The eta isoform of protein kinase C mediates transcriptional activation of the human transglutaminase 1 gene

J Biol Chem. 1996 Apr 19;271(16):9790-4. doi: 10.1074/jbc.271.16.9790.

Abstract

Transglutaminase 1 (TGase 1) is expressed during the terminal differentiation of keratinized squamous epithelium to form cornified cell envelope in differentiated keratinocytes by the epsilon-(gamma-glutamyl) cross-linking reaction. The gene for human TGase 1 is responsible for autosomal recessive lamellar ichthyosis, a severe hereditary keratinizing disorder of the skin. We examined the transcriptional activity of the gene in FRSK, rat keratinocytic cells, transfected with the luciferase reporter gene under control of the 5' upstream region of human TGase 1 gene. Transfection of the reporter gene with an expression vector for the eta isoform of novel protein kinase C (nPKCeta), as well as exposure to 12-0-tetradecanoylphorbol-13-acetate, markedly increased the luciferase activity in FRSK, but not in HT-1080 fibrosarcoma cells, although exogenous nPKCeta was expressed in both. The induction was suppressed by deleting the TGase 1 upstream sequence from -95 to -67 and by deleting the kinase domain from exogenous nPKCeta. In comparison with other PKC isoforms, nPKCeta most effectively induced the luciferase activity. We suggest that nPKCeta, an epithelium-specific isoform of PKC, mediates the activation of the TGase 1 transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Fibrosarcoma
  • Genes, Recessive
  • Humans
  • Ichthyosis / enzymology
  • Ichthyosis / genetics
  • Isoenzymes / metabolism*
  • Keratinocytes / enzymology
  • Luciferases / biosynthesis
  • Mice
  • Protein Kinase C / metabolism*
  • Rats
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Sequence Deletion
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcriptional Activation* / drug effects
  • Transfection
  • Transglutaminases / biosynthesis*
  • Transglutaminases / genetics*
  • Tumor Cells, Cultured

Substances

  • Isoenzymes
  • Recombinant Proteins
  • Luciferases
  • Transglutaminases
  • Protein Kinase C
  • Tetradecanoylphorbol Acetate