Butler J S, Springer M, Dondon J, Grunberg-Manago M
J Bacteriol. 1986 Jan;165(1):198-203. doi: 10.1128/jb.165.1.198-203.1986.
Five mutations in thrS, the gene for threonyl-tRNA synthetase, have been characterized, and the sites of the mutations have been localized to different regions of the thrS gene by recombination with M13 phage carrying portions of the thrS gene. Quantitative immunoblotting shows that some of these mutations cause the overproduction of structurally altered threonyl-tRNA synthetase in vivo. The amounts of in vivo thrS mRNA as measured by quantitative hybridization are, however, the same as wild-type levels for each mutant. These results demonstrate that the expression of threonyl-tRNA synthetase is autoregulated at the posttranscriptional level in vivo.
苏氨酰 - tRNA合成酶基因thrS中的五个突变已被鉴定,并且通过与携带thrS基因部分片段的M13噬菌体进行重组,将突变位点定位到thrS基因的不同区域。定量免疫印迹显示,其中一些突变会导致体内结构改变的苏氨酰 - tRNA合成酶过量产生。然而,通过定量杂交测量的体内thrS mRNA量与每个突变体的野生型水平相同。这些结果表明,苏氨酰 - tRNA合成酶的表达在体内转录后水平受到自动调节。