A Drug Resistance Mutation in the Inhibitor Binding Pocket of Human Immunodeficiency Virus Type 1 Reverse Transcriptase Impairs DNA Synthesis and RNA Degradation

• Published in: Biochemistry (Easton) Vol. 35; no. 30; pp. 9737 - 9745
• Main Authors: Fan, Naisheng, Rank, Kenneth B, Slade, David E, Poppe, Susan M, Evans, David B, Kopta, Laurice A, Olmsted, Robert A, Thomas, Richard C, Tarpley, W. Gary, Sharma, Satish K
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 30-07-1996
• Subjects: Base Sequence; Cloning, Molecular; DNA Primers; DNA Replication; DNA, Viral - biosynthesis; Drug Resistance, Microbial; HIV Reverse Transcriptase; HIV-1 - enzymology; HIV-1 - genetics; HIV-1 - metabolism; human immunodeficiency virus 1; Humans; Kinetics; Macromolecular Substances; Molecular Sequence Data; Mutagenesis, Site-Directed; Point Mutation; Polymerase Chain Reaction; Recombinant Proteins - metabolism; RNA, Viral - metabolism; RNA-Directed DNA Polymerase - genetics; RNA-Directed DNA Polymerase - metabolism; Sequence Tagged Sites; Substrate Specificity
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi9600308

Selection of the IIIB strain of human immunodeficiency virus type (HIV-1) resistant to the (alkylamino)piperidine-bis(heteroaryl)piperazine (AAP-BHAP) U-104489 results in substitution of a glycine to glutamate at residue 190 (G190E) of reverse transcriptase (RT). The AAP-BHAP resistant HIV-1 displays reduced in vitro replication capacity [Olmsted, R. A., et al. (1966) J. Virol. 70, 3698−3705]. We report here that the G190E mutation in recombinant heterodimeric HIV-1 RT, compared to the wild-type RT (G190) or a G190A control mutant, results in a 40% and 80% reduction in the polymerase and RNase H specific enzymatic activities, respectively. A primer-extension assay that allowed determination of DNA elongation by the G190E mutant RT on a heteropolymeric HIV-1 gag-based RNA template showed an overall decrease in DNA polymerization. The size distribution of products generated by G190E RT-associated RNase H digestion of RNA from [35S]poly(rA)·poly(dT) was markedly distinct from that of the G190A RT and was consistent with the observed reduction in RT-associated RNase H activity of the G190E RT. When challenged with unlabeled substrates, the G190E RT was relatively nonprocessive with respect to DNA synthesis and RNA degradation. It is concluded that the deleterious effect of the G190E resistance mutation on both of these RT functions is most likely involved in the observed retarded replication capacity of the AAP-BHAP- (U-104489-) resistant HIV-1.