The interaction of animal cytoplasmic RNA viruses with the nucleus to facilitate replication

被引:65
作者
Hiscox, JA [1 ]
机构
[1] Univ Leeds, Sch Biochem & Mol Biol, Leeds LS2 9JT, W Yorkshire, England
基金
英国生物技术与生命科学研究理事会;
关键词
RNA; viruses; nucleus; nucleolus; replication;
D O I
10.1016/S0168-1702(03)00160-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A number of positive and negative strand RNA viruses whose primary site of replication is the cytoplasm use the nucleus and/or nuclear components in order to facilitate their replicative processes and alter host cell function. The nucleus itself is divided into a number of different sub-domains including structures such as the nucleolus. Many of the nuclear proteins that localise to these domains are involved in RNA processing, and because of their limited coding capacity, it may be necessary for RNA viruses to sequester such cellular factors in order to facilitate the replication, transcription and translation of their genomes. Amongst the best-studied examples of this are the picornaviruses, whose infection results in the redistribution of nuclear proteins to the cytoplasm and their interaction with the internal ribosome entry site (IRES) to facilitate translation of the picornavirus polyprotein. Examples can be found of other positive and also negative strand RNA virus proteins that localise to the nucleus and sub-domains (especially the nucleolus) during virus infection, and several localisation motifs have been defined. Apart from sequestering nuclear proteins for a role in replication, such viruses may also target the nucleus to disrupt nuclear functions and to inhibit antiviral responses. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 22
页数:10
相关论文
共 111 条
[1]   INDUCTION OF MEMBRANE PROLIFERATION BY POLIOVIRUS PROTEINS 2C AND 2BC [J].
ALDABE, R ;
CARRASCO, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 206 (01) :64-76
[2]  
Andersen JS, 2002, CURR BIOL, V12, P1, DOI 10.1016/S0960-9822(01)00650-9
[3]   CDNA CLONING AND SEQUENCING OF HUMAN FIBRILLARIN, A CONSERVED NUCLEOLAR PROTEIN RECOGNIZED BY AUTOIMMUNE ANTISERA [J].
ARIS, JP ;
BLOBEL, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :931-935
[4]  
AZUMGELADE MC, 1994, J CELL SCI, V107, P463
[5]   Translation of polioviral mRNA is inhibited by cleavage of polypyrimidine tract-binding proteins executed by polioviral 3Cpro [J].
Back, SH ;
Kim, YK ;
Kim, WJ ;
Cho, S ;
Oh, HR ;
Kim, JE ;
Jang, SK .
JOURNAL OF VIROLOGY, 2002, 76 (05) :2529-2542
[6]   Inhibition of beta interferon transcription by noncytopathogenic bovine viral diarrhea virus is through an interferon regulatory factor 3-dependent mechanism [J].
Baigent, SJ ;
Zhang, G ;
Fray, MD ;
Flick-Smith, H ;
Goodbourn, S ;
McCauley, JW .
JOURNAL OF VIROLOGY, 2002, 76 (18) :8979-8988
[7]   Early alteration of nucleocytoplasmic traffic induced by some RNA viruses [J].
Belov, GA ;
Evstafieva, AG ;
Rubtsov, YP ;
Mikitas, OV ;
Vartapetian, AB ;
Agol, VI .
VIROLOGY, 2000, 275 (02) :244-248
[8]   Picornavirus RNA translation: roles for cellular proteins [J].
Belsham, GJ ;
Sonenberg, N .
TRENDS IN MICROBIOLOGY, 2000, 8 (07) :330-335
[9]  
Belsham GJ, 1995, CURR TOP MICROBIOL, V203, P85
[10]   THE ROLE OF VESICULAR STOMATITIS-VIRUS MATRIX PROTEIN IN INHIBITION OF HOST-DIRECTED GENE-EXPRESSION IS GENETICALLY SEPARABLE FROM ITS FUNCTION IN VIRUS ASSEMBLY [J].
BLACK, BL ;
RHODES, RB ;
MCKENZIE, M ;
LYLES, DS .
JOURNAL OF VIROLOGY, 1993, 67 (08) :4814-4821