| Title: |
Claspin haploinsufficiency leads to defects in fertility, hyperplasia and an increased oncogenic potential |
| Authors: |
Madgwick S; Luli S; Sellier H; Butterworth JA; Leslie J; Moore AJ; Corbin EK; Yemm AI; Chiremba RT; Tiniakos D; Oakley F; Perkins ND; Hunter JE |
| Source: |
Biochemical Journal, 14 October 2022 |
| Publisher Information: |
Portland Press |
| Publication Year: |
2022 |
| Collection: |
Newcastle University Library ePrints Service |
| Description: |
© 2022 The Author(s).Claspin is an adaptor protein required for ATR-dependent phosphorylation of CHK1 during S-phase following DNA replication stress. Claspin expression is highly variable in cancer, with low levels frequently correlating with poor patient survival. To learn more about the biological consequences of reduced Claspin expression and its effects on tumorigenesis, we investigated mice with a heterozygous knockout of the Clspn gene. Claspin haploinsufficiency resulted in reduced female fertility and a maternally inherited defect in oocyte meiosis I cell cycle progression. Furthermore, aged Clspn+/- mice developed spontaneous lymphoid hyperplasia and increased susceptibility to non-alcoholic fatty liver disease. Importantly, we demonstrate a tumour suppressor role for Claspin. Reduced Claspin levels result in increased liver damage and tumourigenesis in the DEN model of hepatocellular carcinoma. These data reveal that Clspn haploinsufficiency has widespread unanticipated biological effects and establishes the importance of Claspin as a regulatory node controlling tumorigenesis and multiple disease aetiologies. |
| Document Type: |
article in journal/newspaper |
| File Description: |
application/pdf |
| Language: |
unknown |
| Relation: |
https://eprints.ncl.ac.uk/287338; https://eprints.ncl.ac.uk/fulltext.aspx?url=287338/986CE218-3E43-4BCC-83BB-F73F79ED34AD.pdf&pub_id=287338 |
| Availability: |
https://eprints.ncl.ac.uk/287338 |
| Rights: |
https://creativecommons.org/licenses/by/4.0/ |
| Accession Number: |
edsbas.D36DF8B5 |
| Database: |
BASE |