| 水稻齿叶矮缩病毒Pns10蛋白在水稻原生质体内的表达 |
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| 引用本文： | 张洁＃,陈晓敏＃,吴锦鸿,朱重庆,丁新伦,吴祖建.水稻齿叶矮缩病毒Pns10蛋白在水稻原生质体内的表达[J].中国水稻科学,2017,31(3):232-237. |
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| 作者姓名： | 张洁＃ 陈晓敏＃ 吴锦鸿 朱重庆 丁新伦 吴祖建 |
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| 作者单位： | 福建农林大学 植物病毒研究所/福建省植物病毒学重点实验室，福州 350002； |
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| 基金项目： | 高等学校博士学科点专项科研基金资助项目(20133515120004)；国家自然科学基金资助项目(31301640)；福建教育厅科技项目(JA13103)。 |
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| 摘 要： | 【目的】水稻齿叶矮缩病毒(Rice ragged stunt virus,RRSV)Pns10蛋白在介体昆虫细胞内可形成类似病毒原质(viroplasm)的内含体,是RRSV侵染介体所必需。然而Pns10蛋白在水稻寄主中是否具有类似功能及其表达情况如何未见报道。【方法】利用大肠杆菌系统表达Pns10蛋白,免疫家兔制备多克隆抗体;通过水稻原生质体病毒侵染体系,利用免疫荧光技术分析Pns10蛋白在水稻原生质体内的分布情况,利用实时定量PCR技术和Western blot技术分别检测Pns10 RNA和Pns10蛋白在水稻原生质体内的积累情况。【结果】将Pns10基因克隆到Gateway系统原核表达载体p DEST17中,IPTG诱导表达成功后,制备融合蛋白抗血清。Western blot检测显示,该抗血清可检测感病水稻叶片中的Pns10蛋白。病毒侵染水稻原生质体后,Pns10蛋白可形成类似病毒原质的内含体;Pns10 RNA在病毒接种8 h后开始积累,24 h后达到最大值,随后开始下降;Pns10蛋白在24 h后开始表达,之后维持较高水平,60 h后略有下降。【结论】成功获得了Pns10抗血清;Pns10在水稻原生质体内成功表达,可形成类似病毒原质的内含体,并且Pns10 RNA的表达先于其蛋白的表达。
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| 关 键 词： | 水稻齿叶矮缩病毒 水稻原生质体 Pns10抗体 Pns10 RNA Pns10蛋白 |
| 收稿时间： | 2016-11-09 |
Expression of Pns10 Protein of Rice ragged stunt virus in Rice Protoplasts |
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| ZHANG Jie＃,CHEN Xiaomin＃,WU Jinhong,ZHU Chongqing,DING Xinlun,WU Zujian.Expression of Pns10 Protein of Rice ragged stunt virus in Rice Protoplasts[J].Chinese Journal of Rice Science,2017,31(3):232-237. |
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| Authors: | ZHANG Jie＃ CHEN Xiaomin＃ WU Jinhong ZHU Chongqing DING Xinlun WU Zujian |
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| Institution: | Institute of Plant Virology, Fujian Agriculture and Forestry University/Key Laboratory of Plant Virology of Fujian Province, Fuzhou 350002, China; |
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| Abstract: | 【Objective】Pns10 of Rice ragged stunt virus (RRSV) forms viroplasm-like inclusion bodies which are essential for virus infection to vector insects. However, the expression pattern and function of Pns10 in rice remain unknown.【Method】Polyclonal antibody against Pns10 protein was prepared by immunizing rabbits with a bacterially expressed Pns10; the cellular distribution of Pns10 protein in rice protoplasts was observed with an immunofluorescence microscopy; the accumulation of Pns10 RNA in rice protoplasts infected by RRSV was quantified with real-time quantitative RT-PCR and that of the Pns10 protein was investigated using Western blot.【Result】Pns10 ORF was cloned into the Gateway prokaryotic expression vector pDEST17 and its expression was induced by IPTG. Polyclonal antiserum against the Pns10 was obtained and it can react with the Pns10 protein from the naturally RRSV-infected rice by Western blot detecting. Pns10 formed viroplasm-like inclusion bodies in protoplasts. The Pns10 RNA was first detected at 8 h post RRSV inoculation. The accumulation of Pns10 RNA peaked at 24 h post virus inoculation but began to decline thereafter. The Pns10 protein was first detected at 24 h post virus inoculation. A high level of Pns10 protein was maintained until 60 h post virus inoculation.【Conclusion】Antiserum against RRSV Pns10 protein was obtained. Pns10 was expressed and viroplasm-like inclusion bodies formed in rice protoplasts. In addition, the expression of Pns10 RNA was earlier than that of the Pns10 protein. |
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| Keywords: | Rice ragged stunt virus rice protoplast Pns10 antibody Pns10 RNA Pns10 protein |
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