Increased global transcription activity as a mechanism of replication stress in cancer
Cancer cells proliferate at high rates and incur replication stress. Here, the authors show that this can be the consequence of oncogene-induced higher transcriptional activity, which, through increased RNA synthesis and R-loop accumulation, results in replication fork slowing and DNA damage.
Enregistré dans:
Auteurs principaux: | Panagiotis Kotsantis, Lara Marques Silva, Sarah Irmscher, Rebecca M. Jones, Lisa Folkes, Natalia Gromak, Eva Petermann |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2016
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/11549dd2c7d8445a96d11f1f28cfaa77 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Hypoxia-induced SETX links replication stress with the unfolded protein response
par: Shaliny Ramachandran, et autres
Publié: (2021) -
H3K4 methylation at active genes mitigates transcription-replication conflicts during replication stress
par: Shin Yen Chong, et autres
Publié: (2020) -
Topoisomerase 1 prevents replication stress at R-loop-enriched transcription termination sites
par: Alexy Promonet, et autres
Publié: (2020) -
P-body proteins regulate transcriptional rewiring to promote DNA replication stress resistance
par: Raphael Loll-Krippleber, et autres
Publié: (2017) -
Elucidating the regulatory mechanism of Swi1 prion in global transcription and stress responses
par: Zhiqiang Du, et autres
Publié: (2020)