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本文引用的文献

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In vivo protein architecture of the eukaryotic kinetochore with nanometer scale accuracy.真核生物动粒的体内蛋白质结构,精度达纳米级别。
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Kinetochore-microtubule attachment relies on the disordered N-terminal tail domain of Hec1.动粒微管附着依赖于Hec1无序的N端尾部结构域。
Curr Biol. 2008 Nov 25;18(22):1778-84. doi: 10.1016/j.cub.2008.08.012.
4
Kinetochore attachments require an interaction between unstructured tails on microtubules and Ndc80(Hec1).动粒附着需要微管上的无结构尾部与Ndc80(Hec1)之间相互作用。
Curr Biol. 2008 Nov 25;18(22):1785-91. doi: 10.1016/j.cub.2008.11.007.
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Epigenetic regulation of centromeric chromatin: old dogs, new tricks?着丝粒染色质的表观遗传调控:老问题,新方法?
Nat Rev Genet. 2008 Dec;9(12):923-37. doi: 10.1038/nrg2466.
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Toward a molecular structure of the eukaryotic kinetochore.迈向真核生物动粒的分子结构。
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Fibrils connect microtubule tips with kinetochores: a mechanism to couple tubulin dynamics to chromosome motion.原纤维将微管末端与动粒相连:一种将微管蛋白动力学与染色体运动相耦合的机制。
Cell. 2008 Oct 17;135(2):322-33. doi: 10.1016/j.cell.2008.08.038.
8
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果蝇Spc105的动粒内定位及重要功能结构域

Intrakinetochore localization and essential functional domains of Drosophila Spc105.

作者信息

Schittenhelm Ralf B, Chaleckis Romanas, Lehner Christian F

机构信息

Institute of Zoology, University of Zurich, Zurich, Switzerland.

出版信息

EMBO J. 2009 Aug 19;28(16):2374-86. doi: 10.1038/emboj.2009.188. Epub 2009 Jul 9.

DOI:10.1038/emboj.2009.188
PMID:19590494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2735171/
Abstract

The kinetochore is assembled during mitotic and meiotic divisions within the centromeric region of chromosomes. It is composed of more than eighty different proteins. Spc105 (also designated as Spc7, KNL-1 or Blinkin in different eukaryotes) is a comparatively large kinetochore protein, which can bind to the Mis12/MIND and Ndc80 complexes and to the spindle assembly checkpoint components Bub1 and BubR1. Our genetic characterization of Drosophila Spc105 shows that a truncated version lacking the rapidly evolving, repetitive central third still provides all essential functions. Moreover, in comparison with Cenp-C that has previously been observed to extend from the inner to the outer kinetochore region, full-length Spc105 is positioned further out and is not similarly extended along the spindle axis. Thus, our results indicate that Spc105 forms neither an extended link connecting inner Cenp-A chromatin with outer kinetochore regions nor a scaffold constraining kinetochore subcomplexes and spindle assembly checkpoint components together into a geometrically rigid supercomplex. Spc105 seems to provide a platform within the outer kinetochore allowing independent assembly of various kinetochore components.

摘要

动粒在有丝分裂和减数分裂期间于染色体的着丝粒区域组装而成。它由八十多种不同的蛋白质组成。Spc105(在不同真核生物中也被称为Spc7、KNL-1或Blinkin)是一种相对较大的动粒蛋白,它可以与Mis12/MIND和Ndc80复合体以及纺锤体组装检查点组件Bub1和BubR1结合。我们对果蝇Spc105的遗传学特征分析表明,一个缺少快速进化的、重复性的中央三分之一区域的截短版本仍然具备所有基本功能。此外,与之前观察到的从内动粒区域延伸到外动粒区域的Cenp-C相比,全长Spc105的位置更靠外,并且不会沿着纺锤体轴类似地延伸。因此,我们的结果表明,Spc105既不形成连接内部Cenp-A染色质与外动粒区域的延伸连接,也不形成将动粒子复合体和纺锤体组装检查点组件约束在一起形成几何刚性超复合体的支架。Spc105似乎在外动粒内提供了一个平台,允许各种动粒组件独立组装。