Cargando…

Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags

Next-generation sequencing technology provides novel opportunities for gathering genome-scale sequence data in natural populations, laying the empirical foundation for the evolving field of population genomics. Here we conducted a genome scan of nucleotide diversity and differentiation in natural po...

Descripción completa

Detalles Bibliográficos
Autores principales: Hohenlohe, Paul A., Bassham, Susan, Etter, Paul D., Stiffler, Nicholas, Johnson, Eric A., Cresko, William A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829049/
https://www.ncbi.nlm.nih.gov/pubmed/20195501
http://dx.doi.org/10.1371/journal.pgen.1000862
_version_ 1782178068073283584
author Hohenlohe, Paul A.
Bassham, Susan
Etter, Paul D.
Stiffler, Nicholas
Johnson, Eric A.
Cresko, William A.
author_facet Hohenlohe, Paul A.
Bassham, Susan
Etter, Paul D.
Stiffler, Nicholas
Johnson, Eric A.
Cresko, William A.
author_sort Hohenlohe, Paul A.
collection PubMed
description Next-generation sequencing technology provides novel opportunities for gathering genome-scale sequence data in natural populations, laying the empirical foundation for the evolving field of population genomics. Here we conducted a genome scan of nucleotide diversity and differentiation in natural populations of threespine stickleback (Gasterosteus aculeatus). We used Illumina-sequenced RAD tags to identify and type over 45,000 single nucleotide polymorphisms (SNPs) in each of 100 individuals from two oceanic and three freshwater populations. Overall estimates of genetic diversity and differentiation among populations confirm the biogeographic hypothesis that large panmictic oceanic populations have repeatedly given rise to phenotypically divergent freshwater populations. Genomic regions exhibiting signatures of both balancing and divergent selection were remarkably consistent across multiple, independently derived populations, indicating that replicate parallel phenotypic evolution in stickleback may be occurring through extensive, parallel genetic evolution at a genome-wide scale. Some of these genomic regions co-localize with previously identified QTL for stickleback phenotypic variation identified using laboratory mapping crosses. In addition, we have identified several novel regions showing parallel differentiation across independent populations. Annotation of these regions revealed numerous genes that are candidates for stickleback phenotypic evolution and will form the basis of future genetic analyses in this and other organisms. This study represents the first high-density SNP–based genome scan of genetic diversity and differentiation for populations of threespine stickleback in the wild. These data illustrate the complementary nature of laboratory crosses and population genomic scans by confirming the adaptive significance of previously identified genomic regions, elucidating the particular evolutionary and demographic history of such regions in natural populations, and identifying new genomic regions and candidate genes of evolutionary significance.
format Text
id pubmed-2829049
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-28290492010-03-02 Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags Hohenlohe, Paul A. Bassham, Susan Etter, Paul D. Stiffler, Nicholas Johnson, Eric A. Cresko, William A. PLoS Genet Research Article Next-generation sequencing technology provides novel opportunities for gathering genome-scale sequence data in natural populations, laying the empirical foundation for the evolving field of population genomics. Here we conducted a genome scan of nucleotide diversity and differentiation in natural populations of threespine stickleback (Gasterosteus aculeatus). We used Illumina-sequenced RAD tags to identify and type over 45,000 single nucleotide polymorphisms (SNPs) in each of 100 individuals from two oceanic and three freshwater populations. Overall estimates of genetic diversity and differentiation among populations confirm the biogeographic hypothesis that large panmictic oceanic populations have repeatedly given rise to phenotypically divergent freshwater populations. Genomic regions exhibiting signatures of both balancing and divergent selection were remarkably consistent across multiple, independently derived populations, indicating that replicate parallel phenotypic evolution in stickleback may be occurring through extensive, parallel genetic evolution at a genome-wide scale. Some of these genomic regions co-localize with previously identified QTL for stickleback phenotypic variation identified using laboratory mapping crosses. In addition, we have identified several novel regions showing parallel differentiation across independent populations. Annotation of these regions revealed numerous genes that are candidates for stickleback phenotypic evolution and will form the basis of future genetic analyses in this and other organisms. This study represents the first high-density SNP–based genome scan of genetic diversity and differentiation for populations of threespine stickleback in the wild. These data illustrate the complementary nature of laboratory crosses and population genomic scans by confirming the adaptive significance of previously identified genomic regions, elucidating the particular evolutionary and demographic history of such regions in natural populations, and identifying new genomic regions and candidate genes of evolutionary significance. Public Library of Science 2010-02-26 /pmc/articles/PMC2829049/ /pubmed/20195501 http://dx.doi.org/10.1371/journal.pgen.1000862 Text en Hohenlohe et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hohenlohe, Paul A.
Bassham, Susan
Etter, Paul D.
Stiffler, Nicholas
Johnson, Eric A.
Cresko, William A.
Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
title Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
title_full Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
title_fullStr Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
title_full_unstemmed Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
title_short Population Genomics of Parallel Adaptation in Threespine Stickleback using Sequenced RAD Tags
title_sort population genomics of parallel adaptation in threespine stickleback using sequenced rad tags
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829049/
https://www.ncbi.nlm.nih.gov/pubmed/20195501
http://dx.doi.org/10.1371/journal.pgen.1000862
work_keys_str_mv AT hohenlohepaula populationgenomicsofparalleladaptationinthreespinesticklebackusingsequencedradtags
AT basshamsusan populationgenomicsofparalleladaptationinthreespinesticklebackusingsequencedradtags
AT etterpauld populationgenomicsofparalleladaptationinthreespinesticklebackusingsequencedradtags
AT stifflernicholas populationgenomicsofparalleladaptationinthreespinesticklebackusingsequencedradtags
AT johnsonerica populationgenomicsofparalleladaptationinthreespinesticklebackusingsequencedradtags
AT creskowilliama populationgenomicsofparalleladaptationinthreespinesticklebackusingsequencedradtags