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DNA double-strand breaks caused by replication arrest.

机译:复制停滞引起的DNA双链断裂。

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摘要

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.
机译:我们在这里报告DNA双链断裂(DSBs)在大肠杆菌中形成复制叉被缺陷或抑制复制DNA解旋酶的逮捕后形成。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基因突变取消了通过重组修复或线性DNA降解进行的DSB处理。测试了两种大肠杆菌复制性解旋酶,即recBC突变体中必不可少的Rep和DnaB。当rep recBTS recCTS细胞转移到限制性温度时,线性DNA的比例增加高达50%。在不存在复制染色体的情况下,未观察到线性DNA的增加,表明rep菌株中DSB的形成需要复制。通过强大的复制终止子或dnaBTS突变对DnaB解旋酶的抑制导致线性DNA的形成,表明受阻的复制叉易于形成DSB。在野生型大肠杆菌中,在没有RecBC或没有RecA和RecD的情况下检测到线性DNA。这表明存在大量自发DSB。我们建议其中的一些也可能是由于复制叉进程的损害所致。

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