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A role for the Adenomatous Polyposis Coli protein in chromosome segregation.

Mutations in the Adenomatous Polyposis Coli (APC) gene are responsible for familial colon cancer and also occur in the early stages of sporadic colon cancer. APC functions in the Wnt signalling pathway to regulate the degradation of beta-catenin (reviewed in refs 1-3). APC also binds to and stabilizes microtubules in vivo and in vitro, localizes to clusters at the ends of microtubules near the plasma membrane of interphase cells, and is an important regulator of cytoskeletal function. Here we show that cells carrying a truncated APC gene (Min) are defective in chromosome segregation. Moreover, during mitosis, APC localizes to the ends of microtubules embedded in kinetochores and forms a complex with the checkpoint proteins Bub1 and Bub3. In vitro, APC is a high-affinity substrate for Bub kinases. Our data are consistent with a role for APC in kinetochore-microtubule attachment and suggest that truncations in APC that eliminate microtubule binding may contribute to chromosomal instability in cancer cells.

Pubmed ID: 11283619


  • Kaplan KB
  • Burds AA
  • Swedlow JR
  • Bekir SS
  • Sorger PK
  • N√§thke IS


Nature cell biology

Publication Data

April 3, 2001

Associated Grants


Mesh Terms

  • Adenomatous Polyposis Coli Protein
  • Animals
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Cell Cycle Proteins
  • Cell Line
  • Chromosome Segregation
  • Cytoskeletal Proteins
  • Glycogen Synthase Kinase 3
  • HT29 Cells
  • HeLa Cells
  • Humans
  • Kinetochores
  • Microtubules
  • Neoplasm Proteins
  • Protein Kinases
  • Protein-Serine-Threonine Kinases
  • Proteins
  • Recombinant Fusion Proteins
  • Spodoptera