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MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus

Embryos of the annual killifish Austrofundulus limnaeus are the most anoxia-tolerant vertebrate. Annual killifish inhabit ephemeral ponds, producing drought and anoxia-tolerant embryos, which allows the species to persist generation after generation. Anoxia tolerance and physiology vary by developme...

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Autores principales: Riggs, Claire L., Woll, Steven Cody, Podrabsky, Jason E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930250/
https://www.ncbi.nlm.nih.gov/pubmed/31874982
http://dx.doi.org/10.1038/s41598-019-56231-2
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author Riggs, Claire L.
Woll, Steven Cody
Podrabsky, Jason E.
author_facet Riggs, Claire L.
Woll, Steven Cody
Podrabsky, Jason E.
author_sort Riggs, Claire L.
collection PubMed
description Embryos of the annual killifish Austrofundulus limnaeus are the most anoxia-tolerant vertebrate. Annual killifish inhabit ephemeral ponds, producing drought and anoxia-tolerant embryos, which allows the species to persist generation after generation. Anoxia tolerance and physiology vary by developmental stage, creating a unique opportunity for comparative study within the species. A recent study of small ncRNA expression in A. limnaeus embryos in response to anoxia and aerobic recovery revealed small ncRNAs with expression patterns that suggest a role in supporting anoxia tolerance. MitosRNAs, small ncRNAs derived from the mitochondrial genome, emerged as an interesting group of these sequences. MitosRNAs derived from mitochondrial tRNAs were differentially expressed in developing embryos and isolated cells exhibiting extreme anoxia tolerance. In this study we focus on expression of mitosRNAs derived from tRNA-cysteine, and their subcellular and organismal localization in order to consider possible function. These tRNA-cys mitosRNAs appear enriched in the mitochondria, particularly near the nucleus, and also appear to be present in the cytoplasm. We provide evidence that mitosRNAs are generated in the mitochondria in response to anoxia, though the precise mechanism of biosynthesis remains unclear. MitosRNAs derived from tRNA-cys localize to numerous tissues, and increase in the anterior brain during anoxia. We hypothesize that these RNAs may play a role in regulating gene expression that supports extreme anoxia tolerance.
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spelling pubmed-69302502019-12-27 MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus Riggs, Claire L. Woll, Steven Cody Podrabsky, Jason E. Sci Rep Article Embryos of the annual killifish Austrofundulus limnaeus are the most anoxia-tolerant vertebrate. Annual killifish inhabit ephemeral ponds, producing drought and anoxia-tolerant embryos, which allows the species to persist generation after generation. Anoxia tolerance and physiology vary by developmental stage, creating a unique opportunity for comparative study within the species. A recent study of small ncRNA expression in A. limnaeus embryos in response to anoxia and aerobic recovery revealed small ncRNAs with expression patterns that suggest a role in supporting anoxia tolerance. MitosRNAs, small ncRNAs derived from the mitochondrial genome, emerged as an interesting group of these sequences. MitosRNAs derived from mitochondrial tRNAs were differentially expressed in developing embryos and isolated cells exhibiting extreme anoxia tolerance. In this study we focus on expression of mitosRNAs derived from tRNA-cysteine, and their subcellular and organismal localization in order to consider possible function. These tRNA-cys mitosRNAs appear enriched in the mitochondria, particularly near the nucleus, and also appear to be present in the cytoplasm. We provide evidence that mitosRNAs are generated in the mitochondria in response to anoxia, though the precise mechanism of biosynthesis remains unclear. MitosRNAs derived from tRNA-cys localize to numerous tissues, and increase in the anterior brain during anoxia. We hypothesize that these RNAs may play a role in regulating gene expression that supports extreme anoxia tolerance. Nature Publishing Group UK 2019-12-24 /pmc/articles/PMC6930250/ /pubmed/31874982 http://dx.doi.org/10.1038/s41598-019-56231-2 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
Riggs, Claire L.
Woll, Steven Cody
Podrabsky, Jason E.
MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus
title MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus
title_full MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus
title_fullStr MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus
title_full_unstemmed MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus
title_short MitosRNAs and extreme anoxia tolerance in embryos of the annual killifish Austrofundulus limnaeus
title_sort mitosrnas and extreme anoxia tolerance in embryos of the annual killifish austrofundulus limnaeus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930250/
https://www.ncbi.nlm.nih.gov/pubmed/31874982
http://dx.doi.org/10.1038/s41598-019-56231-2
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