The fork protection complex generates DNA topological stress–induced DNA damage while ensuring full and faithful genome duplication

The fork protection complex (FPC), composed of Mrc1, Tof1, and Csm3, supports rapid and stable DNA replication. Here, we show that FPC activity also introduces DNA damage by increasing DNA topological stress during replication. Mrc1 action increases DNA topological stress during plasmid replication, while Mrc1 or Tof1 activity causes replication stress and DNA damage within topologically constrained regions. We show that the recruitment of Top1 to the fork by Tof1 suppresses the DNA damage generated in these loci. While FPC activity introduces some DNA damage due to increased topological stress, the FPC is also necessary to prevent DNA damage in long replicons across the genome, indicating that the FPC is required for complete and faithful genome duplication. We conclude that FPC regulation must balance ensuring full genome duplication through rapid replication with minimizing the consequential DNA topological stress-induced DNA damage caused by rapid replication through constrained regions.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2024-11-26
DOI
https://doi.org/10.1073/pnas.2413631121
Citations
1
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.23

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article

The fork protection complex generates DNA topological stress–induced DNA damage while ensuring full and faithful genome duplication

Jonathan Houseley, Jonathan Baxter, Alex Whale, Sahar Mansoubi et al.
1 citations
Proceedings of the National Academy of Sciences
DNA Repair Mechanisms
0.23
article

The fork protection complex generates DNA topological stress–induced DNA damage while ensuring full and faithful genome duplication

Jonathan Houseley, Jonathan Baxter, Alex Whale, Sahar Mansoubi, Andrea Keszthelyi
article en
1 citations

Abstract

The fork protection complex (FPC), composed of Mrc1, Tof1, and Csm3, supports rapid and stable DNA replication. Here, we show that FPC activity also introduces DNA damage by increasing DNA topological stress during replication. Mrc1 action increases DNA topological stress during plasmid replication, while Mrc1 or Tof1 activity causes replication stress and DNA damage within topologically constrained regions. We show that the recruitment of Top1 to the fork by Tof1 suppresses the DNA damage generated in these loci. While FPC activity introduces some DNA damage due to increased topological stress, the FPC is also necessary to prevent DNA damage in long replicons across the genome, indicating that the FPC is required for complete and faithful genome duplication. We conclude that FPC regulation must balance ensuring full genome duplication through rapid replication with minimizing the consequential DNA topological stress-induced DNA damage caused by rapid replication through constrained regions.

Proceedings of the National Academy of SciencesVol. 121(49)
Babraham Institute (GB), University of Sussex (GB), Islamic Azad University North Tehran Branch (IR)
Wellcome Trust, Directorate for Biological Sciences, Medical Research Council, Biotechnology and Biological Sciences Research Council
Life in Land
Openalex Percentile: Top 41%
DNA Repair Mechanisms
0.23
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