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Genome-wide distribution of 5-formylcytosine in embryonic stem cells is associated with transcription and depends on thymine DNA glycosylase.

Genome biology | 2012

Methylation of cytosine in DNA (5mC) is an important epigenetic mark that is involved in the regulation of genome function. During early embryonic development in mammals, the methylation landscape is dynamically reprogrammed in part through active demethylation. Recent advances have identified key players involved in active demethylation pathways, including oxidation of 5mC to 5-hydroxymethylcytosine (5hmC) and 5-formylcytosine (5fC) by the TET enzymes, and excision of 5fC by the base excision repair enzyme thymine DNA glycosylase (TDG). Here, we provide the first genome-wide map of 5fC in mouse embryonic stem (ES) cells and evaluate potential roles for 5fC in differentiation.

Pubmed ID: 22902005 RIS Download

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Associated grants

  • Agency: Wellcome Trust, United Kingdom
    Id: 095645
  • Agency: Cancer Research UK, United Kingdom
    Id: 12488
  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BBS/E/B/0000H112
  • Agency: Cancer Research UK, United Kingdom
    Id: 11961
  • Agency: Medical Research Council, United Kingdom
    Id: G0801156

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RRID:SCR_010233

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