Mountain H A, Byström A S, Korch C
Department of Microbiology, Umeå University, Sweden.
Mol Microbiol. 1993 Jan;7(2):215-28. doi: 10.1111/j.1365-2958.1993.tb01113.x.
A met4 mutant of Saccharomyces cerevisiae was unable to transcribe a number of genes encoding enzymes of the methionine biosynthetic pathway. The sequence of the cloned MET4 gene allowed the previously sequenced flanking LEU4 and POL1 genes to be linked to MET4 into a 10,327 bp contiguous region of chromosome XIV. From the sequence and mapping of the transcriptional start points, MET4 is predicted to encode a protein of 634 amino acids (as opposed to 666 amino acids published by others) with a leucine zipper domain at the C-terminus, preceded by both acidic and basic regions. Thus, MET4 belongs to the family of basic leucine zipper trans-activator proteins. Disruption of MET4 resulted in methionine auxotrophy with no other phenotype. Transcriptional studies showed that MET4 was regulated by the general amino acid control and hence by another bZIP protein encoded by GCN4. GCN4 binding sequences are present between the divergently transcribed MET4 and LEU4 genes. Over-expression of MET4 resulted in leaky expression from the otherwise tightly regulated MET3 promoter under its control. The presence of consensus sequences for other potential regulatory elements in the MET4 promoter suggests a complex regulation of this gene.
酿酒酵母的met4突变体无法转录许多编码甲硫氨酸生物合成途径中酶的基因。克隆的MET4基因序列使得先前测序的侧翼LEU4和POL1基因能够与MET4连接,形成十四号染色体上一个10327 bp的连续区域。根据转录起始点的序列和定位,预测MET4编码一个634个氨基酸的蛋白质(与其他人发表的666个氨基酸不同),其C端有一个亮氨酸拉链结构域,前面是酸性和碱性区域。因此,MET4属于碱性亮氨酸拉链反式激活蛋白家族。MET4的破坏导致甲硫氨酸营养缺陷,没有其他表型。转录研究表明,MET4受一般氨基酸控制调节,因此受GCN4编码的另一种bZIP蛋白调节。GCN4结合序列存在于反向转录的MET4和LEU4基因之间。MET4的过表达导致其控制下原本严格调控的MET3启动子出现渗漏表达。MET4启动子中存在其他潜在调控元件的共有序列,表明该基因存在复杂的调控。