File:Demethylation of 5-methylcytosine.svg

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Summary[edit]

Summary
Description Demethylation of 5-Methylcytosine (5mC) in DNA. As reviewed in 2018,[1] 5mC is oxidized by the ten-eleven translocation (TET) family of dioxygenases (TET1, TET2, TET3) to generate 5-hydroxymethylcytosine (5hmC). In successive steps TET enzymes further hydroxylate 5hmC to generate 5-formylcytosine (5fC) and 5-carboxylcytosine (5caC). Thymine-DNA glycosylase (TDG) recognizes the intermediate bases 5fC and 5caC and excises the glycosidic bond resulting in an apyrimidinic site (AP site). In an alternative oxidative deamination pathway, 5hmC can be oxidatively deaminated by activity-induced cytidine deaminase/apolipoprotein B mRNA editing complex (AID/APOBEC) deaminases to form 5-hydroxymethyluracil (5hmU) or 5mC can be converted to thymine (Thy). 5hmU can be cleaved by TDG, single-strand-selective monofunctional uracil-DNA glycosylase 1 (SMUG1), Nei-Like DNA Glycosylase 1 (NEIL1), or methyl-CpG binding protein 4 (MBD4). AP sites and T:G mismatches are then repaired by base excision repair (BER) enzymes to yield cytosine (Cyt).
Source Wikimedia Commons file page
Author Bernstein0275, User:Innerstream
Permission See original Commons license details.

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current03:31, 5 June 2026Thumbnail for version as of 03:31, 5 June 2026816 × 1,056 (127 KB)Maintenance script (talk | contribs)== Summary == Importing file

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