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.

Highlights

  • In mammals, caloric restriction consistently results in extended lifespan

  • We found that DNA methylation drifts with age in an analogous manner in three mammalian species and that the rate of drift generally correlates with lifespan (Figs. 1, 3)

  • Changes in DNA methylation occur during the aging process in mammals, and this age-related change in DNA methylation is accelerated in tumorigenesis

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Summary

Introduction

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. 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. The effects of caloric restriction on DNA methylation were detectable across different tissues and correlated with gene expression. CR prolongs lifespan in most mouse strains examined[2] This phenomenon has been extended to primates in a long-term experiment showing increased survival and reduction of age-related diseases including diabetes, cancer, cardiovascular disease, and brain atrophy in CR monkeys (rhesus macaques)[3]. Age-related DNA methylation drift is accelerated in age-related diseases including cancers, diabetes, and chronic inflammation[19,20,21,22,23,24]

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