Schüller H J, Schütz A, Knab S, Hoffmann B, Schweizer E
Institut für Mikrobiologie, Biochemie und Genetik, Universität Erlangen/Nürnberg, Germany.
Eur J Biochem. 1994 Oct 1;225(1):213-22. doi: 10.1111/j.1432-1033.1994.00213.x.
The fatty acid synthase genes FAS1 and FAS2 of the yeast Saccharomyces cerevisiae are under transcriptional control of pathway-specific regulators of phospholipid biosynthesis. However, site-directed mutagenesis of the respective cis-acting elements upstream of FAS1 and FAS2 revealed that additional sequences activating both genes must exist. A deletion analysis of the FAS1 promoter lacking the previously characterized inositol/choline-responsive-element motif defined a region (nucleotides -760 to -850) responsible for most of the remaining activation potency. Gel-retardation experiments and in-vitro DNase footprint studies proved the binding of the general regulatory factors Rap1p, Abf1p and Reb1p to this FAS1 upstream region. Mutation of the respective binding sites led to a drop of gene activation to 8% of the wild-type level. Similarly, we also demonstrated the presence of a Reb1p-binding site upstream of FAS2 and its importance for gene activation. Thus, in addition to the previously characterized FAS-binding factor 1 interacting with the inositol/choline-responsive-element motif, a second motif common to the promoter regions of both FAS genes could be identified. Transcription of yeast fatty acid synthase genes is therefore subjected to both the pathway-specific control affecting genes of phospholipid biosynthesis and to the activation by general transcription factors allowing a sufficiently high level of constitutive gene expression.
酿酒酵母的脂肪酸合酶基因FAS1和FAS2受磷脂生物合成途径特异性调节因子的转录控制。然而,对FAS1和FAS2上游各自的顺式作用元件进行定点诱变后发现,必定存在激活这两个基因的其他序列。对缺乏先前鉴定的肌醇/胆碱反应元件基序的FAS1启动子进行缺失分析,确定了一个负责大部分剩余激活能力的区域(核苷酸-760至-850)。凝胶阻滞实验和体外DNase足迹研究证明了一般调节因子Rap1p、Abf1p和Reb1p与该FAS1上游区域的结合。各自结合位点的突变导致基因激活降至野生型水平的8%。同样,我们也证明了FAS2上游存在一个Reb1p结合位点及其对基因激活的重要性。因此,除了先前鉴定的与肌醇/胆碱反应元件基序相互作用的FAS结合因子1外,还可以鉴定出两个FAS基因启动子区域共有的第二个基序。因此,酵母脂肪酸合酶基因的转录既受到影响磷脂生物合成基因的途径特异性控制,也受到一般转录因子的激活,从而允许足够高水平的组成型基因表达。