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A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska

In studying the causative mechanisms behind migration and life history, the salmonids–salmon, trout, and charr–are an exemplary taxonomic group, as life history development is known to have a strong genetic component. A double inversion located on chromosome 5 in rainbow trout (Oncorhynchus mykiss)...

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Autores principales: Weinstein, Spencer Y., Thrower, Frank P., Nichols, Krista M., Hale, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754156/
https://www.ncbi.nlm.nih.gov/pubmed/31539414
http://dx.doi.org/10.1371/journal.pone.0223018
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author Weinstein, Spencer Y.
Thrower, Frank P.
Nichols, Krista M.
Hale, Matthew C.
author_facet Weinstein, Spencer Y.
Thrower, Frank P.
Nichols, Krista M.
Hale, Matthew C.
author_sort Weinstein, Spencer Y.
collection PubMed
description In studying the causative mechanisms behind migration and life history, the salmonids–salmon, trout, and charr–are an exemplary taxonomic group, as life history development is known to have a strong genetic component. A double inversion located on chromosome 5 in rainbow trout (Oncorhynchus mykiss) is associated with life history development in multiple populations, but the importance of this inversion has not been thoroughly tested in conjunction with other polymorphisms in the genome. To that end, we used a high-density SNP chip to genotype 192 F(1) migratory and resident rainbow trout and focused our analyses to determine whether this inversion is important in life history development in a well-studied population of rainbow trout from Southeast Alaska. We identified 4,994 and 436 SNPs–predominantly outside of the inversion region–associated with life history development in the migrant and resident familial lines, respectively. Although F(1) samples showed genomic patterns consistent with the double inversion on chromosome 5 (reduced observed and expected heterozygosity and an increase in linkage disequilibrium), we found no statistical association between the inversion and life history development. Progeny produced by crossing resident trout and progeny produced by crossing migrant trout both consisted of a mix of migrant and resident individuals, irrespective of the individuals’ inversion haplotype on chromosome 5. This suggests that although the inversion is present at a low frequency, it is not strongly associated with migration as it is in populations of Oncorhynchus mykiss from lower latitudes.
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spelling pubmed-67541562019-10-03 A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska Weinstein, Spencer Y. Thrower, Frank P. Nichols, Krista M. Hale, Matthew C. PLoS One Research Article In studying the causative mechanisms behind migration and life history, the salmonids–salmon, trout, and charr–are an exemplary taxonomic group, as life history development is known to have a strong genetic component. A double inversion located on chromosome 5 in rainbow trout (Oncorhynchus mykiss) is associated with life history development in multiple populations, but the importance of this inversion has not been thoroughly tested in conjunction with other polymorphisms in the genome. To that end, we used a high-density SNP chip to genotype 192 F(1) migratory and resident rainbow trout and focused our analyses to determine whether this inversion is important in life history development in a well-studied population of rainbow trout from Southeast Alaska. We identified 4,994 and 436 SNPs–predominantly outside of the inversion region–associated with life history development in the migrant and resident familial lines, respectively. Although F(1) samples showed genomic patterns consistent with the double inversion on chromosome 5 (reduced observed and expected heterozygosity and an increase in linkage disequilibrium), we found no statistical association between the inversion and life history development. Progeny produced by crossing resident trout and progeny produced by crossing migrant trout both consisted of a mix of migrant and resident individuals, irrespective of the individuals’ inversion haplotype on chromosome 5. This suggests that although the inversion is present at a low frequency, it is not strongly associated with migration as it is in populations of Oncorhynchus mykiss from lower latitudes. Public Library of Science 2019-09-20 /pmc/articles/PMC6754156/ /pubmed/31539414 http://dx.doi.org/10.1371/journal.pone.0223018 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Weinstein, Spencer Y.
Thrower, Frank P.
Nichols, Krista M.
Hale, Matthew C.
A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska
title A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska
title_full A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska
title_fullStr A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska
title_full_unstemmed A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska
title_short A large-scale chromosomal inversion is not associated with life history development in rainbow trout from Southeast Alaska
title_sort large-scale chromosomal inversion is not associated with life history development in rainbow trout from southeast alaska
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754156/
https://www.ncbi.nlm.nih.gov/pubmed/31539414
http://dx.doi.org/10.1371/journal.pone.0223018
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