Sumoylation of Oct4 enhances its stability, DNA binding, and transactivation

Journal of Biological Chemistry

Volumn 282, Issue 29, 2007, Pages 21551-21560

  Wei, Fang ^a   Schöler, Hans R ^b   Atchison, Michael L ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b MAX PLANCK INSTITUTE FOR MOLECULAR BIOMEDICINE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; BINDING SITES; CELLS; GROWTH KINETICS; ONCOLOGY; PHOSPHORYLATION;

DNA BINDING; SUMOYLATION; TRANSACTIVATION; TRANSCRIPTIONAL ACTIVITY;

TRANSCRIPTION;

DNA; LYSINE; OCTAMER TRANSCRIPTION FACTOR 4; SUMO 1 PROTEIN; TRANSCRIPTION FACTOR POU;

ANIMAL CELL; ARTICLE; CELL NUCLEUS; CONTROLLED STUDY; EMBRYO; GENE SEQUENCE; HUMAN; HUMAN CELL; IN VITRO STUDY; IN VIVO STUDY; MOUSE; MUTATION; NONHUMAN; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DNA BINDING; PROTEIN DOMAIN; PROTEIN LOCALIZATION; PROTEIN MODIFICATION; PROTEIN STABILITY; PROTEIN TARGETING; REGULATORY MECHANISM; SUMOYLATION; TRANSACTIVATION;

ANIMALS; BINDING SITES; CELL LINE; DNA; GENE EXPRESSION REGULATION; HUMANS; LYSINE; MICE; NIH 3T3 CELLS; OCTAMER TRANSCRIPTION FACTOR-3; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; SMALL UBIQUITIN-RELATED MODIFIER PROTEINS; TRANS-ACTIVATION (GENETICS);

EID: 34547113757     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M611041200     Document Type: Article

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