Imrichova Denisa, Sarinova Marcela, Cernicka Jana, Gbelska Yvetta, Subik Julius
Department of Microbiology and Virology, Comenius University in Bratislava, Mlynska dolina B-2, 842 15 Bratislava, Slovak Republic.
FEMS Yeast Res. 2005 Feb;5(4-5):323-9. doi: 10.1016/j.femsyr.2004.11.004.
The b-Zip transcription factor Yap1p plays an important role in oxidative stress response and multidrug resistance in Saccharomyces cerevisiae. We have previously demonstrated that the KNQ1 gene, encoding a multidrug transporter of the major facilitator superfamily in Kluyveromyces lactis and containing two potential Yap1p response elements in its promoter, is a putative transcriptional target of KlYap1p, the structural and functional homologue of ScYap1p. In this work, we provide evidence that KlYAP1 controls the expression of the KNQ1 gene. Using a P(KNQ1)-gusA fusion construct we showed that the expression of KNQ1 is induced upon cell treatment with the oxidizing agents H2O2 and menadione and that this induction is mediated by KlYap1p. These results were confirmed by Northern-blot analysis showing that the expression of KNQ1 is responsive to hydrogen peroxide and dependent on the presence of KlYap1p. The role of KlYAP1 in the control of KNQ1 expression was further demonstrated by EMSA experiments and drug resistance assays. These results clearly demonstrate the involvement of the KlYap1p transcription factor in the control of KNQ1 gene expression.
b-Zip转录因子Yap1p在酿酒酵母的氧化应激反应和多药耐药性中发挥着重要作用。我们之前已经证明,KNQ1基因编码乳酸克鲁维酵母主要易化子超家族的一种多药转运蛋白,其启动子中含有两个潜在的Yap1p反应元件,是ScYap1p的结构和功能同源物KlYap1p的一个假定转录靶点。在这项研究中,我们提供证据表明KlYAP1控制KNQ1基因的表达。使用P(KNQ1)-gusA融合构建体,我们发现用氧化剂H2O2和甲萘醌处理细胞后,KNQ1的表达被诱导,并且这种诱导是由KlYap1p介导的。Northern杂交分析证实了这些结果,表明KNQ基因的表达对过氧化氢有反应,并且依赖于KlYap1p的存在。EMSA实验和耐药性分析进一步证明了KlYAP1在控制KNQ1表达中的作用。这些结果清楚地证明了KlYap1p转录因子参与了KNQ1基因表达的调控。