Molecular architecture of the DNA replication origin activation checkpoint

Perturbation of DNA replication initiation arrests human cells in G1, pointing towards an origin activation checkpoint. We used RNAi against Cdc7 kinase to inhibit replication initiation and dissect this checkpoint in fibroblasts. We show that the checkpoint response is dependent on three axes coordinated through the transcription factor FoxO3a. In arrested cells, FoxO3a activates the ARF‐∣Hdm2‐∣p53 → p21 pathway and mediates p15 INK4B upregulation; p53 in turn activates expression of the Wnt/β‐catenin signalling antagonist Dkk3, leading to Myc and cyclin D1 downregulation. The resulting loss of CDK activity inactivates the Rb‐E2F pathway and overrides the G1‐S transcriptional programme. Fibroblasts concomitantly depleted of Cdc7/FoxO3a, Cdc7/p15, Cdc7/p53 or Cdc7/Dkk3 can bypass the arrest and proceed into an abortive S phase followed by apoptosis. The lack of redundancy between the checkpoint axes and reliance on several tumour suppressor proteins commonly inactivated in human tumours provides a mechanistic basis for the cancer‐cell‐specific killing observed with emerging Cdc7 inhibitors. The tumour suppressors Foxo3a, p15INK4B and Dkk3 serve as non‐redundant molecular protectors against a Cdc7‐depletion‐induced DNA replication checkpoint.