机构地区:[1]State Key Laboratory of Common Mechanism Research for Major Diseases,Department of Molecular Biology and Biochemistry,Medical Primate Research Center,Neuroscience Center,Institute of Basic Medical Sciences Chinese Academy of Medical Sciences&School of Basic Medicine Peking Union Medical College,Beijing 100005,China [2]Institute of Medical Biology,Chinese Academy of Medical Sciences&Peking Union Medical College,Kunming 650031,China [3]State Key Laboratory of Respiratory Health and Multimorbidity,Chinese Academy of Medical Sciences&Peking Union Medical College,Beijing 100021,China [4]Institute of Laboratory Animal Science,Chinese Academy of Medical Sciences&Peking Union Medical College,Beijing 100021,China
出 处:《Chinese Medical Sciences Journal》2024年第3期163-172,共10页中国医学科学杂志(英文版)
基 金:国家自然科学基金创新研究群体项目(82221004)。
摘 要:Objectives To identify the 5'untranslated region of Zika virus(ZIKV 5'UTR)RNA-binding proteins and to investigate the impact of the binding protein on the activity of internal ribosomal entry site(IRES)located in ZIKV 5'UTR and virus production.Methods Interacting proteins in U251 cells were captured using tRSA-tagged ZIKV 5'UTR RNA and tRSA-ZIKV 5'UTR RNA-binding proteins were visualized by SDS-PAGE silver staining,Subsequently,liquid chromatographytandem mass spectrometry(LC-MS/MS),bioinformatics analysis,and Western blot were used to identify the candidate proteins binding to ZIKV 5'UTR.Dicistronic expression assay and plaque forming assay were performed to analyze the effect of the binding protein on ZIKV IRES activity and ZIKV production,respecitvely.Results tRSA RNA pull-down assay,LC-MS/MS,and Western blot analysis showed that polypyrimidine tractbinding protein(PTB)bound to the ZIKV 5'UTR.Furthermore,dual luciferase reporter assay revealed that overexpression of PTB significantly enhanced the IRES activity of ZIKV(t=10.220,P<0.001),while PTB knockdown had the opposite effect(t=4.897,P<0.01).Additionally,virus plaque forming assay demonstrated that up-regulation of PTB expression significantly enhanced viral titer(t=6.400,P<0.01),whereas reducing PTB expression level weakened virus infectivity(t=5.055,P<0.01).Conclusion PTB positively interacts with the ZIKV 5'UTR and enhances IRES activity and virus production.目的识别寨卡病毒(Zika virus,ZIKV)5’非翻译区(5’untranslated region,5’UTR)的RNA结合蛋白,并探讨结合蛋白对位于ZIKV5’UTR的内部核糖体进入位点(internal ribosomal entry site,IRES)活性及病毒产生的影响。方法使用tRSA标记的ZIKV5’UTRRNA捕获U251细胞中与之相互作用的蛋白,采用SDS-PAGE银染法获得tRSA-ZIKV5’UTRRNA候选结合蛋白的条带。随后,利用液相色谱-串联质谱法、生物信息学分析和Westernblot分析研究与ZIKV5’UTR结合的候选蛋白。采用双顺反子表达实验和蚀斑形成实验分析结合蛋白对ZIKVIRES活性和ZIKV产生的影响。结果tRSARNA pull-down分析、液相色谱-串联质谱法和Western blot分析显示多嘧啶束结合蛋白(polypyrimidine tract-binding protein,PTB)为与ZIKV5'UTR结合的蛋白。双荧光素酶报告基因检测结果显示:PTB过表达能显著增强ZIKV的IRES活性(t=10.220,P<0.001),而降低PTB表达则效果相反(t=4.897,P<0.01)。此外,病毒噬斑形成实验表明:上调PTB表达能显著提高病毒滴度(t=6.400,P<0.01),而降低PTB表达水平则会削弱病毒的感染能力(t=5.055,P<0.01)。结论PTB对ZIKV5’UTR发挥正向调节作用,能增强IRES活性和提高病毒产量。
关 键 词:internal ribosomal entry site polypyrimidine tract-binding protein Zika virus tRSA RNA pull-down dual-luciferase reporter assay
分 类 号:R373[医药卫生—病原生物学]
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