| Literature DB >> 24825349 |
Benjamin Delatte1, Rachel Deplus1, François Fuks2.
Abstract
Methylation of the fifth carbon of cytosine was the first epigenetic modification to be discovered in DNA. Recently, three new DNA modifications have come to light: hydroxymethylcytosine, formylcytosine, and carboxylcytosine, all generated by oxidation of methylcytosine by Ten Eleven Translocation (TET) enzymes. These modifications can initiate full DNA demethylation, but they are also likely to participate, like methylcytosine, in epigenetic signalling per se. A scenario is emerging in which coordinated regulation at multiple levels governs the participation of TETs in a wide range of physiological functions, sometimes via a mechanism unrelated to their enzymatic activity. Although still under construction, a sophisticated picture is rapidly forming where, according to the function to be performed, TETs ensure epigenetic marking to create specific landscapes, and whose improper build-up can lead to diseases such as cancer and neurodegenerative disorders.Entities:
Keywords: DNA modifications; TET proteins; epigenetics; human diseases; hydroxymethylation
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Year: 2014 PMID: 24825349 PMCID: PMC4198024 DOI: 10.15252/embj.201488290
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598