Hairpin-mediated amplification method

Patent metadata

Field	Value
Publication number	US-10697006-B2
Application number	US-201715692215-A
Country	US
Kind code	B2
Filing date	Aug 31, 2017
Priority date	Sep 15, 2016
Publication date	Jun 30, 2020
Grant date	Jun 30, 2020

Abstract

In some embodiments, the amplification method may comprise producing a reaction mix comprising: a nucleic acid sample, a polymerase, nucleotides, a forward primer that hybridizes to a sequence in the bottom strand of a fragment in the sample, and a reverse primer. The reverse primer has a hairpin structure comprising a loop, a stem and a 3′ overhang of at least 8 nucleotides, wherein the 3′ overhang hybridizes to a sequence in the top strand of the fragment. Subjecting the reaction mix at least two rounds of denaturation, renaturation and primer extension conditions results in extension the forward and reverse primers to produce an amplification product that contains: a double stranded region comprising a nick adjacent to the 5′ end of the reverse primer, and the loop of the first hairpin primer. Primer sets and kits for performing the methods are also provided.

First claim

The invention claimed is:

1. A method for amplifying a nucleic acid, comprising:
(a) producing a reaction mix comprising:
i. a nucleic acid sample;
ii. a polymerase;
iii. nucleotides;
iv. a forward primer that hybridizes to a sequence in the bottom strand of a fragment in the sample; and
v. a reverse primer, wherein the reverse primer has a hairpin structure comprising a loop, a stem and a 3′ overhang of at least 8 nucleotides, wherein the 3′ overhang hybridizes to a sequence in the top strand of the fragment; and
(b) subjecting the reaction mix to at least two rounds of denaturation, renaturation and primer extension conditions to extend the forward and reverse primers to produce an amplification product that contains:
i. a double stranded region comprising a nick adjacent to the 5′ end of the reverse primer, and
ii. the loop of the reverse primer.

2. The method of claim 1 , further comprising sealing the nick with a ligase.

3. The method of claim 1 , wherein step (b) results in a concatemerized amplification product.

4. The method of claim 1 , wherein the forward primer is a linear primer.

5. The method of claim 1 , wherein the forward primer has a hairpin structure comprising a loop, a stem and a 3′ overhang of at least 8 nucleotides, wherein the 3′ overhang hybridizes to a sequence in the bottom strand of the fragment, and wherein the amplification product further comprises the loop of the forward primer at the opposite end to loop of the reverse primer.

6. The method of claim 5 , wherein the 5′ end of the forward primer is not a 5′ phosphate.

7. The method of claim 5 , wherein the 5′ end of the reverse primer is a 5′ phosphate.

8. The method of claim 1 , wherein the forward primer is attached to a surface.

9. The method of claim 8 , wherein step (b) results in an amplification product that is anchored to the surface.

10. The method of claim 1 , wherein the top strand of the fragment and the bottom strand of the fragment in the sample are asymmetrically tagged with a 5′ adaptor sequence and a 3′ adaptor sequence.

11. The method of claim 1 , wherein step (b) is done by thermocycling.

12. The method of claim 1 , wherein the polymerase is a non-strand displacing polymerase.

13. The method of claim 1 , wherein the polymerase is Pfu or a mutant thereof.

Assignees

• Agilent Technologies Inc

Inventors

• Peter Brian Jon
• Ach Robert A

Classifications

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q1/6853 Primary

  using modified primers or templates · CPC title

• C12Q2525/151

  repeat or repeated sequences, e.g. VNTR, microsatellite, concatemer · CPC title

• C12Q2521/501

  Ligase · CPC title

• C12Q2525/301

  Hairpin oligonucleotides · CPC title