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The response to DNA damage in heterochromatin domains
Eukaryotic genomes are organized into chromatin, divided into structurally and functionally distinct euchromatin and heterochromatin compartments. The high level of compaction and the abundance of repeated sequences in heterochromatin pose multiple challenges for the maintenance of genome stability....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440646/ https://www.ncbi.nlm.nih.gov/pubmed/29594515 http://dx.doi.org/10.1007/s00412-018-0669-6 |
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author | Fortuny, Anna Polo, Sophie E. |
author_facet | Fortuny, Anna Polo, Sophie E. |
author_sort | Fortuny, Anna |
collection | PubMed |
description | Eukaryotic genomes are organized into chromatin, divided into structurally and functionally distinct euchromatin and heterochromatin compartments. The high level of compaction and the abundance of repeated sequences in heterochromatin pose multiple challenges for the maintenance of genome stability. Cells have evolved sophisticated and highly controlled mechanisms to overcome these constraints. Here, we summarize recent findings on how the heterochromatic state influences DNA damage formation, signaling and repair. By focusing on distinct heterochromatin domains in different eukaryotic species, we highlight heterochromatin contribution to the compartmentalization of DNA damage repair in the cell nucleus and to repair pathway choice. We also describe the diverse chromatin alterations associated with the DNA damage response in heterochromatin domains and present our current understanding of their regulatory mechanisms. Finally, we discuss the biological significance and the evolutionary conservation of these processes. |
format | Online Article Text |
id | pubmed-6440646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64406462019-03-29 The response to DNA damage in heterochromatin domains Fortuny, Anna Polo, Sophie E. Chromosoma Article Eukaryotic genomes are organized into chromatin, divided into structurally and functionally distinct euchromatin and heterochromatin compartments. The high level of compaction and the abundance of repeated sequences in heterochromatin pose multiple challenges for the maintenance of genome stability. Cells have evolved sophisticated and highly controlled mechanisms to overcome these constraints. Here, we summarize recent findings on how the heterochromatic state influences DNA damage formation, signaling and repair. By focusing on distinct heterochromatin domains in different eukaryotic species, we highlight heterochromatin contribution to the compartmentalization of DNA damage repair in the cell nucleus and to repair pathway choice. We also describe the diverse chromatin alterations associated with the DNA damage response in heterochromatin domains and present our current understanding of their regulatory mechanisms. Finally, we discuss the biological significance and the evolutionary conservation of these processes. 2018-03-29 2018-09 /pmc/articles/PMC6440646/ /pubmed/29594515 http://dx.doi.org/10.1007/s00412-018-0669-6 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Fortuny, Anna Polo, Sophie E. The response to DNA damage in heterochromatin domains |
title | The response to DNA damage in heterochromatin domains |
title_full | The response to DNA damage in heterochromatin domains |
title_fullStr | The response to DNA damage in heterochromatin domains |
title_full_unstemmed | The response to DNA damage in heterochromatin domains |
title_short | The response to DNA damage in heterochromatin domains |
title_sort | response to dna damage in heterochromatin domains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440646/ https://www.ncbi.nlm.nih.gov/pubmed/29594515 http://dx.doi.org/10.1007/s00412-018-0669-6 |
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