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dnaB and dnaI temperature-sensitive mutants of Staphylococcus aureus: evidence for involvement of DnaB and DnaI in synchrony regulation of chromosome replication

机译:金黄色葡萄球菌的DNAB和DNAi温度敏感突变体:DNAB和DNAi参与染色体复制同步调节的证据

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DnaB and DnaI proteins conserved in low-GC content Gram-positive bacteria are apparently involved in helicase loading at the replication initiation site and during the restarting of stalled replication forks. In this study, we found five novel dnaB mutants and three novel dnaI mutants by screening 750 temperature-sensitive Gram-positive Staphylococcus aureus mutants. All of the mutants had a single amino acid substitution in either DnaB or DnaI that controlled temperature-sensitive growth, as confirmed by transduction experiments using phage 80α. DNA synthesis as measured by [3H]thymine incorporation, origin-to-terminus ratios and flow cytometric analysis revealed that the dnaB and dnaI mutants were unable to initiate DNA replication at restrictive temperatures, which is similar to previous findings in Bacillus subtilis. Furthermore, some of the mutants were found to exhibit asynchrony in the initiation of DNA replication. Also, a fraction of the dnaI mutant cells showed arrested replication, and the dnaI mutant tested was sensitive to mitomycin C, which causes DNA lesions. These results suggest that DnaB and DnaI are required not only for replication initiation and but also for regulation of its synchrony, and they provide support for the involvement of DnaI activity in the restart of arrested replication forks in vivo.
机译:在低GC含量革兰氏阳性细菌中保守的DNAB和DNAi蛋白显然参与了复制起始位点的螺旋酶负载,并且在重新启动停滞复制叉期间。在这项研究中,通过筛选750个温度敏感的革兰阳性葡萄球菌突变体,发现了五种新的DNAB突变体和三种新型DNAI突变体。所有突变体在控制温度敏感生长的DNAB或DNAi中的单个氨基酸取代,通过使用噬菌体80α的转导实验证实。通过[3H]胸腺嘧啶掺入测量的DNA合成,末端末端比率和流式细胞术分析显示,DNAB和DNAi突变体无法在限制温度下启动DNA复制,这类似于枯草芽孢杆菌的先前发现。此外,发现一些突变体在发起DNA复制中表现出异步。而且,DNAi突变细胞的一部分显示被捕的复制,并且测试的DNai突变体对丝霉素C敏感,这导致DNA病变。这些结果表明,DNAB和DNAI不仅需要进行复制启动,而且还需要对其同步的监管,并且他们为达到达到活动的参与提供支持在体内逮捕的复制叉中的延期。

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