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TAR RNA decoys inhibit Tat-activated HIV-1 transcription after preinitiation complex formation
被引:27
作者:
Bohjanen, PR
Liu, Y
GarciaBlanco, MA
机构:
[1] DUKE UNIV,MED CTR,DEPT PHARMACOL & CANC BIOL,LEVINE SCI RES CTR,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT MED,LEVINE SCI RES CTR,DIV INFECT DIS,DURHAM,NC 27710
[3] DUKE UNIV,MED CTR,DEPT MICROBIOL,LEVINE SCI RES CTR,DURHAM,NC 27710
基金:
美国国家卫生研究院;
关键词:
D O I:
10.1093/nar/25.22.4481
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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-I transcription after preinitiation complex formation, perhaps by interacting with components of transcription complexes.
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页码:4481 / 4486
页数:6
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