Butler G, McConnell D J
Department of Genetics, Trinity College, Dublin, Ireland.
Curr Genet. 1988 Nov;14(5):405-12. doi: 10.1007/BF00521261.
The upstream region of the Saccharomyces cerevisiae pyruvate decarboxylase structural gene, PDC1, has been isolated and fused to the indicator gene Escherichia coli lacZ. 1.2 kb of the upstream region has been sequenced. The PDC1-lacZ fusion has been integrated at the ura3-52 locus in the yeast genome, and has a basal level of expression on ethanol. On glucose media this level is increased 30-50 fold. An upstream activation site, UASpdc, between 793 and 535 bp upstream from the ATG of PDC1, which mediates the response to glucose has been identified by deletion analysis. The UASpdc contains a consensus RPG box, originally identified in ribosomal protein genes (Leer et al. 1985). The function of UASpdc is independent of distance from the ATG. There is also an upstream repressing sequence located between 535 and 385 bp upstream from the translational start of PDC1.
已分离出酿酒酵母丙酮酸脱羧酶结构基因PDC1的上游区域,并将其与指示基因大肠杆菌lacZ融合。已对1.2 kb的上游区域进行了测序。PDC1-lacZ融合基因已整合到酵母基因组的ura3-52位点,在乙醇上具有基础表达水平。在葡萄糖培养基上,该水平会增加30至50倍。通过缺失分析确定了PDC1的ATG上游793至535 bp之间的一个上游激活位点UASpdc,它介导对葡萄糖的反应。UASpdc包含一个共有RPG框,最初在核糖体蛋白基因中鉴定到(Leer等人,1985年)。UASpdc的功能与距ATG的距离无关。在PDC1翻译起始上游535至385 bp之间还存在一个上游抑制序列。