首页> 美国卫生研究院文献>Journal of Bacteriology >ChvD a Chromosomally Encoded ATP-Binding Cassette Transporter-Homologous Protein Involved in Regulation of Virulence Gene Expression in Agrobacterium tumefaciens
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ChvD a Chromosomally Encoded ATP-Binding Cassette Transporter-Homologous Protein Involved in Regulation of Virulence Gene Expression in Agrobacterium tumefaciens

机译:ChvD染色体编码的ATP结合盒式转运蛋白同源蛋白参与根癌农杆菌中毒力基因表达的调控。

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摘要

A yeast two-hybrid screen searching for chromosomally encoded proteins that interact with the Agrobacterium tumefaciens VirB8 protein was carried out. This screen identified an interaction candidate homologous to the partial sequence of a gene that had previously been identified in a transposon screen as a potential regulator of virG expression, chvD. In this report, the cloning of the entire chvD gene is described and the gene is sequenced and characterized. Insertion of a promoterless lacZ gene into the chvD locus greatly attenuated virulence and vir gene expression. Compared to that of the wild-type strain, growth of the chvD mutant was reduced in rich, but not minimal, medium. Expression of chvD, as monitored by expression of β-galactosidase activity from the chvD-lacZ fusion, occurred in both rich and minimal media as well as under conditions that induce virulence gene expression. The ChvD protein is highly homologous to a family of ATP-binding cassette transporters involved in antibiotic export from bacteria and has two complete Walker box motifs. Molecular genetic analysis demonstrated that disruption of either Walker A box, singly, does not inactivate this protein's effect on virulence but that mutations in both Walker A boxes renders it incapable of complementing a chvD mutant strain. Constitutive expression of virG in the chvD mutant strain restored virulence, supporting the hypothesis that ChvD controls virulence through effects on virG expression.
机译:酵母双杂交筛选搜索与根癌土壤杆菌VirB8蛋白相互作用的染色体编码蛋白。该筛选确定了与基因的部分序列同源的相互作用候选物,该基因先前已在转座子筛选中被鉴定为virG表达chvD的潜在调节剂。在此报告中,描述了整个chvD基因的克隆,并对基因进行了测序和表征。无启动子的lacZ基因插入chvD基因座大大削弱了毒力和vir基因表达。与野生型菌株相比,chvD突变体的生长在丰富而不是最少的培养基中减少了。 chvD的表达,通过来自chvD-lacZ融合的β-半乳糖苷酶活性的表达来监测,既发生在丰富的培养基中,也发生在最基本的培养基中,并且在诱导毒力基因表达的条件下发生。 ChvD蛋白与涉及从细菌输出抗生素的ATP结合盒式转运蛋白家族高度同源,并具有两个完整的Walker盒基序。分子遗传学分析表明,单独破坏任意一个Walker A盒并不会使该蛋白对毒力的作用失活,但是两个Walker A盒中的突变均使其无法补充chvD突变株。 chvD突变株中virG的组成型表达恢复了毒力,支持了ChvD通过影响virG表达来控制毒力的假说。

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