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CTCF participates in DNA damage response via poly(ADP-ribosyl)ation
CCCTC-binding factor (CTCF) plays an essential role in regulating the structure of chromatin by binding DNA strands for defining the boundary between active and heterochromatic DNA. However, the role of CTCF in DNA damage response remains elusive. Here, we show that CTCF is quickly recruited to the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337984/ https://www.ncbi.nlm.nih.gov/pubmed/28262757 http://dx.doi.org/10.1038/srep43530 |
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author | Han, Deqiang Chen, Qian Shi, Jiazhong Zhang, Feng Yu, Xiaochun |
author_facet | Han, Deqiang Chen, Qian Shi, Jiazhong Zhang, Feng Yu, Xiaochun |
author_sort | Han, Deqiang |
collection | PubMed |
description | CCCTC-binding factor (CTCF) plays an essential role in regulating the structure of chromatin by binding DNA strands for defining the boundary between active and heterochromatic DNA. However, the role of CTCF in DNA damage response remains elusive. Here, we show that CTCF is quickly recruited to the sites of DNA damage. The fast recruitment is mediated by the zinc finger domain and poly (ADP-ribose) (PAR). Further analyses show that only three zinc finger motifs are essential for PAR recognition. Moreover, CTCF-deficient cells are hypersensitive to genotoxic stress such as ionizing radiation (IR). Taken together, these results suggest that CTCF participate in DNA damage response via poly(ADP-ribosylation). |
format | Online Article Text |
id | pubmed-5337984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53379842017-03-08 CTCF participates in DNA damage response via poly(ADP-ribosyl)ation Han, Deqiang Chen, Qian Shi, Jiazhong Zhang, Feng Yu, Xiaochun Sci Rep Article CCCTC-binding factor (CTCF) plays an essential role in regulating the structure of chromatin by binding DNA strands for defining the boundary between active and heterochromatic DNA. However, the role of CTCF in DNA damage response remains elusive. Here, we show that CTCF is quickly recruited to the sites of DNA damage. The fast recruitment is mediated by the zinc finger domain and poly (ADP-ribose) (PAR). Further analyses show that only three zinc finger motifs are essential for PAR recognition. Moreover, CTCF-deficient cells are hypersensitive to genotoxic stress such as ionizing radiation (IR). Taken together, these results suggest that CTCF participate in DNA damage response via poly(ADP-ribosylation). Nature Publishing Group 2017-03-06 /pmc/articles/PMC5337984/ /pubmed/28262757 http://dx.doi.org/10.1038/srep43530 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Han, Deqiang Chen, Qian Shi, Jiazhong Zhang, Feng Yu, Xiaochun CTCF participates in DNA damage response via poly(ADP-ribosyl)ation |
title | CTCF participates in DNA damage response via poly(ADP-ribosyl)ation |
title_full | CTCF participates in DNA damage response via poly(ADP-ribosyl)ation |
title_fullStr | CTCF participates in DNA damage response via poly(ADP-ribosyl)ation |
title_full_unstemmed | CTCF participates in DNA damage response via poly(ADP-ribosyl)ation |
title_short | CTCF participates in DNA damage response via poly(ADP-ribosyl)ation |
title_sort | ctcf participates in dna damage response via poly(adp-ribosyl)ation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5337984/ https://www.ncbi.nlm.nih.gov/pubmed/28262757 http://dx.doi.org/10.1038/srep43530 |
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