Internal translation initiation of picornaviruses and hepatitis C virus

被引:57
作者
Niepmann, Michael [1 ]
机构
[1] Univ Giessen, Fac Med, Inst Biochem, D-35392 Giessen, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2009年 / 1789卷 / 9-10期
关键词
IRES; FMDV; EMCV; Poliovirus; HAV; HCV; eIF; microRNA; miR-122; Picornavirus; RIBOSOME ENTRY SITE; TRACT-BINDING-PROTEIN; MOUTH-DISEASE VIRUS; CAP-INDEPENDENT TRANSLATION; 5 NONTRANSLATED REGION; FACTOR 4G EIF4G; RNA-BINDING; ENCEPHALOMYOCARDITIS VIRUS; MESSENGER-RNA; POLIOVIRUS RNA;
D O I
10.1016/j.bbagrm.2009.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Picornaviruses and other positive-strand RNA viruses like hepatitis C virus (HCV) enter the cell with a single RNA genome that directly serves as the template for translation. Accordingly. the viral RNA genome needs to recruit the cellular translation machinery for viral protein synthesis. By the use of internal ribosome entry site (IRES) elements in their genomic RNAs, these viruses bypass translation competition with the bulk of capped cellular mRNAs and, moreover, establish the option to largely shut-down cellular protein synthesis. In this review, I discuss the structure and function of viral IRES elements, focusing on the recruitment of the cellular translation machinery by the IRES and on factors that may contribute to viral tissue tropism on the level of translation. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:529 / 541
页数:13
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