Src-mediated activation of the human neurotensin/neuromedin N promoter

Surgery. 1997 Aug;122(2):180-5; discussion 185-6. doi: 10.1016/s0039-6060(97)90007-6.

Abstract

Background: Expression of the gene encoding the neurotensin/neuromedin N (NT/N) is developmentally regulated in the gut in a distinctive temporal and spatial fashion. Src kinase, a nonreceptor tyrosine kinase, has been implicated in the growth and differentiation of various tissues; its role in gut differentiation is not known. The purpose of this study was to determine whether the Src signaling pathway plays a role in the activation of the human NT/N promoter.

Methods: Caco-2 cells, a human colon cancer cell line that can differentiate to a small bowel phenotype, were transiently transfected with human NT/N promoter fragments linked to luciferase and various amounts of Src expression plasmids or dominant negative Raf; luciferase and beta-galactosidase activities were measured after 48 hours.

Results: Cotransfection of Src resulted in an approximate eightfold increase of NT/N promoter activity; mutation of a proximal activating protein-1/cyclic adenosine monophosphate responsive element site resulted in a dramatic decrease of Src-mediated NT/N induction. Cotransfection with a dominant negative Raf plasmid partially blocked Src-mediated NT/N activation.

Conclusions: Src increases NT/N promoter activity in Caco-2 cells acting, in part, through a proximal AP-1/CRE promoter element. In addition, Src regulation of the NT/N promoter appears to be mediated through a Raf-dependent pathway. We propose that Src may play a role in tissue-specific gene expression in the gut.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • CSK Tyrosine-Protein Kinase
  • Colonic Neoplasms
  • Gene Expression Regulation
  • Humans
  • Luciferases / biosynthesis
  • Neurotensin / biosynthesis*
  • Neurotensin / genetics*
  • Peptide Fragments / biosynthesis*
  • Peptide Fragments / genetics*
  • Promoter Regions, Genetic*
  • Protein Serine-Threonine Kinases / metabolism
  • Protein-Tyrosine Kinases / biosynthesis
  • Protein-Tyrosine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-raf
  • Recombinant Fusion Proteins / biosynthesis
  • Transfection
  • Tumor Cells, Cultured
  • beta-Galactosidase / biosynthesis
  • ras Proteins / metabolism
  • src-Family Kinases

Substances

  • Peptide Fragments
  • Proto-Oncogene Proteins
  • Recombinant Fusion Proteins
  • neuromedin N
  • Neurotensin
  • Luciferases
  • Protein-Tyrosine Kinases
  • CSK Tyrosine-Protein Kinase
  • src-Family Kinases
  • CSK protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf
  • beta-Galactosidase
  • ras Proteins