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中心碳代谢影响大肠杆菌中 DNA 复制的保真度。

Central carbon metabolism influences fidelity of DNA replication in Escherichia coli.

机构信息

Department of Molecular Biology, University of Gdańsk, Gdańsk, Poland.

出版信息

Mutat Res. 2012 Mar 1;731(1-2):99-106. doi: 10.1016/j.mrfmmm.2011.12.005. Epub 2011 Dec 17.

Abstract

Recent studies indicated that there is a direct link between central carbon metabolism (CCM) and initiation and elongation of DNA replication in Eschericha coli. Namely, effects of certain mutations in genes coding for replication proteins (dnaA, dnaB, dnaE, dnaG, and dnaN) could be specifically suppressed by deletions of some genes, whose products are involved in CCM reactions (pta, ackA, pgi, tktB, and gpmA). Here, we demonstrate that the link between CCM and DNA synthesis can be extended to the DNA replication fidelity, as we report changes of the mutator phenotypes of E. coli dnaQ49 and dnaX36 mutants (either suppression or enhancement) by dysfunctions of zwf, pta, ackA, acnB, and icdA genes. Overexpression of appropriate wild-type CCM genes in double mutants resulted in reversions to the initial mutator phenotypes, indicating that the effects were specific. Moreover, the observed suppression and enhancement effects were not caused by changes in bacterial growth rates. These results suggest that there is a genetic correlation between CCM and DNA replication fidelity in E. coli, apart from the already documented link between CCM and DNA replication initiation control and elongation efficiency.

摘要

最近的研究表明,大肠杆菌中心碳代谢(CCM)与 DNA 复制的起始和延伸之间存在直接联系。也就是说,编码复制蛋白(dnaA、dnaB、dnaE、dnaG 和 dnaN)的某些基因突变的影响可以通过删除某些基因来特异性抑制,这些基因的产物参与 CCM 反应(pta、ackA、pgi、tktB 和 gpmA)。在这里,我们证明 CCM 与 DNA 合成之间的联系可以扩展到 DNA 复制保真度,因为我们报告了 E. coli dnaQ49 和 dnaX36 突变体(抑制或增强)的突变表型变化通过 zwf、pta、ackA、acnB 和 icdA 基因的功能障碍。在双突变体中过量表达适当的野生型 CCM 基因导致回复到初始突变体表型,表明这些影响是特异性的。此外,观察到的抑制和增强效应不是由细菌生长速率的变化引起的。这些结果表明,除了已经记录的 CCM 与 DNA 复制起始控制和延伸效率之间的联系之外,大肠杆菌中 CCM 和 DNA 复制保真度之间存在遗传相关性。

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