Two distinct phosphorylation pathways have additive effects on Abl family kinase activation

Mol Cell Biol. 2003 Jun;23(11):3884-96. doi: 10.1128/MCB.23.11.3884-3896.2003.

Abstract

The activities of the related Abl and Arg nonreceptor tyrosine kinases are kept under tight control in cells, but exposure to several different stimuli results in a two- to fivefold stimulation of kinase activity. Following the breakdown of inhibitory intramolecular interactions, Abl activation requires phosphorylation on several tyrosine residues, including a tyrosine in its activation loop. These activating phosphorylations have been proposed to occur either through autophosphorylation by Abl in trans or through phosphorylation of Abl by the Src nonreceptor tyrosine kinase. We show here that these two pathways mediate phosphorylation at distinct sites in Abl and Arg and have additive effects on Abl and Arg kinase activation. Abl and Arg autophosphorylate at several sites outside the activation loop, leading to 5.2- and 6.2-fold increases in kinase activity, respectively. We also find that the Src family kinase Hck phosphorylates the Abl and Arg activation loops, leading to an additional twofold stimulation of kinase activity. The autoactivation pathway may allow Abl family kinases to integrate or amplify cues relayed by Src family kinases from cell surface receptors.

Publication types

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

MeSH terms

  • Animals
  • Cell Line
  • Enzyme Activation
  • Enzyme Inhibitors / metabolism
  • Humans
  • Mice
  • Molecular Structure
  • Multigene Family
  • Phosphorylation
  • Protein Conformation
  • Protein-Tyrosine Kinases / chemistry
  • Protein-Tyrosine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-abl / chemistry
  • Proto-Oncogene Proteins c-abl / metabolism*
  • Proto-Oncogene Proteins c-hck
  • Recombinant Fusion Proteins / metabolism
  • Tyrosine / metabolism

Substances

  • Enzyme Inhibitors
  • Proto-Oncogene Proteins
  • Recombinant Fusion Proteins
  • Tyrosine
  • ARG tyrosine kinase
  • Protein-Tyrosine Kinases
  • HCK protein, human
  • Hck protein, mouse
  • Proto-Oncogene Proteins c-abl
  • Proto-Oncogene Proteins c-hck