Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
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
_version_ 1782419141510037504
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
work_keys_str_mv AT stantongeddesjohn thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT nguyenandrew thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT chicklacy thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT vincentjames thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT vangalamahesh thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT dunnrobertr thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT ellisonaaronm thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT sandersnathanj thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT gotellinicholasj thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies
AT cahansarahelms thermalreactionomesrevealdivergentresponsestothermalextremesinwarmandcoolclimateantspecies