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Journal articles
Quantitative variations of the mitochondrial proteome and phosphoproteome during fermentative and respiratory growth in $Saccharomyces\ cerevisiae$
Abstract : The yeast $Saccharomyces\ cerevisiae$ is a facultative aerobe able to adapt its metabolism according to the carbon substrate. The mechanisms of these adaptations involve at least partly the mitochondria but are not yet well understood. To address the possible role of protein phosphorylation event in their regulation, it is necessary in a first instance to determine precisely the phosphorylation sites that show changes depending on the carbon source. In this aim we performed an overall quantitative proteomic and phosphoproteomic study of isolated mitochondria extracted from yeast grown on fermentative (glucose or galactose) and respiratory (lactate) media. Label free quantitative analysis of protein accumulation revealed significant variation of 176 mitochondrial proteins including 108 proteins less accumulated in glucose medium than in lactate and galactose media. We also showed that the responses to galactose and glucose are not similar. Stable isotope dimethyl labeling allowed the quantitative comparison of phosphorylation levels between the different growth conditions. This study enlarges significantly the map of yeast mitochondrial phosphosites as 670 phosphorylation sites were identified, of which 214 were new and quantified. Above all, we showed that 90 phosphosites displayed a significant variation according to the medium and that variation of phosphorylation level is site-dependent.
Cited literature [31 references]
https://hal-cea.archives-ouvertes.fr/cea-02462405
Contributor : Bruno Savelli <>
Submitted on : Friday, January 31, 2020 - 3:22:29 PM
Last modification on : Wednesday, May 27, 2020 - 6:39:54 AM
Document(s) archivé(s) le : Friday, May 1, 2020 - 4:12:15 PM
Contributor : Bruno Savelli <>
Submitted on : Friday, January 31, 2020 - 3:22:29 PM
Last modification on : Wednesday, May 27, 2020 - 6:39:54 AM
Document(s) archivé(s) le : Friday, May 1, 2020 - 4:12:15 PM
