• 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

着丝粒的三个明智功能:不见错误、不闻断裂、不说延迟。

Three wise centromere functions: see no error, hear no break, speak no delay.

作者信息

Tanaka Tomoyuki U, Clayton Lesley, Natsume Toyoaki

机构信息

Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.

出版信息

EMBO Rep. 2013 Dec;14(12):1073-83. doi: 10.1038/embor.2013.181. Epub 2013 Nov 15.

DOI:10.1038/embor.2013.181
PMID:24232185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3849490/
Abstract

The main function of the centromere is to promote kinetochore assembly for spindle microtubule attachment. Two additional functions of the centromere, however, are becoming increasingly clear: facilitation of robust sister-chromatid cohesion at pericentromeres and advancement of replication of centromeric regions. The combination of these three centromere functions ensures correct chromosome segregation during mitosis. Here, we review the mechanisms of the kinetochore-microtubule interaction, focusing on sister-kinetochore bi-orientation (or chromosome bi-orientation). We also discuss the biological importance of robust pericentromeric cohesion and early centromere replication, as well as the mechanisms orchestrating these two functions at the microtubule attachment site.

摘要

着丝粒的主要功能是促进动粒组装以便纺锤体微管附着。然而,着丝粒的另外两个功能正变得越来越清晰:促进着丝粒周围区域姐妹染色单体的牢固黏连以及推进着丝粒区域的复制。这三种着丝粒功能的结合确保了有丝分裂过程中染色体的正确分离。在此,我们综述动粒与微管相互作用的机制,重点关注姐妹动粒双定向(或染色体双定向)。我们还讨论了着丝粒周围区域牢固黏连和着丝粒早期复制的生物学重要性,以及在微管附着位点协调这两种功能的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/b4411aa9b8ef/embor2013181i3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/f50fb19ca77f/embor2013181f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/db92a048d3ef/embor2013181f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/5e77cd052505/embor2013181f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/1b4867b5741c/embor2013181f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/2e7dde3b4c10/embor2013181f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/01c78b5df2c8/embor2013181f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/6a6f7ec3fcac/embor2013181i1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/a84b54dde1c1/embor2013181i2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/b4411aa9b8ef/embor2013181i3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/f50fb19ca77f/embor2013181f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/db92a048d3ef/embor2013181f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/5e77cd052505/embor2013181f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/1b4867b5741c/embor2013181f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/2e7dde3b4c10/embor2013181f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/01c78b5df2c8/embor2013181f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/6a6f7ec3fcac/embor2013181i1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/a84b54dde1c1/embor2013181i2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5815/3849490/b4411aa9b8ef/embor2013181i3.jpg

相似文献

1
Three wise centromere functions: see no error, hear no break, speak no delay.着丝粒的三个明智功能:不见错误、不闻断裂、不说延迟。
EMBO Rep. 2013 Dec;14(12):1073-83. doi: 10.1038/embor.2013.181. Epub 2013 Nov 15.
2
Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing.着丝粒内区定位的 CPC 维持着丝粒的黏合,并允许有丝分裂检验点失活。
Nat Commun. 2017 May 31;8:15542. doi: 10.1038/ncomms15542.
3
Aurora B/AIR-2 regulates sister centromere resolution and CENP-A/HCP-3 organization to prevent merotelic attachments.极光激酶B/AIR-2调节姐妹着丝粒分离及着丝粒蛋白A/组蛋白H2A变体HCP-3的组织,以防止染色体错向连接。
J Mol Cell Biol. 2025 May 2;16(10). doi: 10.1093/jmcb/mjae045.
4
Kinetochore geometry defined by cohesion within the centromere.由着丝粒内的黏连所定义的动粒几何结构。
Nature. 2009 Apr 16;458(7240):852-8. doi: 10.1038/nature07876.
5
Correcting aberrant kinetochore microtubule attachments: a hidden regulation of Aurora B on microtubules.纠正异常的动粒微管附着:极光 B 对微管的隐性调节。
Curr Opin Cell Biol. 2019 Jun;58:34-41. doi: 10.1016/j.ceb.2018.12.007. Epub 2019 Jan 23.
6
Regulation of kinetochore-microtubule attachments by Aurora B kinase.极光激酶B对动粒微管附着的调控
Biochem Soc Trans. 2009 Oct;37(Pt 5):976-80. doi: 10.1042/BST0370976.
7
Spatiotemporal dynamics of Aurora B-PLK1-MCAK signaling axis orchestrates kinetochore bi-orientation and faithful chromosome segregation.极光激酶B-丝氨酸/苏氨酸蛋白激酶1-微管蛋白去酪氨酸化酶信号轴的时空动态调控动粒双定向和准确的染色体分离。
Sci Rep. 2015 Jul 24;5:12204. doi: 10.1038/srep12204.
8
Aurora A kinase phosphorylates Hec1 to regulate metaphase kinetochore-microtubule dynamics.极光激酶 A 将 Hec1 磷酸化以调节中期着丝粒-微管动力学。
J Cell Biol. 2018 Jan 2;217(1):163-177. doi: 10.1083/jcb.201707160. Epub 2017 Nov 29.
9
Centromere-localized Aurora B kinase is required for the fidelity of chromosome segregation.着丝粒定位的极光激酶B对于染色体分离的准确性是必需的。
J Cell Biol. 2020 Feb 3;219(2). doi: 10.1083/jcb.201907092.
10
Phosphorylation of CENP-R by Aurora B regulates kinetochore-microtubule attachment for accurate chromosome segregation.着丝粒结合蛋白 R 由 Aurora B 激酶磷酸化调控微管与动粒的连接,从而保证染色体的精确分离。
J Mol Cell Biol. 2022 Sep 27;14(7). doi: 10.1093/jmcb/mjac051.

引用本文的文献

1
Nuclear localization of MTHFD2 is required for correct mitosis progression.MTHFD2 的核定位对于正确的有丝分裂进程是必需的。
Nat Commun. 2024 Nov 12;15(1):9529. doi: 10.1038/s41467-024-51847-z.
2
HDAC6 decreases H4K16 and α-tubulin acetylation during porcine oocyte maturation.组蛋白去乙酰化酶 6 在猪卵母细胞成熟过程中降低 H4K16 和 α-微管蛋白的乙酰化。
Cell Cycle. 2023 Sep;22(18):2057-2069. doi: 10.1080/15384101.2023.2275907. Epub 2023 Nov 23.
3
TRF1 Depletion Reveals Mutual Regulation Between Telomeres, Kinetochores, and Inner Centromeres in Mouse Oocytes.

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
Aurora B and Cdk1 mediate Wapl activation and release of acetylated cohesin from chromosomes by phosphorylating Sororin.极光 B 和 Cdk1 通过磷酸化 Sororin 介导 Wapl 的激活和乙酰化黏连蛋白从染色体上的释放。
Proc Natl Acad Sci U S A. 2013 Aug 13;110(33):13404-9. doi: 10.1073/pnas.1305020110. Epub 2013 Jul 30.
3
Kinetochores coordinate pericentromeric cohesion and early DNA replication by Cdc7-Dbf4 kinase recruitment.
TRF1缺失揭示了小鼠卵母细胞中端粒、动粒和内着丝粒之间的相互调控。
Front Cell Dev Biol. 2021 Sep 17;9:749116. doi: 10.3389/fcell.2021.749116. eCollection 2021.
4
Geographic distribution of sex chromosome polymorphism in Anastrepha fraterculus sp. 1 from Argentina.阿根廷小实蝇种组1性染色体多态性的地理分布
BMC Genet. 2020 Dec 18;21(Suppl 2):149. doi: 10.1186/s12863-020-00944-1.
5
LKB1 inactivation leads to centromere defects and genome instability via p53-dependent upregulation of survivin.LKB1 失活通过 p53 依赖性上调 survivin 导致着丝粒缺陷和基因组不稳定性。
Aging (Albany NY). 2020 Jul 16;12(14):14341-14354. doi: 10.18632/aging.103473.
6
Progress, Challenges, and Surprises in Annotating the Human Genome.注释人类基因组的进展、挑战和惊喜。
Annu Rev Genomics Hum Genet. 2020 Aug 31;21:55-79. doi: 10.1146/annurev-genom-121119-083418. Epub 2020 May 18.
7
HDAC11 promotes meiotic apparatus assembly during mouse oocyte maturation via decreasing H4K16 and α-tubulin acetylation.HDAC11 通过降低 H4K16 和 α-微管蛋白乙酰化促进小鼠卵母细胞成熟过程中的减数分裂装置组装。
Cell Cycle. 2020 Feb;19(3):354-362. doi: 10.1080/15384101.2019.1711315. Epub 2020 Jan 7.
8
Aurora B-INCENP Localization at Centromeres/Inner Kinetochores Is Required for Chromosome Bi-orientation in Budding Yeast.着丝粒/内动粒处 Aurora B-INENP 的定位对于芽殖酵母染色体的双向定向是必需的。
Curr Biol. 2019 May 6;29(9):1536-1544.e4. doi: 10.1016/j.cub.2019.03.051. Epub 2019 Apr 18.
9
Overlapping Roles in Chromosome Segregation for Heterochromatin Protein 1 (Swi6) and DDK in .在. 中异染色质蛋白 1(Swi6)和 DDK 的染色体分离中重叠的作用
Genetics. 2019 Jun;212(2):417-430. doi: 10.1534/genetics.119.302125. Epub 2019 Apr 18.
10
The dark side of centromeres: types, causes and consequences of structural abnormalities implicating centromeric DNA.着丝粒的阴暗面:涉及着丝粒 DNA 的结构异常的类型、原因和后果。
Nat Commun. 2018 Oct 18;9(1):4340. doi: 10.1038/s41467-018-06545-y.
动粒通过 Cdc7-Dbf4 激酶募集来协调着丝粒周围的黏合和早期 DNA 复制。
Mol Cell. 2013 Jun 6;50(5):661-74. doi: 10.1016/j.molcel.2013.05.011.
4
DROMPA: easy-to-handle peak calling and visualization software for the computational analysis and validation of ChIP-seq data.DROMPA:用于ChIP-seq数据计算分析和验证的易于操作的峰检测与可视化软件。
Genes Cells. 2013 Jul;18(7):589-601. doi: 10.1111/gtc.12058. Epub 2013 May 15.
5
Tension sensing by Aurora B kinase is independent of survivin-based centromere localization.极光 B 激酶通过感应张力来实现基于 survivin 的着丝粒定位。
Nature. 2013 May 2;497(7447):118-21. doi: 10.1038/nature12057. Epub 2013 Apr 21.
6
Phosphoregulation promotes release of kinetochores from dynamic microtubules via multiple mechanisms.磷酸化调控通过多种机制促进动粒从动态微管上的释放。
Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7282-7. doi: 10.1073/pnas.1220700110. Epub 2013 Apr 15.
7
Cohesin-dependent association of scc2/4 with the centromere initiates pericentromeric cohesion establishment.着丝粒蛋白 scc2/4 通过依赖黏合蛋白的方式与着丝粒结合,从而起始着丝粒周围的黏合结构的形成。
Curr Biol. 2013 Apr 8;23(7):599-606. doi: 10.1016/j.cub.2013.02.022. Epub 2013 Mar 14.
8
Chromosome engineering allows the efficient isolation of vertebrate neocentromeres.染色体工程允许脊椎动物新着丝粒的高效分离。
Dev Cell. 2013 Mar 25;24(6):635-48. doi: 10.1016/j.devcel.2013.02.009. Epub 2013 Mar 14.
9
Functions of the centromere and kinetochore in chromosome segregation.着丝粒和动粒在染色体分离中的功能。
Curr Opin Cell Biol. 2013 Jun;25(3):334-40. doi: 10.1016/j.ceb.2013.02.001. Epub 2013 Mar 13.
10
Family matters: structural and functional conservation of centromere-associated proteins from yeast to humans.家族事务:从酵母到人,着丝粒相关蛋白的结构和功能保守性。
Trends Cell Biol. 2013 Jun;23(6):260-9. doi: 10.1016/j.tcb.2013.01.010. Epub 2013 Mar 5.