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Agrobacterium-mediated transient expression in citrus leaves: a rapid tool for gene expression and functional gene assay

机译:农杆菌介导的柑橘叶片瞬时表达:基因表达和功能基因测定的快速工具

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摘要

In this study, we present a method for transient expression of the type III effector AvrGf1 from Xanthomonas citri subsp. citri strain Aw in grapefruit leaves (Citrus paradisi) via Agrobacterium tumefaciens. The coding sequence of avrGf1 was placed under the control of the constitutive CaMV 35S promoter in the binary vectors pGWB2 and pGWB5. Infiltration of grapefruit leaves with A. tumefaciens carrying these constructs triggered a hypersensitive response (HR) in grapefruit 4 days after inoculation. When transiently expressed in grapefruit leaves, two mutants, AvrGf1ΔN116 and AvrGf1ΔC83, failed to induce an HR. Moreover, using bioinformatics tools, a chloroplast transit signal was predicted at the N terminus of AvrGf1. We demonstrated chloroplast localization by using an AvrGf1::GFP fusion protein, where confocal images revealed that GFP fluorescence was accumulating in the stomatal cells that are abundant in chloroplasts. Transient expression in citrus has the potential for aiding in the development of new disease defense strategies in citrus.
机译:在这项研究中,我们提出了一种从柠檬黄单胞菌亚种瞬时表达III型效应子AvrGf1的方法。通过根癌农杆菌在柚子叶片(Citrus paradisi)中的柠檬菌株A w 。将avrGf1的编码序列置于二元载体pGWB2和pGWB5的组成型CaMV 35S启动子的控制下。接种后4天,带有这些构建体的根癌农杆菌渗入葡萄柚叶片会触发葡萄柚的超敏反应(HR)。当在葡萄柚叶片中瞬时表达时,两个突变体AvrGf1ΔN116和AvrGf1ΔC83无法诱导HR。此外,使用生物信息学工具,在AvrGf1的N端预测了叶绿体转运信号。我们通过使用AvrGf1 :: GFP融合蛋白证明叶绿体定位,共聚焦图像显示GFP荧光在叶绿体中丰富的气孔细胞中积累。柑橘中的瞬时表达具有帮助开发柑橘中新的疾病防御策略的潜力。

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