生物
解旋酶
DNA复制
原点识别复合体
复制的起源
遗传学
染色体复制控制
微小染色体维持
复制前复合体
回复
细胞生物学
真核细胞DNA复制
DNA
计算生物学
基因
核糖核酸
作者
Riki Terui,Scott E. Berger,Larissa A. Sambel,Dan Song,Gheorghe Chistol
出处
期刊:Cell
[Elsevier]
日期:2024-06-12
卷期号:187 (15): 3992-4009.e25
被引量:3
标识
DOI:10.1016/j.cell.2024.05.024
摘要
Metazoan genomes are copied bidirectionally from thousands of replication origins. Replication initiation entails the assembly and activation of two CMG helicases (Cdc45⋅Mcm2-7⋅GINS) at each origin. This requires several replication firing factors (including TopBP1, RecQL4, and DONSON) whose exact roles are still under debate. How two helicases are correctly assembled and activated at each origin is a long-standing question. By visualizing the recruitment of GINS, Cdc45, TopBP1, RecQL4, and DONSON in real time, we uncovered that replication initiation is surprisingly dynamic. First, TopBP1 transiently binds to the origin and dissociates before the start of DNA synthesis. Second, two Cdc45 are recruited together, even though Cdc45 alone cannot dimerize. Next, two copies of DONSON and two GINS simultaneously arrive at the origin, completing the assembly of two CMG helicases. Finally, RecQL4 is recruited to the CMG⋅DONSON⋅DONSON⋅CMG complex and promotes DONSON dissociation and CMG activation via its ATPase activity.
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