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本文引用的文献

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A quantitative map of human Condensins provides new insights into mitotic chromosome architecture.人类凝缩蛋白的定量图谱为有丝分裂染色体结构提供了新的见解。
J Cell Biol. 2018 Jul 2;217(7):2309-2328. doi: 10.1083/jcb.201801048. Epub 2018 Apr 9.
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Ki-67 and condensins support the integrity of mitotic chromosomes through distinct mechanisms.Ki-67 和凝聚素通过不同的机制支持有丝分裂染色体的完整性。
J Cell Sci. 2018 Mar 22;131(6):jcs212092. doi: 10.1242/jcs.212092.
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A pathway for mitotic chromosome formation.有丝分裂染色体形成的一条途径。
Science. 2018 Feb 9;359(6376). doi: 10.1126/science.aao6135. Epub 2018 Jan 18.
4
Metaphase chromosome structure is dynamically maintained by condensin I-directed DNA (de)catenation.中期染色体结构通过凝聚素I介导的DNA(解)连环作用而动态维持。
Elife. 2017 May 6;6:e26120. doi: 10.7554/eLife.26120.
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The supercoiling state of DNA determines the handedness of both H3 and CENP-A nucleosomes.DNA 的超螺旋状态决定了 H3 和 CENP-A 核小体的手性。
Nanoscale. 2017 Feb 2;9(5):1862-1870. doi: 10.1039/c6nr06245h.
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Physical Proximity of Sister Chromatids Promotes Top2-Dependent Intertwining.姐妹染色单体的物理接近促进了拓扑异构酶II(Top2)依赖性的缠绕。
Mol Cell. 2016 Oct 6;64(1):134-147. doi: 10.1016/j.molcel.2016.09.007.
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PICH promotes mitotic chromosome segregation: Identification of a novel role in rDNA disjunction.PICH促进有丝分裂染色体分离:核糖体DNA分离中一个新作用的鉴定。
Cell Cycle. 2016 Oct 17;15(20):2704-11. doi: 10.1080/15384101.2016.1222336. Epub 2016 Aug 26.
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Ki-67 acts as a biological surfactant to disperse mitotic chromosomes.Ki-67作为一种生物表面活性剂来分散有丝分裂染色体。
Nature. 2016 Jul 14;535(7611):308-12. doi: 10.1038/nature18610. Epub 2016 Jun 29.
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Sister chromatid resolution is an intrinsic part of chromosome organization in prophase.姐妹染色单体分离是前期染色体组织的固有部分。
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10
Rapid Protein Depletion in Human Cells by Auxin-Inducible Degron Tagging with Short Homology Donors.通过与短同源供体的生长素诱导 Degron 标记实现人细胞中的快速蛋白质耗竭。
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拓扑异构酶 IIα 对于维持有丝分裂染色体结构至关重要。

Topoisomerase IIα is essential for maintenance of mitotic chromosome structure.

机构信息

Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC 3052, Australia.

Center for Chromosome Stability, Department of Cellular and Molecular Medicine, University of Copenhagen, 2200 Copenhagen, Denmark.

出版信息

Proc Natl Acad Sci U S A. 2020 Jun 2;117(22):12131-12142. doi: 10.1073/pnas.2001760117. Epub 2020 May 15.

DOI:10.1073/pnas.2001760117
PMID:32414923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7275761/
Abstract

Topoisomerase IIα (TOP2A) is a core component of mitotic chromosomes and important for establishing mitotic chromosome condensation. The primary roles of TOP2A in mitosis have been difficult to decipher due to its multiple functions across the cell cycle. To more precisely understand the role of TOP2A in mitosis, we used the auxin-inducible degron (AID) system to rapidly degrade the protein at different stages of the human cell cycle. Removal of TOP2A prior to mitosis does not affect prophase timing or the initiation of chromosome condensation. Instead, it prevents chromatin condensation in prometaphase, extends the length of prometaphase, and ultimately causes cells to exit mitosis without chromosome segregation occurring. Surprisingly, we find that removal of TOP2A from cells arrested in prometaphase or metaphase cause dramatic loss of compacted mitotic chromosome structure and conclude that TOP2A is crucial for maintenance of mitotic chromosomes. Treatments with drugs used to poison/inhibit TOP2A function, such as etoposide and ICRF-193, do not phenocopy the effects on chromosome structure of TOP2A degradation by AID. Our data point to a role for TOP2A as a structural chromosome maintenance enzyme locking in condensation states once sufficient compaction is achieved.

摘要

拓扑异构酶 IIα(TOP2A)是有丝分裂染色体的核心组成部分,对于建立有丝分裂染色体凝聚非常重要。由于 TOP2A 在细胞周期中具有多种功能,因此其在有丝分裂中的主要作用一直难以破译。为了更精确地理解 TOP2A 在有丝分裂中的作用,我们使用了生长素诱导的降解系统(AID)在人类细胞周期的不同阶段快速降解该蛋白。在有丝分裂之前去除 TOP2A 不会影响前期的时间或染色体凝聚的起始。相反,它会阻止前期的染色质凝聚,延长前期的长度,最终导致细胞在没有发生染色体分离的情况下退出有丝分裂。令人惊讶的是,我们发现从处于前期或中期的细胞中去除 TOP2A 会导致压缩的有丝分裂染色体结构的显著丢失,我们得出结论,TOP2A 对于维持有丝分裂染色体至关重要。用用于毒害/抑制 TOP2A 功能的药物(如依托泊苷和 ICRF-193)处理不会模拟 AID 降解对染色体结构的影响。我们的数据表明,TOP2A 作为一种结构性染色体维持酶的作用,一旦达到足够的压缩,就会锁定凝聚状态。