Jovanovic Milija, Lawton Edward, Schumacher Jörg, Buck Martin
Department of Life Sciences, Imperial College London, London, UK.
FEMS Microbiol Lett. 2014 Jul;356(2):201-11. doi: 10.1111/1574-6968.12476. Epub 2014 Jun 19.
Pseudomonas syringae pv. tomato DC3000, a plant pathogenic gram-negative bacterium, employs the type III secretion system (T3SS) to cause disease in tomato and Arabidopsis and to induce the hypersensitive response in nonhost plants. The expression of T3SS is regulated by the HrpL extracytoplasmic sigma factor. Expression of HrpL is controlled by transcriptional activators HrpR and HrpS and negative regulator HrpV. In this study, we analysed the organization of HrpRS and HrpV regulatory proteins and interplay between them. We identified one key residue I26 in HrpS required for repression by HrpV. Substitution of I26 in HrpS abolishes its interaction with HrpV and impairs interactions between HrpS and HrpR and the self-association of HrpS. We show that HrpS self-associates and can associate simultaneously with HrpR and HrpV. We now propose that HrpS has a central role in the assembly of the regulatory HrpRSV complex. Deletion analysis of HrpR and HrpS proteins showed that C-terminal parts of HrpR and HrpS confer determinants indispensable for their self-assembly.
丁香假单胞菌番茄致病变种DC3000是一种植物致病革兰氏阴性细菌,它利用III型分泌系统(T3SS)在番茄和拟南芥中引发病害,并在非寄主植物中诱导过敏反应。T3SS的表达受胞外HrpLσ因子调控。HrpL的表达由转录激活因子HrpR和HrpS以及负调控因子HrpV控制。在本研究中,我们分析了HrpRS和HrpV调控蛋白的结构及其相互作用。我们鉴定出HrpS中一个对HrpV抑制作用至关重要的关键残基I26。HrpS中I26的替换消除了其与HrpV的相互作用,并损害了HrpS与HrpR之间的相互作用以及HrpS的自缔合。我们发现HrpS能自缔合,且能同时与HrpR和HrpV缔合。我们现在提出HrpS在调控HrpRSV复合体的组装中起核心作用。对HrpR和HrpS蛋白的缺失分析表明,HrpR和HrpS的C末端部分赋予了它们自组装所必需的决定因素。