TY - JOUR
T1 - TAR RNA decoys inhibit Tat-activated HIV-1 transcription after preinitiation complex formation
AU - Bohjanen, Paul R.
AU - Liu, Yi
AU - Garcia-Blanco, Mariano A.
N1 - Funding Information:
We thank Carlos Suñé for his critical review of this manuscript. The Keck Foundation is acknowledged for their generous support of the Levine Science Research Center at Duke University, where this work was performed. P.R.B. was supported by a Howard Hughes Medical Institute Postdoctoral Fellowship for Physicians. Y.L. was supported by a grant from the NIH to M.A.G.-B. This work was also supported by a grant from the VA to M.A.G.-B.
PY - 1997
Y1 - 1997
N2 - 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.
AB - 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.
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U2 - 10.1093/nar/25.22.4481
DO - 10.1093/nar/25.22.4481
M3 - Article
C2 - 9358155
AN - SCOPUS:0030728119
SN - 0305-1048
VL - 25
SP - 4481
EP - 4486
JO - Nucleic acids research
JF - Nucleic acids research
IS - 22
ER -