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构建染色体汇聚的整合模型。

Building an integrated model of chromosome congression.

作者信息

Auckland Philip, McAinsh Andrew D

机构信息

Mechanochemical Cell Biology Building, Division of Biomedical Cell Biology, Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK.

Mechanochemical Cell Biology Building, Division of Biomedical Cell Biology, Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK

出版信息

J Cell Sci. 2015 Sep 15;128(18):3363-74. doi: 10.1242/jcs.169367. Epub 2015 Sep 1.

DOI:10.1242/jcs.169367
PMID:26330530
Abstract

A universal feature of mitosis is that all chromosomes become aligned at the spindle equator--the halfway point between the two spindle poles--prior to anaphase onset. This migratory event is called congression, and is powered by centromere-bound protein machines called kinetochores. This Commentary aims to document recent advances concerning the two kinetochore-based force-generating mechanisms that drive mitotic chromosome congression in vertebrate cells: depolymerisation-coupled pulling (DCP) and lateral sliding. We aim to explore how kinetochores can 'read-out' their spatial position within the spindle, and adjust these force-generating mechanisms to ensure chromosomes reach, and then remain, at the equator. Finally, we will describe the 'life history' of a chromosome, and provide a working model for how individual mechanisms are integrated to ensure efficient and successful congression.

摘要

有丝分裂的一个普遍特征是,在后期开始之前,所有染色体都会在纺锤体赤道面(两个纺锤体极之间的中点)对齐。这种迁移事件称为染色体列队,由称为动粒的着丝粒结合蛋白机器驱动。本评论旨在记录关于驱动脊椎动物细胞有丝分裂染色体列队的两种基于动粒的力产生机制的最新进展:解聚耦合牵拉(DCP)和侧向滑动。我们旨在探讨动粒如何“读取”其在纺锤体内的空间位置,并调整这些力产生机制,以确保染色体到达并停留在赤道面。最后,我们将描述染色体的“生命历程”,并提供一个工作模型,说明各个机制是如何整合以确保高效且成功的染色体列队的。

相似文献

1
Building an integrated model of chromosome congression.构建染色体汇聚的整合模型。
J Cell Sci. 2015 Sep 15;128(18):3363-74. doi: 10.1242/jcs.169367. Epub 2015 Sep 1.
2
Mechanisms of Chromosome Congression during Mitosis.有丝分裂期间染色体排列到赤道板的机制。
Biology (Basel). 2017 Feb 17;6(1):13. doi: 10.3390/biology6010013.
3
Physical limits on kinesin-5-mediated chromosome congression in the smallest mitotic spindles.在最小有丝分裂纺锤体中驱动蛋白-5介导染色体排列的物理限制
Mol Biol Cell. 2015 Nov 5;26(22):3999-4014. doi: 10.1091/mbc.E14-10-1454. Epub 2015 Sep 9.
4
Micromanipulation of chromosomes in mitotic vertebrate tissue cells: tension controls the state of kinetochore movement.有丝分裂脊椎动物组织细胞中染色体的显微操作:张力控制着动粒运动的状态。
Exp Cell Res. 1997 Sep 15;235(2):314-24. doi: 10.1006/excr.1997.3691.
5
Kinetochore dynein generates a poleward pulling force to facilitate congression and full chromosome alignment.动粒动力蛋白产生向极拉力,以促进染色体移向赤道板并完全对齐。
Cell Res. 2007 Aug;17(8):701-12. doi: 10.1038/cr.2007.65.
6
Chromosome fragments possessing only one kinetochore can congress to the spindle equator.仅拥有一个动粒的染色体片段能够汇聚到纺锤体赤道面。
J Cell Biol. 1997 Jan 27;136(2):229-40. doi: 10.1083/jcb.136.2.229.
7
Kinetochore motors drive congression of peripheral polar chromosomes by overcoming random arm-ejection forces.动粒马达通过克服随机的臂伸出力来驱动周边极染色体的聚集。
Nat Cell Biol. 2014 Dec;16(12):1249-56. doi: 10.1038/ncb3060. Epub 2014 Nov 10.
8
Directional instability of kinetochore motility during chromosome congression and segregation in mitotic newt lung cells: a push-pull mechanism.有丝分裂蝾螈肺细胞中染色体汇聚和分离过程中动粒运动的方向不稳定性:一种推拉机制。
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9
Chromokinesin Kid and kinetochore kinesin CENP-E differentially support chromosome congression without end-on attachment to microtubules.染色单体运动蛋白 Kid 和着丝粒运动蛋白 CENP-E 无需微管末端连接即可支持染色体向心运动。
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10
Merotelic kinetochores in mammalian tissue cells.哺乳动物组织细胞中的错动着丝粒。
Philos Trans R Soc Lond B Biol Sci. 2005 Mar 29;360(1455):553-68. doi: 10.1098/rstb.2004.1610.

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2
CENP-E activation by Aurora A and B controls kinetochore fibrous corona disassembly.极光激酶 A 和 B 对 CENP-E 的激活控制着着丝粒纤维冠状结构的解体。
Nat Commun. 2023 Sep 1;14(1):5317. doi: 10.1038/s41467-023-41091-2.
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Nucleolin is required for multiple centrosome-associated functions in early vertebrate mitosis.
核仁蛋白在早期脊椎动物有丝分裂中多个与中心体相关的功能中不可或缺。
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4
Self-organization of kinetochore-fibers in human mitotic spindles.人类有丝分裂纺锤体中动粒纤维的自组织。
Elife. 2022 Jul 25;11:e75458. doi: 10.7554/eLife.75458.
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Polar Chromosomes-Challenges of a Risky Path.极体染色体——冒险之路的挑战。
Cells. 2022 May 3;11(9):1531. doi: 10.3390/cells11091531.
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The Role of Mitotic Kinases and the RZZ Complex in Kinetochore-Microtubule Attachments: Doing the Right Link.有丝分裂激酶和RZZ复合体在动粒-微管附着中的作用:建立正确连接
Front Cell Dev Biol. 2022 Jan 28;10:787294. doi: 10.3389/fcell.2022.787294. eCollection 2022.
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Shake It Off: The Elimination of Erroneous Kinetochore-Microtubule Attachments and Chromosome Oscillation.《摇掉它:错误的动粒-微管连接的消除和染色体震荡》。
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Chiasmata and the kinetochore component Dam1 are crucial for elimination of erroneous chromosome attachments and centromere oscillation at meiosis I.交叉和动粒组件 Dam1 对于消除减数分裂 I 中错误的染色体附着和着丝粒震荡至关重要。
Open Biol. 2021 Feb;11(2):200308. doi: 10.1098/rsob.200308. Epub 2021 Feb 3.
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Ensemble-Level Organization of Human Kinetochores and Evidence for Distinct Tension and Attachment Sensors.人类着丝粒的整体水平组织及其对不同张力和附着传感器的证据。
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