解旋酶
生物
微小染色体维持
回复
dnaB解旋酶
DNA复制
真核细胞DNA复制
原点识别复合体
DNA
细胞生物学
计算生物学
遗传学
复制的起源
基因
核糖核酸
作者
Matthew L. Bochman,Anthony Schwacha
标识
DOI:10.1128/mmbr.00019-09
摘要
SUMMARY The Mcm2-7 complex serves as the eukaryotic replicative helicase, the molecular motor that both unwinds duplex DNA and powers fork progression during DNA replication. Consistent with its central role in this process, much prior work has illustrated that Mcm2-7 loading and activation are landmark events in the regulation of DNA replication. Unlike any other hexameric helicase, Mcm2-7 is composed of six unique and essential subunits. Although the unusual oligomeric nature of this complex has long hampered biochemical investigations, recent advances with both the eukaryotic as well as the simpler archaeal Mcm complexes provide mechanistic insight into their function. In contrast to better-studied homohexameric helicases, evidence suggests that the six Mcm2-7 complex ATPase active sites are functionally distinct and are likely specialized to accommodate the regulatory constraints of the eukaryotic process.
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