Sawers G, Böck A
Lehrstuhl für Mikrobiologie, Universität München, Federal Republic of Germany.
J Bacteriol. 1989 May;171(5):2485-98. doi: 10.1128/jb.171.5.2485-2498.1989.
The sequence of the 5' regulatory region of the gene encoding pyruvate formate-lyase is presented together with a detailed analysis of the transcriptional signals required for its expression. The sequence data revealed that a gene coding for an open reading frame (orf) of unknown function is situated just upstream of the pfl gene. Analysis of RNA transcripts by Northern blot hybridization demonstrated that the genes for orf and pfl were cotranscribed as an operon but that the pfl gene was also transcribed alone. S1 nuclease protection analysis, primer extension, and construction of lacZ fusions with sequential deletions in the pfl 5' regulatory sequence revealed that transcription initiated from at least six promoters which spanned 1.2 kilobases of DNA. Three of these lay within the orf structural gene and were responsible for the high expression of pfl. All transcripts originating from these promoters terminated in the 3' untranslated region of the pfl gene at a strong rho-independent transcription terminator. All of the promoters were coordinately regulated by anaerobiosis, pyruvate, nitrate, and the fnr gene product, and the sequences thought to be responsible for this regulation lay 0.8 to 1.3 kilobases upstream of the translational initiation codon of the pfl gene. There were two sequences within this region which showed strong homology with that proposed to be required for recognition by the Fnr protein.
本文展示了编码丙酮酸甲酸裂解酶基因5'调控区的序列,并对其表达所需的转录信号进行了详细分析。序列数据显示,一个编码功能未知的开放阅读框(orf)的基因位于pfl基因的上游。通过Northern印迹杂交对RNA转录本进行分析表明,orf和pfl基因作为一个操纵子共同转录,但pfl基因也可单独转录。S1核酸酶保护分析、引物延伸以及构建在pfl 5'调控序列中具有连续缺失的lacZ融合体,结果表明转录起始于至少六个启动子,这些启动子跨越了1.2千碱基的DNA区域。其中三个启动子位于orf结构基因内,负责pfl基因的高表达。所有源自这些启动子的转录本在pfl基因的3'非翻译区的一个强rho非依赖性转录终止子处终止。所有启动子均受厌氧、丙酮酸、硝酸盐和fnr基因产物的协同调控,并且被认为负责这种调控的序列位于pfl基因翻译起始密码子上游0.8至1.3千碱基处。该区域内有两个序列与Fnr蛋白识别所需的序列具有高度同源性。