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利用酵母双杂交技术筛选鉴定与番茄环纹斑点病毒NSs蛋白互作的西花蓟马蛋白
引用本文:赵星月,陈建斌,王曙光,张晓林,穆野,魏辉,赵立华,陈永对,郑雪,陈勇,郑立敏,张洁. 利用酵母双杂交技术筛选鉴定与番茄环纹斑点病毒NSs蛋白互作的西花蓟马蛋白[J]. 昆虫学报, 2020, 63(6): 735-743. DOI: 10.16380/j.kcxb.2020.06.009
作者姓名:赵星月  陈建斌  王曙光  张晓林  穆野  魏辉  赵立华  陈永对  郑雪  陈勇  郑立敏  张洁
作者单位:(1. 西南林业大学生命科学学院, 昆明 650224; 2. 云南省农业科学院生物技术与种质资源研究所, 云南省农业生物技术重点实验室, 农业部西南作物基因资源与种质创制重点实验室, 昆明 650205; 3. 湖南省农业科学院植物保护研究所, 长沙 410125; 4. 福建省农业科学院植物保护研究所, 福建省作物有害生物监测与治理重点实验室, 农业部福州作物有害生物科学观测试验站, 福州 350003)
基金项目:国家自然科学基金项目(31560499,31871936,31860498,31960531,31871935);;云南省应用基础研究计划重点项目(2018FA020);;国家重点研发计划政府间/港澳台重点专项项目(2018YFE0112600);
摘    要:【目的】筛选鉴定西花蓟马Franiklinella ocicdentalis体内与番茄环纹斑点病毒(tomato zonate spot virus, TZSV)NSs蛋白互作的介体因子。【方法】利用酵母双杂交技术筛选与TZSV NSs互作的西花蓟马蛋白;进行序列分析鉴定后,将捕获的蛋白与NSs基因回转到酵母细胞,利用营养缺陷型培养基鉴定蛋白互作情况。再利用GST Pull-down技术验证TZSV NSs与鉴定出的西花蓟马蛋白的体外互作关系。【结果】构建了TZSV NSs的酵母双杂交诱饵质粒pGBKT7-NSs,确定了诱饵质粒对酵母AH109细胞无毒性,并且无自激活活性。序列分析发现与TZSV NSs互作的西花蓟马蛋白为类电压依赖性阴离子通道(voltage-dependent anion-selective channel-like, VDAC)。酵母回转实验显示TZSV NSs与西花蓟马VDAC在酵母细胞内存在特异性互作。GST Pull-down结果表明TZSV NSs与西花蓟马VDAC在体外存在相互作用。【结论】通过酵母双杂交和GST Pull-down技术,分别在酵母细胞内...

关 键 词:西花蓟马  酵母双杂交  番茄环纹斑点病毒  NSs蛋白  VDAC

Screening and identification of the protein interacting with the NSs protein ofTomato zonate spot virusinFraniklinella ocicdentalis(Thysanoptera: Thripidae) by yeast two-hybrid technique
ZHAO Xing-Yue,CHEN Jian-Bin,WANG Shu-Guang,ZHANG Xiao-Lin,MU Ye,WEI Hui,ZHAO Li-Hua,CHEN Yong-Dui,ZHENG Xue,CHEN Yong,ZHENG Li-Min,ZHANG Jie. Screening and identification of the protein interacting with the NSs protein ofTomato zonate spot virusinFraniklinella ocicdentalis(Thysanoptera: Thripidae) by yeast two-hybrid technique[J]. Acta Entomologica Sinica, 2020, 63(6): 735-743. DOI: 10.16380/j.kcxb.2020.06.009
Authors:ZHAO Xing-Yue  CHEN Jian-Bin  WANG Shu-Guang  ZHANG Xiao-Lin  MU Ye  WEI Hui  ZHAO Li-Hua  CHEN Yong-Dui  ZHENG Xue  CHEN Yong  ZHENG Li-Min  ZHANG Jie
Abstract:【Aim】 To screen and identify the protein interacting with the tomato zonate spot virus (TZSV) NSs protein in the western flower thrips, Franiklinella ocicdentalis. 【Methods】 The protein in F. ocicdentalis interacting with TZSV NSs was screened by yeast two-hybrid technique. After sequence analysis, the captured protein and NSs genes were cotransformed into yeast cells, and their interaction was identified by nutrient deficient medium. Furthermore, GST Pull-down was used to confirm the interaction of NSs and the identified protein in F. ocicdentalis in vitro. 【Results】 pGBKT7-NSs, a yeast two-hybrid bait plasmid of TZSV NSs, was constructed, and it showed no toxicity and no autoactivition to AH109 yeast cell. Sequence analysis showed that a voltage-dependent anion-selective channel-like (VDAC) protein of F. ocicdentalis interacted with TZSV NSs. The cotransformation test results showed that there was a specific interaction between TZSV NSs and VDAC in yeast cell. The GST Pull-down results showed that there was interaction between TZSV NSs and VDAC in vitro. 【Conclusion】 The specific interaction between TZSV NSs and F. ocicdentalis VDAC was confirmed in yeast cell and in vitro by yeast two-hybrid and GST Pull-down techniques, respectively. The results are helpful to reveal the mechanism of the protein VDAC regulating the transmission of persistent-propagative plant viruses in F. ocicdentalis and provide a theoretical basis for the prevention and control of insect-borne virus diseases.
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