Arkadia Induces Degradation of SnoN and c-Ski to Enhance Transforming Growth Factor-β Signaling
pmid: 17510063
Arkadia Induces Degradation of SnoN and c-Ski to Enhance Transforming Growth Factor-β Signaling
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.
- Imperial College London United Kingdom
- National University of Singapore Singapore
- National University of Singapore Libraries Singapore
- MRC London Institute of Medical Sciences United Kingdom
- Japanese Foundation For Cancer Research Japan
Transcription, Genetic, Ubiquitin, Ubiquitin-Protein Ligases, Intracellular Signaling Peptides and Proteins, Down-Regulation, Smad7 Protein, DNA-Binding Proteins, Mice, Transforming Growth Factor beta, Proto-Oncogene Proteins, COS Cells, Chlorocebus aethiops, Animals, Humans, HeLa Cells, Protein Binding, Signal Transduction
Transcription, Genetic, Ubiquitin, Ubiquitin-Protein Ligases, Intracellular Signaling Peptides and Proteins, Down-Regulation, Smad7 Protein, DNA-Binding Proteins, Mice, Transforming Growth Factor beta, Proto-Oncogene Proteins, COS Cells, Chlorocebus aethiops, Animals, Humans, HeLa Cells, Protein Binding, Signal Transduction
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