Ow D W, Sundaresan V, Rothstein D M, Brown S E, Ausubel F M
Proc Natl Acad Sci U S A. 1983 May;80(9):2524-8. doi: 10.1073/pnas.80.9.2524.
We have determined the nucleotide sequences of the Klebsiella pneumoniae nifL (regulation of N2 fixation genes) and the Escherichia coli glnA (glutamine synthetase) promoters. We compared these sequences with the published sequences of three other promoters that, like the nifL and glnA promoters, are activated by the general nitrogen regulators glnF (ntrA) and glnG (ntrC). The three promoters are the argTr (arginine transport) and dhuA (histidine transport) promoters of Salmonella typhimurium and the nifH (nitrogenase) promoter of Rhizobium meliloti. All five sequences (with at most one mismatch) contain the heptameric consensus sequence T-T-T-T-G-C-A. In the R. meliloti nifH and K. pneumoniae nifL promoters, in which the transcription initiation sites have been determined, the consensus sequence is situated in the -15 region. We recently reported that the K. pneumoniae nifA product, which activates nif genes, can substitute for the glnG (ntrC) product in activating promoters of several genes involved in nitrogen assimilation, including the nifL, the glnA, and the R. meliloti nifH promoters. It is likely that nifA also activates the S. typhimurium argTr and dhuA promoters. In contrast, the glnG product cannot substitute for the nifA product in the activation of the K. pneumoniae nifH (nitrogenase) promoter. Consistent with this latter observation, and supporting the conclusion that the T-T-T-T-G-C-A sequence is a regulatory site for glnG product activation, the K. pneumoniae nifH promoter (C-C-C-T-G-C-A) has only partial similarity with the T-T-T-T-G-C-A consensus sequence in the -15 region.
我们已经测定了肺炎克雷伯菌nifL(固氮基因调控)和大肠杆菌glnA(谷氨酰胺合成酶)启动子的核苷酸序列。我们将这些序列与其他三个启动子已发表的序列进行了比较,这三个启动子与nifL和glnA启动子一样,由通用氮调节因子glnF(ntrA)和glnG(ntrC)激活。这三个启动子分别是鼠伤寒沙门氏菌的argTr(精氨酸转运)和dhuA(组氨酸转运)启动子以及苜蓿根瘤菌的nifH(固氮酶)启动子。所有五个序列(最多有一个错配)都包含七聚体共有序列T-T-T-T-G-C-A。在已确定转录起始位点的苜蓿根瘤菌nifH和肺炎克雷伯菌nifL启动子中,共有序列位于-15区域。我们最近报道,激活nif基因的肺炎克雷伯菌nifA产物在激活参与氮同化的几个基因的启动子时,可以替代glnG(ntrC)产物,这些基因包括nifL、glnA和苜蓿根瘤菌nifH启动子。nifA很可能也激活鼠伤寒沙门氏菌的argTr和dhuA启动子。相反,glnG产物在激活肺炎克雷伯菌nifH(固氮酶)启动子时不能替代nifA产物。与后一观察结果一致,并支持T-T-T-T-G-C-A序列是glnG产物激活的调控位点这一结论,肺炎克雷伯菌nifH启动子(C-C-C-T-G-C-A)在-15区域与T-T-T-T-G-C-A共有序列只有部分相似性。