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Aging Cell· 2026Q1

Mutation Accumulation Underpins Evolution of Lifespan Extension by Dietary Restriction

Sara D. Irish, A Jordan Kimberley, Simone Immler, Jacob A. Moorad et al.

Short summary

Dietary restriction (DR) extends lifespan in C. elegans, but this benefit evolves not from resource reallocation but from mutation accumulation driven by suppressed fertility in poor environments.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Dietary restriction (DR) extends lifespan in C. elegans, independent of resource reallocation from reproduction.
  • Experimentally increasing reproduction under DR did not negate its survival benefits.
  • Fertility suppression under DR is a restraint from reproducing in a poor environment.
  • Lifespan extension under DR evolves via mutation accumulation, driven by suppressed fertility increasing selection against mortality.

AI-generated from the title and abstract; the full text is not read.

Abstract

Dietary restriction (DR) extends lifespan in animals and plants, but its evolutionary causes are elusive. The prevailing explanation is that DR prolongs life by shifting resources from reproduction to somatic maintenance. To test this idea in Caenorhabditis elegans we developed an experimental paradigm that tricks nematodes into increasing their reproductive effort under DR via food odour cues. Although DR improved survival, experimentally increased reproduction under DR did not reduce either immediate or long-term survival benefits, thus contradicting resource allocation theory. Our results suggest that much of the fertility suppression under DR reflects restraint from reproducing in a poor environment. We developed a model based on Hamilton's forces of selection showing that lifespan extension under DR can evolve because DR suppresses fertility, thereby directly increasing selection against mortality in that environment. Our novel analytical approach demonstrates that DR-driven lifespan extension can evolve under a broader range of conditions than previously anticipated, such as a relaxed need for physiological or genetic trade-offs. Instead, we show how reduced survival on plentiful food can evolve via mutation accumulation.

The authors' abstract, as published at the source. Aging Cell, 2026 · DOI ↗

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AgingBiochemistry, Genetics and Molecular Biology