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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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Mitotic regulator SKAP forms a link between kinetochore core complex KMN and dynamic spindle microtubules.有丝分裂调节因子 SKAP 连接着动粒核心复合物 KMN 和动态纺锤体微管。
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本文引用的文献

1
Spindle microtubules generate tension-dependent changes in the distribution of inner kinetochore proteins.纺锤体微管产生依赖张力的内在动粒蛋白分布变化。
J Cell Biol. 2011 Apr 4;193(1):125-40. doi: 10.1083/jcb.201012050.
2
Direct binding of Cenp-C to the Mis12 complex joins the inner and outer kinetochore.Cenp-C 与 Mis12 复合物的直接结合将内、外着丝粒连接在一起。
Curr Biol. 2011 Mar 8;21(5):391-8. doi: 10.1016/j.cub.2010.12.039. Epub 2011 Feb 25.
3
CENP-C is a structural platform for kinetochore assembly.着丝粒蛋白 C 是着丝粒装配的结构平台。
Curr Biol. 2011 Mar 8;21(5):399-405. doi: 10.1016/j.cub.2011.02.005. Epub 2011 Feb 25.
4
The Ndc80 complex uses a tripartite attachment point to couple microtubule depolymerization to chromosome movement.Ndc80 复合物使用三部分附着点将微管解聚与染色体运动偶联。
Mol Biol Cell. 2011 Apr 15;22(8):1217-26. doi: 10.1091/mbc.E10-07-0626. Epub 2011 Feb 16.
5
The NDC80 complex proteins Nuf2 and Hec1 make distinct contributions to kinetochore-microtubule attachment in mitosis.NDC80 复合物蛋白 Nuf2 和 Hec1 在有丝分裂中对动粒-微管附着有不同的贡献。
Mol Biol Cell. 2011 Mar 15;22(6):759-68. doi: 10.1091/mbc.E10-08-0671. Epub 2011 Jan 26.
6
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.
7
Ndc80 internal loop interacts with Dis1/TOG to ensure proper kinetochore-spindle attachment in fission yeast.Ndc80 内环与 Dis1/TOG 相互作用,以确保裂殖酵母中正确的着丝粒-纺锤体附着。
Curr Biol. 2011 Feb 8;21(3):214-20. doi: 10.1016/j.cub.2010.12.048. Epub 2011 Jan 20.
8
The Ndc80 loop region facilitates formation of kinetochore attachment to the dynamic microtubule plus end.Ndc80 环区有助于动粒与微管正极端的连接形成。
Curr Biol. 2011 Feb 8;21(3):207-13. doi: 10.1016/j.cub.2010.12.050. Epub 2011 Jan 20.
9
Protein interaction domain mapping of human kinetochore protein Blinkin reveals a consensus motif for binding of spindle assembly checkpoint proteins Bub1 and BubR1.人着丝粒蛋白 Blinkin 的蛋白相互作用结构域作图揭示了纺锤体组装检验点蛋白 Bub1 和 BubR1 结合的一个共识基序。
Mol Cell Biol. 2011 Mar;31(5):998-1011. doi: 10.1128/MCB.00815-10. Epub 2011 Jan 3.
10
The Dam1 ring binds to the E-hook of tubulin and diffuses along the microtubule.Dam1 环结合于微管蛋白的 E 环,并沿微管扩散。
Mol Biol Cell. 2011 Feb 15;22(4):457-66. doi: 10.1091/mbc.E10-10-0841. Epub 2010 Dec 17.

可视化着丝粒结构。

Visualizing kinetochore architecture.

机构信息

Biophysics Graduate Group, UC Berkeley, Berkeley, CA 94720, United States.

出版信息

Curr Opin Struct Biol. 2011 Oct;21(5):661-9. doi: 10.1016/j.sbi.2011.07.009. Epub 2011 Aug 22.

DOI:10.1016/j.sbi.2011.07.009
PMID:21862320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3189262/
Abstract

Kinetochores are large macromolecular assemblies that link chromosomes to spindle microtubules (MTs) during mitosis. Here we review recent advances in the study of core MT-binding kinetochore complexes using electron microcopy methods in vitro and nanometer-accuracy fluorescence microscopy in vivo. We synthesize these findings in novel three-dimensional models of both the budding yeast and vertebrate kinetochore in different stages of mitosis. There is a growing consensus that kinetochores are highly dynamic, supra-molecular machines that undergo dramatic structural rearrangements in response to MT capture and spindle forces during mitosis.

摘要

着丝粒是在有丝分裂过程中将染色体与纺锤体微管(MTs)连接起来的大型大分子组装体。在这里,我们综述了使用体外电子显微镜方法和体内纳米精度荧光显微镜研究核心 MT 结合着丝粒复合物的最新进展。我们在新型三维模型中综合了芽殖酵母和脊椎动物着丝粒在有丝分裂不同阶段的这些发现。越来越多的共识认为,着丝粒是高度动态的、超分子机器,在有丝分裂过程中,为了捕获 MT 和纺锤体力,会发生剧烈的结构重排。