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C. elegans ageing is accelerated by a self-destructive reproductive programme

In post-reproductive C. elegans, destructive somatic biomass repurposing supports production of yolk which, it was recently shown, is vented and can serve as a foodstuff for larval progeny. This is reminiscent of the suicidal reproductive effort (reproductive death) typical of semelparous organisms...

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Autores principales: Kern, Carina C., Srivastava, Shivangi, Ezcurra, Marina, Hsiung, Kuei Ching, Hui, Nancy, Townsend, StJohn, Maczik, Dominik, Zhang, Bruce, Tse, Victoria, Konstantellos, Viktoras, Bähler, Jürg, Gems, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359416/
https://www.ncbi.nlm.nih.gov/pubmed/37474586
http://dx.doi.org/10.1038/s41467-023-40088-1
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author Kern, Carina C.
Srivastava, Shivangi
Ezcurra, Marina
Hsiung, Kuei Ching
Hui, Nancy
Townsend, StJohn
Maczik, Dominik
Zhang, Bruce
Tse, Victoria
Konstantellos, Viktoras
Bähler, Jürg
Gems, David
author_facet Kern, Carina C.
Srivastava, Shivangi
Ezcurra, Marina
Hsiung, Kuei Ching
Hui, Nancy
Townsend, StJohn
Maczik, Dominik
Zhang, Bruce
Tse, Victoria
Konstantellos, Viktoras
Bähler, Jürg
Gems, David
author_sort Kern, Carina C.
collection PubMed
description In post-reproductive C. elegans, destructive somatic biomass repurposing supports production of yolk which, it was recently shown, is vented and can serve as a foodstuff for larval progeny. This is reminiscent of the suicidal reproductive effort (reproductive death) typical of semelparous organisms such as Pacific salmon. To explore the possibility that C. elegans exhibits reproductive death, we have compared sibling species pairs of the genera Caenorhabditis and Pristionchus with hermaphrodites and females. We report that yolk venting and constitutive, early pathology involving major anatomical changes occur only in hermaphrodites, which are also shorter lived. Moreover, only in hermaphrodites does germline removal suppress senescent pathology and markedly increase lifespan. This is consistent with the hypothesis that C. elegans exhibit reproductive death that is suppressed by germline ablation. If correct, this would imply a major difference in the ageing process between C. elegans and most higher organisms, and potentially explain the exceptional plasticity in C. elegans ageing.
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spelling pubmed-103594162023-07-22 C. elegans ageing is accelerated by a self-destructive reproductive programme Kern, Carina C. Srivastava, Shivangi Ezcurra, Marina Hsiung, Kuei Ching Hui, Nancy Townsend, StJohn Maczik, Dominik Zhang, Bruce Tse, Victoria Konstantellos, Viktoras Bähler, Jürg Gems, David Nat Commun Article In post-reproductive C. elegans, destructive somatic biomass repurposing supports production of yolk which, it was recently shown, is vented and can serve as a foodstuff for larval progeny. This is reminiscent of the suicidal reproductive effort (reproductive death) typical of semelparous organisms such as Pacific salmon. To explore the possibility that C. elegans exhibits reproductive death, we have compared sibling species pairs of the genera Caenorhabditis and Pristionchus with hermaphrodites and females. We report that yolk venting and constitutive, early pathology involving major anatomical changes occur only in hermaphrodites, which are also shorter lived. Moreover, only in hermaphrodites does germline removal suppress senescent pathology and markedly increase lifespan. This is consistent with the hypothesis that C. elegans exhibit reproductive death that is suppressed by germline ablation. If correct, this would imply a major difference in the ageing process between C. elegans and most higher organisms, and potentially explain the exceptional plasticity in C. elegans ageing. Nature Publishing Group UK 2023-07-20 /pmc/articles/PMC10359416/ /pubmed/37474586 http://dx.doi.org/10.1038/s41467-023-40088-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kern, Carina C.
Srivastava, Shivangi
Ezcurra, Marina
Hsiung, Kuei Ching
Hui, Nancy
Townsend, StJohn
Maczik, Dominik
Zhang, Bruce
Tse, Victoria
Konstantellos, Viktoras
Bähler, Jürg
Gems, David
C. elegans ageing is accelerated by a self-destructive reproductive programme
title C. elegans ageing is accelerated by a self-destructive reproductive programme
title_full C. elegans ageing is accelerated by a self-destructive reproductive programme
title_fullStr C. elegans ageing is accelerated by a self-destructive reproductive programme
title_full_unstemmed C. elegans ageing is accelerated by a self-destructive reproductive programme
title_short C. elegans ageing is accelerated by a self-destructive reproductive programme
title_sort c. elegans ageing is accelerated by a self-destructive reproductive programme
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359416/
https://www.ncbi.nlm.nih.gov/pubmed/37474586
http://dx.doi.org/10.1038/s41467-023-40088-1
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