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The many faces of ubiquitinated histone H2A: insights from the DUBs

Monoubiquitination of H2A is a major histone modification in mammalian cells. Understanding how monoubiquitinated H2A (uH2A) regulates DNA-based processes in the context of chromatin is a challenging question. Work in the past years linked uH2A to transcriptional repression by the Polycomb group pro...

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Autores principales: Vissers, Joseph HA, Nicassio, Francesco, van Lohuizen, Maarten, Di Fiore, Pier Paolo, Citterio, Elisabetta
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373781/
https://www.ncbi.nlm.nih.gov/pubmed/18430235
http://dx.doi.org/10.1186/1747-1028-3-8
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author Vissers, Joseph HA
Nicassio, Francesco
van Lohuizen, Maarten
Di Fiore, Pier Paolo
Citterio, Elisabetta
author_facet Vissers, Joseph HA
Nicassio, Francesco
van Lohuizen, Maarten
Di Fiore, Pier Paolo
Citterio, Elisabetta
author_sort Vissers, Joseph HA
collection PubMed
description Monoubiquitination of H2A is a major histone modification in mammalian cells. Understanding how monoubiquitinated H2A (uH2A) regulates DNA-based processes in the context of chromatin is a challenging question. Work in the past years linked uH2A to transcriptional repression by the Polycomb group proteins of developmental regulators. Recently, a number of mammalian deubiquitinating enzymes (DUBs) that catalyze the removal of ubiquitin from H2A have been discovered. These studies provide convincing evidence that H2A deubiquitination is connected with gene activation. In addition, uH2A regulatory enzymes have crucial roles in the cellular response to DNA damage and in cell cycle progression. In this review we will discuss new insights into uH2A biology, with emphasis on the H2A DUBs.
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spelling pubmed-23737812008-05-08 The many faces of ubiquitinated histone H2A: insights from the DUBs Vissers, Joseph HA Nicassio, Francesco van Lohuizen, Maarten Di Fiore, Pier Paolo Citterio, Elisabetta Cell Div Review Monoubiquitination of H2A is a major histone modification in mammalian cells. Understanding how monoubiquitinated H2A (uH2A) regulates DNA-based processes in the context of chromatin is a challenging question. Work in the past years linked uH2A to transcriptional repression by the Polycomb group proteins of developmental regulators. Recently, a number of mammalian deubiquitinating enzymes (DUBs) that catalyze the removal of ubiquitin from H2A have been discovered. These studies provide convincing evidence that H2A deubiquitination is connected with gene activation. In addition, uH2A regulatory enzymes have crucial roles in the cellular response to DNA damage and in cell cycle progression. In this review we will discuss new insights into uH2A biology, with emphasis on the H2A DUBs. BioMed Central 2008-04-22 /pmc/articles/PMC2373781/ /pubmed/18430235 http://dx.doi.org/10.1186/1747-1028-3-8 Text en Copyright © 2008 Vissers et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Vissers, Joseph HA
Nicassio, Francesco
van Lohuizen, Maarten
Di Fiore, Pier Paolo
Citterio, Elisabetta
The many faces of ubiquitinated histone H2A: insights from the DUBs
title The many faces of ubiquitinated histone H2A: insights from the DUBs
title_full The many faces of ubiquitinated histone H2A: insights from the DUBs
title_fullStr The many faces of ubiquitinated histone H2A: insights from the DUBs
title_full_unstemmed The many faces of ubiquitinated histone H2A: insights from the DUBs
title_short The many faces of ubiquitinated histone H2A: insights from the DUBs
title_sort many faces of ubiquitinated histone h2a: insights from the dubs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373781/
https://www.ncbi.nlm.nih.gov/pubmed/18430235
http://dx.doi.org/10.1186/1747-1028-3-8
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