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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....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6733842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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