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dc.contributor.authorDraga, M
dc.contributor.authorMadgett, EB
dc.contributor.authorVandenberg, CJ
dc.contributor.authordu Plessis, D
dc.contributor.authorKaufmann, A
dc.contributor.authorWerler, P
dc.contributor.authorChakraborty, P
dc.contributor.authorLowndes, NF
dc.contributor.authorHiom, K
dc.date.accessioned2020-12-18T02:42:27Z
dc.date.available2020-12-18T02:42:27Z
dc.date.issued2015-11
dc.identifierpii: MCB.01497-14
dc.identifier.citationDraga, M., Madgett, E. B., Vandenberg, C. J., du Plessis, D., Kaufmann, A., Werler, P., Chakraborty, P., Lowndes, N. F. & Hiom, K. (2015). BRCA1 Is Required for Maintenance of Phospho-Chk1 and G2/M Arrest during DNA Cross-Link Repair in DT40 Cells.. Mol Cell Biol, 35 (22), pp.3829-3840. https://doi.org/10.1128/MCB.01497-14.
dc.identifier.issn0270-7306
dc.identifier.urihttp://hdl.handle.net/11343/255463
dc.description.abstractThe Fanconi anemia DNA repair pathway is pivotal for the efficient repair of DNA interstrand cross-links. Here, we show that FA-defective (Fancc(-)) DT40 cells arrest in G2 phase following cross-link damage and trigger apoptosis. Strikingly, cell death was reduced in Fancc(-) cells by additional deletion of the BRCA1 tumor suppressor, resulting in elevated clonogenic survival. Increased resistance to cross-link damage was not due to loss of toxic BRCA1-mediated homologous recombination but rather through the loss of a G2 checkpoint. This proapoptotic role also required the BRCA1-A complex member ABRAXAS (FAM175A). Finally, we show that BRCA1 promotes G2 arrest and cell death by prolonging phosphorylation of Chk1 on serine 345 after DNA damage to sustain arrest. Our data imply that DNA-induced cross-link death in cells defective in the FA pathway is dependent on the ability of BRCA1 to prolong cell cycle arrest in G2 phase.
dc.languageeng
dc.publisherAmerican Society for Microbiology
dc.titleBRCA1 Is Required for Maintenance of Phospho-Chk1 and G2/M Arrest during DNA Cross-Link Repair in DT40 Cells.
dc.typeJournal Article
dc.identifier.doi10.1128/MCB.01497-14
melbourne.affiliation.departmentMedical Biology (W.E.H.I.)
melbourne.source.titleMolecular and Cellular Biology
melbourne.source.volume35
melbourne.source.issue22
melbourne.source.pages3829-3840
dc.rights.licenseCC BY
melbourne.elementsid1281089
melbourne.openaccess.pmchttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609749
melbourne.contributor.authorVandenberg, Cassandra
dc.identifier.eissn1098-5549
melbourne.accessrightsOpen Access


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