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Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation
A substantial part of biodiversity is thought to have arisen from adaptive radiations in which one lineage rapidly diversified into multiple lineages adapted to many different niches. However, selection and drift reduce genetic variation during adaptation to new niches and may thus prevent or slow d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519129/ https://www.ncbi.nlm.nih.gov/pubmed/29942074 http://dx.doi.org/10.1038/s41559-018-0581-8 |
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author | Marques, David A. Jones, Felicity C. Di Palma, Federica Kingsley, David M. Reimchen, Thomas E. |
author_facet | Marques, David A. Jones, Felicity C. Di Palma, Federica Kingsley, David M. Reimchen, Thomas E. |
author_sort | Marques, David A. |
collection | PubMed |
description | A substantial part of biodiversity is thought to have arisen from adaptive radiations in which one lineage rapidly diversified into multiple lineages adapted to many different niches. However, selection and drift reduce genetic variation during adaptation to new niches and may thus prevent or slow down further niche shifts. We tested whether rapid adaptation is still possible from a highly derived ecotype in the adaptive radiation of threespine stickleback on the Haida Gwaii archipelago, Western Canada. In a 19-years selection experiment, we let giant stickleback from a large blackwater lake evolve in a small clearwater pond without vertebrate predators. 56 whole genomes from the experiment and 26 natural populations revealed that adaptive genomic change was rapid in many small genomic regions and encompassed 75% of the adaptive genomic change between 12,000 years old ecotypes. Adaptive genomic change was as fast as phenotypic change in defence and trophic morphology and both were largely parallel between the short-term selection experiment and long-term natural adaptive radiation. Our results show that functionally relevant standing genetic variation can persist in derived adaptive radiation members, allowing adaptive radiations to unfold very rapidly. |
format | Online Article Text |
id | pubmed-6519129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-65191292019-05-15 Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation Marques, David A. Jones, Felicity C. Di Palma, Federica Kingsley, David M. Reimchen, Thomas E. Nat Ecol Evol Article A substantial part of biodiversity is thought to have arisen from adaptive radiations in which one lineage rapidly diversified into multiple lineages adapted to many different niches. However, selection and drift reduce genetic variation during adaptation to new niches and may thus prevent or slow down further niche shifts. We tested whether rapid adaptation is still possible from a highly derived ecotype in the adaptive radiation of threespine stickleback on the Haida Gwaii archipelago, Western Canada. In a 19-years selection experiment, we let giant stickleback from a large blackwater lake evolve in a small clearwater pond without vertebrate predators. 56 whole genomes from the experiment and 26 natural populations revealed that adaptive genomic change was rapid in many small genomic regions and encompassed 75% of the adaptive genomic change between 12,000 years old ecotypes. Adaptive genomic change was as fast as phenotypic change in defence and trophic morphology and both were largely parallel between the short-term selection experiment and long-term natural adaptive radiation. Our results show that functionally relevant standing genetic variation can persist in derived adaptive radiation members, allowing adaptive radiations to unfold very rapidly. 2018-06-25 2018-07 /pmc/articles/PMC6519129/ /pubmed/29942074 http://dx.doi.org/10.1038/s41559-018-0581-8 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 Marques, David A. Jones, Felicity C. Di Palma, Federica Kingsley, David M. Reimchen, Thomas E. Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
title | Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
title_full | Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
title_fullStr | Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
title_full_unstemmed | Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
title_short | Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
title_sort | experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519129/ https://www.ncbi.nlm.nih.gov/pubmed/29942074 http://dx.doi.org/10.1038/s41559-018-0581-8 |
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