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解析聚合酶链反应:理解并纠正与引物简并性和引物-模板错配相关的偏差。

Deconstructing the polymerase chain reaction: understanding and correcting bias associated with primer degeneracies and primer-template mismatches.

作者信息

Green Stefan J, Venkatramanan Raghavee, Naqib Ankur

机构信息

DNA Services Facility, Research Resources Center, University of Illinois at Chicago, Chicago, Illinois, United States of America; Dept. of Biological Sciences, University of Illinois at Chicago, Chicago, Illinois, United States of America.

DNA Services Facility, Research Resources Center, University of Illinois at Chicago, Chicago, Illinois, United States of America; Dept. of Bioengineering, University of Illinois at Chicago, Chicago, Illinois, United States of America.

出版信息

PLoS One. 2015 May 21;10(5):e0128122. doi: 10.1371/journal.pone.0128122. eCollection 2015.

Abstract

The polymerase chain reaction (PCR) is sensitive to mismatches between primer and template, and mismatches can lead to inefficient amplification of targeted regions of DNA template. In PCRs in which a degenerate primer pool is employed, each primer can behave differently. Therefore, inefficiencies due to different primer melting temperatures within a degenerate primer pool, in addition to mismatches between primer binding sites and primers, can lead to a distortion of the true relative abundance of targets in the original DNA pool. A theoretical analysis indicated that a combination of primer-template and primer-amplicon interactions during PCR cycles 3-12 is potentially responsible for this distortion. To test this hypothesis, we developed a novel amplification strategy, entitled "Polymerase-exonuclease (PEX) PCR", in which primer-template interactions and primer-amplicon interactions are separated. The PEX PCR method substantially and significantly improved the evenness of recovery of sequences from a mock community of known composition, and allowed for amplification of templates with introduced mismatches near the 3' end of the primer annealing sites. When the PEX PCR method was applied to genomic DNA extracted from complex environmental samples, a significant shift in the observed microbial community was detected. Furthermore, the PEX PCR method provides a mechanism to identify which primers in a primer pool are annealing to target gDNA. Primer utilization patterns revealed that at high annealing temperatures in the PEX PCR method, perfect match annealing predominates, while at lower annealing temperatures, primers with up to four mismatches with templates can contribute substantially to amplification. The PEX PCR method is simple to perform, is limited to PCR mixes and a single exonuclease step which can be performed without reaction cleanup, and is recommended for reactions in which degenerate primer pools are used or when mismatches between primers and template are possible.

摘要

聚合酶链反应(PCR)对引物与模板之间的错配很敏感,错配会导致DNA模板靶向区域的扩增效率低下。在使用简并引物库的PCR中,每个引物的表现可能不同。因此,除了引物结合位点与引物之间的错配外,简并引物库中不同引物解链温度导致的效率低下,可能会导致原始DNA库中靶标的真实相对丰度发生扭曲。理论分析表明,PCR循环3至12期间引物 - 模板和引物 - 扩增子相互作用的组合可能是造成这种扭曲的原因。为了验证这一假设,我们开发了一种名为“聚合酶 - 核酸外切酶(PEX)PCR”的新型扩增策略,其中引物 - 模板相互作用和引物 - 扩增子相互作用是分开的。PEX PCR方法显著提高了从已知组成的模拟群落中回收序列的均匀性,并允许扩增在引物退火位点3'端附近引入错配的模板。当PEX PCR方法应用于从复杂环境样品中提取的基因组DNA时,检测到观察到的微生物群落发生了显著变化。此外,PEX PCR方法提供了一种机制来识别引物库中的哪些引物正在与目标基因组DNA退火。引物利用模式显示,在PEX PCR方法的高退火温度下,完美匹配退火占主导,而在较低退火温度下,与模板有多达四个错配的引物可以对扩增做出重大贡献。PEX PCR方法操作简单,仅限于PCR混合物和单个核酸外切酶步骤,无需反应清理即可进行,推荐用于使用简并引物库或引物与模板之间可能存在错配的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5894/4440812/1082c6f6c6c7/pone.0128122.g001.jpg

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