Saliola Michele, Getuli Claudia, Mazzoni Cristina, Fantozzi Ivana, Falcone Claudio
Department of Cell and Developmental Biology, University of Rome 'La Sapienza', Piazzale Aldo Moro, Rome, Italy.
FEMS Yeast Res. 2007 Aug;7(5):693-701. doi: 10.1111/j.1567-1364.2007.00250.x. Epub 2007 May 16.
KlADH3 is a Kluyveromyces lactis alcohol dehydrogenase gene induced in the presence of all respiratory carbon sources except ethanol, which specifically represses this gene. Deletion analysis of the KlADH3 promoter revealed the presence of both positive and negative elements. However, by site-directed mutagenesis and gel retardation experiments, we identified a 15-bp element responsible for the transcriptional repression of this gene by ethanol. In particular, this element showed putative sites required for the sequential binding of ethanol-induced factors responsible for the repressed conditions, and the binding of additional factors relieved repression. In addition, we showed that the ethanol element was required for in vivo repression of KlAdh3 activity.
KlADH3是乳酸克鲁维酵母的乙醇脱氢酶基因,在除乙醇以外的所有呼吸性碳源存在时被诱导,而乙醇会特异性抑制该基因。对KlADH3启动子的缺失分析揭示了正调控元件和负调控元件的存在。然而,通过定点诱变和凝胶阻滞实验,我们鉴定出一个15碱基对的元件,它负责乙醇对该基因的转录抑制。特别地,该元件显示出乙醇诱导因子顺序结合所需的假定位点,这些因子负责抑制条件,而其他因子的结合则解除抑制。此外,我们表明乙醇元件对于体内抑制KlAdh3活性是必需的。