Increased stress in early life epigenetically rewires pathways related to aging and longevity

Olova, Nelly N., Zhou, Tianchi, Boner, Winnie, Gillespie, Robert, Ivimey-Cook, Edward R. ORCID: https://orcid.org/0000-0003-4910-0443, Marioni, Riccardo, Cunningham, Emma J. A., Chandra, Tamir, Little, Tom J., Monaghan, Pat and Dominoni, Davide M. (2026) Increased stress in early life epigenetically rewires pathways related to aging and longevity.

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Abstract

Environmental conditions experienced early in life have profound consequences for vertebrate health, yet the molecular pathways linking developmental stress to aging and reduced lifespan remain poorly understood. Through a novel highly accurate epigenetic clock, developed from RRBS-based blood DNA methylation profiles, we show that experimental lifespan-reducing early-life stress rapidly accelerates epigenetic age in zebra finch chicks (Taeniopygia guttata). Corticosterone-treated 29-day-old chicks share differentially methylated loci with non-treated aged birds and cluster with 6-month-old birds. The transcriptional repressor ZBTB16 emerges as an epigenetically top age-correlated gene and is strongest affected by corticosterone. Elevated developmental corticosterone causes rapid epigenetic remodelling of metabolic pathways well-established in aging and longevity. Our results demonstrate epigenetic rewiring of the aging trajectory through conserved stress-survival mechanisms immediately following elevated early-life stress exposure.

Item Type: Article
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Faculty of Science
Faculty of Science > School of Biological Sciences
Related URLs:
Depositing User: LivePure Connector
Date Deposited: 05 Oct 2026 23:05
Last Modified: 05 Oct 2026 23:05
URI: https://ueaeprints.uea.ac.uk/id/eprint/104730
DOI: 10.64898/2026.09.30.755600

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