1. Academic Validation
  2. FACT relieves DSIF/NELF-mediated inhibition of transcriptional elongation and reveals functional differences between P-TEFb and TFIIH

FACT relieves DSIF/NELF-mediated inhibition of transcriptional elongation and reveals functional differences between P-TEFb and TFIIH

  • Mol Cell. 2000 Jun;5(6):1067-72. doi: 10.1016/s1097-2765(00)80272-5.
T Wada 1 G Orphanides J Hasegawa D K Kim D Shima Y Yamaguchi A Fukuda K Hisatake S Oh D Reinberg H Handa
Affiliations

Affiliation

  • 1 Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama, Japan.
Abstract

We report that the chromatin-specific transcription elongation factor FACT functions in conjunction with the RNA polymerase II CTD kinase P-TEFb to alleviate transcription inhibition by DSIF (DRB sensitivity-inducing factor) and NELF (negative elongation factor). We find that the kinase activity of TFIIH is dispensable for this activity, demonstrating that TFIIH-mediated CTD phosphorylation is not involved in the regulation of FACT and DSIF/NELF activities. Thus, we propose a novel transcriptional regulatory network in which DSIF/NELF inhibition of transcription is prevented by P-TEFb in cooperation with FACT. This study uncovers a novel role for FACT in the regulation of transcription on naked DNA that is independent of its activities on chromatin templates. In addition, this study reveals functional differences between P-TEFb and TFIIH in the regulation of transcription.

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