Johnston S A, Hopper J E
Proc Natl Acad Sci U S A. 1982 Nov;79(22):6971-5. doi: 10.1073/pnas.79.22.6971.
GAL4 is a classically defined positive regulatory gene controlling the five inducible structural genes of galactose/melibiose utilization in yeast. The positive regulatory function of the GAL4 gene product in turn is controlled by the product of another gene, the negative regulator GAL80. We have cloned a 3.1-kilobase fragment containing GAL4 by homologous complementation using the multicopy chimeric vector YEp24 and demonstrated that multiple copies of GAL4 in yeast have pronounced dosage effects on the expression of the structural genes. Yeast transformed with GAL4-bearing plasmid become constitutive for expression of the galactose/melibiose genes, even in normally repressing (glucose) medium. Multiple copies of the GAL4 plasmid also increase expression of the structural genes in inducing (galactose) medium and can partially overcome the effects of a dominant super-repressor mutant, GAL80S. Using an internal deletion in GAL4, we have demonstrated that these dosage effects are due to overproduction of GAL4 positive regulatory product rather than an effect of the flanking sequences titrating out a negative regulator. These results point to the importance of competitive interplay between the positive and negative regulatory proteins in the control of this system. We have also used the dosage effect of GAL4 plasmid in combination with different GAL4 and GAL80 alleles to create new phenotypes. We interpret these phenotypes as indicating that (i) the repressing effects of glucose, at least in part, are mediated by the product of the negative regulatory gene, GAL80, and (ii) the GAL80 protein may have specific interactions with the control regions of the structural genes.
GAL4是一个经典定义的正向调节基因,它控制酵母中半乳糖/蜜二糖利用的五个可诱导结构基因。GAL4基因产物的正向调节功能反过来又受另一个基因——负调节因子GAL80的产物控制。我们使用多拷贝嵌合载体YEp24通过同源互补克隆了一个包含GAL4的3.1千碱基片段,并证明酵母中GAL4的多个拷贝对结构基因的表达有显著的剂量效应。用携带GAL4的质粒转化的酵母即使在通常起抑制作用的(葡萄糖)培养基中也会组成型表达半乳糖/蜜二糖基因。GAL4质粒的多个拷贝还会增加诱导(半乳糖)培养基中结构基因的表达,并能部分克服显性超阻遏突变体GAL80S的影响。利用GAL4中的内部缺失,我们证明这些剂量效应是由于GAL4正向调节产物的过量产生,而不是侧翼序列滴定出负调节因子的效应。这些结果表明正向和负向调节蛋白之间的竞争性相互作用在该系统的控制中很重要。我们还利用GAL4质粒的剂量效应与不同的GAL4和GAL80等位基因相结合来创造新的表型。我们将这些表型解释为表明:(i)葡萄糖的抑制作用至少部分是由负调节基因GAL80的产物介导的,以及(ii)GAL80蛋白可能与结构基因的控制区域有特异性相互作用。