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半位点特异性引物PCR:一种简单但可靠的基因组步移工具。

Semi-Site-Specific Primer PCR: A Simple but Reliable Genome-Walking Tool.

作者信息

Wei Cheng, Lin Zhiyu, Pei Jinfeng, Pan Hao, Li Haixing

机构信息

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China.

Sino-German Joint Research Institute, Nanchang University, Nanchang 330047, China.

出版信息

Curr Issues Mol Biol. 2023 Jan 5;45(1):512-523. doi: 10.3390/cimb45010034.

Abstract

Genome-walking has been frequently applied to molecular biology and related areas. Herein, a simple but reliable genome-walking technique, termed semi-site-specific primer PCR (3SP-PCR), is presented. The key to 3SP-PCR is the use of a semi-site-specific primer in secondary PCR that partially overlaps its corresponding primary site-specific primer. A 3SP-PCR set comprises two rounds of nested amplification reactions. In each round of reaction, any primer is allowed to partially anneal to the DNA template once only in the single relaxed-stringency cycle, creating a pool of single-stranded DNAs. The target single-stranded DNA can be converted into a double-stranded molecule directed by the site-specific primer, and thus can be exponentially amplified by the subsequent high-stringency cycles. The non-target one cannot be converted into a double-strand due to the lack of a perfect binding site to any primer, and thus fails to be amplified. We validated the 3SP-PCR method by using it to probe the unknown DNA regions of rice hygromycin genes and CD0817 glutamic acid decarboxylase genes.

摘要

基因组步移技术已被广泛应用于分子生物学及相关领域。在此,我们介绍一种简单可靠的基因组步移技术,称为半位点特异性引物PCR(3SP-PCR)。3SP-PCR的关键在于在二次PCR中使用半位点特异性引物,该引物与相应的一次位点特异性引物部分重叠。一个3SP-PCR试剂盒包括两轮巢式扩增反应。在每一轮反应中,任何引物只允许在单个宽松严格度循环中与DNA模板部分退火一次,从而产生一单链DNA文库。目标单链DNA可以在位点特异性引物的引导下转化为双链分子,因此可以在随后的高严格度循环中进行指数扩增。非目标单链DNA由于缺乏与任何引物的完美结合位点,无法转化为双链,因此无法被扩增。我们通过用3SP-PCR方法探测水稻潮霉素基因和CD0817谷氨酸脱羧酶基因的未知DNA区域,对该方法进行了验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f95f/9857434/27572480d1e9/cimb-45-00034-g001.jpg

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