Gendron N, Putzer H, Grunberg-Manago M
Service de Biochimie, Centre National de la Recherche Scientifique URA 1139, Institut de Biologie Physico-Chimique, Paris, France.
J Bacteriol. 1994 Jan;176(2):486-94. doi: 10.1128/jb.176.2.486-494.1994.
The "housekeeping" threonyl-tRNA synthetase gene (thrS) of Bacillus subtilis is shown to be transcribed in vivo and in vitro from a single promoter. In vitro, 85% of all messages transcribed from the thrS promoter are terminated at a strong factor-independent terminator localized upstream of the thrS Shine-Dalgarno sequence, within the 305-nucleotide-long leader region. Overexpression of thrS represses transcriptional and translational thrS-lacZ fusions to a similar extent, suggesting that thrS is autoregulated at the transcriptional level. We show that autogenous control does not act at the level of transcription initiation but involves antitermination of the transcription mechanism. thrZ, the second threonyl-tRNA synthetase gene, is also autogenously regulated. However, the ability of the ThrS synthetase to repress thrS as well as thrZ expression is much greater than that of the ThrZ synthetase.
枯草芽孢杆菌的“管家”苏氨酰 - tRNA合成酶基因(thrS)在体内和体外均从单一启动子转录。在体外,从thrS启动子转录的所有信使RNA中,85% 在位于thrS Shine-Dalgarno序列上游、305个核苷酸长的前导区内的一个强的不依赖因子的终止子处终止。thrS的过表达对转录和翻译的thrS - lacZ融合体有相似程度的抑制作用,这表明thrS在转录水平上是自我调节的。我们表明,自身调节并非作用于转录起始水平,而是涉及转录机制的抗终止作用。第二个苏氨酰 - tRNA合成酶基因thrZ也受到自身调节。然而,ThrS合成酶抑制thrS以及thrZ表达的能力远大于ThrZ合成酶。