Author
Listed:
- Alexy Promonet
(Equipe labélisée Ligue contre le Cancer)
- Ismaël Padioleau
(Equipe labélisée Ligue contre le Cancer
Institut Gustave Roussy)
- Yaqun Liu
(Sorbonne Université)
- Lionel Sanz
(University of California)
- Anna Biernacka
(University of Warsaw)
- Anne-Lyne Schmitz
(Equipe labélisée Ligue contre le Cancer)
- Magdalena Skrzypczak
(University of Warsaw)
- Amélie Sarrazin
(CNRS et Université de Montpellier)
- Clément Mettling
(CNRS et Université de Montpellier)
- Maga Rowicka
(University of Texas Medical Branch at Galveston)
- Krzysztof Ginalski
(University of Warsaw)
- Frédéric Chedin
(University of California)
- Chun-Long Chen
(Sorbonne Université)
- Yea-Lih Lin
(Equipe labélisée Ligue contre le Cancer)
- Philippe Pasero
(Equipe labélisée Ligue contre le Cancer)
Abstract
R-loops have both positive and negative impacts on chromosome functions. To identify toxic R-loops in the human genome, here, we map RNA:DNA hybrids, replication stress markers and DNA double-strand breaks (DSBs) in cells depleted for Topoisomerase I (Top1), an enzyme that relaxes DNA supercoiling and prevents R-loop formation. RNA:DNA hybrids are found at both promoters (TSS) and terminators (TTS) of highly expressed genes. In contrast, the phosphorylation of RPA by ATR is only detected at TTS, which are preferentially replicated in a head-on orientation relative to the direction of transcription. In Top1-depleted cells, DSBs also accumulate at TTS, leading to persistent checkpoint activation, spreading of γ-H2AX on chromatin and global replication fork slowdown. These data indicate that fork pausing at the TTS of highly expressed genes containing R-loops prevents head-on conflicts between replication and transcription and maintains genome integrity in a Top1-dependent manner.
Suggested Citation
Alexy Promonet & Ismaël Padioleau & Yaqun Liu & Lionel Sanz & Anna Biernacka & Anne-Lyne Schmitz & Magdalena Skrzypczak & Amélie Sarrazin & Clément Mettling & Maga Rowicka & Krzysztof Ginalski & Frédé, 2020.
"Topoisomerase 1 prevents replication stress at R-loop-enriched transcription termination sites,"
Nature Communications, Nature, vol. 11(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17858-2
DOI: 10.1038/s41467-020-17858-2
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17858-2. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.