Gangloff S P, Marguet D, Lauquin G J
Institut de Biochimie Cellulaire et Neurochimie, Centre National de la Recherche Scientifique, Bordeaux, France.
Mol Cell Biol. 1990 Jul;10(7):3551-61. doi: 10.1128/mcb.10.7.3551-3561.1990.
We have isolated genomic clones complementing the aconitase-deficient strain (glu1-1) of Saccharomyces cerevisiae. Identification of the aconitase gene was established by enzymatic assays and molecular analyses. The corresponding mRNA has been characterized, and its direction of transcription has been determined. The complete nucleotide sequence revealed strong amino acid homologies with the sequences of some peptides isolated from the mammalian protein. Disruption of the gene by deletion-insertion led to glutamate auxotrophy. Expression of the aconitase gene was sensitive to glucose repression and was synergistically down regulated by glucose and glutamate.
我们已分离出可互补酿酒酵母乌头酸酶缺陷型菌株(glu1-1)的基因组克隆。通过酶学分析和分子分析确定了乌头酸酶基因。已对相应的mRNA进行了表征,并确定了其转录方向。完整的核苷酸序列显示与从哺乳动物蛋白质中分离出的一些肽的序列具有很强的氨基酸同源性。通过缺失插入破坏该基因导致谷氨酸营养缺陷。乌头酸酶基因的表达对葡萄糖阻遏敏感,并受到葡萄糖和谷氨酸的协同下调。