Identification and characterization of murine IRAK-M

Biochem Biophys Res Commun. 2002 May 24;293(5):1472-7. doi: 10.1016/S0006-291X(02)00411-4.

Abstract

Interleukin-1 receptor-associated-kinases (IRAKs) are signal transduction mediators of the Toll/IL-1 receptor family, which comprise several transmembrane proteins involved in host defense mechanisms. Today four different human IRAKs (hu-IRAK-1, hu-IRAK-2, hu-IRAK-M, hu-IRAK-4) and two murine IRAKs (mouse pelle like kinase (mPLK) and mu-IRAK-4) have been described. Here we report the identification and characterization of murine IRAK-M (mu-IRAK-M), a mouse homologue to human IRAK-M (hu-IRAK-M). These IRAK-M molecules show 71% sequence identity, a comparable cellular expression, and functional similarities with respect to signal transduction capacity and kinase activity, suggesting functional homology in signalling in human and mouse cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Cells, Cultured
  • DNA, Complementary / metabolism
  • Genes, Reporter
  • Humans
  • Immunoblotting
  • Interleukin-1 / metabolism
  • Interleukin-1 Receptor-Associated Kinases
  • Mice
  • NF-kappa B / metabolism
  • Phosphorylation
  • Polymerase Chain Reaction
  • Precipitin Tests
  • Protein Kinases / chemistry*
  • Protein Kinases / metabolism*
  • Protein Structure, Tertiary
  • RNA / metabolism
  • Recombinant Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Tissue Distribution

Substances

  • DNA, Complementary
  • Interleukin-1
  • NF-kappa B
  • Recombinant Proteins
  • RNA
  • Protein Kinases
  • IRAK3 protein, human
  • Interleukin-1 Receptor-Associated Kinases
  • Irak3 protein, mouse