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Mismatch repair inhibits homeologous recombination via coordinated directional unwinding of trapped DNA structures

机译:错配修复通过捕获的DNA结构的定向解链抑制同源重组

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Homeologous recombination between divergent DNA sequences is inhibited by DNA mismatch repair. In Escherichia coli, MutS and MutL respond to DNA mismatches within recombination intermediates and prevent strand exchange via an unknown mechanism. Here, using purified proteins and DNA substrates, we find that in addition to mismatches within the heteroduplex region, secondary structures within the displaced single-stranded DNA formed during branch migration within the recombination intermediate are involved in the inhibition. We present a model that explains how higher-order complex formation of MutS, MutL, and DNA blocks branch migration by preventing rotation of the DNA strands within the recombination intermediate. Furthermore, we find that the helicase UvrD is recruited to directionally resolve these trapped intermediates toward DNA substrates. Thus, our results explain on a mechanistic level how the coordinated action between MutS, MutL, and UvrD prevents homeologous recombination and maintains genome stability.
机译:DNA错配修复抑制了不同DNA序列之间的同源重组。在大肠杆菌中,MutS和MutL对重组中间体中的DNA错配作出反应,并通过未知机制阻止链交换。在这里,使用纯化的蛋白质和DNA底物,我们发现除了异源双链体区域内的错配外,在重组中间体内分支迁移过程中形成的置换单链DNA内的二级结构也参与了抑制作用。我们提出了一个模型,该模型解释了MutS,MutL和DNA的高阶复合物如何通过防止重组中间的DNA链旋转来阻止分支迁移。此外,我们发现解旋酶UvrD被募集以将这些被捕获的中间体定向解析为DNA底物。因此,我们的结果在机制水平上解释了MutS,MutL和UvrD之间的协同作用如何防止同源重组并保持基因组稳定性。

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