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解读衰老甲基化组。

Making sense of the ageing methylome.

作者信息

Seale Kirsten, Horvath Steve, Teschendorff Andrew, Eynon Nir, Voisin Sarah

机构信息

Institute for Health and Sport (iHeS), Victoria University, Footscray, Melbourne, Victoria, Australia.

Department of Human Genetics, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.

出版信息

Nat Rev Genet. 2022 Oct;23(10):585-605. doi: 10.1038/s41576-022-00477-6. Epub 2022 May 2.

Abstract

Over time, the human DNA methylation landscape accrues substantial damage, which has been associated with a broad range of age-related diseases, including cardiovascular disease and cancer. Various age-related DNA methylation changes have been described, including at the level of individual CpGs, such as differential and variable methylation, and at the level of the whole methylome, including entropy and correlation networks. Here, we review these changes in the ageing methylome as well as the statistical tools that can be used to quantify them. We detail the evidence linking DNA methylation to ageing phenotypes and the longevity strategies aimed at altering both DNA methylation patterns and machinery to extend healthspan and lifespan. Lastly, we discuss theories on the mechanistic causes of epigenetic ageing.

摘要

随着时间的推移,人类DNA甲基化图谱会积累大量损伤,这与包括心血管疾病和癌症在内的多种与年龄相关的疾病有关。已经描述了各种与年龄相关的DNA甲基化变化,包括在单个CpG水平上,如差异甲基化和可变甲基化,以及在整个甲基化组水平上,包括熵和相关网络。在这里,我们回顾了衰老甲基化组中的这些变化以及可用于量化它们的统计工具。我们详细阐述了将DNA甲基化与衰老表型联系起来的证据,以及旨在改变DNA甲基化模式和机制以延长健康寿命和寿命的长寿策略。最后,我们讨论了表观遗传衰老机制原因的理论。

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