Polaczek P, Wright A
Department of Molecular Biology and Microbiology, Tufts University, Boston, MA 02111.
New Biol. 1990 Jun;2(6):574-82.
The dnaA gene of Escherichia coli specifies a product that is a key element in the initiation of DNA replication. Expression of dnaA occurs from two promoters, 1P and 2P, which flank a DnaA protein binding site (DnaA box). In this paper we describe the effects of DnaA box mutations on transcription from the two promoters, measured with the use of dnaA-galK gene fusions. All of the mutations examined led to a five-fold increase in expression from the upstream promoter, 1P, suggesting that expression from this promoter is negatively autoregulated by binding of DnaA protein to the box. The same mutations led to a decrease in expression from promoter 2P, suggesting that the DnaA box plays a role in activating promoter 2P under normal conditions. Overproduction of DnaA protein, above normal physiological levels, led to decreased transcription from both promoters. We present evidence from analysis of both dnaA mRNA and DnaA protein that promoter 2P is subject to growth rate-dependent control and that this promoter, but not promoter 1P, is completely shut off in the stationary phase of growth.
大肠杆菌的dnaA基因编码一种产物,它是DNA复制起始过程中的关键元件。dnaA基因的表达由两个启动子1P和2P驱动,这两个启动子位于一个DnaA蛋白结合位点(DnaA框)两侧。在本文中,我们描述了利用dnaA-galK基因融合技术检测到的DnaA框突变对这两个启动子转录的影响。所有检测的突变均导致上游启动子1P的表达增加了五倍,这表明该启动子的表达受到DnaA蛋白与该框结合的负向自动调节。相同的突变导致启动子2P的表达下降,这表明在正常条件下DnaA框在激活启动子2P中发挥作用。DnaA蛋白在高于正常生理水平下过量表达,导致两个启动子的转录均下降。我们通过对dnaA mRNA和DnaA蛋白的分析提供证据表明,启动子2P受到生长速率依赖性调控,并且在生长稳定期该启动子(而非启动子1P)完全关闭。