Merighi Massimo, Majerczak Doris R, Zianni Michael, Tessanne Kimberly, Coplin David L
Department of Plant Pathology, The Ohio State University, 201 Kottman Hall, 2021 Coffey Rd., Columbus, OH 43210-1087, USA.
J Bacteriol. 2006 Jul;188(14):5089-100. doi: 10.1128/JB.01929-05.
Pantoea stewartii subsp. stewartii is a bacterial pathogen of corn. Its pathogenicity depends on the translocation of effector proteins into host cells by the Hrp type III secretion system. We previously showed by genetic analysis that the HrpX sensor kinase and the HrpY response regulator are at the head of a complex cascade of regulators controlling hrp/hrc secretion and wts effector genes. This cascade also includes the HrpS response regulator and the HrpL alternative sigma factor. These regulators are shared among many important plant pathogens in the genera Pantoea, Erwinia, and Pseudomonas. In this study, we dissect the regulatory elements in the hrpS promoter region, using genetic and biochemical approaches, and show how it integrates various environmental signals, only some of which are dependent on phosphorylation of HrpY. Primer extension located the transcriptional start site of hrpS at a sigma70 promoter 601 bp upstream of the open reading frame. Electrophoretic mobility shift assays and DNase I footprinting analysis demonstrated that HrpY binds to conserved regulatory elements immediately adjacent to this promoter, and its binding affinity was increased by phosphorylation at D57. A consensus sequence for the two direct repeats bound by HrpY is proposed. Deletion analysis of the promoter region revealed that both the HrpY binding site and additional sequences farther upstream, including a putative integration host factor binding site, are required for hrpS expression. This finding suggests that other unknown regulatory proteins may act cooperatively with HrpY.
斯氏泛菌斯氏亚种是玉米的一种细菌病原体。其致病性取决于效应蛋白通过Hrp III型分泌系统转运到宿主细胞中。我们之前通过遗传分析表明,HrpX传感激酶和HrpY反应调节因子处于控制hrp/hrc分泌和wts效应基因的复杂调节因子级联反应的顶端。该级联反应还包括HrpS反应调节因子和HrpL替代σ因子。这些调节因子在泛菌属、欧文氏菌属和假单胞菌属的许多重要植物病原体中是共有的。在本研究中,我们使用遗传和生化方法剖析了hrpS启动子区域中的调节元件,并展示了它如何整合各种环境信号,其中只有一些信号依赖于HrpY的磷酸化。引物延伸将hrpS的转录起始位点定位在开放阅读框上游601 bp处的一个σ70启动子处。电泳迁移率变动分析和DNase I足迹分析表明,HrpY与紧邻该启动子的保守调节元件结合,并且其结合亲和力在D57处通过磷酸化而增加。提出了HrpY结合的两个直接重复序列的共有序列。启动子区域的缺失分析表明,hrpS表达需要HrpY结合位点和更上游的其他序列,包括一个假定的整合宿主因子结合位点。这一发现表明,其他未知的调节蛋白可能与HrpY协同作用。