IRES特异性IRNA对HCV IRES启动蛋白翻译细胞内抑制作用  被引量:4

Inhibitory effect of IRES specific inhibitor RNA on HCV IRES mediated protein translation

在线阅读下载全文

作  者:梁雪松[1] 连建奇[1] 周永兴[1] 聂青和[1] 郝春秋[1] 

机构地区:[1]中国人民解放军第四军医大学唐都医院全军感染病诊疗中心,陕西省西安市710038

出  处:《世界华人消化杂志》2003年第2期157-160,共4页World Chinese Journal of Digestology

基  金:国家自然科学基金课题;No:3000147~~

摘  要:目的:研究核糖体内部进入位点(internalribosomeentrysite,IRES)特异性抑制性RNA(inhibitorRNA,IRNA)细胞内对丙型肝炎病毒(HCV)IRES介导蛋白翻译的抑制作用.方法:体外应用脂质体细胞转染法,将IRNA及其突变体mIRNA真核表达载体pcRz-IRNA/pcRz-mIRNA转染人肝癌细胞株(HHCC),经G418筛选4wk后建立IRNA及mIRNA表达株;以相同的方法构建pcHCVcluc转染株;以脂质体介导细胞转染法将pCMVNCRLuc转染IRNA及mIRNA细胞株,于转染后48h检测荧光素酶表达量;将IRNA及mIRNA真核表达体转染pcHCVcLuc表达株,于转染后不同时间检测荧光素酶表达量.结果:HCVIRES介导蛋白翻译在IRNA表达株明显受到抑制,同样IRNA对HCV翻译复制子的蛋白翻译作用有明显抑制性;突变体mIRNA表达株和空载体对照株中未见相似的抑制性.结论:pcHCVcluc在HHCC细胞中获得有效表达;IRES特异性IRNA能有效的抑制HCVIRES介导细胞内蛋白翻译作用.AIM:To explore the inhibitory effect of internal ribosome entry site (IRES) specific inhibitor RNA (IRNA) on HCV IRES mediated protein translation in vivo. METHODS:Human hepatic carcinoma cell line (HHCC) was transfected with the eukaryotic vectors of IRNA or mIRNA (pcRz-IRNA or pcRz-mIRNA),and then selected with G418 for 4 weeks.HHCC expressing IRNA or mIRNA was cotransfected with pCMVNCRluc containing HCV IRES.HHCC stably expressing pcHCVcluc was transfected with pcRz-IRNA, and pcRz-mIRNA,respectively, the luciferase activity was examined at desired time post-transfection. RESULTS:The pCMVNCRluc was efficiently suppressed in HHCC expressing IRNA rather than the cell line expressing mIRNA.The IRES specific IRNA inhibited expression of HCV IRES mediated luc gene by 20 % to 80 % in pcHCVcluc expressing cell after transfection; However, no inhibitory effect of the mutant IRNA was observed. CONCLUSION:pcHCVcluc could be expressed successfully in HHCC, and IRNA inhibited HCV IRES mediated gene expression in vivo.

关 键 词:IRES 特异性IRNA HCV IRES 启动蛋白翻译 细胞内 抑制作用 

分 类 号:R373.21[医药卫生—病原生物学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象