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2
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本文引用的文献

1
Sgo1 establishes the centromeric cohesion protection mechanism in G2 before subsequent Bub1-dependent recruitment in mitosis.Sgo1 在有丝分裂中 Bub1 依赖性招募之前,在 G2 中建立着丝粒凝聚体的保护机制。
J Cell Sci. 2010 Mar 1;123(Pt 5):653-9. doi: 10.1242/jcs.059501. Epub 2010 Feb 2.
2
A pharmacodynamic model of Aurora kinase inhibitors in the spindle assembly checkpoint.纺锤体组装检查点中 Aurora 激酶抑制剂的药效动力学模型。
Front Biosci (Landmark Ed). 2010 Jan 1;15(1):249-58. doi: 10.2741/3619.
3
Phosphorylation of H2A by Bub1 prevents chromosomal instability through localizing shugoshin.Bub1 对 H2A 的磷酸化作用通过定位 shugoshin 来防止染色体不稳定性。
Science. 2010 Jan 8;327(5962):172-7. doi: 10.1126/science.1180189. Epub 2009 Nov 19.
4
Serine/threonine phosphatases: mechanism through structure.丝氨酸/苏氨酸磷酸酶:基于结构的作用机制
Cell. 2009 Oct 30;139(3):468-84. doi: 10.1016/j.cell.2009.10.006.
5
Covalent modifications of histones during mitosis and meiosis.有丝分裂和减数分裂过程中组蛋白的共价修饰。
Cell Cycle. 2009 Nov 15;8(22):3688-94. doi: 10.4161/cc.8.22.9908. Epub 2009 Nov 24.
6
How cohesin and CTCF cooperate in regulating gene expression.黏连蛋白和CTCF如何协同调节基因表达。
Chromosome Res. 2009;17(2):201-14. doi: 10.1007/s10577-008-9017-7. Epub 2009 Mar 24.
7
The crystal structure of the N-terminal region of BUB1 provides insight into the mechanism of BUB1 recruitment to kinetochores.BUB1蛋白N端区域的晶体结构为深入了解BUB1蛋白定位于动粒的机制提供了线索。
Structure. 2009 Jan 14;17(1):105-16. doi: 10.1016/j.str.2008.10.015.
8
Multiple anaphase-promoting complex/cyclosome degrons mediate the degradation of human Sgo1.多个后期促进复合体/细胞周期体降解结构域介导人类Sgo1的降解。
J Biol Chem. 2009 Jan 16;284(3):1772-80. doi: 10.1074/jbc.M807083200. Epub 2008 Nov 17.
9
Polo-like kinase 1 reaches beyond mitosis--cytokinesis, DNA damage response, and development.Polo样激酶1的作用超出有丝分裂范畴——涉及胞质分裂、DNA损伤反应及发育过程。
Curr Opin Cell Biol. 2008 Dec;20(6):650-60. doi: 10.1016/j.ceb.2008.10.005. Epub 2008 Nov 27.
10
Structure and substrate recruitment of the human spindle checkpoint kinase Bub1.人类纺锤体检查点激酶Bub1的结构与底物募集
Mol Cell. 2008 Nov 7;32(3):394-405. doi: 10.1016/j.molcel.2008.09.017.

有丝分裂检查点控制与染色质重塑。

Mitotic checkpoint control and chromatin remodeling.

机构信息

Department of Environmental Medicine, New York University School of Medicine, Tuxedo, New York 10987, USA.

出版信息

Front Biosci (Landmark Ed). 2012 Jan 1;17(3):976-83. doi: 10.2741/3968.

DOI:10.2741/3968
PMID:22201785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3762472/
Abstract

In order to maintain chromosomal stability during cell division, eukaryotic cells have evolved a number of surveillance mechanisms termed checkpoints. These checkpoints monitor the completion of essential molecular and cellular processes of one stage before entering another. The spindle checkpoint watches the bi-orientation attachment of spindle microtubules to all condensed chromosomes before initiation of nuclear division during mitosis. Histones are subject to a number of post-translational modifications during the cell cycle, which may in turn modify or facilitate cell cycle progression. Recent studies suggest that mitotic proteins including Bub1 and Sgo1 that are involved in the spindle checkpoint also play a major role in the regulation of histone modifications and chromatin remodeling. This mini-review summarizes emerging information about the new role of spindle checkpoint proteins in chromatin remodeling.

摘要

为了在细胞分裂过程中维持染色体稳定性,真核细胞进化出了许多称为检查点的监控机制。这些检查点在进入下一个阶段之前,监控一个阶段的重要分子和细胞过程的完成情况。纺锤体检查点在有丝分裂过程中核分裂开始之前,观察纺锤体微管与所有浓缩染色体的双定向附着。组蛋白在细胞周期中受到许多翻译后修饰的影响,这反过来又可能改变或促进细胞周期进程。最近的研究表明,参与纺锤体检查点的有丝分裂蛋白,包括 Bub1 和 Sgo1,也在组蛋白修饰和染色质重塑的调控中发挥主要作用。这篇综述总结了纺锤体检查点蛋白在染色质重塑中发挥新作用的新信息。