4.6 Article

5-hydroxymethylcytosine in DNA repair: A new player or a red herring?

Journal

CELL CYCLE
Volume 16, Issue 16, Pages 1499-1501

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15384101.2017.1346761

Keywords

5hmC; 5-hydroxymethylcytosine; DNA demethylation; DNA methylation; DNA repair; ten-eleven translocation; TET

Categories

Funding

  1. Russian Science Foundation [14-24-00022]
  2. Russian Science Foundation [17-24-00005] Funding Source: Russian Science Foundation

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Active DNA demethylation performed by ten-eleven translocation (TET) enzymes produces 5-hydroxymethylcytosines, 5-formylcytosines, and 5-carboxylcytosines. Recent observations suggest that 5-hydroxymethylcytosine is a stable epigenetic mark rather than merely an intermediate of DNA demethylation. However, the clear functional role of this new epigenetic player is elusive. The contribution of 5-hydroxymethylation to DNA repair is being discussed currently. Recently, Jiang and colleagues have demonstrated that DNA damage response-activated ATR kinase phosphorylates TET3 in mammalian cells and promotes DNA demethylation and 5-hydroxymethylcytosine accumulation. Moreover, TET3 catalytic activity is important for proper DNA repair and cell survival. Here, we discuss recent studies on the potential role of 5-hydroxymethylation in DNA repair and genome integrity maintenance.

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