Brisco P R, Cunningham T S, Kohlhaw G B
Genetics. 1987 Jan;115(1):91-9. doi: 10.1093/genetics/115.1.91.
The LEU3 gene of the yeast Saccharomyces cerevisiae, which is involved in the regulation of at least two LEU structural genes (LEU1 and LEU2), has been cloned by complementation of leu3 mutations and shown to reside within a 5.6-kb fragment. Transformation of leu3 mutants with LEU3-carrying multicopy plasmids restored normal, leucine-independent growth behavior in the recipients. It also restored approximately wild-type levels of isopropylmalate isomerase (LEU1) and beta-isopropylmalate dehydrogenase (LEU2), which were strongly reduced when exogenous leucine was supplied. Strains containing a disrupted leu3 allele were constructed by deleting 0.7-kb of LEU3 DNA and inserting the yeast HIS3 gene in its place. Like other leu3 mutants, these strains were leaky leucine auxotrophs, owing to a basal level of expression of LEU1 and LEU2. Southern transfer and genetic analyses of strains carrying a disrupted leu3 allele demonstrated that the cloned gene was LEU3, as opposed to a suppressor. Disruption of LEU3 was performed also with a diploid and shown to be nonlethal by tetrad analysis. Northern transfer experiments showed that the LEU3 gene produces mRNA approximately 2.9 kilonucleotides in length. The leu3 marker was mapped to chromosome XII by the spo11 method. Linkage to ura4 by about 44 centiMorgans places leu3 on the right arm of this chromosome.
酿酒酵母的LEU3基因参与至少两个亮氨酸结构基因(LEU1和LEU2)的调控,通过对leu3突变体的互补作用进行了克隆,并显示位于一个5.6kb的片段内。用携带LEU3的多拷贝质粒转化leu3突变体可使受体恢复正常的、不依赖亮氨酸的生长行为。它还恢复了异丁基苹果酸异构酶(LEU1)和β-异丁基苹果酸脱氢酶(LEU2)的近似野生型水平,当提供外源亮氨酸时,这两种酶的水平会大幅降低。通过缺失0.7kb的LEU3 DNA并插入酵母HIS3基因来构建含有破坏的leu3等位基因的菌株。与其他leu3突变体一样,由于LEU1和LEU2的基础表达水平,这些菌株是渗漏型亮氨酸营养缺陷型。对携带破坏的leu3等位基因的菌株进行Southern转移和遗传分析表明,克隆的基因是LEU3,而不是一个抑制子。还用二倍体进行了LEU3的破坏,并通过四分体分析表明其是非致死的。Northern转移实验表明,LEU3基因产生长度约为2.9千核苷酸的mRNA。通过spo11方法将leu3标记定位到第十二号染色体上。与ura4的连锁距离约为44厘摩,将leu3定位在该染色体的右臂上。