4.4 Review

DNA demethylation pathways: Additional players and regulators

Journal

BIOESSAYS
Volume 39, Issue 1, Pages -

Publisher

WILEY
DOI: 10.1002/bies.201600178

Keywords

5-carboxylcytosine; 5-formylcytosine; 5-hydroxymethylcytosine; 5-hydroxymethyluracil; active DNA demethylation; AID; deamination; oxidation; TDG; TET

Funding

  1. Polish National Science Centre (NCN) [UMO-2014/13/B/NZ1/03991, UMO-2011/02/A/NZ1/00052, UMO-2014/14/M/NZ5/00558]
  2. REGPOT Grant FishMed, European Commission (EC) [316125]

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DNA demethylation can occur passively by dilution'' of methylation marks by DNA replication, or actively and independently of DNA replication. Direct conversion of 5-methylcytosine(5mC) tocytosine(C), as originally proposed, does not occur. Instead, active DNA methylation involves oxidation of the methylated base by ten-eleven translocations (TETs), or deamination of the methylated or a nearby base by activation induced deaminase (AID). The modified nucleotide, possibly together with surrounding nucleotides, is then replaced by the BER pathway. Recent data clarify the roles and the regulation of well-known enzymes in this process. They identify base excision repair (BER) glycosylases that may cooperate with or replace thymine DNA glycosylase (TDG) in the base excision step, and suggest possible involvement of DNA damage repair pathways other than BER in active DNA demethylation. Here, we review these new developments. Review essays

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