New Insights into the Mechanism of DNA Duplication by the Eukaryotic Replisome

被引:37
|
作者
Pellegrini, Luca [1 ]
Costa, Alessandro [2 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
[2] Francis Crick Inst, Clare Hall Lab, Macromol Machines Lab, Blanche Lane, S Mimms EN6 3LD, Herts, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
POLYMERASE ALPHA; STRUCTURAL BASIS; HEXAMERIC HELICASE; REPLICATION FORK; MCM2-7; HELICASE; CMG HELICASE; POL EPSILON; PROTEIN; CTF4; COMPLEX;
D O I
10.1016/j.tibs.2016.07.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The DNA replication machinery, or replisome, is a macromolecular complex that combines DNA unwinding, priming and synthesis activities. In eukaryotic cells, the helicase and polymerases are multi-subunit, highly-dynamic assemblies whose structural characterization requires an integrated approach. Recent studies have combined single-particle electron cryo-microscopy and protein crystallography to gain insights into the mechanism of DNA duplication by the eukaryotic replisome. We review current understanding of how replication fork unwinding by the CMG helicase is coupled to leading-strand synthesis by polymerase (Pol) epsilon and lagging-strand priming by Pol alpha/primase, and discuss emerging principles of replisome organization.
引用
收藏
页码:859 / 871
页数:13
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