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极光激酶的有丝分裂后期功能。

Late mitotic functions of Aurora kinases.

作者信息

Afonso Olga, Figueiredo Ana C, Maiato Helder

机构信息

Instituto de Biologia Molecular e Celular, Universidade do Porto, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.

Chromosome Instability & Dynamics Laboratory, Instituto de Investigação e Inovação em Saúde da Universidade do Porto - i3S, Rua Alfredo Allen, 208, 4200-135, Porto, Portugal.

出版信息

Chromosoma. 2017 Feb;126(1):93-103. doi: 10.1007/s00412-016-0594-5. Epub 2016 Apr 22.

DOI:10.1007/s00412-016-0594-5
PMID:27106516
Abstract

The coordination between late mitotic events such as poleward chromosome motion, spindle elongation, DNA decondensation, and nuclear envelope reformation (NER) is crucial for the completion of chromosome segregation at the anaphase-telophase transition. Mitotic exit is driven by a decrease of Cdk1 kinase activity and an increase of PP1/PP2A phosphatase activities. More recently, Aurora kinases have also emerged as master regulators of late mitotic events and cytokinesis. Aurora A is mainly associated with spindle poles throughout mitosis and midbody during telophase, whereas Aurora B re-localizes from centromeres in early mitosis to the spindle midzone and midbody as cells progress from anaphase to the completion of cytokinesis. Functional studies, together with the identification of a phosphorylation gradient during anaphase, established Aurora B as a major player in the organization of the spindle midzone and in the spatiotemporal coordination between chromosome segregation and NER. Aurora A has been less explored, but a cooperative role in spindle midzone stability has also been proposed, implying that both Aurora A and B contribute to accurate chromosome segregation during mitotic exit. Here, we review the roles of the Aurora kinases in the regulation of late mitotic events and discuss how they work together with other mitotic players to ensure an error-free mitosis.

摘要

后期有丝分裂事件(如染色体向极运动、纺锤体伸长、DNA解聚和核膜重建(NER))之间的协调对于在后期-末期转变时完成染色体分离至关重要。有丝分裂退出由Cdk1激酶活性的降低和PP1/PP2A磷酸酶活性的增加驱动。最近,极光激酶也已成为后期有丝分裂事件和胞质分裂的主要调节因子。极光A在整个有丝分裂过程中主要与纺锤体极相关,在末期与中间体相关,而随着细胞从后期进展到胞质分裂完成,极光B从有丝分裂早期的着丝粒重新定位到纺锤体中间区和中间体。功能研究以及后期磷酸化梯度的鉴定,确立了极光B在纺锤体中间区组织以及染色体分离与NER之间的时空协调中的主要作用。对极光A的研究较少,但也有人提出它在纺锤体中间区稳定性方面具有协同作用,这意味着极光A和B在有丝分裂退出期间都有助于准确的染色体分离。在这里,我们综述了极光激酶在调节后期有丝分裂事件中的作用,并讨论它们如何与其他有丝分裂参与者协同工作以确保无差错的有丝分裂。

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Late mitotic functions of Aurora kinases.极光激酶的有丝分裂后期功能。
Chromosoma. 2017 Feb;126(1):93-103. doi: 10.1007/s00412-016-0594-5. Epub 2016 Apr 22.
2
The active form of the metabolic sensor: AMP-activated protein kinase (AMPK) directly binds the mitotic apparatus and travels from centrosomes to the spindle midzone during mitosis and cytokinesis.代谢传感器的活性形式:AMP 活化蛋白激酶(AMPK)直接与有丝分裂装置结合,并在有丝分裂和胞质分裂过程中从中心体移动到纺锤体中间区。
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Spatiotemporal control of mitotic exit during anaphase by an aurora B-Cdk1 crosstalk.通过 Aurora B-Cdk1 相互作用对后期有丝分裂退出进行时空调控。
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A chromosome separation checkpoint: A midzone Aurora B gradient mediates a chromosome separation checkpoint that regulates the anaphase-telophase transition.一种染色体分离检查点:中间区极光激酶B梯度介导一种调节后期至末期转变的染色体分离检查点。
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Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins.极光闪耀:相互作用蛋白对 Aurora A 和 B 激酶功能的调节。
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Endomitotic megakaryocytes form a midzone in anaphase but have a deficiency in cleavage furrow formation.核内有丝分裂的巨核细胞在后期形成一个中间区,但在分裂沟形成方面存在缺陷。
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Double-checking chromosome segregation.检查染色体分离情况。

本文引用的文献

1
Ubiquitin Receptor Protein UBASH3B Drives Aurora B Recruitment to Mitotic Microtubules.泛素受体蛋白UBASH3B驱动Aurora B募集至有丝分裂微管。
Dev Cell. 2016 Jan 11;36(1):63-78. doi: 10.1016/j.devcel.2015.12.017.
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Bistability of a coupled Aurora B kinase-phosphatase system in cell division.细胞分裂中Aurora B激酶-磷酸酶偶联系统的双稳性
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Cdk1 orders mitotic events through coordination of a chromosome-associated phosphatase switch.细胞周期蛋白依赖性激酶1(Cdk1)通过协调一种与染色体相关的磷酸酶开关来调控有丝分裂事件。
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4
Insights on the Role of PGRMC1 in Mitotic and Meiotic Cell Division.PGRMC1在有丝分裂和减数分裂细胞分裂中的作用见解
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Dephosphorylation in nuclear reassembly after mitosis.有丝分裂后细胞核重新组装过程中的去磷酸化作用。
Front Cell Dev Biol. 2022 Oct 4;10:1012768. doi: 10.3389/fcell.2022.1012768. eCollection 2022.
6
The ubiquitin-ligase TRAF6 and TGFβ type I receptor form a complex with Aurora kinase B contributing to mitotic progression and cytokinesis in cancer cells.泛素连接酶 TRAF6 和 TGFβ 型 I 受体与 Aurora 激酶 B 形成复合物,促进癌细胞的有丝分裂进程和胞质分裂。
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7
LiveCellMiner: A new tool to analyze mitotic progression.LiveCellMiner:一种分析有丝分裂进程的新工具。
PLoS One. 2022 Jul 7;17(7):e0270923. doi: 10.1371/journal.pone.0270923. eCollection 2022.
8
An anaphase surveillance mechanism prevents micronuclei formation from frequent chromosome segregation errors.一种后期检测机制可防止频繁的染色体分离错误导致微核的形成。
Cell Rep. 2021 Nov 9;37(6):109783. doi: 10.1016/j.celrep.2021.109783.
9
The Aurora B gradient sustains kinetochore stability in anaphase.极光 B 梯度在后期维持着动粒的稳定性。
Cell Rep. 2021 Nov 9;37(6):109818. doi: 10.1016/j.celrep.2021.109818.
10
Aurora B-dependent polarization of the cortical actomyosin network during mitotic exit.有丝分裂后期皮层肌动球蛋白网络的 Aurora B 依赖性极化。
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Kinetochore-localized PP1-Sds22 couples chromosome segregation to polar relaxation.着丝粒定位的 PP1-Sds22 将染色体分离与极区松弛偶联。
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Dev Cell. 2015 Apr 20;33(2):204-15. doi: 10.1016/j.devcel.2015.03.015.
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Aurora B-mediated localized delays in nuclear envelope formation facilitate inclusion of late-segregating chromosome fragments.极光激酶B介导的核膜形成局部延迟有助于纳入后期分离的染色体片段。
Mol Biol Cell. 2015 Jun 15;26(12):2227-41. doi: 10.1091/mbc.E15-01-0026. Epub 2015 Apr 15.