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Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions

Nucleosomal histones are barriers to the DNA repair process particularly at DNA double-strand breaks (DSBs). However, the molecular mechanism by which these histone barriers are removed from the sites of DNA damage remains elusive. Here, we have generated a single specific inducible DSB in the cells...

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Autores principales: Yang, Guang, Chen, Yibin, Wu, Jiaxue, Chen, Shih-Hsun, Liu, Xiuhua, Singh, Anup Kumar, Yu, Xiaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102957/
https://www.ncbi.nlm.nih.gov/pubmed/31965183
http://dx.doi.org/10.1093/nar/gkaa022
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author Yang, Guang
Chen, Yibin
Wu, Jiaxue
Chen, Shih-Hsun
Liu, Xiuhua
Singh, Anup Kumar
Yu, Xiaochun
author_facet Yang, Guang
Chen, Yibin
Wu, Jiaxue
Chen, Shih-Hsun
Liu, Xiuhua
Singh, Anup Kumar
Yu, Xiaochun
author_sort Yang, Guang
collection PubMed
description Nucleosomal histones are barriers to the DNA repair process particularly at DNA double-strand breaks (DSBs). However, the molecular mechanism by which these histone barriers are removed from the sites of DNA damage remains elusive. Here, we have generated a single specific inducible DSB in the cells and systematically examined the histone removal process at the DNA lesion. We found that histone removal occurred immediately following DNA damage and could extend up to a range of few kilobases from the lesion. To examine the molecular mechanism underlying DNA damage-induced histone removal, we screened histone modifications and found that histone ADP-ribosylation was associated with histone removal at DNA lesions. PARP inhibitor treatment suppressed the immediate histone eviction at DNA lesions. Moreover, we examined histone chaperones and found that the FACT complex recognized ADP-ribosylated histones and mediated the removal of histones in response to DNA damage. Taken together, our results reveal a pathway that regulates early histone barrier removal at DNA lesions. It may also explain the mechanism by which PARP inhibitor regulates early DNA damage repair.
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spelling pubmed-71029572020-04-02 Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions Yang, Guang Chen, Yibin Wu, Jiaxue Chen, Shih-Hsun Liu, Xiuhua Singh, Anup Kumar Yu, Xiaochun Nucleic Acids Res Genome Integrity, Repair and Replication Nucleosomal histones are barriers to the DNA repair process particularly at DNA double-strand breaks (DSBs). However, the molecular mechanism by which these histone barriers are removed from the sites of DNA damage remains elusive. Here, we have generated a single specific inducible DSB in the cells and systematically examined the histone removal process at the DNA lesion. We found that histone removal occurred immediately following DNA damage and could extend up to a range of few kilobases from the lesion. To examine the molecular mechanism underlying DNA damage-induced histone removal, we screened histone modifications and found that histone ADP-ribosylation was associated with histone removal at DNA lesions. PARP inhibitor treatment suppressed the immediate histone eviction at DNA lesions. Moreover, we examined histone chaperones and found that the FACT complex recognized ADP-ribosylated histones and mediated the removal of histones in response to DNA damage. Taken together, our results reveal a pathway that regulates early histone barrier removal at DNA lesions. It may also explain the mechanism by which PARP inhibitor regulates early DNA damage repair. Oxford University Press 2020-04-06 2020-01-22 /pmc/articles/PMC7102957/ /pubmed/31965183 http://dx.doi.org/10.1093/nar/gkaa022 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genome Integrity, Repair and Replication
Yang, Guang
Chen, Yibin
Wu, Jiaxue
Chen, Shih-Hsun
Liu, Xiuhua
Singh, Anup Kumar
Yu, Xiaochun
Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions
title Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions
title_full Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions
title_fullStr Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions
title_full_unstemmed Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions
title_short Poly(ADP-ribosyl)ation mediates early phase histone eviction at DNA lesions
title_sort poly(adp-ribosyl)ation mediates early phase histone eviction at dna lesions
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102957/
https://www.ncbi.nlm.nih.gov/pubmed/31965183
http://dx.doi.org/10.1093/nar/gkaa022
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