
pmid: 2460924
The human immunodeficiency virus type 1 (HIV-1) shows extensive genetic variation and undergoes rapid evolution. The fidelity of purified HIV-1 reverse transcriptase was measured during DNA polymerization in vitro by means of three different assays. Reverse transcriptase from HIV-1 introduced base-substitution errors in DNA from the bacteriophage φX174 amber 3 at estimated frequencies of 1/2000 to 1/4000. Analyses of misincorporation rates opposite a single template adenine residue showed that HIV-1 reverse transcriptase catalyzed nucleotide mismatches with a specificity of A:C >> A:G > A:A. The high error rate of HIV-1 reverse transcriptase in vitro translates to approximately five to ten errors per HIV-1 genome per round of replication in vivo. This high error rate suggests that misincorporation by HIV-1 reverse transcriptase is, at least in part, responsible for the hypermutability of the AIDS virus. The specificity of misincorporation may provide a basis for the systematic construction of antiviral nucleosides.
Avian Myeloblastosis Virus, Nucleotides, HIV, RNA-Directed DNA Polymerase, DNA, DNA Polymerase II, Kinetics, DNA, Viral, Mutation, Electrophoresis, Polyacrylamide Gel, Moloney murine leukemia virus, Bacteriophage phi X 174
Avian Myeloblastosis Virus, Nucleotides, HIV, RNA-Directed DNA Polymerase, DNA, DNA Polymerase II, Kinetics, DNA, Viral, Mutation, Electrophoresis, Polyacrylamide Gel, Moloney murine leukemia virus, Bacteriophage phi X 174
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