• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Kinetochore fiber formation in animal somatic cells: dueling mechanisms come to a draw.动物体细胞中动粒微管的形成:两种竞争机制不分胜负
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.在动物有丝分裂过程中,动粒驱动的动粒纤维形成有助于纺锤体组装。
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.星体有丝分裂纺锤体的形成:中心体-动粒相互作用的超微结构基础
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.核仁基质蛋白缺失通过检查点不敏感的 k 纤维从有丝分裂纺锤体极末端脱离导致微核的形成。
Curr Biol. 2023 Feb 6;33(3):572-580.e2. doi: 10.1016/j.cub.2022.12.017. Epub 2023 Jan 9.
5
Kinetochores are transported poleward along a single astral microtubule during chromosome attachment to the spindle in newt lung cells.在蝾螈肺细胞中,着丝粒在染色体附着到纺锤体的过程中沿着单根星体微管向两极运输。
J Cell Biol. 1990 Jan;110(1):81-95. doi: 10.1083/jcb.110.1.81.
6
Direct kinetochore-spindle pole connections are not required for chromosome segregation.直接的动粒-纺锤极连接对于染色体分离并非必需。
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.动粒产生的推力在双极纺锤体组装过程中分离中心体。
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.果蝇 Dgt6 与 Ndc80、Msps/XMAP215 和 γ-微管蛋白相互作用,促进动粒驱动的微管形成。
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.仅拥有一个动粒的染色体片段能够汇聚到纺锤体赤道面。
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.预先形成的动粒纤维的负端捕获有助于纺锤体形态发生。
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.不对称着丝粒通过与有丝分裂机制的差异化协调,确保生殖干细胞中姐妹染色单体的偏分离。
Cell Stem Cell. 2019 Nov 7;25(5):666-681.e5. doi: 10.1016/j.stem.2019.08.014. Epub 2019 Sep 26.
2
The microtubule-associated protein HURP recruits the centrosomal protein TACC3 to regulate K-fiber formation and support chromosome congression.微管相关蛋白 HURP 将中心体蛋白 TACC3 募集到调节 K-纤维的形成和支持染色体的汇聚。
J Biol Chem. 2018 Oct 5;293(40):15733-15747. doi: 10.1074/jbc.RA118.003676. Epub 2018 Jul 27.
3
Microtubules assemble near most kinetochores during early prometaphase in human cells.在人类细胞的早前期,微管在大多数着丝粒附近组装。
J Cell Biol. 2018 Aug 6;217(8):2647-2659. doi: 10.1083/jcb.201710094. Epub 2018 Jun 15.
4
FGFR3-TACC3 cancer gene fusions cause mitotic defects by removal of endogenous TACC3 from the mitotic spindle.FGFR3-TACC3 癌基因融合通过将内源性 TACC3 从有丝纺锤体中移除而导致有丝分裂缺陷。
Open Biol. 2017 Aug;7(8). doi: 10.1098/rsob.170080.
5
Mitotic spindle: kinetochore fibers hold on tight to interpolar bundles.有丝分裂纺锤体:动粒纤维紧紧附着于极间束。
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.动物细胞有丝分裂纺锤体的组装:精细的平衡行为。
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.在有丝分裂过程中,极光激酶A调节MCRS1的功能。
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.RanGTP 通路:从核质转运到纺锤体组装及其他。
Front Cell Dev Biol. 2016 Jan 11;3:82. doi: 10.3389/fcell.2015.00082. eCollection 2015.
9
Super-resolution kinetochore tracking reveals the mechanisms of human sister kinetochore directional switching.超分辨率动粒追踪揭示了人类姐妹动粒方向转换的机制。
Elife. 2015 Oct 13;4:e09500. doi: 10.7554/eLife.09500.
10
The deubiquitinating enzyme complex BRISC is required for proper mitotic spindle assembly in mammalian cells.去泛素化酶复合物BRISC是哺乳动物细胞中正常有丝分裂纺锤体组装所必需的。
J Cell Biol. 2015 Jul 20;210(2):209-24. doi: 10.1083/jcb.201503039.

本文引用的文献

1
Mitotic Behavior of Induced Chromosomal Fragments Lacking Spindle Attachments in the Neuroblasts of the Grasshopper.蝗虫神经母细胞中缺乏纺锤体附着的诱导染色体片段的有丝分裂行为
Proc Natl Acad Sci U S A. 1938 Nov;24(11):500-7. doi: 10.1073/pnas.24.11.500.
2
Efficient chromosome capture requires a bias in the 'search-and-capture' process during mitotic-spindle assembly.高效的染色体捕获需要在有丝分裂纺锤体组装过程中的“搜索与捕获”过程中存在偏差。
Curr Biol. 2005 May 10;15(9):828-32. doi: 10.1016/j.cub.2005.03.019.
3
Spindle microtubules in flux.处于动态变化中的纺锤体微管。
J Cell Sci. 2005 Mar 15;118(Pt 6):1105-16. doi: 10.1242/jcs.02284.
4
Kinetochore-spindle microtubule interactions during mitosis.有丝分裂期间动粒与纺锤体微管的相互作用。
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.果蝇CLASP是微管亚基整合到动态动粒纤维中所必需的。
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.在动物有丝分裂过程中,动粒驱动的动粒纤维形成有助于纺锤体组装。
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.Hec1和nuf2是动粒外板的核心组成部分,对组织微管附着位点至关重要。
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.动态动粒-微管界面
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.纺锤体组装机制:Ran及其靶点TPX2的功能
J Cell Biol. 2004 Sep 27;166(7):949-55. doi: 10.1083/jcb.200312112.
10
Mechanisms and molecules of the mitotic spindle.有丝分裂纺锤体的机制与分子
Curr Biol. 2004 Sep 21;14(18):R797-805. doi: 10.1016/j.cub.2004.09.021.

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.

DOI:10.1007/s00412-005-0028-2
PMID:16270218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2570760/
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。