HIV-1 reverse transcription:: A brief overview focused on structure-function relationships among molecules involved in initiation of the reaction

被引:82
作者
Götte, M [1 ]
Li, XG [1 ]
Wainberg, MA [1 ]
机构
[1] Jewish Gen Hosp, Lady Davis Inst, McGill AIDS Ctr, Montreal, PQ H3T 1E2, Canada
基金
英国医学研究理事会;
关键词
HIV; reverse transcriptase; RNase H; nucleocapsid; initiation;
D O I
10.1006/abbi.1999.1209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An early step in the life cycle of the human immunodeficiency virus type 1 (HIV-1) is reverse transcription of viral RNA into proviral DNA, which can then be integrated into the host cell genome. Reverse transcription is a discontinuous process carried out by the viral encoded reverse transcriptase that displays DNA polymerase activities on RNA and DNA templates as well as an RNase H activity that degrades transcribed RNA. DNA synthesis is initiated by cellular tRNA(Lys3) that binds at its 3'-terminus to the complementary primer binding site of the genomic RNA. The initiation of reverse transcription is itself a complex reaction that requires tRNA placement onto viral RNA and the formation of a specific primer/template complex that is recognized by reverse transcriptase. After initiation takes place, the enzyme translocates from the initially bound RNA/RNA duplex into chimeric replication intermediates and finally accommodates newly synthesized DNA/RNA hybrids, This review focuses on structure-function relationships among these various molecules that are involved in the initiation of HIV-1 reverse transcription. (C) 1999 Academic Press.
引用
收藏
页码:199 / 210
页数:12
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