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根癌土壤杆菌中VirA异源二聚体糖信号转导的亚基间互补及VirA活性的翻译后调控

Intersubunit complementation of sugar signal transduction in VirA heterodimers and posttranslational regulation of VirA activity in Agrobacterium tumefaciens.

作者信息

Wise Arlene A, Voinov Luba, Binns Andrew N

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, PA 19104-6018, USA.

出版信息

J Bacteriol. 2005 Jan;187(1):213-23. doi: 10.1128/JB.187.1.213-223.2005.

Abstract

The VirA/VirG two-component regulatory system of Agrobacterium tumefaciens regulates expression of the virulence (vir) genes that control the infection process leading to crown gall tumor disease on susceptible plants. VirA, a membrane-bound homodimer, initiates vir gene induction by communicating the presence of molecular signals found at the site of a plant wound through phosphorylation of VirG. Inducing signals include phenols, monosaccharides, and acidic pH. While sugars are not essential for gene induction, their presence greatly increases vir gene expression when levels of the essential phenolic signal are low. Reception of the sugar signal depends on a direct interaction between ChvE, a sugar-binding protein, and VirA. Here we show that the sugar signal received in the periplasmic region of one subunit within a VirA heterodimer can enhance the kinase function of the second subunit. However, sugar enhancement of vir gene expression was vector dependent. virA alleles expressed from pSa-derived vectors inhibited signal transduction by endogenous VirA. Inhibition was conditional, depending on the induction medium and the virA allele tested. Moreover, constitutive expression of virG overcame the inhibitory effect of some but not all virA alleles, suggesting that there may be more than one inhibitory mechanism.

摘要

根癌土壤杆菌的VirA/VirG双组分调节系统调控着毒性(vir)基因的表达,这些基因控制着导致易感植物发生冠瘿瘤病的感染过程。VirA是一种膜结合同型二聚体,通过对VirG进行磷酸化来传递植物伤口处发现的分子信号的存在,从而启动vir基因的诱导。诱导信号包括酚类、单糖和酸性pH值。虽然糖类对于基因诱导并非必不可少,但当必需酚类信号水平较低时,它们的存在会大大增加vir基因的表达。糖类信号的接收取决于糖结合蛋白ChvE与VirA之间的直接相互作用。在此我们表明,在VirA异源二聚体一个亚基的周质区域接收到的糖类信号可以增强第二个亚基的激酶功能。然而,糖类对vir基因表达的增强作用取决于载体。从pSa衍生载体表达的virA等位基因会抑制内源性VirA的信号转导。抑制作用是有条件的,取决于诱导培养基和所测试的virA等位基因。此外,virG的组成型表达克服了一些但并非所有virA等位基因的抑制作用,这表明可能存在不止一种抑制机制。

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