Chromatin Remodeling at DNA Double-Strand Breaks
Open accessAbstract
DNA double-strand breaks (DSBs) can arise from multiple sources, including exposure to ionizing radiation. The repair of DSBs involves both posttranslational modification of nucleosomes and concentration of DNA-repair proteins at the site of damage. Consequently, nucleosome packing and chromatin architecture surrounding the DSB may limit the ability of the DNA-damage response to access and repair the break. Here, we review early chromatin-based events that promote the formation of open, relaxed chromatin structures at DSBs and that allow the DNA-repair machinery to access the spatially confined region surrounding the DSB, thereby facilitating mammalian DSB repair.
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This structure then allows further chromatin processing to create open, flexible chromatin structures, which are essential for DSB repair.
“This structure then allows further chromatin processing to create open, flexible chromatin structures, which are essential for DSB repair (11).”
From DNA double-strand breaks promote methylation of histone H3 on lysine 9 and transient formation of repressive chromatin (2014) · cites this paper as [11]
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- Authors
- Price, B. D., & D’Andrea, A. D.
- Affiliations
- Harvard University (US)
- Corresponding author
- D’Andrea, Alan D.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2013-03
- Volume
- 152
- Issue
- 6
- Pages
- 1344-1354
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC3670600
- OpenAlex
- W1969503475
- Cited by
- 588
- References
- 104
- Citations by year
- 2026: 24 · 2025: 25 · 2024: 30 · 2023: 35 · 2022: 42 · 2021: 39 · 2020: 49 · 2019: 48 · 2018: 53 · 2017: 58 · 2016: 44 · 2015: 52 · 2014: 62 · 2013: 25 · 2012: 1
- FWCI
- 5.62
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute (R37HL052725)
- National Cancer Institute (R01CA177884, R01CA064585, R01CA093602, CA64585, CA93602)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK043889)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- DNA double-strand breaks, chromatin remodeling, DNA repair, ionizing radiation, chromatin structure, DNA damage response, nucleosome packing
- MeSH terms
- Animals, DNA Repair, Histones, Humans, Neoplasms, Chromatin Assembly and Disassembly, Genomic Instability, DNA Breaks, Double-Stranded
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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