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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >A topoisomerase II-dependent mechanism for resetting replicons at the S-M-phase transition.
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A topoisomerase II-dependent mechanism for resetting replicons at the S-M-phase transition.

机译:拓扑异构酶II依赖性机制,用于在S-M相转变时重置复制子。

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摘要

Topoisomerase II (topo II) is required for chromosome segregation and for reprogramming replicons. Here, we show that topo II couples DNA replication termination with the clearing of replication complexes for resetting replicons at mitosis. Topo II inhibition impairs completion of DNA replication, accounting for replication protein A (RPA) stabilization onto ssDNA. Topo II inhibition does not affect the caffeine-sensitive ORC1 degradation found upon origin firing, but it impairs the cdk-dependent degradation/chromatin dissociation of an ORC1/2 reservoir at mitosis. Our results show that ORC1 degradation is rescued by Pin1 depletion and that this topo II-dependent clearing of ORC1/2 from chromatin involves the APC.
机译:染色体分离和复制子重编程需要拓扑异构酶II(拓扑II)。在这里,我们显示topo II将DNA复制终止与复制复合物的清除结合起来,以在有丝分裂时重置复制子。 Topo II抑制作用会破坏DNA复制的完成,这说明复制蛋白A(RPA)稳定在ssDNA上。 Topo II抑制作用不会影响原产地激发后发现的对咖啡因敏感的ORC1降解,但会损害有丝分裂时ORC1 / 2储库的cdk依赖性降解/染色质解离。我们的结果表明,Pin1耗尽可挽救ORC1降解,并且这种从染色质中ORC1 / 2的拓扑II依赖性清除涉及APC。

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