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Transcription-replication coordination revealed in single live cells
The coexistence of DNA replication and transcription during S-phase requires their tight coordination to prevent harmful conflicts. While extensive research revealed important mechanisms for minimizing these conflicts and their consequences, little is known regarding how the replication and transcri...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887460/ https://www.ncbi.nlm.nih.gov/pubmed/35137218 http://dx.doi.org/10.1093/nar/gkac069 |
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author | Tsirkas, Ioannis Dovrat, Daniel Thangaraj, Manikandan Brouwer, Ineke Cohen, Amit Paleiov, Zohar Meijler, Michael M Lenstra, Tineke Aharoni, Amir |
author_facet | Tsirkas, Ioannis Dovrat, Daniel Thangaraj, Manikandan Brouwer, Ineke Cohen, Amit Paleiov, Zohar Meijler, Michael M Lenstra, Tineke Aharoni, Amir |
author_sort | Tsirkas, Ioannis |
collection | PubMed |
description | The coexistence of DNA replication and transcription during S-phase requires their tight coordination to prevent harmful conflicts. While extensive research revealed important mechanisms for minimizing these conflicts and their consequences, little is known regarding how the replication and transcription machinery are coordinated in real-time. Here, we developed a live-cell imaging approach for the real-time monitoring of replisome progression and transcription dynamics during a transcription-replication encounter. We found a wave of partial transcriptional repression ahead of the moving replication fork, which may contribute to efficient fork progression through the transcribed gene. Real-time detection of conflicts revealed their negative impact on both processes, leading to fork stalling or slowdown as well as lower transcription levels during gene replication, with different trade-offs observed in defined subpopulations of cells. Our real-time measurements of transcription-replication encounters demonstrate how these processes can proceed simultaneously while maintaining genomic stability, and how conflicts can arise when coordination is impaired. |
format | Online Article Text |
id | pubmed-8887460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88874602022-03-02 Transcription-replication coordination revealed in single live cells Tsirkas, Ioannis Dovrat, Daniel Thangaraj, Manikandan Brouwer, Ineke Cohen, Amit Paleiov, Zohar Meijler, Michael M Lenstra, Tineke Aharoni, Amir Nucleic Acids Res Molecular Biology The coexistence of DNA replication and transcription during S-phase requires their tight coordination to prevent harmful conflicts. While extensive research revealed important mechanisms for minimizing these conflicts and their consequences, little is known regarding how the replication and transcription machinery are coordinated in real-time. Here, we developed a live-cell imaging approach for the real-time monitoring of replisome progression and transcription dynamics during a transcription-replication encounter. We found a wave of partial transcriptional repression ahead of the moving replication fork, which may contribute to efficient fork progression through the transcribed gene. Real-time detection of conflicts revealed their negative impact on both processes, leading to fork stalling or slowdown as well as lower transcription levels during gene replication, with different trade-offs observed in defined subpopulations of cells. Our real-time measurements of transcription-replication encounters demonstrate how these processes can proceed simultaneously while maintaining genomic stability, and how conflicts can arise when coordination is impaired. Oxford University Press 2022-02-08 /pmc/articles/PMC8887460/ /pubmed/35137218 http://dx.doi.org/10.1093/nar/gkac069 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Molecular Biology Tsirkas, Ioannis Dovrat, Daniel Thangaraj, Manikandan Brouwer, Ineke Cohen, Amit Paleiov, Zohar Meijler, Michael M Lenstra, Tineke Aharoni, Amir Transcription-replication coordination revealed in single live cells |
title | Transcription-replication coordination revealed in single live cells |
title_full | Transcription-replication coordination revealed in single live cells |
title_fullStr | Transcription-replication coordination revealed in single live cells |
title_full_unstemmed | Transcription-replication coordination revealed in single live cells |
title_short | Transcription-replication coordination revealed in single live cells |
title_sort | transcription-replication coordination revealed in single live cells |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887460/ https://www.ncbi.nlm.nih.gov/pubmed/35137218 http://dx.doi.org/10.1093/nar/gkac069 |
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