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Radiation-induced DNA damage and repair effects on 3D genome organization
The three-dimensional structure of chromosomes plays an important role in gene expression regulation and also influences the repair of radiation-induced DNA damage. Genomic aberrations that disrupt chromosome spatial domains can lead to diseases including cancer, but how the 3D genome structure resp...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710719/ https://www.ncbi.nlm.nih.gov/pubmed/33268790 http://dx.doi.org/10.1038/s41467-020-20047-w |
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author | Sanders, Jacob T. Freeman, Trevor F. Xu, Yang Golloshi, Rosela Stallard, Mary A. Hill, Ashtyn M. San Martin, Rebeca Balajee, Adayabalam S. McCord, Rachel Patton |
author_facet | Sanders, Jacob T. Freeman, Trevor F. Xu, Yang Golloshi, Rosela Stallard, Mary A. Hill, Ashtyn M. San Martin, Rebeca Balajee, Adayabalam S. McCord, Rachel Patton |
author_sort | Sanders, Jacob T. |
collection | PubMed |
description | The three-dimensional structure of chromosomes plays an important role in gene expression regulation and also influences the repair of radiation-induced DNA damage. Genomic aberrations that disrupt chromosome spatial domains can lead to diseases including cancer, but how the 3D genome structure responds to DNA damage is poorly understood. Here, we investigate the impact of DNA damage response and repair on 3D genome folding using Hi-C experiments on wild type cells and ataxia telangiectasia mutated (ATM) patient cells. We irradiate fibroblasts, lymphoblasts, and ATM-deficient fibroblasts with 5 Gy X-rays and perform Hi-C at 30 minutes, 24 hours, or 5 days after irradiation. We observe that 3D genome changes after irradiation are cell type-specific, with lymphoblastoid cells generally showing more contact changes than irradiated fibroblasts. However, all tested repair-proficient cell types exhibit an increased segregation of topologically associating domains (TADs). This TAD boundary strengthening after irradiation is not observed in ATM deficient fibroblasts and may indicate the presence of a mechanism to protect 3D genome structure integrity during DNA damage repair. |
format | Online Article Text |
id | pubmed-7710719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77107192020-12-03 Radiation-induced DNA damage and repair effects on 3D genome organization Sanders, Jacob T. Freeman, Trevor F. Xu, Yang Golloshi, Rosela Stallard, Mary A. Hill, Ashtyn M. San Martin, Rebeca Balajee, Adayabalam S. McCord, Rachel Patton Nat Commun Article The three-dimensional structure of chromosomes plays an important role in gene expression regulation and also influences the repair of radiation-induced DNA damage. Genomic aberrations that disrupt chromosome spatial domains can lead to diseases including cancer, but how the 3D genome structure responds to DNA damage is poorly understood. Here, we investigate the impact of DNA damage response and repair on 3D genome folding using Hi-C experiments on wild type cells and ataxia telangiectasia mutated (ATM) patient cells. We irradiate fibroblasts, lymphoblasts, and ATM-deficient fibroblasts with 5 Gy X-rays and perform Hi-C at 30 minutes, 24 hours, or 5 days after irradiation. We observe that 3D genome changes after irradiation are cell type-specific, with lymphoblastoid cells generally showing more contact changes than irradiated fibroblasts. However, all tested repair-proficient cell types exhibit an increased segregation of topologically associating domains (TADs). This TAD boundary strengthening after irradiation is not observed in ATM deficient fibroblasts and may indicate the presence of a mechanism to protect 3D genome structure integrity during DNA damage repair. Nature Publishing Group UK 2020-12-02 /pmc/articles/PMC7710719/ /pubmed/33268790 http://dx.doi.org/10.1038/s41467-020-20047-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sanders, Jacob T. Freeman, Trevor F. Xu, Yang Golloshi, Rosela Stallard, Mary A. Hill, Ashtyn M. San Martin, Rebeca Balajee, Adayabalam S. McCord, Rachel Patton Radiation-induced DNA damage and repair effects on 3D genome organization |
title | Radiation-induced DNA damage and repair effects on 3D genome organization |
title_full | Radiation-induced DNA damage and repair effects on 3D genome organization |
title_fullStr | Radiation-induced DNA damage and repair effects on 3D genome organization |
title_full_unstemmed | Radiation-induced DNA damage and repair effects on 3D genome organization |
title_short | Radiation-induced DNA damage and repair effects on 3D genome organization |
title_sort | radiation-induced dna damage and repair effects on 3d genome organization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710719/ https://www.ncbi.nlm.nih.gov/pubmed/33268790 http://dx.doi.org/10.1038/s41467-020-20047-w |
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