Identification and partial characterization of FRAG-6, a novel interferon-stimulated gene that is expressed in an IRF-1-INDEPENDENT manner

Cytokine. 1999 Nov;11(11):813-21. doi: 10.1006/cyto.1999.0493.

Abstract

In order to identify new interferon-stimulated genes that could help in the better understanding of the mechanism of action of interferons (IFNs), we decided to compare, by differential display RT-PCR (DDRT-PCR), the pattern of gene expression between IFN-alpha treated and untreated mouse embryonic fibroblasts (MEFs). Here we describe the initial characterization of a new cDNA fragment, named FRAG-6, that is expressed only upon IFN stimulation. The IFN-induced expression of this new gene can be observed in both wild-type and IRF-1-deficient MEF. FRAG-6 cDNA hybridizes with an mRNA of 6-9 kb that is induced by IFNs in a time-dependent manner. Analysis of the cloned nucleotide sequence revealed a 174 amino acid (aa) open reading frame (ORF) contained within the 576 bp. No significant homology with known nucleotide or protein sequences was observed. FRAG-6 is induced in vitro upon treatment of wild type or IRF-1-null cells with IFN-alpha or -gamma, but not with TNF or IL-1. Treatment of mice with imiquimod, a potent inducer of IFN, led to induced expression of FRAG-6 mRNA in various organs from wild type or IRF-1-deficient mice, but not from STAT-1 or type I IFN receptor deficient animals. Our results demonstrate that FRAG-6 mRNA induction by interferons is IRF-1-independent and it is likely to be activated by the JAK/STAT pathway. Further characterization of FRAG-6 will help us in the understanding of the mechanism of action of IFNs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Aminoquinolines / pharmacology
  • Animals
  • Base Sequence
  • Cells, Cultured
  • DNA, Complementary / genetics
  • DNA, Complementary / isolation & purification
  • DNA-Binding Proteins / deficiency*
  • DNA-Binding Proteins / genetics
  • Embryo, Mammalian
  • Fibroblasts / metabolism
  • Gene Expression / drug effects*
  • Imiquimod
  • Interferon Inducers / pharmacology
  • Interferon Regulatory Factor-1
  • Interferons / pharmacology*
  • Interleukin-1 / pharmacology
  • Membrane Proteins
  • Mice
  • Molecular Sequence Data
  • Phosphoproteins / deficiency*
  • Phosphoproteins / genetics
  • Proteins / genetics*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptor, Interferon alpha-beta
  • Receptors, Interferon / deficiency
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT1 Transcription Factor
  • Sequence Analysis, DNA
  • Signal Transduction / drug effects
  • Signal Transduction / genetics
  • Trans-Activators / deficiency
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Aminoquinolines
  • DNA, Complementary
  • DNA-Binding Proteins
  • FRAG-6 protein, mouse
  • Interferon Inducers
  • Interferon Regulatory Factor-1
  • Interleukin-1
  • Irf1 protein, mouse
  • Membrane Proteins
  • Phosphoproteins
  • Proteins
  • RNA, Messenger
  • Receptors, Interferon
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Trans-Activators
  • Tumor Necrosis Factor-alpha
  • Receptor, Interferon alpha-beta
  • Interferons
  • Imiquimod

Associated data

  • GENBANK/U76754