mRNA profiling of rat islet tumors reveals nkx 6.1 as a beta-cell-specific homeodomain transcription factor

J Biol Chem. 1996 Aug 2;271(31):18749-58. doi: 10.1074/jbc.271.31.18749.

Abstract

Development of a high capacity multiplex reverse transcriptase-polymerase chain reaction protocol has allowed us to screen lineage related rat islet tumors classified as alpha-, beta-, and delta-like as judged by their hormone profile for differential expression of more than 50 selected genes. We find that in addition to insulin the insulinoma express the normal beta-cell markers Pdx-1, IAPP, and Glut-2, and that these markers are absent from the glucagonoma: a reflection of the normal alpha-cell. Furthermore, this study suggests that the GLP-1, glucagon, GIP, IGF-1, and insulin receptors as well as E-cadherin, R-cadherin, Id-1, and Id-2 are differentially expressed within the islet of Langerhans. Importantly, insulinoma-specific expression of the recently cloned homeodomain protein Nkx 6.1 predicted beta-cell-specific expression in the normal islet. Immunohistochemistry using antibodies raised against recombinant Nkx 6.1 did indeed localize Nkx 6.1 expression exclusively to the nuclei of normal islet beta-cells. Apart from pancreatic islets only the antral part of the stomach contained Nkx 6.1 mRNA. We conclude that multiplex reverse transcriptase-polymerase chain reaction-based mRNA profiling is a powerful tool to identify differentially expressed genes within phenotypically related cells and propose that Nkx 6.1 is involved in specifying the unique characteristics of the beta-cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma, Islet Cell / genetics
  • Adenoma, Islet Cell / metabolism*
  • Animals
  • Base Sequence
  • Biomarkers
  • DNA Primers / genetics
  • DNA, Complementary / genetics
  • Gene Expression
  • Hexokinase / genetics
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / immunology
  • Homeodomain Proteins / metabolism*
  • Immunohistochemistry
  • Islets of Langerhans / metabolism*
  • Molecular Sequence Data
  • Monosaccharide Transport Proteins / genetics
  • Pancreatic Hormones / genetics
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism*
  • Phenotype
  • Polymerase Chain Reaction
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism*
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism*
  • Rats
  • Receptors, Cell Surface / genetics
  • Transcription Factors / genetics
  • Transcription Factors / immunology
  • Transcription Factors / metabolism*

Substances

  • Biomarkers
  • DNA Primers
  • DNA, Complementary
  • Homeodomain Proteins
  • Monosaccharide Transport Proteins
  • Pancreatic Hormones
  • RNA, Messenger
  • RNA, Neoplasm
  • Receptors, Cell Surface
  • Transcription Factors
  • Hexokinase