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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...

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Autores principales: Tsirkas, Ioannis, Dovrat, Daniel, Thangaraj, Manikandan, Brouwer, Ineke, Cohen, Amit, Paleiov, Zohar, Meijler, Michael M, Lenstra, Tineke, Aharoni, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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