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Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts

Industrial yeast strains of economic importance used in winemaking and beer production are genomically diverse and subjected to harsh environmental conditions during fermentation. In the present study, we investigated wine yeast adaptation to chronic mild alcohol stress when cells were cultured for...

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Autores principales: Adamczyk, Jagoda, Deregowska, Anna, Skoneczny, Marek, Skoneczna, Adrianna, Kwiatkowska, Aleksandra, Potocki, Leszek, Rawska, Ewa, Pabian, Sylwia, Kaplan, Jakub, Lewinska, Anna, Wnuk, Maciej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058656/
https://www.ncbi.nlm.nih.gov/pubmed/27074556
http://dx.doi.org/10.18632/oncotarget.8673
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author Adamczyk, Jagoda
Deregowska, Anna
Skoneczny, Marek
Skoneczna, Adrianna
Kwiatkowska, Aleksandra
Potocki, Leszek
Rawska, Ewa
Pabian, Sylwia
Kaplan, Jakub
Lewinska, Anna
Wnuk, Maciej
author_facet Adamczyk, Jagoda
Deregowska, Anna
Skoneczny, Marek
Skoneczna, Adrianna
Kwiatkowska, Aleksandra
Potocki, Leszek
Rawska, Ewa
Pabian, Sylwia
Kaplan, Jakub
Lewinska, Anna
Wnuk, Maciej
author_sort Adamczyk, Jagoda
collection PubMed
description Industrial yeast strains of economic importance used in winemaking and beer production are genomically diverse and subjected to harsh environmental conditions during fermentation. In the present study, we investigated wine yeast adaptation to chronic mild alcohol stress when cells were cultured for 100 generations in the presence of non-cytotoxic ethanol concentration. Ethanol-induced reactive oxygen species (ROS) and superoxide signals promoted growth rate during passages that was accompanied by increased expression of sirtuin proteins, Sir1, Sir2 and Sir3, and DNA-binding transcription regulator Rap1. Genome-wide array-CGH analysis revealed that yeast genome was shaped during passages. The gains of chromosomes I, III and VI and significant changes in the gene copy number in nine functional gene categories involved in metabolic processes and stress responses were observed. Ethanol-mediated gains of YRF1 and CUP1 genes were the most accented. Ethanol also induced nucleolus fragmentation that confirms that nucleolus is a stress sensor in yeasts. Taken together, we postulate that wine yeasts of different origin may adapt to mild alcohol stress by shifts in intracellular redox state promoting growth capacity, upregulation of key regulators of longevity, namely sirtuins and changes in the dosage of genes involved in the telomere maintenance and ion detoxification.
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spelling pubmed-50586562016-10-15 Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts Adamczyk, Jagoda Deregowska, Anna Skoneczny, Marek Skoneczna, Adrianna Kwiatkowska, Aleksandra Potocki, Leszek Rawska, Ewa Pabian, Sylwia Kaplan, Jakub Lewinska, Anna Wnuk, Maciej Oncotarget Research Paper: Gerotarget (Focus on Aging) Industrial yeast strains of economic importance used in winemaking and beer production are genomically diverse and subjected to harsh environmental conditions during fermentation. In the present study, we investigated wine yeast adaptation to chronic mild alcohol stress when cells were cultured for 100 generations in the presence of non-cytotoxic ethanol concentration. Ethanol-induced reactive oxygen species (ROS) and superoxide signals promoted growth rate during passages that was accompanied by increased expression of sirtuin proteins, Sir1, Sir2 and Sir3, and DNA-binding transcription regulator Rap1. Genome-wide array-CGH analysis revealed that yeast genome was shaped during passages. The gains of chromosomes I, III and VI and significant changes in the gene copy number in nine functional gene categories involved in metabolic processes and stress responses were observed. Ethanol-mediated gains of YRF1 and CUP1 genes were the most accented. Ethanol also induced nucleolus fragmentation that confirms that nucleolus is a stress sensor in yeasts. Taken together, we postulate that wine yeasts of different origin may adapt to mild alcohol stress by shifts in intracellular redox state promoting growth capacity, upregulation of key regulators of longevity, namely sirtuins and changes in the dosage of genes involved in the telomere maintenance and ion detoxification. Impact Journals LLC 2016-04-10 /pmc/articles/PMC5058656/ /pubmed/27074556 http://dx.doi.org/10.18632/oncotarget.8673 Text en Copyright: © 2016 Adamczyk et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Gerotarget (Focus on Aging)
Adamczyk, Jagoda
Deregowska, Anna
Skoneczny, Marek
Skoneczna, Adrianna
Kwiatkowska, Aleksandra
Potocki, Leszek
Rawska, Ewa
Pabian, Sylwia
Kaplan, Jakub
Lewinska, Anna
Wnuk, Maciej
Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts
title Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts
title_full Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts
title_fullStr Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts
title_full_unstemmed Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts
title_short Adaptive response to chronic mild ethanol stress involves ROS, sirtuins and changes in chromosome dosage in wine yeasts
title_sort adaptive response to chronic mild ethanol stress involves ros, sirtuins and changes in chromosome dosage in wine yeasts
topic Research Paper: Gerotarget (Focus on Aging)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058656/
https://www.ncbi.nlm.nih.gov/pubmed/27074556
http://dx.doi.org/10.18632/oncotarget.8673
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