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Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster
Experimental evolution combined with whole-genome sequencing (evolve and resequence (E&R)) is a powerful approach to study the adaptive architecture of selected traits. Nevertheless, so far the focus has been on the selective response triggered by a single stressor. Building on the highly parall...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579754/ https://www.ncbi.nlm.nih.gov/pubmed/36259211 http://dx.doi.org/10.1098/rspb.2022.1857 |
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author | Burny, Claire Nolte, Viola Dolezal, Marlies Schlötterer, Christian |
author_facet | Burny, Claire Nolte, Viola Dolezal, Marlies Schlötterer, Christian |
author_sort | Burny, Claire |
collection | PubMed |
description | Experimental evolution combined with whole-genome sequencing (evolve and resequence (E&R)) is a powerful approach to study the adaptive architecture of selected traits. Nevertheless, so far the focus has been on the selective response triggered by a single stressor. Building on the highly parallel selection response of founder populations with reduced variation, we evaluated how the presence of a second stressor affects the genomic selection response. After 20 generations of adaptation to laboratory conditions at either 18°C or 29°C, strong genome-wide selection signatures were observed. Only 38% of the selection signatures can be attributed to laboratory adaptation (no difference between temperature regimes). The remaining selection responses are either caused by temperature-specific effects, or reflect the joint effects of temperature and laboratory adaptation (same direction, but the magnitude differs between temperatures). The allele frequency changes resulting from the combined effects of temperature and laboratory adaptation were more extreme in the hot environment for 83% of the affected genomic regions—indicating widespread synergistic effects of the two stressors. We conclude that E&R with reduced genetic variation is a powerful approach to study genome-wide fitness consequences driven by the combined effects of multiple environmental factors. |
format | Online Article Text |
id | pubmed-9579754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-95797542022-10-28 Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster Burny, Claire Nolte, Viola Dolezal, Marlies Schlötterer, Christian Proc Biol Sci Evolution Experimental evolution combined with whole-genome sequencing (evolve and resequence (E&R)) is a powerful approach to study the adaptive architecture of selected traits. Nevertheless, so far the focus has been on the selective response triggered by a single stressor. Building on the highly parallel selection response of founder populations with reduced variation, we evaluated how the presence of a second stressor affects the genomic selection response. After 20 generations of adaptation to laboratory conditions at either 18°C or 29°C, strong genome-wide selection signatures were observed. Only 38% of the selection signatures can be attributed to laboratory adaptation (no difference between temperature regimes). The remaining selection responses are either caused by temperature-specific effects, or reflect the joint effects of temperature and laboratory adaptation (same direction, but the magnitude differs between temperatures). The allele frequency changes resulting from the combined effects of temperature and laboratory adaptation were more extreme in the hot environment for 83% of the affected genomic regions—indicating widespread synergistic effects of the two stressors. We conclude that E&R with reduced genetic variation is a powerful approach to study genome-wide fitness consequences driven by the combined effects of multiple environmental factors. The Royal Society 2022-10-26 2022-10-19 /pmc/articles/PMC9579754/ /pubmed/36259211 http://dx.doi.org/10.1098/rspb.2022.1857 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Burny, Claire Nolte, Viola Dolezal, Marlies Schlötterer, Christian Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster |
title | Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster |
title_full | Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster |
title_fullStr | Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster |
title_full_unstemmed | Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster |
title_short | Genome-wide selection signatures reveal widespread synergistic effects of two different stressors in Drosophila melanogaster |
title_sort | genome-wide selection signatures reveal widespread synergistic effects of two different stressors in drosophila melanogaster |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579754/ https://www.ncbi.nlm.nih.gov/pubmed/36259211 http://dx.doi.org/10.1098/rspb.2022.1857 |
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