Cumulative effects of mutation accumulation on mitochondrial function and fitness

Mitochondrion. 2025 Jan:80:101976. doi: 10.1016/j.mito.2024.101976. Epub 2024 Oct 31.

Abstract

The impact of mutations on the mitochondria deserves specific interest due to the crucial role played by these organelles on numerous cellular functions. This study examines the effects of repeated bottlenecks on mitochondrial function and fitness. Daphnia pulex mutation accumulation lines (MA) lines were maintained for over 120 generations under copper and no copper conditions. Following the MA propagation, Daphnia from MA lines were raised under optimal and high temperatures for two generations before assessing mitochondrial and phenotypic traits. Spontaneous mutation accumulation under copper led to a later age at maturity and lowered fecundity in the MA lines. Mitochondrial respiration was found to be 10% lower in all mutation accumulation (MA) lines as compared to the non-MA control. MtDNA copy number was elevated in MA lines compared to the control under optimal temperature suggesting a compensatory mechanism. Three MA lines propagated under low copper had very low mtDNA copy number and fitness, suggesting mutations might have affected genes involved in mtDNA replication or mitochondrial biogenesis. Overall, our study suggests that mutation accumulation had an impact on life history traits, mtDNA copy number, and mitochondrial respiration. Some phenotypic effects were magnified under high temperatures. MtDNA copy number appears to be an important mitigation factor to allow mitochondria to cope with mutation accumulation up to a certain level beyond which it can no longer compensate.

Keywords: Daphnia; Fitness; Mitochondria; Mitochondria copy number; Mutation accumulation.

MeSH terms

  • Animals
  • Copper / metabolism
  • DNA Copy Number Variations
  • DNA, Mitochondrial* / genetics
  • Daphnia* / genetics
  • Daphnia* / physiology
  • Genetic Fitness
  • Mitochondria* / genetics
  • Mitochondria* / metabolism
  • Mutation
  • Mutation Accumulation*

Substances

  • DNA, Mitochondrial
  • Copper