Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

0

Subtelomeric p53 Binding Prevents Accumulation of DNA Damage at Human Telomeres


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. p53 binding was analyzed by ChIP-Seq in HCT116 cells treated with camptothecin or untreated control.

ORGANISM(S): Homo sapiens

SUBMITTER: Priyankara Wickramasinghe 

PROVIDER: E-GEOD-75528 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

altmetric image

Publications


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 subtelome  ...[more]

Similar Datasets

2016-01-07 | GSE75528 | GEO
2022-08-24 | GSE193623 | GEO
2020-07-17 | MSV000085772 | MassIVE
2013-08-01 | E-GEOD-44599 | biostudies-arrayexpress
2013-02-28 | E-GEOD-36792 | biostudies-arrayexpress
2017-05-11 | PXD006074 | Pride
2020-11-20 | PXD021085 | Pride
2013-08-01 | GSE44599 | GEO
2022-08-10 | GSE190759 | GEO
2022-08-09 | GSE195972 | GEO