Concurrent D-loop cleavage by Mus81 and Yen1 yields half-crossover precursors

Author:

Carreira Raquel1ORCID,Lama-Diaz Tomas1,Crugeiras Maria1,Aguado F Javier1,Sebesta Marek2ORCID,Krejci Lumir2ORCID,Blanco Miguel G1ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, CIMUS, Universidade de Santiago de Compostela-Instituto de Investigación Sanitaria (IDIS) , Santiago de Compostela , A Coruña  15782 , Spain

2. Department of Biology and National Centre for Biomolecular Research, Masaryk University , Brno  62500 , Czech Republic

Abstract

Abstract Homologous recombination involves the formation of branched DNA molecules that may interfere with chromosome segregation. To resolve these persistent joint molecules, cells rely on the activation of structure-selective endonucleases (SSEs) during the late stages of the cell cycle. However, the premature activation of SSEs compromises genome integrity, due to untimely processing of replication and/or recombination intermediates. Here, we used a biochemical approach to show that the budding yeast SSEs Mus81 and Yen1 possess the ability to cleave the central recombination intermediate known as the displacement loop or D-loop. Moreover, we demonstrate that, consistently with previous genetic data, the simultaneous action of Mus81 and Yen1, followed by ligation, is sufficient to recreate the formation of a half-crossover precursor in vitro. Our results provide not only mechanistic explanation for the formation of a half-crossover, but also highlight the critical importance for precise regulation of these SSEs to prevent chromosomal rearrangements.

Funder

Ministerio de Ciencia e Innovación

Agencia Estatal de Investigación

Fondo Europeo de Desarrollo Regional

Czech Science Foundation

Wellcome Trust

Xunta de Galicia

Asociación Española Contra el Cáncer

Publisher

Oxford University Press (OUP)

Reference85 articles.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3