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由复制停滞引起的DNA双链断裂。

DNA double-strand breaks caused by replication arrest.

作者信息

Michel B, Ehrlich S D, Uzest M

机构信息

Laboratoire de Génétique Microbienne, Institut National de la Recherche Agronomique, Jouy en Josas, France.

出版信息

EMBO J. 1997 Jan 15;16(2):430-8. doi: 10.1093/emboj/16.2.430.

Abstract

We report here that DNA double-strand breaks (DSBs) form in Escherichia coli upon arrest of replication forks due to a defect in, or the inhibition of, replicative DNA helicases. The formation of DSBs was assessed by the appearance of linear DNA detected by pulse-field gel electrophoresis. Processing of DSBs by recombination repair or linear DNA degradation was abolished by mutations in recBCD genes. Two E. coli replicative helicases were tested, Rep, which is essential in recBC mutants, and DnaB. The proportion of linear DNA increased up to 50% upon shift of rep recBTS recCTS cells to restrictive temperature. No increase in linear DNA was observed in the absence of replicating chromosomes, indicating that the formation of DSBs in rep strains requires replication. Inhibition of the DnaB helicase either by a strong replication terminator or by a dnaBTS mutation led to the formation of linear DNA, showing that blocked replication forks are prone to DSB formation. In wild-type E. coli, linear DNA was detected in the absence of RecBC or of both RecA and RecD. This reveals the existence of a significant amount of spontaneous DSBs. We propose that some of them may also result from the impairment of replication fork progression.

摘要

我们在此报告,由于复制性DNA解旋酶存在缺陷或受到抑制,导致复制叉停滞时,大肠杆菌中会形成DNA双链断裂(DSB)。通过脉冲场凝胶电泳检测到的线性DNA的出现来评估DSB的形成。recBCD基因的突变消除了通过重组修复或线性DNA降解对DSB的处理。测试了两种大肠杆菌复制性解旋酶,在recBC突变体中必不可少的Rep以及DnaB。将rep recBTS recCTS细胞转移至限制温度后,线性DNA的比例增加至50%。在没有复制染色体的情况下未观察到线性DNA增加,这表明rep菌株中DSB的形成需要复制。强复制终止子或dnaBTS突变对DnaB解旋酶的抑制导致线性DNA的形成,表明停滞的复制叉易于形成DSB。在野生型大肠杆菌中,在没有RecBC或同时没有RecA和RecD的情况下检测到线性DNA。这揭示了存在大量自发DSB。我们认为其中一些也可能是由于复制叉进展受损所致。

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