Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1997 Nov 15;25(22):4481-6.
doi: 10.1093/nar/25.22.4481.

TAR RNA decoys inhibit tat-activated HIV-1 transcription after preinitiation complex formation

Affiliations

TAR RNA decoys inhibit tat-activated HIV-1 transcription after preinitiation complex formation

P R Bohjanen et al. Nucleic Acids Res. .

Abstract

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.

PubMed Disclaimer

References

    1. J Biol Chem. 1982 Dec 10;257(23):14419-27 - PubMed
    1. J Virol. 1995 Oct;69(10):6572-6 - PubMed
    1. Science. 1985 Jul 5;229(4708):69-73 - PubMed
    1. Cell. 1986 Sep 26;46(7):973-82 - PubMed
    1. Nature. 1987 Dec 3-9;330(6147):489-93 - PubMed

Publication types

Substances