MacGregor B J, Karls R K, Donohue T J
Department of Bacteriology, University of Wisconsin-Madison, 53706, USA.
J Bacteriol. 1998 Jan;180(1):1-9. doi: 10.1128/JB.180.1.1-9.1998.
These experiments sought to identify what form of RNA polymerase transcribes the P1 promoter for the Rhodobacter sphaeroides cytochrome c2 gene (cycA). In vitro, cycA P1 was recognized by an RNA polymerase holoenzyme fraction that transcribes several well-characterized Escherichia coli heat shock (sigma32) promoters. The in vivo effects of mutations flanking the transcription initiation site (+1) also suggested that cycA P1 was recognized by an RNA polymerase similar to E. coli Esigma32. Function of cycA P1 was not altered by mutations more than 35 bp upstream of position +1 or by alterations downstream of -7. A point mutation at position -34 that is towards the E. coli Esigma32 -35 consensus sequence (G34T) increased cycA P1 activity approximately 20-fold, while several mutations that reduced or abolished promoter function changed highly conserved bases in presumed -10 or -35 elements. In addition, cycA P1 function was retained in mutant promoters with a spacer region as short as 14 nucleotides. When either wild-type or G34T promoters were incubated with reconstituted RNA polymerase holoenzymes, cycA P1 transcription was observed only with samples containing either a 37-kDa subunit that is a member of the heat shock sigma factor family (Esigma37) or a 38-kDa subunit that also allows core RNA polymerase to recognize E. coli heat shock promoters (Esigma38). (R. K. Karls, J. Brooks, P. Rossmeissl, J. Luedke, and T. J. Donohue, J. Bacteriol. 180:10-19, 1998).
这些实验旨在确定何种形式的RNA聚合酶转录球形红细菌细胞色素c2基因(cycA)的P1启动子。在体外,cycA P1被一种RNA聚合酶全酶组分识别,该组分可转录几个特征明确的大肠杆菌热休克(sigma32)启动子。转录起始位点(+1)侧翼突变的体内效应也表明,cycA P1被一种类似于大肠杆菌Esigma32的RNA聚合酶识别。+1位置上游超过35 bp的突变或-7下游的改变均未改变cycA P1的功能。-34位置朝向大肠杆菌Esigma32 -35共有序列(G34T)的点突变使cycA P1活性增加了约20倍,而几个降低或消除启动子功能的突变改变了推测的-10或-35元件中的高度保守碱基。此外,cycA P1功能在间隔区短至14个核苷酸的突变启动子中得以保留。当野生型或G34T启动子与重组RNA聚合酶全酶一起孵育时,仅在含有热休克sigma因子家族成员的37-kDa亚基(Esigma37)或也能使核心RNA聚合酶识别大肠杆菌热休克启动子的38-kDa亚基(Esigma38)的样品中观察到cycA P1转录。(R.K.卡尔斯、J.布鲁克斯、P.罗斯迈斯尔、J.吕德克和T.J.多诺霍,《细菌学杂志》180:10 - 19,1998年)