Tutton Stephen, Azzam Greggory A, Stong Nicholas, Vladimirova Olga, Wiedmer Andreas, Monteith Jessica A, Beishline Kate, Wang Zhuo, Deng Zhong, Riethman Harold, McMahon Steven B, Murphy Maureen, Lieberman Paul M
The Wistar Institute, Philadelphia, PA, USA.
Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.
EMBO J. 2016 Jan 18;35(2):193-207. doi: 10.15252/embj.201490880. Epub 2015 Dec 12.
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.
端粒和肿瘤抑制蛋白TP53(p53)在基因组保护中发挥作用,但p53在端粒上的直接作用尚未见报道。在此,我们在人类亚端粒区域鉴定出非典型p53结合位点,这些位点可抑制端粒重复DNA处DNA损伤的积累。这些非典型亚端粒p53结合位点具有类似转录增强子的功能,包括局部组蛋白H3K9和H3K27乙酰化增加以及对亚端粒转录本(包括含端粒重复序列的RNA,即TERRA)的刺激作用。p53可抑制端粒相关γH2AX的形成,并在DNA损伤应激时防止端粒DNA降解。我们的研究结果表明,p53为人类端粒以及其他脆弱的基因组位点提供了直接的染色质相关保护。我们提出,p53相关的染色质修饰可增强局部DNA修复或保护作用,从而提供一种此前未被认识到的p53的肿瘤抑制功能。
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