Literature DB >> 8906991

Forward mutation rate of human immunodeficiency virus type 1 in a T lymphoid cell line.

L M Mansky1.   

Abstract

An in vivo assay was previously developed for detecting forward mutations in human immunodeficiency virus type 1 (HIV-1) in a single cycle of replication. This system uses the lacZalpha peptide gene as a reporter for mutations, and allows for the rates and types of mutations that occur to be determined. The forward mutation rate for HIV-1 in HeLa cells was found to be 3 x 10(-5) mutations per target base pair per cycle. To test whether the mutation rate was influenced by cell type, the mutation rate of HIV-1 in CEM-A cells, a T lymphoid cell line, was determined. The mutation rate of HIV-1 reverse transcription in CEM-A cells was found to be 4 x 10(-5) mutations per target base pair per cycle. The number and types of mutations observed were similar to that in HeLa cells. Specifically, base substitution mutations predominated, and G-to-A transition mutations were the most common base substitution. G-to-A hypermutants were also characterized. The difference in HIV-1 mutation rate between HeLa and CEM-A cells was not significant, indicating that the accuracy of HIV-1 reverse transcription is comparable in both the HeLa and CEM-A cell lines.

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Year:  1996        PMID: 8906991     DOI: 10.1089/aid.1996.12.307

Source DB:  PubMed          Journal:  AIDS Res Hum Retroviruses        ISSN: 0889-2229            Impact factor:   2.205


  54 in total

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5.  Nature, position, and frequency of mutations made in a single cycle of HIV-1 replication.

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7.  Mutations in HIV-1 reverse transcriptase affect the errors made in a single cycle of viral replication.

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8.  Fitness costs and diversity of the cytotoxic T lymphocyte (CTL) response determine the rate of CTL escape during acute and chronic phases of HIV infection.

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9.  Influence of random genetic drift on human immunodeficiency virus type 1 env evolution during chronic infection.

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10.  Lack of mutational hot spots during decitabine-mediated HIV-1 mutagenesis.

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