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Mediation of the DCC apoptotic signal by DIP13 alpha.

DCC (deleted in colorectal cancer) is a candidate tumor suppressor gene. However the function of DCC remains elusive. Previously, we demonstrated that forced expression of DCC induces apoptosis or cell cycle arrest (Chen, Y. Q., Hsieh, J. T., Yao, F., Fang, B., Pong, R. C., Cipriano, S. C. & Krepulat, F. (1999) Oncogene 18, 2747-2754). To delineate the DCC-induced apoptotic pathway, we have identified a protein, DIP13 alpha, which interacts with DCC. The DIP13 alpha protein has a pleckstrin homology domain and a phosphotyrosine binding domain. It interacts with a region on the DCC cytoplasmic domain that is required for the induction of apoptosis. Although ectopic expression of DIP13 alpha alone causes only a slight increase in apoptosis, co-expression of DCC and DIP13 alpha results in an approximately 5-fold increase in apoptosis. Removal of the DCC-interacting domain on DIP13 alpha abolishes its ability to enhance DCC-induced apoptosis. Inhibition of endogenous DIP13 alpha expression by small interfering RNA blocks DCC-induced apoptosis. Our data suggest that DIP13 alpha is a mediator of the DCC apoptotic pathway.

Pubmed ID: 12011067


  • Liu J
  • Yao F
  • Wu R
  • Morgan M
  • Thorburn A
  • Finley RL
  • Chen YQ


The Journal of biological chemistry

Publication Data

July 19, 2002

Associated Grants

  • Agency: NCI NIH HHS, Id: R01CA77489

Mesh Terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Apoptosis
  • Carrier Proteins
  • Colorectal Neoplasms
  • Genes, DCC
  • Molecular Sequence Data
  • Peptide Mapping
  • Phosphotyrosine
  • RNA, Small Interfering
  • RNA, Untranslated
  • Rabbits
  • Tumor Cells, Cultured
  • Yeasts