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MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)

Hibernation is a physiological state employed by many animals that are exposed to limited food and adverse winter conditions. Controlling tissue-specific and organism wide changes in metabolism and cellular function requires precise regulation of gene expression, including by microRNAs (miRNAs). Her...

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Autores principales: Capraro, Alexander, O‘Meally, Denis, Waters, Shafagh A., Patel, Hardip R., Georges, Arthur, Waters, Paul D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576210/
https://www.ncbi.nlm.nih.gov/pubmed/33082398
http://dx.doi.org/10.1038/s41598-020-73706-9
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author Capraro, Alexander
O‘Meally, Denis
Waters, Shafagh A.
Patel, Hardip R.
Georges, Arthur
Waters, Paul D.
author_facet Capraro, Alexander
O‘Meally, Denis
Waters, Shafagh A.
Patel, Hardip R.
Georges, Arthur
Waters, Paul D.
author_sort Capraro, Alexander
collection PubMed
description Hibernation is a physiological state employed by many animals that are exposed to limited food and adverse winter conditions. Controlling tissue-specific and organism wide changes in metabolism and cellular function requires precise regulation of gene expression, including by microRNAs (miRNAs). Here we profile miRNA expression in the central bearded dragon (Pogona vitticeps) using small RNA sequencing of brain, heart, and skeletal muscle from individuals in late hibernation and four days post-arousal. A total of 1295 miRNAs were identified in the central bearded dragon genome; 664 of which were novel to central bearded dragon. We identified differentially expressed miRNAs (DEmiRs) in all tissues and correlated mRNA expression with known and predicted target mRNAs. Functional analysis of DEmiR targets revealed an enrichment of differentially expressed mRNA targets involved in metabolic processes. However, we failed to reveal biologically relevant tissue-specific processes subjected to miRNA-mediated regulation in heart and skeletal muscle. In brain, neuroprotective pathways were identified as potential targets regulated by miRNAs. Our data suggests that miRNAs are necessary for modulating the shift in cellular metabolism during hibernation and regulating neuroprotection in the brain. This study is the first of its kind in a hibernating reptile and provides key insight into this ephemeral phenotype.
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spelling pubmed-75762102020-10-21 MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps) Capraro, Alexander O‘Meally, Denis Waters, Shafagh A. Patel, Hardip R. Georges, Arthur Waters, Paul D. Sci Rep Article Hibernation is a physiological state employed by many animals that are exposed to limited food and adverse winter conditions. Controlling tissue-specific and organism wide changes in metabolism and cellular function requires precise regulation of gene expression, including by microRNAs (miRNAs). Here we profile miRNA expression in the central bearded dragon (Pogona vitticeps) using small RNA sequencing of brain, heart, and skeletal muscle from individuals in late hibernation and four days post-arousal. A total of 1295 miRNAs were identified in the central bearded dragon genome; 664 of which were novel to central bearded dragon. We identified differentially expressed miRNAs (DEmiRs) in all tissues and correlated mRNA expression with known and predicted target mRNAs. Functional analysis of DEmiR targets revealed an enrichment of differentially expressed mRNA targets involved in metabolic processes. However, we failed to reveal biologically relevant tissue-specific processes subjected to miRNA-mediated regulation in heart and skeletal muscle. In brain, neuroprotective pathways were identified as potential targets regulated by miRNAs. Our data suggests that miRNAs are necessary for modulating the shift in cellular metabolism during hibernation and regulating neuroprotection in the brain. This study is the first of its kind in a hibernating reptile and provides key insight into this ephemeral phenotype. Nature Publishing Group UK 2020-10-20 /pmc/articles/PMC7576210/ /pubmed/33082398 http://dx.doi.org/10.1038/s41598-020-73706-9 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Capraro, Alexander
O‘Meally, Denis
Waters, Shafagh A.
Patel, Hardip R.
Georges, Arthur
Waters, Paul D.
MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)
title MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)
title_full MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)
title_fullStr MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)
title_full_unstemmed MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)
title_short MicroRNA dynamics during hibernation of the Australian central bearded dragon (Pogona vitticeps)
title_sort microrna dynamics during hibernation of the australian central bearded dragon (pogona vitticeps)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7576210/
https://www.ncbi.nlm.nih.gov/pubmed/33082398
http://dx.doi.org/10.1038/s41598-020-73706-9
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