The rate of epigenetic drift scales with maximum lifespan across mammals

Abstract Epigenetic drift or “disorder” increases across the mouse lifespan and is suggested to underlie epigenetic clock signals. While the role of epigenetic drift in determining maximum lifespan across species has been debated, robust tests of this hypothesis are lacking. Here, we test if epigene...

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Main Authors: Emily M. Bertucci-Richter, Benjamin B. Parrott
Format: Article
Language:English
Published: Nature Portfolio 2023-11-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-023-43417-6
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author Emily M. Bertucci-Richter
Benjamin B. Parrott
author_facet Emily M. Bertucci-Richter
Benjamin B. Parrott
author_sort Emily M. Bertucci-Richter
collection DOAJ
description Abstract Epigenetic drift or “disorder” increases across the mouse lifespan and is suggested to underlie epigenetic clock signals. While the role of epigenetic drift in determining maximum lifespan across species has been debated, robust tests of this hypothesis are lacking. Here, we test if epigenetic disorder at various levels of genomic resolution explains maximum lifespan across four mammal species. We show that epigenetic disorder increases with age in all species and at all levels of genomic resolution tested. The rate of disorder accumulation occurs faster in shorter lived species and corresponds to species adjusted maximum lifespan. While the density of cytosine-phosphate-guanine dinucleotides (“CpGs”) is negatively associated with the rate of age-associated disorder accumulation, it does not fully explain differences across species. Our findings support the hypothesis that the rate of epigenetic drift explains maximum lifespan and provide partial support for the hypothesis that CpG density buffers against epigenetic drift.
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spelling doaj.art-2de6a7075ab4408f86c3a33ecff5b8572023-11-26T13:45:04ZengNature PortfolioNature Communications2041-17232023-11-011411810.1038/s41467-023-43417-6The rate of epigenetic drift scales with maximum lifespan across mammalsEmily M. Bertucci-Richter0Benjamin B. Parrott1Savannah River Ecology Laboratory, University of GeorgiaSavannah River Ecology Laboratory, University of GeorgiaAbstract Epigenetic drift or “disorder” increases across the mouse lifespan and is suggested to underlie epigenetic clock signals. While the role of epigenetic drift in determining maximum lifespan across species has been debated, robust tests of this hypothesis are lacking. Here, we test if epigenetic disorder at various levels of genomic resolution explains maximum lifespan across four mammal species. We show that epigenetic disorder increases with age in all species and at all levels of genomic resolution tested. The rate of disorder accumulation occurs faster in shorter lived species and corresponds to species adjusted maximum lifespan. While the density of cytosine-phosphate-guanine dinucleotides (“CpGs”) is negatively associated with the rate of age-associated disorder accumulation, it does not fully explain differences across species. Our findings support the hypothesis that the rate of epigenetic drift explains maximum lifespan and provide partial support for the hypothesis that CpG density buffers against epigenetic drift.https://doi.org/10.1038/s41467-023-43417-6
spellingShingle Emily M. Bertucci-Richter
Benjamin B. Parrott
The rate of epigenetic drift scales with maximum lifespan across mammals
Nature Communications
title The rate of epigenetic drift scales with maximum lifespan across mammals
title_full The rate of epigenetic drift scales with maximum lifespan across mammals
title_fullStr The rate of epigenetic drift scales with maximum lifespan across mammals
title_full_unstemmed The rate of epigenetic drift scales with maximum lifespan across mammals
title_short The rate of epigenetic drift scales with maximum lifespan across mammals
title_sort rate of epigenetic drift scales with maximum lifespan across mammals
url https://doi.org/10.1038/s41467-023-43417-6
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