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在中性选择条件下检测复制DNA中错配与替代切除依赖修复的动力学

Dynamics of Mismatch and Alternative Excision-Dependent Repair in Replicating DNA Examined Under Conditions of Neutral Selection.

作者信息

Patlán-Vázquez Adriana G, Ayala-García Víctor M, Vallin Carmen, Cortés Jonathan, Vásquez-Morales Suria G, Robleto Eduardo A, Nudler Evgeny, Pedraza-Reyes Mario

机构信息

Division of Natural and Exact Sciences, Department of Biology, University of Guanajuato, Guanajuato, Mexico.

Faculty of Chemical Sciences, Juarez University of Durango State, Durango, Mexico.

出版信息

Front Microbiol. 2022 Jun 30;13:866089. doi: 10.3389/fmicb.2022.866089. eCollection 2022.

Abstract

Spontaneous DNA deamination is a potential source of transition mutations. In , EndoV, a component of the alternative excision repair pathway (AER), counteracts the mutagenicity of base deamination-induced mispairs. Here, we report that the mismatch repair (MMR) system, MutSL, prevents the harmful effects of HNO, a deaminating agent of Cytosine (C), Adenine (A), and Guanine (G). Using Maximum Depth Sequencing (MDS), which measures mutagenesis under conditions of neutral selection, in strains proficient or deficient in MutSL and/or EndoV, revealed asymmetric and heterogeneous patterns of mutations in both DNA template strands. While the lagging template strand showed a higher frequency of C → T substitutions; G → A mutations, occurred more frequently in the leading template strand in different genetic backgrounds. In summary, our results unveiled a role for MutSL in preventing the deleterious effects of base deamination and uncovered differential patterns of base deamination processing by the AER and MMR systems that are influenced by the sequence context and the replicating DNA strand.

摘要

自发的DNA脱氨基作用是转换突变的一个潜在来源。在替代切除修复途径(AER)的一个组成部分EndoV中,它可抵消碱基脱氨基诱导的错配的致突变性。在此,我们报告错配修复(MMR)系统MutSL可防止HNO(一种胞嘧啶(C)、腺嘌呤(A)和鸟嘌呤(G)的脱氨基剂)的有害影响。使用最大深度测序(MDS)(其在中性选择条件下测量诱变作用),在MutSL和/或EndoV功能正常或缺陷的菌株中,揭示了两条DNA模板链中不对称且异质的突变模式。虽然滞后模板链显示出较高频率的C→T替换;而G→A突变在不同遗传背景下的前导模板链中更频繁发生。总之,我们的结果揭示了MutSL在防止碱基脱氨基的有害影响方面的作用,并揭示了受序列背景和复制DNA链影响的AER和MMR系统处理碱基脱氨基的差异模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97b2/9280176/1b83207199a9/fmicb-13-866089-g001.jpg

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