首页> 外文OA文献 >The Pseudomonas syringae HopPtoV Protein Is Secreted in Culture and Translocated into Plant Cells via the Type III Protein Secretion System in a Manner Dependent on the ShcV Type III Chaperone
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The Pseudomonas syringae HopPtoV Protein Is Secreted in Culture and Translocated into Plant Cells via the Type III Protein Secretion System in a Manner Dependent on the ShcV Type III Chaperone

机译:丁香假单胞菌HopPtoV蛋白在文化中分泌,并通过依赖于ShcV III型分子伴侣的III型蛋白分泌系统转移到植物细胞中。

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摘要

The bacterial plant pathogen Pseudomonas syringae depends on a type III protein secretion system and the effector proteins that it translocates into plant cells to cause disease and to elicit the defense-associated hypersensitive response on resistant plants. The availability of the P. syringae pv. tomato DC3000 genome sequence has resulted in the identification of many novel effectors. We identified the hopPtoV effector gene on the basis of its location next to a candidate type III chaperone (TTC) gene, shcV, and within a pathogenicity island in the DC3000 chromosome. A DC3000 mutant lacking ShcV was unable to secrete detectable amounts of HopPtoV into culture supernatants or translocate HopPtoV into plant cells, based on an assay that tested whether HopPtoV-AvrRpt2 fusions were delivered into plant cells. Coimmunoprecipitation and Saccharomyces cerevisiae two-hybrid experiments showed that ShcV and HopPtoV interact directly with each other. The ShcV binding site was delimited to an N-terminal region of HopPtoV between amino acids 76 and 125 of the 391-residue full-length protein. Our results demonstrate that ShcV is a TTC for the HopPtoV effector. DC3000 overexpressing ShcV and HopPtoV and DC3000 mutants lacking either HopPtoV or both ShcV and HopPtoV were not significantly impaired in disease symptoms or bacterial multiplication in planta, suggesting that HopPtoV plays a subtle role in pathogenesis or that other effectors effectively mask the contribution of HopPtoV in plant pathogenesis.
机译:细菌性植物病原体丁香假单胞菌依赖于III型蛋白分泌系统及其效应蛋白,该蛋白易位到植物细胞中引起疾病​​并在抗性植物上引发与防御相关的超敏反应。丁香假单胞菌PV的可用性。番茄DC3000基因组序列已鉴定出许多新型效应子。我们根据HopPtoV效应基因的位置确定其位置,该基因位于候选III型伴侣(TTC)基因shcV的旁边,并位于DC3000染色体的致病岛内。缺少ShcV的DC3000突变体无法检测可检测量的HopPtoV到培养上清液中,也无法将HopPtoV易位到植物细胞中,这是根据一种检测HopPtoV-AvrRpt2融合物是否已递送到植物细胞中的分析方法进行的。免疫共沉淀和酿酒酵母两个杂交实验表明,ShcV和HopPtoV彼此直接相互作用。 ShcV结合位点被界定为在391个残基的全长蛋白质的第76和125位氨基酸之间的HopPtoV的N端区域。我们的结果表明ShcV是HopPtoV效应子的TTC。过度表达ShcV和HopPtoV的DC3000以及缺少HopPtoV或ShcV和HopPtoV的DC3000突变体在疾病症状或植物中细菌繁殖方面均未受到明显损害,这表明HopPtoV在发病机理中起着微妙的作用,或者其他效应子有效地掩盖了HopPtoV在植物中的作用发病。

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