Xiao Y, Heu S, Yi J, Lu Y, Hutcheson S W
Department of Botany, University of Maryland, College Park 20742.
J Bacteriol. 1994 Feb;176(4):1025-36. doi: 10.1128/jb.176.4.1025-1036.1994.
The Pseudomonas syringae hrp and hrmA genes controlling pathogenicity and elicitation of the hypersensitive response and the avr genes controlling host range have been shown previously to be regulated by carbon, nitrogen, pH, osmolarity, and hypothetical plant factors. In P. syringae pv. syringae Pss61, inactivation of hrp complementation groups II and XIII reduced expression of a plasmid-borne hrmA'-lacZ fusion. The hrp regions II and XIII were cloned on separate plasmids and shown to enhance the activity of the hrmA promoter in Escherichia coli MC4100 transformants at least 100-fold. The nucleotide sequence of region XIII revealed two open reading frames (hrpR and hrpS) whose deduced products share homology with P. syringae pv. phaseolicola NPS3121 HrpS and are both related to the NtrC family of two-component signal transduction systems. HrpR and HrpS differ from most members of the protein family by lacking an amino-terminal domain which modulates the regulatory activity. A single open reading frame, hrpL, whose product shares homology with AlgU, a putative alternate sigma factor of P. aeruginosa, as well as with the related alternate sigma factors was identified within region II. Key domains are partially conserved. Inactivation of hrpS in Pss61 repressed expression of a plasmid-borne hrpL'-lacZ fusion carried by pYXPL1R, and transformation of MC4100(pYXPL1R) with a plasmid carrying hrpRS increased hrpL promoter activity at least 200-fold. Neither hrpS nor hrpR, when cloned on separate plasmids, activated the hrpL promoter activity individually. The expression of hrpL when directed by a lac promoter was sufficient to express a set of plasmid-borne hrmA'-, hrpJ'-, and hrpZ'-lacZ fusions independently of other hrp genes. The results indicate that hrpRS and hrpL are part of a regulatory cascade in which HrpR and HrpS activate expression of hrpL and HrpL, a putative sigma factor, induces expression of HrpL-responsive genes.
先前已表明,丁香假单胞菌中控制致病性、激发超敏反应的hrp和hrmA基因以及控制宿主范围的avr基因受碳、氮、pH、渗透压和假定的植物因子调控。在丁香假单胞菌丁香致病变种Pss61中,hrp互补群II和XIII的失活降低了质粒携带的hrmA'-lacZ融合基因的表达。hrp区域II和XIII被克隆到不同的质粒上,并显示在大肠杆菌MC4100转化子中可将hrmA启动子的活性增强至少100倍。区域XIII的核苷酸序列揭示了两个开放阅读框(hrpR和hrpS),其推导产物与菜豆假单胞菌NPS3121的HrpS具有同源性,且二者均与双组分信号转导系统的NtrC家族相关。HrpR和HrpS与该蛋白家族的大多数成员不同,它们缺少一个调节调节活性的氨基末端结构域。在区域II内鉴定出一个单一的开放阅读框hrpL,其产物与铜绿假单胞菌的假定替代σ因子AlgU以及相关的替代σ因子具有同源性。关键结构域部分保守。Pss61中hrpS的失活抑制了pYXPL1R携带的质粒携带的hrpL'-lacZ融合基因的表达,用携带hrpRS的质粒转化MC4100(pYXPL1R)可使hrpL启动子活性增加至少200倍。当hrpS和hrpR分别克隆到不同的质粒上时,二者均不能单独激活hrpL启动子活性。由lac启动子指导的hrpL的表达足以独立于其他hrp基因表达一组质粒携带的hrmA'-、hrpJ'-和hrpZ'-lacZ融合基因。结果表明,hrpRS和hrpL是调控级联的一部分,其中HrpR和HrpS激活hrpL的表达,而HrpL(一种假定的σ因子)诱导HrpL反应性基因的表达。