Qi Z T, Kalkeri G, Hanible J, Prabhu R, Bastian F, Garry R F, Dash S
Department of Pathology and Laboratory Medicine, Tulane University Health Sciences Center, New Orleans, LA 70112, U.S.A.
Arch Virol. 2003 Mar;148(3):449-67. doi: 10.1007/s00705-002-0933-0.
The 5' and 3' untranslated regions (UTR) of the hepatitis C virus (HCV) genome contain stem-loop structures, which are important in viral gene expression and replication. In this study, the functional roles of the predicted stem-loop structures of HCV 5' UTR and 3' UTR in viral gene expression were examined using a chimeric clone of full-length HCV genomic cDNA clone and the gene for green fluorescent protein (GFP). High level expression of the HCV-GFP chimera in Huh-7 cells was accomplished by using a replication defective adenovirus that expresses T7 RNA polymerase and transcription plasmid containing full-length HCV-GFP chimera under the control of a T7 promoter. The HCV-GFP clone, with deletion of stem-loop I, expressed proteins in transfected Huh-7 cells at comparable levels to the wild type HCV clone. Other mutations of the 5' UTR, which either deleted or altered the base pairing of stem-loops II to IV, completely abolished the expression of HCV-GFP chimera. In contrast, deletion of 3' UTR sequences had no effect on HCV protein expression. These findings suggest that the stem-loop structures II to IV of HCV 5' UTR are necessary for protein expression, but that stem loop I is dispensable for protein translation. The stem-loop structures of 3' UTR of HCV genome appear to have no direct role in viral gene expression.
丙型肝炎病毒(HCV)基因组的5'和3'非翻译区(UTR)含有茎环结构,这些结构在病毒基因表达和复制中很重要。在本研究中,使用全长HCV基因组cDNA克隆与绿色荧光蛋白(GFP)基因的嵌合克隆,检测了HCV 5'UTR和3'UTR预测的茎环结构在病毒基因表达中的功能作用。通过使用表达T7 RNA聚合酶的复制缺陷型腺病毒和在T7启动子控制下含有全长HCV-GFP嵌合体的转录质粒,在Huh-7细胞中实现了HCV-GFP嵌合体的高水平表达。缺失茎环I的HCV-GFP克隆在转染的Huh-7细胞中表达的蛋白水平与野生型HCV克隆相当。5'UTR的其他突变,即删除或改变茎环II至IV的碱基配对,完全消除了HCV-GFP嵌合体的表达。相反,删除3'UTR序列对HCV蛋白表达没有影响。这些发现表明,HCV 5'UTR的茎环结构II至IV是蛋白表达所必需的,但茎环I对于蛋白翻译是可有可无的。HCV基因组3'UTR的茎环结构似乎在病毒基因表达中没有直接作用。