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DNA methylation dynamics in muscle development and disease

DNA methylation is an essential epigenetic modification for mammalian development and is crucial for the establishment and maintenance of cellular identity. Traditionally, DNA methylation has been considered as a permanent repressive epigenetic mark. However, the application of genome-wide approache...

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Detalles Bibliográficos
Autores principales: Carrió, Elvira, Suelves, Mònica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350440/
https://www.ncbi.nlm.nih.gov/pubmed/25798107
http://dx.doi.org/10.3389/fnagi.2015.00019
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author Carrió, Elvira
Suelves, Mònica
author_facet Carrió, Elvira
Suelves, Mònica
author_sort Carrió, Elvira
collection PubMed
description DNA methylation is an essential epigenetic modification for mammalian development and is crucial for the establishment and maintenance of cellular identity. Traditionally, DNA methylation has been considered as a permanent repressive epigenetic mark. However, the application of genome-wide approaches has allowed the analysis of DNA methylation in different genomic contexts revealing a more dynamic regulation than originally thought, since active DNA methylation and demethylation occur during cellular differentiation and tissue specification. Satellite cells are the primary stem cells in adult skeletal muscle and are responsible for postnatal muscle growth, hypertrophy, and muscle regeneration. This review outlines the published data regarding DNA methylation changes along the skeletal muscle program, in both physiological and pathological conditions, to better understand the epigenetic mechanisms that control myogenesis.
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spelling pubmed-43504402015-03-20 DNA methylation dynamics in muscle development and disease Carrió, Elvira Suelves, Mònica Front Aging Neurosci Neuroscience DNA methylation is an essential epigenetic modification for mammalian development and is crucial for the establishment and maintenance of cellular identity. Traditionally, DNA methylation has been considered as a permanent repressive epigenetic mark. However, the application of genome-wide approaches has allowed the analysis of DNA methylation in different genomic contexts revealing a more dynamic regulation than originally thought, since active DNA methylation and demethylation occur during cellular differentiation and tissue specification. Satellite cells are the primary stem cells in adult skeletal muscle and are responsible for postnatal muscle growth, hypertrophy, and muscle regeneration. This review outlines the published data regarding DNA methylation changes along the skeletal muscle program, in both physiological and pathological conditions, to better understand the epigenetic mechanisms that control myogenesis. Frontiers Media S.A. 2015-03-05 /pmc/articles/PMC4350440/ /pubmed/25798107 http://dx.doi.org/10.3389/fnagi.2015.00019 Text en Copyright © 2015 Carrió and Suelves. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Carrió, Elvira
Suelves, Mònica
DNA methylation dynamics in muscle development and disease
title DNA methylation dynamics in muscle development and disease
title_full DNA methylation dynamics in muscle development and disease
title_fullStr DNA methylation dynamics in muscle development and disease
title_full_unstemmed DNA methylation dynamics in muscle development and disease
title_short DNA methylation dynamics in muscle development and disease
title_sort dna methylation dynamics in muscle development and disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350440/
https://www.ncbi.nlm.nih.gov/pubmed/25798107
http://dx.doi.org/10.3389/fnagi.2015.00019
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