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Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change

Organisms rely upon external cues to avoid detrimental conditions during environmental change. Rapid water loss, or desiccation, is a universal threat for terrestrial plants and animals, especially under climate change, but the cues that facilitate plastic responses to avoid desiccation are unclear....

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Autores principales: Riddell, Eric A., Roback, Emma Y., Wells, Christina E., Zamudio, Kelly R., Sears, Michael W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733842/
https://www.ncbi.nlm.nih.gov/pubmed/31501425
http://dx.doi.org/10.1038/s41467-019-11990-4
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author Riddell, Eric A.
Roback, Emma Y.
Wells, Christina E.
Zamudio, Kelly R.
Sears, Michael W.
author_facet Riddell, Eric A.
Roback, Emma Y.
Wells, Christina E.
Zamudio, Kelly R.
Sears, Michael W.
author_sort Riddell, Eric A.
collection PubMed
description Organisms rely upon external cues to avoid detrimental conditions during environmental change. Rapid water loss, or desiccation, is a universal threat for terrestrial plants and animals, especially under climate change, but the cues that facilitate plastic responses to avoid desiccation are unclear. We integrate acclimation experiments with gene expression analyses to identify the cues that regulate resistance to water loss at the physiological and regulatory level in a montane salamander (Plethodon metcalfi). Here we show that temperature is an important cue for developing a desiccation-resistant phenotype and might act as a reliable cue for organisms across the globe. Gene expression analyses consistently identify regulation of stem cell differentiation and embryonic development of vasculature. The temperature-sensitive blood vessel development suggests that salamanders regulate water loss through the regression and regeneration of capillary beds in the skin, indicating that tissue regeneration may be used for physiological purposes beyond replacing lost limbs.
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spelling pubmed-67338422019-09-11 Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change Riddell, Eric A. Roback, Emma Y. Wells, Christina E. Zamudio, Kelly R. Sears, Michael W. Nat Commun Article Organisms rely upon external cues to avoid detrimental conditions during environmental change. Rapid water loss, or desiccation, is a universal threat for terrestrial plants and animals, especially under climate change, but the cues that facilitate plastic responses to avoid desiccation are unclear. We integrate acclimation experiments with gene expression analyses to identify the cues that regulate resistance to water loss at the physiological and regulatory level in a montane salamander (Plethodon metcalfi). Here we show that temperature is an important cue for developing a desiccation-resistant phenotype and might act as a reliable cue for organisms across the globe. Gene expression analyses consistently identify regulation of stem cell differentiation and embryonic development of vasculature. The temperature-sensitive blood vessel development suggests that salamanders regulate water loss through the regression and regeneration of capillary beds in the skin, indicating that tissue regeneration may be used for physiological purposes beyond replacing lost limbs. Nature Publishing Group UK 2019-09-09 /pmc/articles/PMC6733842/ /pubmed/31501425 http://dx.doi.org/10.1038/s41467-019-11990-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Riddell, Eric A.
Roback, Emma Y.
Wells, Christina E.
Zamudio, Kelly R.
Sears, Michael W.
Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
title Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
title_full Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
title_fullStr Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
title_full_unstemmed Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
title_short Thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
title_sort thermal cues drive plasticity of desiccation resistance in montane salamanders with implications for climate change
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733842/
https://www.ncbi.nlm.nih.gov/pubmed/31501425
http://dx.doi.org/10.1038/s41467-019-11990-4
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