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质膜相关阳离子结合蛋白 1 样蛋白负调控 BaMV 的细胞间运动。

Plasma membrane-associated cation-binding protein 1-like protein negatively regulates intercellular movement of BaMV.

机构信息

Graduate Institute of Biotechnology, National Chung Hsing University, Taichung, 402, Taiwan.

Research Center for Sustainable Energy and Nanotechnology, National Chung Hsing University, Taichung, 402, Taiwan.

出版信息

J Exp Bot. 2017 Oct 13;68(17):4765-4774. doi: 10.1093/jxb/erx307.

DOI:10.1093/jxb/erx307
PMID:28992255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5853580/
Abstract

To establish a successful infection, a virus needs to replicate and move cell-to-cell efficiently. We investigated whether one of the genes upregulated in Nicotiana benthamiana after Bamboo mosaic virus (BaMV) inoculation was involved in regulating virus movement. We revealed the gene to be a plasma membrane-associated cation-binding protein 1-like protein, designated NbPCaP1L. The expression of NbPCaP1L in N. benthamiana was knocked down using Tobacco rattle virus-based gene silencing and consequently the accumulation of BaMV increased significantly to that of control plants. Further analysis indicated no significant difference in the accumulation of BaMV in NbPCaP1L knockdown and control protoplasts, suggesting NbPCaP1L may affect cell-to-cell movement of BaMV. Using a viral vector expressing green fluorescent protein in the knockdown plants, the mean area of viral focus, as determined by fluorescence, was found to be larger in NbPCaP1L knockdown plants. Orange fluorescence protein (OFP)-fused NbPCaP1L, NbPCaP1L-OFP, was expressed in N. benthamiana and reduced the accumulation of BaMV to 46%. To reveal the possible interaction of viral protein with NbPCaP1L, we performed yeast two-hybrid and co-immunoprecipitation experiments. The results indicated that NbPCaP1L interacted with BaMV replicase. The results also suggested that NbPCaP1L could trap the BaMV movement RNP complex via interaction with the viral replicase in the complex and so restricted viral cell-to-cell movement.

摘要

为了建立成功的感染,病毒需要有效地复制和细胞间移动。我们研究了在感染竹花叶病毒(BaMV)后,拟南芥中上调的一个基因是否参与调节病毒运动。我们发现该基因是一种质膜相关阳离子结合蛋白 1 样蛋白,命名为 NbPCaP1L。利用烟草脆裂病毒(TRV)介导的基因沉默技术敲低了 NbPCaP1L 在拟南芥中的表达,结果导致 BaMV 的积累显著增加,达到对照植物的水平。进一步分析表明,在 NbPCaP1L 敲低和对照原生质体中,BaMV 的积累没有显著差异,这表明 NbPCaP1L 可能影响 BaMV 的细胞间运动。在敲低植物中,利用表达绿色荧光蛋白的病毒载体,通过荧光测定发现,病毒焦点的平均面积在 NbPCaP1L 敲低植物中更大。橙色荧光蛋白(OFP)融合的 NbPCaP1L,NbPCaP1L-OFP,在拟南芥中表达,并将 BaMV 的积累减少到 46%。为了揭示病毒蛋白与 NbPCaP1L 之间可能的相互作用,我们进行了酵母双杂交和免疫共沉淀实验。结果表明,NbPCaP1L 与 BaMV 复制酶相互作用。结果还表明,NbPCaP1L 可以通过与复合物中的病毒复制酶相互作用,捕获 BaMV 运动 RNA 蛋白复合物,从而限制病毒的细胞间运动。

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