首页> 外文期刊>Molecular Plant-Microbe Interactions >At-4/1, an interactor of the Tomato spotted wilt virus movement protein, belongs to a new family of plant proteins capable of directed intra- and intercellular trafficking
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At-4/1, an interactor of the Tomato spotted wilt virus movement protein, belongs to a new family of plant proteins capable of directed intra- and intercellular trafficking

机译:At-4 / 1是番茄斑萎病毒运动蛋白的相互作用因子,属于一种新的植物蛋白家族,能够指导细胞内和细胞间运输

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The Tomato spotted wilt virus (TSWV) encoded NSm movement protein facilitates cell-to-cell spread of the viral genome through structurally modified plasmodesmata. NSm has been utilized as bait in yeast two-hybrid interaction trap screenings. As a result, a protein of unknown function, called At-4/1, was isolated from an Arabidopsis thaliana GAL4 activation domain-tagged cDNA library. Using polyclonal antibodies against bacterially expressed At-4/1, Western blot analysis of protein extracts isolated from different plant species as well as genome database screenings showed that homologues of At-4/1 seemed to be encoded by many vascular plants. For subcellular localization studies, At-4/1 was fused to green fluorescent protein, and corresponding expression vectors were used in particle bombardment and agroinfiltration assays. Confocal laser scannings revealed that At-4/1 assembled in punctate spots at the cell periphery. The protein accumulated intracellularly in a polarized fashion, appearing in only one-half of a bombarded epidermal cell, and, moreover, moved from cell to cell, forming twin-structured bodies seemingly located at both orifices of the plasmodesmatal pore. In coexpression studies, At-4/1 colocalized with a plant virus movement protein TGBp3 known to reside in endoplasmic reticulum-derived membrane structures located in close vicinity to plasmodesmata. Thus, At-4/1 belongs to a new family of plant proteins capable of directed intra- and intercellular trafficking.
机译:番茄斑萎病毒(TSWV)编码的NSm运动蛋白可通过结构修饰的胞质瘤促进病毒基因组的细胞间传播。 NSm已被用作酵母双杂交相互作用陷阱筛选的诱饵。结果,从拟南芥GAL4激活结构域标记的cDNA文库中分离了一种功能未知的蛋白,称为At-4 / 1。使用针对细菌表达的At-4 / 1的多克隆抗体,对从不同植物物种分离的蛋白质提取物进行的蛋白质印迹分析以及基因组数据库筛选显示,At-4 / 1的同源物似乎由许多维管植物编码。对于亚细胞定位研究,将At-4 / 1与绿色荧光蛋白融合,并将相应的表达载体用于粒子轰击和农业浸润试验。共聚焦激光扫描显示At-4 / 1聚集在细胞外围的点状斑点中。该蛋白质以极化的方式在细胞内积累,仅在轰击的表皮细胞的一半中出现,而且在细胞之间移动,形成似乎位于胞浆孔两个孔口的双结构体。在共表达研究中,At-4 / 1与一种植物病毒运动蛋白TGBp3共定位,该蛋白已知位于内质网衍生的膜结构中,该膜结构紧邻胞质。因此,At-4 / 1属于能够指导细胞内和细胞间运输的植物蛋白新家族。

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