The evolution of CpG density and lifespan in conserved primate and mammalian promoters

Gene promoters are evolutionarily conserved across holozoans and enriched in CpG sites, the target for DNA methylation. As animals age, the epigenetic pattern of DNA methylation degrades, with highly methylated CpG sites gradually becoming demethylated while CpG islands increase in methylation. Acro...

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Bibliographic Details
Published in:Aging (Albany, NY.) NY.), 2018-04, Vol.10 (4), p.561-572
Main Authors: McLain, Adam T, Faulk, Christopher
Format: Article
Language:English
Subjects:
Animals
Biological Evolution
CpG Islands - genetics
DNA Methylation - genetics
Humans
Longevity - genetics
Mammals - genetics
Phylogeny
Primates - genetics
Promoter Regions, Genetic - genetics
Research Paper
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Summary:Gene promoters are evolutionarily conserved across holozoans and enriched in CpG sites, the target for DNA methylation. As animals age, the epigenetic pattern of DNA methylation degrades, with highly methylated CpG sites gradually becoming demethylated while CpG islands increase in methylation. Across vertebrates, aging is a trait that varies among species. We used this variation to determine whether promoter CpG density correlates with species' maximum lifespan. Human promoter sequences were used to identify conserved regions in 131 mammals and a subset of 28 primate genomes. We identified approximately 1000 gene promoters (5% of the total), that significantly correlated CpG density with lifespan. The correlations were performed via the phylogenetic least squares method to account for trait similarity by common descent using phylogenetic branch lengths. Gene set enrichment analysis revealed no significantly enriched pathways or processes, consistent with the hypothesis that aging is not under positive selection. However, within both mammals and primates, 95% of the promoters showed a positive correlation between increasing CpG density and species lifespan, and two thirds were shared between the primate subset and mammalian datasets. Thus, these genes may require greater buffering capacity against age-related dysregulation of DNA methylation in longer-lived species.
ISSN:1945-4589
1945-4589
DOI:10.18632/aging.101413