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TOPBP1 regulates RAD51 phosphorylation and chromatin loading and determines PARP inhibitor sensitivity
P. Moudry, K. Watanabe, KM. Wolanin, J. Bartkova, IE. Wassing, S. Watanabe, R. Strauss, R. Troelsgaard Pedersen, VH. Oestergaard, M. Lisby, M. Andújar-Sánchez, A. Maya-Mendoza, F. Esashi, J. Lukas, J. Bartek,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1962 do Před 6 měsíci
Freely Accessible Science Journals
od 1962 do Před 6 měsíci
Europe PubMed Central
od 1962 do Před 6 měsíci
Open Access Digital Library
od 1955-01-25
Open Access Digital Library
od 1959-01-01
Open Access Digital Library
od 1962-01-01
PubMed
26811421
DOI
10.1083/jcb.201507042
Knihovny.cz E-zdroje
- MeSH
- časové faktory MeSH
- chromatin metabolismus MeSH
- DNA vazebné proteiny genetika metabolismus MeSH
- fosforylace MeSH
- ftalaziny farmakologie MeSH
- HEK293 buňky MeSH
- HeLa buňky MeSH
- homologní rekombinace * MeSH
- interakční proteinové domény a motivy MeSH
- jaderné proteiny genetika metabolismus MeSH
- lidé MeSH
- nádory vaječníků farmakoterapie enzymologie genetika patologie MeSH
- PARP inhibitory farmakologie MeSH
- piperaziny farmakologie MeSH
- protein-serin-threoninkinasy metabolismus MeSH
- proteiny buněčného cyklu metabolismus MeSH
- protoonkogenní proteiny metabolismus MeSH
- rekombinasa Rad51 genetika metabolismus MeSH
- restrukturace chromatinu * MeSH
- RNA interference MeSH
- signální transdukce účinky léků MeSH
- transfekce MeSH
- transportní proteiny genetika metabolismus MeSH
- vazba proteinů MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Topoisomerase IIβ-binding protein 1 (TOPBP1) participates in DNA replication and DNA damage response; however, its role in DNA repair and relevance for human cancer remain unclear. Here, through an unbiased small interfering RNA screen, we identified and validated TOPBP1 as a novel determinant whose loss sensitized human cells to olaparib, an inhibitor of poly(ADP-ribose) polymerase. We show that TOPBP1 acts in homologous recombination (HR) repair, impacts olaparib response, and exhibits aberrant patterns in subsets of human ovarian carcinomas. TOPBP1 depletion abrogated RAD51 loading to chromatin and formation of RAD51 foci, but without affecting the upstream HR steps of DNA end resection and RPA loading. Furthermore, TOPBP1 BRCT domains 7/8 are essential for RAD51 foci formation. Mechanistically, TOPBP1 physically binds PLK1 and promotes PLK1 kinase-mediated phosphorylation of RAD51 at serine 14, a modification required for RAD51 recruitment to chromatin. Overall, our results provide mechanistic insights into TOPBP1's role in HR, with potential clinical implications for cancer treatment.
Danish Cancer Society Research Center DK 2100 Copenhagen Denmark
Department of Biology University of Copenhagen DK 2200 Copenhagen Denmark
The Sir William Dunn School of Pathology University of Oxford Oxford OX1 3RE England UK
Citace poskytuje Crossref.org
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