Takayanagi Y, Tanaka K, Takahashi H
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.
Mol Gen Genet. 1994 Jun 3;243(5):525-31. doi: 10.1007/BF00284200.
The nucleotide sequence of the 5' upstream region of the Escherichia coli rpoS gene was determined and analyzed. At least four promoters responsible for rpoS transcription were identified, and designated P1, P2, P3 and P4, P1 being furthest from the upstream. Using lacZ fusion genes, the P2 promoter was found to be the strongest of the four. All of these promoters are regulated similarly, and their activity is enhanced 2 to 3-fold in stationary phase. P1 and P2 transcription start sites were determined by primer extension analyses. The P2 promoter region shows similarity to the consensus sigma 70-type promoter sequence, and was recognized by both E sigma 70 and E sigma 38 holoenzymes in vitro. The mRNA transcribed from the most distal promoter, P1, appears to include another open reading frame (orf-281), indicating that the two open reading frames comprise an operon. The rpoS gene product (sigma 38) was rapidly degraded after addition of chloramphenicol to cultures in the exponential, but not the stationary phase. This strongly suggests that posttranslational regulation is involved in the control of rpoS expression.
测定并分析了大肠杆菌rpoS基因5'上游区域的核苷酸序列。确定了至少四个负责rpoS转录的启动子,分别命名为P1、P2、P3和P4,其中P1距离上游最远。利用lacZ融合基因发现,P2启动子是这四个启动子中最强的。所有这些启动子的调控方式相似,且它们的活性在稳定期提高2至3倍。通过引物延伸分析确定了P1和P2的转录起始位点。P2启动子区域与共有σ70型启动子序列相似,并且在体外能被Eσ70和Eσ38全酶识别。从最远端启动子P1转录的mRNA似乎包含另一个开放阅读框(orf-281),这表明这两个开放阅读框构成一个操纵子。在对数期而非稳定期的培养物中添加氯霉素后,rpoS基因产物(σ38)迅速降解。这有力地表明,翻译后调控参与了rpoS表达的控制。