Comparative proteomic analysis of transition of saccharomyces cerevisiae from glucose-deficient medium to glucose-rich medium

Proteome Science

Hui-Ling Chiang¹  Bruce A Stanley²  Bennett J Giardina¹ 

[1] Department of Cellular and Molecular Physiology, Penn State University College of Medicine, 500 University Drive, Hershey, PA, 17033, USA;Section of Research Resources, Penn State University College of Medicine, 500 University Drive, Hershey, PA, 17033, USA

关键词: MALDI;    iTRAQ;    Saccharomyces cerevisiae;    FBPase;    Gluconeogenesis;    Glycolysis;    Catabolite repression;    Catabolite inactivation;   

Others  :  817246
DOI  :  10.1186/1477-5956-10-40

 received in 2011-12-09, accepted in 2012-05-29,  发布年份 2012

【 摘 要 】

Background

When glucose is added to Saccharomyces cerevisiae grown in non-fermentable carbon sources, genes encoding ribosomal, cell-cycle, and glycolytic proteins are induced. By contrast, genes involved in mitochondrial functions, gluconeogenesis, and the utilization of other carbon sources are repressed. Glucose also causes the activation of the plasma membrane ATPase and the inactivation of gluconeogenic enzymes and mitochondrial enzymes. The goals of this study were to use the iTRAQ-labeling mass spectrometry technique to identify proteins whose relative levels change in response to glucose re-feeding and to correlate changes in protein abundance with changes in transcription and enzymatic activities. We used an experimental condition that causes the degradation of gluconeogenic enzymes when glucose starved cells are replenished with glucose. Identification of these enzymes as being down-regulated by glucose served as an internal control. Furthermore, we sought to identify new proteins that were either up-regulated or down-regulated by glucose.

Results

We have identified new and known proteins that change their relative levels in cells that were transferred from medium containing low glucose to medium containing high glucose. Up-regulated proteins included ribosomal subunits, proteins involved in protein translation, and the plasma membrane ATPase. Down-regulated proteins included small heat shock proteins, mitochondrial proteins, glycolytic enzymes, and gluconeogenic enzymes. Ach1p is involved in acetate metabolism and is also down-regulated by glucose.

Conclusions

We have identified known proteins that have previously been reported to be regulated by glucose as well as new glucose-regulated proteins. Up-regulation of ribosomal proteins and proteins involved in translation may lead to an increase in protein synthesis and in nutrient uptake. Down-regulation of glycolytic enzymes, gluconeogenic enzymes, and mitochondrial proteins may result in changes in glycolysis, gluconeogenesis, and mitochondrial functions. These changes may be beneficial for glucose-starved cells to adapt to the addition of glucose.

【 授权许可】

   
2012 Giardina et al.; licensee BioMed Central Ltd.

【 图 表 】

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