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本文引用的文献

1
Cohesin, condensin, and the intramolecular centromere loop together generate the mitotic chromatin spring.黏合蛋白、凝聚素和分子内着丝粒环共同产生有丝分裂染色质弹簧。
J Cell Biol. 2011 Jun 27;193(7):1167-80. doi: 10.1083/jcb.201103138.
2
A cell cycle phosphoproteome of the yeast centrosome.酵母中心体的细胞周期磷酸化蛋白质组。
Science. 2011 Jun 24;332(6037):1557-61. doi: 10.1126/science.1205193.
3
Phosphorylation of the yeast γ-tubulin Tub4 regulates microtubule function.酵母γ-微管蛋白 Tub4 的磷酸化调节微管功能。
PLoS One. 2011 May 5;6(5):e19700. doi: 10.1371/journal.pone.0019700.
4
Regulated offloading of cytoplasmic dynein from microtubule plus ends to the cortex.细胞质动力蛋白从微管正端向质膜卸载的调控。
Dev Cell. 2011 May 17;20(5):639-51. doi: 10.1016/j.devcel.2011.04.011.
5
Tobacco leaves and roots differ in the expression of proline metabolism-related genes in the course of drought stress and subsequent recovery.在干旱胁迫及随后恢复过程中,烟草叶片和根系中转录脯氨酸代谢相关基因的表达存在差异。
J Plant Physiol. 2011 Sep 1;168(13):1588-97. doi: 10.1016/j.jplph.2011.02.009. Epub 2011 Apr 8.
6
Structure-function analysis of the C-terminal domain of CNM67, a core component of the Saccharomyces cerevisiae spindle pole body.酿酒酵母纺锤体极体核心组件 CNM67 的 C 末端结构与功能分析。
J Biol Chem. 2011 May 20;286(20):18240-50. doi: 10.1074/jbc.M111.227371. Epub 2011 Mar 24.
7
XMAP215 polymerase activity is built by combining multiple tubulin-binding TOG domains and a basic lattice-binding region.XMAP215 聚合酶的活性是通过结合多个微管结合 TOG 结构域和一个基本晶格结合区域构建而成的。
Proc Natl Acad Sci U S A. 2011 Feb 15;108(7):2741-6. doi: 10.1073/pnas.1016498108. Epub 2011 Jan 31.
8
Monitoring spindle orientation: Spindle position checkpoint in charge.监测纺锤体方向:纺锤体位置检查点负责。
Cell Div. 2010 Dec 11;5:28. doi: 10.1186/1747-1028-5-28.
9
Identification of Saccharomyces cerevisiae spindle pole body remodeling factors.鉴定酿酒酵母中心体重塑因子。
PLoS One. 2010 Nov 12;5(11):e15426. doi: 10.1371/journal.pone.0015426.
10
Mitotic spindle disassembly occurs via distinct subprocesses driven by the anaphase-promoting complex, Aurora B kinase, and kinesin-8.有丝分裂纺锤体的解体是通过后期促进复合物、极光激酶 B 和驱动蛋白-8 驱动的不同亚过程发生的。
J Cell Biol. 2010 Nov 15;191(4):795-808. doi: 10.1083/jcb.201006028.

有丝分裂纺锤体的形成和功能。

Mitotic spindle form and function.

机构信息

Molecular Cell and Developmental Biology, University of Colorado, Boulder, Colorado 80309, USA.

出版信息

Genetics. 2012 Apr;190(4):1197-224. doi: 10.1534/genetics.111.128710.

DOI:10.1534/genetics.111.128710
PMID:22491889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3316638/
Abstract

The Saccharomyces cerevisiae mitotic spindle in budding yeast is exemplified by its simplicity and elegance. Microtubules are nucleated from a crystalline array of proteins organized in the nuclear envelope, known as the spindle pole body in yeast (analogous to the centrosome in larger eukaryotes). The spindle has two classes of nuclear microtubules: kinetochore microtubules and interpolar microtubules. One kinetochore microtubule attaches to a single centromere on each chromosome, while approximately four interpolar microtubules emanate from each pole and interdigitate with interpolar microtubules from the opposite spindle to provide stability to the bipolar spindle. On the cytoplasmic face, two to three microtubules extend from the spindle pole toward the cell cortex. Processes requiring microtubule function are limited to spindles in mitosis and to spindle orientation and nuclear positioning in the cytoplasm. Microtubule function is regulated in large part via products of the 6 kinesin gene family and the 1 cytoplasmic dynein gene. A single bipolar kinesin (Cin8, class Kin-5), together with a depolymerase (Kip3, class Kin-8) or minus-end-directed kinesin (Kar3, class Kin-14), can support spindle function and cell viability. The remarkable feature of yeast cells is that they can survive with microtubules and genes for just two motor proteins, thus providing an unparalleled system to dissect microtubule and motor function within the spindle machine.

摘要

酿酒酵母的有丝分裂纺锤体以其简单性和优雅性为特点。微管从核膜中组织成的蛋白质的晶体阵列中发芽,在酵母中称为纺锤体极体(类似于较大真核生物中的中心体)。纺锤体有两类核微管:动粒微管和极间微管。一个动粒微管附着在每个染色体上的一个单一着丝粒上,而大约四个极间微管从每个极发出并与来自相反纺锤体的极间微管交织,为双极纺锤体提供稳定性。在细胞质面上,两个到三个微管从纺锤体极伸向细胞皮质。需要微管功能的过程仅限于有丝分裂中的纺锤体以及细胞质中的纺锤体定向和核定位。微管功能在很大程度上受到 6 个驱动蛋白基因家族和 1 个细胞质动力蛋白基因的产物调节。单个双极驱动蛋白(Cin8,类 Kin-5),加上解聚酶(Kip3,类 Kin-8)或负端导向驱动蛋白(Kar3,类 Kin-14),可以支持纺锤体功能和细胞活力。酵母细胞的显著特点是,它们可以仅使用微管和两个运动蛋白基因存活,从而为剖析纺锤体中的微管和运动蛋白功能提供了无与伦比的系统。