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生物
DNA聚合酶
DNA复制
遗传学
DNA
聚合酶
初级
细菌圆形染色体
进化生物学
计算生物学
聚合酶链反应
基因
逆转录酶
作者
James E. Graham,Kenneth J. Marians,Stephen C. Kowalczykowski
出处
期刊:Cell
[Elsevier]
日期:2017-06-01
卷期号:169 (7): 1201-1213.e17
被引量:167
标识
DOI:10.1016/j.cell.2017.05.041
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 ∼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. PAPERCLIP.
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