Uncoupling of acetylation from phosphorylation regulates FoxO1 function independent of its subcellular localization

Journal of Biological Chemistry

Volumn 285, Issue 35, 2010, Pages 27396-27401

  Qiang, Li ^a   Banks, Alexander S ^b   Accili, Domenico ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DEACETYLATION; DEPHOSPHORYLATIONS; HEK293 CELLS; NUCLEAR LOCALIZATION; POST-TRANSLATIONAL MODIFICATIONS; RESVERATROL; SUBCELLULAR LOCALIZATIONS;

PHOSPHORYLATION; TRANSCRIPTION FACTORS;

ACETYLATION;

COMPLEMENTARY DNA; HYDROGEN PEROXIDE; PROTEIN KINASE B; RESVERATROL; SERINE; THREONINE; TRANSCRIPTION FACTOR FKHR;

ACETYLATION; ADENOVIRUS; ARTICLE; CELL CULTURE; CELL NUCLEUS; CELL STRAIN HEK293; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DEACETYLATION; GENE MUTATION; OXIDATIVE STRESS; PLASMID; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN MODIFICATION; PROTEIN PHOSPHORYLATION; REGULATORY MECHANISM;

ACETYLATION; ACTIVE TRANSPORT, CELL NUCLEUS; ANIMALS; CELL LINE; CELL NUCLEUS; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; HYDROGEN PEROXIDE; INSULIN; MICE; OXIDANTS; OXIDATIVE STRESS; PHOSPHORYLATION; PROTO-ONCOGENE PROTEINS C-AKT; SIRTUIN 1;

EID: 77956260966     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.140228     Document Type: Article

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