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Epigenetic Drift Is a Determinant of Mammalian Lifespan
Changes in Gene Regulation Over Time May Influence Mammal Lifespan
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Abstract
A new DNA methylation clock may be slowed by caloric restriction, correlating with lifespan and healthspan extension.
- The epigenome is not maintained perfectly in somatic animal cells, leading to epigenetic drift, a hallmark of aging.
- DNA methylation clocks have been linked to increasing age and epigenetic drift.
- Caloric restriction appears to slow a specific DNA methylation clock, suggesting a relationship between epigenetic drift and lifespan.
- Genomic editing of DNA methylation homeostatic genes may demonstrate a causal role for DNA methylation in lifespan differences between species.
- Transient methods to erase DNA methylation patterns in somatic cells could potentially reset aging effects, but this remains to be validated.
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