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Dynamics of leading-strand lesion skipping by the replisome

机译:复制体跳过前导病变的动力学

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The E.coli replisome stalls transiently when it encounters a lesion in the leading-strand template, skipping over the damage by reinitiating replication at a new primer synthesized downstream by the primase. We report here that template unwinding and lagging-strand synthesis continue downstream of the lesion at a reduced rate after replisome stalling, that one replisome is capable of skipping multiple lesions, and that the rate-limiting steps of replication restart involve the synthesis and activation of the new primer downstream. We also find little support for the concept that polymerase uncoupling, where extensive lagging-strand synthesis proceeds downstream in the absence of leading-strand synthesis, involves physical separation of the leading-strand polymerase from the replisome. Instead, our data indicate that extensive uncoupled replication likely results from a failure of the leading-strand polymerase still associated with the DNA helicase and thelagging-strand polymerase that are proceeding downstream to reinitiate synthesis.
机译:大肠杆菌复制体在前导链模板中遇到病灶时会暂时停止,通过在酶的下游合成的新引物上重新启动复制来跳过损伤。我们在这里报告说,模板解旋和滞后链合成在复制子停滞后以降低的速率继续在病变的下游,一个复制子能够跳过多个损伤,并且复制重启的限速步骤涉及合成和激活下游的新底漆。我们也很少支持聚合酶解偶联的概念,即在没有前导链合成的情况下,大量的滞后链合成在下游进行,涉及从复制体中物理分离前导链聚合酶。取而代之的是,我们的数据表明,广泛的未偶联复制可能是由仍与下游继续重新启动合成的DNA解旋酶和落后链聚合酶相关的前导链聚合酶的失败导致的。

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