Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544, USA.
Microbiol Mol Biol Rev. 2009 Dec;73(4):652-83. doi: 10.1128/MMBR.00019-09.
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.
Mcm2-7 复合物是真核复制解旋酶,即分子马达,它既能解开双链 DNA,又能在 DNA 复制过程中推动叉进行。与该复合物在这一过程中的核心作用相一致,先前的大量研究表明,Mcm2-7 的加载和激活是 DNA 复制调控的标志性事件。与任何其他六聚体解旋酶不同,Mcm2-7 由六个独特且必需的亚基组成。尽管该复合物的这种特殊寡聚状态长期以来一直阻碍了生化研究,但最近在真核生物和更简单的古菌 Mcm 复合物方面的进展为其功能提供了机制上的见解。与研究更为充分的同型六聚体解旋酶相比,有证据表明,六个 Mcm2-7 复合物 ATP 酶活性位点在功能上是不同的,并且可能专门适应真核生物过程的调节限制。