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Postnatal DNA demethylation and its role in tissue maturation.

Yitzhak ReizelOfra SabagYael SkverskyAdam SpiroBenjamin SteinbergDiana BernsteinAmber WangJulia KieckhaeferCatherine LiEli PikarskyRena Levin-KleinAlon GorenKlaus RajewskyKlaus H KaestnerHoward Cedar
Published in: Nature communications (2018)
Development in mammals is accompanied by specific de novo and demethylation events that are thought to stabilize differentiated cell phenotypes. We demonstrate that a large percentage of the tissue-specific methylation pattern is generated postnatally. Demethylation in the liver is observed in thousands of enhancer-like sequences associated with genes that undergo activation during the first few weeks of life. Using. conditional gene ablation strategy we show that the removal of these methyl groups is stable and necessary for assuring proper hepatocyte gene expression and function through its effect on chromatin accessibility. These postnatal changes in methylation come about through exposure to hormone signaling. These results define the molecular rules of 5-methyl-cytosine regulation as an epigenetic mechanism underlying cellular responses to. changing environment.
Keyphrases
  • genome wide
  • dna methylation
  • gene expression
  • preterm infants
  • copy number
  • transcription factor
  • single molecule
  • genome wide identification
  • single cell
  • cell therapy
  • stem cells
  • dna damage
  • liver injury
  • drug induced