A small circular TAR RNA decoy specifically inhibits Tat-activated HIV-1 transcription

Paul R. Bohjanen, Richard A. Colvin, M. Puttaraju, Michael D. Been, Mariano A. Garcia-Blanco

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Linear TAR RNA has previously been used as a decoy to inhibit HIV-1 transcription in vitro and HIV-1 replication in vivo, A 48 nucleotide circular RNA containing the stem, bulge and loop of the HIV-1 TAR element was synthesized using the self-splicing activity of a group I permuted intron-exon and was tested for its ability to function as a TAR decoy in vitro. This small circular TAR molecule was exceptionally stable in HeLa nuclear extracts, whereas a similar linear TAR molecule was rapidly degraded. The TAR circle bound specifically to Tfr38, a peptide containing the TAR-binding region of Tat. The ability of Tat to trans-activate transcription from the HIV-1 promoter in vitro was efficiently inhibited by circular TAR RNA but not by TAR circles that contained either bulge or loop mutations. TAR circles did not inhibit transactivation exclusively by binding to Tat since this inhibition was not reversed by adding excess Tat to the transcription reaction. Together, these data suggest that TAR circles act as decoys that inhibit transactivation by binding to Tat and at least one cellular factor. These data also demonstrate the utility of small circular RNA molecules as tools for biochemical studies.

Original languageEnglish (US)
Pages (from-to)3733-3738
Number of pages6
JournalNucleic acids research
Issue number19
StatePublished - 1996

Bibliographical note

Funding Information:
We thank K. Weeks and D. Crothers for the kind gift of the Tfr38 peptide. We also thank C. Suñé, Z. Pasman and M. Velaz-Faircloth for their critical reading of this manuscript. The Keck Foundation is acknowledged for their generous support of the Levine Science Research Center at Duke University, where much of this work was performed. P.R.B. was supported by a Howard Hughes Medical Institute Postdoctoral Fellowship for Physicians. R.A.C. was a predoctoral fellow in the MSTP at Duke University. This work was supported by grants from the VA to M.A.G.-B. and from the NIH to M.D.B.


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