Syk-mediated tyrosine phosphorylation of mule promotes TNF-induced JNK activation and cell death

Oncogene. 2016 Apr 14;35(15):1988-95. doi: 10.1038/onc.2015.275. Epub 2015 Jul 27.

Abstract

The transcription factor Miz1 negatively regulates TNF-induced JNK activation and cell death by suppressing TRAF2 K63-polyubiquitination; upon TNF stimulation, the suppression is relieved by Mule/ARF-BP1-mediated Miz1 ubiquitination and subsequent degradation. It is not known how Mule is activated by TNF. Here we report that TNF activates Mule by inducing the dissociation of Mule from its inhibitor ARF. ARF binds to and thereby inhibits the E3 ligase activity of Mule in the steady state. TNF induces tyrosine phosphorylation of Mule, which subsequently dissociates from ARF and becomes activated. Inhibition of Mule phosphorylation by silencing of the Spleen Tyrosine Kinase (Syk) prevents its dissociation from ARF, thereby inhibiting Mule E3 ligase activity and TNF-induced JNK activation and cell death. Our data provides a missing link in TNF signaling pathway that leads to JNK activation and cell death.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Cell Line
  • Cyclin-Dependent Kinase Inhibitor p16 / genetics
  • Cyclin-Dependent Kinase Inhibitor p16 / metabolism
  • Enzyme Activation
  • Fibroblasts
  • HEK293 Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Kruppel-Like Transcription Factors / metabolism
  • MAP Kinase Signaling System / physiology*
  • Mice
  • Nuclear Proteins / metabolism
  • Phosphorylation
  • Proteasome Endopeptidase Complex
  • Protein Inhibitors of Activated STAT / metabolism
  • Protein Processing, Post-Translational / physiology*
  • Protein-Tyrosine Kinases / metabolism*
  • Proteolysis
  • RNA, Small Interfering / genetics
  • Syk Kinase
  • Transfection
  • Tumor Necrosis Factor-alpha / physiology*
  • Tumor Suppressor Proteins
  • Ubiquitin-Protein Ligases / metabolism*
  • Ubiquitination / physiology

Substances

  • Cdkn2a protein, mouse
  • Cyclin-Dependent Kinase Inhibitor p16
  • Intracellular Signaling Peptides and Proteins
  • Kruppel-Like Transcription Factors
  • Nuclear Proteins
  • Protein Inhibitors of Activated STAT
  • RNA, Small Interfering
  • Tumor Necrosis Factor-alpha
  • Tumor Suppressor Proteins
  • ZBTB17 protein, human
  • HUWE1 protein, human
  • Huwe1 protein, mouse
  • Miz1 protein, mouse
  • Ubiquitin-Protein Ligases
  • Protein-Tyrosine Kinases
  • SYK protein, human
  • Syk Kinase
  • Syk protein, mouse
  • JNK Mitogen-Activated Protein Kinases
  • Proteasome Endopeptidase Complex