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Exchange between Escherichia coli polymerases II and III on a processivity clamp

机译:大肠埃希氏大肠杆菌聚合酶II和III之间的交换

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Escherichia coli has three DNA polymerases implicated in the bypass of DNA damage, a process called translesion synthesis (TLS) that alleviates replication stalling. Although these polymerases are specialized for different DNA lesions, it is unclear if they interact differently with the replication machinery. Of the three, DNA polymerase (Pol) II remains the most enigmatic. Here we report a stable ternary complex of Pol II, the replicative polymerase Pol III core complex and the dimeric processivity clamp, beta. Single-molecule experiments reveal that the interactions of Pol II and Pol III with beta allow for rapid exchange during DNA synthesis. As with another TLS polymerase, Pol IV, increasing concentrations of Pol II displace the Pol III core during DNA synthesis in a minimal reconstitution of primer extension. However, in contrast to Pol IV, Pol II is inefficient at disrupting rolling-circle synthesis by the fully reconstituted Pol III replisome. Together, these data suggest a beta-mediated mechanism of exchange between Pol II and Pol III that occurs outside the replication fork.
机译:大肠埃希菌具有绕过DNA损伤的三种DNA聚合酶,这一过程称为跨病变合成(TLS),可减轻复制停滞。尽管这些聚合酶专门针对不同的DNA损伤,但尚不清楚它们与复制机制的相互作用是否不同。在这三者中,DNA聚合酶(Pol)II仍然是最令人费解的。在这里,我们报告一个稳定的三元复合物Pol II,复制性聚合酶Pol III核心复合物和二聚体合成钳位β。单分子实验表明,Pol II和Pol III与β的相互作用可以在DNA合成过程中快速交换。与另一种TLS聚合酶Pol IV一样,增加的Pol II浓度会在DNA合成过程中以最小的引物延伸重构来置换Pol III核心。但是,与Pol IV相比,Pol II在完全重组的Pol III复制体破坏滚动环合成方面效率低下。总之,这些数据表明在复制叉之外发生的由β介导的Pol II和Pol III之间的交换机制。

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