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Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2

Class I histone deacetylases (HDACs) are cellular enzymes expressed in many tissues and play crucial roles in differentiation, proliferation, and cancer. HDAC1 and HDAC2 in particular are highly homologous proteins that show redundant or specific roles in different cell types or in response to diffe...

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Detalles Bibliográficos
Autores principales: Segré, Chiara V., Chiocca, Susanna
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004424/
https://www.ncbi.nlm.nih.gov/pubmed/21197454
http://dx.doi.org/10.1155/2011/690848
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author Segré, Chiara V.
Chiocca, Susanna
author_facet Segré, Chiara V.
Chiocca, Susanna
author_sort Segré, Chiara V.
collection PubMed
description Class I histone deacetylases (HDACs) are cellular enzymes expressed in many tissues and play crucial roles in differentiation, proliferation, and cancer. HDAC1 and HDAC2 in particular are highly homologous proteins that show redundant or specific roles in different cell types or in response to different stimuli and signaling pathways. The molecular details of this dual regulation are largely unknown. HDAC1 and HDAC2 are not only protein modifiers, but are in turn regulated by post-translational modifications (PTMs): phosphorylation, acetylation, ubiquitination, SUMOylation, nitrosylation, and carbonylation. Some of these PTMs occur and crosstalk specifically on HDAC1 or HDAC2, creating a rational “code” for a differential, context-related regulation. The global comprehension of this PTM code is central for dissecting the role of single HDAC1 and HDAC2 in physiology and pathology.
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spelling pubmed-30044242010-12-30 Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2 Segré, Chiara V. Chiocca, Susanna J Biomed Biotechnol Review Article Class I histone deacetylases (HDACs) are cellular enzymes expressed in many tissues and play crucial roles in differentiation, proliferation, and cancer. HDAC1 and HDAC2 in particular are highly homologous proteins that show redundant or specific roles in different cell types or in response to different stimuli and signaling pathways. The molecular details of this dual regulation are largely unknown. HDAC1 and HDAC2 are not only protein modifiers, but are in turn regulated by post-translational modifications (PTMs): phosphorylation, acetylation, ubiquitination, SUMOylation, nitrosylation, and carbonylation. Some of these PTMs occur and crosstalk specifically on HDAC1 or HDAC2, creating a rational “code” for a differential, context-related regulation. The global comprehension of this PTM code is central for dissecting the role of single HDAC1 and HDAC2 in physiology and pathology. Hindawi Publishing Corporation 2011 2010-12-09 /pmc/articles/PMC3004424/ /pubmed/21197454 http://dx.doi.org/10.1155/2011/690848 Text en Copyright © 2011 C. V. Segré and S. Chiocca. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Segré, Chiara V.
Chiocca, Susanna
Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2
title Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2
title_full Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2
title_fullStr Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2
title_full_unstemmed Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2
title_short Regulating the Regulators: The Post-Translational Code of Class I HDAC1 and HDAC2
title_sort regulating the regulators: the post-translational code of class i hdac1 and hdac2
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004424/
https://www.ncbi.nlm.nih.gov/pubmed/21197454
http://dx.doi.org/10.1155/2011/690848
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