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Talking to chromatin: post-translational modulation of polycomb group function

Polycomb Group proteins are important epigenetic regulators of gene expression. Epigenetic control by polycomb Group proteins involves intrinsic as well as associated enzymatic activities. Polycomb target genes change with cellular context, lineage commitment and differentiation status, revealing dy...

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Detalles Bibliográficos
Autores principales: Niessen, Hanneke EC, Demmers, Jeroen A, Voncken, Jan Willem
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745409/
https://www.ncbi.nlm.nih.gov/pubmed/19723311
http://dx.doi.org/10.1186/1756-8935-2-10
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author Niessen, Hanneke EC
Demmers, Jeroen A
Voncken, Jan Willem
author_facet Niessen, Hanneke EC
Demmers, Jeroen A
Voncken, Jan Willem
author_sort Niessen, Hanneke EC
collection PubMed
description Polycomb Group proteins are important epigenetic regulators of gene expression. Epigenetic control by polycomb Group proteins involves intrinsic as well as associated enzymatic activities. Polycomb target genes change with cellular context, lineage commitment and differentiation status, revealing dynamic regulation of polycomb function. It is currently unclear how this dynamic modulation is controlled and how signaling affects polycomb-mediated epigenetic processes at the molecular level. Experimental evidence on regulation of polycomb function by post-translational mechanisms is steadily emerging: Polycomb Group proteins are targeted for ubiquitylation, sumoylation and phosphorylation. In addition, specific Polycomb Group proteins modify other (chromatin) associated proteins via similar post-translational modifications. Such modifications affect protein function by affecting protein stability, protein-protein interactions and enzymatic activities. Here, we review current insights in covalent modification of Polycomb Group proteins in the context of protein function and present a tentative view of integrated signaling to chromatin in the context of phosphorylation. Clearly, the available literature reveals just the tip of the iceberg, and exact molecular mechanisms in, and the biological relevance of post-translational regulation of polycomb function await further elucidation. Our understanding of causes and consequences of post-translational modification of polycomb proteins will gain significantly from in vivo validation experiments. Impaired polycomb function has important repercussions for stem cell function, development and disease. Ultimately, increased understanding of signaling to chromatin and the mechanisms involved in epigenetic remodeling will contribute to the development of therapeutic interventions in cell fate decisions in development and disease.
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spelling pubmed-27454092009-09-17 Talking to chromatin: post-translational modulation of polycomb group function Niessen, Hanneke EC Demmers, Jeroen A Voncken, Jan Willem Epigenetics Chromatin Review Polycomb Group proteins are important epigenetic regulators of gene expression. Epigenetic control by polycomb Group proteins involves intrinsic as well as associated enzymatic activities. Polycomb target genes change with cellular context, lineage commitment and differentiation status, revealing dynamic regulation of polycomb function. It is currently unclear how this dynamic modulation is controlled and how signaling affects polycomb-mediated epigenetic processes at the molecular level. Experimental evidence on regulation of polycomb function by post-translational mechanisms is steadily emerging: Polycomb Group proteins are targeted for ubiquitylation, sumoylation and phosphorylation. In addition, specific Polycomb Group proteins modify other (chromatin) associated proteins via similar post-translational modifications. Such modifications affect protein function by affecting protein stability, protein-protein interactions and enzymatic activities. Here, we review current insights in covalent modification of Polycomb Group proteins in the context of protein function and present a tentative view of integrated signaling to chromatin in the context of phosphorylation. Clearly, the available literature reveals just the tip of the iceberg, and exact molecular mechanisms in, and the biological relevance of post-translational regulation of polycomb function await further elucidation. Our understanding of causes and consequences of post-translational modification of polycomb proteins will gain significantly from in vivo validation experiments. Impaired polycomb function has important repercussions for stem cell function, development and disease. Ultimately, increased understanding of signaling to chromatin and the mechanisms involved in epigenetic remodeling will contribute to the development of therapeutic interventions in cell fate decisions in development and disease. BioMed Central 2009-09-01 /pmc/articles/PMC2745409/ /pubmed/19723311 http://dx.doi.org/10.1186/1756-8935-2-10 Text en Copyright © 2009 Niessen 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
Niessen, Hanneke EC
Demmers, Jeroen A
Voncken, Jan Willem
Talking to chromatin: post-translational modulation of polycomb group function
title Talking to chromatin: post-translational modulation of polycomb group function
title_full Talking to chromatin: post-translational modulation of polycomb group function
title_fullStr Talking to chromatin: post-translational modulation of polycomb group function
title_full_unstemmed Talking to chromatin: post-translational modulation of polycomb group function
title_short Talking to chromatin: post-translational modulation of polycomb group function
title_sort talking to chromatin: post-translational modulation of polycomb group function
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2745409/
https://www.ncbi.nlm.nih.gov/pubmed/19723311
http://dx.doi.org/10.1186/1756-8935-2-10
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