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lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy
Skeletal muscle exhibits remarkable plasticity in its ability to modulate its mass in response to the physiologic changes associated with functional use, systemic disease, and aging. Although a gradual loss of muscle mass normally occurs with advancing age, its increasingly rapid progression results...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674882/ https://www.ncbi.nlm.nih.gov/pubmed/28855249 http://dx.doi.org/10.1083/jcb.201612100 |
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author | Neppl, Ronald L Wu, Chia-Ling Walsh, Kenneth |
author_facet | Neppl, Ronald L Wu, Chia-Ling Walsh, Kenneth |
author_sort | Neppl, Ronald L |
collection | PubMed |
description | Skeletal muscle exhibits remarkable plasticity in its ability to modulate its mass in response to the physiologic changes associated with functional use, systemic disease, and aging. Although a gradual loss of muscle mass normally occurs with advancing age, its increasingly rapid progression results in sarcopenia in a subset of individuals. The identities of muscle-enriched, long noncoding RNAs that regulate this process are unknown. Here, we identify a long noncoding RNA, named Chronos, whose expression in muscle is positively regulated with advancing age and negatively regulated during Akt1-mediated growth. Inhibition of Chronos induces myofiber hypertrophy both in vitro and in vivo, in part, through the epigenetic modulation of Bmp7 signaling. |
format | Online Article Text |
id | pubmed-5674882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56748822018-05-06 lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy Neppl, Ronald L Wu, Chia-Ling Walsh, Kenneth J Cell Biol Research Articles Skeletal muscle exhibits remarkable plasticity in its ability to modulate its mass in response to the physiologic changes associated with functional use, systemic disease, and aging. Although a gradual loss of muscle mass normally occurs with advancing age, its increasingly rapid progression results in sarcopenia in a subset of individuals. The identities of muscle-enriched, long noncoding RNAs that regulate this process are unknown. Here, we identify a long noncoding RNA, named Chronos, whose expression in muscle is positively regulated with advancing age and negatively regulated during Akt1-mediated growth. Inhibition of Chronos induces myofiber hypertrophy both in vitro and in vivo, in part, through the epigenetic modulation of Bmp7 signaling. The Rockefeller University Press 2017-11-06 /pmc/articles/PMC5674882/ /pubmed/28855249 http://dx.doi.org/10.1083/jcb.201612100 Text en © 2017 Neppl et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Neppl, Ronald L Wu, Chia-Ling Walsh, Kenneth lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy |
title | lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy |
title_full | lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy |
title_fullStr | lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy |
title_full_unstemmed | lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy |
title_short | lncRNA Chronos is an aging-induced inhibitor of muscle hypertrophy |
title_sort | lncrna chronos is an aging-induced inhibitor of muscle hypertrophy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674882/ https://www.ncbi.nlm.nih.gov/pubmed/28855249 http://dx.doi.org/10.1083/jcb.201612100 |
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