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A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1
Trehalose metabolism in yeast has been linked to a variety of phenotypes, including heat resistance, desiccation tolerance, carbon-source utilization, and sporulation. The relationships among the several phenotypes of mutants unable to synthesize trehalose are not understood, even though the pathway...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259636/ https://www.ncbi.nlm.nih.gov/pubmed/32470059 http://dx.doi.org/10.1371/journal.pone.0233779 |
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author | Gibney, Patrick A. Chen, Anqi Schieler, Ariel Chen, Jonathan C. Xu, Yifan Hendrickson, David G. McIsaac, R. Scott Rabinowitz, Joshua D. Botstein, David |
author_facet | Gibney, Patrick A. Chen, Anqi Schieler, Ariel Chen, Jonathan C. Xu, Yifan Hendrickson, David G. McIsaac, R. Scott Rabinowitz, Joshua D. Botstein, David |
author_sort | Gibney, Patrick A. |
collection | PubMed |
description | Trehalose metabolism in yeast has been linked to a variety of phenotypes, including heat resistance, desiccation tolerance, carbon-source utilization, and sporulation. The relationships among the several phenotypes of mutants unable to synthesize trehalose are not understood, even though the pathway is highly conserved. One of these phenotypes is that tps1Δ strains cannot reportedly grow on media containing glucose or fructose, even when another carbon source they can use (e.g. galactose) is present. Here we corroborate the recent observation that a small fraction of yeast tps1Δ cells do grow on glucose, unlike the majority of the population. This is not due to a genetic alteration, but instead resembles the persister phenotype documented in many microorganisms and cancer cells undergoing lethal stress. We extend these observations to show that this phenomenon is glucose-specific, as it does not occur on another highly fermented carbon source, fructose. We further demonstrate that this phenomenon appears to be related to mitochondrial complex III function, but unrelated to inorganic phosphate levels in the cell, as had previously been suggested. Finally, we found that this phenomenon is specific to S288C-derived strains, and is the consequence of a variant in the MKT1 gene. |
format | Online Article Text |
id | pubmed-7259636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72596362020-06-08 A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 Gibney, Patrick A. Chen, Anqi Schieler, Ariel Chen, Jonathan C. Xu, Yifan Hendrickson, David G. McIsaac, R. Scott Rabinowitz, Joshua D. Botstein, David PLoS One Research Article Trehalose metabolism in yeast has been linked to a variety of phenotypes, including heat resistance, desiccation tolerance, carbon-source utilization, and sporulation. The relationships among the several phenotypes of mutants unable to synthesize trehalose are not understood, even though the pathway is highly conserved. One of these phenotypes is that tps1Δ strains cannot reportedly grow on media containing glucose or fructose, even when another carbon source they can use (e.g. galactose) is present. Here we corroborate the recent observation that a small fraction of yeast tps1Δ cells do grow on glucose, unlike the majority of the population. This is not due to a genetic alteration, but instead resembles the persister phenotype documented in many microorganisms and cancer cells undergoing lethal stress. We extend these observations to show that this phenomenon is glucose-specific, as it does not occur on another highly fermented carbon source, fructose. We further demonstrate that this phenomenon appears to be related to mitochondrial complex III function, but unrelated to inorganic phosphate levels in the cell, as had previously been suggested. Finally, we found that this phenomenon is specific to S288C-derived strains, and is the consequence of a variant in the MKT1 gene. Public Library of Science 2020-05-29 /pmc/articles/PMC7259636/ /pubmed/32470059 http://dx.doi.org/10.1371/journal.pone.0233779 Text en © 2020 Gibney et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gibney, Patrick A. Chen, Anqi Schieler, Ariel Chen, Jonathan C. Xu, Yifan Hendrickson, David G. McIsaac, R. Scott Rabinowitz, Joshua D. Botstein, David A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 |
title | A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 |
title_full | A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 |
title_fullStr | A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 |
title_full_unstemmed | A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 |
title_short | A tps1Δ persister-like state in Saccharomyces cerevisiae is regulated by MKT1 |
title_sort | tps1δ persister-like state in saccharomyces cerevisiae is regulated by mkt1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259636/ https://www.ncbi.nlm.nih.gov/pubmed/32470059 http://dx.doi.org/10.1371/journal.pone.0233779 |
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