Literature DB >> 10575014

c-Ski acts as a transcriptional co-repressor in transforming growth factor-beta signaling through interaction with smads.

S Akiyoshi1, H Inoue, J Hanai, K Kusanagi, N Nemoto, K Miyazono, M Kawabata.   

Abstract

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 Smad3 with a transcriptional co-activator, p300, and in turn recruits HDAC. c-Ski is thus a transcriptional co-repressor that links Smads to HDAC in TGF-beta signaling.

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Year:  1999        PMID: 10575014     DOI: 10.1074/jbc.274.49.35269

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  101 in total

1.  Ski represses bone morphogenic protein signaling in Xenopus and mammalian cells.

Authors:  W Wang; F V Mariani; R M Harland; K Luo
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

Review 2.  Transcriptional control by the TGF-beta/Smad signaling system.

Authors:  J Massagué; D Wotton
Journal:  EMBO J       Date:  2000-04-17       Impact factor: 11.598

3.  Smad3 recruits the anaphase-promoting complex for ubiquitination and degradation of SnoN.

Authors:  S L Stroschein; S Bonni; J L Wrana; K Luo
Journal:  Genes Dev       Date:  2001-11-01       Impact factor: 11.361

4.  Tissue- and stage-specific modulation of Wingless signaling by the segment polarity gene lines.

Authors:  V Hatini; P Bokor; R Goto-Mandeville; S DiNardo
Journal:  Genes Dev       Date:  2000-06-01       Impact factor: 11.361

5.  Ligand-dependent degradation of Smad3 by a ubiquitin ligase complex of ROC1 and associated proteins.

Authors:  M Fukuchi; T Imamura; T Chiba; T Ebisawa; M Kawabata; K Tanaka; K Miyazono
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

6.  Transposon mutagenesis with coat color genotyping identifies an essential role for Skor2 in sonic hedgehog signaling and cerebellum development.

Authors:  Baiping Wang; Wilbur Harrison; Paul A Overbeek; Hui Zheng
Journal:  Development       Date:  2011-10       Impact factor: 6.868

7.  Smad6 recruits transcription corepressor CtBP to repress bone morphogenetic protein-induced transcription.

Authors:  Xia Lin; Yao-Yun Liang; Baohua Sun; Min Liang; Yujiang Shi; F Charles Brunicardi; Yang Shi; Xin-Hua Feng
Journal:  Mol Cell Biol       Date:  2003-12       Impact factor: 4.272

8.  Content and localization of myostatin in mouse skeletal muscles during aging, mechanical unloading and reloading.

Authors:  S Kawada; C Tachi; N Ishii
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

9.  Intercellular variation in signaling through the TGF-β pathway and its relation to cell density and cell cycle phase.

Authors:  Agata Zieba; Katerina Pardali; Ola Söderberg; Lena Lindbom; Erik Nyström; Aristidis Moustakas; Carl-Henrik Heldin; Ulf Landegren
Journal:  Mol Cell Proteomics       Date:  2012-03-22       Impact factor: 5.911

10.  Zinc finger protein 451 is a novel Smad corepressor in transforming growth factor-β signaling.

Authors:  Yili Feng; Hongxing Wu; Yongxian Xu; Zhengmao Zhang; Ting Liu; Xia Lin; Xin-Hua Feng
Journal:  J Biol Chem       Date:  2013-12-09       Impact factor: 5.157

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