Cargando…
Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin
The three-dimensional arrangement of chromatin encodes regulatory traits important for nuclear processes such as transcription and replication. Chromatin topology is in part mediated by the architectural protein CCCTC-binding factor (CTCF) that binds to the boundaries of topologically associating do...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Biophysical Society
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444008/ https://www.ncbi.nlm.nih.gov/pubmed/28487148 http://dx.doi.org/10.1016/j.bpj.2017.04.018 |
_version_ | 1783238659206545408 |
---|---|
author | Agarwal, Harsha Reisser, Matthias Wortmann, Celina Gebhardt, J. Christof M. |
author_facet | Agarwal, Harsha Reisser, Matthias Wortmann, Celina Gebhardt, J. Christof M. |
author_sort | Agarwal, Harsha |
collection | PubMed |
description | The three-dimensional arrangement of chromatin encodes regulatory traits important for nuclear processes such as transcription and replication. Chromatin topology is in part mediated by the architectural protein CCCTC-binding factor (CTCF) that binds to the boundaries of topologically associating domains. Whereas sites of CTCF interactions are well characterized, little is known on how long CTCF binds to chromatin and how binding evolves during the cell cycle. We monitored CTCF-chromatin interactions by live cell single molecule tracking in different phases of the cell cycle. In G1-, S-, and G2-phases, a majority of CTCF molecules was bound transiently (∼0.2 s) to chromatin, whereas minor fractions were bound dynamically (∼4 s) or stably (>15 min). During mitosis, CTCF was mostly excluded from chromatin. Our data suggest that CTCF scans DNA in search for two different subsets of specific target sites and provide information on the timescales over which topologically associating domains might be restructured. During S-phase, dynamic and stable interactions decreased considerably compared to G1-phase, but were resumed in G2-phase, indicating that specific interactions need to be dissolved for replication to proceed. |
format | Online Article Text |
id | pubmed-5444008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Biophysical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-54440082018-05-23 Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin Agarwal, Harsha Reisser, Matthias Wortmann, Celina Gebhardt, J. Christof M. Biophys J Biophysical Letter The three-dimensional arrangement of chromatin encodes regulatory traits important for nuclear processes such as transcription and replication. Chromatin topology is in part mediated by the architectural protein CCCTC-binding factor (CTCF) that binds to the boundaries of topologically associating domains. Whereas sites of CTCF interactions are well characterized, little is known on how long CTCF binds to chromatin and how binding evolves during the cell cycle. We monitored CTCF-chromatin interactions by live cell single molecule tracking in different phases of the cell cycle. In G1-, S-, and G2-phases, a majority of CTCF molecules was bound transiently (∼0.2 s) to chromatin, whereas minor fractions were bound dynamically (∼4 s) or stably (>15 min). During mitosis, CTCF was mostly excluded from chromatin. Our data suggest that CTCF scans DNA in search for two different subsets of specific target sites and provide information on the timescales over which topologically associating domains might be restructured. During S-phase, dynamic and stable interactions decreased considerably compared to G1-phase, but were resumed in G2-phase, indicating that specific interactions need to be dissolved for replication to proceed. The Biophysical Society 2017-05-23 2017-05-06 /pmc/articles/PMC5444008/ /pubmed/28487148 http://dx.doi.org/10.1016/j.bpj.2017.04.018 Text en © 2017 Biophysical Society. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Biophysical Letter Agarwal, Harsha Reisser, Matthias Wortmann, Celina Gebhardt, J. Christof M. Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin |
title | Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin |
title_full | Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin |
title_fullStr | Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin |
title_full_unstemmed | Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin |
title_short | Direct Observation of Cell-Cycle-Dependent Interactions between CTCF and Chromatin |
title_sort | direct observation of cell-cycle-dependent interactions between ctcf and chromatin |
topic | Biophysical Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444008/ https://www.ncbi.nlm.nih.gov/pubmed/28487148 http://dx.doi.org/10.1016/j.bpj.2017.04.018 |
work_keys_str_mv | AT agarwalharsha directobservationofcellcycledependentinteractionsbetweenctcfandchromatin AT reissermatthias directobservationofcellcycledependentinteractionsbetweenctcfandchromatin AT wortmanncelina directobservationofcellcycledependentinteractionsbetweenctcfandchromatin AT gebhardtjchristofm directobservationofcellcycledependentinteractionsbetweenctcfandchromatin |