Abstract

The whole genome analysis has demonstrated that wine yeasts undergo changes in promoter regions and variations in gene copy number, which make them different to lab strains and help them better adapt to stressful conditions during winemaking, where oxidative stress plays a critical role. Since cytoplasmic thioredoxin II, a small protein with thiol-disulphide oxidoreductase activity, has been seen to perform important functions under biomass propagation conditions of wine yeasts, we studied the involvement of Trx2p in the molecular regulation of the oxidative stress transcriptional response on these strains. In this study, we analyzed the expression levels of several oxidative stress-related genes regulated by either Yap1p or the co-operation between Yap1p and Skn7p. The results revealed a lowered expression for all the tested Skn7p dependent genes in a Trx2p-deficient strain and that Trx2p is essential for the oxidative stress response during respiratory metabolism in wine yeast. Additionally, activity of Yap1p and Skn7p dependent promoters by β-galactosidase assays clearly demonstrated that Skn7p-dependent promoter activation is affected by TRX2 gene deficiency. Finally we showed that deleting the TRX2 gene causes Skn7p hyperphosphorylation under oxidative stress conditions. We propose Trx2p to be a new positive efector in the regulation of the Skn7p transcription factor that controls phosphorylation events and, therefore, modulates the oxidative stress response in yeast.

Highlights

  • The TRX2 gene encodes the cytoplasmic thioredoxin II in Saccharomyces cerevisiae, which is a small protein (11 kDa) with thiol-disulfide oxidoreductase activity [1]

  • We selected T73 for our study, a widely used wine yeast model strain, and we analyzed the effects of TRX2 gene deficiency on the oxidative stress response

  • We focused our experiments on analyzing H2O2 toxicity in wine strains as a common oxidant compound

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Summary

Introduction

The TRX2 gene encodes the cytoplasmic thioredoxin II in Saccharomyces cerevisiae, which is a small protein (11 kDa) with thiol-disulfide oxidoreductase activity [1]. Further evidence that supports the existence of different antioxidant transcriptional responses yet to be described is that Tsa1p deficiency alters the expression of several Yap1p-targeted genes (TRX2, SOD2, CTT1) in the presence of H2O2 without affecting Yap1p nuclear localization [27] All these reports suggest that alternative mechanisms for the oxidative stress response still to be described may exist, which coordinate Trx2p, Tsa1p, Yap1p, Skn7p, and other putative regulatory proteins. We outline that Trx2p is involved mainly in the oxidative stress response under respiratory conditions by modulating Skn7p transcription factor activity by hyper-phosphorylation events to regulate the OSR gene expression

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