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General amino acid control and specific arginine repression in Saccharomyces cerevisiae: physical study of the bifunctional regulatory region of the ARG3 gene.

机译:酿酒酵母中的一般氨基酸控制和特异精氨酸抑制:ARG3基因双功能调节区的物理研究。

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摘要

To characterize further the regulatory mechanism modulating the expression of the Saccharomyces cerevisiae ARG3 gene, i.e., the specific repression by arginine and the general amino acid control, we analyzed by deletion the region upstream of that gene, determined the nucleotide sequence of operator-constitutive-like mutations affecting the specific regulation, and examined the behavior of an ARG3-galK fusion engineered at the initiating codon of ARG3. Similarly to what was observed in previous studies on the HIS3 and HIS4 genes, our data show that the general regulation acts as a positive control and that a sequence containing the nucleotide TGACTC, between positions -364 and -282 upstream of the transcription start, functions as a regulatory target site. This sequence contains the most proximal of the two TGACTC boxes identified in front of ARG3. While the general control appears to modulate transcription efficiency, the specific repression by arginine displays a posttranscriptional component (F. Messenguy and E. Dubois, Mol. Gen. Genet. 189:148-156, 1983). Our deletion and gene fusion analyses confirm that the specific and general controls operate independently of each other and assign the site responsible for arginine-specific repression to between positions -170 and +22. In keeping with this assignment, the two operator-constitutive-like mutations were localized at positions -80 and -46, respectively, and thus in a region which is not transcribed. We discuss a hypothesis accounting for the involvement of untranscribed DNA in a posttranscriptional control.
机译:为了进一步表征酿酒酵母ARG3基因表达的调控机制,即精氨酸的特异性抑制和一般氨基酸控制,我们通过删除该基因上游区域进行分析,确定了操纵子-组成-核苷酸序列例如影响特定调控的突变,并研究了在ARG3起始密码子处工程改造的ARG3-galK融合蛋白的行为。与以前对HIS3和HIS4基因的研究相似,我们的数据表明,一般调控可作为阳性对照,并且转录起始上游-364和-282位之间含有TGACTC核苷酸的序列起作用作为监管目标网站。该序列包含在ARG3前面识别的两个TGACTC框中最接近的框。虽然一般的对照似乎调节转录效率,但是精氨酸的特异性阻遏表现出转录后的成分(F. Messenguy and E. Dubois,Mol。Gen. Genet。189:148-156,1983)。我们的缺失和基因融合分析证实,特异性对照和常规对照彼此独立起作用,并将负责精氨酸特异性阻遏的位点分配在位置-170和+22之间。与该分配一致,这两个类似操纵子组成型的突变分别位于-80和-46位置,因此位于一个未转录的区域。我们讨论一个假说,说明转录后对照中涉及未转录的DNA。

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