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Regulation of DNA Pairing in Homologous Recombination

机译:同源重组中DNA配对的调控

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摘要

Homologous recombination (HR) is a major mechanism for eliminating DNA double-strand breaks from chromosomes. In this process, the break termini are resected nucleolytically to form 3′ ssDNA (single-strand DNA) overhangs. A recombinase (i.e., a protein that catalyzes homologous DNA pairing and strand exchange) assembles onto the ssDNA and promotes pairing with a homologous duplex. DNA synthesis then initiates from the 3′ end of the invading strand, and the extended DNA joint is resolved via one of several pathways to restore the integrity of the injured chromosome. It is crucial that HR be carefully orchestrated because spurious events can create cytotoxic intermediates or cause genomic rearrangements and loss of gene heterozygosity, which can lead to cell death or contribute to the development of cancer. In this review, we will discuss how DNA motor proteins regulate HR via a dynamic balance of the recombination-promoting and -attenuating activities that they possess.
机译:同源重组(HR)是消除染色体DNA双链断裂的主要机制。在此过程中,将断裂末端进行核酶切以形成3'ssDNA(单链DNA)突出端。重组酶(即催化同源DNA配对和链交换的蛋白质)组装到ssDNA上并促进与同源双链体的配对。然后从入侵链的3'端开始DNA合成,并通过几种途径之一解析延伸的DNA接头,以恢复受损染色体的完整性。精心策划HR至关重要,因为虚假事件可能会产生细胞毒性中间体或引起基因组重排以及基因杂合性丧失,从而导致细胞死亡或促进癌症的发展。在这篇综述中,我们将讨论DNA运动蛋白如何通过它们所具有的重组促进和减弱活性的动态平衡来调节HR。

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