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Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation
Speciation events often occur in rapid bursts of diversification, but the ecological and genetic factors that promote these radiations are still much debated. Using whole transcriptomes from all 13 species in the ecologically and reproductively diverse wild tomato clade (Solanum sect. Lycopersicon),...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752443/ https://www.ncbi.nlm.nih.gov/pubmed/26871574 http://dx.doi.org/10.1371/journal.pbio.1002379 |
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author | Pease, James B. Haak, David C. Hahn, Matthew W. Moyle, Leonie C. |
author_facet | Pease, James B. Haak, David C. Hahn, Matthew W. Moyle, Leonie C. |
author_sort | Pease, James B. |
collection | PubMed |
description | Speciation events often occur in rapid bursts of diversification, but the ecological and genetic factors that promote these radiations are still much debated. Using whole transcriptomes from all 13 species in the ecologically and reproductively diverse wild tomato clade (Solanum sect. Lycopersicon), we infer the species phylogeny and patterns of genetic diversity in this group. Despite widespread phylogenetic discordance due to the sorting of ancestral variation, we date the origin of this radiation to approximately 2.5 million years ago and find evidence for at least three sources of adaptive genetic variation that fuel diversification. First, we detect introgression both historically between early-branching lineages and recently between individual populations, at specific loci whose functions indicate likely adaptive benefits. Second, we find evidence of lineage-specific de novo evolution for many genes, including loci involved in the production of red fruit color. Finally, using a “PhyloGWAS” approach, we detect environment-specific sorting of ancestral variation among populations that come from different species but share common environmental conditions. Estimated across the whole clade, small but substantial and approximately equal fractions of the euchromatic portion of the genome are inferred to contribute to each of these three sources of adaptive genetic variation. These results indicate that multiple genetic sources can promote rapid diversification and speciation in response to new ecological opportunity, in agreement with our emerging phylogenomic understanding of the complexity of both ancient and recent species radiations. |
format | Online Article Text |
id | pubmed-4752443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47524432016-02-26 Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation Pease, James B. Haak, David C. Hahn, Matthew W. Moyle, Leonie C. PLoS Biol Research Article Speciation events often occur in rapid bursts of diversification, but the ecological and genetic factors that promote these radiations are still much debated. Using whole transcriptomes from all 13 species in the ecologically and reproductively diverse wild tomato clade (Solanum sect. Lycopersicon), we infer the species phylogeny and patterns of genetic diversity in this group. Despite widespread phylogenetic discordance due to the sorting of ancestral variation, we date the origin of this radiation to approximately 2.5 million years ago and find evidence for at least three sources of adaptive genetic variation that fuel diversification. First, we detect introgression both historically between early-branching lineages and recently between individual populations, at specific loci whose functions indicate likely adaptive benefits. Second, we find evidence of lineage-specific de novo evolution for many genes, including loci involved in the production of red fruit color. Finally, using a “PhyloGWAS” approach, we detect environment-specific sorting of ancestral variation among populations that come from different species but share common environmental conditions. Estimated across the whole clade, small but substantial and approximately equal fractions of the euchromatic portion of the genome are inferred to contribute to each of these three sources of adaptive genetic variation. These results indicate that multiple genetic sources can promote rapid diversification and speciation in response to new ecological opportunity, in agreement with our emerging phylogenomic understanding of the complexity of both ancient and recent species radiations. Public Library of Science 2016-02-12 /pmc/articles/PMC4752443/ /pubmed/26871574 http://dx.doi.org/10.1371/journal.pbio.1002379 Text en © 2016 Pease 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 Pease, James B. Haak, David C. Hahn, Matthew W. Moyle, Leonie C. Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
title | Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
title_full | Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
title_fullStr | Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
title_full_unstemmed | Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
title_short | Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
title_sort | phylogenomics reveals three sources of adaptive variation during a rapid radiation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752443/ https://www.ncbi.nlm.nih.gov/pubmed/26871574 http://dx.doi.org/10.1371/journal.pbio.1002379 |
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