Abstract:The production of the reactive oxygen species superoxide and hydrogen peroxide in Saccharomyces cerevisiae induces the expression of various defence genes involved in an oxidative stress response. Expression of many of these genes has been shown to be coordinated by two transcriptional regulators, Yap1p and Skn7p, either alone or in concert. Here, we investigated the role of the Yap1p and Skn7p-mediated stress response in the defence against singlet oxygen, a non-radical reactive oxygen species produced mainly… Show more
“…The stress-responsive transcription factors Yap1 and Skn7 have also been reported as targets of calcineurin in other conditions (8). The yap1 skn7 double mutant also retained full responsiveness to FK506, Crz1 loss, and Cmk2 loss (Fig.…”
“…The stress-responsive transcription factors Yap1 and Skn7 have also been reported as targets of calcineurin in other conditions (8). The yap1 skn7 double mutant also retained full responsiveness to FK506, Crz1 loss, and Cmk2 loss (Fig.…”
“…Two main transcriptional activators, Yap1 and Skn7, have been implicated in this adaptive response (29)(30)(31). Although many oxidative stress-responsive defense genes are regulated by both factors, it seems that Yap1 and Skn7 respond to different oxidative stimuli (32,33). The Yap1 basic leucine zipper protein preferentially binds to AP-1 sequences (5=-TTACTAA-3=) in promoters of antioxidant genes (34).…”
Fine-tuned activation of gene expression in response to stress is the result of dynamic interactions of transcription factors with specific promoter binding sites. In the study described here we used a time-resolved luciferase reporter assay in living Saccharomyces cerevisiae yeast cells to gain insights into how osmotic and oxidative stress signals modulate gene expression in a dosesensitive manner. Specifically, the dose-response behavior of four different natural promoters (GRE2, CTT1, SOD2, and CCP1) reveals differences in their sensitivity and dynamics in response to different salt and oxidative stimuli. Characteristic dose-response profiles were also obtained for artificial promoters driven by only one type of stress-regulated consensus element, such as the cyclic AMP-responsive element, stress response element, or AP-1 site. Oxidative and osmotic stress signals activate these elements separately and with different sensitivities through different signaling molecules. Combination of stress-activated cis elements does not, in general, enhance the absolute expression levels; however, specific combinations can increase the inducibility of the promoter in response to different stress doses. Finally, we show that the stress tolerance of the cell critically modulates the dynamics of its transcriptional response in the case of oxidative stress.
“…Msn2/Msn4 nuclear localisation and activity are regulated by both TORC1 and PKA (detailed formerly). For the induction of many antioxidant genes, Skn7 and Yap1 act cooperatively upon oxidative stress (Lee et al, 1999;Brombacher et al, 2006;He et al, 2005). The contribution of Skn7 to the oxidative stress response does not occur through any of the cysteines of the protein.…”
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