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本文引用的文献

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Temporal changes in Hec1 phosphorylation control kinetochore-microtubule attachment stability during mitosis.在有丝分裂过程中,Hec1 磷酸化的时空调控着动粒-微管附着的稳定性。
J Cell Sci. 2011 Feb 15;124(Pt 4):622-34. doi: 10.1242/jcs.072629. Epub 2011 Jan 25.
2
Sensing centromere tension: Aurora B and the regulation of kinetochore function.感知着着丝粒张力:Aurora B 激酶与动粒功能的调控。
Trends Cell Biol. 2011 Mar;21(3):133-40. doi: 10.1016/j.tcb.2010.10.007. Epub 2010 Nov 22.
3
Shared and separate functions of polo-like kinases and aurora kinases in cancer.Polo-like 激酶和 Aurora 激酶在癌症中的共同和独立功能。
Nat Rev Cancer. 2010 Dec;10(12):825-41. doi: 10.1038/nrc2964. Epub 2010 Nov 24.
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BUB1 and BUBR1: multifaceted kinases of the cell cycle.BUB1 和 BUBR1:细胞周期的多功能激酶。
Trends Biochem Sci. 2011 Mar;36(3):141-50. doi: 10.1016/j.tibs.2010.08.004. Epub 2010 Oct 15.
5
Mps1 directs the assembly of Cdc20 inhibitory complexes during interphase and mitosis to control M phase timing and spindle checkpoint signaling.Mps1 在细胞间期和有丝分裂期间指导 Cdc20 抑制复合物的组装,以控制 M 期时间和纺锤体检查点信号。
J Cell Biol. 2010 Jul 12;190(1):89-100. doi: 10.1083/jcb.201001050.
6
Dissecting the role of MPS1 in chromosome biorientation and the spindle checkpoint through the small molecule inhibitor reversine.通过小分子抑制剂 reversine 解析 MPS1 在染色体的定向和纺锤体检查点中的作用。
J Cell Biol. 2010 Jul 12;190(1):73-87. doi: 10.1083/jcb.201001036.
7
Sustained Mps1 activity is required in mitosis to recruit O-Mad2 to the Mad1-C-Mad2 core complex.在有丝分裂过程中,需要持续的 Mps1 活性将 O-Mad2 招募到 Mad1-C-Mad2 核心复合物中。
J Cell Biol. 2010 Jul 12;190(1):25-34. doi: 10.1083/jcb.201002133.
8
A chemical tool box defines mitotic and interphase roles for Mps1 kinase.化学工具盒定义了 Mps1 激酶在有丝分裂和间期的作用。
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9
Molecular causes for BUBR1 dysfunction in the human cancer predisposition syndrome mosaic variegated aneuploidy.人类癌症易感性综合征镶嵌性非整倍体中 BUBR1 功能障碍的分子原因。
Cancer Res. 2010 Jun 15;70(12):4891-900. doi: 10.1158/0008-5472.CAN-09-4319. Epub 2010 Jun 1.
10
An overview of Cdk1-controlled targets and processes.Cdk1 调控的靶标和过程概述。
Cell Div. 2010 May 13;5:11. doi: 10.1186/1747-1028-5-11.

Bub1 和 BubR1:位于染色体附着和纺锤体检查点之间的界面上。

Bub1 and BubR1: at the interface between chromosome attachment and the spindle checkpoint.

机构信息

Reproduction, Perinatal Health, and Infant Health, CHUL-CRCHUQ, 2705 Blvd. Laurier, RC-9800, Québec G1V 4G2, Canada.

出版信息

Mol Cell Biol. 2011 Aug;31(15):3085-93. doi: 10.1128/MCB.05326-11. Epub 2011 May 31.

DOI:10.1128/MCB.05326-11
PMID:21628528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3147602/
Abstract

The spindle checkpoint ensures genome fidelity by temporarily halting chromosome segregation and the ensuing mitotic exit until the last kinetochore is productively attached to the mitotic spindle. At the interface between proper chromosome attachment and the metaphase-to-anaphase transition are the mammalian spindle checkpoint kinases. Compelling evidence indicates that the checkpoint kinases Bub1 and BubR1 have the added task of regulating kinetochore-microtubule attachments. However, the debate on the requirement of kinase activity is in full swing. This minireview summarizes recent advances in our understanding of the core spindle checkpoint kinases Bub1 and BubR1 and considers evidence that supports and opposes the role of kinase activity in regulating their functions during mitosis.

摘要

纺锤体检查点通过暂时停止染色体分离和随后的有丝分裂退出,直到最后一个动粒与有丝分裂纺锤体有效连接,从而确保基因组的完整性。在正确的染色体连接和从中期到后期过渡的交界处是哺乳动物纺锤体检查点激酶。令人信服的证据表明,检查点激酶 Bub1 和 BubR1 还有额外的任务,即调节动粒微管连接。然而,关于激酶活性的必要性的争论正在激烈进行。这篇综述总结了我们对核心纺锤体检查点激酶 Bub1 和 BubR1 的理解的最新进展,并考虑了支持和反对激酶活性在调节它们在有丝分裂过程中的功能的证据。