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Dissecting the Molecular Mechanism of the Subcellular Localization and Cell-to-cell Movement of the Sugarcane mosaic virus P3N-PIPO

机译:解剖甘蔗花叶病毒P3N-PIPO亚细胞定位和细胞间运动的分子机制

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摘要

The coding sequence of P3N-PIPO was cloned by fusion PCR from Sugarcane mosaic virus (SCMV), a main causal agent of sugarcane (Saccharum spp. hybrid) mosaic disease. SCMV P3N-PIPO preferentially localized to the plasma membrane (PM) compared with the plasmodesmata (PD), as demonstrated by transient expression and plasmolysis assays in the leaf epidermal cells of Nicotiana benthamiana. The subcellular localization of the P3N-PIPO mutants P3N-PIPOT1 and P3N-PIPOT2 with 29 and 63 amino acids deleted from the C-terminus of PIPO, respectively, revealed that the 19 amino acids at the N-terminus of PIPO contributed to the PD localization. Interaction assays showed that the 63 amino acids at the C-terminus of PIPO determined the P3N-PIPO interaction with PM-associated Ca2+-binding protein 1, ScPCaP1, which was isolated from the SCMV-susceptible sugarcane cultivar Badila. Like wild-type P3N-PIPO, P3N-PIPOT1 and P3N-PIPOT2 could translocate to neighbouring cells and recruit the SCMV cylindrical inclusion protein to the PM. Thus, interactions with ScPCaP1 may contribute to, but not determine, SCMV Pm3N-PIPO’s localization to the PM or PD. These results also imply the existence of truncated P3N-PIPO in nature.
机译:通过融合PCR从甘蔗花叶病毒(SCMV)(甘蔗(Saccharum spp。hybrid)花叶病的主要病原体)中通过融合PCR克隆了P3N-PIPO的编码序列。 SCMV P3N-PIPO与质膜(PD)相比,优先定位在质膜(PM)上,如本特尼烟草(Nicotiana benthamiana)叶片的表皮细胞中的瞬时表达和质解分析所证明的。 P3N-PIPO突变体P3N-PIPOT1和P3N-PIPOT2在PIPO C末端分别缺失29和63个氨基酸的亚细胞定位显示,PIPO N末端的19个氨基酸有助于PD本土化。相互作用分析表明,PIPO C末端的63个氨基酸决定了P3N-PIPO与PM相关的Ca 2 + 结合蛋白1 ScPCaP1的相互作用,该蛋白从SCMV易感人群中分离出来。甘蔗品种巴迪拉。像野生型P3N-PIPO一样,P3N-PIPOT1和P3N-PIPOT2可以易位到邻近细胞,并将SCMV圆柱形包涵蛋白募集到PM。因此,与ScPCaP1的交互可能有助于(但不能确定)SCMV Pm3N-PIPO定位于PM或PD。这些结果还暗示自然界中存在截短的P3N-PIPO。

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