Subtelomeric p53 binding prevents accumulation of DNA damage at human telomeres.

نویسندگان

  • Stephen Tutton
  • Greggory A Azzam
  • Nicholas Stong
  • Olga Vladimirova
  • Andreas Wiedmer
  • Jessica A Monteith
  • Kate Beishline
  • Zhuo Wang
  • Zhong Deng
  • Harold Riethman
  • Steven B McMahon
  • Maureen Murphy
  • Paul M Lieberman
چکیده

Telomeres and tumor suppressor protein TP53 (p53) function in genome protection, but a direct role of p53 at telomeres has not yet been described. Here, we have identified non-canonical p53-binding sites within the human subtelomeres that suppress the accumulation of DNA damage at telomeric repeat DNA. These non-canonical subtelomeric p53-binding sites conferred transcription enhancer-like functions that include an increase in local histone H3K9 and H3K27 acetylation and stimulation of subtelomeric transcripts, including telomere repeat-containing RNA (TERRA). p53 suppressed formation of telomere-associated γH2AX and prevented telomere DNA degradation in response to DNA damage stress. Our findings indicate that p53 provides a direct chromatin-associated protection to human telomeres, as well as other fragile genomic sites. We propose that p53-associated chromatin modifications enhance local DNA repair or protection to provide a previously unrecognized tumor suppressor function of p53.

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عنوان ژورنال:
  • The EMBO journal

دوره 35 2  شماره 

صفحات  -

تاریخ انتشار 2016