Winans S C
Department of Microbiology, Cornell University, Ithaca, New York 14853-7201.
J Bacteriol. 1990 May;172(5):2433-8. doi: 10.1128/jb.172.5.2433-2438.1990.
Transcription of the virG gene of Agrobacterium tumefaciens was previously shown to be expressed from two tandem promoters and to be responsive to three stimuli: plant-released phenolic compounds, phosphate starvation, and acidic media. In this report, I describe a set of deletions and other alterations of the 5' end of virG that show that the upstream promoter (P1) is necessary for induction by phenolic compounds and by phosphate starvation, whereas the downstream promoter (P2) is induced by acidic media. Upstream of promoter P1 there are three copies of a family of sequences (vir boxes) found near all VirA, VirG-inducible promoters. Site-directed mutagenesis of these sequences showed that vir box I and vir box III but not vir box II are needed for induction of P1 by acetosyringone. Induction of P1 by phosphate starvation requires vir box III (or an overlapping site), whereas vir box I and vir box II are not needed. The relative importance of promoters P1 and P2 in vir gene induction was tested by measuring the expression of a virB::lacZ fusion in strains containing mutations at either promoter P1 or P2. Mutations in either promoter significantly attenuated the expression of virB, indicating that both promoters play important roles in vir gene induction.
根癌土壤杆菌virG基因的转录先前已表明是由两个串联启动子表达,并对三种刺激有反应:植物释放的酚类化合物、磷饥饿和酸性培养基。在本报告中,我描述了一组virG 5'端的缺失和其他改变,结果表明上游启动子(P1)对于酚类化合物和磷饥饿诱导是必需的,而下游启动子(P2)由酸性培养基诱导。在启动子P1上游有一个序列家族(vir框)的三个拷贝,在所有VirA、VirG可诱导启动子附近都能找到。这些序列的定点诱变表明,vir框I和vir框III而非vir框II是乙酰丁香酮诱导P1所必需的。磷饥饿诱导P1需要vir框III(或一个重叠位点),而不需要vir框I和vir框II。通过测量在启动子P1或P2处含有突变的菌株中virB::lacZ融合蛋白的表达,测试了启动子P1和P2在vir基因诱导中的相对重要性。任一启动子中的突变都显著减弱了virB的表达,表明两个启动子在vir基因诱导中都起重要作用。