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首页> 外文期刊>Journal of bacteriology >Identification of a putative alternate sigma factor and characterization of a multicomponent regulatory cascade controlling the expression of Pseudomonas syringae pv. syringae Pss61 hrp and hrmA genes.
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Identification of a putative alternate sigma factor and characterization of a multicomponent regulatory cascade controlling the expression of Pseudomonas syringae pv. syringae Pss61 hrp and hrmA genes.

机译:推定的备用sigma因子的鉴定和控制丁香假单胞菌pv表达的多组分调节级联反应的表征。丁香属植物Pss61 hrp和hrmA基因。

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摘要

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.
机译:先前已经显示,控制致病性和过敏反应诱发的丁香假单胞菌hrp和hrmA基因以及控制宿主范围的avr基因受碳,氮,pH,摩尔渗透压浓度和假想植物因子的调节。在丁香假单胞菌pv。丁香属植物Pss61,hrp互补基团II和XIII的失活减少了质粒携带的hrmA'-lacZ融合蛋白的表达。将hrp区II和XIII克隆在单独的质粒上,显示出它们可增强hrMC启动子在大肠杆菌MC4100转化子中的活性至少100倍。 XIII区的核苷酸序列揭示了两个开放阅读框(hrpR和hrpS),其推论产物与丁香假单胞菌pv具有同源性。 phaseolicola NPS3121 HrpS和两者都与NtrC系列的两组分信号转导系统有关。 HrpR和HrpS与蛋白质家族的大多数成员有所不同,因为缺少调节调节活性的氨基末端结构域。在区域II中鉴定出一个单一的开放阅读框hrpL,其产物与AlgU,铜绿假单胞菌的一个候补sigma因子以及相关的另一些sigma因子具有同源性。关键域是部分保守的。在Pss61中,hrpS的失活抑制了pYXPL1R携带的质粒携带的hrpL'-lacZ融合蛋白的表达,而用携带hrpRS的质粒转化MC4100(pYXPL1R)可以使hrpL启动子活性增加至少200倍。当hrpS和hrpR克隆在单独的质粒上时,它们都不会分别激活hrpL启动子活性。当由lac启动子指导时,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融合体。结果表明,hrpRS和hrpL是调节级联反应的一部分,其中HrpR和HrpS激活hrpL的表达,而HrpL(假定的sigma因子)诱导HrpL响应基因的表达。

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