The Journal of Cell Biology · 2009 · 62 citations · 31 references
Life SciencesCell BiologyMolecular BiologyCell SignalingDna RepairMolecular Cell BiologyCell Cycle ControlCell Cycle SignalingDna DamageDna Damage SignalingDna Strand BreaksDouble-strand Break RepairCdk ActivationDna Damage Checkpoint SignalingDna Damage Response PathwaysDna Damage Response SignalingDna Damage ResponsesMurine ModelsPhosphorylation-based SignalingProtein Phosphorylation Signaling
In response to DNA damage, cells activate a phosphorylation-based signaling cascade known as the DNA damage response (DDR). One of the main outcomes of DDR activation is inhibition of cyclin-dependent kinase (Cdk) activity to restrain cell cycle progression until lesions are healed. Recent studies have revealed a reverse connection by which Cdk activity modulates processing of DNA break ends and DDR activation. However, the specific contribution of individual Cdks to this process remains poorly understood. To address this issue, we have examined the DDR in murine cells carrying a defined set of Cdks. Our results reveal that genome maintenance programs of postreplicative cells, including DDR, are regulated by the overall level of Cdk activity and not by specific Cdks.
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Megabase Chromatin Domains Involved in DNA Double-Strand Breaks in Vivo
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Human CtIP promotes DNA end resection
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