Nafiseh Chalabi Hagkarim
Disruption of the Mammalian Ccr4–Not Complex Contributes to Transcription-Mediated Genome Instability
Hagkarim, Nafiseh Chalabi; Hajkarim, Morteza Chalabi; Suzuki, Toru; Fujiwara, Toshinobu; Winkler, G. Sebastiaan; Stewart, Grant S.; Grand, Roger J.
Authors
Morteza Chalabi Hajkarim
Toru Suzuki
Toshinobu Fujiwara
Dr SEBASTIAAN WINKLER SEBASTIAAN.WINKLER@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Grant S. Stewart
Roger J. Grand
Contributors
Majid Momeny
Editor
Vishnu Suresh Babu
Editor
Avisek Majumder
Editor
Abstract
The mammalian Ccr4–Not complex, carbon catabolite repression 4 (Ccr4)-negative on TATA-less (Not), is a large, highly conserved, multifunctional assembly of proteins that acts at different cellular levels to regulate gene expression. It is involved in the control of the cell cycle, chromatin modification, activation and inhibition of transcription initiation, control of transcription elongation, RNA export, and nuclear RNA surveillance; the Ccr4–Not complex also plays a central role in the regulation of mRNA decay. Growing evidence suggests that gene transcription has a vital role in shaping the landscape of genome replication and is also a potent source of replication stress and genome instability. Here, we have examined the effects of the inactivation of the Ccr4–Not complex, via the depletion of the scaffold subunit CNOT1, on DNA replication and genome integrity in mammalian cells. In CNOT1-depleted cells, the elevated expression of the general transcription factor TATA-box binding protein (TBP) leads to increased RNA synthesis, which, together with R-loop accumulation, results in replication fork slowing, DNA damage, and senescence. Furthermore, we have shown that the stability of TBP mRNA increases in the absence of CNOT1, which may explain its elevated protein expression in CNOT1-depleted cells. Finally, we have shown the activation of mitogen-activated protein kinase signalling as evidenced by ERK1/2 phosphorylation in the absence of CNOT1, which may be responsible for the observed cell cycle arrest at the border of G1/S.
Citation
Hagkarim, N. C., Hajkarim, M. C., Suzuki, T., Fujiwara, T., Winkler, G. S., Stewart, G. S., & Grand, R. J. (2023). Disruption of the Mammalian Ccr4–Not Complex Contributes to Transcription-Mediated Genome Instability. Cells, 12(14), Article 1868. https://doi.org/10.3390/cells12141868
Journal Article Type | Article |
---|---|
Acceptance Date | Jul 5, 2023 |
Online Publication Date | Jul 17, 2023 |
Publication Date | 2023-07 |
Deposit Date | Aug 16, 2023 |
Publicly Available Date | Aug 16, 2023 |
Journal | Cells |
Electronic ISSN | 2073-4409 |
Publisher | MDPI |
Peer Reviewed | Peer Reviewed |
Volume | 12 |
Issue | 14 |
Article Number | 1868 |
DOI | https://doi.org/10.3390/cells12141868 |
Keywords | CNOT8, transcription, genome instability, DNA repair, CNOT complex, CNOT7, CNOT1 |
Public URL | https://nottingham-repository.worktribe.com/output/24138918 |
Publisher URL | https://www.mdpi.com/2073-4409/12/14/1868 |
Files
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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