PLoS Genetics (Sep 2020)

Cis-regulatory differences in isoform expression associate with life history strategy variation in Atlantic salmon.

  • Jukka-Pekka Verta,
  • Paul Vincent Debes,
  • Nikolai Piavchenko,
  • Annukka Ruokolainen,
  • Outi Ovaskainen,
  • Jacqueline Emmanuel Moustakas-Verho,
  • Seija Tillanen,
  • Noora Parre,
  • Tutku Aykanat,
  • Jaakko Erkinaro,
  • Craig Robert Primmer

DOI
https://doi.org/10.1371/journal.pgen.1009055
Journal volume & issue
Vol. 16, no. 9
p. e1009055

Abstract

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A major goal in biology is to understand how evolution shapes variation in individual life histories. Genome-wide association studies have been successful in uncovering genome regions linked with traits underlying life history variation in a range of species. However, lack of functional studies of the discovered genotype-phenotype associations severely restrains our understanding how alternative life history traits evolved and are mediated at the molecular level. Here, we report a cis-regulatory mechanism whereby expression of alternative isoforms of the transcription co-factor vestigial-like 3 (vgll3) associate with variation in a key life history trait, age at maturity, in Atlantic salmon (Salmo salar). Using a common-garden experiment, we first show that vgll3 genotype associates with puberty timing in one-year-old salmon males. By way of temporal sampling of vgll3 expression in ten tissues across the first year of salmon development, we identify a pubertal transition in vgll3 expression where maturation coincided with a 66% reduction in testicular vgll3 expression. The late maturation allele was not only associated with a tendency to delay puberty, but also with expression of a rare transcript isoform of vgll3 pre-puberty. By comparing absolute vgll3 mRNA copies in heterozygotes we show that the expression difference between the early and late maturity alleles is largely cis-regulatory. We propose a model whereby expression of a rare isoform from the late allele shifts the liability of its carriers towards delaying puberty. These results exemplify the potential importance of regulatory differences as a mechanism for the evolution of life history traits.