Cheema A K, Choudhury N R, Das H K
Genetic Engineering Unit and Centre for Biotechnology, Jawaharlal Nehru University, New Delhi 110067, India.
J Bacteriol. 1999 Sep;181(17):5296-302. doi: 10.1128/JB.181.17.5296-5302.1999.
The nif promoters of Klebsiella pneumoniae must be activated by proteins bound to upstream sequences which are thought to interact with the sigma54-RNA polymerase holoenzyme by DNA looping. NifA is the activator for most of the promoters, and integration host factor (IHF) mediates the DNA looping. While NtrC is the activator for the nifLA promoter, no IHF appears to be involved. There are two A tracts and one T tract between the upstream enhancer and the nifLA promoter. This DNA segment exhibits anomalous electrophoretic mobility, suggesting intrinsic sequence-induced curvature in the DNA. On the one hand, mutation of the A tracts or T tract individually or together, or deletion of the A tracts and the T tract reduces the anomaly; on the other hand, creation of two additional A tracts enhances the anomaly. Intrinsic curvature in the DNA has been confirmed by circular permutation analysis after cloning the DNA fragment in the vector pBend 2 and also by electron microscopy. Computer simulation with the DNA base sequence is also suggestive of intrinsic curvature. A transcriptional fusion with the Escherichia coli lacZ gene of the DNA fragment containing the nifLA promoter and the wild-type or the mutated upstream sequences was constructed, and in vivo transcription in K. pneumoniae and E. coli was monitored. There was indeed very good correlation between the extent of intrinsic curvature of the DNA and transcription from the promoter, suggesting that DNA curvature due to the A tracts and the T tract was necessary for transcription in vivo from the nifLA promoter of K. pneumoniae.
肺炎克雷伯菌的nif启动子必须被与上游序列结合的蛋白质激活,这些上游序列被认为通过DNA环化与σ54 - RNA聚合酶全酶相互作用。NifA是大多数启动子的激活因子,整合宿主因子(IHF)介导DNA环化。而NtrC是nifLA启动子的激活因子,似乎没有IHF参与其中。在上游增强子和nifLA启动子之间有两个A序列和一个T序列。该DNA片段表现出异常的电泳迁移率,表明DNA中存在内在序列诱导的弯曲。一方面,单独或一起突变A序列或T序列,或缺失A序列和T序列会降低这种异常;另一方面,额外创建两个A序列会增强这种异常。在将DNA片段克隆到载体pBend 2中后,通过环形置换分析以及电子显微镜证实了DNA中的内在弯曲。对DNA碱基序列进行计算机模拟也提示存在内在弯曲。构建了包含nifLA启动子和野生型或突变上游序列的DNA片段与大肠杆菌lacZ基因的转录融合体,并监测了肺炎克雷伯菌和大肠杆菌中的体内转录情况。DNA的内在弯曲程度与启动子的转录之间确实存在非常好的相关性,这表明由A序列和T序列导致的DNA弯曲对于肺炎克雷伯菌nifLA启动子的体内转录是必要的。