Vis enkel innførsel

dc.contributor.authorSinclair-Waters, Marion
dc.contributor.authorØdegård, Jørgen
dc.contributor.authorKorsvoll, Sven Arild
dc.contributor.authorMoen, Thomas
dc.contributor.authorLien, Sigbjørn
dc.contributor.authorPrimmer, Craig R.
dc.contributor.authorBarson, Nicola
dc.date.accessioned2020-11-11T08:45:55Z
dc.date.available2020-11-11T08:45:55Z
dc.date.created2020-10-21T12:42:22Z
dc.date.issued2020
dc.identifier.citationGenetics Selection Evolution. 2020, 52 (1), 1-11.en_US
dc.identifier.issn0999-193X
dc.identifier.urihttps://hdl.handle.net/11250/2687260
dc.description.abstractBackground. Understanding genetic architecture is essential for determining how traits will change in response to evolutionary processes such as selection, genetic drift and/or gene flow. In Atlantic salmon, age at maturity is an important life history trait that affects factors such as survival, reproductive success, and growth. Furthermore, age at maturity can seriously impact aquaculture production. Therefore, characterizing the genetic architecture that underlies variation in age at maturity is of key interest. Results. Here, we refine our understanding of the genetic architecture for age at maturity of male Atlantic salmon using a genome-wide association study of 11,166 males from a single aquaculture strain, using imputed genotypes at 512,397 single nucleotide polymorphisms (SNPs). All individuals were genotyped with a 50K SNP array and imputed to higher density using parents genotyped with a 930K SNP array and pedigree information. We found significant association signals on 28 of 29 chromosomes (P-values: 8.7 × 10−133–9.8 × 10−8), including two very strong signals spanning the six6 and vgll3 gene regions on chromosomes 9 and 25, respectively. Furthermore, we identified 116 independent signals that tagged 120 candidate genes with varying effect sizes. Five of the candidate genes found here were previously associated with age at maturity in other vertebrates, including humans. Discussion. These results reveal a mixed architecture of large-effect loci and a polygenic component that consists of multiple smaller-effect loci, suggesting a more complex genetic architecture of Atlantic salmon age at maturity than previously thought. This more complex architecture will have implications for selection on this key trait in aquaculture and for management of wild salmon populations.en_US
dc.language.isoengen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleBeyond large-effect loci: Large-scale GWAS reveals a mixed large-effect and polygenic architecture for age at maturity of Atlantic salmonen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-11en_US
dc.source.volume52en_US
dc.source.journalGenetics Selection Evolutionen_US
dc.source.issue1en_US
dc.identifier.doi10.1186/s12711-020-0529-8
dc.identifier.cristin1841177
dc.relation.projectNorges forskningsråd: 254852en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel

Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Med mindre annet er angitt, så er denne innførselen lisensiert som Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal