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一个复杂的网络调节茄科青枯雷尔氏菌的eps及其他毒力基因的表达。

A complex network regulates expression of eps and other virulence genes of Pseudomonas solanacearum.

作者信息

Huang J, Carney B F, Denny T P, Weissinger A K, Schell M A

机构信息

Department of Microbiology, University of Georgia, Athens 30602.

出版信息

J Bacteriol. 1995 Mar;177(5):1259-67. doi: 10.1128/jb.177.5.1259-1267.1995.

Abstract

We have discovered an unusual and complex regulatory network used by the phytopathogen Pseudomonas solanacearum to control transcription of eps, which encodes for production of its primary virulence factor, the exopolysaccharide EPS I. The major modules of this network were shown to be three separate signal transduction systems: PhcA, a LysR-type transcriptional regulator, an dual two-component regulatory systems, VsrA/VsrD and VsrB/VsrC. Using lacZ fusions and RNA analysis, we found that both PhcA and VsrA/VsrD control transcription of another network component, xpsR, which in turn acts in conjunction with vsrB/vsrC to increase transcription of the eps promoter by > 25-fold. Moreover, gel shift DNA binding assays showed that PhcA specifically binds to the xpsR promoter region. Thus, the unique XpsR protein interconnects the three signal transduction systems, forming a network for convergent control of EPS I in simultaneous response to multiple environmental inputs. In addition, we demonstrate that each individual signaling system of the network also acts independently to divergently regulate other unique sets of virulence factors. The purpose of this complex network may be to allow this phytopathogen to both coordinately or independently regulate diverse virulence factors in order to cope with the dynamic situations and conditions encountered during interactions with plants.

摘要

我们发现了植物病原体青枯雷尔氏菌(Pseudomonas solanacearum)用于控制eps转录的一个不同寻常且复杂的调控网络,eps编码其主要毒力因子胞外多糖EPS I的产生。该网络的主要模块显示为三个独立的信号转导系统:PhcA,一种LysR型转录调节因子,以及两个双组分调节系统,VsrA/VsrD和VsrB/VsrC。通过使用lacZ融合和RNA分析,我们发现PhcA和VsrA/VsrD都控制另一个网络组件xpsR的转录,而xpsR又与vsrB/vsrC协同作用,使eps启动子的转录增加超过25倍。此外,凝胶迁移DNA结合试验表明,PhcA特异性结合xpsR启动子区域。因此,独特的XpsR蛋白将这三个信号转导系统相互连接,形成一个网络,以便在同时响应多种环境输入时对EPS I进行汇聚控制。此外,我们证明该网络的每个单独信号系统也独立发挥作用,以不同方式调节其他独特的毒力因子组。这个复杂网络的目的可能是使这种植物病原体能够协调或独立地调节多种毒力因子,以便应对与植物相互作用过程中遇到的动态情况和条件。

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