Positive and negative effects on translation of the hepatitis C virus 3' untranslated region.

Journal of human virology Pub Date : 2002-01-01
Lisa Wiklund, Karin Spångberg, Stefan Schwartz
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Abstract

Objectives: To determine the role of the hepatitis C virus 3' untranslated region in viral mRNA translation in transfected cells and in cell extracts.

Study design/methods: Noninfectious hepatitis C virus mini-genome RNAs with various deletions in the viral 3' untranslated region were transfected into cells or translated in vitro, and the translation efficiency was determined.

Results: We have found that the presence of the hepatitis C virus 3' untranslated region modestly increases mRNA translation. The positive effect correlated with the binding of a 45-kDa cytoplasmic factor to the hepatitis C virus 3' untranslated region. Furthermore, the U-rich sequence in the hepatitis C virus 3' untranslated region inhibits translation of capped and polyadenylated mRNAs as a result of the hybridization.

Conclusions: The modest effect of the hepatitis C virus 3' untranslated region on translation suggests that it does not play a major role in mRNA translation. The inhibitory effect of the hepatitis C virus 3' untranslated region on translation of polyadenylated mRNAs supports the notion that translation of hepatitis C virus mRNAs occurs independently of a polyA tail.

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对丙型肝炎病毒3'非翻译区翻译的正面和负面影响。
目的:确定丙型肝炎病毒3′非翻译区在转染细胞和细胞提取物中病毒mRNA翻译中的作用。研究设计/方法:将病毒3'非翻译区不同缺失的非传染性丙型肝炎病毒小基因组rna转染细胞或体外翻译,并测定翻译效率。结果:我们发现丙型肝炎病毒3'非翻译区存在适度增加mRNA翻译。这种积极作用与一个45 kda的细胞质因子与丙型肝炎病毒3'非翻译区结合有关。此外,丙型肝炎病毒3'非翻译区的富u序列由于杂交而抑制了带帽和多腺苷化mrna的翻译。结论:丙型肝炎病毒3'非翻译区对mRNA翻译的影响不大,表明它在mRNA翻译中不起主要作用。丙型肝炎病毒3'非翻译区对多聚腺苷化mrna翻译的抑制作用支持了丙型肝炎病毒mrna翻译独立于多聚a尾部发生的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Associations between MHC class I and susceptibility to HIV-2 disease progression. Positive and negative effects on translation of the hepatitis C virus 3' untranslated region. Development of vaccination strategies that elicit broadly neutralizing antibodies against human immunodeficiency virus type 1 in both the mucosal and systemic immune compartments. Abstracts of the 2002 International Meeting of the Institute of Human Virology. September 9-13, 2002, Baltimore, Maryland, USA. The hepatitis C virus NS5B RNA-dependent RNA polymerase activity and susceptibility to inhibitors is modulated by metal cations.
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