pubmed-article:12482968 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C1257890 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C1367177 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C0439855 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C1549781 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C1515021 | lld:lifeskim |
pubmed-article:12482968 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
pubmed-article:12482968 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:12482968 | pubmed:dateCreated | 2002-12-16 | lld:pubmed |
pubmed-article:12482968 | pubmed:abstractText | Many transcription coactivators interact with nuclear receptors in a ligand- and C-terminal transactivation function (AF2)-dependent manner. These include activating signal cointegrator 2 (ASC-2), a recently isolated transcriptional coactivator molecule, which is amplified in human cancers and stimulates transactivation by nuclear receptors and numerous other transcription factors. In this report, we show that ASC-2 belongs to a steady-state complex of approximately 2 MDa (ASC-2 complex [ASCOM]) in HeLa nuclei. ASCOM contains retinoblastoma-binding protein RBQ-3, alpha/beta-tubulins, and trithorax group proteins ALR-1, ALR-2, HALR, and ASH2. In particular, ALR-1/2 and HALR contain a highly conserved 130- to 140-amino-acid motif termed the SET domain, which was recently implicated in histone H3 lysine-specific methylation activities. Indeed, recombinant ALR-1, HALR, and immunopurified ASCOM exhibit very weak but specific H3-lysine 4 methylation activities in vitro, and transactivation by retinoic acid receptor appears to involve ligand-dependent recruitment of ASCOM and subsequent transient H3-lysine 4 methylation of the promoter region in vivo. Thus, ASCOM may represent a distinct coactivator complex of nuclear receptors. Further characterization of ASCOM will lead to a better understanding of how nuclear receptors and other transcription factors mediate transcriptional activation. | lld:pubmed |
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pubmed-article:12482968 | pubmed:language | eng | lld:pubmed |
pubmed-article:12482968 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12482968 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:12482968 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12482968 | pubmed:month | Jan | lld:pubmed |
pubmed-article:12482968 | pubmed:issn | 0270-7306 | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:JungDong-JuDJ | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:LeeJae WoonJW | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:RoederRobert... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:BergerShelley... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:LeeKong-JooKJ | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:SongEun JooEJ | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:MeltzerPaul... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:LeeYoung... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:ChowVincent... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:KangMin-JungM... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:KimSeung-Whan... | lld:pubmed |
pubmed-article:12482968 | pubmed:author | pubmed-author:GooYoung-HwaY... | lld:pubmed |