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Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae

In Saccharomyces cerevisiae, mitochondrial morphology changes when cells are shifted between nonfermentative and fermentative carbon sources. Here, we show that cells of S. cerevisiae grown in different glucose concentrations display different mitochondrial morphologies. The morphology of mitochondr...

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Autores principales: Aung-Htut, May T., Lam, Yuen T., Lim, Yu-Leng, Rinnerthaler, Mark, Gelling, Cristy L., Yang, Hongyuan, Breitenbach, Michael, Dawes, Ian W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727090/
https://www.ncbi.nlm.nih.gov/pubmed/23936612
http://dx.doi.org/10.1155/2013/636287
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author Aung-Htut, May T.
Lam, Yuen T.
Lim, Yu-Leng
Rinnerthaler, Mark
Gelling, Cristy L.
Yang, Hongyuan
Breitenbach, Michael
Dawes, Ian W.
author_facet Aung-Htut, May T.
Lam, Yuen T.
Lim, Yu-Leng
Rinnerthaler, Mark
Gelling, Cristy L.
Yang, Hongyuan
Breitenbach, Michael
Dawes, Ian W.
author_sort Aung-Htut, May T.
collection PubMed
description In Saccharomyces cerevisiae, mitochondrial morphology changes when cells are shifted between nonfermentative and fermentative carbon sources. Here, we show that cells of S. cerevisiae grown in different glucose concentrations display different mitochondrial morphologies. The morphology of mitochondria in the cells growing in 0.5% glucose was similar to that of mitochondria in respiring cells. However, the mitochondria of cells growing in higher glucose concentrations (2% and 4%) became fragmented after growth in these media, due to the production of acetic acid; however, the fragmentation was not due to intracellular acidification. From a screen of mutants involved in sensing and utilizing nutrients, cells lacking TOR1 had reduced mitochondrial fragmentation, and autophagy was found to be essential for this reduction. Mitochondrial fragmentation in cells grown in high glucose was reversible by transferring them into conditioned medium from a culture grown on 0.5% glucose. Similarly, the chronological lifespan of cells grown in high glucose medium was reduced, and this phenotype could be reversed when cells were transferred to low glucose conditioned medium. These data indicate that chronological lifespan seems correlated with mitochondrial morphology of yeast cells and that both phenotypes can be influenced by factors from conditioned medium of cultures grown in low glucose medium.
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spelling pubmed-37270902013-08-09 Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae Aung-Htut, May T. Lam, Yuen T. Lim, Yu-Leng Rinnerthaler, Mark Gelling, Cristy L. Yang, Hongyuan Breitenbach, Michael Dawes, Ian W. Oxid Med Cell Longev Research Article In Saccharomyces cerevisiae, mitochondrial morphology changes when cells are shifted between nonfermentative and fermentative carbon sources. Here, we show that cells of S. cerevisiae grown in different glucose concentrations display different mitochondrial morphologies. The morphology of mitochondria in the cells growing in 0.5% glucose was similar to that of mitochondria in respiring cells. However, the mitochondria of cells growing in higher glucose concentrations (2% and 4%) became fragmented after growth in these media, due to the production of acetic acid; however, the fragmentation was not due to intracellular acidification. From a screen of mutants involved in sensing and utilizing nutrients, cells lacking TOR1 had reduced mitochondrial fragmentation, and autophagy was found to be essential for this reduction. Mitochondrial fragmentation in cells grown in high glucose was reversible by transferring them into conditioned medium from a culture grown on 0.5% glucose. Similarly, the chronological lifespan of cells grown in high glucose medium was reduced, and this phenotype could be reversed when cells were transferred to low glucose conditioned medium. These data indicate that chronological lifespan seems correlated with mitochondrial morphology of yeast cells and that both phenotypes can be influenced by factors from conditioned medium of cultures grown in low glucose medium. Hindawi Publishing Corporation 2013 2013-07-11 /pmc/articles/PMC3727090/ /pubmed/23936612 http://dx.doi.org/10.1155/2013/636287 Text en Copyright © 2013 May T. Aung-Htut et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Aung-Htut, May T.
Lam, Yuen T.
Lim, Yu-Leng
Rinnerthaler, Mark
Gelling, Cristy L.
Yang, Hongyuan
Breitenbach, Michael
Dawes, Ian W.
Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae
title Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae
title_full Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae
title_fullStr Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae
title_full_unstemmed Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae
title_short Maintenance of Mitochondrial Morphology by Autophagy and Its Role in High Glucose Effects on Chronological Lifespan of Saccharomyces cerevisiae
title_sort maintenance of mitochondrial morphology by autophagy and its role in high glucose effects on chronological lifespan of saccharomyces cerevisiae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727090/
https://www.ncbi.nlm.nih.gov/pubmed/23936612
http://dx.doi.org/10.1155/2013/636287
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