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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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