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Journal of Virology, August 2000, p. 7039-7047, Vol. 74, No. 15
Department of Molecular Virology, Immunology,
and Medical Genetics, Center for Retrovirus Research, and Comprehensive
Cancer Center, Ohio State University Medical Center, Columbus, Ohio
43210,1 and INSERM U529, ICGM,
Université Paris V, Paris, France2
Received 8 March 2000/Accepted 1 May 2000
The Vpr protein of human immunodeficiency virus type 1 (HIV-1)
influences the in vivo mutation rate of the virus. Since Vpr interacts
with a cellular protein implicated in the DNA repair process, uracil
DNA glycosylase (UNG), we have explored the contribution of this
interaction to the mutation rate of HIV-1. Single-amino-acid variants
of Vpr were characterized for their differential UNG-binding properties
and used to trans complement vpr null mutant
HIV-1. A striking correlation was established between the abilities of Vpr to interact with UNG and to influence the HIV-1 mutation rate. We
demonstrate that Vpr incorporation into virus particles is required to
influence the in vivo mutation rate and to mediate virion packaging of
the nuclear form of UNG. The recruitment of UNG into virions indicates
a mechanism for how Vpr can influence reverse transcription accuracy.
Our data suggest that distinct mechanisms evolved in primate and
nonprimate lentiviruses to reconcile uracil misincorporation into
lentiviral DNA.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
The Interaction of Vpr with Uracil DNA Glycosylase Modulates the
Human Immunodeficiency Virus Type 1 In Vivo Mutation Rate

*
Corresponding author. Mailing address: Department of
Molecular Virology, Immunology, and Medical Genetics, 2078 Graves Hall, 333 West 10th Ave., Columbus, OH 43210. Phone: (614) 292-5525. Fax:
(614) 292-9805. E-mail: mansky.3{at}osu.edu.
Present address: Hybrigenics, Inc., Paris, France.
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