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Journal of Virology, September 1999, p. 7132-7137, Vol. 73, No. 9
Departments of Microbiology & Immunology and
Medicine, University of California
Received 21 January 1999/Accepted 3 May 1999
The human immunodeficiency virus type 1 (HIV-1) Vpr protein induces
cell cycle arrest at the border of G2 and M similar to the
arrest caused by agents which damage DNA. We determined whether the
presence of Vpr would affect the ability of cells to repair DNA. We
developed a shuttle vector system to analyze the effect of Vpr upon the
repair of UV-damaged DNA. Our results demonstrated that the presence of
Vpr decreased the rate of deletions in this system. Of note, cells
arrested in G2 by other genotoxic agents also increased the
frequency of DNA repair of UV-damaged shuttle vectors. We did not
observe any direct effect of Vpr upon the rate of double-strand break
repair and/or nucleotide excision repair of genomic DNA in cells. Our
results suggest a role for HIV-1 Vpr in altering the frequency of DNA
repair, a property which may have importance for HIV-1 replication and pathogenesis.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The Presence of Human Immunodeficiency Virus Type 1 Vpr Correlates with a Decrease in the Frequency of Mutations in a
Plasmid Shuttle Vector
Los Angeles School of Medicine, Los
Angeles, California 90095-1678,1 and
International Diabetes Institute, Caulfield, Victoria 3162, Australia2
*
Corresponding author. Mailing address: Departments of
Microbiology & Immunology and Medicine, UCLA School of Medicine, Los Angeles, CA 90095-1678. Phone: (310) 825-4793. Fax: (310) 794-7682. E-mail: rtaweesu{at}ucla.edu.
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