Simian virus 40 large T antigen targets the spindle assembly checkpoint protein Bub1

Proc Natl Acad Sci U S A. 2004 Jan 27;101(4):947-52. doi: 10.1073/pnas.0308006100. Epub 2004 Jan 19.

Abstract

The mitotic spindle checkpoint protein Bub1 has been found to be mutated at low frequency in certain human cancers characterized by aneuploidy. Simian virus 40 large T antigen efficiently immortalizes rodent cells and occasionally transforms them to tumorigenicity. T antigen can also cause genomic instability, inducing chromosomal aberrations and aneuploidy. Here, we report an interaction between Bub1 and T antigen. T antigen coimmunoprecipitates with endogenous Bub1 and Bub3, another component of the spindle checkpoint complex. Genetic analysis demonstrates that the interaction of T antigen with Bub1 is not required for immortalization but is closely correlated with transformation. T antigen induces an override of the spindle checkpoint dependent on Bub1 binding. This interaction with proteins of the spindle checkpoint machinery suggests another role for T antigen and provides insight into its ability to cause chromosomal aberrations, aneuploidy, and transformation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigens, Polyomavirus Transforming / metabolism*
  • Mice
  • Molecular Sequence Data
  • Precipitin Tests
  • Protein Binding
  • Protein Kinases / metabolism*
  • Protein Serine-Threonine Kinases
  • Sequence Homology, Amino Acid
  • Two-Hybrid System Techniques

Substances

  • Antigens, Polyomavirus Transforming
  • Protein Kinases
  • BUB1 protein, human
  • Bub1 protein, mouse
  • Bub1 spindle checkpoint protein
  • Protein Serine-Threonine Kinases