Izui K, Miwa T, Kajitani M, Fujita N, Sabe H, Ishihama A, Katsuki H
Nucleic Acids Res. 1985 Jan 11;13(1):59-71. doi: 10.1093/nar/13.1.59.
In order to find the promoter region of phosphoenolpyruvate carboxylase [EC 4.1.1.31] gene (ppc), in vitro transcription was performed using truncated DNA fragments as templates. Transcription mapping showed three promoters as candidates, but only one of them could be assigned to the promoter of ppc gene, considering the nucleotide sequence of its coding region (Fujita, N., Miwa, T., Ishijima, S., Izui, K. and Katsuki, H. (1984) J. Biochem. 95, 909-916). Nuclease S1 mapping showed that the in vivo and in vitro transcription initiation sites are identical and that the site lies 91 or 92 nucleotides upstream the translation initiation site. No alteration of the transcription initiation site was observed whether the cells were starved for an amino acid or grown on various carbon sources. The sequences of the -10 and -35 regions were fairly in accordance with the consensus sequences hitherto reported. Some features of the sequence around the promoter region were discussed.
为了找到磷酸烯醇丙酮酸羧化酶[EC 4.1.1.31]基因(ppc)的启动子区域,以截短的DNA片段为模板进行了体外转录。转录图谱显示有三个启动子作为候选,但考虑到其编码区的核苷酸序列,其中只有一个可被确定为ppc基因的启动子(藤田,N.,三泽,T.,石岛,S.,井井,K.和胜木,H.(1984年)《生物化学杂志》95,909 - 916)。核酸酶S1图谱显示体内和体外转录起始位点相同,该位点位于翻译起始位点上游91或92个核苷酸处。无论细胞是氨基酸饥饿还是在各种碳源上生长,均未观察到转录起始位点的改变。-10和-35区域的序列与迄今报道的共有序列相当一致。讨论了启动子区域周围序列的一些特征。