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Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio)
Regulatory mechanisms underlying thermal plasticity determine its evolution and potential to confer resilience to climate change. Here we show that class I and II histone deacetylases (HDAC) mediated thermal plasticity globally by shifting metabolomic profiles of cold acclimated zebrafish (Danio rer...
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/PMC6546753/ https://www.ncbi.nlm.nih.gov/pubmed/31160672 http://dx.doi.org/10.1038/s41598-019-44726-x |
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author | Seebacher, Frank Simmonds, Alec I. M. |
author_facet | Seebacher, Frank Simmonds, Alec I. M. |
author_sort | Seebacher, Frank |
collection | PubMed |
description | Regulatory mechanisms underlying thermal plasticity determine its evolution and potential to confer resilience to climate change. Here we show that class I and II histone deacetylases (HDAC) mediated thermal plasticity globally by shifting metabolomic profiles of cold acclimated zebrafish (Danio rerio) away from warm acclimated animals. HDAC activity promoted swimming performance, but reduced slow and fast myosin heavy chain content in cardiac and skeletal muscle. HDAC increased sarco-endoplasmic reticulum ATPase activity in cold-acclimated fish but not in warm-acclimated animals, and it promoted cardiac function (heart rate and relative stroke volume) in cold but not in warm-acclimated animals. HDAC are an evolutionarily ancient group of proteins, and our data show that they mediate the capacity for thermal plasticity, although the actual manifestation of plasticity is likely to be determined by interactions with other regulators such as AMP-activated protein kinase and thyroid hormone. |
format | Online Article Text |
id | pubmed-6546753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65467532019-06-10 Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) Seebacher, Frank Simmonds, Alec I. M. Sci Rep Article Regulatory mechanisms underlying thermal plasticity determine its evolution and potential to confer resilience to climate change. Here we show that class I and II histone deacetylases (HDAC) mediated thermal plasticity globally by shifting metabolomic profiles of cold acclimated zebrafish (Danio rerio) away from warm acclimated animals. HDAC activity promoted swimming performance, but reduced slow and fast myosin heavy chain content in cardiac and skeletal muscle. HDAC increased sarco-endoplasmic reticulum ATPase activity in cold-acclimated fish but not in warm-acclimated animals, and it promoted cardiac function (heart rate and relative stroke volume) in cold but not in warm-acclimated animals. HDAC are an evolutionarily ancient group of proteins, and our data show that they mediate the capacity for thermal plasticity, although the actual manifestation of plasticity is likely to be determined by interactions with other regulators such as AMP-activated protein kinase and thyroid hormone. Nature Publishing Group UK 2019-06-03 /pmc/articles/PMC6546753/ /pubmed/31160672 http://dx.doi.org/10.1038/s41598-019-44726-x 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 Seebacher, Frank Simmonds, Alec I. M. Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) |
title | Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) |
title_full | Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) |
title_fullStr | Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) |
title_full_unstemmed | Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) |
title_short | Histone deacetylase activity mediates thermal plasticity in zebrafish (Danio rerio) |
title_sort | histone deacetylase activity mediates thermal plasticity in zebrafish (danio rerio) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546753/ https://www.ncbi.nlm.nih.gov/pubmed/31160672 http://dx.doi.org/10.1038/s41598-019-44726-x |
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