Satola S, Kirchman P A, Moran C P
Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
Proc Natl Acad Sci U S A. 1991 May 15;88(10):4533-7. doi: 10.1073/pnas.88.10.4533.
Examination of the effects of 56 single-base-pair substitutions in the spoIIG promoter and studies of the interaction of the spo0A product (Spo0A) with this promoter in vitro demonstrated that Spo0A acts directly to enable this promoter to be used by sigma A-associated RNA polymerase (EC 2.7.7.6). The spoIIG operon from Bacillus subtilis is transcribed during sporulation by a form o RNA polymerase containing sigma A, the primary sigma factor in vegetative cells. The spoIIG promoter is unusual in that it contains sequences that are similar to those found at the -10 and -35 regions of promoters that are used by sigma A-associated RNA polymerase, but these sigma A-like recognition sequences are separated by 22 base pairs rather than the typical 17 or 18 base pairs. We found that single-base-pair substitutions in the around the -35-like sequence, and substitutions in a region upstream from this position, around position -87, reduced promoter activity. DNase I protection and electrophoretic gel mobility shift assays were used to demonstrate that Spo0A binds specifically to these regions in vitro. Evidently, the -35-like sequence is part of a Spo0A binding site and therefore is possibly not a sigma A-recognition sequence. These results support a model in which Spo0A activates the spoIIG promoter after the onset of endospore formation.
对枯草芽孢杆菌spoIIG启动子中56个单碱基对替换的效应进行检测,并对spo0A产物(Spo0A)与该启动子在体外的相互作用进行研究,结果表明,Spo0A直接发挥作用,使该启动子能够被与σA相关的RNA聚合酶(EC 2.7.7.6)所利用。枯草芽孢杆菌的spoIIG操纵子在芽孢形成过程中由一种含有σA的RNA聚合酶转录,σA是营养细胞中的主要σ因子。spoIIG启动子不同寻常之处在于,它含有与那些被与σA相关的RNA聚合酶所利用的启动子的-10和-35区域中发现的序列相似的序列,但这些类似σA的识别序列被22个碱基对隔开,而不是典型的17或18个碱基对。我们发现,-35样序列周围的单碱基对替换,以及该位置上游约-87位区域的替换,都会降低启动子活性。利用DNase I保护和电泳凝胶迁移率变动分析来证明Spo0A在体外特异性结合这些区域。显然,-35样序列是Spo0A结合位点的一部分,因此可能不是σA识别序列。这些结果支持了一个模型,即Spo0A在芽孢形成开始后激活spoIIG启动子。