Oxygen-regulated erythropoietin gene expression is dependent on a CpG methylation-free hypoxia-inducible factor-1 DNA-binding site

Eur J Biochem. 1998 May 1;253(3):771-7. doi: 10.1046/j.1432-1327.1998.2530771.x.

Abstract

The hypoxia-inducible factor-1 (HIF-1) is a transcriptional activator involved in the expression of oxygen-regulated genes such as that for erythropoietin. Following exposure to low oxygen partial pressure (hypoxia), HIF-1 binds to an hypoxia-response element located 3' to the erythropoietin gene and confers activation of erythropoietin expression. The conserved core HIF-1 binding site (HBS) of the erythropoietin 3' enhancer (CGTG) contains a CpG dinucleotide known to be a potential target of cytosine methylation. We found that methylation of the HBS abolishes HIF-1 DNA binding as well as hypoxic reporter gene activation, suggesting that a methylation-free HBS is mandatory for HIF-1 function. The in vivo methylation pattern of the erythropoietin 3' HBS in various human cell lines and mouse organs was assessed by genomic Southern blotting using a methylation-sensitive restriction enzyme. Whereas this site was essentially methylation-free in the erythropoietin-producing cell line Hep3B, a direct correlation between erythropoietin protein expression and the degree of erythropoietin 3' HBS methylation was found in different HepG2 sublines. However, the finding that this site is partially methylation-free in human cell lines and mouse tissues that do not express erythropoietin suggests that there might be a general selective pressure to keep this site methylation-free, independent of erythropoietin expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Carcinoma, Hepatocellular
  • Cell Hypoxia*
  • Cell Nucleus / metabolism
  • DNA Methylation
  • DNA-Binding Proteins / metabolism*
  • Dinucleoside Phosphates / metabolism*
  • Erythropoietin / biosynthesis*
  • Gene Expression Regulation*
  • Gene Expression Regulation, Neoplastic
  • Genes, Reporter
  • HeLa Cells
  • Humans
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Kidney / embryology
  • Kidney / growth & development
  • Kidney / metabolism
  • L Cells
  • Leukemia
  • Liver / embryology
  • Liver / growth & development
  • Liver / metabolism
  • Liver Neoplasms
  • Luciferases / biosynthesis
  • Mice
  • Neuroblastoma
  • Nuclear Proteins / metabolism*
  • Organ Specificity
  • Recombinant Fusion Proteins / biosynthesis
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Transfection
  • Tumor Cells, Cultured

Substances

  • DNA-Binding Proteins
  • Dinucleoside Phosphates
  • HIF1A protein, human
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Nuclear Proteins
  • Recombinant Fusion Proteins
  • Transcription Factors
  • Erythropoietin
  • cytidylyl-3'-5'-guanosine
  • Luciferases