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大肠杆菌dnaE抗突变等位基因在缺乏校对功能的mutD5菌株中的作用。

Effects of Escherichia coli dnaE antimutator alleles in a proofreading-deficient mutD5 strain.

作者信息

Fijalkowska I J, Schaaper R M

机构信息

Laboratory of Molecular Genetics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.

出版信息

J Bacteriol. 1995 Oct;177(20):5979-86. doi: 10.1128/jb.177.20.5979-5986.1995.

Abstract

We have previously isolated seven mutants of Escherichia coli which replicate their DNA with increased fidelity. These mutants were isolated as suppressors of the elevated mutability of a mismatch-repair-defective mutL strain. Each mutant was shown to contain a single amino acid substitution in the dnaE gene product, the alpha (i.e., polymerase) subunit of DNA polymerase III holoenzyme responsible for replicating the E. coli chromosome. The mechanism(s) by which these antimutators exert their effect is of interest. Here, we have examined the effects of the antimutator alleles in a mutD5 mutator strain. This strain carries a mutation in the dnaQ gene, which results in defective exonucleolytic proofreading. Our results show that dnaE mutations also confer a strong antimutator phenotype in this background, the effects being generally much greater than those observed previously in the mutL background. The results suggest that the dnaE antimutator alleles can exert their effect independently of exonucleolytic proofreading activity. The large magnitude of the antimutator effects in the mutD5 background can be ascribed, at least in part, to the (additional) restoration of DNA mismatch repair, which is generally impaired in mutD5 strains because of error saturation. The high mutability of mutD5 strains was exploited to isolate a strong new dnaE antimutator allele on the basis of its ability to suppress the high reversion rate of an A.T-->T.A transversion in this background. A model suggesting how the dnaE antimutator alleles might exert their effects in proofreading-proficient and -deficient backgrounds is presented.

摘要

我们之前分离出了七株大肠杆菌突变体,它们复制DNA时保真度更高。这些突变体是作为错配修复缺陷型mutL菌株高突变率的抑制子而分离出来的。已证明每个突变体在dnaE基因产物中都有一个氨基酸替换,dnaE基因产物是DNA聚合酶III全酶的α(即聚合酶)亚基,负责复制大肠杆菌染色体。这些抗突变基因发挥作用的机制令人感兴趣。在这里,我们研究了抗突变基因等位基因在mutD5突变菌株中的作用。该菌株在dnaQ基因中携带一个突变,导致核酸外切酶校对功能缺陷。我们的结果表明,在这种背景下,dnaE突变也赋予了很强的抗突变表型,其效果通常比之前在mutL背景中观察到的要大得多。结果表明,dnaE抗突变基因等位基因可以独立于核酸外切酶校对活性发挥作用。在mutD5背景中抗突变效果的大幅增强至少部分可归因于DNA错配修复的(额外)恢复,由于错误饱和,mutD5菌株中的DNA错配修复通常受损。利用mutD5菌株的高突变率,基于其在这种背景下抑制A.T→T.A颠换高回复率的能力,分离出了一个新的强dnaE抗突变基因等位基因。本文提出了一个模型,说明dnaE抗突变基因等位基因在校对功能正常和缺陷背景下可能如何发挥作用。

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