Dna Crosslinking for Primer Extension Assays

• US 20090011514A1
• Filed: 02/22/2006
• Published: 01/08/2009
• Est. Priority Date: 02/22/2005
• Status: Abandoned Application

• Current Assignee: Arizona Board of Regents (University of Arizona)
• Original Assignee: Arizona Board of Regents (University of Arizona)
• Inventors: Aksyonov, Sergei, Williams, Peter
• Application Number:
  US11/884,908
• Publication Number:
  US 20090011514A1
• Time in Patent Office: Days
• US Class Current: 436/94
• CPC Class Codes: C12Q 1/6823 Release of bound markers
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2523/101 Crosslinking agents, e.g. psoralen
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2527/125 Specific component of sample, medium or buffer
• CPC Class Codes: C12Q 2533/101 Primer extension
• CPC Class Codes: Y10T 436/143333 Saccharide [e.g., DNA, etc.]

Abstract

Provided herein are compositions and methods for inhibiting false signals associated with mispriming in primer extension assays.

Claims

1. A method of identifying nucleotides in a nucleic acid template comprising contacting a primer with a nucleic acid template, crosslinking the primer to the template, and extending the primer under conditions that denature undesirable secondary structures and detecting extension of the primer, thereby identifying one or more nucleotides in the template.

2. The method of claim 1, wherein the primer is extended by a single nucleotide type at a time, wherein extension of the primer is detected after each extension by a single nucleotide type, and wherein extension and detection of extension are repeated one or more times, thereby identifying a plurality of nucleotides in the template.

3. The method of claim 1, wherein the primer comprises a crosslinking agent.

4. The method of claim 3, wherein the crosslinking agent is photoactivated.

5. The method of claim 4, wherein the crosslinking agent is psoralen.

6. The method of claim 4, wherein the primer-template duplex is exposed to a quantity of UV light sufficient to activate the crosslinking agent.

7. The method of claim 1, wherein primer extension conditions comprise conditions more stringent than condition under which the template contacts the primer.

8. The method of claim 7, wherein stringency is increased by raising the temperature.

9. The method of claim 7, wherein stringency is increased by lowering the salt concentration.

10. The method of claim 7, wherein stringency is increased by adding a denaturing agent.

11. The method of claim 10, wherein the denaturing agent is urea or formamide.

12. The method of claim 1, wherein the primer is immobilized on a solid substrate.

13. The method of claim 1, wherein the template is immobilized on a solid substrate.

14. The method of claim 12, wherein the solid substrate is glass or silica.

15. The method of claim 1, wherein extending the primer comprises contacting the primer-template duplex with a polymerase and a single type of nucleotide under conditions that allow extension of the primer.

16. The method of claim 15, wherein the nucleotide comprises a fluorescent moiety, and wherein primer extension is detected by detecting a fluorescent signal emitted by the fluorescent moiety.

17. The method of claim 1, wherein primer extension is detected by measuring the heat generated by nucleotide incorporation.

18. The method of claim 1, wherein primer extension is detected by measuring the concentration of pyrophosphate release by addition of a nucleotide to the primer,

19. The method of claim 18, wherein the concentration of pyrophosphate is detected by hydrolyzing the pyrophosphate and measuring heat generated by hydrolysis of the pyrophosphate.

20. The method of claim 18, wherein the pyrophosphate is converted into ATP by ATP sulfurylase in the presence of adenosine 5′

phosphosulfate, wherein ATP drives the luciferase-mediated conversion of luciferin to oxyluciferin that generates visible light in amounts that are proportional to the amount of ATP, wherein the concentration of pyrophosphate is detected by measuring visible light.

21. The method of claim 1, wherein primer extension is detected by measuring the refractive index of the buffer.

22. The method of claim 1, wherein the polymerase has reduced exonuclease activity.

23. The method of claim 13, wherein the solid substrate is glass or silica.