Crabeel M, Huygen R, Verschueren K, Messenguy F, Tinel K, Cunin R, Glansdorff N
Mol Cell Biol. 1985 Nov;5(11):3139-48. doi: 10.1128/mcb.5.11.3139-3148.1985.
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.
为了进一步表征调节酿酒酵母ARG3基因表达的调控机制,即精氨酸的特异性阻遏和一般氨基酸控制,我们通过缺失分析该基因上游区域,确定影响特异性调控的类操纵子组成型突变的核苷酸序列,并检测在ARG3起始密码子处构建的ARG3-galK融合体的行为。与先前对HIS3和HIS4基因的研究结果相似,我们的数据表明,一般调控起正调控作用,转录起始上游-364至-282位之间包含核苷酸TGACTC的序列作为调控靶位点发挥作用。该序列包含在ARG3前鉴定出的两个TGACTC框中最靠近近端的一个。虽然一般调控似乎调节转录效率,但精氨酸的特异性阻遏表现出转录后成分(F. Messenguy和E. Dubois,《分子遗传学与普通遗传学》189:148 - 156,1983)。我们的缺失和基因融合分析证实,特异性调控和一般调控相互独立运作,并将负责精氨酸特异性阻遏的位点定位在-170至+22位之间。与此定位一致,两个类操纵子组成型突变分别位于-80和-46位,因此位于一个不被转录的区域。我们讨论了一个假说,解释未转录DNA在转录后调控中的作用。