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Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species
BACKGROUND: The distributions of species and their responses to climate change are in part determined by their thermal tolerances. However, little is known about how thermal tolerance evolves. To test whether evolutionary extension of thermal limits is accomplished through enhanced cellular stress r...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776372/ https://www.ncbi.nlm.nih.gov/pubmed/26934985 http://dx.doi.org/10.1186/s12864-016-2466-z |
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author | Stanton-Geddes, John Nguyen, Andrew Chick, Lacy Vincent, James Vangala, Mahesh Dunn, Robert R. Ellison, Aaron M. Sanders, Nathan J. Gotelli, Nicholas J. Cahan, Sara Helms |
author_facet | Stanton-Geddes, John Nguyen, Andrew Chick, Lacy Vincent, James Vangala, Mahesh Dunn, Robert R. Ellison, Aaron M. Sanders, Nathan J. Gotelli, Nicholas J. Cahan, Sara Helms |
author_sort | Stanton-Geddes, John |
collection | PubMed |
description | BACKGROUND: The distributions of species and their responses to climate change are in part determined by their thermal tolerances. However, little is known about how thermal tolerance evolves. To test whether evolutionary extension of thermal limits is accomplished through enhanced cellular stress response (enhanced response), constitutively elevated expression of protective genes (genetic assimilation) or a shift from damage resistance to passive mechanisms of thermal stability (tolerance), we conducted an analysis of the reactionome: the reaction norm for all genes in an organism’s transcriptome measured across an experimental gradient. We characterized thermal reactionomes of two common ant species in the eastern U.S, the northern cool-climate Aphaenogaster picea and the southern warm-climate Aphaenogaster carolinensis, across 12 temperatures that spanned their entire thermal breadth. RESULTS: We found that at least 2 % of all genes changed expression with temperature. The majority of upregulation was specific to exposure to low temperatures. The cool-adapted A. picea induced expression of more genes in response to extreme temperatures than did A. carolinensis, consistent with the enhanced response hypothesis. In contrast, under high temperatures the warm-adapted A. carolinensis downregulated many of the genes upregulated in A. picea, and required more extreme temperatures to induce down-regulation in gene expression, consistent with the tolerance hypothesis. We found no evidence for a trade-off between constitutive and inducible gene expression as predicted by the genetic assimilation hypothesis. CONCLUSIONS: These results suggest that increases in upper thermal limits may require an evolutionary shift in response mechanism away from damage repair toward tolerance and prevention. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2466-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4776372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47763722016-03-04 Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species Stanton-Geddes, John Nguyen, Andrew Chick, Lacy Vincent, James Vangala, Mahesh Dunn, Robert R. Ellison, Aaron M. Sanders, Nathan J. Gotelli, Nicholas J. Cahan, Sara Helms BMC Genomics Research Article BACKGROUND: The distributions of species and their responses to climate change are in part determined by their thermal tolerances. However, little is known about how thermal tolerance evolves. To test whether evolutionary extension of thermal limits is accomplished through enhanced cellular stress response (enhanced response), constitutively elevated expression of protective genes (genetic assimilation) or a shift from damage resistance to passive mechanisms of thermal stability (tolerance), we conducted an analysis of the reactionome: the reaction norm for all genes in an organism’s transcriptome measured across an experimental gradient. We characterized thermal reactionomes of two common ant species in the eastern U.S, the northern cool-climate Aphaenogaster picea and the southern warm-climate Aphaenogaster carolinensis, across 12 temperatures that spanned their entire thermal breadth. RESULTS: We found that at least 2 % of all genes changed expression with temperature. The majority of upregulation was specific to exposure to low temperatures. The cool-adapted A. picea induced expression of more genes in response to extreme temperatures than did A. carolinensis, consistent with the enhanced response hypothesis. In contrast, under high temperatures the warm-adapted A. carolinensis downregulated many of the genes upregulated in A. picea, and required more extreme temperatures to induce down-regulation in gene expression, consistent with the tolerance hypothesis. We found no evidence for a trade-off between constitutive and inducible gene expression as predicted by the genetic assimilation hypothesis. CONCLUSIONS: These results suggest that increases in upper thermal limits may require an evolutionary shift in response mechanism away from damage repair toward tolerance and prevention. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2466-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-02 /pmc/articles/PMC4776372/ /pubmed/26934985 http://dx.doi.org/10.1186/s12864-016-2466-z Text en © Stanton-Geddes et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Stanton-Geddes, John Nguyen, Andrew Chick, Lacy Vincent, James Vangala, Mahesh Dunn, Robert R. Ellison, Aaron M. Sanders, Nathan J. Gotelli, Nicholas J. Cahan, Sara Helms Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
title | Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
title_full | Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
title_fullStr | Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
title_full_unstemmed | Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
title_short | Thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
title_sort | thermal reactionomes reveal divergent responses to thermal extremes in warm and cool-climate ant species |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776372/ https://www.ncbi.nlm.nih.gov/pubmed/26934985 http://dx.doi.org/10.1186/s12864-016-2466-z |
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