METHOD FOR AMPLIFYING A TARGET SEQUENCE INCLUDED IN A DOUBLE-STRANDED DNA
the present invention provides an amplification method capable of inhibiting the generating of the undesired amplified double-stranded DNA sequence. In the present method, DNA polymerase, deoxynucleoside triphosphate, the double-stranded DNA, a forward primer, a reverse primer, and a first block nucleic acid are mixed so as to amplify the double-stranded target sequence with use of a polymerase chain reaction. The first block nucleic acid does not serve as an origin for the elongation reaction with the DNA polymerase. The first block nucleic acid is complementary with a part of the third non-amplified sequence which is interposed between the 5′ end and the complimentary single-stranded target sequence. Due to the first block nucleic acid, the generating of the undesired amplified double-stranded DNA sequence is inhibited.
1 . A method for amplifying a double-stranded target sequence included in a double-stranded DNA, the method comprising steps of:
a step (a) of mixing DNA polymerase, deoxynucleoside triphosphate, the double-stranded DNA, a forward primer, a reverse primer, and a first block nucleic acid 20 , and amplifying the double-stranded target sequence using a PCR method, wherein,
the double-stranded DNA consists of a first single-stranded DNA 6 and a second single-stranded DNA 7 ,
the double-stranded target sequence consist of a single-stranded target sequence 1 a and a complementary single-stranded target sequence 1 b,
the first single-stranded DNA 6 consists of 3′ end—a first sequence 6 a —the single-stranded target sequence 1 a —a second sequence 6 b— 5′ end, the second single-stranded DNA 7 consists of 5′-end—a third sequence 7 a —the complementary single-stranded target sequence 1 b —a fourth sequence 7 b— 3′-end,
the complementary single-stranded target sequence 1 b , the third sequence 7 a , and the fourth sequence 7 b are complementary to the single-stranded target sequence 1 a , the first sequence 6 a , and the second sequence 6 b , respectively,
both of the forward primer 4 and the reverse primer 5 serve as an origin for elongation reaction with the DNA polymerase,
the forward primer 4 is complementary to a sequence 6 c located at the 3′-end side of the single-stranded target sequence 1 a,
the reverse primer 5 is complementary to a sequence 7 c located at the 3′-end side of the complementary single-stranded target sequence 1 b,
the first block nucleic acid 20 does not serve as an origin for elongation reaction with the DNA polymerase,
the first block nucleic acid 20 is complementary to a part of the third sequence 7 a.
2 . The method according to claim 1 , wherein
the first block nucleic acid consists of a DNA where an OH group at a position 3 of a sugar molecule included in a nucleotide located at the 3′-end thereof is substituted or modified with a hydrogen atom, a phosphate group, an amino group, a biotin group, a thiol group, or the derivative thereof.
3 . The method according to claim 1 , wherein
the first block nucleic acid consists of a Locked Nucleic Acid where an OH group at a position 3 of a sugar molecule included in a nucleotide located at the 3′-end thereof is substituted or modified with a hydrogen atom, a phosphate group, an amino group, a biotin group, a thiol group, or the derivative thereof.
4 . The method according to claim 1 , wherein
The first block nucleic acid consists of a peptide nucleic acid.
5 . The method according to claim 1 , wherein
in the step (a), a second block nucleic acid is added,
the second block nucleic acid does not serves as an origin for elongation reaction with the DNA polymerase, and
the second block nucleic acid is complementary with a part of the second sequence.
6 . The method according to claim 5 , wherein
The second block nucleic acid consists of a DNA where an OH group at a position 3 of a sugar molecule included in a nucleotide located at the 3′-end thereof is substituted or modified with a hydrogen atom, a phosphate group, an amino group, a biotin group, a thiol group, or the derivative thereof.
7 . The method according to claim 5 , wherein
The second block nucleic acid consists of a Locked Nucleic Acid where an OH group at a position 3 of a sugar molecule included in a nucleotide located at the 3′-end thereof is substituted or modified with a hydrogen atom, a phosphate group, an amino group, a biotin group, a thiol group, or the derivative thereof.
8 . The method according to claim 5 , wherein
The second block nucleic acid consists of a peptide nucleic acid.