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Parallel Evolution of Cold Tolerance within Drosophila melanogaster

Drosophila melanogaster originated in tropical Africa before expanding into strikingly different temperate climates in Eurasia and beyond. Here, we find elevated cold tolerance in three distinct geographic regions: beyond the well-studied non-African case, we show that populations from the highlands...

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Autores principales: Pool, John E., Braun, Dylan T., Lack, Justin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526443/
https://www.ncbi.nlm.nih.gov/pubmed/27777283
http://dx.doi.org/10.1093/molbev/msw232
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author Pool, John E.
Braun, Dylan T.
Lack, Justin B.
author_facet Pool, John E.
Braun, Dylan T.
Lack, Justin B.
author_sort Pool, John E.
collection PubMed
description Drosophila melanogaster originated in tropical Africa before expanding into strikingly different temperate climates in Eurasia and beyond. Here, we find elevated cold tolerance in three distinct geographic regions: beyond the well-studied non-African case, we show that populations from the highlands of Ethiopia and South Africa have significantly increased cold tolerance as well. We observe greater cold tolerance in outbred versus inbred flies, but only in populations with higher inversion frequencies. Each cold-adapted population shows lower inversion frequencies than a closely-related warm-adapted population, suggesting that inversion frequencies may decrease with altitude in addition to latitude. Using the F(ST)-based “Population Branch Excess” statistic (PBE), we found only limited evidence for parallel genetic differentiation at the scale of ∼4 kb windows, specifically between Ethiopian and South African cold-adapted populations. And yet, when we looked for single nucleotide polymorphisms (SNPs) with codirectional frequency change in two or three cold-adapted populations, strong genomic enrichments were observed from all comparisons. These findings could reflect an important role for selection on standing genetic variation leading to “soft sweeps”. One SNP showed sufficient codirectional frequency change in all cold-adapted populations to achieve experiment-wide significance: an intronic variant in the synaptic gene Prosap. Another codirectional outlier SNP, at senseless-2, had a strong association with our cold trait measurements, but in the opposite direction as predicted. More generally, proteins involved in neurotransmission were enriched as potential targets of parallel adaptation. The ability to study cold tolerance evolution in a parallel framework will enhance this classic study system for climate adaptation.
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spelling pubmed-55264432017-07-27 Parallel Evolution of Cold Tolerance within Drosophila melanogaster Pool, John E. Braun, Dylan T. Lack, Justin B. Mol Biol Evol Discoveries Drosophila melanogaster originated in tropical Africa before expanding into strikingly different temperate climates in Eurasia and beyond. Here, we find elevated cold tolerance in three distinct geographic regions: beyond the well-studied non-African case, we show that populations from the highlands of Ethiopia and South Africa have significantly increased cold tolerance as well. We observe greater cold tolerance in outbred versus inbred flies, but only in populations with higher inversion frequencies. Each cold-adapted population shows lower inversion frequencies than a closely-related warm-adapted population, suggesting that inversion frequencies may decrease with altitude in addition to latitude. Using the F(ST)-based “Population Branch Excess” statistic (PBE), we found only limited evidence for parallel genetic differentiation at the scale of ∼4 kb windows, specifically between Ethiopian and South African cold-adapted populations. And yet, when we looked for single nucleotide polymorphisms (SNPs) with codirectional frequency change in two or three cold-adapted populations, strong genomic enrichments were observed from all comparisons. These findings could reflect an important role for selection on standing genetic variation leading to “soft sweeps”. One SNP showed sufficient codirectional frequency change in all cold-adapted populations to achieve experiment-wide significance: an intronic variant in the synaptic gene Prosap. Another codirectional outlier SNP, at senseless-2, had a strong association with our cold trait measurements, but in the opposite direction as predicted. More generally, proteins involved in neurotransmission were enriched as potential targets of parallel adaptation. The ability to study cold tolerance evolution in a parallel framework will enhance this classic study system for climate adaptation. Oxford University Press 2017-02 2016-10-24 /pmc/articles/PMC5526443/ /pubmed/27777283 http://dx.doi.org/10.1093/molbev/msw232 Text en © The Author 2016. 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
Pool, John E.
Braun, Dylan T.
Lack, Justin B.
Parallel Evolution of Cold Tolerance within Drosophila melanogaster
title Parallel Evolution of Cold Tolerance within Drosophila melanogaster
title_full Parallel Evolution of Cold Tolerance within Drosophila melanogaster
title_fullStr Parallel Evolution of Cold Tolerance within Drosophila melanogaster
title_full_unstemmed Parallel Evolution of Cold Tolerance within Drosophila melanogaster
title_short Parallel Evolution of Cold Tolerance within Drosophila melanogaster
title_sort parallel evolution of cold tolerance within drosophila melanogaster
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5526443/
https://www.ncbi.nlm.nih.gov/pubmed/27777283
http://dx.doi.org/10.1093/molbev/msw232
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