Cargando…
Coupling chromatin structure and dynamics by live super-resolution imaging
Chromatin conformation regulates gene expression and thus, constant remodeling of chromatin structure is essential to guarantee proper cell function. To gain insight into the spatiotemporal organization of the genome, we use high-density photoactivated localization microscopy and deep learning to ob...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458449/ https://www.ncbi.nlm.nih.gov/pubmed/32937447 http://dx.doi.org/10.1126/sciadv.aaz2196 |
_version_ | 1783576199544438784 |
---|---|
author | Barth, R. Bystricky, K. Shaban, H. A. |
author_facet | Barth, R. Bystricky, K. Shaban, H. A. |
author_sort | Barth, R. |
collection | PubMed |
description | Chromatin conformation regulates gene expression and thus, constant remodeling of chromatin structure is essential to guarantee proper cell function. To gain insight into the spatiotemporal organization of the genome, we use high-density photoactivated localization microscopy and deep learning to obtain temporally resolved super-resolution images of chromatin in living cells. In combination with high-resolution dense motion reconstruction, we find elongated ~45- to 90-nm-wide chromatin “blobs.” A computational chromatin model suggests that these blobs are dynamically associating chromatin fragments in close physical and genomic proximity and adopt topologically associated domain–like interactions in the time-average limit. Experimentally, we found that chromatin exhibits a spatiotemporal correlation over ~4 μm in space and tens of seconds in time, while chromatin dynamics are correlated over ~6 μm and last 40 s. Notably, chromatin structure and dynamics are closely related, which may constitute a mechanism to grant access to regions with high local chromatin concentration. |
format | Online Article Text |
id | pubmed-7458449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74584492020-09-16 Coupling chromatin structure and dynamics by live super-resolution imaging Barth, R. Bystricky, K. Shaban, H. A. Sci Adv Research Articles Chromatin conformation regulates gene expression and thus, constant remodeling of chromatin structure is essential to guarantee proper cell function. To gain insight into the spatiotemporal organization of the genome, we use high-density photoactivated localization microscopy and deep learning to obtain temporally resolved super-resolution images of chromatin in living cells. In combination with high-resolution dense motion reconstruction, we find elongated ~45- to 90-nm-wide chromatin “blobs.” A computational chromatin model suggests that these blobs are dynamically associating chromatin fragments in close physical and genomic proximity and adopt topologically associated domain–like interactions in the time-average limit. Experimentally, we found that chromatin exhibits a spatiotemporal correlation over ~4 μm in space and tens of seconds in time, while chromatin dynamics are correlated over ~6 μm and last 40 s. Notably, chromatin structure and dynamics are closely related, which may constitute a mechanism to grant access to regions with high local chromatin concentration. American Association for the Advancement of Science 2020-07-01 /pmc/articles/PMC7458449/ /pubmed/32937447 http://dx.doi.org/10.1126/sciadv.aaz2196 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Barth, R. Bystricky, K. Shaban, H. A. Coupling chromatin structure and dynamics by live super-resolution imaging |
title | Coupling chromatin structure and dynamics by live super-resolution imaging |
title_full | Coupling chromatin structure and dynamics by live super-resolution imaging |
title_fullStr | Coupling chromatin structure and dynamics by live super-resolution imaging |
title_full_unstemmed | Coupling chromatin structure and dynamics by live super-resolution imaging |
title_short | Coupling chromatin structure and dynamics by live super-resolution imaging |
title_sort | coupling chromatin structure and dynamics by live super-resolution imaging |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458449/ https://www.ncbi.nlm.nih.gov/pubmed/32937447 http://dx.doi.org/10.1126/sciadv.aaz2196 |
work_keys_str_mv | AT barthr couplingchromatinstructureanddynamicsbylivesuperresolutionimaging AT bystrickyk couplingchromatinstructureanddynamicsbylivesuperresolutionimaging AT shabanha couplingchromatinstructureanddynamicsbylivesuperresolutionimaging |