细胞周期
DNA复制
细胞生物学
真核细胞DNA复制
原点识别复合体
染色体复制控制
复制(统计)
DNA
许可因素
细胞周期检查点
生物
S相
真核细胞
DNA再复制
化学
遗传学
细胞
病毒学
作者
Aftab Amin,Rentian Wu,Man Hei Cheung,John F. Scott,Ziyi Wang,Zijing Zhou,Changdong Liu,Guang Zhu,Chris K.C. Wong,Zhi‐Ling Yu,Chun Liang
出处
期刊:Cell Reports
[Cell Press]
日期:2020-03-01
卷期号:30 (10): 3323-3338.e6
被引量:16
标识
DOI:10.1016/j.celrep.2020.02.046
摘要
Eukaryotic DNA replication licensing is a prerequisite for, and plays a role in, regulating genome duplication that occurs exactly once per cell cycle. ORC (origin recognition complex) binds to and marks replication origins throughout the cell cycle and loads other replication-initiation proteins onto replication origins to form pre-replicative complexes (pre-RCs), completing replication licensing. However, how an asymmetric single-heterohexameric ORC structure loads the symmetric MCM (minichromosome maintenance) double hexamers is controversial, and importantly, it remains unknown when and how ORC proteins associate with the newly replicated origins to protect them from invasion by histones. Here, we report an essential and cell-cycle-dependent ORC "dimerization cycle" that plays three fundamental roles in the regulation of DNA replication: providing a symmetric platform to load the symmetric pre-RCs, marking and protecting the nascent sister replication origins for the next licensing, and playing a crucial role to prevent origin re-licensing within the same cell cycle.
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