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Mapping the Synthetic Dosage Lethality Network of CDK1/CDC28.
Zimmermann, Christine; Garcia, Ignacio; Omerzu, Manja; Chymkowitch, Pierre; Zhang, Beibei; Enserink, Jorrit M.
Affiliation
  • Zimmermann C; Department of Molecular Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0379 Oslo, Norway.
  • Garcia I; Department of Molecular Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0379 Oslo, Norway.
  • Omerzu M; Department of Molecular Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0379 Oslo, Norway.
  • Chymkowitch P; Department of Molecular Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0379 Oslo, Norway.
  • Zhang B; Department of Molecular Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0379 Oslo, Norway.
  • Enserink JM; Department of Molecular Cell Biology, Institute for Cancer Research, The Norwegian Radium Hospital, Montebello, 0379 Oslo, Norway jorrit.enserink@rr-research.no.
G3 (Bethesda) ; 7(6): 1753-1766, 2017 06 07.
Article in En | MEDLINE | ID: mdl-28428242
Cdk1 (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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Mapping / CDC2-CDC28 Kinases / Epistasis, Genetic / Synthetic Lethal Mutations Language: En Journal: G3 (Bethesda) Year: 2017 Document type: Article Affiliation country: Norway Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Mapping / CDC2-CDC28 Kinases / Epistasis, Genetic / Synthetic Lethal Mutations Language: En Journal: G3 (Bethesda) Year: 2017 Document type: Article Affiliation country: Norway Country of publication: United kingdom