Nucleic Acids Research, Vol 25, Issue 22 4481-4486, Copyright © 1997 by Oxford University Press
PR Bohjanen, Y Liu and MA Garcia-Blanco
The ability of the HIV-1 Tat protein to trans -activate HIV-1 transcription
in vitro is specifically inhibited by a circular TAR RNA decoy. This
inhibition is not overcome by adding an excess of Tat to the reaction but
is partially overcome by adding Tat in combination with nuclear extract,
suggesting that TAR RNA might function by interacting with a complex
containing Tat and cellular factor(s). A cell-free transcription system
involving immobilized DNA templates was used to further define the
factor(s) that interact with TAR RNA. Preinitiation complexes formed in the
presence or absence of Tat were purified on immobilized templates
containing the HIV-1 promoter. After washing, nucleotides and radiolabelled
UTP were added and transcription was measured. The presence of Tat during
preinitiation complex formation resulted in an increase in the level of
full-length HIV-1 transcripts. This Tat-activated increase in HIV-1
transcription was not inhibited by circular TAR decoys added during
preinitiation complex formation but was inhibited by circular TAR decoys
subsequently added during the transcription reaction. These results suggest
that TAR decoys inhibit Tat-activated HIV-1 transcription after
preinitiation complex formation, perhaps by interacting with components of
transcription complexes.
ARTICLES
TAR RNA decoys inhibit tat-activated HIV-1 transcription after preinitiation complex formation
Department of Pharmacology and Cancer Biology, Levine Science Research Center, Duke University Medical Center, Durham, NC 27710, USA.
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