原点识别复合体
微小染色体维持
真核细胞DNA复制
复制的起源
染色体复制控制
细胞生物学
复制因子C
DNA
作者
Linhua Fang,Megan J. Davey,Michael O’Donnell
出处
期刊:Molecular Cell
[Elsevier]
日期:1999-10-01
卷期号:4 (4): 541-553
被引量:180
标识
DOI:10.1016/s1097-2765(00)80205-1
摘要
This study outlines the events downstream of origin unwinding by DnaA, leading to assembly of two replication forks at the E. coli origin, oriC. We show that two hexamers of DnaB assemble onto the opposing strands of the resulting bubble, expanding it further, yet helicase action is not required. Primase cannot act until the helicases move 65 nucleotides or more. Once primers are formed, two molecules of the large DNA polymerase III holoenzyme machinery assemble into the bubble, forming two replication forks. Primer locations are heterogeneous; some are even outside oriC. This observation generalizes to many systems, prokaryotic and eukaryotic. Heterogeneous initiation sites are likely explained by primase functioning with a moving helicase target.
科研通智能强力驱动
Strongly Powered by AbleSci AI