ASXL1 represses retinoic acid receptor-mediated transcription through associating with HP1 and LSD1

Journal of Biological Chemistry

Volumn 285, Issue 1, 2010, Pages 18-29

  Lee, Sang Wang ^a   Cho, Yang Sook ^a   Na, Jung Min ^a   Park, Ui Hyun ^a   Kang, Myengmo ^a   Kim, Eun Joo ^b   Um, Soo Jong ^a  

^a Sejong University   (South Korea)

^b Dankook University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; CELL TYPES; CHROMATIN IMMUNOPRECIPITATION ASSAY; COACTIVATORS; COMB-LIKE; COREPRESSORS; DEMETHYLASE; DIRECT INTERACTIONS; H3K9 METHYLATION; HEK-293; HISTONE H3; IN-VITRO; MEDIATED TRANSCRIPTION; N-TERMINALS; OVER-EXPRESSION; RETINOIC ACID RECEPTORS; RETINOID X RECEPTOR; TERNARY COMPLEX; TRANSCRIPTION ASSAYS; TRANSCRIPTIONAL ACTIVATIONS; TRANSCRIPTIONAL REPRESSION; TRANSFECTION ASSAYS;

ALKYLATION; AMINO ACIDS; BINDING ENERGY; COMPLEXATION; METHYLATION; NUCLEIC ACIDS; ORGANIC ACIDS; TRANSCRIPTION;

PROTEINS;

ADDITIONAL SEX COMB LIKE 1 PROTEIN; HETEROCHROMATIN PROTEIN 1; HISTONE H3; LYSINE SPECIFIC DEMETHYLASE 1; RETINOIC ACID RECEPTOR; RETINOID X RECEPTOR; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ARTICLE; BINDING SITE; CANCER CELL CULTURE; CELL STRAIN H1299; CELL STRAIN HEK293; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; ENZYME ACTIVITY; GENE DELETION; GENE FUNCTION; GENE OVEREXPRESSION; GENE REPRESSION; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; IN VITRO STUDY; IN VIVO STUDY; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN BINDING; PROTEIN METHYLATION; SEQUENCE ANALYSIS; TRANSCRIPTION INITIATION; TRANSCRIPTION REGULATION;

AMINO ACID SEQUENCE; BINDING SITES; CELL LINE; CHROMOSOMAL PROTEINS, NON-HISTONE; CO-REPRESSOR PROTEINS; HISTONE DEMETHYLASES; HISTONES; HUMANS; LIGANDS; METHYLATION; MOLECULAR SEQUENCE DATA; MULTIPROTEIN COMPLEXES; PROMOTER REGIONS, GENETIC; PROTEIN BINDING; RECEPTORS, RETINOIC ACID; REPRESSOR PROTEINS; REPRODUCIBILITY OF RESULTS; TRANSCRIPTION, GENETIC; TRETINOIN;

EID: 73649142039     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M109.065862     Document Type: Article

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