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

被引:137
作者
Nagano, Yoshiko
Mavrakis, Konstantinos J.
Lee, Kian Leong
Fujii, Tomoko
Koinuma, Daizo
Sase, Hitoshi
Yuki, Keiko
Isogaya, Kazunobu
Saitoh, Masao
Imamura, Takeshi
Episkopou, Vasso
Miyazono, Kohei [1 ]
Miyazawa, Keiji
机构
[1] Univ Tokyo, Grad Sch Med, Dept Mol Pathol, Tokyo 1130033, Japan
[2] Imperial Coll Sch Med, Hammersmith Hosp, Mammalian Neurogenesis Med Res Council, London W12 0NN, England
[3] Japanese Fdn Canc Res, Inst Canc, Dept Biochem, Tokyo 1358550, Japan
基金
英国医学研究理事会;
关键词
D O I
10.1074/jbc.M701294200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:20492 / 20501
页数:10
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