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Small Rad51 and Dmc1 Complexes Often Co-occupy Both Ends of a Meiotic DNA Double Strand Break

机译:小Rad51和Dmc1复杂往往共同占据减数分裂DNA双链断裂的两端。

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摘要

The Eukaryotic RecA-like proteins Rad51 and Dmc1 cooperate during meiosis to promote recombination between homologous chromosomes by repairing programmed DNA double strand breaks (DSBs). Previous studies showed that Rad51 and Dmc1 form partially overlapping co-foci. Here we show these Rad51-Dmc1 co-foci are often arranged in pairs separated by distances of up to 400 nm. Paired co-foci remain prevalent when DSBs are dramatically reduced or when strand exchange or synapsis is blocked. Super-resolution dSTORM microscopy reveals that individual foci observed by conventional light microscopy are often composed of two or more substructures. The data support a model in which the two tracts of ssDNA formed by a single DSB separate from one another by distances of up to 400 nm, with both tracts often bound by one or more short (about 100 nt) Rad51 filaments and also by one or more short Dmc1 filaments.
机译:真核RecA样蛋白Rad51和Dmc1在减数分裂过程中合作,通过修复程序化的DNA双链断裂(DSB)来促进同源染色体之间的重组。先前的研究表明Rad51和Dmc1形成部分重叠的共灶。在这里,我们显示了这些Rad51-Dmc1共病灶通常成对排列,最远间隔为400 nm。当DSB显着减少或链交换或突触受阻时,成对的共灶仍很普遍。超分辨率dSTORM显微镜显示,常规光学显微镜观察到的单个病灶通常由两个或多个子结构组成。数据支持一种模型,在该模型中,单个DSB形成的两条ssDNA片段彼此分开,最远可达400 nm,两个片段通常由一个或多个短(约100 nt)Rad51细丝以及一个或更短的Dmc1细丝。

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