High social status males experience accelerated epigenetic aging in wild baboons

Author:

Anderson Jordan A1ORCID,Johnston Rachel A1ORCID,Lea Amanda J234ORCID,Campos Fernando A25ORCID,Voyles Tawni N1,Akinyi Mercy Y6ORCID,Alberts Susan C12ORCID,Archie Elizabeth A7ORCID,Tung Jenny1289ORCID

Affiliation:

1. Department of Evolutionary Anthropology, Duke University, Durham, United States

2. Department of Biology, Duke University, Durham, United States

3. Lewis-Sigler Institute for Integrative Genomics, Carl Icahn Laboratory, Princeton University, Princeton, United States

4. Department of Ecology and Evolution, Princeton University, Princeton, United States

5. Department of Anthropology, University of Texas at San Antonio, San Antonio, United States

6. Institute of Primate Research, National Museums of Kenya, Nairobi, Kenya

7. Department of Biological Sciences, University of Notre Dame, Notre Dame, United States

8. Duke Population Research Institute, Duke University, Durham, United States

9. Canadian Institute for Advanced Research, Toronto, Canada

Abstract

Aging, for virtually all life, is inescapable. However, within populations, biological aging rates vary. Understanding sources of variation in this process is central to understanding the biodemography of natural populations. We constructed a DNA methylation-based age predictor for an intensively studied wild baboon population in Kenya. Consistent with findings in humans, the resulting ‘epigenetic clock’ closely tracks chronological age, but individuals are predicted to be somewhat older or younger than their known ages. Surprisingly, these deviations are not explained by the strongest predictors of lifespan in this population, early adversity and social integration. Instead, they are best predicted by male dominance rank: high-ranking males are predicted to be older than their true ages, and epigenetic age tracks changes in rank over time. Our results argue that achieving high rank for male baboons – the best predictor of reproductive success – imposes costs consistent with a ‘live fast, die young’ life-history strategy.

Funder

National Science Foundation

National Institutes of Health

Foerster-Bernstein Foundation

North Carolina Biotechnology Center

Center for Population Health and Aging

Canadian Institute for Advanced Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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