Lee J, Godon C, Lagniel G, Spector D, Garin J, Labarre J, Toledano M B
Department of Pharmacology and Toxicology, College of Pharmacy, Rutgers University, Piscataway, New Jersey 08855, USA.
J Biol Chem. 1999 Jun 4;274(23):16040-6. doi: 10.1074/jbc.274.23.16040.
Yap1 and Skn7 are two yeast transcriptional regulators that co-operate to activate thioredoxin (TRX2) and thioredoxin reductase (TRR1) in response to redox stress signals. Although they are both important for resistance to H2O2, only Yap1 is important for cadmium resistance, whereas Skn7 has a negative effect upon this response. The respective roles of Yap1 and Skn7 in the induction of defense genes by H2O2 were analyzed by two-dimensional gel electrophoresis. Yap1 controls a large oxidative stress response regulon of at least 32 proteins. Fifteen of these proteins also require the presence of Skn7 for their induction by H2O2. Although about half of the Yap1 target genes do not contain a consensus Yap1 recognition motif, the control of one such gene, TSA1, involves the binding of Yap1 and Skn7 to its promoter in vitro. The co-operative control of the oxidative stress response by Yap1 and Skn7 delineates two gene subsets. Remarkably, these two gene subsets separate antioxidant scavenging enzymes from the metabolic pathways regenerating the main cellular reducing power, glutathione and NADPH. Such a specialization may explain, at least in part, the dissociated function of Yap1 and Skn7 in H2O2 and cadmium resistance.
Yap1和Skn7是两种酵母转录调节因子,它们共同作用以响应氧化还原应激信号激活硫氧还蛋白(TRX2)和硫氧还蛋白还原酶(TRR1)。尽管它们对于抵抗过氧化氢都很重要,但只有Yap1对镉抗性很重要,而Skn7对这种反应有负面影响。通过二维凝胶电泳分析了Yap1和Skn7在过氧化氢诱导防御基因中的各自作用。Yap1控制着一个至少由32种蛋白质组成的大型氧化应激反应调节子。其中15种蛋白质在被过氧化氢诱导时也需要Skn7的存在。尽管约一半的Yap1靶基因不包含一致的Yap1识别基序,但对其中一个这样的基因TSA1的调控涉及Yap1和Skn7在体外与它的启动子结合。Yap1和Skn7对氧化应激反应的协同调控划定了两个基因子集。值得注意的是,这两个基因子集将抗氧化清除酶与再生主要细胞还原能力(谷胱甘肽和NADPH)的代谢途径区分开来。这种专业化至少可以部分解释Yap1和Skn7在过氧化氢和镉抗性中的解离功能。