DNA damage-induced phosphorylation of TRF2 is required for the fast pathway of DNA double-strand break repair

Research output: Contribution to journalArticle

30 Scopus citations

Abstract

Protein kinases of the phosphatidylinositol 3-kinase-like kinase family, originally known to act in maintaining genomic integrity via DNA repair pathways, have been shown to also function in telomere maintenance. Here we focus on the functional role of DNA damage-induced phosphorylation of the essential mammalian telomeric DNA binding protein TRF2, which coordinates the assembly of the proteinaceous cap to disguise the chromosome end from being recognized as a double-stand break (DSB). Previous results suggested a link between the transient induction of human TRF2 phosphorylation at threonine 188 (T188) by the ataxia telangiectasia mutated protein kinase (ATM) and the DNA damage response. Here, we report evidence that X-ray-induced phosphorylation of TRF2 at T188 plays a role in the fast pathway of DNA DSB repair. These results connect the highly transient induction of human TRF2 phosphorylation to the DNA damage response machinery. Thus, we find that a protein known to function in telomere maintenance, TRF2, also plays a functional role in DNA DSB repair.

Original languageEnglish (US)
Pages (from-to)3597-3604
Number of pages8
JournalMolecular and cellular biology
Volume29
Issue number13
DOIs
StatePublished - Jul 1 2009

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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