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Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual

The theory that ageing evolves because of competitive resource allocation between the soma and the germline has been challenged by studies showing that somatic maintenance can be improved without impairing reproduction. However, it has been suggested that cost‐free improvement in somatic maintenance...

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Detalles Bibliográficos
Autores principales: Carlsson, Hanne, Ivimey‐Cook, Edward, Duxbury, Elizabeth M. L., Edden, Nathan, Sales, Kris, Maklakov, Alexei A.
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/PMC8484722/
https://www.ncbi.nlm.nih.gov/pubmed/34621540
http://dx.doi.org/10.1002/evl3.254
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author Carlsson, Hanne
Ivimey‐Cook, Edward
Duxbury, Elizabeth M. L.
Edden, Nathan
Sales, Kris
Maklakov, Alexei A.
author_facet Carlsson, Hanne
Ivimey‐Cook, Edward
Duxbury, Elizabeth M. L.
Edden, Nathan
Sales, Kris
Maklakov, Alexei A.
author_sort Carlsson, Hanne
collection PubMed
description The theory that ageing evolves because of competitive resource allocation between the soma and the germline has been challenged by studies showing that somatic maintenance can be improved without impairing reproduction. However, it has been suggested that cost‐free improvement in somatic maintenance is possible only under a narrow range of benign conditions. Here, we show that experimental downregulation of insulin/IGF‐1 signaling (IIS) in C. elegans nematodes, a robustly reproducible life span‐ and health span‐extending treatment, reduces fitness in a complex variable environment when initiated during development but does not reduce fitness when initiated in adulthood. Thus, our results show that the costs and benefits of reduced IIS can be uncoupled when organisms inhabit variable environments, and, therefore, do not provide support for the resource allocation theory. Our findings support the theory that the force of natural selection on gene expression in evolutionarily conserved signaling pathways that shape life‐history traits declines after the onset of reproduction resulting in organismal senescence.
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spelling pubmed-84847222021-10-06 Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual Carlsson, Hanne Ivimey‐Cook, Edward Duxbury, Elizabeth M. L. Edden, Nathan Sales, Kris Maklakov, Alexei A. Evol Lett Letters The theory that ageing evolves because of competitive resource allocation between the soma and the germline has been challenged by studies showing that somatic maintenance can be improved without impairing reproduction. However, it has been suggested that cost‐free improvement in somatic maintenance is possible only under a narrow range of benign conditions. Here, we show that experimental downregulation of insulin/IGF‐1 signaling (IIS) in C. elegans nematodes, a robustly reproducible life span‐ and health span‐extending treatment, reduces fitness in a complex variable environment when initiated during development but does not reduce fitness when initiated in adulthood. Thus, our results show that the costs and benefits of reduced IIS can be uncoupled when organisms inhabit variable environments, and, therefore, do not provide support for the resource allocation theory. Our findings support the theory that the force of natural selection on gene expression in evolutionarily conserved signaling pathways that shape life‐history traits declines after the onset of reproduction resulting in organismal senescence. John Wiley and Sons Inc. 2021-09-08 /pmc/articles/PMC8484722/ /pubmed/34621540 http://dx.doi.org/10.1002/evl3.254 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
Carlsson, Hanne
Ivimey‐Cook, Edward
Duxbury, Elizabeth M. L.
Edden, Nathan
Sales, Kris
Maklakov, Alexei A.
Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual
title Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual
title_full Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual
title_fullStr Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual
title_full_unstemmed Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual
title_short Ageing as “early‐life inertia”: Disentangling life‐history trade‐offs along a lifetime of an individual
title_sort ageing as “early‐life inertia”: disentangling life‐history trade‐offs along a lifetime of an individual
topic Letters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484722/
https://www.ncbi.nlm.nih.gov/pubmed/34621540
http://dx.doi.org/10.1002/evl3.254
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