The interferon-inducible protein kinase PKR modulates the transcriptional activation of immunoglobulin kappa gene

J Biol Chem. 1995 Oct 27;270(43):25426-34. doi: 10.1074/jbc.270.43.25426.

Abstract

PKR is an interferon (IFN)-induced serine/threonine protein kinase that regulates protein synthesis through phosphorylation of eukaryotic translation initiation factor-2 (eIF-2). In addition to its demonstrated role in translational control, recent findings suggest that PKR plays an important role in regulation of gene transcription, as PKR phosphorylates I kappa B alpha upon double-stranded RNA treatment resulting in activation of NF-kappa B DNA binding in vitro (Kumar, A., Haque, J., Lacoste, J., Hiscott, J., and Williams, B.R.G. (1994) Proc. Natl. Acad. Sci. U.S.A. 91, 6288-6292). To further investigate the role of PKR in transcriptional signaling, we expressed the wild type human PKR and a catalytically inactive dominant negative PKR mutant in the murine pre-B lymphoma 70Z/3 cells. Here, we report that expression of wild type PKR had no effect on kappa-chain transcriptional activation induced by lipopolysaccharide or IFN-gamma. However, expression of the dominant negative PKR mutant inhibited kappa gene transcription independently of NF-kappa B activation. Phosphorylation of eIF-2 alpha was not increased by lipopolysaccharide or IFN-gamma, suggesting that PKR mediates kappa gene transcriptional activation without affecting protein synthesis. Our findings further support a transcriptional role for PKR and demonstrate that there are at least two distinct PKR-mediated signal transduction pathways to the transcriptional machinery depending on cell type and stimuli, NF-kappa B-dependent and NF-kappa B-independent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Enzyme Induction
  • Eukaryotic Initiation Factor-2 / metabolism
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Neoplastic*
  • Genes, Immunoglobulin*
  • Humans
  • Immunoglobulin M / biosynthesis
  • Immunoglobulin kappa-Chains / genetics*
  • Lymphoma, B-Cell
  • Mice
  • Molecular Sequence Data
  • Mutation
  • NF-kappa B / metabolism
  • Phosphorylation
  • Precancerous Conditions
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • RNA, Neoplasm / biosynthesis
  • Receptors, Antigen, B-Cell / biosynthesis
  • Recombinant Proteins / metabolism
  • Sequence Deletion
  • Signal Transduction*
  • Transcription, Genetic
  • Tumor Cells, Cultured
  • eIF-2 Kinase

Substances

  • Eukaryotic Initiation Factor-2
  • Immunoglobulin M
  • Immunoglobulin kappa-Chains
  • NF-kappa B
  • RNA, Neoplasm
  • Receptors, Antigen, B-Cell
  • Recombinant Proteins
  • Protein Serine-Threonine Kinases
  • eIF-2 Kinase