PTK6 promotes degradation of c-Cbl through PTK6-mediated phosphorylation

Biochem Biophys Res Commun. 2013 Feb 22;431(4):734-9. doi: 10.1016/j.bbrc.2013.01.046. Epub 2013 Jan 23.

Abstract

PTK6 (also known as Brk) is an intracellular tyrosine kinase which induces proliferation, anti-apoptosis, migration, and anchorage-independent growth. Herein we report that PTK6 phosphorylates and down-regulates E3 ubiquitin ligase c-Cbl. Tyr(700), Tyr(731), and Tyr(774) residues in the C-terminal domain of c-Cbl are major phosphorylation sites targeted by PTK6. The phosphorylated c-Cbl is subjected to auto-ubiquitination and degraded through the ubiquitin-proteasome pathway. These results provide evidence for a novel mechanism demonstrating the oncogenic potential of PTK6 through degradation of c-Cbl, which is an E3 ligase important in down-regulation of oncoproteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism*
  • Down-Regulation
  • Gene Knockdown Techniques
  • Humans
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Phosphorylation
  • Proteasome Endopeptidase Complex / metabolism
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism*
  • Proteolysis
  • Proto-Oncogene Proteins c-cbl / metabolism*
  • Tyrosine / genetics
  • Tyrosine / metabolism

Substances

  • Neoplasm Proteins
  • Tyrosine
  • Proto-Oncogene Proteins c-cbl
  • Protein-Tyrosine Kinases
  • PTK6 protein, human
  • Proteasome Endopeptidase Complex