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Journal of Virology, June 1999, p. 5191-5195, Vol. 73, No. 6
Department of Microbiology and
Immunology,1 Department of Biological
Chemistry,3 and Department of
Internal Medicine,4 University of Michigan, Ann
Arbor, Michigan 48109, and Department of Molecular Biology,
Beckman Research Institute of the City of Hope, Duarte, California
910102
Received 2 November 1998/Accepted 28 February 1999
Tat activation-response region (TAR) decoys have been developed for
use in gene therapy for people infected with human immunodeficiency virus type 1 (HIV-1). When a TAR RNA decoy is overexpressed, it will
bind Tat, thus leaving less of this crucial protein to bind to and
activate the natural transcriptional promoter of HIV-1. Previous TAR
decoy constructs have used HIV-1 TAR. However, recent epidemiological
and biological data began to suggest that the TAR region from the human
immunodeficiency virus type 2 (HIV-2) may suppress HIV-1 transcription
and hence replication. We created a vector which overexpresses TAR-2
under the control of the human U6 small nuclear RNA gene promoter and
here show that the U6-TAR-2 decoy construct potently inhibits both
HIV-2 and HIV-1 gene expression. Further, this decoy construct is able
to markedly suppress HIV-1 replication. Thus, we have directly proven
that TAR-2 can suppress HIV-1 replication and suggest that the HIV-2
TAR decoy may prove useful for combating HIV-1 infection.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Potent Inhibition of Human Immunodeficiency Virus
Type 1 (HIV-1) Gene Expression and Virus Production by an HIV-2 Tat
Activation-Response RNA Decoy
*
Corresponding author. Mailing address: 5220 MSRB III,
University of Michigan Medical Center, 1150 W. Medical Center Dr., Ann Arbor, MI 48109-0640. Phone: (734) 647-1786. Fax: (734) 764-0101. E-mail: DMARKOV{at}UMICH.EDU.
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