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拓扑异构酶 II 对于脊椎动物复制终止时叉的汇聚至关重要。

Topoisomerase II Is Crucial for Fork Convergence during Vertebrate Replication Termination.

机构信息

Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA; Department of Medicine (Hematology, Oncology), Vanderbilt University School of Medicine, Nashville, TN 37232, USA; VA Tennessee Valley Healthcare System, Nashville, TN 37212, USA.

出版信息

Cell Rep. 2019 Oct 8;29(2):422-436.e5. doi: 10.1016/j.celrep.2019.08.097.

Abstract

Termination of DNA replication occurs when two replication forks converge upon the same stretch of DNA. Resolution of topological stress by topoisomerases is crucial for fork convergence in bacteria and viruses, but it is unclear whether similar mechanisms operate during vertebrate termination. Using Xenopus egg extracts, we show that topoisomerase II (Top2) resolves topological stress to prevent converging forks from stalling during termination. Under these conditions, stalling arises due to an inability to unwind the final stretch of DNA ahead of each fork. By promoting fork convergence, Top2 facilitates all downstream events of termination. Converging forks ultimately overcome stalling independently of Top2, indicating that additional mechanisms support fork convergence. Top2 acts throughout replication to prevent the accumulation of topological stress that would otherwise stall converging forks. Thus, termination poses evolutionarily conserved topological problems that can be mitigated by careful execution of the earlier stages of replication.

摘要

当两个复制叉在同一 DNA 片段上汇聚时,DNA 复制就会终止。拓扑异构酶对拓扑张力的解决对于细菌和病毒中的叉汇聚至关重要,但在脊椎动物终止过程中是否存在类似的机制尚不清楚。利用非洲爪蟾卵提取物,我们发现拓扑异构酶 II(Top2)可以解决拓扑张力问题,以防止汇聚的叉在终止过程中停滞。在这些条件下,停滞是由于无法在每个叉的前方解开最后一段 DNA 引起的。通过促进叉汇聚,Top2 促进了终止的所有下游事件。汇聚的叉最终独立于 Top2 克服停滞,表明存在其他机制支持叉汇聚。Top2 在整个复制过程中发挥作用,以防止拓扑张力的积累,否则会使汇聚的叉停滞不前。因此,终止会产生进化保守的拓扑问题,可以通过仔细执行复制的早期阶段来缓解这些问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf27/6919565/ec70bee2176f/nihms-1544142-f0002.jpg

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