Evidence map›Paper›PMID 26536110›Full record

ArticleNature2015

Sex-dependent dominance at a single locus maintains variation in age at maturity in salmon.

Nicola J Barson, Tutku Aykanat, Kjetil Hindar, Matthew Baranski, Geir H Bolstad, Peder Fiske, Céleste Jacq, Arne J Jensen, Susan E Johnston, Sten Karlsson and 12 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 252 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
252citing papers in PubMed, 1 pooled it
70.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

252 citing papers in PubMed, 1 synthesis or guideline pooled it, 693 citations in OpenAlex.

  1. Pooled it
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  10. Review
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  13. A century of theories of balancing selection.Biological reviews of the Cambridge Philosophical Society · 2026
    Review
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192 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 6 institutions in 3 countries.

Nicola J BarsonCentre for Integrative Genetics (CIGENE), Department of Animal and Aquacultural Sciences, Norwegian University of Life Sciences, NO-1432 Ås, Norway.
Tutku AykanatDepartment of Biology, University of Turku, FI-20014, Finland.
Kjetil HindarNorwegian Institute for Nature Research (NINA), NO-7485 Trondheim, Norway.
Matthew BaranskiNofima - Norwegian Institute of Food, Fisheries and Aquaculture Research, NO-1431 Ås, Norway.
Geir H BolstadNorwegian Institute for Nature Research (NINA), NO-7485 Trondheim, Norway.
Peder FiskeNorwegian Institute for Nature Research (NINA), NO-7485 Trondheim, Norway.
Céleste JacqNofima - Norwegian Institute of Food, Fisheries and Aquaculture Research, NO-1431 Ås, Norway.
Arne J JensenNorwegian Institute for Nature Research (NINA), NO-7485 Trondheim, Norway.
Susan E JohnstonInstitute of Evolutionary Biology, University of Edinburgh, Edinburgh EH9 3FL, UK.
Sten KarlssonNorwegian Institute for Nature Research (NINA), NO-7485 Trondheim, Norway.
Matthew KentCentre for Integrative Genetics (CIGENE), Department of Animal and Aquacultural Sciences, Norwegian University of Life Sciences, NO-1432 Ås, Norway.
Thomas MoenAquaGen, NO-7462 Trondheim, Norway.
Eero NiemeläNatural Resources Institute Finland, Oulu, FI-90014, Finland.
Torfinn NomeCentre for Integrative Genetics (CIGENE), Department of Animal and Aquacultural Sciences, Norwegian University of Life Sciences, NO-1432 Ås, Norway.
Tor F NæsjeNorwegian Institute for Nature Research (NINA), NO-7485 Trondheim, Norway.
Panu OrellNatural Resources Institute Finland, Oulu, FI-90014, Finland.
Atso RomakkaniemiNatural Resources Institute Finland, Oulu, FI-90014, Finland.
Harald SægrovRadgivende Biologer, NO-5003 Bergen, Norway.
Kurt UrdalRadgivende Biologer, NO-5003 Bergen, Norway.
Jaakko ErkinaroNatural Resources Institute Finland, Oulu, FI-90014, Finland.
Sigbjørn LienCentre for Integrative Genetics (CIGENE), Department of Animal and Aquacultural Sciences, Norwegian University of Life Sciences, NO-1432 Ås, Norway.
Craig R PrimmerDepartment of Biology, University of Turku, FI-20014, Finland.
Norwegian Institute for Nature Research · NONorwegian University of Life Sciences · NONofima · NOUniversity of Turku · FIAquaGen (Norway) · NOUniversity of Edinburgh · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Males and females share many traits that have a common genetic basis; however, selection on these traits often differs between the sexes, leading to sexual conflict. Under such sexual antagonism, theory predicts the evolution of genetic architectures that resolve this sexual conflict. Yet, despite intense theoretical and empirical interest, the specific loci underlying sexually antagonistic phenotypes have rarely been identified, limiting our understanding of how sexual conflict impacts genome evolution and the maintenance of genetic diversity. Here we identify a large effect locus controlling age at maturity in Atlantic salmon (Salmo salar), an important fitness trait in which selection favours earlier maturation in males than females, and show it is a clear example of sex-dependent dominance that reduces intralocus sexual conflict and maintains adaptive variation in wild populations. Using high-density single nucleotide polymorphism data across 57 wild populations and whole genome re-sequencing, we find that the vestigial-like family member 3 gene (VGLL3) exhibits sex-dependent dominance in salmon, promoting earlier and later maturation in males and females, respectively. VGLL3, an adiposity regulator associated with size and age at maturity in humans, explained 39% of phenotypic variation, an unexpectedly large proportion for what is usually considered a highly polygenic trait. Such large effects are predicted under balancing selection from either sexually antagonistic or spatially varying selection. Our results provide the first empirical example of dominance reversal allowing greater optimization of phenotypes within each sex, contributing to the resolution of sexual conflict in a major and widespread evolutionary trade-off between age and size at maturity. They also provide key empirical evidence for how variation in reproductive strategies can be maintained over large geographical scales. We anticipate these findings will have a substantial impact on population management in a range of harvested species where trends towards earlier maturation have been observed.

Indexed as

Sex CharacteristicsAgingAnimalsBiological EvolutionBody SizeFemaleFish ProteinsGenetic VariationGenome-Wide Association StudyGrowthHumansMaleModels, BiologicalPhenotypeReproductionSalmo salarFish ProteinsTranscription Factors

Identifiers

PMID26536110
OpenAlexW2140124881

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.