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2000
Volume 9, Issue 3
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

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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/content/journals/mrmc/10.2174/138955709787583014
2009-03-01
2025-09-19
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  • Article Type:
    Research Article
Keyword(s): HIV-1; P-TEFb; TAR; Tat; transcription inhibitor
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