c-Ski acts as a transcriptional co-repressor in transforming growth factor-β signaling through interaction with Smads

被引:325
作者
Akiyoshi, S
Inoue, H
Hanai, J
Kusanagi, K
Nemoto, N
Miyazono, K
Kawabata, M
机构
[1] Japanese Fdn Canc Res, Inst Canc, Dept Biochem, Toshima Ku, Tokyo 1708455, Japan
[2] Japan Soc Promot Sci, Res Future Program, Dept Biochem, Toshima Ku, Tokyo 1708455, Japan
[3] Toyama Med & Pharmaceut Univ, Fac Pharmaceut Sci, Dept Toxicol, Toyama 9300194, Japan
关键词
D O I
10.1074/jbc.274.49.35269
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
Smads are intracellular signaling mediators of the transforming growth factor-beta (TGF-beta) superfamily that regulates a wide variety of biological processes. Among them, Smads 2 and 3 are activated specifically by TGF-beta. We identified c-Ski as a Smad2 interacting protein. c-Ski is the cellular homologue of the v-ski oncogene product and has been shown to repress transcription by recruiting histone deacetylase (HDAC). Smad2/3 interacts with c-Ski through its C-terminal MH2 domain in a TGF-beta-dependent manner. c-Ski contains two distinct Smad-binding sites with different binding properties. c-Ski strongly inhibits transactivation of various reporter genes by TGF-beta. c-Ski is incorporated in the Smad DNA binding complex, interferes with the interaction of Smads with a transcriptional co-activator, p300, and in turn recruits HDAC. c-Ski is thus a transcriptional corepressor that links Smads to HDAC in TGF-beta signaling.
引用
收藏
页码:35269 / 35277
页数:9
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