Characterization of a novel isoform of murine interferon regulatory factor 3

Biochem Biophys Res Commun. 2008 Dec 12;377(2):384-388. doi: 10.1016/j.bbrc.2008.09.147. Epub 2008 Oct 11.

Abstract

Interferon (IFN) regulatory factors (IRFs) are a family of transcription mediators involved in the regulation of type I IFN (IFN-alpha/beta) transcription. Among the nine already identified IRFs, IRF-3 is a constitutively and ubiquitously expressed and plays a critical role in the transcriptional activation of type I IFN and IFN-stimulated genes including IFN-alpha1, IFN-beta and RANTES. In the present study, we report the identification of a novel alternatively spliced transcript of murine Irf-3 gene (mIrf-3) designated mIRF-3a. mIRF-3a is ubiquitously present in mouse tissues along with mIRF-3 and could be translocated into the nucleus in uninfected L929 cells. EMSA and reporter assay demonstrated that mIRF-3a binds to ISRE sequences in murine Ifn-beta promoter and represses Ifn-beta promoter activation induced by Newcastle disease virus infection. These results suggest that mIRF-3a may act as a modulator of mIRF-3 functions in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Nucleus / metabolism
  • Electrophoretic Mobility Shift Assay
  • Female
  • Interferon Regulatory Factor-3 / genetics
  • Interferon Regulatory Factor-3 / metabolism*
  • Interferon-beta / genetics*
  • Liver / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Newcastle Disease / genetics
  • Newcastle Disease / metabolism
  • Promoter Regions, Genetic
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Transport
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tissue Distribution
  • Transcription, Genetic
  • Transcriptional Activation*

Substances

  • Interferon Regulatory Factor-3
  • Irf3 protein, mouse
  • Protein Isoforms
  • RNA, Messenger
  • Interferon-beta