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RESEARCH PAPER / 2024-12-22

An epigenetic clock for Xenopus tropicalis reveals age-associated sites enriched in H4K20me3-marked heterochromatin

Bennett, R., Morselli, M., Peshkin, L., Pellegrini, M.

Department of Molecular, Cell and Developmental Biology, University of California Los Angeles, Los Angeles, CA, USA · biorxiv

Abstract

DNA methylation clocks have been widely used for accurate age prediction, but most studies have been carried out on mammals. Here we present a clock for the aquatic frog Xenopus tropicalis, a widely used model organism in developmental biology and genomics. The clock, trained on targeted bisulfite sequencing data, achieved a cross-validation median absolute error of 0.70 years. To construct the clock, we collected DNA methylation data from 192 frogs at genomic regions containing CpG sites previously shown to have age-associated methylation in Xenopus. We found that CpG sites with methylation levels significantly increasing or decreasing with age are enriched in heterochromatic regions marked with H4K20me3 and H3K9me3. CpG sites with positively age-associated methylation levels are enriched in bivalent chromatin and gene bodies with H3K36me3, and tend to be proximal to lowly expressed genes. These epigenetic features of aging are similar to those found in mammals, suggesting evolutionary conservation of epigenetic aging mechanisms. Our clock enables future aging biology experiments that leverage the unique properties of amphibians.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper presents a novel epigenetic clock for Xenopus tropicalis, which is relevant to aging research as it explores the mechanisms of aging through DNA methylation and epigenetic changes. However, while it contributes to the understanding of aging in a model organism, the findings are primarily incremental and do not directly address the root causes of aging or lifespan extension in a significant way. The implications for broader aging biology are limited, thus the impact score reflects a solid but not groundbreaking contribution.

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