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Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms

Queens of eusocial species live extraordinarily long compared to their workers. So far, it has been argued that these lifespan divergences are readily explained by the classical evolutionary theory of ageing. As workers predominantly perform risky tasks, such as foraging and nest defense, and queens...

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Autores principales: Kreider, Jan J., Pen, Ido, Kramer, Boris H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190452/
https://www.ncbi.nlm.nih.gov/pubmed/34136267
http://dx.doi.org/10.1002/evl3.230
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author Kreider, Jan J.
Pen, Ido
Kramer, Boris H.
author_facet Kreider, Jan J.
Pen, Ido
Kramer, Boris H.
author_sort Kreider, Jan J.
collection PubMed
description Queens of eusocial species live extraordinarily long compared to their workers. So far, it has been argued that these lifespan divergences are readily explained by the classical evolutionary theory of ageing. As workers predominantly perform risky tasks, such as foraging and nest defense, and queens stay in the well‐protected nests, selection against harmful genetic mutations expressed in old age should be weaker in workers than in queens due to caste differences in extrinsic mortality risk, and thus, lead to the evolution of longer queen and shorter worker lifespans. However, these arguments have not been supported by formal models. Here, we present a model for the evolution of caste‐specific ageing in social insects, based on Williams’ antagonistic pleiotropy theory of ageing. In individual‐based simulations, we assume that mutations with antagonistic fitness effects can act within castes, that is, mutations in early life are accompanied by an antagonistic effect acting in later life, or between castes, where antagonistic effects emerge due to caste antagonism or indirect genetic effects between castes. In monogynous social insect species with sterile workers, large lifespan divergences between castes evolved under all different scenarios of antagonistic effects, but regardless of the degree of caste‐specific extrinsic mortality. Mutations with antagonistic fitness effects within castes reduced lifespans of both castes, while mutations with between‐caste antagonistic effects decreased worker lifespans more than queen lifespans, and consequently increased lifespan divergences. Our results challenge the central explanatory role of extrinsic mortality for caste‐specific ageing in eusocial organisms and suggest that antagonistic pleiotropy affects castes differently due to reproductive monopolization by queens, hence, reproductive division of labor. Finally, these findings provide new insights into the evolution of tissue‐specific ageing in multicellular organisms in general.
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spelling pubmed-81904522021-06-15 Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms Kreider, Jan J. Pen, Ido Kramer, Boris H. Evol Lett Letters Queens of eusocial species live extraordinarily long compared to their workers. So far, it has been argued that these lifespan divergences are readily explained by the classical evolutionary theory of ageing. As workers predominantly perform risky tasks, such as foraging and nest defense, and queens stay in the well‐protected nests, selection against harmful genetic mutations expressed in old age should be weaker in workers than in queens due to caste differences in extrinsic mortality risk, and thus, lead to the evolution of longer queen and shorter worker lifespans. However, these arguments have not been supported by formal models. Here, we present a model for the evolution of caste‐specific ageing in social insects, based on Williams’ antagonistic pleiotropy theory of ageing. In individual‐based simulations, we assume that mutations with antagonistic fitness effects can act within castes, that is, mutations in early life are accompanied by an antagonistic effect acting in later life, or between castes, where antagonistic effects emerge due to caste antagonism or indirect genetic effects between castes. In monogynous social insect species with sterile workers, large lifespan divergences between castes evolved under all different scenarios of antagonistic effects, but regardless of the degree of caste‐specific extrinsic mortality. Mutations with antagonistic fitness effects within castes reduced lifespans of both castes, while mutations with between‐caste antagonistic effects decreased worker lifespans more than queen lifespans, and consequently increased lifespan divergences. Our results challenge the central explanatory role of extrinsic mortality for caste‐specific ageing in eusocial organisms and suggest that antagonistic pleiotropy affects castes differently due to reproductive monopolization by queens, hence, reproductive division of labor. Finally, these findings provide new insights into the evolution of tissue‐specific ageing in multicellular organisms in general. John Wiley and Sons Inc. 2021-05-17 /pmc/articles/PMC8190452/ /pubmed/34136267 http://dx.doi.org/10.1002/evl3.230 Text en © 2021 The Authors. Evolution Letters published by Wiley Periodicals LLC on behalf of Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEB). https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters
Kreider, Jan J.
Pen, Ido
Kramer, Boris H.
Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
title Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
title_full Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
title_fullStr Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
title_full_unstemmed Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
title_short Antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
title_sort antagonistic pleiotropy and the evolution of extraordinary lifespans in eusocial organisms
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190452/
https://www.ncbi.nlm.nih.gov/pubmed/34136267
http://dx.doi.org/10.1002/evl3.230
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