Mutations in the 1,25-dihydroxyvitamin D3 receptor identifying C-terminal amino acids required for transcriptional activation that are functionally dissociated from hormone binding, heterodimeric DNA binding, and interaction with basal transcription factor IIB, in vitro

J Biol Chem. 1997 Jun 6;272(23):14592-9. doi: 10.1074/jbc.272.23.14592.

Abstract

To investigate a potential ligand-dependent transcriptional activation domain (AF-2) in the C-terminal region of the human vitamin D receptor (hVDR), two conserved residues, Leu-417 and Glu-420, were replaced with alanines by site-directed mutagenesis (L417A and E420A). Transcriptional activation in response to 1, 25-dihydroxyvitamin D3 (1,25-(OH)2D3) was virtually eliminated when either point mutant was transfected into several mammalian cell lines. Furthermore, both mutants exhibited a dominant negative phenotype when expressed in COS-7 cells. Scatchard analysis at 4 degrees C and a ligand-dependent DNA binding assay at 25 degrees C revealed essentially normal 1,25-(OH)2D3 binding for the mutant hVDRs, which were also equivalent to native receptor in associating with the rat osteocalcin vitamin D responsive element as a presumed heterodimer with retinoid X receptor. Glutathione S-transferase-human transcription factor IIB (TFIIB) fusion protein linked to Sepharose equally coprecipitated the wild-type hVDR and the AF-2 mutants. These data implicate amino acids Leu-417 and Glu-420, residing in a putative alpha-helical region at the extreme C terminus of hVDR, as critical in the mechanism of 1, 25-(OH)2D3-stimulated transcription, likely mediating an interaction with a coactivator(s) or a component of the basal transcriptional machinery distinct from TFIIB.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • COS Cells
  • Calcitriol / pharmacology
  • Conserved Sequence
  • DNA / metabolism*
  • Dimerization
  • Glutamic Acid
  • Humans
  • Kinetics
  • Leucine
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Osteocalcin / biosynthesis
  • Phenotype
  • Point Mutation
  • Protein Structure, Secondary
  • Rats
  • Receptors, Calcitriol / biosynthesis
  • Receptors, Calcitriol / chemistry
  • Receptors, Calcitriol / metabolism*
  • Receptors, Retinoic Acid / chemistry
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Retinoid X Receptors
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Transcription Factor TFIIB
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*
  • Transcriptional Activation*
  • Transfection

Substances

  • Receptors, Calcitriol
  • Receptors, Retinoic Acid
  • Recombinant Proteins
  • Retinoid X Receptors
  • Transcription Factor TFIIB
  • Transcription Factors
  • Osteocalcin
  • Glutamic Acid
  • DNA
  • Calcitriol
  • Leucine