THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 TAT ANTAGONIST, RO-5-3335, PREDOMINANTLY INHIBITS TRANSCRIPTION INITIATION FROM THE VIRAL PROMOTER

被引:29
作者
CUPELLI, LA [1 ]
HSU, MC [1 ]
机构
[1] HOFFMANN LA ROCHE INC,ROCHE RES CTR,NUTLEY,NJ 07110
关键词
D O I
10.1128/JVI.69.4.2640-2643.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tat, the transcriptional transactivator protein of the human immunodeficiency virus type 1 (HIV-1), is required for viral replication in vitro. The Tat antagonist, Ro 5-3335, and its analog, Ro 24-7429, have been shown to inhibit replication of HIV-1 and to reduce steady-state viral RNA in infected cells (M.-C. Hsu et al., Science 254:1799-1802, 1991, and M.-C. Hsu et al., Proc. Natl. scad. Sci. USA 90:6395-6399, 1993). Analysis of HIV-1 long terminal repeat-driven reporter gene transcription in a recombinant adenovirus by nuclear run-on assay indicated that the drug predominantly inhibits Tat-dependent initiation and also exerts a measurable effect on elongation. This result may imply a common mechanism for Tat-mediated transcription initiation and elongation.
引用
收藏
页码:2640 / 2643
页数:4
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