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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...

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Detalles Bibliográficos
Autores principales: Han, Deqiang, Chen, Qian, Shi, Jiazhong, Zhang, Feng, Yu, Xiaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
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).
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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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