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      Role of the HIV-1 positive elongation factor P-TEFb and inhibitors thereof.

      Mini Reviews in Medicinal Chemistry
      Flavonoids, chemistry, pharmacology, HIV Infections, drug therapy, metabolism, virology, HIV-1, drug effects, physiology, Humans, Models, Biological, Piperidines, Positive Transcriptional Elongation Factor B, antagonists & inhibitors, Protein Kinase Inhibitors, Purines, RNA, Small Nuclear, Transcription, Genetic

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          Abstract

          Transcription is considered to be a crucial step in the replication cycle of HIV-1. Tat regulates an early step of transcription elongation. The positive elongation factor P-TEFb, a heterodimer containing a catalytic subunit (CDK9) and unique regulatory cyclins (CycT1), is required for HIV-1 Tat transcriptional activation. This is a potential target for new HIV-1 transcription inhibitors. Without P-TEFb, transactivation is restrained and only short transcripts are generated. All the P-TEFb inhibitors can suppress the HIV-1 transactivation process by inhibition of CycT1, CDK9 or their interaction. Several low-molecular-weight compounds such as flavopiridol, roscovitine and the human small nuclear RNA 7SK which have been showed to possess potent anti-HIV activity by interfering with P-TEFb functions are reviewed in this article.

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