Cargando…
High social status males experience accelerated epigenetic aging in wild baboons
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 st...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087445/ https://www.ncbi.nlm.nih.gov/pubmed/33821798 http://dx.doi.org/10.7554/eLife.66128 |
_version_ | 1783686664014528512 |
---|---|
author | Anderson, Jordan A Johnston, Rachel A Lea, Amanda J Campos, Fernando A Voyles, Tawni N Akinyi, Mercy Y Alberts, Susan C Archie, Elizabeth A Tung, Jenny |
author_facet | Anderson, Jordan A Johnston, Rachel A Lea, Amanda J Campos, Fernando A Voyles, Tawni N Akinyi, Mercy Y Alberts, Susan C Archie, Elizabeth A Tung, Jenny |
author_sort | Anderson, Jordan A |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8087445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80874452021-05-03 High social status males experience accelerated epigenetic aging in wild baboons Anderson, Jordan A Johnston, Rachel A Lea, Amanda J Campos, Fernando A Voyles, Tawni N Akinyi, Mercy Y Alberts, Susan C Archie, Elizabeth A Tung, Jenny eLife Evolutionary Biology 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. eLife Sciences Publications, Ltd 2021-04-06 /pmc/articles/PMC8087445/ /pubmed/33821798 http://dx.doi.org/10.7554/eLife.66128 Text en © 2021, Anderson et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Anderson, Jordan A Johnston, Rachel A Lea, Amanda J Campos, Fernando A Voyles, Tawni N Akinyi, Mercy Y Alberts, Susan C Archie, Elizabeth A Tung, Jenny High social status males experience accelerated epigenetic aging in wild baboons |
title | High social status males experience accelerated epigenetic aging in wild baboons |
title_full | High social status males experience accelerated epigenetic aging in wild baboons |
title_fullStr | High social status males experience accelerated epigenetic aging in wild baboons |
title_full_unstemmed | High social status males experience accelerated epigenetic aging in wild baboons |
title_short | High social status males experience accelerated epigenetic aging in wild baboons |
title_sort | high social status males experience accelerated epigenetic aging in wild baboons |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087445/ https://www.ncbi.nlm.nih.gov/pubmed/33821798 http://dx.doi.org/10.7554/eLife.66128 |
work_keys_str_mv | AT andersonjordana highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT johnstonrachela highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT leaamandaj highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT camposfernandoa highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT voylestawnin highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT akinyimercyy highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT albertssusanc highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT archieelizabetha highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons AT tungjenny highsocialstatusmalesexperienceacceleratedepigeneticaginginwildbaboons |