Snap-back primers and detectable hairpin structures
View Patent ↗The present invention provides methods, compositions, and kits comprising snap-back primers used for forming 3′ hairpin structures, 5′ hairpin structures, and double hairpin structures. The hairpin structures may be used for detecting target sequences (e.g., such as small RNA target sequence), for detecting polymorphisms in target sequences (e.g., such as polymorphisms located near the 5′ or 3′ ends of the target sequence), or other nucleic acid characterization methods. In certain embodiments, the hairpin structures form invasive cleavage structures (e.g., in combination with a probe or upstream oligonucleotide) which may be cleaved by structure-specific enzymes in order to detect the presence or absence of a particular nucleotide or nucleotide sequence.
1. A composition, selected from the group consisting of:
I) a first composition, configured for generating a 3′ hairpin structure from a target nucleic acid, said first composition comprising a snap-back primer and a reverse primer,
wherein said snap-back primer comprises:
i) a 3′ region configured to hybridize to said target nucleic acid such that it can be extended by a polymerase to generate a first amplification product, and
ii) a 5′ region configured to not hybridize to said target nucleic when said 3′ region of said snap-back primer is hybridized to said target nucleic acid;
wherein said reverse primer comprises a 3′ region configured to hybridize to said first amplification product such that said reverse primer can be extended by a polymerase to generate a second amplification product comprising a 3′ snap-back portion capable of hybridizing to a non-adjacent portion of said second amplification product to form a 3′ hairpin structure, wherein said 3′ hairpin structure comprises a 3′ terminal portion configured to not hybridize to said second amplification product; and
II) a second composition, configured for generating a 5′ hairpin structure from a target nucleic acid, said second composition comprising a snap-back primer, wherein said snap-back primer comprises:
i) a 3′ region configured to hybridize to said target nucleic acid such that it can be extended by a polymerase to generate an amplification product, and
ii) a 5′ region configured to not hybridize to said target nucleic when said 3′ region of said snap-back primer is hybridized to said target nucleic acid;
wherein said amplification product comprises a 5′ snap-back portion capable of hybridizing to a non-adjacent portion of said amplification product to form a 5′ hairpin structure, wherein said 5′ hairpin structure comprises a 5′ terminal portion not hybridized to said amplification product.
2. The composition of claim 1 , wherein in said first composition, said 3′ hairpin structure comprises a first nucleotide located immediately 5′ of said non-adjacent portion, wherein said first nucleotide corresponds to a second nucleotide at a polymorphic position in said target nucleic acid.
3. The composition of claim 1 , wherein said first composition further comprises a downstream probe comprising a 3′ region configured to hybridize to said 3′ hairpin structure and a 5′ region configured to not hybridize to said 3′ hairpin structure.
4. The composition of claim 3 , wherein said downstream probe is configured to hybridize to said 3′ hairpin structure immediately 5′ of said non-adjacent portion, thereby forming an invasive cleavage structure.
5. The composition of claim 1 , wherein in said first composition, said 3′ region of said snap-back primer comprises a sequence capable of hybridizing to said non-adjacent portion of said second amplification product.
6. The composition of claim 1 , wherein in said first composition, said 3′ region of said snap-back primer is not capable of hybridizing to said non-adjacent portion of said second amplification product.
7. The composition of claim 1 , wherein in said first composition, said 3′ terminal portion of said 3′ hairpin structure is less than 10 nucleotides in length.
8. The composition of claim 1 , wherein in said first composition, said 3′ snap-back portion is partially complementary to said non-adjacent portion.
9. The composition of claim 1 , wherein in said second composition, the 3′ terminal nucleotide of said non-adjacent portion of said amplification product corresponds to, and is complementary to, a target nucleotide at a polymorphic position in said target nucleic acid.
10. The composition of claim 1 , wherein said second composition further comprises an upstream probe comprising a 5′ region configured to hybridize to said amplification product and a 3′ region configured to not hybridize to said amplification product.
11. The composition of claim 10 , wherein said upstream probe hybridizes to said amplification product immediately 3′ of said non-adjacent portion thereby forming an invasive cleavage structure.
12. The composition of claim 1 , wherein in said second composition, said 3′ region of said snap-back primer comprises a sequence capable of hybridizing to the complement of said non-adjacent portion of said amplification product.
13. The composition of claim 1 , wherein in said second composition, said 3′ region of said snap-back primer is not capable of hybridizing to the complement of said non-adjacent portion of said amplification product.
14. The composition of claim 1 , wherein in said second composition, said 5′ terminal portion of said 5′ hairpin structure is between 10 and 30 bases in length.
15. The composition of claim 1 , further comprising a polymerase.
16. The composition of claim 1 , further comprising a deoxynucleoside triphosphate.
17. The composition of claim 1 , further comprising a FEN-1 flap endonuclease.
18. A kit for forming an invasive cleavage structure from a target nucleic acid, selected from the group consisting of:
I) a first kit, comprising a snap-back primer and a reverse primer configured to amplify a target sequence, and a downstream probe,
wherein said snap-back primer comprises:
i) a 3′ region configured to hybridize to said target nucleic acid such that it can be extended by a polymerase to generate a first amplification product, and
ii) a 5′ region configured to not hybridize to said target nucleic when said 3′ region of said snap-back primer is hybridized to said target nucleic acid;
wherein said reverse primer comprises a 3′ region configured to hybridize to said first amplification product such that it can be extended by a polymerase to generate a second amplification product having a 3′ hairpin structure; and
wherein said downstream probe is configured to form an invasive cleavage structure with said 3′ hairpin structure of said second amplification product, wherein said downstream probe comprises a 3′ region configured to hybridize to second amplification product, and a 5′ region configured to not hybridize to second amplification product;
and
II) a second kit, comprising a snap-back primer and an upstream probe, wherein said snap-back primer comprises:
i) a 5′ region configured to not hybridize to said target nucleic when said 3′ region of said snap-back primer is hybridized to said target nucleic acid, and
ii) a 3′ region configured to hybridize to said target nucleic acid such that it can be extended by a polymerase to generate an amplification product comprising a 5′ hairpin structure;
wherein said upstream probe is configured to form an invasive cleavage structure with said 5′ hairpin structure of said amplification product, wherein said upstream probe comprises a 5′ region configured to hybridize to said amplification product and a 3′ region configured to not hybridize to said amplification product.
19. The kit of claim 18 , further comprising a polymerase.
20. The kit of claim 18 , further comprising a deoxynucleoside triphosphate.
21. The kit of claim 18 , further comprising a FEN-1 flap endonuclease.