Compositions and methods for producing single-stranded circular DNA
The present invention provides methods, kits, and compositions for producing single-stranded circular DNA by PCR. In particular, hairpin primers are provided, and methods of use thereof to produce single-stranded circular DNA molecules.
1. A method of producing single-stranded circular DNA molecules comprising the steps of:
(a) annealing a pair of hairpin primers to a target nucleic acid, wherein said hairpin primers comprise a target-hybridization region complementary to a sequence of said target nucleic acid, wherein said hairpin primers are configured to hybridize to opposing strands at different ends of said target nucleic acid in such a manner as to prime polymerization along each strand, wherein said hairpin primers comprise a hairpin-forming region capable of folding back on itself to form an intramolecular hairpin and wherein at least one primer of said pair of hairpin primers comprises a 5′ terminal phosphate in the hairpin-forming region of said primer;
(b) amplifying said target nucleic acid with said pair of hairpin primers to produce a duplex of amplicon sequences, wherein said amplicon sequences comprise target sequence flanked on both ends by hairpin primer sequences wherein said hairpin primer sequences form hairpin sequences;
(c) altering the solution conditions to promote denaturation of said duplex and formation of said intramolecular hairpins; and
(d) treating said amplicons with non-strand displacing polymerase to extend amplicon sequence and ligase to unite the 5′ and 3′ ends of the extended sequence.
2. The method of claim 1 , wherein said target nucleic acid comprises DNA.
3. The method of claim 1 , wherein said amplifying is by polymerase chain reaction.
4. The method of claim 1 , wherein altering the solution conditions comprises the steps of:
(i) applying denaturing conditions;
(ii) altering said solution conditions to favor intramolecular interactions over intermolecular interactions; and
(iii) applying reannealing condition.
5. The method of claim 4 , wherein denaturing conditions comprise heating above the T m of said duplex.
6. The method of claim 4 , wherein solution conditions that favor intramolecular interactions over intermolecular interactions comprise more dilute conditions.
7. The method of claim 4 , wherein reannealing conditions comprise controlled cooling below the T m of said intramolecular hairpins.
8. The method of claim 1 , wherein said non-strand displacing polymerase comprises a DNA polymerase.
9. The method of claim 8 , wherein said non-strand displacing polymerase lacks 5′ to 3′ exonuclease activity.
10. The method of claim 9 , wherein said non-strand displacing polymerase comprises T4 or T7 DNA polymerase.
11. The method of claim 1 , wherein said non-strand displacing polymerase extends the amplicon sequence from the 3′ end of the hairpin primer until the extended 3′ end reaches the 5′ end of the other hairpin primer, using the target-hybridization regions of the hairpin primers and the target sequence as a template.
12. The method of claim 1 , wherein said ligase comprises a DNA ligase.
13. The method of claim 12 , wherein said ligase comprises T4, T. aquaticus , or E. coli DNA ligase.
14. The method of claim 1 , wherein said ligase repairs the nick between the 3′ end and the 5′ end of said extended sequence.
15. A method of producing single-stranded circular DNA molecules comprising the steps of:
(a) annealing a pair of hairpin primers to a target nucleic acid wherein said target nucleic acid comprises DNA, wherein said hairpin primers comprise a target-hybridization region complementary to a sequence of said target nucleic acid, wherein said hairpin primers are configured to hybridize to opposing strands at different ends of said target nucleic acid in such a manner as to prime polymerization along each strand, wherein said hairpin primers comprise a hairpin-forming region capable of folding back on itself to form an intramolecular hairpin, and wherein at least one primer of said pair of hairpin primers comprises a 5′ terminal phosphate in the hairpin-forming region of said primer;
(b) amplifying said target nucleic acid with said pair of hairpin primers to produce a duplex of amplicon sequences, wherein said amplicon sequences comprise target sequence flanked on both ends by hairpin primer sequences wherein said hairpin primer sequences form hairpin sequences, and wherein said amplifying is by polymerase chain reaction;
(c) altering the solution conditions to promote denaturation of said duplex and formation of said intramolecular hairpins wherein said altering the solution conditions comprises the steps of:
(i) applying denaturing conditions wherein said denaturing conditions comprise heating above the T m of said duplex;
(ii) altering said solution conditions to favor intramolecular interactions over intermolecular interactions wherein said solution conditions that favor intramolecular interactions over intermolecular interactions comprise more dilute conditions; and
(iii) applying reannealing conditions wherein said reannealing conditions comprise controlled cooling below the T m of said intramolecular hairpins;
(d) treating said amplicons with non-strand displacing polymerase to extend amplicon sequence and ligase to unite the 5′ and 3′ ends of the extended sequence wherein said non-strand displacing polymerase comprises a DNA polymerase, wherein said non-strand displacing polymerase lacks 5′ to 3′ exonuclease activity, wherein said non-strand displacing polymerase comprises T4 or T7 DNA polymerase, and wherein said non-strand displacing polymerase extends the amplicon sequence from the 3′ end of the hairpin primer until the extended 3′ end reaches the 5′ end of the other hairpin primer using the target-hybridization regions of the hairpin primers and the target sequence as a template, wherein said ligase comprises a DNA ligase selected from the group consisting of T4, T. aquaticus , or E. coli DNA ligase, and wherein said ligase repairs the nick between the 3′ end and the 5′ end of said extended sequence; and
(e) testing for successful creation of said single-stranded circular DNA molecules.
16. The method of claim 15 , wherein said testing comprises exonuclease treatment, gel electrophoresis, and mass spectrometry.
17. The method of claim 16 wherein said exonuclease treatment comprises exo III and/or exo VII treatment.