Abstract

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.

Caenorhabditis elegans is used as a model species to investigate ageing, yet has a very high degree of plasticity in lifespan. This study argues that ageing in C. elegans is driven by suicidal reproductive effort, unlike many other organisms.

Details

Title
C. elegans ageing is accelerated by a self-destructive reproductive programme
Author
Kern, Carina C. 1 ; Srivastava, Shivangi 1 ; Ezcurra, Marina 2   VIAFID ORCID Logo  ; Hsiung, Kuei Ching 1 ; Hui, Nancy 1 ; Townsend, StJohn 3 ; Maczik, Dominik 1   VIAFID ORCID Logo  ; Zhang, Bruce 1   VIAFID ORCID Logo  ; Tse, Victoria 1 ; Konstantellos, Viktoras 1 ; Bähler, Jürg 1   VIAFID ORCID Logo  ; Gems, David 1   VIAFID ORCID Logo 

 University College London, Institute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201) 
 University College London, Institute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201); University of Kent, Canterbury, School of Biosciences, Stacey Building, Kent, UK (GRID:grid.9759.2) (ISNI:0000 0001 2232 2818) 
 University College London, Institute of Healthy Ageing, and Research Department of Genetics, Evolution and Environment, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201); The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London, UK (GRID:grid.451388.3) (ISNI:0000 0004 1795 1830) 
Pages
4381
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2840080443
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.