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本文引用的文献

1
An EB1-binding motif acts as a microtubule tip localization signal.一个EB1结合基序作为微管尖端定位信号。
Cell. 2009 Jul 23;138(2):366-76. doi: 10.1016/j.cell.2009.04.065.
2
Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores.通过着丝粒处依赖通量的力平衡来同步染色体分离。
J Cell Biol. 2009 Jul 13;186(1):11-26. doi: 10.1083/jcb.200904153. Epub 2009 Jul 6.
3
TIP150 interacts with and targets MCAK at the microtubule plus ends.TIP150在微管正端与MCAK相互作用并以其为靶点。
EMBO Rep. 2009 Aug;10(8):857-65. doi: 10.1038/embor.2009.94. Epub 2009 Jun 19.
4
Plk1 and Aurora A regulate the depolymerase activity and the cellular localization of Kif2a.Plk1和Aurora A调节Kif2a的解聚酶活性和细胞定位。
J Cell Sci. 2009 May 1;122(Pt 9):1334-41. doi: 10.1242/jcs.044321. Epub 2009 Apr 7.
5
ICIS and Aurora B coregulate the microtubule depolymerase Kif2a.ICIS与极光激酶B共同调节微管解聚酶Kif2a。
Curr Biol. 2009 May 12;19(9):758-63. doi: 10.1016/j.cub.2009.03.018. Epub 2009 Mar 26.
6
Kinetochore-generated pushing forces separate centrosomes during bipolar spindle assembly.动粒产生的推力在双极纺锤体组装过程中分离中心体。
J Cell Biol. 2009 Feb 9;184(3):365-72. doi: 10.1083/jcb.200809055.
7
MCAK and paclitaxel have differential effects on spindle microtubule organization and dynamics.MCAK和紫杉醇对纺锤体微管的组织和动力学有不同的影响。
Mol Biol Cell. 2009 Mar;20(6):1639-51. doi: 10.1091/mbc.e08-09-0985. Epub 2009 Jan 21.
8
Genome stability is ensured by temporal control of kinetochore-microtubule dynamics.基因组稳定性通过动粒-微管动力学的时间控制得以确保。
Nat Cell Biol. 2009 Jan;11(1):27-35. doi: 10.1038/ncb1809. Epub 2008 Dec 7.
9
Aurora kinase-A regulates kinetochore/chromatin associated microtubule assembly in human cells.极光激酶A调节人类细胞中动粒/染色质相关微管组装。
Cell Cycle. 2008 Sep 1;7(17):2691-704. doi: 10.4161/cc.7.17.6460.
10
Aurora-A and ch-TOG act in a common pathway in control of spindle pole integrity.极光激酶A和驱动蛋白样蛋白Ch-TOG在控制纺锤体极完整性的共同途径中发挥作用。
Oncogene. 2008 Nov 20;27(51):6539-49. doi: 10.1038/onc.2008.252. Epub 2008 Jul 28.

有丝分裂中的驱动蛋白-13 家族:纺锤体微管空间和时间组织的关键因子。

Kinesin-13s in mitosis: Key players in the spatial and temporal organization of spindle microtubules.

机构信息

Medical Science Program, Indiana University, Bloomington, IN 47405, USA.

出版信息

Semin Cell Dev Biol. 2010 May;21(3):276-82. doi: 10.1016/j.semcdb.2010.01.016. Epub 2010 Jan 28.

DOI:10.1016/j.semcdb.2010.01.016
PMID:20109574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2844478/
Abstract

Dynamic microtubules are essential for the process of mitosis. Thus, elucidating when, where, and how microtubule dynamics are regulated is key to understanding this process. One important class of proteins that directly regulates microtubule dynamics is the Kinesin-13 family. Kinesin-13 proteins induce depolymerization uniquely from both ends of the microtubule. This activity coincides with their cellular localization and with their ability to regulate microtubule dynamics to control spindle assembly and kinetochore-microtubule attachments. In this review, we highlight recent findings that dissect the important actions of Kinesin-13 family members and summarize important studies on the regulation of their activity by phosphorylation and by protein-protein interactions.

摘要

动态微管对于有丝分裂过程是必不可少的。因此,阐明微管动力学何时、何地以及如何受到调节对于理解这一过程至关重要。一类能够直接调节微管动力学的重要蛋白质是驱动蛋白-13 家族。驱动蛋白-13 蛋白能够从微管的两端诱导解聚。这种活性与其细胞定位以及调节微管动力学以控制纺锤体组装和动粒-微管连接的能力相一致。在这篇综述中,我们强调了最近的发现,这些发现剖析了驱动蛋白-13 家族成员的重要作用,并总结了关于其磷酸化和蛋白-蛋白相互作用调节其活性的重要研究。