Literature DB >> 10049357

Ski is a component of the histone deacetylase complex required for transcriptional repression by Mad and thyroid hormone receptor.

T Nomura1, M M Khan, S C Kaul, H D Dong, R Wadhwa, C Colmenares, I Kohno, S Ishii.   

Abstract

The N-CoR/SMRT complex containing mSin3 and histone deacetylase (HDAC) mediates transcriptional repression by nuclear hormone receptors and Mad. The proteins encoded by the ski proto-oncogene family directly bind to N-CoR/SMRT and mSin3A, and forms a complex with HDAC. c-Ski and its related gene product Sno are required for transcriptional repression by Mad and thyroid hormone receptor (TRbeta). The oncogenic form, v-Ski, which lacks the mSin3A-binding domain, acts in a dominant-negative fashion, and abrogates transcriptional repression by Mad and TRbeta. In ski-deficient mouse embryos, the ornithine decarboxylase gene, whose expression is normally repressed by Mad-Max, is expressed ectopically. These results show that Ski is a component of the HDAC complex and that Ski is required for the transcriptional repression mediated by this complex. The involvement of c-Ski in the HDAC complex indicates that the function of the HDAC complex is important for oncogenesis.

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Year:  1999        PMID: 10049357      PMCID: PMC316468          DOI: 10.1101/gad.13.4.412

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  54 in total

1.  Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor.

Authors:  A J Hörlein; A M Näär; T Heinzel; J Torchia; B Gloss; R Kurokawa; A Ryan; Y Kamei; M Söderström; C K Glass
Journal:  Nature       Date:  1995-10-05       Impact factor: 49.962

2.  A transcriptional co-repressor that interacts with nuclear hormone receptors.

Authors:  J D Chen; R M Evans
Journal:  Nature       Date:  1995-10-05       Impact factor: 49.962

3.  The tau 4 activation domain of the thyroid hormone receptor is required for release of a putative corepressor(s) necessary for transcriptional silencing.

Authors:  A Baniahmad; X Leng; T P Burris; S Y Tsai; M J Tsai; B W O'Malley
Journal:  Mol Cell Biol       Date:  1995-01       Impact factor: 4.272

4.  A switch from Myc:Max to Mad:Max heterocomplexes accompanies monocyte/macrophage differentiation.

Authors:  D E Ayer; R N Eisenman
Journal:  Genes Dev       Date:  1993-11       Impact factor: 11.361

5.  Mad: a heterodimeric partner for Max that antagonizes Myc transcriptional activity.

Authors:  D E Ayer; L Kretzner; R N Eisenman
Journal:  Cell       Date:  1993-01-29       Impact factor: 41.582

6.  Mediation of c-Myc-induced apoptosis by p53.

Authors:  H Hermeking; D Eick
Journal:  Science       Date:  1994-09-30       Impact factor: 47.728

7.  Contrasting roles for Myc and Mad proteins in cellular growth and differentiation.

Authors:  L Chin; N Schreiber-Agus; I Pellicer; K Chen; H W Lee; M Dudast; C Cordon-Cardo; R A DePinho
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-29       Impact factor: 11.205

Review 8.  The retinoid signaling pathway: molecular and genetic analyses.

Authors:  P Chambon
Journal:  Semin Cell Biol       Date:  1994-04

Review 9.  Regulation of vertebrate muscle differentiation by thyroid hormone: the role of the myoD gene family.

Authors:  G E Muscat; M Downes; D H Dowhan
Journal:  Bioessays       Date:  1995-03       Impact factor: 4.345

Review 10.  The nuclear receptor superfamily: the second decade.

Authors:  D J Mangelsdorf; C Thummel; M Beato; P Herrlich; G Schütz; K Umesono; B Blumberg; P Kastner; M Mark; P Chambon; R M Evans
Journal:  Cell       Date:  1995-12-15       Impact factor: 41.582

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  95 in total

Review 1.  The Max network gone mad.

Authors:  T A Baudino; J L Cleveland
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

2.  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

3.  SKIP, a CBF1-associated protein, interacts with the ankyrin repeat domain of NotchIC To facilitate NotchIC function.

Authors:  S Zhou; M Fujimuro; J J Hsieh; L Chen; A Miyamoto; G Weinmaster; S D Hayward
Journal:  Mol Cell Biol       Date:  2000-04       Impact factor: 4.272

4.  A role for SKIP in EBNA2 activation of CBF1-repressed promoters.

Authors:  S Zhou; M Fujimuro; J J Hsieh; L Chen; S D Hayward
Journal:  J Virol       Date:  2000-02       Impact factor: 5.103

5.  Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation.

Authors:  T A Heanue; R Reshef; R J Davis; G Mardon; G Oliver; S Tomarev; A B Lassar; C J Tabin
Journal:  Genes Dev       Date:  1999-12-15       Impact factor: 11.361

6.  Functional interaction of STAT5 and nuclear receptor co-repressor SMRT: implications in negative regulation of STAT5-dependent transcription.

Authors:  H Nakajima; P K Brindle; M Handa; J N Ihle
Journal:  EMBO J       Date:  2001-12-03       Impact factor: 11.598

7.  Nuclear localization of CBF1 is regulated by interactions with the SMRT corepressor complex.

Authors:  S Zhou; S D Hayward
Journal:  Mol Cell Biol       Date:  2001-09       Impact factor: 4.272

8.  Ski interacts with the evolutionarily conserved SNW domain of Skip.

Authors:  T Prathapam; C Kühne; M Hayman; L Banks
Journal:  Nucleic Acids Res       Date:  2001-09-01       Impact factor: 16.971

9.  HERP, a novel heterodimer partner of HES/E(spl) in Notch signaling.

Authors:  T Iso; V Sartorelli; C Poizat; S Iezzi; H Y Wu; G Chung; L Kedes; Y Hamamori
Journal:  Mol Cell Biol       Date:  2001-09       Impact factor: 4.272

10.  Skip interacts with the retinoblastoma tumor suppressor and inhibits its transcriptional repression activity.

Authors:  Tulasiram Prathapam; Christian Kühne; Lawrence Banks
Journal:  Nucleic Acids Res       Date:  2002-12-01       Impact factor: 16.971

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