Appleman J A, Ross W, Salomon J, Gourse R L
Department of Bacteriology, University of Wisconsin, Madison 53706, USA.
J Bacteriol. 1998 Mar;180(6):1525-32. doi: 10.1128/JB.180.6.1525-1532.1998.
rRNA transcription in Escherichia coli is activated by the FIS protein, which binds upstream of rrnp1 promoters and interacts directly with RNA polymerase. Analysis of the contribution of FIS to rrn transcription under changing physiological conditions is complicated by several factors: the wide variation in cellular FIS concentrations with growth conditions, the contributions of several other regulatory systems to rRNA synthesis, and the pleiotropy of fis mutations. In this report, we show by in vivo footprinting and Western blot analysis that occupancy of the rrnBp1 FIS sites correlates with cellular levels of FIS. We find, using two methods of measurement (pulse induction of a FIS-activated hybrid promoter and primer extension from an unstable transcript made from rrnBp1), that the extent of transcription activation by FIS parallels the degree of FIS site occupancy and therefore cellular FIS levels. FIS activates transcription throughout exponential growth at low culture density, but rrnp1 transcription increases independently of FIS immediately following upshift, before FIS accumulates. These results support the model that FIS is one of a set of overlapping signals that together contribute to transcription from rrnp1 promoters during steady-state growth.
在大肠杆菌中,rRNA转录由FIS蛋白激活,该蛋白结合在rrnp1启动子的上游并直接与RNA聚合酶相互作用。在不断变化的生理条件下分析FIS对rrn转录的贡献会受到几个因素的影响而变得复杂:细胞中FIS浓度随生长条件的广泛变化、其他几个调节系统对rRNA合成的贡献以及fis突变的多效性。在本报告中,我们通过体内足迹法和蛋白质免疫印迹分析表明,rrnBp1 FIS位点的占有率与细胞内FIS水平相关。我们使用两种测量方法(对FIS激活的杂交启动子进行脉冲诱导以及对由rrnBp1产生的不稳定转录本进行引物延伸)发现,FIS激活转录的程度与FIS位点占有率以及细胞内FIS水平的程度平行。在低培养密度下的整个指数生长期,FIS都能激活转录,但在培养条件改变后,在FIS积累之前,rrnp1转录立即独立于FIS增加。这些结果支持了这样一种模型,即FIS是一组重叠信号之一,这些信号共同有助于在稳态生长期间从rrnp1启动子进行转录。