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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8484722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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