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. 1995 Sep;69(9):5883-9.
doi: 10.1128/JVI.69.9.5883-5889.1995.

Fate of the human immunodeficiency virus type 1 provirus in infected cells: a role for vpr

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Fate of the human immunodeficiency virus type 1 provirus in infected cells: a role for vpr

V Planelles et al. J Virol. 1995 Sep.

Abstract

We investigated the fate of human immunodeficiency virus type 1 (HIV-1) viral DNA in infected peripheral blood lymphocytes and immortalized T-cell lines by using a replication-defective HIV-1. We observed that integrated HIV-1 DNA and viral gene expression decrease over time. A frameshift mutation in vpr resulted in maintenance of the HIV-1 provirus and stable persistence of viral expression. Transfection of vpr together with the neomycin resistance gene in the absence of other viral genes decreased the formation of geneticin-resistant colonies, indicating either a cytotoxic or a cytostatic effect upon cells. Therefore, maintenance of HIV-1 infection within an infected proliferating population is due to two competing processes, the rate of viral spread and the degree of cell growth inhibition and/or death induced by Vpr.

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References

    1. Science. 1976 Jun 11;192(4244):1075-80 - PubMed
    1. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7311-5 - PubMed
    1. Mol Cell Biol. 1987 Feb;7(2):725-37 - PubMed
    1. Science. 1987 May 15;236(4803):819-22 - PubMed
    1. Gene. 1987;52(1):71-82 - PubMed

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