Thyroid-specific enhancer-binding protein (T/EBP): cDNA cloning, functional characterization, and structural identity with thyroid transcription factor TTF-1

Mol Cell Biol. 1991 Oct;11(10):4927-33. doi: 10.1128/mcb.11.10.4927-4933.1991.

Abstract

A cDNA clone encoding a thyroid-specific enhancer-binding protein (T/EBP) was isolated from a rat thyroid-derived FRTL-5 cell lambda gt 11 expression library, using a double-stranded oligonucleotide probe. This oligonucleotide was previously demonstrated to have the strongest binding affinity among three cis-acting DNA elements within the thyroid-specific enhancer region located 5.5 kbp upstream of the human thyroid peroxidase gene transcription start site. Nucleotide and deduced amino acid sequences of the cDNA revealed that T/EBP is identical to the previously reported thyroid-specific transcription factor 1 (TTF-1), which binds to the promoter of the rat thyroglobulin gene and controls its thyroid-specific expression. Expression of the T/EBP cDNA under control of the human cytomegalovirus major immediate-early gene promoter conferred thyroid-specific enhancer activity of as high as 26-fold to nonpermissive human hepatoma HepG2 cells when cotransfected with a vector containing 6.3 kbp of upstream sequence of the human thyroid peroxidase gene connected to a luciferase reporter gene. T/EBP was further expressed in HepG2 cells by using the vaccinia virus expression system. The expressed protein was partially purified by using sequence-specific affinity column chromatography and was further shown, by gel mobility shift experiments, to specifically bind to the enhancer-derived double-stranded oligonucleotide. These results clearly indicate that the binding of T/EBP (TTF-1) to the specific cis-acting enhancer element is largely responsible for thyroid-specific enhancer activity.

MeSH terms

  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cell Line
  • Cloning, Molecular
  • Enhancer Elements, Genetic / physiology
  • Gene Expression / physiology
  • Humans
  • Iodide Peroxidase / genetics*
  • Luciferases / genetics
  • Molecular Sequence Data
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Oligonucleotides / metabolism
  • Rats
  • Recombinant Fusion Proteins / biosynthesis
  • Sequence Homology, Nucleic Acid
  • Thyroid Nuclear Factor 1
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Tumor Cells, Cultured
  • Vaccinia virus / genetics

Substances

  • NKX2-1 protein, human
  • Nkx2-1 protein, rat
  • Nuclear Proteins
  • Oligonucleotides
  • Recombinant Fusion Proteins
  • Thyroid Nuclear Factor 1
  • Transcription Factors
  • Iodide Peroxidase
  • Luciferases