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提高PCR中简并引物效率和特异性的策略

Strategies to Improve Efficiency and Specificity of Degenerate Primers in PCR.

作者信息

Campos Maria Jorge, Quesada Alberto

机构信息

MARE - Marine and Environmental Sciences Centre, ESTM, Instituto Politécnico de Leiria, Apartado 4133, 2520-641, Peniche, Portugal.

Facultad de Veterinaria, Departamento de Bioquímica, Biología Molecular y Genética, Universidad de Extremadura, Extremadura, Spain.

出版信息

Methods Mol Biol. 2017;1620:75-85. doi: 10.1007/978-1-4939-7060-5_4.

Abstract

PCR with degenerate primers can be used to identify the coding sequence of an unknown protein or to detect a genetic variant within a gene family. These primers, which are complex mixtures of slightly different oligonucleotide sequences, can be optimized to increase the efficiency and/or specificity of PCR in the amplification of a sequence of interest by the introduction of mismatches with the target sequence and balancing their position toward the primers 5'- or 3'-ends. In this work, we explain in detail examples of rational design of primers in two different applications, including the use of specific determinants at the 3'-end, to: (1) improve PCR efficiency with coding sequences for members of a protein family by fully degeneration at a core box of conserved genetic information, with the reduction of degeneration at the 5'-end, and (2) optimize specificity of allelic discrimination of closely related orthologous by 5'-end degenerate primers.

摘要

使用简并引物进行聚合酶链反应(PCR)可用于鉴定未知蛋白质的编码序列,或检测基因家族内的遗传变异。这些引物是略有不同的寡核苷酸序列的复杂混合物,可通过引入与靶序列的错配并平衡其朝向引物5'端或3'端的位置来进行优化,以提高PCR在扩增目标序列时的效率和/或特异性。在这项工作中,我们详细解释了两种不同应用中引物合理设计的示例,包括在3'端使用特异性决定因素,以:(1)通过在保守遗传信息的核心框处完全简并,并减少5'端的简并度,提高蛋白质家族成员编码序列的PCR效率;(2)通过5'端简并引物优化密切相关直系同源基因的等位基因鉴别特异性。

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