Kang J G, Hahn M Y, Ishihama A, Roe J H
Department of Microbiology, College of Natural Sciences, and Research Center for Molecular Microbiology, Seoul National University, Seoul 151-742, Korea.
Nucleic Acids Res. 1997 Jul 1;25(13):2566-73. doi: 10.1093/nar/25.13.2566.
We examined the promoter selectivity of RNA polymerase (RNAP) from Streptomyces coelicolor at two growth phases by in vitro transcription. Distinct sets of promoters were preferentially recognized by either exponential or stationary phase RNAP. No change in molecular weight or net charge of the core subunits was observed, suggesting that the associated specificity factors determined phase-specific promoter selectivity of the holoenzyme. Five different specificity factors and their cognate promoters were identified by in vitro holoenzyme reconstitution and transcription assays. sigma66 (sigma hrdB) and sigma46 (sigma hrdD) recognized promoters (rrnD p2 and dagA p4 for sigma66, actII-orf4 p and whiB p2 for sigma46) preferentially transcribed by the exponential phase RNAP. sigma52 recognized promoters (dagA p3 and actIII px1) preferentially transcribed by the stationary phase RNAP. Sigma28 (sigma sigE) recognized promoters (hrdD p1, whiB p1 and dagA p2) transcribed equally by both RNAPs. A novel 31 kDa specificity factor recognized actIII px2, glnR p2 and hrdD p2 promoters preferentially transcribed by the stationary phase RNAP. This factor was isolated from the stationary phase RNAP and reconstituted holoenzyme in vitro as a sigma factor. The N-terminal sequence suggests that it is a novel factor. By examining phase-specific promoter recognition pattern we can predict that holoenzyme Esigma52 and Esigma31 activities are higher in the stationary phase, whereas Esigma66 and Esigma46activities are higher in the exponential phase. Possible promoter sequences recognized by some of these sigma factors were suggested.
我们通过体外转录研究了天蓝色链霉菌在两个生长阶段的RNA聚合酶(RNAP)的启动子选择性。指数期或稳定期的RNAP优先识别不同的启动子组。未观察到核心亚基的分子量或净电荷发生变化,这表明相关的特异性因子决定了全酶的阶段特异性启动子选择性。通过体外全酶重组和转录分析鉴定了五种不同的特异性因子及其同源启动子。sigma66(sigma hrdB)和sigma46(sigma hrdD)识别优先由指数期RNAP转录的启动子(sigma66对应的rrnD p2和dagA p4,sigma46对应的actII-orf4 p和whiB p2)。sigma52识别优先由稳定期RNAP转录的启动子(dagA p3和actIII px1)。Sigma28(sigma sigE)识别由两种RNAP同等转录的启动子(hrdD p1、whiB p1和dagA p2)。一种新的31 kDa特异性因子识别优先由稳定期RNAP转录的actIII px2、glnR p2和hrdD p2启动子。该因子从稳定期RNAP中分离出来,并在体外作为sigma因子重组全酶。N端序列表明它是一个新因子。通过检查阶段特异性启动子识别模式,我们可以预测全酶Esigma52和Esigma31的活性在稳定期较高,而Esigma66和Esigma46的活性在指数期较高。还提出了其中一些sigma因子可能识别的启动子序列。