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dc.date.accessioned2018-09-20T09:39:59Z
dc.date.available2018-09-20T09:39:59Z
dc.date.created2017-09-05T14:31:40Z
dc.date.issued2017
dc.identifier.citationZimmermann, Christine Garcia, Ignacio Omerzu, Manja Chymkowitch, Pierre Zhang, Beibei Enserink, Jorrit . Mapping the synthetic dosage lethality network of CDK1/CDC28. G3: Genes, Genomes, Genetics. 2017, 7(6), 1753-1766
dc.identifier.urihttp://hdl.handle.net/10852/64840
dc.description.abstractCdk1 (Cdc28 in yeast) is a cyclin-dependent kinase (CDK) essential for cell cycle progression and cell division in normal cells. However, CDK activity also underpins proliferation of tumor cells, making it a relevant study subject. While numerous targets and processes regulated by Cdc28 have been identified, the exact functions of Cdc28 are only partially understood. To further explore the functions of Cdc28, we systematically overexpressed ∼4800 genes in wild-type (WT) cells and in cells with artificially reduced Cdc28 activity. This screen identified 366 genes that, when overexpressed, specifically compromised cell viability under conditions of reduced Cdc28 activity. Consistent with the crucial functions of Cdc28 in cell cycle regulation and chromosome metabolism, most of these genes have functions in the cell cycle, DNA replication, and transcription. However, a substantial number of genes control processes not directly associated with the cell cycle, indicating that Cdc28 may also regulate these processes. Finally, because the dataset was enriched for direct Cdc28 targets, the results from this screen will aid in identifying novel targets and process regulated by Cdc28.en_US
dc.languageEN
dc.publisherGenetics Society of America
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleMapping the synthetic dosage lethality network of CDK1/CDC28en_US
dc.typeJournal articleen_US
dc.creator.authorZimmermann, Christine
dc.creator.authorGarcia, Ignacio
dc.creator.authorOmerzu, Manja
dc.creator.authorChymkowitch, Pierre
dc.creator.authorZhang, Beibei
dc.creator.authorEnserink, Jorrit
cristin.unitcode185,15,29,40
cristin.unitnameSeksjon for biokjemi og molekylærbiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1491142
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=G3: Genes, Genomes, Genetics&rft.volume=7&rft.spage=1753&rft.date=2017
dc.identifier.jtitleG3: Genes, Genomes, Genetics
dc.identifier.volume7
dc.identifier.issue6
dc.identifier.startpage1753
dc.identifier.endpage1766
dc.identifier.doihttp://dx.doi.org/10.1534/g3.117.042317
dc.identifier.urnURN:NBN:no-67394
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2160-1836
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/64840/1/enserink%2Bpost%2B1491142_1753.full63718.pdf
dc.type.versionPublishedVersion


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