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Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons

In humans and other hierarchical species, social status is tightly linked to variation in health and fitness-related traits. Experimental manipulations of social status in female rhesus macaques suggest that this relationship is partially explained by status effects on immune gene regulation. Howeve...

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Autores principales: Lea, Amanda J., Akinyi, Mercy Y., Nyakundi, Ruth, Mareri, Peter, Nyundo, Fred, Kariuki, Thomas, Alberts, Susan C., Archie, Elizabeth A., Tung, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310778/
https://www.ncbi.nlm.nih.gov/pubmed/30538194
http://dx.doi.org/10.1073/pnas.1811967115
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author Lea, Amanda J.
Akinyi, Mercy Y.
Nyakundi, Ruth
Mareri, Peter
Nyundo, Fred
Kariuki, Thomas
Alberts, Susan C.
Archie, Elizabeth A.
Tung, Jenny
author_facet Lea, Amanda J.
Akinyi, Mercy Y.
Nyakundi, Ruth
Mareri, Peter
Nyundo, Fred
Kariuki, Thomas
Alberts, Susan C.
Archie, Elizabeth A.
Tung, Jenny
author_sort Lea, Amanda J.
collection PubMed
description In humans and other hierarchical species, social status is tightly linked to variation in health and fitness-related traits. Experimental manipulations of social status in female rhesus macaques suggest that this relationship is partially explained by status effects on immune gene regulation. However, social hierarchies are established and maintained in different ways across species: While some are based on kin-directed nepotism, others emerge from direct physical competition. We investigated how this variation influences the relationship between social status and immune gene regulation in wild baboons, where hierarchies in males are based on fighting ability but female hierarchies are nepotistic. We measured rank-related variation in gene expression levels in adult baboons of both sexes at baseline and in response to ex vivo stimulation with the bacterial endotoxin lipopolysaccharide (LPS). We identified >2,000 rank-associated genes in males, an order of magnitude more than in females. In males, high status predicted increased expression of genes involved in innate immunity and preferential activation of the NF-κB–mediated proinflammatory pathway, a pattern previously associated with low status in female rhesus macaques. Using Mendelian randomization, we reconcile these observations by demonstrating that high status-associated gene expression patterns are precursors, not consequences, of high social status in males, in support of the idea that physiological condition determines who attains high rank. Together, our work provides a test of the relationship between social status and immune gene regulation in wild primates. It also emphasizes the importance of social context in shaping the relationship between social status and immune function.
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spelling pubmed-63107782019-01-04 Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons Lea, Amanda J. Akinyi, Mercy Y. Nyakundi, Ruth Mareri, Peter Nyundo, Fred Kariuki, Thomas Alberts, Susan C. Archie, Elizabeth A. Tung, Jenny Proc Natl Acad Sci U S A PNAS Plus In humans and other hierarchical species, social status is tightly linked to variation in health and fitness-related traits. Experimental manipulations of social status in female rhesus macaques suggest that this relationship is partially explained by status effects on immune gene regulation. However, social hierarchies are established and maintained in different ways across species: While some are based on kin-directed nepotism, others emerge from direct physical competition. We investigated how this variation influences the relationship between social status and immune gene regulation in wild baboons, where hierarchies in males are based on fighting ability but female hierarchies are nepotistic. We measured rank-related variation in gene expression levels in adult baboons of both sexes at baseline and in response to ex vivo stimulation with the bacterial endotoxin lipopolysaccharide (LPS). We identified >2,000 rank-associated genes in males, an order of magnitude more than in females. In males, high status predicted increased expression of genes involved in innate immunity and preferential activation of the NF-κB–mediated proinflammatory pathway, a pattern previously associated with low status in female rhesus macaques. Using Mendelian randomization, we reconcile these observations by demonstrating that high status-associated gene expression patterns are precursors, not consequences, of high social status in males, in support of the idea that physiological condition determines who attains high rank. Together, our work provides a test of the relationship between social status and immune gene regulation in wild primates. It also emphasizes the importance of social context in shaping the relationship between social status and immune function. National Academy of Sciences 2018-12-26 2018-12-11 /pmc/articles/PMC6310778/ /pubmed/30538194 http://dx.doi.org/10.1073/pnas.1811967115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Lea, Amanda J.
Akinyi, Mercy Y.
Nyakundi, Ruth
Mareri, Peter
Nyundo, Fred
Kariuki, Thomas
Alberts, Susan C.
Archie, Elizabeth A.
Tung, Jenny
Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
title Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
title_full Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
title_fullStr Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
title_full_unstemmed Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
title_short Dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
title_sort dominance rank-associated gene expression is widespread, sex-specific, and a precursor to high social status in wild male baboons
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310778/
https://www.ncbi.nlm.nih.gov/pubmed/30538194
http://dx.doi.org/10.1073/pnas.1811967115
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