Stress responses and dynamic equilibrium: key determinants of ageing in the Caenorhabditis elegans clk-1 mutant

Abstract Systems biology offers valuable insights into ageing by integrating experimental data with mathematical models and bioinformatics tools. Long-lived mutants of Caenorhabditis elegans, particularly clk-1, have provided extensive data on the ageing mechanisms. The clk-1 gene, which encodes a ubiquitin precursor, shows a pleiotropic phenotype characterized by slow behaviour, high mitochondrial reactive oxygen species levels, autophagy and metabolic changes. However, the link between these changes and lifespan extension remains unclear. Using a Boolean network, we modelled genetic interactions and derived differential equations for a continuous approach. Our results highlight that aak-2 (AMPK) is crucial for clk-1 lifespan extension owing to its role in stress-response regulation. We introduced a health index based on the attrition of neuromuscular behaviours to assess the health of various strains. Our findings suggest that while stress responses may enhance lifespan, overall health is determined by the extent of the damage.

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Publication Details

Journal
Royal Society Open Science
Published
2026-08-26
DOI
https://doi.org/10.1098/rsos.251736
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
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article

Stress responses and dynamic equilibrium: key determinants of ageing in the Caenorhabditis elegans clk-1 mutant

Roberto Álvarez-Martínez, Fausto Arellano‐Carbajal, Etzel Garrido, Jose Carracedo-Gonzalez
Royal Society Open Science
Genetics, Aging, and Longevity in Model Organisms
article

Stress responses and dynamic equilibrium: key determinants of ageing in the Caenorhabditis elegans clk-1 mutant

Roberto Álvarez-Martínez, Fausto Arellano‐Carbajal, Etzel Garrido, Jose Carracedo-Gonzalez
article en

Abstract

Abstract Systems biology offers valuable insights into ageing by integrating experimental data with mathematical models and bioinformatics tools. Long-lived mutants of Caenorhabditis elegans, particularly clk-1, have provided extensive data on the ageing mechanisms. The clk-1 gene, which encodes a ubiquitin precursor, shows a pleiotropic phenotype characterized by slow behaviour, high mitochondrial reactive oxygen species levels, autophagy and metabolic changes. However, the link between these changes and lifespan extension remains unclear. Using a Boolean network, we modelled genetic interactions and derived differential equations for a continuous approach. Our results highlight that aak-2 (AMPK) is crucial for clk-1 lifespan extension owing to its role in stress-response regulation. We introduced a health index based on the attrition of neuromuscular behaviours to assess the health of various strains. Our findings suggest that while stress responses may enhance lifespan, overall health is determined by the extent of the damage.

Royal Society Open ScienceVol. 13(8)
Autonomous University of Queretaro (MX)
Zero hunger
Openalex Percentile: Top 14%
Genetics, Aging, and Longevity in Model Organisms
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