Suppr超能文献

动物体细胞中动粒微管的形成:两种竞争机制不分胜负

Kinetochore fiber formation in animal somatic cells: dueling mechanisms come to a draw.

作者信息

Rieder Conly L

机构信息

Laboratory of Cell Regulation, Division of Molecular Medicine, Wadsworth Center, New York State Department of Health, 509, Albany, NY 12201-0509, USA.

出版信息

Chromosoma. 2005 Nov;114(5):310-8. doi: 10.1007/s00412-005-0028-2. Epub 2005 Nov 12.

Abstract

The attachment to and movement of a chromosome on the mitotic spindle are mediated by the formation of a bundle of microtubules (MTs) that tethers the kinetochore on the chromosome to a spindle pole. The origin of these "kinetochore fibers" (K fibers) has been investigated for over 125 years. As noted in 1944 by Schrader [Mitosis, Columbia University Press, New York, 110 pp.], there are three possible ways to form a K fiber: (a) it grows from the pole until it contacts the kinetochore, (b) it grows directly from the kinetochore, or (c) it forms as a result of an interaction between the pole and the chromosome. Since Schrader's time, it has been firmly established that K fibers in centrosome-containing animal somatic cells form as kinetochores capture MTs growing from the spindle pole (route a). It is now similarly clear that in cells lacking centrosomes, including higher plants and many animal oocytes, K fibers "self-assemble" from MTs generated by the chromosomes (route b). Can animal somatic cells form K fibers in the absence of centrosomes by the "self-assembly" pathway? In 2000, the answer to this question was shown to be a resounding "yes." With this result, the next question became whether the presence of a centrosome normally suppresses K fiber self-assembly or if this route works concurrently with centrosome-mediated K-fiber formation. This question, too, has recently been answered: observations on untreated live animal cells expressing green fluorescent protein-tagged tubulin clearly show that kinetochores can nucleate the formation of their associated MTs in a unique manner in the presence of functional centrosomes. The concurrent operation of these two "dueling" routes for forming K fibers in animal cells helps explain why the attachment of kinetochores and the maturation of K fibers occur as quickly as they do on all chromosomes within a cell.

摘要

染色体在有丝分裂纺锤体上的附着和移动是由一束微管(MTs)介导的,这束微管将染色体上的动粒与纺锤体极连接起来。这些“动粒纤维”(K纤维)的起源已经研究了125多年。正如施拉德在1944年所指出的[《有丝分裂》,哥伦比亚大学出版社,纽约,110页],形成K纤维有三种可能的方式:(a)它从纺锤体极生长直到接触到动粒,(b)它直接从动粒生长,或者(c)它是由于纺锤体极与染色体之间的相互作用而形成。自施拉德时代以来,已经确凿地证实,含有中心体的动物体细胞中的K纤维是在动粒捕获从纺锤体极生长的MTs时形成的(途径a)。现在同样清楚的是,在缺乏中心体的细胞中,包括高等植物和许多动物卵母细胞,K纤维由染色体产生的MTs“自我组装”而成(途径b)。动物体细胞在没有中心体的情况下能否通过“自我组装”途径形成K纤维呢?2000年,这个问题的答案被证明是响亮的“能”。有了这个结果,下一个问题就变成了中心体的存在通常是抑制K纤维的自我组装,还是这条途径与中心体介导的K纤维形成同时起作用。这个问题最近也得到了答案:对表达绿色荧光蛋白标记微管蛋白的未处理活动物细胞的观察清楚地表明,在有功能的中心体存在的情况下,动粒能够以独特的方式使其相关MTs成核。在动物细胞中这两条“竞争”的K纤维形成途径的同时运作,有助于解释为什么动粒的附着和K纤维的成熟在细胞内所有染色体上都能如此迅速地发生。

相似文献

1
Kinetochore fiber formation in animal somatic cells: dueling mechanisms come to a draw.
Chromosoma. 2005 Nov;114(5):310-8. doi: 10.1007/s00412-005-0028-2. Epub 2005 Nov 12.
2
Kinetochore-driven formation of kinetochore fibers contributes to spindle assembly during animal mitosis.
J Cell Biol. 2004 Dec 6;167(5):831-40. doi: 10.1083/jcb.200407090. Epub 2004 Nov 29.
3
Formation of the astral mitotic spindle: ultrastructural basis for the centrosome-kinetochore interaction.
Electron Microsc Rev. 1990;3(2):269-300. doi: 10.1016/0892-0354(90)90005-d.
4
NuMA deficiency causes micronuclei via checkpoint-insensitive k-fiber minus-end detachment from mitotic spindle poles.
Curr Biol. 2023 Feb 6;33(3):572-580.e2. doi: 10.1016/j.cub.2022.12.017. Epub 2023 Jan 9.
6
Direct kinetochore-spindle pole connections are not required for chromosome segregation.
J Cell Biol. 2014 Jul 21;206(2):231-43. doi: 10.1083/jcb.201401090. Epub 2014 Jul 14.
7
Kinetochore-generated pushing forces separate centrosomes during bipolar spindle assembly.
J Cell Biol. 2009 Feb 9;184(3):365-72. doi: 10.1083/jcb.200809055.
8
Drosophila Dgt6 interacts with Ndc80, Msps/XMAP215, and gamma-tubulin to promote kinetochore-driven MT formation.
Curr Biol. 2009 Nov 17;19(21):1839-45. doi: 10.1016/j.cub.2009.09.043. Epub 2009 Oct 15.
9
Chromosome fragments possessing only one kinetochore can congress to the spindle equator.
J Cell Biol. 1997 Jan 27;136(2):229-40. doi: 10.1083/jcb.136.2.229.
10
Minus-end capture of preformed kinetochore fibers contributes to spindle morphogenesis.
J Cell Biol. 2003 Mar 3;160(5):671-83. doi: 10.1083/jcb.200208143. Epub 2003 Feb 25.

引用本文的文献

1
Asymmetric Centromeres Differentially Coordinate with Mitotic Machinery to Ensure Biased Sister Chromatid Segregation in Germline Stem Cells.
Cell Stem Cell. 2019 Nov 7;25(5):666-681.e5. doi: 10.1016/j.stem.2019.08.014. Epub 2019 Sep 26.
3
Microtubules assemble near most kinetochores during early prometaphase in human cells.
J Cell Biol. 2018 Aug 6;217(8):2647-2659. doi: 10.1083/jcb.201710094. Epub 2018 Jun 15.
5
Mitotic spindle: kinetochore fibers hold on tight to interpolar bundles.
Eur Biophys J. 2018 Apr;47(3):191-203. doi: 10.1007/s00249-017-1244-4. Epub 2017 Jul 19.
6
Mitotic spindle assembly in animal cells: a fine balancing act.
Nat Rev Mol Cell Biol. 2017 Mar;18(3):187-201. doi: 10.1038/nrm.2016.162. Epub 2017 Feb 8.
7
Aurora-A regulates MCRS1 function during mitosis.
Cell Cycle. 2016 Jul 2;15(13):1779-86. doi: 10.1080/15384101.2016.1187342. Epub 2016 May 18.
8
The RanGTP Pathway: From Nucleo-Cytoplasmic Transport to Spindle Assembly and Beyond.
Front Cell Dev Biol. 2016 Jan 11;3:82. doi: 10.3389/fcell.2015.00082. eCollection 2015.

本文引用的文献

1
3
Spindle microtubules in flux.
J Cell Sci. 2005 Mar 15;118(Pt 6):1105-16. doi: 10.1242/jcs.02284.
4
Kinetochore-spindle microtubule interactions during mitosis.
Curr Opin Cell Biol. 2005 Feb;17(1):35-46. doi: 10.1016/j.ceb.2004.12.009.
5
Drosophila CLASP is required for the incorporation of microtubule subunits into fluxing kinetochore fibres.
Nat Cell Biol. 2005 Jan;7(1):42-7. doi: 10.1038/ncb1207. Epub 2004 Dec 12.
6
Kinetochore-driven formation of kinetochore fibers contributes to spindle assembly during animal mitosis.
J Cell Biol. 2004 Dec 6;167(5):831-40. doi: 10.1083/jcb.200407090. Epub 2004 Nov 29.
7
Hec1 and nuf2 are core components of the kinetochore outer plate essential for organizing microtubule attachment sites.
Mol Biol Cell. 2005 Feb;16(2):519-31. doi: 10.1091/mbc.e04-09-0852. Epub 2004 Nov 17.
8
The dynamic kinetochore-microtubule interface.
J Cell Sci. 2004 Nov 1;117(Pt 23):5461-77. doi: 10.1242/jcs.01536.
9
The mechanism of spindle assembly: functions of Ran and its target TPX2.
J Cell Biol. 2004 Sep 27;166(7):949-55. doi: 10.1083/jcb.200312112.
10
Mechanisms and molecules of the mitotic spindle.
Curr Biol. 2004 Sep 21;14(18):R797-805. doi: 10.1016/j.cub.2004.09.021.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验