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Contrasting models for kinetochore microtubule attachment in mammalian cells.哺乳动物细胞中着丝粒微管附着的对比模型。
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2
The Hec1/Ndc80 tail domain is required for force generation at kinetochores, but is dispensable for kinetochore-microtubule attachment formation and Ska complex recruitment.Hec1/Ndc80 尾部结构域对于动粒产生力是必需的,但对于动粒-微管连接的形成和 Ska 复合物的招募是可有可无的。
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Multivalency of NDC80 in the outer kinetochore is essential to track shortening microtubules and generate forces.NDC80 在着丝粒外的多价性对于追踪缩短的微管并产生力是必不可少的。
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Aurora B Tension Sensing Mechanisms in the Kinetochore Ensure Accurate Chromosome Segregation.动粒中的Aurora B张力感应机制确保染色体准确分离。
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Emergent complexity of the cytoskeleton: from single filaments to tissue.细胞骨架的突发复杂性:从单丝到组织
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SUMOylation in control of accurate chromosome segregation during mitosis.SUMOylation 在有丝分裂过程中控制染色体正确分离的作用。
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Mitotic spindle form and function.有丝分裂纺锤体的形成和功能。
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Reconstituting the kinetochore–microtubule interface: what, why, and how.重建动粒-微管界面:是什么、为什么以及如何实现。
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本文引用的文献

1
CENP-H-containing complex facilitates centromere deposition of CENP-A in cooperation with FACT and CHD1.含CENP-H的复合物与FACT和CHD1协同作用,促进CENP-A在着丝粒上的沉积。
Mol Biol Cell. 2009 Sep;20(18):3986-95. doi: 10.1091/mbc.e09-01-0065. Epub 2009 Jul 22.
2
The CENP-S complex is essential for the stable assembly of outer kinetochore structure.着丝粒蛋白S复合体对于外着丝粒结构的稳定组装至关重要。
J Cell Biol. 2009 Jul 27;186(2):173-82. doi: 10.1083/jcb.200903100. Epub 2009 Jul 20.
3
Boveri revisited: chromosomal instability, aneuploidy and tumorigenesis.重访博韦里:染色体不稳定、非整倍体与肿瘤发生
Nat Rev Mol Cell Biol. 2009 Jul;10(7):478-87. doi: 10.1038/nrm2718.
4
Protein architecture of the human kinetochore microtubule attachment site.人类动粒微管附着位点的蛋白质结构
Cell. 2009 May 15;137(4):672-84. doi: 10.1016/j.cell.2009.03.035.
5
Centromere-specific assembly of CENP-a nucleosomes is mediated by HJURP.CENP-A核小体的着丝粒特异性组装由HJURP介导。
Cell. 2009 May 1;137(3):472-84. doi: 10.1016/j.cell.2009.02.039.
6
Comparative profiling identifies C13orf3 as a component of the Ska complex required for mammalian cell division.比较分析表明C13orf3是哺乳动物细胞分裂所需的Ska复合体的一个组成部分。
EMBO J. 2009 May 20;28(10):1453-65. doi: 10.1038/emboj.2009.114. Epub 2009 Apr 23.
7
Stable kinetochore-microtubule interactions depend on the Ska complex and its new component Ska3/C13Orf3.稳定的动粒-微管相互作用依赖于Ska复合体及其新组分Ska3/C13Orf3。
EMBO J. 2009 May 20;28(10):1442-52. doi: 10.1038/emboj.2009.96. Epub 2009 Apr 9.
8
The human kinetochore Ska1 complex facilitates microtubule depolymerization-coupled motility.人类动粒Ska1复合体促进微管解聚偶联的运动。
Dev Cell. 2009 Mar;16(3):374-85. doi: 10.1016/j.devcel.2009.01.011.
9
Releasing the spindle assembly checkpoint without tension.在无张力情况下释放纺锤体组装检查点。
J Cell Biol. 2009 Feb 9;184(3):355-6. doi: 10.1083/jcb.200812016. Epub 2009 Feb 3.
10
Intrakinetochore stretch is associated with changes in kinetochore phosphorylation and spindle assembly checkpoint activity.动粒内张力与动粒磷酸化及纺锤体组装检查点活性的变化相关。
J Cell Biol. 2009 Feb 9;184(3):373-81. doi: 10.1083/jcb.200808130. Epub 2009 Feb 3.

哺乳动物细胞中着丝粒微管附着的对比模型。

Contrasting models for kinetochore microtubule attachment in mammalian cells.

机构信息

Wadsworth Center, New York State Department of Health, Albany, NY 12201, USA.

出版信息

Cell Mol Life Sci. 2010 Jul;67(13):2163-72. doi: 10.1007/s00018-010-0322-x. Epub 2010 Mar 25.

DOI:10.1007/s00018-010-0322-x
PMID:20336345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2883615/
Abstract

Kinetochore function is mediated through its interaction with microtubule plus ends embedded in the kinetochore outer plate. Here, we compare and evaluate current models for kinetochore microtubule attachment, beginning with a brief review of the molecular, biochemical, cellular, and structural studies upon which these models are based. The majority of these studies strongly support a model in which the kinetochore outer plate is a network of fibers that form multiple weak attachments to each microtubule, chiefly through the Ndc80 complex. Multiple weak attachments enable kinetochores to remain attached to microtubule plus ends that are continually growing and shrinking. It is unlikely that rings or "kinetochore fibrils" have a significant role in kinetochore microtubule attachment, but such entities could have a role in stabilizing attachment, modifying microtubule dynamics, and harnessing the energy released from microtubule disassembly. It is currently unclear whether kinetochores control and coordinate the dynamics of individual kinetochore microtubules.

摘要

动粒功能是通过与嵌入动粒外板的微管正端相互作用来介导的。在这里,我们将比较和评估当前的动粒微管附着模型,首先简要回顾这些模型所基于的分子、生化、细胞和结构研究。这些研究中的大多数强烈支持这样一种模型,即动粒外板是一个纤维网络,通过 Ndc80 复合物与每个微管形成多个弱附着,主要是通过 Ndc80 复合物。多个弱附着使动粒能够保持与不断生长和收缩的微管正端相连。环或“动粒原纤维”不太可能在动粒微管附着中起重要作用,但这些实体可能在稳定附着、修饰微管动力学以及利用微管解聚释放的能量方面发挥作用。目前尚不清楚动粒是否控制和协调单个动粒微管的动力学。