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Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis

The novel extremophilic yeast Rhodotorula frigidialcoholis, formerly R. JG1b, was isolated from ice-cemented permafrost in University Valley (Antarctic), one of coldest and driest environments on Earth. Phenotypic and phylogenetic analyses classified R. frigidialcoholis as a novel species. To charac...

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Autores principales: Touchette, D., Altshuler, I., Gostinčar, C., Zalar, P., Raymond-Bouchard, I., Zajc, J., McKay, C. P., Gunde-Cimerman, N., Whyte, L. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692454/
https://www.ncbi.nlm.nih.gov/pubmed/34294882
http://dx.doi.org/10.1038/s41396-021-01030-9
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author Touchette, D.
Altshuler, I.
Gostinčar, C.
Zalar, P.
Raymond-Bouchard, I.
Zajc, J.
McKay, C. P.
Gunde-Cimerman, N.
Whyte, L. G.
author_facet Touchette, D.
Altshuler, I.
Gostinčar, C.
Zalar, P.
Raymond-Bouchard, I.
Zajc, J.
McKay, C. P.
Gunde-Cimerman, N.
Whyte, L. G.
author_sort Touchette, D.
collection PubMed
description The novel extremophilic yeast Rhodotorula frigidialcoholis, formerly R. JG1b, was isolated from ice-cemented permafrost in University Valley (Antarctic), one of coldest and driest environments on Earth. Phenotypic and phylogenetic analyses classified R. frigidialcoholis as a novel species. To characterize its cold-adaptive strategies, we performed mRNA and sRNA transcriptomic analyses, phenotypic profiling, and assessed ethanol production at 0 and 23 °C. Downregulation of the ETC and citrate cycle genes, overexpression of fermentation and pentose phosphate pathways genes, growth without reduction of tetrazolium dye, and our discovery of ethanol production at 0 °C indicate that R. frigidialcoholis induces a metabolic switch from respiration to ethanol fermentation as adaptation in Antarctic permafrost. This is the first report of microbial ethanol fermentation utilized as the major energy pathway in response to cold and the coldest temperature reported for natural ethanol production. R. frigidialcoholis increased its diversity and abundance of sRNAs when grown at 0 versus 23 °C. This was consistent with increase in transcription of Dicer, a key protein for sRNA processing. Our results strongly imply that post-transcriptional regulation of gene expression and mRNA silencing may be a novel evolutionary fungal adaptation in the cryosphere.
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spelling pubmed-86924542022-01-10 Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis Touchette, D. Altshuler, I. Gostinčar, C. Zalar, P. Raymond-Bouchard, I. Zajc, J. McKay, C. P. Gunde-Cimerman, N. Whyte, L. G. ISME J Article The novel extremophilic yeast Rhodotorula frigidialcoholis, formerly R. JG1b, was isolated from ice-cemented permafrost in University Valley (Antarctic), one of coldest and driest environments on Earth. Phenotypic and phylogenetic analyses classified R. frigidialcoholis as a novel species. To characterize its cold-adaptive strategies, we performed mRNA and sRNA transcriptomic analyses, phenotypic profiling, and assessed ethanol production at 0 and 23 °C. Downregulation of the ETC and citrate cycle genes, overexpression of fermentation and pentose phosphate pathways genes, growth without reduction of tetrazolium dye, and our discovery of ethanol production at 0 °C indicate that R. frigidialcoholis induces a metabolic switch from respiration to ethanol fermentation as adaptation in Antarctic permafrost. This is the first report of microbial ethanol fermentation utilized as the major energy pathway in response to cold and the coldest temperature reported for natural ethanol production. R. frigidialcoholis increased its diversity and abundance of sRNAs when grown at 0 versus 23 °C. This was consistent with increase in transcription of Dicer, a key protein for sRNA processing. Our results strongly imply that post-transcriptional regulation of gene expression and mRNA silencing may be a novel evolutionary fungal adaptation in the cryosphere. Nature Publishing Group UK 2021-07-22 2022-01 /pmc/articles/PMC8692454/ /pubmed/34294882 http://dx.doi.org/10.1038/s41396-021-01030-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Touchette, D.
Altshuler, I.
Gostinčar, C.
Zalar, P.
Raymond-Bouchard, I.
Zajc, J.
McKay, C. P.
Gunde-Cimerman, N.
Whyte, L. G.
Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis
title Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis
title_full Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis
title_fullStr Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis
title_full_unstemmed Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis
title_short Novel Antarctic yeast adapts to cold by switching energy metabolism and increasing small RNA synthesis
title_sort novel antarctic yeast adapts to cold by switching energy metabolism and increasing small rna synthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692454/
https://www.ncbi.nlm.nih.gov/pubmed/34294882
http://dx.doi.org/10.1038/s41396-021-01030-9
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