The Regulation of Replisome Dynamics during Replication Fork Collapse
Project/Area Number |
15K06955
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Molecular biology
|
Research Institution | Tokyo University of Pharmacy and Life Science |
Principal Investigator |
|
Project Period (FY) |
2015-04-01 – 2018-03-31
|
Project Status |
Completed (Fiscal Year 2017)
|
Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
|
Keywords | DNA複製フォーク / レプリソーム / 無細胞複製系 / CDK / ユビキチン化 / Mre11ヌクレアーゼ / 細胞周期 / アフリカツメガエル卵抽出液 / 複製フォーク / p97/VCP / アフリカツメガエル卵無細胞系 / Cdc45 / GINS / ユビキチン / Mre11 / 複製チェックポイント / PLK1 |
Outline of Final Research Achievements |
The DNA Replication machinery, or replisome is displaced from chromatin at the end of DNA replication and during the collapse of stalled replication forks. In this study, I aimed to elucidate the molecular mechanism of the replisome displacement during fork collapse by utilizing cell-free DNA replication system, and found that the replisome displacement was efficiently induced at stalled forks by enforcing cell cycle transit from interphase into mitotic phase. I also demonstrated that this mitotic displacement pathway is a novel one that requires CDK activity, ubiquitylation and Mre11 nuclease activatey.
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Report
(4 results)
Research Products
(3 results)