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Genomics of Parallel Experimental Evolution in Drosophila
What are the genomic foundations of adaptation in sexual populations? We address this question using fitness–character and whole-genome sequence data from 30 Drosophila laboratory populations. These 30 populations are part of a nearly 40-year laboratory radiation featuring 3 selection regimes, each...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400383/ https://www.ncbi.nlm.nih.gov/pubmed/28087779 http://dx.doi.org/10.1093/molbev/msw282 |
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author | Graves, J.L. Hertweck, K.L. Phillips, M.A. Han, M.V. Cabral, L.G. Barter, T.T. Greer, L.F. Burke, M.K. Mueller, L.D. Rose, M.R. |
author_facet | Graves, J.L. Hertweck, K.L. Phillips, M.A. Han, M.V. Cabral, L.G. Barter, T.T. Greer, L.F. Burke, M.K. Mueller, L.D. Rose, M.R. |
author_sort | Graves, J.L. |
collection | PubMed |
description | What are the genomic foundations of adaptation in sexual populations? We address this question using fitness–character and whole-genome sequence data from 30 Drosophila laboratory populations. These 30 populations are part of a nearly 40-year laboratory radiation featuring 3 selection regimes, each shared by 10 populations for up to 837 generations, with moderately large effective population sizes. Each of 3 sets of the 10 populations that shared a selection regime consists of 5 populations that have long been maintained under that selection regime, paired with 5 populations that had only recently been subjected to that selection regime. We find a high degree of evolutionary parallelism in fitness phenotypes when most-recent selection regimes are shared, as in previous studies from our laboratory. We also find genomic parallelism with respect to the frequencies of single-nucleotide polymorphisms, transposable elements, insertions, and structural variants, which was expected. Entirely unexpected was a high degree of parallelism for linkage disequilibrium. The evolutionary genetic changes among these sexual populations are rapid and genomically extensive. This pattern may be due to segregating functional genetic variation that is abundantly maintained genome-wide by selection, variation that responds immediately to changes of selection regime. |
format | Online Article Text |
id | pubmed-5400383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54003832017-04-28 Genomics of Parallel Experimental Evolution in Drosophila Graves, J.L. Hertweck, K.L. Phillips, M.A. Han, M.V. Cabral, L.G. Barter, T.T. Greer, L.F. Burke, M.K. Mueller, L.D. Rose, M.R. Mol Biol Evol Discoveries What are the genomic foundations of adaptation in sexual populations? We address this question using fitness–character and whole-genome sequence data from 30 Drosophila laboratory populations. These 30 populations are part of a nearly 40-year laboratory radiation featuring 3 selection regimes, each shared by 10 populations for up to 837 generations, with moderately large effective population sizes. Each of 3 sets of the 10 populations that shared a selection regime consists of 5 populations that have long been maintained under that selection regime, paired with 5 populations that had only recently been subjected to that selection regime. We find a high degree of evolutionary parallelism in fitness phenotypes when most-recent selection regimes are shared, as in previous studies from our laboratory. We also find genomic parallelism with respect to the frequencies of single-nucleotide polymorphisms, transposable elements, insertions, and structural variants, which was expected. Entirely unexpected was a high degree of parallelism for linkage disequilibrium. The evolutionary genetic changes among these sexual populations are rapid and genomically extensive. This pattern may be due to segregating functional genetic variation that is abundantly maintained genome-wide by selection, variation that responds immediately to changes of selection regime. Oxford University Press 2017-04 2017-01-12 /pmc/articles/PMC5400383/ /pubmed/28087779 http://dx.doi.org/10.1093/molbev/msw282 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Graves, J.L. Hertweck, K.L. Phillips, M.A. Han, M.V. Cabral, L.G. Barter, T.T. Greer, L.F. Burke, M.K. Mueller, L.D. Rose, M.R. Genomics of Parallel Experimental Evolution in Drosophila |
title | Genomics of Parallel Experimental Evolution in Drosophila |
title_full | Genomics of Parallel Experimental Evolution in Drosophila |
title_fullStr | Genomics of Parallel Experimental Evolution in Drosophila |
title_full_unstemmed | Genomics of Parallel Experimental Evolution in Drosophila |
title_short | Genomics of Parallel Experimental Evolution in Drosophila |
title_sort | genomics of parallel experimental evolution in drosophila |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400383/ https://www.ncbi.nlm.nih.gov/pubmed/28087779 http://dx.doi.org/10.1093/molbev/msw282 |
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