PRIMER SET, METHOD FOR AMPLIFYING TARGET NUCLEIC ACID SEQUENCE USING SAME, AND METHOD FOR DETECTING MUTATED NUCLEIC ACID USING SAME

• US 20140295447A1
• Filed: 09/07/2012
• Published: 10/02/2014
• Est. Priority Date: 09/08/2011
• Status: Active Grant

• Current Assignee: Kabushiki Kaisha Dnaform
• Original Assignee: Kabushiki Kaisha Dnaform, Riken
• Inventors: Kawai, Yuki, Hayashizaki, Yoshihide, Kimura, Yasumasa, Usui, Kengo, Tanaka, Yuki
• Granted Patent: US 9,586,987 B2
• Time in Patent Office: Days
• US Class Current: 435/6.12
• CPC Class Codes: C07H 21/04 with deoxyribosyl as saccharide radical
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 2525/155 incorporating/generating a new priming site
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2527/101 Temperature
• CPC Class Codes: C12Q 2531/119 Strand displacement amplification [SDA]
• CPC Class Codes: C12Q 2531/125 Rolling circle

Abstract

The present invention provides a primer set including primers that can be designed easily, with which an amplification distance can be shortened. Provided is a primer set for use in a method for isothermally amplifying a target nucleic acid sequence 4. The primer set includes a first primer 1F and a second primer 1R. The first primer 1F includes, on the 3′ side thereof, a sequence (A′) that can hybridize to a sequence (A) on the 3′ side of the target nucleic acid sequence. The second primer 1R includes, on the 3′ side thereof, a sequence (B′) that can hybridize to a sequence (B) on the 3′ side of either a strand extended from the first primer or a complementary strand of the target nucleic acid sequence 4. The first primer 1F and the second primer 1R include, on the 5′ sides thereof, sequences (C) that are substantially identical to each other.

Claims

1. A primer set for use in a method for isothermally amplifying a target nucleic acid sequence, the primer set comprising:

a first primer; and

a second primer,

wherein the first primer comprises, on the 3′

side thereof, a sequence (A′

) that can hybridize to a sequence (A) on the 3′

side of the target nucleic acid sequence,

the second primer comprises, on the 3′

side thereof, a sequence (B′

) that can hybridize to a sequence (B) on the 3′

side of either a strand extended from the first primer or a strand complementary to the target nucleic acid sequence, and

the first primer and the second primer comprise, on the 5′

sides thereof, sequences (C) that are substantially identical to each other.

2. The primer set according to claim 1, wherein

at least one of the first primer and the second primer further comprises, on the 5′

side of the sequence (C), a folding sequence (D-D′

) comprising, on the same strand, two sequences that hybridize to each other.

3. The primer set according to claim 1, wherein

the first primer further comprises, on the 5′

side of the sequence (C), a folding sequence (D-D′

) comprising, on the same strand, two sequences that hybridize to each other,

the second primer further comprises, on the 5′

side of the sequence (C), a folding sequence (E-E′

) comprising, on the same strand, two sequences that hybridize to each other, and

the sequence (D-D′

) and the sequence (E-E′

) are different from each other.

4. The primer set according to claim 1, further comprising a third primer,

wherein the third primer hybridizes to the target nucleic acid sequence, a sequence complementary to the target nucleic acid sequence, or a strand extended from the first primer or the second primer, and

the hybridization of the third primer does not compete with the first primer and the second primer.

5. A method for isothermally amplifying a target nucleic acid sequence using a primer set, wherein

the primer set is the primer set according to claim 1.

6. A method for detecting a mutation in a nucleic acid sequence in a nucleic acid sample by an isothermal amplification method using a primer set, wherein

the primer set is the primer set according to claim 1,

the primer set is designed so that the primer set targets a nucleic acid sequence having or not having the mutation and that a nucleotide residue corresponding to the mutation is included in the sequence (A) complementary to the sequence (A′

) in the first primer or in the sequence (B) complementary to the sequence (B′

) in the second primer, and

an isothermal amplification reaction using the primer set is carried out in the presence of the nucleic acid sample.

9. The nucleic acid synthesis method according to claim 7, wherein

the single-stranded template nucleic acid provided in the step (A1) is a single-stranded template nucleic acid formed by an isothermal amplification reaction using the primer set according to claim 2 wherein only the first primer comprises the folding sequence (D-D′

), and

the primer hybridized to the loop in the step (A2) is the first primer comprising the folding sequence (D-D′

).

7. A nucleic acid synthesis method for isothermally synthesizing a double-stranded nucleic acid composed of a single-stranded nucleic acid in which the order of at least two different sequences is repeated to a total of two or more times and a nucleic acid complementary to the single-stranded nucleic acid, the nucleic acid synthesis method comprising the following steps (A1) to (A6):

(A1) providing a single-stranded template nucleic acid having a stem-loop structure in which a 3′

side stem sequence comprising the 3′

end and a 5′

side stem sequence comprising the 5′

end are linked to each other via a loop sequence, with a folding sequence comprising, on the same strand, two sequences that hybridize to each other being linked to the 3′

end of the 3′

side stem sequence;

(A2) hybridizing a primer to the loop of the single-stranded template nucleic acid and extending the primer toward the 5′

end of the 5′

side stem sequence;

(A3) successively continuing the extension of the primer that has reached the 5′

end of the 5′

side stem sequence from the 5′

end of the 5′

side stem sequence to the 3′

end of the folding sequence;

(A4) successively continuing the extension of the primer that has reached the 3′

end of the folding sequence in the step (A3) toward the 5′

end of the 5′

side stem sequence again, and, by the continuing primer extension, rendering the primer-extended strand hybridizing to the single-stranded template nucleic acid formed in the step (A2) single-stranded through a strand displacement reaction;

(A5) terminating the extension of the primer in the step (A4) at the 5′

end of the 5′

side stem sequence; and

(A6) extending the 3′

end of the folding sequence in the single-stranded template nucleic acid using the primer-extended strand that has been rendered single-stranded in the step (A4) as a template.

8. The nucleic acid synthesis method according to claim 7, wherein the step (A3) and the step (A4) are repeated to a total of two or more times.

10. The nucleic acid synthesis method according to claim 7, wherein

the single-stranded template nucleic acid provided in the step (A1) further comprises a folding sequence comprising, on the same strand, two sequences that hybridize to each other and being linked to the 5′

end of the 5′

side stem-loop sequence, and

the nucleic acid synthesis method comprises, instead of the step (A3), the following step (A3-2);

(A3-2) successively continuing the extension of the primer that has reached the 5′

end of the 5′

side stem sequence from the 5′

end of the 5′

side stem sequence directly to the 3′

end of the folding sequence, without mediation of the folding sequence linked to the 5′

end of the 5′

side stem sequence.

11. The nucleic acid synthesis method according to claim 10, wherein

the step (A3-2) and the step (A4) are repeated to a total of two or more times.

12. The nucleic acid synthesis method according to claim 10, wherein

the single-stranded template nucleic acid provided in the step (A1) is a single-stranded template nucleic acid formed by an isothermal amplification method using the primer set according to claim 3, and

the primer hybridized to the loop in the step (A2) is the first primer or the second primer of the primer set according to claim 3.

13. A nucleic acid amplification method comprising the step of:

isothermally synthesizing a double-stranded nucleic acid composed of a single-stranded nucleic acid in which the order of at least two different sequences is repeated to a total of two or more times and a nucleic acid complementary to the single-stranded nucleic acid,

wherein the step of synthesizing the nucleic acid is carried out by the nucleic acid synthesis method according to claim 7.

14. A nucleic acid synthesis method for isothermally synthesizing a double-stranded nucleic acid composed of a single-stranded nucleic acid in which the order of at least two different sequences is repeated to a total of two or more times and a nucleic acid complementary to the single-stranded nucleic acid, the nucleic acid synthesis method comprising at least one of:

a first reaction step; and

a second reaction step,

the first reaction step comprising the following steps (B1) to (B3);

(B1) providing two double strands in a state where their sequences are in opposite orientations, the double strands each being composed of a single-stranded nucleic acid that comprises, in a region comprising the 3′

end, a folding sequence comprising, on the same strand, two sequences that hybridize to each other and a single-stranded nucleic acid complementary to the single-stranded nucleic acid;

(B2) extending, through a strand displacement reaction, the 3′

end of the folding sequence in the single-stranded nucleic acid in one of the two double strands provided in the step (B1) using the complementary single-stranded nucleic acid in the other double strand as a template, thereby forming a partial double strand in which part of the extended strand of the single-stranded nucleic acid in said one of the double strands hybridizes to the complementary single-stranded nucleic acid in the other double strand; and

(B3) extending, in the partial double strand in the step (B2), the 3′

end of the complementary single-stranded nucleic acid using the single-stranded nucleic acid as a template, thereby forming a complete double strand,

the second reaction step comprising the following steps (C1) to (C3);

(C1) providing one double strand composed of a single-stranded nucleic acid that comprises, in a region comprising the 3′

end, a folding sequence comprising, on the same strand, two sequences that hybridize to each other and a single-stranded nucleic acid complementary to the single-stranded nucleic acid;

(C2) extending, through a strand displacement reaction, the 3′

end of the folding sequence in the single-stranded nucleic acid in the double strand provided in the step (C1) using the complementary single-stranded nucleic acid as a template from the 3′

end to the 5′

end of the complementary single-stranded nucleic acid, thereby forming a partial double strand in which part of the extended strand of the single-stranded nucleic acid hybridizes to the complementary single-stranded nucleic acid; and

(C3) extending, in the partial double strand in the step (C2), the 3′

end of the complementary single-stranded nucleic acid using the single-stranded nucleic acid as a template, thereby forming a complete double strand.

15. The nucleic acid synthesis method according to claim 14, wherein

each double strand in the steps (B1) and (C1) is a double strand formed by an isothermal amplification reaction using the primer set according to claim 3.

16. A nucleic acid amplification method comprising the step of:

isothermally synthesizing a double-stranded nucleic acid composed of a single-stranded nucleic acid in which the order of at least two different sequences is repeated to a total of two or more times and a nucleic acid complementary to the single-stranded nucleic acid,

wherein the step of synthesizing the nucleic acid is carried out by the nucleic acid synthesis method according to claim 14.

17. The nucleic acid synthesis method according to claim 15, wherein

each double strand in the steps (B1) and (C1) is a double strand formed by an isothermal amplification reaction using the primer set according to claim 2.