Marconi R, Wigboldus J, Weissbach H, Brot N
Roche Research Center, Nutley, NJ 07110.
Biochem Biophys Res Commun. 1991 Mar 29;175(3):1057-63. doi: 10.1016/0006-291x(91)91672-y.
The 5' upstream region of the Escherichia coli metH gene has been sequenced. Primer extension analysis revealed a transcription start site at 324 bases upstream of the initiator codon. An 8 base sequence homologous to the MetR binding region on the E. coli metE gene is present 217 bp downstream of the transcription start site. Gel retardation experiments showed that purified MetR protein could bind to a 30 base oligonucleotide containing the putative MetR binding region. No "met box" was present which explains the relative lack of regulation of the expression of the metH gene by methionine.
已对大肠杆菌metH基因的5'上游区域进行了测序。引物延伸分析揭示了在起始密码子上游324个碱基处的一个转录起始位点。在转录起始位点下游217 bp处存在一个与大肠杆菌metE基因上的MetR结合区域同源的8碱基序列。凝胶阻滞实验表明,纯化的MetR蛋白可与包含假定MetR结合区域的30碱基寡核苷酸结合。不存在“met框”,这解释了metH基因表达相对缺乏甲硫氨酸调控的原因。