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Phosphatases in the cellular response to DNA damage

In the last fifteen years, rapid progress has been made in delineating the cellular response to DNA damage. The DNA damage response network is composed of a large number of proteins with different functions that detect and signal the presence of DNA damage in order to coordinate DNA repair with a va...

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Detalles Bibliográficos
Autores principales: Freeman, Alyson K, Monteiro, Alvaro NA
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954851/
https://www.ncbi.nlm.nih.gov/pubmed/20860841
http://dx.doi.org/10.1186/1478-811X-8-27
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author Freeman, Alyson K
Monteiro, Alvaro NA
author_facet Freeman, Alyson K
Monteiro, Alvaro NA
author_sort Freeman, Alyson K
collection PubMed
description In the last fifteen years, rapid progress has been made in delineating the cellular response to DNA damage. The DNA damage response network is composed of a large number of proteins with different functions that detect and signal the presence of DNA damage in order to coordinate DNA repair with a variety of cellular processes, notably cell cycle progression. This signal, which radiates from the chromatin template, is driven primarily by phosphorylation events, mainly on serine and threonine residues. While we have accumulated detailed information about kinases and their substrates our understanding of the role of phosphatases in the DNA damage response is still preliminary. Identifying the phosphatases and their regulation will be instrumental to obtain a complete picture of the dynamics of the DNA damage response. Here we give an overview of the DNA damage response in mammalian cells and then review the data on the role of different phosphatases and discuss their biological relevance.
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spelling pubmed-29548512010-10-15 Phosphatases in the cellular response to DNA damage Freeman, Alyson K Monteiro, Alvaro NA Cell Commun Signal Review In the last fifteen years, rapid progress has been made in delineating the cellular response to DNA damage. The DNA damage response network is composed of a large number of proteins with different functions that detect and signal the presence of DNA damage in order to coordinate DNA repair with a variety of cellular processes, notably cell cycle progression. This signal, which radiates from the chromatin template, is driven primarily by phosphorylation events, mainly on serine and threonine residues. While we have accumulated detailed information about kinases and their substrates our understanding of the role of phosphatases in the DNA damage response is still preliminary. Identifying the phosphatases and their regulation will be instrumental to obtain a complete picture of the dynamics of the DNA damage response. Here we give an overview of the DNA damage response in mammalian cells and then review the data on the role of different phosphatases and discuss their biological relevance. BioMed Central 2010-09-22 /pmc/articles/PMC2954851/ /pubmed/20860841 http://dx.doi.org/10.1186/1478-811X-8-27 Text en Copyright ©2010 Freeman and Monteiro; 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
Freeman, Alyson K
Monteiro, Alvaro NA
Phosphatases in the cellular response to DNA damage
title Phosphatases in the cellular response to DNA damage
title_full Phosphatases in the cellular response to DNA damage
title_fullStr Phosphatases in the cellular response to DNA damage
title_full_unstemmed Phosphatases in the cellular response to DNA damage
title_short Phosphatases in the cellular response to DNA damage
title_sort phosphatases in the cellular response to dna damage
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954851/
https://www.ncbi.nlm.nih.gov/pubmed/20860841
http://dx.doi.org/10.1186/1478-811X-8-27
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