• 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

动力蛋白轻链Tctex-1在动粒上的非依赖动力蛋白的作用。

A dynein independent role of Tctex-1 at the kinetochore.

作者信息

Liu Chenshu, Chuang Jen-Zen, Sung Ching-Hwa, Mao Yinghui

机构信息

a Department of Pathology and Cell Biology ; Columbia University College of Physicians and Surgeons ; New York , NY USA.

出版信息

Cell Cycle. 2015;14(9):1379-88. doi: 10.1080/15384101.2014.1000217.

DOI:10.1080/15384101.2014.1000217
PMID:25928583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4614829/
Abstract

Dynein light chains are accessory subunits of the cytoplasmic dynein complex, a minus-end directed microtubule motor. Here, we demonstrate that the dynein light chain Tctex-1 associates with unattached kinetochores and is essential for accurate chromosome segregation. Tctex-1 knockdown in cells does not affect the localization and function of dynein at the kinetochore, but produces a prolonged mitotic arrest with a few misaligned chromosomes, which are subsequently missegregated during anaphase. This function is independent of Tctex-1's association with dynein. The kinetochore localization of Tctex-1 is independent of the ZW10-dynein pathway, but requires the Ndc80 complex. Thus, our findings reveal a dynein independent role of Tctex-1 at the kinetochore to enhance the stability of kinetochore-microtubule attachment.

摘要

动力蛋白轻链是胞质动力蛋白复合体的辅助亚基,胞质动力蛋白复合体是一种向微管负端移动的马达蛋白。在此,我们证明动力蛋白轻链Tctex-1与未附着的动粒相关联,并且对于精确的染色体分离至关重要。在细胞中敲低Tctex-1不会影响动力蛋白在动粒处的定位和功能,但会导致有丝分裂长期停滞,并出现一些染色体排列错误,这些染色体随后在后期会发生错误分离。该功能独立于Tctex-1与动力蛋白的关联。Tctex-1在动粒处的定位独立于ZW10-动力蛋白途径,但需要Ndc80复合体。因此,我们的研究结果揭示了Tctex-1在动粒处具有独立于动力蛋白的作用,可增强动粒-微管附着的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/1113744003a8/kccy-14-09-1000217-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/050fcc611391/kccy-14-09-1000217-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/b8b68f1a913d/kccy-14-09-1000217-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/d12ecad0e52e/kccy-14-09-1000217-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/83ad3d85dcfe/kccy-14-09-1000217-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/6671e28e48c2/kccy-14-09-1000217-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/1113744003a8/kccy-14-09-1000217-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/050fcc611391/kccy-14-09-1000217-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/b8b68f1a913d/kccy-14-09-1000217-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/d12ecad0e52e/kccy-14-09-1000217-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/83ad3d85dcfe/kccy-14-09-1000217-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/6671e28e48c2/kccy-14-09-1000217-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8495/4614829/1113744003a8/kccy-14-09-1000217-g006.jpg

相似文献

1
A dynein independent role of Tctex-1 at the kinetochore.动力蛋白轻链Tctex-1在动粒上的非依赖动力蛋白的作用。
Cell Cycle. 2015;14(9):1379-88. doi: 10.1080/15384101.2014.1000217.
2
Kinetochore dynein generates a poleward pulling force to facilitate congression and full chromosome alignment.动粒动力蛋白产生向极拉力,以促进染色体移向赤道板并完全对齐。
Cell Res. 2007 Aug;17(8):701-12. doi: 10.1038/cr.2007.65.
3
Phosphorylation regulates targeting of cytoplasmic dynein to kinetochores during mitosis.磷酸化作用在有丝分裂过程中调节胞质动力蛋白向动粒的靶向定位。
J Cell Biol. 2008 Dec 1;183(5):819-34. doi: 10.1083/jcb.200804114. Epub 2008 Nov 24.
4
Antagonism between the dynein and Ndc80 complexes at kinetochores controls the stability of kinetochore-microtubule attachments during mitosis.在有丝分裂过程中,动粒上的动力蛋白和 Ndc80 复合物之间的拮抗作用控制着动粒-微管连接的稳定性。
J Biol Chem. 2018 Apr 20;293(16):5755-5765. doi: 10.1074/jbc.RA117.001699. Epub 2018 Feb 23.
5
Dynein prevents erroneous kinetochore-microtubule attachments in mitosis.动力蛋白可防止有丝分裂过程中动粒与微管的错误连接。
Cell Cycle. 2015;14(21):3356-61. doi: 10.1080/15384101.2015.1089369.
6
Coordination between the Ndc80 complex and dynein is essential for microtubule plus-end capture by kinetochores during early mitosis.在有丝分裂早期,Ndc80 复合物与动力蛋白之间的协调对于动粒对微管正极的捕获是必不可少的。
J Biol Chem. 2023 Jun;299(6):104711. doi: 10.1016/j.jbc.2023.104711. Epub 2023 Apr 14.
7
NudE regulates dynein at kinetochores but is dispensable for other dynein functions in the early embryo.NudE 在动粒处调控动力蛋白,但对于早期胚胎中的其他动力蛋白功能是可有可无的。
J Cell Sci. 2018 Jan 8;131(1):jcs212159. doi: 10.1242/jcs.212159.
8
CLIP-170 tethers kinetochores to microtubule plus ends against poleward force by dynein for stable kinetochore-microtubule attachment.CLIP-170通过动力蛋白将动粒与微管正端相连,以抵抗向极的力,从而实现稳定的动粒-微管附着。
FEBS Lett. 2015 Sep 14;589(19 Pt B):2739-46. doi: 10.1016/j.febslet.2015.07.036. Epub 2015 Jul 29.
9
Dynein and mast/orbit/CLASP have antagonistic roles in regulating kinetochore-microtubule plus-end dynamics.动力蛋白与纺锤体微管组织中心/轨道/微管结合蛋白在调控动粒微管正端动力学方面具有拮抗作用。
J Cell Sci. 2009 Jul 15;122(Pt 14):2543-53. doi: 10.1242/jcs.044818. Epub 2009 Jun 23.
10
Dynamic kinetochore size regulation promotes microtubule capture and chromosome biorientation in mitosis.动态着丝粒大小调节促进有丝分裂中微管的捕获和染色体的双定向。
Nat Cell Biol. 2018 Jul;20(7):800-810. doi: 10.1038/s41556-018-0130-3. Epub 2018 Jun 18.

引用本文的文献

1
MAST4 promotes primary ciliary resorption through phosphorylation of Tctex-1.MAST4 通过磷酸化 Tctex-1 促进初级纤毛吸收。
Life Sci Alliance. 2023 Sep 19;6(11). doi: 10.26508/lsa.202301947. Print 2023 Nov.
2
A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in .核膜上的一个合作网络在 卵子发生过程中抵消了 LINC 介导的力。
Sci Adv. 2023 Jul 14;9(28):eabn5709. doi: 10.1126/sciadv.abn5709. Epub 2023 Jul 12.
3
Dynein Light Chain Protein Tctex1: A Novel Prognostic Marker and Molecular Mediator in Glioblastoma.

本文引用的文献

1
Linked in: formation and regulation of microtubule attachments during chromosome segregation.着丝粒连接:染色体分离过程中微管连接的形成和调控。
Curr Opin Cell Biol. 2014 Feb;26:113-22. doi: 10.1016/j.ceb.2013.12.005. Epub 2014 Jan 7.
2
IGF-1 activates a cilium-localized noncanonical Gβγ signaling pathway that regulates cell-cycle progression.IGF-1 激活了一种定位于纤毛的非经典 Gβγ 信号通路,该通路调节细胞周期进程。
Dev Cell. 2013 Aug 26;26(4):358-68. doi: 10.1016/j.devcel.2013.07.014. Epub 2013 Aug 15.
3
Review series: The functions and consequences of force at kinetochores.
动力蛋白轻链蛋白Tctex1:胶质母细胞瘤中的一种新型预后标志物和分子介质。
Cancers (Basel). 2021 May 27;13(11):2624. doi: 10.3390/cancers13112624.
4
Centrifugal Displacement of Nuclei Reveals Multiple LINC Complex Mechanisms for Homeostatic Nuclear Positioning.离心力驱动核迁移揭示了 LINC 复合物维持核定位的多种机制。
Curr Biol. 2017 Oct 23;27(20):3097-3110.e5. doi: 10.1016/j.cub.2017.08.073. Epub 2017 Oct 5.
5
Tctex-1 controls ciliary resorption by regulating branched actin polymerization and endocytosis.Tctex-1通过调节分支肌动蛋白聚合和内吞作用来控制纤毛的吸收。
EMBO Rep. 2017 Aug;18(8):1460-1472. doi: 10.15252/embr.201744204. Epub 2017 Jun 12.
6
Set Theory, Logic, and Probability: The Integration of Qualitative Reasoning into Teaching Statistics for Quantitative Biology.集合论、逻辑与概率:将定性推理融入定量生物学统计学教学
CBE Life Sci Educ. 2016 winter;15(4). doi: 10.1187/cbe.16-06-0184.
7
Formin-mediated epigenetic maintenance of centromere identity.成膜蛋白介导的着丝粒身份的表观遗传维持。
Small GTPases. 2017 Oct 2;8(4):245-250. doi: 10.1080/21541248.2016.1215658. Epub 2016 Jul 22.
8
Diaphanous formin mDia2 regulates CENP-A levels at centromeres.透明形态发生素mDia2调节着丝粒处的CENP-A水平。
J Cell Biol. 2016 May 23;213(4):415-24. doi: 10.1083/jcb.201512034. Epub 2016 May 16.
9
Non-Overlapping Distributions and Functions of the VDAC Family in Ciliogenesis.电压依赖性阴离子通道(VDAC)家族在纤毛发生中的非重叠分布与功能
Cells. 2015 Jul 31;4(3):331-53. doi: 10.3390/cells4030331.
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.
4
New insights into the mechanism for chromosome alignment in metaphase.中期染色体排列机制的新见解。
Int Rev Cell Mol Biol. 2013;303:237-62. doi: 10.1016/B978-0-12-407697-6.00006-4.
5
The MRN-CtIP pathway is required for metaphase chromosome alignment.MRN-CtIP 通路对于中期染色体的排列是必需的。
Mol Cell. 2013 Mar 28;49(6):1097-107. doi: 10.1016/j.molcel.2013.01.023. Epub 2013 Feb 21.
6
The KMN protein network--chief conductors of the kinetochore orchestra.KMN 蛋白网络——动粒乐团的首席指挥家。
J Cell Sci. 2012 Dec 15;125(Pt 24):5927-36. doi: 10.1242/jcs.093724. Epub 2013 Feb 15.
7
Microtubule plus-ends within a mitotic cell are 'moving platforms' with anchoring, signalling and force-coupling roles.有丝分裂细胞内的微管正端是具有锚定、信号和力偶联作用的“活动平台”。
Open Biol. 2012 Nov;2(11):120132. doi: 10.1098/rsob.120132.
8
CENP-A: the key player behind centromere identity, propagation, and kinetochore assembly.着丝粒蛋白A:着丝粒身份、遗传及动粒组装背后的关键因子。
Chromosoma. 2012 Dec;121(6):527-38. doi: 10.1007/s00412-012-0386-5. Epub 2012 Oct 26.
9
CENP-E--dependent BubR1 autophosphorylation enhances chromosome alignment and the mitotic checkpoint.CENP-E 依赖性 BubR1 自磷酸化增强染色体排列和有丝分裂检查点。
J Cell Biol. 2012 Jul 23;198(2):205-17. doi: 10.1083/jcb.201202152. Epub 2012 Jul 16.
10
FORMIN a link between kinetochores and microtubule ends.形成动粒与微管末端之间的连接。
Trends Cell Biol. 2011 Nov;21(11):625-9. doi: 10.1016/j.tcb.2011.08.005. Epub 2011 Sep 13.