Tanaka K, Kusano S, Fujita N, Ishihama A, Takahashi H
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.
Nucleic Acids Res. 1995 Mar 11;23(5):827-34. doi: 10.1093/nar/23.5.827.
Sequence determinants responsible for promoter recognition by RNA polymerase holoenzyme containing sigma 38, the rpoS gene product, were analyzed. In a previous study [Tanaka et al. (1993) Proc. Natl. Acad. Sci. USA, 90, 3511-3515], Escherichia coli promoters were classified into three groups: promoters recognized only by RNA polymerase holoenzyme containing sigma 70 (E sigma 70); promoters recognized preferentially by that containing sigma 38 (E sigma 38); promoters recognized by both E sigma 70 and E sigma 38. As representatives of each group of promoter, we chose the alaS, fic and lacUV5 promoters. Making use of a restriction enzyme site inserted between the -10 and -35 hexamer sequences, promoters were divided into the upstream (UE) and downstream (DE) elements. These UEs and DEs were combined in all possible combinations and used for in vitro transcription reactions. Promoters containing DE from the fic or lacUV5 promoter were found to be recognized by E sigma 38, while those containing DE from the alaS promoter were not. Moreover, fic DE alone functioned as an efficient promoter for E sigma 38. Thus we conclude that the discrimination signal resides within the DE sequence. To test the activator response of E sigma 38, in vitro transcription reactions were also performed with the gal and lac promoters. For both CRP-responsive P1 promoters, E sigma 38 was found to be activated by the CRP-cAMP complex.
对负责含σ38(rpoS基因产物)的RNA聚合酶全酶识别启动子的序列决定因素进行了分析。在先前的一项研究中[田中等人(1993年)《美国国家科学院院刊》,90,3511 - 3515],大肠杆菌启动子被分为三组:仅由含σ70的RNA聚合酶全酶(Eσ70)识别的启动子;优先由含σ38的全酶(Eσ38)识别的启动子;被Eσ70和Eσ38两者识别的启动子。作为每组启动子的代表,我们选择了alaS、fic和lacUV5启动子。利用插入在 - 10和 - 35六聚体序列之间的一个限制酶位点,将启动子分为上游(UE)和下游(DE)元件。这些UE和DE以所有可能的组合进行组合,并用于体外转录反应。发现含有来自fic或lacUV5启动子的DE的启动子能被Eσ38识别,而含有来自alaS启动子的DE的启动子则不能。此外,单独的fic DE作为Eσ38的有效启动子发挥作用。因此我们得出结论,识别信号存在于DE序列内。为了测试Eσ38的激活剂反应,还对gal和lac启动子进行了体外转录反应。对于两个对CRP有反应的P1启动子,发现Eσ38被CRP - cAMP复合物激活。