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减数分裂重组过程中的RPA同源物与单链DNA加工

RPA homologs and ssDNA processing during meiotic recombination.

作者信息

Ribeiro Jonathan, Abby Emilie, Livera Gabriel, Martini Emmanuelle

机构信息

Laboratory of Development of the Gonads, Unit of Stem Cells and Radiation, University of Paris Diderot, Sorbonne Paris Cité, UMR 967, F-92265, Fontenay-aux-Roses, France.

CEA, DSV, iRCM, SCSR, LDG, F-92265, Fontenay-aux-Roses, France.

出版信息

Chromosoma. 2016 Jun;125(2):265-76. doi: 10.1007/s00412-015-0552-7. Epub 2015 Oct 31.

Abstract

Meiotic homologous recombination is a specialized process that involves homologous chromosome pairing and strand exchange to guarantee proper chromosome segregation and genetic diversity. The formation and repair of DNA double-strand breaks (DSBs) during meiotic recombination differs from those during mitotic recombination in that the homologous chromosome rather than the sister chromatid is the preferred repair template. The processing of single-stranded DNA (ssDNA) formed on intermediate recombination structures is central to driving the specific outcomes of DSB repair during meiosis. Replication protein A (RPA) is the main ssDNA-binding protein complex involved in DNA metabolism. However, the existence of RPA orthologs in plants and the recent discovery of meiosis specific with OB domains (MEIOB), a widely conserved meiosis-specific RPA1 paralog, strongly suggest that multiple RPA complexes evolved and specialized to subdivide their roles during DNA metabolism. Here we review ssDNA formation and maturation during mitotic and meiotic recombination underlying the meiotic specific features. We describe and discuss the existence and properties of MEIOB and multiple RPA subunits in plants and highlight how they can provide meiosis-specific fates to ssDNA processing during homologous recombination. Understanding the functions of these RPA homologs and how they interact with the canonical RPA subunits is of major interest in the fields of meiosis and DNA repair.

摘要

减数分裂同源重组是一个特殊的过程,涉及同源染色体配对和链交换,以确保正确的染色体分离和遗传多样性。减数分裂重组过程中DNA双链断裂(DSB)的形成和修复与有丝分裂重组过程中的不同之处在于,同源染色体而非姐妹染色单体是首选的修复模板。在中间重组结构上形成的单链DNA(ssDNA)的加工对于驱动减数分裂期间DSB修复的特定结果至关重要。复制蛋白A(RPA)是参与DNA代谢的主要ssDNA结合蛋白复合物。然而,植物中RPA直系同源物的存在以及最近对具有OB结构域的减数分裂特异性蛋白(MEIOB)的发现,MEIOB是一种广泛保守的减数分裂特异性RPA1旁系同源物,强烈表明多个RPA复合物在进化过程中专门化,以细分它们在DNA代谢中的作用。在这里,我们回顾了有丝分裂和减数分裂重组过程中ssDNA的形成和成熟,这些过程是减数分裂特异性特征的基础。我们描述并讨论了植物中MEIOB和多个RPA亚基的存在和特性,并强调了它们如何在同源重组过程中为ssDNA加工提供减数分裂特异性的结果。了解这些RPA同源物的功能以及它们如何与经典RPA亚基相互作用,是减数分裂和DNA修复领域的主要研究兴趣所在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dd1/4830875/95c32b9cccfe/412_2015_552_Fig1_HTML.jpg

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