The selective packaging and annealing of primer tRNALys3 in HIV-1

被引:39
作者
Kleiman, L [1 ]
Halwani, R
Javanbakht, H
机构
[1] Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[2] Jewish Gen Hosp, McGill AIDS Ctr, Montreal, PQ H3T 1E2, Canada
关键词
primer tRNA(Lys3); tRNA-(Lys) packaging complex; lysyl-tRNA synthetase; Gag; GagPol; tRNA(Lys3) annealing to viral RNA;
D O I
10.2174/1570162043484988
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In HIV-1, tRNA(Lys3) serves as the primer for reverse transcriptase, and during viral assembly, the tRNA(Lys) isoacceptors, tRNA(Lys1,2), and tRNA(Lys3) are selectively packaged into the virion. In this review, we shall first discuss the evidence for the formation of a tRNA(Lys) packaging complex, whose components include Gag, GagPol, genomic RNA, lysyl-tRNA synthetase (LysRS), and tRNA(Lys). Evidence suggests that the formation of this complex involves a Gag/GagPol/viral genomic RNA complex interacting with a tRNA(Lys)/LysRS complex, with Gag interacting with both GagPol and LysRS, and GagPol interacting with the tRNA(Lys). The interaction of Gag with LysRS is quite specific, does not require the presence of tRNA(Lys), and LysRS is believed to be the target that allows the specific packaging of tRNA(Lys) into the virion. The parameters influencing these interactions, and the molecular sites of interaction, will be discussed. The selective packaging of tRNA(Lys3) into HIV-1 facilitates annealing of tRNA(Lys3) to the 5' region of viral RNA genome. This region contains a series of stem loops, and there exists several regions in both the viral RNA and the tRNA(Lys3) that are believed to be important for tRNA(Lys3) annealing. The annealing is facilitated by vital proteins such as unprocessed Gag, nucleocapsid, and reverse transcriptase.
引用
收藏
页码:163 / 175
页数:13
相关论文
共 152 条
[41]  
FARAS AJ, 1975, P NATL ACAD SCI USA, V72, P859, DOI 10.1073/pnas.72.3.859
[42]   The human immunodeficiency virus type 1 Gag polyprotein has nucleic acid chaperone activity: Possible role in dimerization of genomic RNA and placement of tRNA on the primer binding site [J].
Feng, YX ;
Campbell, S ;
Harvin, D ;
Ehresmann, B ;
Ehresmann, C ;
Rein, A .
JOURNAL OF VIROLOGY, 1999, 73 (05) :4251-4256
[43]   Functional dissection of the eukaryotic-specific tRNA-interacting factor of lysyl-tRNA synthetase [J].
Francin, M ;
Mirande, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) :1472-1479
[44]   The N-terminal domain of mammalian lysyl-tRNA synthetase is a functional tRNA-binding domain [J].
Francin, M ;
Kaminska, M ;
Kerjan, P ;
Mirande, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (03) :1762-1769
[45]   A domain in the N-terminal extension of class IIb eukaryotic aminoacyl-tRNA synthetases is important for tRNA binding [J].
Frugier, M ;
Moulinier, L ;
Giegé, R .
EMBO JOURNAL, 2000, 19 (10) :2371-2380
[46]   Placement of tRNA primer on the primer-binding site requires pol gene expression in avian but not murine retroviruses [J].
Fu, W ;
OrtizConde, BA ;
Gorelick, RJ ;
Hughes, SH ;
Rein, A .
JOURNAL OF VIROLOGY, 1997, 71 (09) :6940-6946
[47]   Effect of altering the tRNA3Lys concentration in human immunodeficiency virus type 1 upon its annealing to viral RNA, GagPol incorporation, and viral infectivity [J].
Gabor, J ;
Cen, S ;
Javanbakht, H ;
Niu, MJ ;
Kleiman, L .
JOURNAL OF VIROLOGY, 2002, 76 (18) :9096-9102
[48]   Structure of the carboxyl-terminal dimerization domain of the HIV-1 capsid protein [J].
Gamble, TR ;
Yoo, SH ;
Vajdos, FF ;
vonSchwedler, UK ;
Worthylake, DK ;
Wang, H ;
McCutcheon, JP ;
Sundquist, WI ;
Hill, CP .
SCIENCE, 1997, 278 (5339) :849-853
[49]   Particle size determinants in the human immunodeficiency virus type 1 Gag protein [J].
Garnier, L ;
Ratner, L ;
Rovinski, B ;
Cao, SX ;
Wills, JW .
JOURNAL OF VIROLOGY, 1998, 72 (06) :4667-4677
[50]  
Geigenmuller U, 1996, J VIROL, V70, P667