Characterization of a novel hexameric repeat DNA sequence in the promoter of the immediate early gene, IEX-1, that mediates 1alpha,25-dihydroxyvitamin D(3)-associated IEX-1 gene repression

Oncogene. 2002 May 23;21(23):3706-14. doi: 10.1038/sj.onc.1205450.

Abstract

1alpha,25-Dihydroxyvitamin D(3)(1alpha,25(OH)(2)D(3)), the active metabolite of vitamin D(3), mediates anti-proliferative effects in cells by regulating the expression of 1alpha,25(OH)(2)D(3)-responsive genes. The expression of the proliferation-promoting Immediate Early gene X-1 (IEX-1) is reduced by 1alpha,25(OH)(2)D(3) through unknown mechanisms. Here we report the presence of a novel inhibitory hexameric repeat DNA response element in the promoter of the human IEX-1 gene that mediates 1alpha,25(OH)(2)D(3)-associated IEX-1 gene repression. To localize a vitamin D sensitive DNA response element we transfected the keratinocyte-like cell line, HaCaT, (referred as HaCaT) with a series of plasmids containing full-length and truncated IEX-1 promoter elements fused to the luciferase reporter gene in the absence or presence of 1alpha,25(OH)(2)D(3), and we performed electrophoretic gel mobility assays in the presence of receptors for 1alpha,25(OH)(2)D(3) (vitamin D receptor, VDR) and 9-cis-retinoic acid (RXRalpha). We mapped a negative response element between nt -405 and -391(15 bp) of theIEX-1 promoter (5'-TGAACC AGG GAGTCA-3') that mediates transcriptional inhibition in response to 1alpha,25(OH)(2)D(3) and which requires expression of both nuclear receptors for 1alpha,25(OH)(2)D(3) and 9-cis-retinoic acid. Our data indicate that the physiological repression of IEX-1 gene expression by 1alpha,25(OH)(2)D(3) is directly mediated by nuclear VDR/RXRalpha heterodimers through a specific transcriptional element.

Publication types

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

MeSH terms

  • Apoptosis Regulatory Proteins
  • Base Sequence
  • Cell Line
  • Dimerization
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation*
  • Humans
  • Immediate-Early Proteins / genetics*
  • Membrane Glycoproteins / genetics*
  • Membrane Proteins
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Mutation
  • Neoplasm Proteins*
  • Promoter Regions, Genetic / genetics*
  • Receptors, Retinoic Acid / metabolism
  • Response Elements / genetics
  • Retinoid X Receptors
  • Terminal Repeat Sequences
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Vitamin D / analogs & derivatives*
  • Vitamin D / chemistry
  • Vitamin D / metabolism*

Substances

  • 2-methyl-1,25-dihydroxyvitamin D3
  • Apoptosis Regulatory Proteins
  • IER3 protein, human
  • Immediate-Early Proteins
  • Membrane Glycoproteins
  • Membrane Proteins
  • Neoplasm Proteins
  • Receptors, Retinoic Acid
  • Retinoid X Receptors
  • Transcription Factors
  • Vitamin D