Urbanowski M L, Stauffer G V
Department of Microbiology, University of Iowa, Iowa City 52242.
Gene. 1988 Dec 15;73(1):193-200. doi: 10.1016/0378-1119(88)90325-3.
The control region of the Salmonella typhimurium metH gene was sequenced and the transcription start point was determined by S1 nuclease mapping experiments. Activation of the metH gene by the metR gene product was shown to occur at the level of transcription. The translation start site was determined by amino acid sequence analysis of the amino terminus of a chimeric Met-Lac fusion protein encoded by a metH-lacZ gene fusion. Analysis of the nucleotide sequence of the metH promoter region showed that two sequence elements, present in the promoters of all other met biosynthetic genes thus far examined, are not present in the metH promoter region, namely, the repeated MetJ repressor recognition sequence 5'-AGACGTCT-3' and a highly conserved sequence 5'-TGGA----TAAAC-3' of unknown function.
对鼠伤寒沙门氏菌metH基因的调控区进行了测序,并通过S1核酸酶图谱实验确定了转录起始点。结果表明,metR基因产物对metH基因的激活发生在转录水平。通过对由metH-lacZ基因融合体编码的嵌合Met-Lac融合蛋白氨基末端的氨基酸序列分析,确定了翻译起始位点。对metH启动子区域核苷酸序列的分析表明,在迄今为止所研究的所有其他met生物合成基因的启动子中存在的两个序列元件,在metH启动子区域中不存在,即重复的MetJ阻遏物识别序列5'-AGACGTCT-3'和功能未知的高度保守序列5'-TGGA----TAAAC-3'。