The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination

The INO80 complex (INO80-C) is an evolutionarily conserved nucleosome remodeler that acts in transcription, replication, and genome stability. It is required for resistance against genotoxic agents and is involved in the repair of DNA double-strand breaks (DSBs) by homologous recombination (HR). How...

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Main Authors: Claudio A. Lademann, Jörg Renkawitz, Boris Pfander, Stefan Jentsch
Format: Article
Language:English
Published: Elsevier 2017-05-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124717305454
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spelling doaj-6e382995778d47c2b6f68def3ce672f92020-11-25T01:32:30ZengElsevierCell Reports2211-12472017-05-011971294130310.1016/j.celrep.2017.04.051The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous RecombinationClaudio A. Lademann0Jörg Renkawitz1Boris Pfander2Stefan Jentsch3Molecular Cell Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, GermanyMolecular Cell Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, GermanyDNA Replication and Genome Integrity, Max Planck Institute of Biochemistry, 82152 Martinsried, GermanyMolecular Cell Biology, Max Planck Institute of Biochemistry, 82152 Martinsried, GermanyThe INO80 complex (INO80-C) is an evolutionarily conserved nucleosome remodeler that acts in transcription, replication, and genome stability. It is required for resistance against genotoxic agents and is involved in the repair of DNA double-strand breaks (DSBs) by homologous recombination (HR). However, the causes of the HR defect in INO80-C mutant cells are controversial. Here, we unite previous findings using a system to study HR with high spatial resolution in budding yeast. We find that INO80-C has at least two distinct functions during HR—DNA end resection and presynaptic filament formation. Importantly, the second function is linked to the histone variant H2A.Z. In the absence of H2A.Z, presynaptic filament formation and HR are restored in INO80-C-deficient mutants, suggesting that presynaptic filament formation is the crucial INO80-C function during HR.http://www.sciencedirect.com/science/article/pii/S2211124717305454homologous recombinationdouble-strand breakschromatinnucleosome remodelinggenome stabilityINO80-CH2A.ZRad51 filament formationDNA end resection
collection DOAJ
language English
format Article
sources DOAJ
author Claudio A. Lademann
Jörg Renkawitz
Boris Pfander
Stefan Jentsch
spellingShingle Claudio A. Lademann
Jörg Renkawitz
Boris Pfander
Stefan Jentsch
The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination
Cell Reports
homologous recombination
double-strand breaks
chromatin
nucleosome remodeling
genome stability
INO80-C
H2A.Z
Rad51 filament formation
DNA end resection
author_facet Claudio A. Lademann
Jörg Renkawitz
Boris Pfander
Stefan Jentsch
author_sort Claudio A. Lademann
title The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination
title_short The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination
title_full The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination
title_fullStr The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination
title_full_unstemmed The INO80 Complex Removes H2A.Z to Promote Presynaptic Filament Formation during Homologous Recombination
title_sort ino80 complex removes h2a.z to promote presynaptic filament formation during homologous recombination
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2017-05-01
description The INO80 complex (INO80-C) is an evolutionarily conserved nucleosome remodeler that acts in transcription, replication, and genome stability. It is required for resistance against genotoxic agents and is involved in the repair of DNA double-strand breaks (DSBs) by homologous recombination (HR). However, the causes of the HR defect in INO80-C mutant cells are controversial. Here, we unite previous findings using a system to study HR with high spatial resolution in budding yeast. We find that INO80-C has at least two distinct functions during HR—DNA end resection and presynaptic filament formation. Importantly, the second function is linked to the histone variant H2A.Z. In the absence of H2A.Z, presynaptic filament formation and HR are restored in INO80-C-deficient mutants, suggesting that presynaptic filament formation is the crucial INO80-C function during HR.
topic homologous recombination
double-strand breaks
chromatin
nucleosome remodeling
genome stability
INO80-C
H2A.Z
Rad51 filament formation
DNA end resection
url http://www.sciencedirect.com/science/article/pii/S2211124717305454
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