McLean B G, Greene E A, Zambryski P C
Department of Plant Biology, University of California, Berkeley 94720.
J Biol Chem. 1994 Jan 28;269(4):2645-51.
In the presence of inducer molecules produced by wounded plants, the VirA/VirG two-component positive regulatory system of Agrobacterium tumefaciens initiates transcription of virulence genes required for crown gall tumor formation. Exactly how this system enables the bacterium to respond to an environmental signal is not known, but phosphorylation of VirA and VirG plays a role. To analyze further the function of VirA, we chemically mutagenized the virA gene. Two mutants that activate vir transcription without the plant inducer acetosyringone were found; these mutants alter VirA function by distinct mechanisms. One mutant functions entirely independently of acetosyringone, whereas the activity of the second mutant is enhanced by acetosyringone. Both mutants function best at acid pH, but respond differently to specific monosaccharides that stimulate induction by wild-type VirA. Both mutant phenotypes are dominant over wild-type VirA, and both need the conserved histidine at the autophosphorylation site for strong inducer-independent vir transcription.
在受伤植物产生的诱导分子存在的情况下,根癌土壤杆菌的VirA/VirG双组分正调控系统启动了冠瘿瘤形成所需的毒力基因的转录。该系统究竟如何使细菌对环境信号做出反应尚不清楚,但VirA和VirG的磷酸化起了作用。为了进一步分析VirA的功能,我们对virA基因进行了化学诱变。发现了两个在没有植物诱导剂乙酰丁香酮的情况下激活vir转录的突变体;这些突变体通过不同的机制改变了VirA的功能。一个突变体完全独立于乙酰丁香酮发挥作用,而第二个突变体的活性则被乙酰丁香酮增强。两个突变体在酸性pH下功能最佳,但对刺激野生型VirA诱导的特定单糖反应不同。两种突变体表型均显性于野生型VirA,且都需要自磷酸化位点上保守的组氨酸来实现强诱导剂非依赖性vir转录。