c-Jun associates with the oncoprotein Ski and suppresses Smad2 transcriptional activity

J Biol Chem. 2002 Aug 9;277(32):29094-100. doi: 10.1074/jbc.M202831200. Epub 2002 May 28.

Abstract

The Smad proteins are key intracellular effectors of transforming growth factor-beta (TGF-beta) cytokines. The ability of Smads to modulate transcription results from a functional cooperativity with the coactivators p300/cAMP-response element-binding protein-binding protein (CBP), or the corepressors TGIF and Ski. The c-Jun N-terminal kinase (JNK) pathway, another downstream target activated by TGF-beta receptors, has also been suggested to inhibit TGF-beta signaling through interaction of c-Jun with Smad2 and Smad3. Here we show that c-Jun directly interacts with Ski to enhance the association of Ski with Smad2 in the basal state. Interestingly, TGF-beta signaling induces dissociation of c-Jun from Ski, thereby relieving active repression by c-Jun. Moreover, activation of JNK pathway suppressed the ability of TGF-beta to induce dissociation of c-Jun from ski. Thus, the formation of a c-Jun/Ski complex maintains the repressed state of Smad2-responsive genes in the absence of ligand and participates in negative feedback regulation of TGF-beta signaling by the JNK cascade.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Cell Line
  • DNA-Binding Proteins / metabolism*
  • Enzyme Activation
  • Glutathione Transferase / metabolism
  • Humans
  • Immunoblotting
  • Mice
  • Precipitin Tests
  • Protein Binding
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-jun / metabolism*
  • Signal Transduction
  • Smad2 Protein
  • Trans-Activators / metabolism*
  • Transcription Factor AP-1 / metabolism
  • Transcription, Genetic*
  • Transfection
  • Transforming Growth Factor beta / metabolism

Substances

  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-jun
  • SMAD2 protein, human
  • Ski protein, mouse
  • Smad2 Protein
  • Smad2 protein, mouse
  • Trans-Activators
  • Transcription Factor AP-1
  • Transforming Growth Factor beta
  • SKI protein, human
  • Glutathione Transferase