Method for constructing nucleic acid molecule
The present invention provides a method for constructing a single-stranded nucleic acid molecule for nucleic acid sequencing by means of a nanopore sequencer, said method including: a step in which at least one hairpin primer including a single-stranded region on the 3′ side and a pair of primers are used to synthesize a complementary strand of template DNA that includes the target sequence; and a step in which the synthesized complementary strand forms a hairpin structure inside a molecule and a template extension reaction is carried out. The obtained nucleic acid molecule includes both the target sequence and the complementary strand thereof in the sequence. Single strand construction enables analysis by nanopore sequencing, and the sequence of only the target nucleic acid, which does not include information of the complementary strand, is repeatedly analyzed, thus enabling analysis to be conducted with greater precision by addressing the problem of sequence errors.
1. A method for constructing a single-stranded nucleic acid molecule, the method comprising: synthesizing a complementary strand of a template DNA including a target sequence by using at least one hairpin primer including a single-stranded region at the 3′ terminal end and a primer in a pair, wherein the hairpin primer comprise a stem region that has a Tm value at least 5° C. higher than the Tm value of the single strand region to form a hairpin structure from the synthesized complementary strand; and performing a template extension reaction on the hairpin structure to obtain the single stranded nucleic acid molecule wherein the obtained nucleic acid molecule includes both the target sequence and the complementary strand thereof in the sequence.
2. The method according to claim 1 , wherein the synthesized complementary strand sequence performs a template extension reaction in accordance with a reduction in the hairpin primer due to the advance of the reaction.
3. The method according to claim 1 , further comprising of phosphorylating the 5′ terminal end of the hairpin primer before use and decomposing the phosphorylated DNA strand after constructing a target nucleic acid molecule.
4. The method according to claim 3 , wherein the decomposition is performed by using λ exonuclease.
5. The method according to claim 3 , wherein, the extension reaction of self-annealing from the 3′ terminal end of the complementary strand thereof through the hairpin structure is performed after the phosphorylated DNA strand is decomposed.
6. The method according to claim 1 , further comprising an adapter having a hairpin loop structure to the obtained nucleic acid molecule and performing a strand displacement reaction to extend the obtained nucleic acid molecule.
7. The method according to claim 5 , wherein an adapter having a hairpin loop structure is ligated to the obtained nucleic acid molecule and performing a strand displacement reaction to extend the obtained nucleic acid molecule.
8. The method according to claim 1 , wherein the 5′ terminal end formed from the primer in the pair is immobilized and the template extension reaction is performed after the complementary strand DNA is dissociated.
9. The method according to claim 6 , wherein a loop structure part of the adapter includes an extension reaction inhibitor molecule.
10. The method according to claim 1 , wherein the primer in the pair has a chimeric structure of DNA and RNA, and the method further includes a step in which the RNA is decomposed after the extension reaction.
11. The method according to claim 1 further comprising sequencing the obtained nucleic acid molecule using a nanopore sequencer.
12. The method according to claim 11 , wherein the sequencing step comprises obtaining a signal from a known base sequence in the nucleic acid molecule and correcting a detector based on the signal from the known base sequence.
13. The method according to claim 11 , wherein the sequencing step, analysis is performed on the basis of a signal obtained from a known base sequence included in the nucleic acid molecule.
14. The method according to claim 11 , wherein the speed of a reaction product passing through the nanopore is controlled by using a reaction product having a double strand formed therein.
15. The method according to claim 1 , wherein the hairpin primer has a random sequence.
16. The method according to claim 15 , wherein the hairpin primer comprises random sequences equal to or more than the number of mutations in the target sequence.