N7-Ended Walker PCR: An Efficient Genome-Walking Tool

被引:2
|
作者
Tian, Bingkun [1 ,2 ,3 ]
Wu, Hongjing [4 ]
Wang, Rongrong [1 ,2 ,3 ]
Chen, Hong [1 ,2 ,3 ]
Li, Haixing [1 ,2 ,3 ]
机构
[1] Nanchang Univ, State Key Lab Food Sci & Resource, Nanchang 330047, Peoples R China
[2] Nanchang Univ, Int Inst Food Innovat Co Ltd, Nanchang 330020, Peoples R China
[3] Nanchang Univ, Sino German Joint Res Inst, Nanchang 330047, Peoples R China
[4] Nanchang Univ, Coll Sci & Technol, Nanchang 330029, Peoples R China
基金
中国国家自然科学基金;
关键词
Nested PCR; Genome-walking; Primary walker primer; Degenerate walker primer; Intrastrand annealing; ASYMMETRIC INTERLACED PCR; INSERT END FRAGMENTS; AMPLIFICATION; DNA;
D O I
10.1007/s10528-024-10896-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As a tool for acquiring uncharacterized genomic DNA adjacent to characterized DNA, genome-walking is integral to bioscience-related research works. Herein, a new genome-walking tool known as N-7-ended walker PCR (polymerase chain reaction) is presented. The key aspect for this method is the use of a degenerate walker primer in secondary/tertiary PCR. The 7 nt 5' tail of this primer completely degenerates to N-7 relative to its corresponding primary walker primer. The degeneracy reduces the efficiency of annealing this primer to its predecessor site. Clearly, primary nontarget DNA defined by the primary walker primer prefers to form a hairpin structure via the inverted ends rather than hybridizing with the degenerate primer. As a result, N-7-ended walker PCR achieves genome-walking by selectively boosting the DNA of interest. The feasibility of the N-7-ended walker PCR method was proven by acquiring uncharacterized DNAs flanking several characterized DNAs.
引用
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页数:15
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