A selfish genetic element linked to increased lifespan impacts metabolism in female house mice

J Exp Biol. 2020 Jan 2;223(Pt 1):jeb212704. doi: 10.1242/jeb.212704.

Abstract

Gene drive systems can lead to the evolution of traits that further enhance the transmission of the driving element. In gene drive, one allele is transmitted to offspring at a higher frequency than the homologous allele. This has a range of consequences, which generally include a reduction in fitness of the carrier of the driving allele, making such systems 'selfish'. The t haplotype is one such driver, found in house mice. It is linked to a reduction in litter size in matings among heterozygous animals, but also to increased lifespan in wild females that carry it. Here, we tested whether carrying the t haplotype was associated with altered resting metabolic rate (RMR). We show that females carrying the t haplotype decrease RMR as they increase in size, compared with wild-type females or males of either genotype. Our study elucidates a plausible mechanism by which a selfish genetic element increases lifespan.

Keywords: Lifespan; Meiotic drive; Metabolic rate; t haplotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basal Metabolism*
  • Female
  • Haplotypes / physiology*
  • Longevity / genetics*
  • Male
  • Mice / genetics
  • Mice / physiology*
  • Repetitive Sequences, Nucleic Acid / physiology*
  • Sex Factors

Associated data

  • Dryad/10.5061/dryad.k71rd89