Brome mosaic virus RNA replication: Revealing the role of the host in RNA virus replication

被引:112
作者
Noueiry, AO [1 ]
Ahlquist, P
机构
[1] Univ Wisconsin, Inst Mol Virol, Madison, WI 53706 USA
[2] Univ Wisconsin, Howard Hughes Med Inst, Madison, WI 53706 USA
关键词
positive-strand RNA virus; translation initiation; RNA chaperone; endoplasmic reticulum; molecular chaperone; genetic analysis;
D O I
10.1146/annurev.phyto.41.052002.095717
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The replication of positive-strand RNA viruses is a complex multi-step process involving interactions between the viral genome, virus-encoded replication factors, and host factors. The plant virus brome mosaic virus (BMV) has served as a model for positive-strand RNA virus replication, recombination, and virion assembly. This review addresses recent findings on the identification and characterization of host factors in BMV RNA replication. To date, all characterized host factors facilitate steps that lead to assembly of a functional BMV RNA replication complex. Some of these host factors are required for regulation of viral gene expression. Others are needed to co-regulate BMV RNA translation and recruitment of BMV RNAs from translation to viral RNA replication complexes on the endoplasmic reticulum. Other host factors provide essential lipid modifications in the endoplasmic reticulum membrane or function as molecular chaperones to activate the replication complex. Characterizing the functions of these host factors is revealing basic aspects of virus RNA replication and helping to define the normal functions of these factors in the host.
引用
收藏
页码:77 / 98
页数:22
相关论文
共 125 条
[41]   Switch from translation to RNA replication in a positive-stranded RNA virus [J].
Gamarnik, AV ;
Andino, R .
GENES & DEVELOPMENT, 1998, 12 (15) :2293-2304
[42]   Replication of poliovirus in Xenopus oocytes requires two human factors [J].
Gamarnik, AV ;
Andino, R .
EMBO JOURNAL, 1996, 15 (21) :5988-5998
[43]   Transient expression of cellular polypyrimidine-tract binding protein stimulates cap-independent translation directed by both picornaviral and flaviviral internal ribosome entry sites in vivo [J].
Gosert, R ;
Chang, KH ;
Rijnbrand, R ;
Yi, MY ;
Sangar, DV ;
Lemon, SM .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (05) :1583-1595
[44]   PHOSPHOLIPID BIOSYNTHESIS AND POLIOVIRUS GENOME REPLICATION, 2 COUPLED PHENOMENA [J].
GUINEA, R ;
CARRASCO, L .
EMBO JOURNAL, 1990, 9 (06) :2011-2016
[45]   STRIKING SIMILARITIES IN AMINO-ACID-SEQUENCE AMONG NONSTRUCTURAL PROTEINS ENCODED BY RNA VIRUSES THAT HAVE DISSIMILAR GENOMIC ORGANIZATION [J].
HASELOFF, J ;
GOELET, P ;
ZIMMERN, D ;
AHLQUIST, P ;
DASGUPTA, R ;
KAESBERG, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (14) :4358-4362
[46]   Poliovirus RNA replication requires genome circularization through a protein-protein bridge [J].
Herold, J ;
Andino, R .
MOLECULAR CELL, 2001, 7 (03) :581-591
[47]   Mechanisms of mRNA surveillance in eukaryotes [J].
Hilleren, P ;
Parker, R .
ANNUAL REVIEW OF GENETICS, 1999, 33 :229-260
[48]   Hsp90 is required for the activity of a hepatitis B virus reverse transcriptase [J].
Hu, JM ;
Seeger, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1060-1064
[49]   Hepadnavirus assembly and reverse transcription require a multi-component chaperone complex which is incorporated into nucleocapsids [J].
Hu, JM ;
Toft, DO ;
Seeger, C .
EMBO JOURNAL, 1997, 16 (01) :59-68
[50]   In vitro reconstitution of functional hepadnavirus reverse transcriptase with cellular chaperone proteins [J].
Hu, JM ;
Toft, D ;
Anselmo, D ;
Wang, XT .
JOURNAL OF VIROLOGY, 2002, 76 (01) :269-279