Independent and Stochastic Action of DNA Polymerases in the Replisome

被引:124
作者
Graham, James E. [1 ,2 ,4 ]
Marians, Kenneth J. [3 ]
Kowalczykowski, Stephen C. [1 ,2 ]
机构
[1] Univ Calif Davis, Dept Microbiol & Mol Genet, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
[3] Mem Sloan Kettering Canc Ctr, Mol Biol Program, 1275 York Ave, New York, NY 10065 USA
[4] Oxford Nanopore Technol, Edmund Cartwright House,4 Robert Robinson Ave, Oxford OX4 4GA, England
关键词
LAGGING-STRAND SYNTHESIS; SINGLE-MOLECULE OBSERVATION; COORDINATED LEADING-STRAND; REPLICATION FORK; HELICASE; PROTEIN; PRIMASE; DYNAMICS; VISUALIZATION; PURIFICATION;
D O I
10.1016/j.cell.2017.05.041
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
It has been assumed that DNA synthesis by the leading- and lagging-strand polymerases in the replisome must be coordinated to avoid the formation of significant gaps in the nascent strands. Using real-time single-molecule analysis, we establish that leading- and lagging-strand DNA polymerases function independently within a single replisome. Although average rates of DNA synthesis on leading and lagging strands are similar, individual trajectories of both DNA polymerases display stochastically switchable rates of synthesis interspersed with distinct pauses. DNA unwinding by the replicative helicase may continue during such pauses, but a self-governing mechanism, where helicase speed is reduced by similar to 80%, permits recoupling of polymerase to helicase. These features imply a more dynamic, kinetically discontinuous replication process, wherein contacts within the replisome are continually broken and reformed. We conclude that the stochastic behavior of replisome components ensures complete DNA duplication without requiring coordination of leading- and lagging-strand synthesis.
引用
收藏
页码:1201 / +
页数:30
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