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Regulation of Mus81–Eme1 Holliday junction resolvase in response to DNA damage

Authors :
Bertrand Llorente
Pierre-Henri L. Gaillard
Pierre-Marie Dehé
Arato Takedachi
Stéphane Coulon
Paul Shanahan
John R. Yates
Sarah Scaglione
James A. Wohlschlegel
Paul Russell
Centre de Recherche en Cancérologie de Marseille (CRCM)
Aix Marseille Université (AMU)-Institut Paoli-Calmettes
Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
The Scripps Research Institute [La Jolla]
University of California [San Diego] (UC San Diego)
University of California-University of California
Department of Surgical and Radiological Sciences
University of California [Davis] (UC Davis)
Institut Paoli-Calmettes
Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)
Aix Marseille Université (AMU)
Institut National de la Santé et de la Recherche Médicale (INSERM)
Centre National de la Recherche Scientifique (CNRS)
The Scripps Research Institute [La Jolla, San Diego]
University of California (UC)-University of California (UC)
gaillard, pierre-henri
Source :
Nature Structural and Molecular Biology, Nature Structural and Molecular Biology, Nature Publishing Group, 2013, 20 (5), pp.598-603. ⟨10.1038/nsmb.2550⟩, Nature Structural and Molecular Biology, 2013, 20 (5), pp.598-603. ⟨10.1038/nsmb.2550⟩
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

Structure-specific DNA endonucleases have critical roles during DNA replication, repair and recombination, yet they also harbor the potential for causing genome instability. Controlling these enzymes may be essential to ensure efficient processing of ad hoc substrates and to prevent random, unscheduled processing of other DNA structures, but it is unknown whether structure-specific endonucleases are regulated in response to DNA damage. Here, we uncover DNA damage-induced activation of Mus81-Eme1 Holliday junction resolvase in fission yeast. This novel regulation requires both Cdc2CDK1 and Rad3ATR-dependent phosphorylations of Eme1. Mus81-Eme1 activation prevents gross chromosomal rearrangements in cells lacking the BLM-related DNA helicase Rqh1. We propose that linking Mus81-Eme1 DNA damaged-induced activation to cell cycle progression ensures efficient resolution of Holliday junctions that escape dissolution by Rqh1-TopIII while preventing unnecessary DNA cleavages.

Details

ISSN :
15459985 and 15459993
Volume :
20
Database :
OpenAIRE
Journal :
Nature Structural & Molecular Biology
Accession number :
edsair.doi.dedup.....094fac90cdc343c04e1d302819a9c268
Full Text :
https://doi.org/10.1038/nsmb.2550