The genomic basis of adaptive evolution in threespine sticklebacks

Marine stickleback fish have colonized and adapted to innumerable streams and lakes formed since the last ice age, providing an exceptional opportunity to characterize genomic mechanisms underlying repeated ecological adaptation in nature. Here we develop a high quality reference genome assembly for...

Full description

Bibliographic Details
Main Authors: Jones, Felicity C, Grabherr, Manfred G, Chan, Yingguang Frank, Russell, Pamela, Mauceli, Evan, Johnson, Jeremy, Swofford, Ross, Pirun, Mono, Zody, Michael C, White, Simon, Birney, Ewan, Searle, Stephen, Schmutz, Jeremy, Grimwood, Jane, Dickson, Mark C, Myers, Richard M, Miller, Craig T, Summers, Brian R, Knecht, Anne K, Brady, Shannon D, Zhang, Haili, Pollen, Alex A, Howes, Timothy, Amemiya, Chris, Lander, Eric S, Di Palma, Federica, Lindblad-Toh, Kerstin, Kingsley, David M
Format: Online
Language:English
Published: 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322419/
id pubmed-3322419
recordtype oai_dc
spelling pubmed-33224192012-10-05 The genomic basis of adaptive evolution in threespine sticklebacks Jones, Felicity C Grabherr, Manfred G Chan, Yingguang Frank Russell, Pamela Mauceli, Evan Johnson, Jeremy Swofford, Ross Pirun, Mono Zody, Michael C White, Simon Birney, Ewan Searle, Stephen Schmutz, Jeremy Grimwood, Jane Dickson, Mark C Myers, Richard M Miller, Craig T Summers, Brian R Knecht, Anne K Brady, Shannon D Zhang, Haili Pollen, Alex A Howes, Timothy Amemiya, Chris Lander, Eric S Di Palma, Federica Lindblad-Toh, Kerstin Kingsley, David M Article Marine stickleback fish have colonized and adapted to innumerable streams and lakes formed since the last ice age, providing an exceptional opportunity to characterize genomic mechanisms underlying repeated ecological adaptation in nature. Here we develop a high quality reference genome assembly for threespine sticklebacks. By sequencing the genomes of 20 additional individuals from a global set of marine and freshwater populations, we identify a genome-wide set of loci that are consistently associated with marine-freshwater divergence. Our results suggest that reuse of globally-shared standing genetic variation, including chromosomal inversions, plays an important role in repeated evolution of distinct marine and freshwater sticklebacks, and in the maintenance of divergent ecotypes during early stages of reproductive isolation. Both coding and regulatory changes occur in the set of loci underlying marine-freshwater evolution, with regulatory changes likely predominating in this classic example of repeated adaptive evolution in nature. 2012-04-04 /pmc/articles/PMC3322419/ /pubmed/22481358 http://dx.doi.org/10.1038/nature10944 Text en Users may view, print, copy, download and 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
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Jones, Felicity C
Grabherr, Manfred G
Chan, Yingguang Frank
Russell, Pamela
Mauceli, Evan
Johnson, Jeremy
Swofford, Ross
Pirun, Mono
Zody, Michael C
White, Simon
Birney, Ewan
Searle, Stephen
Schmutz, Jeremy
Grimwood, Jane
Dickson, Mark C
Myers, Richard M
Miller, Craig T
Summers, Brian R
Knecht, Anne K
Brady, Shannon D
Zhang, Haili
Pollen, Alex A
Howes, Timothy
Amemiya, Chris
Lander, Eric S
Di Palma, Federica
Lindblad-Toh, Kerstin
Kingsley, David M
spellingShingle Jones, Felicity C
Grabherr, Manfred G
Chan, Yingguang Frank
Russell, Pamela
Mauceli, Evan
Johnson, Jeremy
Swofford, Ross
Pirun, Mono
Zody, Michael C
White, Simon
Birney, Ewan
Searle, Stephen
Schmutz, Jeremy
Grimwood, Jane
Dickson, Mark C
Myers, Richard M
Miller, Craig T
Summers, Brian R
Knecht, Anne K
Brady, Shannon D
Zhang, Haili
Pollen, Alex A
Howes, Timothy
Amemiya, Chris
Lander, Eric S
Di Palma, Federica
Lindblad-Toh, Kerstin
Kingsley, David M
The genomic basis of adaptive evolution in threespine sticklebacks
author_facet Jones, Felicity C
Grabherr, Manfred G
Chan, Yingguang Frank
Russell, Pamela
Mauceli, Evan
Johnson, Jeremy
Swofford, Ross
Pirun, Mono
Zody, Michael C
White, Simon
Birney, Ewan
Searle, Stephen
Schmutz, Jeremy
Grimwood, Jane
Dickson, Mark C
Myers, Richard M
Miller, Craig T
Summers, Brian R
Knecht, Anne K
Brady, Shannon D
Zhang, Haili
Pollen, Alex A
Howes, Timothy
Amemiya, Chris
Lander, Eric S
Di Palma, Federica
Lindblad-Toh, Kerstin
Kingsley, David M
author_sort Jones, Felicity C
title The genomic basis of adaptive evolution in threespine sticklebacks
title_short The genomic basis of adaptive evolution in threespine sticklebacks
title_full The genomic basis of adaptive evolution in threespine sticklebacks
title_fullStr The genomic basis of adaptive evolution in threespine sticklebacks
title_full_unstemmed The genomic basis of adaptive evolution in threespine sticklebacks
title_sort genomic basis of adaptive evolution in threespine sticklebacks
description Marine stickleback fish have colonized and adapted to innumerable streams and lakes formed since the last ice age, providing an exceptional opportunity to characterize genomic mechanisms underlying repeated ecological adaptation in nature. Here we develop a high quality reference genome assembly for threespine sticklebacks. By sequencing the genomes of 20 additional individuals from a global set of marine and freshwater populations, we identify a genome-wide set of loci that are consistently associated with marine-freshwater divergence. Our results suggest that reuse of globally-shared standing genetic variation, including chromosomal inversions, plays an important role in repeated evolution of distinct marine and freshwater sticklebacks, and in the maintenance of divergent ecotypes during early stages of reproductive isolation. Both coding and regulatory changes occur in the set of loci underlying marine-freshwater evolution, with regulatory changes likely predominating in this classic example of repeated adaptive evolution in nature.
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322419/
_version_ 1611519792215228416