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首页> 外文期刊>Nucleic acids research >Chromosomal over-replication in Escherichia coli recG cells is triggered by replication fork fusion and amplified if replichore symmetry is disturbed
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Chromosomal over-replication in Escherichia coli recG cells is triggered by replication fork fusion and amplified if replichore symmetry is disturbed

机译:大肠杆菌recG细胞中的染色体过度复制是由复制叉融合触发的,如果复制对称性受到干扰,则会放大

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Chromosome duplication initiates via the assembly of replication forks at defined origins. Forks proceed in opposite directions until they fuse with a converging fork. Recent work highlights that fork fusions are highly choreographed both in pro- and eukaryotic cells. The circular Escherichia coli chromosome is replicated from a single origin (oriC), and a single fork fusion takes place in a specialised termination area opposite oriC that establishes a fork trap mediated by Tus protein bound at ter sequences that allows forks to enter but not leave. Here we further define the molecular details of fork fusions and the role of RecG helicase in replication termination. Our data support the idea that fork fusions have the potential to trigger local re-replication of the already replicated DNA. In ΔrecG cells this potential is realised in a substantial fraction of cells and is dramatically elevated when one fork is trapped for some time before the converging fork arrives. They also support the idea that the termination area evolved to contain such over-replication and we propose that the stable arrest of replication forks at ter/Tus complexes is an important feature that limits the likelihood of problems arising as replication terminates.
机译:染色体复制通过在定义的起源处组装复制叉而开始。叉以相反的方向前进,直到它们与会聚的叉融合。最近的工作表明,前融合和真核细胞均高度编排了叉子融合。环状大肠杆菌染色体从单个起点(oriC)复制,并且单个叉融合发生在oriC对面的专门终止区域中,该区域建立了由Tus蛋白介导的,在三叉序列处结合的叉陷阱,从而允许叉进入但不能离开。在这里,我们进一步定义了叉子融合的分子细节以及RecG解旋酶在复制终止中的作用。我们的数据支持这样的想法,即叉子融合有可能触发已经复制的DNA的局部复制。在ΔrecG细胞中,这一潜力在相当一部分细胞中得以实现,并且在聚合叉到达之前,将一个叉子夹住一段时间后,电位会显着升高。他们还支持终止区域演变为包含此类过度复制的想法,我们建议稳定地阻止复制叉在ter / Tus复合体上的重要特征,可限制复制终止时出现问题的可能性。

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