Myc recruits P-TEFb to mediate the final step in the transcriptional activation of the cad promoter

J Biol Chem. 2002 Oct 18;277(42):40156-62. doi: 10.1074/jbc.M207441200. Epub 2002 Aug 9.

Abstract

The c-Myc protein is up-regulated in many different types of cancer, suggesting that a detailed understanding of Myc function is an important goal. Our previous studies have focused on determining the mechanism by which Myc activates transcription using the target gene cad as an experimental model. Previously, we found that Myc activates cad transcription at a post-RNA polymerase II recruitment step and that the Myc transactivation domain interacts with a number of cdk-cyclin complexes. We now extend these studies to determine the role of these cyclin-cdk complexes in Myc-mediated transactivation. We have found that cyclin T1 binding to Myc localizes to the highly conserved Myc Box I, whereas cdk8 binding localizes to the amino-terminal 41 amino acids of the Myc transactivation domain. We showed that recruitment of cdk8 is sufficient for activation of a synthetic promoter construct. In contrast, the ability of Myc to activate transcription of the cad promoter correlates with binding of cyclin T1. Furthermore, recruitment of cyclin T1 to the cad promoter via a Gal4 fusion protein or through protein-protein interaction with the HIV-1 Tat protein can also activate cad transcription. These results suggest that Myc activates transcription by stimulating elongation and that P-TEFb is a key mediator of this process.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3T3 Cells
  • Animals
  • Glutathione Transferase / metabolism
  • HeLa Cells
  • Humans
  • Mice
  • Plasmids / metabolism
  • Positive Transcriptional Elongation Factor B
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Structure, Tertiary
  • Proto-Oncogene Proteins c-myc / metabolism*
  • Proto-Oncogene Proteins c-myc / physiology*
  • Recombinant Fusion Proteins / metabolism
  • Transcription, Genetic
  • Transcriptional Activation
  • Transfection

Substances

  • Proto-Oncogene Proteins c-myc
  • Recombinant Fusion Proteins
  • Glutathione Transferase
  • Positive Transcriptional Elongation Factor B
  • Protein Serine-Threonine Kinases