Association of human immunodeficiency virus type 1 vif with RNA and its role in reverse transcription

被引:96
作者
Dettenhofer, M
Cen, S
Carlson, BA
Kleiman, L
Yu, XF
机构
[1] Johns Hopkins Univ, Sch Hyg & Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] NCI, Basic Res Lab, NIH, Bethesda, MD 20892 USA
[3] McGill Univ, Jewish Gen Hosp, McGill AIDS Ctr, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Lady Davis Inst Med Res, Montreal, PQ H3T 1E2, Canada
[5] McGill Univ, Dept Med, Montreal, PQ H3T 1E2, Canada
[6] McGill Univ, Dept Immunol, Montreal, PQ H3T 1E2, Canada
[7] McGill Univ, Dept Microbiol, Montreal, PQ H3T 1E2, Canada
关键词
D O I
10.1128/JVI.74.19.8938-8945.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The vif gene of human immunodeficiency virus type 1 (HIV-1) is essential for viral replication, although the functional target of Vif remains elusive. HIV-1 vif mutant virions derived from nonpermissive H9 cells displayed no significant differences in the amount, ratio, or integrity of their protein composition relative to an isogenic wild-type virion. The amounts of the virion-associated viral genomic RNA and tRNA(3)(Lys) were additionally present at normal levels in vif mutant virions. We demonstrate that Vif associates with RNA. in vitro as well as with viral genomic RNA in virus-infected cells. A functionally conserved lentivirus Vif motif was found in the double-stranded RNA binding domain of Xenopus laevis, Xlrbpa. The natural intravirion reverse transcriptase products were markedly reduced in vif mutant virions. Moreover, purified vif mutant genomic RNA-primer tRNA complexes displayed severe defects in the initiation of reverse transcription with recombinant reverse transcriptase. These data point to a novel role for Vif in the regulation of efficient reverse transcription through modulation of the virion nucleic acid components.
引用
收藏
页码:8938 / 8945
页数:8
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