Rajkumari K, Kusano S, Ishihama A, Mizuno T, Gowrishankar J
Centre for Cellular & Molecular Biology, Hyderabad, India.
J Bacteriol. 1996 Jul;178(14):4176-81. doi: 10.1128/jb.178.14.4176-4181.1996.
We have used supercoiled DNA templates in this study to demonstrate that transcription in vitro from the P1 and P2 promoters of the osmoresponsive proU operon of Escherichia coli is preferentially mediated by the sigma(s) and sigma70-bearing RNA polymerase holoenzymes, respectively. Addition of potassium glutamate resulted in the activation of transcription from both P1 and P2 and also led to a pronounced enhancement of sigma(s) selectivity at the P1 promoter. Transcription from P2, and to a lesser extent from P1, was inhibited by the nucleoid protein H-NS but only in the absence of potassium glutamate. This study validates the existence of dual promoters with dual specificities for proU transcription. Our results also support the proposals that potassium, which is known to accumulate in cells grown at high osmolarity, is at least partially responsible for effecting the in vivo induction of proU transcription and that it does so through two mechanisms, directly by the activation of RNA polymerase and indirectly by the relief of repression imposed by H-NS.
在本研究中,我们使用了超螺旋DNA模板来证明,大肠杆菌渗透压响应性proU操纵子的P1和P2启动子的体外转录分别优先由含σS和σ70的RNA聚合酶全酶介导。添加谷氨酸钾导致P1和P2的转录激活,并且还导致P1启动子处σS选择性的显著增强。P2的转录以及程度较轻的P1的转录受到类核蛋白H-NS的抑制,但仅在没有谷氨酸钾的情况下。这项研究证实了proU转录具有双重特异性的双重启动子的存在。我们的结果还支持以下提议:已知在高渗透压下生长的细胞中积累的钾至少部分负责在体内诱导proU转录,并且它通过两种机制实现,直接通过激活RNA聚合酶,间接通过解除H-NS施加的抑制作用。