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A meiosis-specific BRCA2 binding protein recruits recombinases to DNA double-strand breaks to ensure homologous recombination.

Journal article
Authors Jingjing Zhang
Yasuhiro Fujiwara
Shohei Yamamoto
Hiroki Shibuya
Published in Nature communications
Volume 10
Issue 1
Pages 722
ISSN 2041-1723
Publication year 2019
Published at Department of Chemistry and Molecular Biology
Pages 722
Language en
Links dx.doi.org/10.1038/s41467-019-08676...
www.ncbi.nlm.nih.gov/entrez/query.f...
Subject categories Cell Biology

Abstract

Homologous recombination (HR) repairs DNA double-strand breaks (DSBs) to maintain genomic integrity. Recombinase recruited to the DSBs by the mediator protein BRCA2 catalyzes the homology-directed repair. During meiotic HR, programmed DSBs are introduced genome-wide but their repair mechanisms, including the regulation of BRCA2, have remained largely elusive. Here we identify a meiotic localizer of BRCA2, MEILB2/HSF2BP, that localizes to the site of meiotic DSBs in mice. Disruption of Meilb2 abolishes the localization of RAD51 and DMC1 recombinases in spermatocytes, leading to errors in DSB repair and male sterility. MEILB2 directly binds to BRCA2 and regulates its association to meiotic DSBs. We map the MEILB2-binding domain within BRCA2 that is distinct from the canonical DNA-binding domain but is sufficient to localize to meiotic DSBs in a MEILB2-dependent manner. We conclude that localization of BRCA2 to meiotic DSBs is mediated by MEILB2, which is an integral mechanism to repair abundant meiotic DSBs.

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