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Context-dependent CpG methylation directs cell-specific binding of transcription factor ZBTB38.

Claire MarchalPierre-Antoine DefossezBenoit Miotto
Published in: Epigenetics (2022)
DNA methylation on CpGs regulates transcription in mammals, both by decreasing the binding of methylation-repelled factors and by increasing the binding of methylation-attracted factors. Among the latter, zinc finger proteins have the potential to bind methylated CpGs in a sequence-specific context. The protein ZBTB38 is unique in that it has two independent sets of zinc fingers, which recognize two different methylated consensus sequences in vitro . Here, we identify the binding sites of ZBTB38 in a human cell line, and show that they contain the two methylated consensus sequences identified in vitro . In addition, we show that the distribution of ZBTB38 sites is highly unusual: while 10% of the ZBTB38 sites are also bound by CTCF, the other 90% of sites reside in closed chromatin and are not bound by any of the other factors mapped in our model cell line. Finally, a third of ZBTB38 sites are found upstream of long and active CpG islands. Our work therefore validates ZBTB38 as a methyl-DNA binder in vivo and identifies its unique distribution in the genome.
Keyphrases
  • dna methylation
  • genome wide
  • transcription factor
  • gene expression
  • dna binding
  • endothelial cells
  • binding protein
  • copy number
  • stem cells
  • single cell
  • cell therapy
  • amino acid
  • single molecule
  • genetic diversity