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Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region

In contrast to the well-studied condensation and folding of chromosomes during mitosis, their dynamics during interphase are less understood. We deployed a CRISPR-based DNA imaging system to track the dynamics of genomic loci situated kilobases to megabases apart on a single chromosome. Two distinct...

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Autores principales: Ma, Hanhui, Tu, Li-Chun, Chung, Yu-Chieh, Naseri, Ardalan, Grunwald, David, Zhang, Shaojie, Pederson, Thoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504907/
https://www.ncbi.nlm.nih.gov/pubmed/30846483
http://dx.doi.org/10.1083/jcb.201807162
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author Ma, Hanhui
Tu, Li-Chun
Chung, Yu-Chieh
Naseri, Ardalan
Grunwald, David
Zhang, Shaojie
Pederson, Thoru
author_facet Ma, Hanhui
Tu, Li-Chun
Chung, Yu-Chieh
Naseri, Ardalan
Grunwald, David
Zhang, Shaojie
Pederson, Thoru
author_sort Ma, Hanhui
collection PubMed
description In contrast to the well-studied condensation and folding of chromosomes during mitosis, their dynamics during interphase are less understood. We deployed a CRISPR-based DNA imaging system to track the dynamics of genomic loci situated kilobases to megabases apart on a single chromosome. Two distinct modes of dynamics were resolved: local movements as well as ones that might reflect translational movements of the entire domain within the nucleoplasmic space. The magnitude of both of these modes of movements increased from early to late G1, whereas the translational movements were reduced in early S phase. The local fluctuations decreased slightly in early S and more markedly in mid-late S. These newly observed movements and their cell cycle dependence suggest the existence of a hitherto unrecognized compaction–relaxation dynamic of the interphase chromosome fiber, operating concurrently with changes in the extent of overall movements of loci in the 4D genome.
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spelling pubmed-65049072019-11-06 Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region Ma, Hanhui Tu, Li-Chun Chung, Yu-Chieh Naseri, Ardalan Grunwald, David Zhang, Shaojie Pederson, Thoru J Cell Biol Research Articles In contrast to the well-studied condensation and folding of chromosomes during mitosis, their dynamics during interphase are less understood. We deployed a CRISPR-based DNA imaging system to track the dynamics of genomic loci situated kilobases to megabases apart on a single chromosome. Two distinct modes of dynamics were resolved: local movements as well as ones that might reflect translational movements of the entire domain within the nucleoplasmic space. The magnitude of both of these modes of movements increased from early to late G1, whereas the translational movements were reduced in early S phase. The local fluctuations decreased slightly in early S and more markedly in mid-late S. These newly observed movements and their cell cycle dependence suggest the existence of a hitherto unrecognized compaction–relaxation dynamic of the interphase chromosome fiber, operating concurrently with changes in the extent of overall movements of loci in the 4D genome. Rockefeller University Press 2019-05-06 2019-03-07 /pmc/articles/PMC6504907/ /pubmed/30846483 http://dx.doi.org/10.1083/jcb.201807162 Text en © 2019 Ma et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Ma, Hanhui
Tu, Li-Chun
Chung, Yu-Chieh
Naseri, Ardalan
Grunwald, David
Zhang, Shaojie
Pederson, Thoru
Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
title Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
title_full Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
title_fullStr Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
title_full_unstemmed Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
title_short Cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
title_sort cell cycle– and genomic distance–dependent dynamics of a discrete chromosomal region
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504907/
https://www.ncbi.nlm.nih.gov/pubmed/30846483
http://dx.doi.org/10.1083/jcb.201807162
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