bioRxivMolecular BiologyPreprint
DNA Break-Induced Epigenetic Drift as a Cause of Mammalian Aging
Motoshi HayanoiD, Jae-Hyun YangiD, Michael S. BonkowskiiD, João A. AmorimiD, Jaime M. RossiD, Giuseppe CoppotelliiD, Patrick T. GriffiniD, Yap Ching ChewiD, Wei GuoiD, Xiaojing YangiD, Daniel L. VeraiD, Elias SalfatiiD, Abhirup DasiD, Sachin Thakur, Alice E. KaneiD, Sarah Jayne MitchelliD, Yasuaki Mohri, Emi K. NishimuraiD, Laura R. SchaevitziD, Neha Garg, Ana-Maria BaltaiD, Meghan A. RegoiD, Meredith S. Gregory-KsanderiD, Tatjana JakobsiD, Lei ZhongiD, , David A. SinclairiD
Abstract
There are numerous hallmarks of aging in mammals, but no unifying cause has been identified. In budding yeast, aging is associated with a loss of epigenetic information that occurs in response to genome instability, particularly DNA double-strand breaks (DSBs). Mammals also undergo predictable epigenetic changes with age, including alterations to DNA methylation patterns that serve as epigenetic \"age\" clocks, but what drives these changes is not known. Using a transgenic mouse system called \"ICE\" (for inducible changes to the epigenome), we show that a tissues response to non-mutagenic DSBs reorganizes the epigenome and accelerates physiological, cognitive, and molecular changes normally seen in older mice, including advancement of the epigenetic clock. These findings implicate DSB-induced epigenetic drift as a conserved cause of aging from yeast to mammals.\n\nOne Sentence SummaryDNA breaks induce epigenomic changes that accelerate the aging clock in mammals
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