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Caloric restriction delays age-related methylation drift

In mammals, caloric restriction consistently results in extended lifespan. Epigenetic information encoded by DNA methylation is tightly regulated, but shows a striking drift associated with age that includes both gains and losses of DNA methylation at various sites. Here, we report that epigenetic d...

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Autores principales: Maegawa, Shinji, Lu, Yue, Tahara, Tomomitsu, Lee, Justin T., Madzo, Jozef, Liang, Shoudan, Jelinek, Jaroslav, Colman, Ricki J., Issa, Jean-Pierre J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599616/
https://www.ncbi.nlm.nih.gov/pubmed/28912502
http://dx.doi.org/10.1038/s41467-017-00607-3
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author Maegawa, Shinji
Lu, Yue
Tahara, Tomomitsu
Lee, Justin T.
Madzo, Jozef
Liang, Shoudan
Jelinek, Jaroslav
Colman, Ricki J.
Issa, Jean-Pierre J.
author_facet Maegawa, Shinji
Lu, Yue
Tahara, Tomomitsu
Lee, Justin T.
Madzo, Jozef
Liang, Shoudan
Jelinek, Jaroslav
Colman, Ricki J.
Issa, Jean-Pierre J.
author_sort Maegawa, Shinji
collection PubMed
description In mammals, caloric restriction consistently results in extended lifespan. Epigenetic information encoded by DNA methylation is tightly regulated, but shows a striking drift associated with age that includes both gains and losses of DNA methylation at various sites. Here, we report that epigenetic drift is conserved across species and the rate of drift correlates with lifespan when comparing mice, rhesus monkeys, and humans. Twenty-two to 30-year-old rhesus monkeys exposed to 30% caloric restriction since 7–14 years of age showed attenuation of age-related methylation drift compared to ad libitum-fed controls such that their blood methylation age appeared 7 years younger than their chronologic age. Even more pronounced effects were seen in 2.7–3.2-year-old mice exposed to 40% caloric restriction starting at 0.3 years of age. The effects of caloric restriction on DNA methylation were detectable across different tissues and correlated with gene expression. We propose that epigenetic drift is a determinant of lifespan in mammals.
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spelling pubmed-55996162017-09-18 Caloric restriction delays age-related methylation drift Maegawa, Shinji Lu, Yue Tahara, Tomomitsu Lee, Justin T. Madzo, Jozef Liang, Shoudan Jelinek, Jaroslav Colman, Ricki J. Issa, Jean-Pierre J. Nat Commun Article In mammals, caloric restriction consistently results in extended lifespan. Epigenetic information encoded by DNA methylation is tightly regulated, but shows a striking drift associated with age that includes both gains and losses of DNA methylation at various sites. Here, we report that epigenetic drift is conserved across species and the rate of drift correlates with lifespan when comparing mice, rhesus monkeys, and humans. Twenty-two to 30-year-old rhesus monkeys exposed to 30% caloric restriction since 7–14 years of age showed attenuation of age-related methylation drift compared to ad libitum-fed controls such that their blood methylation age appeared 7 years younger than their chronologic age. Even more pronounced effects were seen in 2.7–3.2-year-old mice exposed to 40% caloric restriction starting at 0.3 years of age. The effects of caloric restriction on DNA methylation were detectable across different tissues and correlated with gene expression. We propose that epigenetic drift is a determinant of lifespan in mammals. Nature Publishing Group UK 2017-09-14 /pmc/articles/PMC5599616/ /pubmed/28912502 http://dx.doi.org/10.1038/s41467-017-00607-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Maegawa, Shinji
Lu, Yue
Tahara, Tomomitsu
Lee, Justin T.
Madzo, Jozef
Liang, Shoudan
Jelinek, Jaroslav
Colman, Ricki J.
Issa, Jean-Pierre J.
Caloric restriction delays age-related methylation drift
title Caloric restriction delays age-related methylation drift
title_full Caloric restriction delays age-related methylation drift
title_fullStr Caloric restriction delays age-related methylation drift
title_full_unstemmed Caloric restriction delays age-related methylation drift
title_short Caloric restriction delays age-related methylation drift
title_sort caloric restriction delays age-related methylation drift
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599616/
https://www.ncbi.nlm.nih.gov/pubmed/28912502
http://dx.doi.org/10.1038/s41467-017-00607-3
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