Sp1 sites in the mouse aprt gene promoter are required to prevent methylation of the CpG island

Genes Dev. 1994 Oct 1;8(19):2282-92. doi: 10.1101/gad.8.19.2282.


In an attempt to find the mechanism by which CpG islands remain free of methylation we have undertaken a detailed examination of the mouse adenine phosphoribosyltransferase (aprt) gene. This housekeeping gene has a CpG island that extends over the gene promoter and includes the first two exons. We show that the island is free of methylation at all CpGs, whereas the flanks are methyated. Detailed patterns of methylation beyond the boundaries of the CpG island vary between cells. In vivo footprinting across the island region shows that three GC boxes clustered at the 5' edge of the CpG island are occupied, most probably by Sp1. No other footprints are detected within the island region. Deletion or mutagenesis of the Sp1 sites causes de novo methylation of the CpG island in a transgenic mouse assay. Thus, the peripherally located Sp1 sites are necessary to keep the aprt island methylation free.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine Phosphoribosyltransferase / genetics*
  • Animals
  • Base Sequence
  • Binding Sites / genetics
  • DNA / genetics
  • DNA / metabolism
  • DNA Primers / genetics
  • Female
  • Male
  • Methylation
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Transgenic
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nucleosomes / metabolism
  • Oligodeoxyribonucleotides / genetics
  • Oligodeoxyribonucleotides / metabolism*
  • Promoter Regions, Genetic
  • Sequence Deletion
  • Sp1 Transcription Factor / metabolism*


  • DNA Primers
  • Nucleosomes
  • Oligodeoxyribonucleotides
  • Sp1 Transcription Factor
  • DNA
  • Adenine Phosphoribosyltransferase