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热量限制延缓与年龄相关的甲基化漂移。

Caloric restriction delays age-related methylation drift.

机构信息

Fels Institute for Cancer Research & Molecular Biology, Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania, 19140, USA.

Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77030, USA.

出版信息

Nat Commun. 2017 Sep 14;8(1):539. doi: 10.1038/s41467-017-00607-3.

DOI:10.1038/s41467-017-00607-3
PMID:28912502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5599616/
Abstract

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.Caloric restriction has been shown to increase lifespan in mammals. Here, the authors provide evidence that age-related methylation drift correlates with lifespan and that caloric restriction in mice and rhesus monkeys results in attenuation of age-related methylation drift.

摘要

在哺乳动物中,热量限制确实会延长寿命。由 DNA 甲基化编码的表观遗传信息受到严格调控,但随着年龄的增长,会出现明显的漂移,包括在不同位点上的 DNA 甲基化的增加和减少。在这里,我们报告说,表观遗传漂移在物种间是保守的,并且当比较小鼠、恒河猴和人类时,漂移的速度与寿命相关。自 7-14 岁起,22-30 岁的恒河猴接受 30%热量限制,与自由喂养的对照组相比,其与年龄相关的甲基化漂移减弱,以至于它们的血液甲基化年龄比实际年龄年轻 7 岁。在从 0.3 岁开始接受 40%热量限制的 2.7-3.2 岁小鼠中,观察到更为显著的效果。热量限制对 DNA 甲基化的影响可以在不同的组织中检测到,并与基因表达相关。作者提出,表观遗传漂移是哺乳动物寿命的决定因素。热量限制已被证明能延长哺乳动物的寿命。在这里,作者提供了证据表明,与年龄相关的甲基化漂移与寿命相关,并且在小鼠和恒河猴中,热量限制导致与年龄相关的甲基化漂移减弱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/cbfc9af3920c/41467_2017_607_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/cd4ac7013d19/41467_2017_607_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/9fa59e619407/41467_2017_607_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/c6b812924025/41467_2017_607_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/deba83af9e5f/41467_2017_607_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/01175c42ddb0/41467_2017_607_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/cbfc9af3920c/41467_2017_607_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/cd4ac7013d19/41467_2017_607_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/9fa59e619407/41467_2017_607_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/c6b812924025/41467_2017_607_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/deba83af9e5f/41467_2017_607_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/01175c42ddb0/41467_2017_607_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66f8/5599616/cbfc9af3920c/41467_2017_607_Fig6_HTML.jpg

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