Cargando…

Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon

Understanding the mechanisms by which populations adapt to their environments is a fundamental aim in biology. However, it remains challenging to identify the genetic basis of traits, provide evidence of genetic changes and quantify phenotypic responses. Age at maturity in Atlantic salmon represents...

Descripción completa

Detalles Bibliográficos
Autores principales: Czorlich, Yann, Aykanat, Tutku, Erkinaro, Jaakko, Orell, Panu, Primmer, Craig Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322654/
https://www.ncbi.nlm.nih.gov/pubmed/30275465
http://dx.doi.org/10.1038/s41559-018-0681-5
_version_ 1783385635412770816
author Czorlich, Yann
Aykanat, Tutku
Erkinaro, Jaakko
Orell, Panu
Primmer, Craig Robert
author_facet Czorlich, Yann
Aykanat, Tutku
Erkinaro, Jaakko
Orell, Panu
Primmer, Craig Robert
author_sort Czorlich, Yann
collection PubMed
description Understanding the mechanisms by which populations adapt to their environments is a fundamental aim in biology. However, it remains challenging to identify the genetic basis of traits, provide evidence of genetic changes and quantify phenotypic responses. Age at maturity in Atlantic salmon represents an ideal trait to study contemporary adaptive evolution as it has been associated with a single locus in the vgll3 region, and has also strongly changed in recent decades. Here, we provide an empirical example of contemporary adaptive evolution of a large effect locus driving contrasting sex-specific evolutionary responses at the phenotypic level. We identified an 18% decrease in the vgll3 allele associated with late maturity (L) in a large and diverse salmon population over 36 years, induced by sex-specific selection during the sea migration. Those genetic changes resulted in a significant evolutionary response in males only, due to sex-specific dominance patterns and vgll3 allelic effects. The vgll3 allelic and dominance effects differed greatly in a second population and were likely to generate different selection and evolutionary patterns. Our study highlights the importance of knowledge of genetic architecture to better understand fitness trait evolution and phenotypic diversity. It also emphasizes the potential role of adaptive evolution in the trend toward earlier maturation observed in numerous Atlantic salmon populations worldwide.
format Online
Article
Text
id pubmed-6322654
institution National Center for Biotechnology Information
language English
publishDate 2018
record_format MEDLINE/PubMed
spelling pubmed-63226542019-04-01 Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon Czorlich, Yann Aykanat, Tutku Erkinaro, Jaakko Orell, Panu Primmer, Craig Robert Nat Ecol Evol Article Understanding the mechanisms by which populations adapt to their environments is a fundamental aim in biology. However, it remains challenging to identify the genetic basis of traits, provide evidence of genetic changes and quantify phenotypic responses. Age at maturity in Atlantic salmon represents an ideal trait to study contemporary adaptive evolution as it has been associated with a single locus in the vgll3 region, and has also strongly changed in recent decades. Here, we provide an empirical example of contemporary adaptive evolution of a large effect locus driving contrasting sex-specific evolutionary responses at the phenotypic level. We identified an 18% decrease in the vgll3 allele associated with late maturity (L) in a large and diverse salmon population over 36 years, induced by sex-specific selection during the sea migration. Those genetic changes resulted in a significant evolutionary response in males only, due to sex-specific dominance patterns and vgll3 allelic effects. The vgll3 allelic and dominance effects differed greatly in a second population and were likely to generate different selection and evolutionary patterns. Our study highlights the importance of knowledge of genetic architecture to better understand fitness trait evolution and phenotypic diversity. It also emphasizes the potential role of adaptive evolution in the trend toward earlier maturation observed in numerous Atlantic salmon populations worldwide. 2018-10-01 2018-11 /pmc/articles/PMC6322654/ /pubmed/30275465 http://dx.doi.org/10.1038/s41559-018-0681-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Czorlich, Yann
Aykanat, Tutku
Erkinaro, Jaakko
Orell, Panu
Primmer, Craig Robert
Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon
title Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon
title_full Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon
title_fullStr Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon
title_full_unstemmed Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon
title_short Rapid sex-specific evolution of age at maturity is shaped by genetic architecture in Atlantic salmon
title_sort rapid sex-specific evolution of age at maturity is shaped by genetic architecture in atlantic salmon
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6322654/
https://www.ncbi.nlm.nih.gov/pubmed/30275465
http://dx.doi.org/10.1038/s41559-018-0681-5
work_keys_str_mv AT czorlichyann rapidsexspecificevolutionofageatmaturityisshapedbygeneticarchitectureinatlanticsalmon
AT aykanattutku rapidsexspecificevolutionofageatmaturityisshapedbygeneticarchitectureinatlanticsalmon
AT erkinarojaakko rapidsexspecificevolutionofageatmaturityisshapedbygeneticarchitectureinatlanticsalmon
AT orellpanu rapidsexspecificevolutionofageatmaturityisshapedbygeneticarchitectureinatlanticsalmon
AT primmercraigrobert rapidsexspecificevolutionofageatmaturityisshapedbygeneticarchitectureinatlanticsalmon