Yu Zhou, Wang Dongying, Lin Zhiyu, Li Haixing
Sino-German Joint Research Institute, Nanchang University, Nanchang, China.
Physical Education Department, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Bio Protoc. 2025 Feb 20;15(4):e5188. doi: 10.21769/BioProtoc.5188.
Genome walking, a molecular technique for mining unknown flanking DNAs, has a wide range of uses in life sciences and related areas. Herein, a simple but reliable genome walking protocol named primer extension refractory PCR (PER-PCR) is detailed. This PER-PCR-based protocol uses a set of three walking primers (WPs): primary WP (PWP), secondary WP (SWP), and tertiary WP (TWP). The 15 nt middle region of PWP overlaps the 3' region of SWP/TWP. The 5' regions of the three WPs are completely different from each other. In the low annealing temperature cycle of secondary or tertiary PER-PCR, the short overlap mediates the annealing of the WP to the previous WP site, thus producing a series of single-stranded DNAs (ssDNA). However, the 5' mismatch between the two WPs prevents the template DNA from synthesizing the WP complement at its 3' end. In the next high annealing temperature cycles, the target ssDNA is exponentially amplified because it is defined by both the WP and sequence-specific primer, while non-target ssDNA cannot be amplified as it lacks a binding site for at least one of the primers. Finally, the target DNA becomes the main PER-PCR product. This protocol has been validated by walking two selected genes. Key features • The current protocol builds upon the technique developed by Li et al. [1], which is universal to any species. • The developed protocol relies on the partial overlap among a set of three WPs. • Two rounds of nested PER-PCRs can generally result in a positive walking result. Graphical overview.
基因组步移是一种用于挖掘未知侧翼DNA的分子技术,在生命科学及相关领域有广泛应用。本文详细介绍了一种名为引物延伸难熔PCR(PER-PCR)的简单而可靠的基因组步移方案。基于PER-PCR的该方案使用一组三种步移引物(WPs):初级WP(PWP)、次级WP(SWP)和三级WP(TWP)。PWP的15个核苷酸中间区域与SWP/TWP的3'区域重叠。三种WPs的5'区域彼此完全不同。在次级或三级PER-PCR的低退火温度循环中,短重叠介导WP与前一个WP位点退火,从而产生一系列单链DNA(ssDNA)。然而,两个WPs之间的5'错配阻止模板DNA在其3'端合成WP互补序列。在下一个高退火温度循环中,目标ssDNA呈指数扩增,因为它由WP和序列特异性引物共同界定,而非目标ssDNA由于缺乏至少一种引物的结合位点而无法扩增。最终,目标DNA成为主要的PER-PCR产物。该方案已通过对两个选定基因的步移进行验证。关键特性 • 本方案基于Li等人[1]开发的技术,该技术对任何物种都通用。 • 所开发的方案依赖于一组三种WPs之间的部分重叠。 • 两轮巢式PER-PCR通常可产生阳性步移结果。图形概述。