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小的Rad51和Dmc1复合体经常共同占据减数分裂DNA双链断裂的两端。

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

作者信息

Brown M Scott, Grubb Jennifer, Zhang Annie, Rust Michael J, Bishop Douglas K

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, Cummings Life Science Center, Chicago, Illinois, United States of America.

Department of Radiation and Cellular Oncology, University of Chicago, Cummings Life Science Center, Chicago, Illinois, United States of America.

出版信息

PLoS Genet. 2015 Dec 31;11(12):e1005653. doi: 10.1371/journal.pgen.1005653. eCollection 2015 Dec.

Abstract

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.

摘要

真核生物中类RecA蛋白Rad51和Dmc1在减数分裂过程中协同作用,通过修复程序性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形成部分重叠的共焦点。在此我们表明,这些Rad51-Dmc1共焦点常常成对排列,间距可达400纳米。当DSB显著减少或链交换或联会被阻断时,成对的共焦点依然普遍存在。超分辨率dSTORM显微镜显示,传统光学显微镜观察到的单个焦点通常由两个或更多子结构组成。这些数据支持一种模型,即由单个DSB形成的两条单链DNA(ssDNA)彼此分开,间距可达400纳米,两条链常常都结合有一条或多条短(约100个核苷酸)的Rad51细丝,同时也结合有一条或多条短的Dmc1细丝。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2306/4697796/f9fa65c8e092/pgen.1005653.g001.jpg

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