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Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing
Adulthood‐only downregulation of insulin/IGF‐1 signaling (IIS), an evolutionarily conserved pathway regulating resource allocation between somatic maintenance and reproduction, increases life span without fecundity cost in the nematode, Caenorhabditis elegans. However, long‐term multigenerational ef...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092551/ https://www.ncbi.nlm.nih.gov/pubmed/36199198 http://dx.doi.org/10.1111/evo.14640 |
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author | Duxbury, Elizabeth M. L. Carlsson, Hanne Sales, Kris Sultanova, Zahida Immler, Simone Chapman, Tracey Maklakov, Alexei A. |
author_facet | Duxbury, Elizabeth M. L. Carlsson, Hanne Sales, Kris Sultanova, Zahida Immler, Simone Chapman, Tracey Maklakov, Alexei A. |
author_sort | Duxbury, Elizabeth M. L. |
collection | PubMed |
description | Adulthood‐only downregulation of insulin/IGF‐1 signaling (IIS), an evolutionarily conserved pathway regulating resource allocation between somatic maintenance and reproduction, increases life span without fecundity cost in the nematode, Caenorhabditis elegans. However, long‐term multigenerational effects of reduced IIS remain unexplored and are proposed to carry costs for offspring quality. To test this hypothesis, we ran a mutation accumulation (MA) experiment and downregulated IIS in half of the 400 MA lines by silencing daf‐2 gene expression using RNA interference (RNAi) across 40 generations. Contrary to the prediction, adulthood‐only daf‐2 RNAi reduced extinction of MA lines both under UV‐induced and spontaneous MA. Fitness of the surviving UV‐induced MA lines was higher under daf‐2 RNAi. Reduced IIS increased intergenerational F1 offspring fitness under UV stress but had no quantifiable transgenerational effects. Functional hrde‐1 was required for the benefits of multigenerational daf‐2 RNAi. Overall, we found net benefit to fitness from multigenerational reduction of IIS and the benefits became more apparent under stress. Because reduced daf‐2 expression during development carries fitness costs, we suggest that our findings are best explained by the developmental theory of ageing, which maintains that the decline in the force of selection with age results in poorly regulated gene expression in adulthood. |
format | Online Article Text |
id | pubmed-10092551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100925512023-04-13 Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing Duxbury, Elizabeth M. L. Carlsson, Hanne Sales, Kris Sultanova, Zahida Immler, Simone Chapman, Tracey Maklakov, Alexei A. Evolution Original Articles Adulthood‐only downregulation of insulin/IGF‐1 signaling (IIS), an evolutionarily conserved pathway regulating resource allocation between somatic maintenance and reproduction, increases life span without fecundity cost in the nematode, Caenorhabditis elegans. However, long‐term multigenerational effects of reduced IIS remain unexplored and are proposed to carry costs for offspring quality. To test this hypothesis, we ran a mutation accumulation (MA) experiment and downregulated IIS in half of the 400 MA lines by silencing daf‐2 gene expression using RNA interference (RNAi) across 40 generations. Contrary to the prediction, adulthood‐only daf‐2 RNAi reduced extinction of MA lines both under UV‐induced and spontaneous MA. Fitness of the surviving UV‐induced MA lines was higher under daf‐2 RNAi. Reduced IIS increased intergenerational F1 offspring fitness under UV stress but had no quantifiable transgenerational effects. Functional hrde‐1 was required for the benefits of multigenerational daf‐2 RNAi. Overall, we found net benefit to fitness from multigenerational reduction of IIS and the benefits became more apparent under stress. Because reduced daf‐2 expression during development carries fitness costs, we suggest that our findings are best explained by the developmental theory of ageing, which maintains that the decline in the force of selection with age results in poorly regulated gene expression in adulthood. John Wiley and Sons Inc. 2022-10-13 2022-12 /pmc/articles/PMC10092551/ /pubmed/36199198 http://dx.doi.org/10.1111/evo.14640 Text en © 2022 The Authors. Evolution published by Wiley Periodicals LLC on behalf of The Society for the Study of Evolution. 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 | Original Articles Duxbury, Elizabeth M. L. Carlsson, Hanne Sales, Kris Sultanova, Zahida Immler, Simone Chapman, Tracey Maklakov, Alexei A. Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing |
title | Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing |
title_full | Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing |
title_fullStr | Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing |
title_full_unstemmed | Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing |
title_short | Multigenerational downregulation of insulin/IGF‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in Caenorhabditis elegans supporting the developmental theory of ageing |
title_sort | multigenerational downregulation of insulin/igf‐1 signaling in adulthood improves lineage survival, reproduction, and fitness in caenorhabditis elegans supporting the developmental theory of ageing |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092551/ https://www.ncbi.nlm.nih.gov/pubmed/36199198 http://dx.doi.org/10.1111/evo.14640 |
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