Sumoylation of the basic helix-loop-helix transcription factor sharp-1 regulates recruitment of the histone methyltransferase G9a and function in myogenesis

Journal of Biological Chemistry

Volumn 288, Issue 24, 2013, Pages 17654-17662

  Wang, Yaju ^a   Shankar, Shilpa Rani ^a   Kher, Devaki ^a   Ling, Belinda Mei Tze ^a   Taneja, Reshma ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

HISTONE METHYLTRANSFERASE; MYOGENIC DIFFERENTIATIONS; POST-TRANSLATIONAL MODIFICATIONS; SKELETAL MUSCLE DIFFERENTIATION; SUBCELLULAR LOCALIZATIONS; TISSUE-SPECIFIC GENE EXPRESSION; TRANSCRIPTIONAL REPRESSION; TRANSCRIPTIONAL REPRESSORS;

AMINO ACIDS; CHROMOSOMES; MUSCLE;

TRANSCRIPTION FACTORS;

BASIC HELIX LOOP HELIX TRANSCRIPTION FACTOR; HISTONE METHYLTRANSFERASE; HISTONE METHYLTRANSFERASE G9A; LYSINE; MYOD PROTEIN; PROTEIN SENP1; SHARP 1 PROTEIN; SUMO PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL DIFFERENTIATION; CELLULAR DISTRIBUTION; CHROMATIN STRUCTURE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME REGULATION; GENE EXPRESSION; HISTONE METHYLATION; HUMAN; MOUSE; MUSCLE DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; RAT; SIGNAL TRANSDUCTION; SKELETAL MUSCLE; SUMOYLATION;

CHROMATIN MODIFICATION; DIFFERENTIATION; EPIGENETICS; HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; HISTONE METHYLATION; MYOGENESIS; SKELETAL MUSCLE; SUMOYLATION; TRANSCRIPTION FACTORS;

AMINO ACID SEQUENCE; ANIMALS; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTORS; BINDING SITES; CELL DIFFERENTIATION; CELL LINE; CERCOPITHECUS AETHIOPS; CONSERVED SEQUENCE; COS CELLS; ENDOPEPTIDASES; HEK293 CELLS; HISTOCOMPATIBILITY ANTIGENS; HISTONE-LYSINE N-METHYLTRANSFERASE; HUMANS; MICE; MOLECULAR SEQUENCE DATA; MUSCLE DEVELOPMENT; MYOD PROTEIN; PROTEIN BINDING; PROTEIN TRANSPORT; SUMOYLATION; TRANSCRIPTION, GENETIC;

EID: 84879044970     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.463257     Document Type: Article

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