Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783511946590420992 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7102957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yangguang polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions AT chenyibin polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions AT wujiaxue polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions AT chenshihhsun polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions AT liuxiuhua polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions AT singhanupkumar polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions AT yuxiaochun polyadpribosylationmediatesearlyphasehistoneevictionatdnalesions |