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The INO80 remodeller in transcription, replication and repair.

Authors :
Poli J
Gasser SM
Papamichos-Chronakis M
Source :
Philosophical transactions of the Royal Society of London. Series B, Biological sciences [Philos Trans R Soc Lond B Biol Sci] 2017 Oct 05; Vol. 372 (1731).
Publication Year :
2017

Abstract

The accessibility of eukaryotic genomes to the action of enzymes involved in transcription, replication and repair is maintained despite the organization of DNA into nucleosomes. This access is often regulated by the action of ATP-dependent nucleosome remodellers. The INO80 class of nucleosome remodellers has unique structural features and it is implicated in a diverse array of functions, including transcriptional regulation, DNA replication and DNA repair. Underlying these diverse functions is the catalytic activity of the main ATPase subunit, which in the context of a multisubunit complex can shift nucleosomes and carry out histone dimer exchange. In vitro studies showed that INO80 promotes replication fork progression on a chromatin template, while in vivo it was shown to facilitate replication fork restart after stalling and to help evict RNA polymerase II at transcribed genes following the collision of a replication fork with transcription. More recent work in yeast implicates INO80 in the general eviction and degradation of nucleosomes following high doses of oxidative DNA damage. Beyond these replication and repair functions, INO80 was shown to repress inappropriate transcription at promoters in the opposite direction to the coding sequence. Here we discuss the ways in which INO80's diverse functions help maintain genome integrity.This article is part of the themed issue 'Chromatin modifiers and remodellers in DNA repair and signalling'.<br /> (© 2017 The Author(s).)

Details

Language :
English
ISSN :
1471-2970
Volume :
372
Issue :
1731
Database :
MEDLINE
Journal :
Philosophical transactions of the Royal Society of London. Series B, Biological sciences
Publication Type :
Academic Journal
Accession number :
28847827
Full Text :
https://doi.org/10.1098/rstb.2016.0290