Evidence map›Paper›PMID 26551894›Full record

ArticlePLoS genetics2015

The vgll3 Locus Controls Age at Maturity in Wild and Domesticated Atlantic Salmon (Salmo salar L.) Males.

Fernando Ayllon, Erik Kjærner-Semb, Tomasz Furmanek, Vidar Wennevik, Monica F Solberg, Geir Dahle, Geir Lasse Taranger, Kevin A Glover, Markus Sällman Almén, Carl J Rubin and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
12.6field-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

91 citing papers in PubMed, 217 citations in OpenAlex.

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  10. Population Genetics of Atlantic Salmon (Ecology and evolution · 2025
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  14. A complex mechanism translating variation of a simple genetic architecture into alternative life histories.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Introgression affectsEvolutionary applications · 2024
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31 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

12 authors at 3 institutions in 2 countries.

Fernando AyllonInstitute of Marine Research, Bergen, Norway.
Erik Kjærner-SembInstitute of Marine Research, Bergen, Norway.
Tomasz FurmanekInstitute of Marine Research, Bergen, Norway.
Vidar WennevikInstitute of Marine Research, Bergen, Norway.
Monica F SolbergInstitute of Marine Research, Bergen, Norway.
Geir DahleInstitute of Marine Research, Bergen, Norway.
Geir Lasse TarangerInstitute of Marine Research, Bergen, Norway.
Kevin A GloverInstitute of Marine Research, Bergen, Norway.
Markus Sällman AlménDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Carl J RubinDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Rolf B EdvardsenInstitute of Marine Research, Bergen, Norway.
Anna WargeliusInstitute of Marine Research, Bergen, Norway.
Norwegian Institute of Marine Research · NOUppsala University · SEUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wild and domesticated Atlantic salmon males display large variation for sea age at sexual maturation, which varies between 1-5 years. Previous studies have uncovered a genetic predisposition for variation of age at maturity with moderate heritability, thus suggesting a polygenic or complex nature of this trait. The aim of this study was to identify associated genetic loci, genes and ultimately specific sequence variants conferring sea age at maturity in salmon. We performed a genome wide association study (GWAS) using a pool sequencing approach (20 individuals per river and phenotype) of male salmon returning to rivers as sexually mature either after one sea winter (2009) or three sea winters (2011) in six rivers in Norway. The study revealed one major selective sweep, which covered 76 significant SNPs in which 74 were found in a 370 kb region of chromosome 25. Genotyping other smolt year classes of wild and domesticated salmon confirmed this finding. Genotyping domesticated fish narrowed the haplotype region to four SNPs covering 2386 bp, containing the vgll3 gene, including two missense mutations explaining 33-36% phenotypic variation. A single locus was found to have a highly significant role in governing sea age at maturation in this species. The SNPs identified may be both used as markers to guide breeding for late maturity in salmon aquaculture and in monitoring programs of wild salmon. Interestingly, a SNP in proximity of the VGLL3 gene in humans (Homo sapiens), has previously been linked to age at puberty suggesting a conserved mechanism for timing of puberty in vertebrates.

Indexed as

AgingAnimalsGenome-Wide Association StudyPolymorphism, Single NucleotideSalmo salarTranscription FactorsTranscription Factors

Identifiers

PMID26551894
PMCPMC4638356
OpenAlexW2329004962

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.