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

Omar L KantidzeSergey V Razin
Published in: Cell cycle (Georgetown, Tex.) (2017)
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.
Keyphrases
  • dna repair
  • dna damage response
  • circulating tumor
  • dna damage
  • cell free
  • single molecule
  • dna methylation
  • gene expression
  • circulating tumor cells
  • oxidative stress
  • protein kinase
  • climate change