CHOP transcription factor phosphorylation by casein kinase 2 inhibits transcriptional activation

J Biol Chem. 2003 Oct 17;278(42):40514-20. doi: 10.1074/jbc.M306404200. Epub 2003 Jul 21.

Abstract

The CAAT/enhancer binding protein homologous transcription factor CHOP, also known as GADD153, is involved in DNA damage, growth arrest, and the induction of apoptosis after endoplasmic reticulum stress and nutrient deprivation. CHOP dimerizes with and inhibits the binding of C/EBP-related transcription factors to their consensus DNA target sequences and also forms novel complexes with other transcriptional proteins (e.g. c-Jun, c-Fos). The transcriptional activation of these complexes is modified by their phosphorylation. Phosphorylation of CHOP at serine 79 and serine 81 by p38-MAP kinase enhances its transcriptional activity. Here we show that an interactive association between CHOP and casein kinase II (CK2) results in the phosphorylation of its amino-terminal transactivation domain. Mapping of the functional domains of CHOP indicates that the region in CHOP required for association with CK2 differs from that required for its phosphorylation. Th binding of CK2 to CHOP requires only the carboxylterminal bZip domain of CHOP, whereas phosphorylation involves residues located in the amino-terminal domain. The presence of the bZip domain, however, facilitates the phosphorylation of CHOP. Analyses of the effect of point mutations of CHOP on its transcriptional activity and the effect of specific inhibitors of CK2 lead us to conclude that CK2-mediated phosphorylation of CHOP inhibits its transcriptional activity. Our findings suggest that inhibition of the proapoptotic functions of CHOP by CK2 may be a mechanism by which CK2 prevents apoptosis and promotes cellular proliferation.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CCAAT-Enhancer-Binding Proteins / chemistry
  • CCAAT-Enhancer-Binding Proteins / metabolism*
  • Casein Kinase II
  • Cell Division
  • Cell Line
  • Dimerization
  • Gene Deletion
  • Glutathione Transferase / metabolism
  • HeLa Cells
  • Humans
  • Luciferases / metabolism
  • Mice
  • Mitogen-Activated Protein Kinases / metabolism
  • Models, Biological
  • Models, Genetic
  • Molecular Sequence Data
  • Mutation
  • NIH 3T3 Cells
  • Phosphorylation
  • Plasmids / metabolism
  • Point Mutation
  • Protein Binding
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein Structure, Tertiary
  • Serine / chemistry
  • Transcription Factor CHOP
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Transcriptional Activation*
  • Transfection
  • p38 Mitogen-Activated Protein Kinases

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DDIT3 protein, human
  • Ddit3 protein, mouse
  • Transcription Factors
  • Transcription Factor CHOP
  • Serine
  • Luciferases
  • Glutathione Transferase
  • Casein Kinase II
  • Protein Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases