| Literature DB >> 26658110 |
Stephen Tutton1, Greggory A Azzam1, Nicholas Stong1, Olga Vladimirova1, Andreas Wiedmer1, Jessica A Monteith2, Kate Beishline1, Zhuo Wang1, Zhong Deng1, Harold Riethman1, Steven B McMahon2, Maureen Murphy1, Paul M Lieberman3.
Abstract
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.Entities:
Keywords: DNA damage; TERRA; TP53; chromatin; telomere; tumor suppressor
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Year: 2015 PMID: 26658110 PMCID: PMC4718461 DOI: 10.15252/embj.201490880
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598