细胞生物学
DNA复制
生物
DNA
复制(统计)
化学
计算生物学
遗传学
基因组
基因
突变
真核细胞DNA复制
染色体复制控制
作者
Samsara Upadhya,Nalin Ratnayeke,Katherine Ferrick,David Rosenthal,Tobias Meyer
标识
DOI:10.1038/s41467-026-75804-0
摘要
Precise temporal control of DNA replication initiation is essential for faithful cell division, yet there are conflicting prevailing models for how cells trigger origin firing. Here, we demonstrate that human origins are not fired at fixed thresholds of cell cycle regulators E2F, APC/CCdh1, CDK2/1, and CDC7. Instead, origin firing is triggered at a tunable CDK2/1 threshold that is gated by either CDC7 or APC/CCdh1 activity. CDC7 phosphorylates MCM helicase, enabling Cyclin E-CDK2 to trigger origin firing at low CDK2/1 activity, independent of APC/CCdh1 inactivation. In contrast, APC/CCdh1 inactivation enables Cyclin A-CDK1 to phosphorylate MCM at distinct CDK2/1-specific sites and trigger origin firing, independent of CDC7 activity. Strikingly, this requires much higher CDK2/1 activity, which CDK2 cannot normally reach alone. Thus, having two distinct routes necessitates blocking both routes to prevent S phase: either by inhibiting CDC7 or CDK2 while also preventing APC/CCdh1 inactivation or inhibiting CDK1. Human DNA replication initiation is triggered at a tunable CDK2/1 activity threshold gated by two parallel pathways. DBF4-CDC7 activity enables origin firing independent of APC/CCdh1 inactivation by phosphorylating MCMs.
科研通智能强力驱动
Strongly Powered by AbleSci AI