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Complex Chromatin Motions for DNA Repair

A number of studies across different model systems revealed that chromatin undergoes significant changes in dynamics in response to DNA damage. These include local motion changes at damage sites, increased nuclear exploration of both damaged and undamaged loci, and directed motions to new nuclear lo...

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Autores principales: Miné-Hattab, Judith, Chiolo, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481375/
https://www.ncbi.nlm.nih.gov/pubmed/33061931
http://dx.doi.org/10.3389/fgene.2020.00800
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author Miné-Hattab, Judith
Chiolo, Irene
author_facet Miné-Hattab, Judith
Chiolo, Irene
author_sort Miné-Hattab, Judith
collection PubMed
description A number of studies across different model systems revealed that chromatin undergoes significant changes in dynamics in response to DNA damage. These include local motion changes at damage sites, increased nuclear exploration of both damaged and undamaged loci, and directed motions to new nuclear locations associated with certain repair pathways. These studies also revealed the need for new analytical methods to identify directed motions in a context of mixed trajectories, and the importance of investigating nuclear dynamics over different time scales to identify diffusion regimes. Here we provide an overview of the current understanding of this field, including imaging and analytical methods developed to investigate nuclear dynamics in different contexts. These dynamics are essential for genome integrity. Identifying the molecular mechanisms responsible for these movements is key to understanding how their misregulation contributes to cancer and other genome instability disorders.
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spelling pubmed-74813752020-10-13 Complex Chromatin Motions for DNA Repair Miné-Hattab, Judith Chiolo, Irene Front Genet Genetics A number of studies across different model systems revealed that chromatin undergoes significant changes in dynamics in response to DNA damage. These include local motion changes at damage sites, increased nuclear exploration of both damaged and undamaged loci, and directed motions to new nuclear locations associated with certain repair pathways. These studies also revealed the need for new analytical methods to identify directed motions in a context of mixed trajectories, and the importance of investigating nuclear dynamics over different time scales to identify diffusion regimes. Here we provide an overview of the current understanding of this field, including imaging and analytical methods developed to investigate nuclear dynamics in different contexts. These dynamics are essential for genome integrity. Identifying the molecular mechanisms responsible for these movements is key to understanding how their misregulation contributes to cancer and other genome instability disorders. Frontiers Media S.A. 2020-08-27 /pmc/articles/PMC7481375/ /pubmed/33061931 http://dx.doi.org/10.3389/fgene.2020.00800 Text en Copyright © 2020 Miné-Hattab and Chiolo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Miné-Hattab, Judith
Chiolo, Irene
Complex Chromatin Motions for DNA Repair
title Complex Chromatin Motions for DNA Repair
title_full Complex Chromatin Motions for DNA Repair
title_fullStr Complex Chromatin Motions for DNA Repair
title_full_unstemmed Complex Chromatin Motions for DNA Repair
title_short Complex Chromatin Motions for DNA Repair
title_sort complex chromatin motions for dna repair
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481375/
https://www.ncbi.nlm.nih.gov/pubmed/33061931
http://dx.doi.org/10.3389/fgene.2020.00800
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