Cheung A Y, Watson L, Söll D
J Bacteriol. 1985 Jan;161(1):212-8. doi: 10.1128/jb.161.1.212-218.1985.
We studied the regulation of in vivo expression of Escherichia coli glutaminyl-tRNA synthetase at the transcriptional and translational level by analysis of glnS mRNA and glutaminyl-tRNA synthetase levels under a variety of growth conditions. In addition, strains carrying fusions of the beta-galactosidase structural gene and the glnS promoter were constructed and subsequently used for glnS regulatory studies. The level of glutaminyl-tRNA synthetase increases with the increasing growth rate, with a concomitant though much larger increase in glnS mRNA levels. Thus, transcriptional control appears to mediate metabolic regulation. It is known that glnR5, a regulatory mutation unlinked to glnS, causes overproduction of glutaminyl-tRNA synthetase. Here we showed that the glnR5 product enhances transcription of glnS 10- to 15-fold. The glnR5 mutation does not affect metabolic control. Thus, glnS appears to be regulated by two different control systems affecting transcription. Furthermore, our results suggest post-transcriptional regulation of glutaminyl-tRNA synthetase.
我们通过分析在多种生长条件下谷氨酰胺-tRNA合成酶(glnS)mRNA和谷氨酰胺-tRNA合成酶的水平,研究了大肠杆菌谷氨酰胺-tRNA合成酶在体内转录和翻译水平的调控。此外,构建了携带β-半乳糖苷酶结构基因与glnS启动子融合的菌株,并随后用于glnS调控研究。谷氨酰胺-tRNA合成酶的水平随着生长速率的增加而增加,同时glnS mRNA水平也有相应的增加,不过增加幅度更大。因此,转录控制似乎介导了代谢调控。已知glnR5是一个与glnS不连锁的调控突变,会导致谷氨酰胺-tRNA合成酶的过量产生。在此我们表明,glnR5产物可将glnS的转录增强10至15倍。glnR5突变不影响代谢调控。因此,glnS似乎受影响转录的两种不同控制系统调控。此外,我们的结果提示了谷氨酰胺-tRNA合成酶的转录后调控。