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Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates

BACKGROUND: Depending on the carbon source, Saccharomyces cerevisiae displays various degrees of respiration. These range from complete respiration as in the case of ethanol, to almost complete fermentation, and thus very low degrees of respiration on glucose. While many key regulators are known for...

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Autores principales: Fendt, Sarah-Maria, Sauer, Uwe
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847992/
https://www.ncbi.nlm.nih.gov/pubmed/20167065
http://dx.doi.org/10.1186/1752-0509-4-12
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author Fendt, Sarah-Maria
Sauer, Uwe
author_facet Fendt, Sarah-Maria
Sauer, Uwe
author_sort Fendt, Sarah-Maria
collection PubMed
description BACKGROUND: Depending on the carbon source, Saccharomyces cerevisiae displays various degrees of respiration. These range from complete respiration as in the case of ethanol, to almost complete fermentation, and thus very low degrees of respiration on glucose. While many key regulators are known for these extreme cases, we focus here on regulators that are relevant at intermediate levels of respiration. RESULTS: We address this question by linking the functional degree of respiration to transcriptional regulation via enzyme abundances. Specifically, we investigated aerobic batch cultures with the differently repressive carbon sources glucose, mannose, galactose and pyruvate. Based on (13)C flux analysis, we found that the respiratory contribution to cellular energy production was largely absent on glucose and mannose, intermediate on galactose and highest on pyruvate. In vivo abundances of 40 respiratory enzymes were quantified by GFP-fusions under each condition. During growth on the partly and fully respired substrates galactose and pyruvate, several TCA cycle and respiratory chain enzymes were significantly up-regulated. From these enzyme levels and the known regulatory network structure, we determined the probability for a given transcription factor to cause the coordinated expression changes. The most probable transcription factors to regulate the different degrees of respiration were Gcr1p, Cat8p, the Rtg-proteins and the Hap-complex. For the latter three ones we confirmed their importance for respiration by quantifying the degree of respiration and biomass yields in the corresponding deletion strains. CONCLUSIONS: Cat8p is required for wild-type like respiration, independent of its known activation of gluconeogenic genes. The Rtg-proteins and the Hap-complex are essential for wild-type like respiration under partially respiratory conditions. Under fully respiratory conditions, the Hap-complex, but not the Rtg-proteins are essential for respiration.
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spelling pubmed-28479922010-04-01 Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates Fendt, Sarah-Maria Sauer, Uwe BMC Syst Biol Research article BACKGROUND: Depending on the carbon source, Saccharomyces cerevisiae displays various degrees of respiration. These range from complete respiration as in the case of ethanol, to almost complete fermentation, and thus very low degrees of respiration on glucose. While many key regulators are known for these extreme cases, we focus here on regulators that are relevant at intermediate levels of respiration. RESULTS: We address this question by linking the functional degree of respiration to transcriptional regulation via enzyme abundances. Specifically, we investigated aerobic batch cultures with the differently repressive carbon sources glucose, mannose, galactose and pyruvate. Based on (13)C flux analysis, we found that the respiratory contribution to cellular energy production was largely absent on glucose and mannose, intermediate on galactose and highest on pyruvate. In vivo abundances of 40 respiratory enzymes were quantified by GFP-fusions under each condition. During growth on the partly and fully respired substrates galactose and pyruvate, several TCA cycle and respiratory chain enzymes were significantly up-regulated. From these enzyme levels and the known regulatory network structure, we determined the probability for a given transcription factor to cause the coordinated expression changes. The most probable transcription factors to regulate the different degrees of respiration were Gcr1p, Cat8p, the Rtg-proteins and the Hap-complex. For the latter three ones we confirmed their importance for respiration by quantifying the degree of respiration and biomass yields in the corresponding deletion strains. CONCLUSIONS: Cat8p is required for wild-type like respiration, independent of its known activation of gluconeogenic genes. The Rtg-proteins and the Hap-complex are essential for wild-type like respiration under partially respiratory conditions. Under fully respiratory conditions, the Hap-complex, but not the Rtg-proteins are essential for respiration. BioMed Central 2010-02-18 /pmc/articles/PMC2847992/ /pubmed/20167065 http://dx.doi.org/10.1186/1752-0509-4-12 Text en Copyright ©2010 Fendt and Sauer; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Fendt, Sarah-Maria
Sauer, Uwe
Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
title Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
title_full Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
title_fullStr Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
title_full_unstemmed Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
title_short Transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
title_sort transcriptional regulation of respiration in yeast metabolizing differently repressive carbon substrates
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847992/
https://www.ncbi.nlm.nih.gov/pubmed/20167065
http://dx.doi.org/10.1186/1752-0509-4-12
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