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WI-38 senescence is associated with global and site-specific hypomethylation

Cellular senescence plays an important role in the age-dependent functional decline of organs and organ systems, as well as in age-related pathologies, such as cancer. Therefore, a better understanding of its underlying molecular mechanisms is crucial in the search for intervening measures. In this...

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Autores principales: Sidler, Corinne, Woycicki, Rafal, Kovalchuk, Igor, Kovalchuk, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153623/
https://www.ncbi.nlm.nih.gov/pubmed/25063771
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author Sidler, Corinne
Woycicki, Rafal
Kovalchuk, Igor
Kovalchuk, Olga
author_facet Sidler, Corinne
Woycicki, Rafal
Kovalchuk, Igor
Kovalchuk, Olga
author_sort Sidler, Corinne
collection PubMed
description Cellular senescence plays an important role in the age-dependent functional decline of organs and organ systems, as well as in age-related pathologies, such as cancer. Therefore, a better understanding of its underlying molecular mechanisms is crucial in the search for intervening measures. In this study, we considered the role of DNA methylation in senescence. We found that senescence is associated with global DNA hypomethylation, but also involves site-specific DNA hypo- and hypermethylation. In some cases, this differential methylation may affect gene expression and thereby modulate functional processes within cells. However, the majority of the CpG sites that were differentially methylated did not correspond with altered gene expression, suggesting that DNA methylation affects senescence by other means also, such as, for instance, genome stability.
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spelling pubmed-41536232014-09-08 WI-38 senescence is associated with global and site-specific hypomethylation Sidler, Corinne Woycicki, Rafal Kovalchuk, Igor Kovalchuk, Olga Aging (Albany NY) Research Paper Cellular senescence plays an important role in the age-dependent functional decline of organs and organ systems, as well as in age-related pathologies, such as cancer. Therefore, a better understanding of its underlying molecular mechanisms is crucial in the search for intervening measures. In this study, we considered the role of DNA methylation in senescence. We found that senescence is associated with global DNA hypomethylation, but also involves site-specific DNA hypo- and hypermethylation. In some cases, this differential methylation may affect gene expression and thereby modulate functional processes within cells. However, the majority of the CpG sites that were differentially methylated did not correspond with altered gene expression, suggesting that DNA methylation affects senescence by other means also, such as, for instance, genome stability. Impact Journals LLC 2014-07-19 /pmc/articles/PMC4153623/ /pubmed/25063771 Text en Copyright: © 2014 Sidler et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Paper
Sidler, Corinne
Woycicki, Rafal
Kovalchuk, Igor
Kovalchuk, Olga
WI-38 senescence is associated with global and site-specific hypomethylation
title WI-38 senescence is associated with global and site-specific hypomethylation
title_full WI-38 senescence is associated with global and site-specific hypomethylation
title_fullStr WI-38 senescence is associated with global and site-specific hypomethylation
title_full_unstemmed WI-38 senescence is associated with global and site-specific hypomethylation
title_short WI-38 senescence is associated with global and site-specific hypomethylation
title_sort wi-38 senescence is associated with global and site-specific hypomethylation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153623/
https://www.ncbi.nlm.nih.gov/pubmed/25063771
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