Identification of a gamma-tubulin-binding domain in BRCA1

Cancer Res. 2001 Nov 1;61(21):7713-8.

Abstract

We previously reported (L-C. Hsu and R. L. White, Proc. Natl. Acad. Sci. USA, 95: 12983-12988, 1998) that hypophosphorylated BRCA1 is associated with mitotic centrosomes in vivo, perhaps through its interaction with gamma-tubulin. In vitro evidence presented here indicates that full-length BRCA1 protein generated by in vitro translation interacts with gamma-tubulin. A specific domain of BRCA1 protein, BRCA1 fragment no. 3 (BF3; amino acids 504-803), is both necessary and sufficient to bind gamma-tubulin. BF3 and gamma-tubulin coimmunoprecipitated when coexpressed in cells. In addition, expression of BF3 interfered with the interaction between BRCA1 and gamma-tubulin. Stable transformants of COS-7 cells that overexpressed BF3 showed a reduced growth rate partly because of increased apoptosis. Furthermore, overexpression of BF3 in COS-7 cells results in the accumulation of mitotic cells with multiple centrosomes and abnormal spindles. Okadaic acid, an inhibitor of protein phosphatases types 1 and 2A, induces hyperphosphorylation of BRCA1, a reduction of both BRCA1 and gamma-tubulin associated with mitotic centrosomes, and an accumulation of abnormal spindle formation. Thus, attenuating the interaction between BRCA1 and gamma-tubulin, and their association with mitotic centrosomes, may induce an increase of aneuploid cell population and contribute to tumorigenesis.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / physiology
  • BRCA1 Protein / genetics
  • BRCA1 Protein / metabolism*
  • Binding Sites
  • COS Cells
  • Cell Division / physiology
  • Centrosome / drug effects
  • Centrosome / metabolism
  • Enzyme Inhibitors / pharmacology
  • Exons
  • Humans
  • Okadaic Acid / pharmacology
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Phosphoprotein Phosphatases / antagonists & inhibitors
  • Phosphorylation / drug effects
  • Precipitin Tests
  • Protein Structure, Tertiary
  • Transfection
  • Tubulin / metabolism*

Substances

  • BRCA1 Protein
  • Enzyme Inhibitors
  • Peptide Fragments
  • Tubulin
  • Okadaic Acid
  • Phosphoprotein Phosphatases