Molecular Basis of Encapsidation of Hepatitis C Virus Genome

被引:13
作者
Shi, Guoli [1 ]
Suzuki, Tetsuro [2 ]
机构
[1] NCI, Ctr Canc Res, HIV Dynam & Replicat Program, Antiviral Immun & Resistance Sect, Frederick, MD 21701 USA
[2] Hamamatsu Univ Sch Med, Dept Virol & Parasitol, Hamamatsu, Shizuoka, Japan
来源
FRONTIERS IN MICROBIOLOGY | 2018年 / 9卷
关键词
hepatitis C virus; encapsidation; packaging signal; cis-acting element; virion assembly; FLAVIVIRUS RNA REPLICATION; NUCLEIC-ACID CHAPERONE; CIS-ACTING REPLICATION; RIBOSOME ENTRY SITE; CORE PROTEIN; TYPE-1; RNA; IN-VITRO; 3' END; DIMERIZATION; REGION;
D O I
10.3389/fmicb.2018.00396
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis C virus (HCV), a major etiologic agent of human liver diseases, is a positive-sense single-stranded RNA virus and is classified in the Flaviviridae family. Although research findings for the assembly of HCV particles are accumulating due to development of HCV cell culture system, the mechanism(s) by which the HCV genome becomes encapsidated remains largely unclear. In general, viral RNA represents only a small fraction of the RNA molecules in the cells infected with RNA viruses, but the viral genomic RNA is considered to selectively packaged into virions. It was recently demonstrated that HCV RNAs containing 3' end of the genome are selectively incorporated into virus particles during the assembly process and the 3' untranslated region functions as a cis-acting element for RNA packaging. Here, we discuss the molecular basis of RNA encapsidation of HCV and classical flaviviruses, contrast with the packaging mechanism of HIV-1.
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页数:7
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