Arkadia induces degradation of SnoN and c-Ski to enhance transforming growth factor-beta signaling

J Biol Chem. 2007 Jul 13;282(28):20492-501. doi: 10.1074/jbc.M701294200. Epub 2007 May 16.

Abstract

Transforming growth factor-beta (TGF-beta) signaling is controlled by a variety of regulators that target either signaling receptors or activated Smad complexes. Among the negative regulators, Smad7 antagonizes TGF-beta signaling mainly through targeting the signaling receptors, whereas SnoN and c-Ski repress signaling at the transcriptional level through inactivation of Smad complexes. We previously found that Arkadia is a positive regulator of TGF-beta signaling that induces ubiquitin-dependent degradation of Smad7 through its C-terminal RING domain. We report here that Arkadia induces degradation of SnoN and c-Ski in addition to Smad7. Arkadia interacts with SnoN and c-Ski in their free forms as well as in the forms bound to Smad proteins, and constitutively down-regulates levels of their expression. Arkadia thus appears to effectively enhance TGF-beta signaling through simultaneous down-regulation of two distinct types of negative regulators, Smad7 and SnoN/c-Ski, and may play an important role in determining the intensity of TGF-beta family signaling in target cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Chlorocebus aethiops
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation / drug effects
  • Down-Regulation / physiology
  • HeLa Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Mice
  • Protein Binding / drug effects
  • Protein Binding / physiology
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Smad7 Protein / genetics
  • Smad7 Protein / metabolism
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / physiology
  • Transforming Growth Factor beta / metabolism*
  • Transforming Growth Factor beta / pharmacology
  • Ubiquitin / genetics
  • Ubiquitin / metabolism*
  • Ubiquitin-Protein Ligases

Substances

  • DNA-Binding Proteins
  • Intracellular Signaling Peptides and Proteins
  • Proto-Oncogene Proteins
  • SKIL protein, human
  • SMAD7 protein, human
  • Smad7 Protein
  • Smad7 protein, mouse
  • Transforming Growth Factor beta
  • Ubiquitin
  • SKI protein, human
  • Rnf111 protein, mouse
  • Ubiquitin-Protein Ligases