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分离大肠杆菌复制酶校对亚基功能的突变

Mutations that Separate the Functions of the Proofreading Subunit of the Escherichia coli Replicase.

作者信息

Whatley Zakiya, Kreuzer Kenneth N

机构信息

University Program in Genetics and Genomics, Duke University, Durham, North Carolina 27705.

University Program in Genetics and Genomics, Duke University, Durham, North Carolina 27705 Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710

出版信息

G3 (Bethesda). 2015 Apr 15;5(6):1301-11. doi: 10.1534/g3.115.017285.

Abstract

The dnaQ gene of Escherichia coli encodes the ε subunit of DNA polymerase III, which provides the 3' → 5' exonuclease proofreading activity of the replicative polymerase. Prior studies have shown that loss of ε leads to high mutation frequency, partially constitutive SOS, and poor growth. In addition, a previous study from our laboratory identified dnaQ knockout mutants in a screen for mutants specifically defective in the SOS response after quinolone (nalidixic acid) treatment. To explain these results, we propose a model whereby, in addition to proofreading, ε plays a distinct role in replisome disassembly and/or processing of stalled replication forks. To explore this model, we generated a pentapeptide insertion mutant library of the dnaQ gene, along with site-directed mutants, and screened for separation of function mutants. We report the identification of separation of function mutants from this screen, showing that proofreading function can be uncoupled from SOS phenotypes (partially constitutive SOS and the nalidixic acid SOS defect). Surprisingly, the two SOS phenotypes also appear to be separable from each other. These findings support the hypothesis that ε has additional roles aside from proofreading. Identification of these mutants, especially those with normal proofreading but SOS phenotype(s), also facilitates the study of the role of ε in SOS processes without the confounding results of high mutator activity associated with dnaQ knockout mutants.

摘要

大肠杆菌的 dnaQ 基因编码 DNA 聚合酶 III 的 ε 亚基,该亚基为复制性聚合酶提供 3'→5' 核酸外切酶校对活性。先前的研究表明,ε 亚基缺失会导致高突变频率、部分组成型 SOS 反应以及生长不良。此外,我们实验室之前的一项研究在喹诺酮(萘啶酸)处理后对 SOS 反应有特异性缺陷的突变体筛选中鉴定出了 dnaQ 基因敲除突变体。为了解释这些结果,我们提出了一个模型,即除了校对功能外,ε 亚基在复制体解体和/或停滞复制叉的处理中发挥独特作用。为了探索这个模型,我们构建了 dnaQ 基因的五肽插入突变体文库以及定点突变体,并筛选功能分离突变体。我们报告了从该筛选中鉴定出的功能分离突变体,表明校对功能可以与 SOS 表型(部分组成型 SOS 和萘啶酸 SOS 缺陷)解偶联。令人惊讶的是,这两种 SOS 表型似乎也彼此可分离。这些发现支持了 ε 亚基除校对功能外还有其他作用的假设。鉴定这些突变体,特别是那些具有正常校对功能但有 SOS 表型的突变体,也有助于研究 ε 亚基在 SOS 过程中的作用而不会受到与 dnaQ 基因敲除突变体相关的高突变活性的混淆结果的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/715d/4478557/4956d09d1dca/1301f1.jpg

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