A novel c-Jun-dependent signal transduction pathway necessary for the transcriptional activation of interferon gamma response genes

J Biol Chem. 2007 Jan 12;282(2):938-46. doi: 10.1074/jbc.M607674200. Epub 2006 Nov 14.

Abstract

The biological effects of interferon gamma (IFNgamma) are mediated by interferon-stimulated genes (ISGs), many of which are activated downstream of Janus kinase (JAK)/signal transducer and activator of transcription 1 (STAT1) signaling. Herein we have shown that IFNgamma rapidly activated AP-1 DNA binding that required c-Jun but was independent of JAK1 and STAT1. IFNgamma-induced c-Jun phosphorylation and AP-1 DNA binding required the MEK1/2 and ERK1/2 signaling pathways, whereas the JNK1/2 and p38 mitogen-activated protein kinase pathways were dispensable. The induction of several ISGs, including ifi-205 and iNOS, was impaired in IFNgamma-treated c-Jun-/- cells, but others, such as IP-10 and SOCS3, were unaffected, and chromatin immunoprecipitation demonstrated that c-Jun binds to the iNOS promoter following treatment with IFNgamma. Thus, IFNgamma induced JAK1- and STAT1-independent activation of the ERK mitogen-activated protein kinase pathway, phosphorylation of c-Jun, and activation of AP-1 DNA binding, which are important for the induction of a subset of ISGs. This represents a novel signal transduction pathway induced by IFNgamma that proceeds in parallel with conventional JAK/STAT signaling to activate ISGs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Transformed
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / physiology
  • Interferon-gamma / metabolism*
  • Interferon-gamma / pharmacology
  • Janus Kinase 1 / genetics
  • Janus Kinase 1 / metabolism
  • MAP Kinase Signaling System / physiology*
  • Mice
  • Nitric Oxide Synthase Type II / genetics
  • Phosphorylation
  • Promoter Regions, Genetic / physiology
  • Proto-Oncogene Proteins c-jun / metabolism*
  • STAT1 Transcription Factor / metabolism
  • Transcription Factor AP-1 / metabolism
  • Transcriptional Activation / physiology*
  • Tumor Suppressor Proteins / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Ifi205 protein, mouse
  • Proto-Oncogene Proteins c-jun
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Transcription Factor AP-1
  • Tumor Suppressor Proteins
  • Interferon-gamma
  • Nitric Oxide Synthase Type II
  • Jak1 protein, mouse
  • Janus Kinase 1
  • Extracellular Signal-Regulated MAP Kinases
  • p38 Mitogen-Activated Protein Kinases