The retrovirus RNA trafficking granule: from birth to maturity

被引:102
作者
Cochrane, Alan W.
T McNally, Mark
Mouland, Andrew J.
机构
[1] Sir Mortimer B Davis Jewish Hosp, RNA Trafficking Lab HIV 1, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Montreal, PQ H3T 1E2, Canada
[3] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
[4] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
关键词
D O I
10.1186/1742-4690-3-18
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Post-transcriptional events in the life of an RNA including RNA processing, transport, translation and metabolism are characterized by the regulated assembly of multiple ribonucleoprotein (RNP) complexes. At each of these steps, there is the engagement and disengagement of RNA-binding proteins until the RNA reaches its final destination. For retroviral genomic RNA, the final destination is the capsid. Numerous studies have provided crucial information about these processes and serve as the basis for studies on the intracellular fate of retroviral RNA. Retroviral RNAs are like cellular mRNAs but their processing is more tightly regulated by multiple cis-acting sequences and the activities of many trans-acting proteins. This review describes the viral and cellular partners that retroviral RNA encounters during its maturation that begins in the nucleus, focusing on important events including splicing, 3' end-processing, RNA trafficking from the nucleus to the cytoplasm and finally, mechanisms that lead to its compartmentalization into progeny virions.
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页数:17
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共 199 条
[1]   Efficient replication of full-length murine leukemia viruses modified at the dimer initiation site regions [J].
Aagaard, L ;
Rasmussen, SV ;
Mikkelsen, JG ;
Pedersen, FS .
VIROLOGY, 2004, 318 (01) :360-370
[2]  
Afonina E, 1997, J BIOL CHEM, V272, P2307, DOI 10.1074/jbc.272.4.2307
[3]   Heat-shock protein 70 can replace viral protein R of HIV-1 during nuclear import of the viral preintegration complex [J].
Agostini, I ;
Popov, S ;
Li, JH ;
Dubrovsky, L ;
Hao, T ;
Bukrinsky, M .
EXPERIMENTAL CELL RESEARCH, 2000, 259 (02) :398-403
[4]   Transport and localization elements in myelin basic protein mRNA [J].
Ainger, K ;
Avossa, D ;
Diana, AS ;
Barry, C ;
Barbarese, E ;
Carson, JH .
JOURNAL OF CELL BIOLOGY, 1997, 138 (05) :1077-1087
[5]   PRESENCE OF NEGATIVE AND POSITIVE CIS-ACTING RNA SPLICING ELEMENTS WITHIN AND FLANKING THE FIRST TAT CODING EXON OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 [J].
AMENDT, BA ;
HESSLEIN, D ;
CHANG, LJ ;
STOLTZFUS, CM .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (06) :3960-3970
[6]   INHIBITION OF RNA SPLICING AT THE ROUS-SARCOMA VIRUS SRC-3' SPLICE-SITE IS MEDIATED BY AN INTERACTION BETWEEN A NEGATIVE CIS-ELEMENT AND A CHICKEN-EMBRYO FIBROBLAST NUCLEAR FACTOR [J].
AMENDT, BA ;
SIMPSON, SB ;
STOLTZFUS, CM .
JOURNAL OF VIROLOGY, 1995, 69 (08) :5068-5076
[7]  
AMENDT BA, 1995, MOL CELL BIOL, V15, P4606
[8]   REGULATION OF ROUS-SARCOMA VIRUS-RNA SPLICING AND STABILITY [J].
ARRIGO, S ;
BEEMON, K .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (11) :4858-4867
[9]   Control of HIV-1 env RNA splicing and transport:: investigating the role of hnRNP A1 in exon splicing silencer (ESS3a) function [J].
Asai, K ;
Platt, C ;
Cochrane, A .
VIROLOGY, 2003, 314 (01) :229-242
[10]   The HIV-1 5' LTR poly(A) site is inactivated by U1 snRNP interaction with the downstream major splice donor site [J].
Ashe, MP ;
Pearson, LH ;
Proudfoot, NJ .
EMBO JOURNAL, 1997, 16 (18) :5752-5763