrayed at corresponding discrete elements in high density.

6. The method of claim 1, wherein each SNP probe comprises a label.

7. The method of claim 1, wherein the SNP probes are a subset of assay probes and the relative affinity of each SNP probe for the corresponding SNP region is increased to provide enhanced discrimination between the corresponding SNP region and regions of the target polynucleotide other than the corresponding SNP region.

8. The method of claim 7, wherein the relative affinity of each SNP probe for the corresponding SNP region is increased at least in part by a method comprising the step of including in the combining step a reagent which normalizes the melting temperatures of the assay probes.

9. The method of claim 7, wherein the relative affinity of each SNP probe for the corresponding SNP region is increased at least in part by the SNP probe interacting with the capture polynucleotide or an auxiliary probe hybridized to the corresponding target polynucleotide.

10. The method of claim 7, wherein the relative affinity of each SNP probe for the corresponding SNP region is increased at least in part by the SNP probe interacting with the capture polynucleotide or an auxiliary probe hybridized to the corresponding target polynucleotide through a minor groove binder tethered to at least one of the SNP probe, the capture polynucleotide and the auxiliary probe.

11. The method of claim 7, wherein the assay probes comprise a degenerate set of all possible same-sized polynucleotides.

12. The method of claim 7, wherein the sample polynucleotides comprise fragmented genomic DNA.

13. The method of claim 7, wherein the capture polynucleotides are a subset of immobilized polynucleotides and the immobilized polynucleotides are a segregated and arrayed cDNA library.

14. The method of claim 7, wherein the capture polynucleotides are immobilized and arrayed at corresponding discrete elements in high density.

15. The method of claim 7, wherein each SNP probe comprises a label.

17. The method of claim 10, wherein the assay probes comprise a degenerate set of all possible same-sized polynucleotides.

18. The method of claim 10, wherein the sample polynucleotides comprise fragmented genomic DNA.

19. The method of claim 10, wherein the capture polynucleotides are a subset of immobilized polynucleotides and the immobilized polynucleotides are a segregated and arrayed cDNA library.

20. The method of claim 10, wherein the capture polynucleotides are immobilized and arrayed at corresponding discrete elements in high density.

16. A method for detecting multiple SNPs in a population of target polynucleotides in parallel, the method comprising the steps of:

(a) combining populations of each of sample polynucleotides, immobilized polynucleotides and assay probe pairs, each assay probe pair comprising first and second assay probes, under conditions wherein;

a subset of the sample polynucleotides are target polynucleotides, each comprising a different capture region and a different SNP region comprising a corresponding different SNP,

a subset of the immobilized polynucleotides are capture polynucleotides which are immobilized and arrayed at corresponding discrete elements on a substrate and each capture polynucleotide comprises a sequence which specifically hybridizes to a corresponding different capture region,

a subset of the assay probe pairs are SNP probe pairs, each comprising a first SNP probe comprising a sequence complementary to a corresponding different SNP region, and a second SNP probe comprising a sequence having a single base mismatch with the same corresponding SNP region;

the target polynucleotides are immobilized by hybridizing to the capture polynucleotides whereby each target polynucleotide is immobilized at a corresponding discrete element of the substrate to provide a first discrimination of the sample polynucleotides; and

the relative affinity of each first SNP probe for the corresponding SNP region is increased at least in part by at least one of (a) a method comprising the step of including in the combining step a reagent which normalizes the melting temperatures of the assay probes and (b) the SNP probe interacting with the capture polynucleotide or an auxiliary probe hybridized to the corresponding target polynucleotide, sufficiently to provide selective hybridization of the first SNP probe to the corresponding SNP region to provide a second discrimination of the sample polynucleotides, whereby the ratio of hybridization of each first SNP probe to the corresponding SNP region to the hybridization of each second SNP probe to the same corresponding SNP region increases as a result of said conditions at least 2-fold; and

(b) detecting the presence of each SNP probe on the substrate, wherein the presence of a given SNP probe at a given element indicates the presence of the corresponding SNP in the corresponding target polynucleotide.