Methods of screening nucleic acids for single nucleotide variations

• US 7,906,287 B2
• Filed: 05/14/2008
• Issued: 03/15/2011
• Est. Priority Date: 05/14/2007
• Status: Expired due to Fees

• Current Assignee: insight genomics limited
• Original Assignee: insight genomics limited
• Inventors: Dahlhauser, Paul A.
• Primary Examiner(s): WHISENANT, ETHAN C
• Application Number:
  US12/152,512
• Publication Number:
  US 20090053715A1
• Time in Patent Office: 1,035 Days
• Field of Search: 435/6, 536/23.1, 536/24.3
• US Class Current: 435/6.11
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 2521/101 DNA polymerase
• CPC Class Codes: C12Q 2521/319 Exonuclease
• CPC Class Codes: C12Q 2525/125 incorporating agents resulting in resistance to degradation
• CPC Class Codes: C12Q 2535/125 Allele specific primer extension

Abstract

Disclosed are methods and compositions for detecting variation in nucleic acids. The disclosed method compares the sequence of a nucleic acid of interest with the sequence of a reference nucleic acid to sensitively identify variations between the sequence of a nucleic acid of interest and the sequence of a reference nucleic acid. The disclosed method generally involves excision and replacement of selected nucleotides in nucleic acid strands hybridized to other strands. In the method, if the excised nucleotide was mismatched with the nucleotide in the other, hybridized strand, then the replacement nucleotide will not be mismatched. If the excised nucleotide was not mismatched with the nucleotide in the other, hybridized strand, then the excised nucleotide is not replaced. This difference allows detection of variation in the nucleic acid of interest. In some forms of the method, by replacing excised nucleotides with nuclease-resistant nucleotides, strands in which excised nucleotides are replaced will be resistant to nuclease digestion while strands in which excised nucleotides are not replaced will be sensitive to nuclease digestion. By exposing the hybridizing nucleic acids to nuclease following replacement of excised nucleotides, the strands in which excised nucleotides are not replaced can be destroyed by the nuclease while strands in which excised nucleotides are replaced can be preserved. The remaining strands can then be detected and whether the strand survived nuclease digestion can be noted. Strands that survive nuclease digestion are indicative of the presence of variation in the nucleic acid of interest.

Claims

1. A method of detecting a nucleotide variation within a nucleic acid of interest comprising:

(a) a step comprising generating a set of extension products from a first nucleic acid and causing modified nucleotides to be present in the extension products, wherein the modified nucleotides comprise a single type of base,

(b) a step comprising hybridizing the extension products to a second nucleic acid,

(c) a step comprising contacting the hybridizing nucleic acid with one or more agents that collectively remove the modified nucleotides,

(d) a step comprising contacting the hybridizing nucleic acid with a first enzyme that extends the extension products in the presence of three types of nuclease-resistant nucleotides and not in the presence of nucleotides that comprise the same type of base as the modified nucleotides, wherein each of the three types of nuclease-resistant nucleotides comprises a different type of base,

(e) a step comprising contacting the hybridizing nucleic acid with a second enzyme that removes nucleotides from the 3′

end of the extension products, wherein the second enzyme does not remove the nuclease-resistant nucleotides,

(f) a step comprising contacting the hybridizing nucleic acid with a third enzyme that extends the extension products in the presence of nucleotides,

(g) a step comprising distinguishing those extension products comprising a nuclease-resistant nucleotide from those extension products not comprising a nuclease-resistant nucleotide, wherein the first nucleic acid is a reference nucleic acid and the second nucleic acid is the nucleic acid of interest or wherein the first nucleic acid is the nucleic acid of interest and the second nucleic acid is a reference nucleic acid, thereby detecting nucleotide variation in the nucleic acid of interest.

2. The method of claim 1, wherein the reference nucleic acid comprises a wild-type sequence.

3. The method of claim 2, wherein the nucleic acid of interest comprises a sequence that corresponds to the wild-type sequence of the reference nucleic acid.

4. The method of claim 1, wherein in step (g) there are substantially no extension products not comprising a nuclease-resistant nucleotide, wherein distinguishing those extension products comprising a nuclease-resistant nucleotide from those extension products not comprising a nuclease-resistant nucleotide comprises detecting the presence of extension products.

5. The method of claim 1, wherein extension products are only present in step (g) if a nuclease-resistant nucleotide was incorporated into an extension product in step (d).

6. The method of claim 1, wherein a nuclease-resistant nucleotide is incorporated into an extension product in step (d) only if a nucleotide variation was present in the nucleic acid of interest.

7. The method of claim 1, wherein a nuclease-resistant nucleotide is incorporated into an extension product in step (d) substantially only if a nucleotide variation was present in the nucleic acid of interest.

8. The method of claim 1, wherein the nucleotide variation was present in the nucleic acid of interest at a site corresponding to the location of a modified nucleotide in the extension products.

9. The method of claim 1, nucleotides 5′

of the nuclease-resistant nucleotide in the extension products are protected from removal by the second enzyme.

10. The method of claim 1, wherein extension products in which no nuclease-resistant nucleotide is present are digested by the second enzyme.

11. The method of claim 1, wherein the first nucleic acid comprises a primer sequence, wherein at least some of the extension products in which a nuclease-resistant nucleotide is present are extended in step (f) at least to the primer sequence in the first nucleic acid.

12. The method of claim 1, wherein the modified nucleotide is 7,8-dihydro-8-oxoguanine (8-oxoguanine), 8-oxoadenine, fapy-guanine, methyl-fapy-guanine, fapy-adenine, aflatoxin B₁-fapy-guanine, 5-hydroxy-cytosine, 5-hydroxy-uracil, ring-opened N-7 guanine adducts (7-methylguanine), ribose, uracil, or a combination.

13. The method of claim 1, wherein steps (c) and (d) are performed simultaneously.

14. The method of claim 1, wherein the one or more of the agents removes the base from the modified nucleotides.

15. The method of claim 1, wherein the one or more agents comprise an endonuclease.

16. The method of claim 1, wherein the one or more agents comprise Endonuclease IV.

17. The method of claim 1, wherein the one or more agents comprise formamidopyrimidine-DNA glycosylase (FPG).

18. The method of claim 1, wherein the first enzyme replaces the modified nucleotide with a labeled nucleotide.

19. The method of claim 1, wherein the first enzyme comprises a polymerase.

20. The method of claim 1, wherein the first enzyme is DNA polymerase.

21. The method of claim 1, wherein the first enzyme is a thermostable polymerase.

22. The method of claim 1, wherein the nuclease-resistant nucleotides comprise thio-modified deoxynucleotides.

23. The method of claim 1, wherein the nuclease-resistant nucleotides comprise borano-modified nucleotides.

24. The method of claim 1, wherein the second enzyme comprises an exonuclease.

25. The method of claim 1, wherein the second enzyme comprises Exonuclease III.

26. The method of claim 1, wherein the extension products are distinguished by real time PCR (rtPCR).

27. The method of claim 26, wherein PCR is mediated by two or more primers, wherein one or more of the primers comprises a fluorescent label.

28. The method of claim 27, wherein one or more of the primers comprises a fluorescent change primer.

29. The method of claim 1, wherein extension of the extension products in step (f) incorporates one or more labeled nucleotides into the extension products.

30. The method of claim 29, wherein one or more of the labeled nucleotides comprises biotin.

31. The method of claim 30, wherein the extension products are distinguished by detecting the labeled nucleotides.

32. The method of claim 1, wherein the extension products are distinguished via probe hybridization, primer extension, or a combination.

33. The method of claim 1, wherein the extension products are distinguished via association of the extension products with a solid support.

34. The method of claim 1, further comprising performing steps (a) through (g) one or more additional times each time using a different type of modified nucleotide comprising a different type of base.

35. The method of claim 1, wherein steps (a) through (g) are performed at least once using each of four different modified nucleotides, wherein each of the four different modified nucleotides comprises a different one of the four types of base.

36. The method of claim 1, further comprising sequencing the extension products with a nucleotide variation and comparing that sequence to a reference sequence, thereby specifically identifying the nucleotide variation in the first nucleic acid.

37. The method of claim 1, wherein the nucleotide variation is a single nucleotide variation.

38. The method of claim 1, wherein the nucleotide variation detected is a nucleotide variation in a single nucleotide.

39. The method of claim 1, wherein the extension products are labeled with a detectable label and the distinguishing step (g) comprises performing gel electrophoresis of the reaction from step (f), wherein the electrophoresis is of sufficient resolution to distinguish between a labeled extension product that is not further extended and a full length nucleic acid.

40. The method of claim 1, where modified nucleotides are caused to be present in the extension products by generating the extension products in the presence of modified nucleotides comprising a single type of base, wherein the extension products incorporate the modified nucleotides.

41. The method of claim 1, wherein modified nucleotides are caused to be present in the extension products by modifying nucleotides in the extension products to produce the modified nucleotides.

42. The method of claim 41, wherein nucleotides are modified in the extension products selectively.

43. The method of claim 41 or 42, wherein nucleotides are modified in the extension products in a limited way.

44. The method of claim 41, wherein nucleotides are modified in the extension products by chemical modification.

45. The method of claim 41, wherein nucleotides are modified in the extension products by enzymatic modification.

46. A method of detecting a nucleotide variation within a first nucleic acid comprising:

a. a step comprising generating a set of extension products from a reference nucleic acid in the presence of modified nucleotides comprising a single type of base, wherein the extension products incorporate the modified nucleotides,

b. a step comprising hybridizing the extension products to the first nucleic acid,

c. a step comprising contacting the hybridizing nucleic acid with one or more agents that collectively remove the modified nucleotides,

d. a step comprising contacting the hybridizing nucleic acid with a first enzyme that extends the extension products in the presence of three types of labeled nucleotides and not in the presence of nucleotides that comprise the same type of base as the modified nucleotides, wherein each of the three types of labeled nucleotides comprises a different type of base,

e. a step comprising distinguishing those extension products comprising a labeled nucleotide from those extension products not comprising a labeled nucleotide, thereby detecting nucleotide variation in the first nucleic acid.