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动粒

The kinetochore.

作者信息

Cheeseman Iain M

机构信息

Whitehead Institute and Department of Biology, MIT Nine Cambridge Center, Cambridge, Massachusetts 02142.

出版信息

Cold Spring Harb Perspect Biol. 2014 Jul 1;6(7):a015826. doi: 10.1101/cshperspect.a015826.

DOI:10.1101/cshperspect.a015826
PMID:24984773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4067989/
Abstract

A critical requirement for mitosis is the distribution of genetic material to the two daughter cells. The central player in this process is the macromolecular kinetochore structure, which binds to both chromosomal DNA and spindle microtubule polymers to direct chromosome alignment and segregation. This review will discuss the key kinetochore activities required for mitotic chromosome segregation, including the recognition of a specific site on each chromosome, kinetochore assembly and the formation of kinetochore-microtubule connections, the generation of force to drive chromosome segregation, and the regulation of kinetochore function to ensure that chromosome segregation occurs with high fidelity.

摘要

有丝分裂的一个关键要求是将遗传物质分配到两个子细胞中。这一过程的核心参与者是大分子动粒结构,它与染色体DNA和纺锤体微管聚合物结合,以指导染色体的排列和分离。本综述将讨论有丝分裂染色体分离所需的关键动粒活动,包括识别每条染色体上的特定位点、动粒组装以及动粒-微管连接的形成、驱动染色体分离的力的产生,以及动粒功能的调节,以确保染色体分离能高度精确地发生。

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本文引用的文献

1
The composition, functions, and regulation of the budding yeast kinetochore.酵母有丝分裂纺锤体着丝粒的组成、功能与调控。
Genetics. 2013 Aug;194(4):817-46. doi: 10.1534/genetics.112.145276.
2
Solo or doppio: how many CENP-As make a centromeric nucleosome?单体还是二聚体:多少个着丝粒蛋白A组成一个着丝粒核小体?
Nat Struct Mol Biol. 2013 Jun;20(6):648-50. doi: 10.1038/nsmb.2602.
3
A conserved mechanism for centromeric nucleosome recognition by centromere protein CENP-C.由着丝粒蛋白 CENP-C 识别着丝粒核小体的保守机制。
Science. 2013 May 31;340(6136):1110-3. doi: 10.1126/science.1235532.
4
CDK-dependent phosphorylation and nuclear exclusion coordinately control kinetochore assembly state.CDK 依赖性磷酸化和核排斥协同控制着动粒组装状态。
J Cell Biol. 2013 Apr 1;201(1):23-32. doi: 10.1083/jcb.201301006. Epub 2013 Mar 25.
5
Review series: The functions and consequences of force at kinetochores.综述系列:着丝粒处力的功能和后果。
J Cell Biol. 2013 Mar 4;200(5):557-65. doi: 10.1083/jcb.201211113.
6
Direct binding between BubR1 and B56-PP2A phosphatase complexes regulate mitotic progression.BubR1 与 B56-PP2A 磷酸酶复合物的直接结合调控有丝分裂进程。
J Cell Sci. 2013 Mar 1;126(Pt 5):1086-92. doi: 10.1242/jcs.122481. Epub 2013 Jan 23.
7
CENP-T provides a structural platform for outer kinetochore assembly.CENP-T 为外中心体装配提供了一个结构平台。
EMBO J. 2013 Feb 6;32(3):424-36. doi: 10.1038/emboj.2012.348. Epub 2013 Jan 18.
8
The CCAN recruits CENP-A to the centromere and forms the structural core for kinetochore assembly.中央复合体招募着丝粒蛋白 A 到着丝粒上,并形成动粒组装的结构核心。
J Cell Biol. 2013 Jan 7;200(1):45-60. doi: 10.1083/jcb.201210106. Epub 2012 Dec 31.
9
The kinetochore-bound Ska1 complex tracks depolymerizing microtubules and binds to curved protofilaments.着丝粒结合的 Ska1 复合物追踪去聚合的微管,并与弯曲的原纤维结合。
Dev Cell. 2012 Nov 13;23(5):968-80. doi: 10.1016/j.devcel.2012.09.012. Epub 2012 Oct 18.
10
Integration of kinase and phosphatase activities by BUBR1 ensures formation of stable kinetochore-microtubule attachments.BUBR1 通过整合激酶和磷酸酶活性来确保稳定的动粒-微管连接的形成。
Dev Cell. 2012 Oct 16;23(4):745-55. doi: 10.1016/j.devcel.2012.09.005.