• 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

NEK7是一种对微管成核至关重要的中心体激酶。

NEK7 is a centrosomal kinase critical for microtubule nucleation.

作者信息

Kim Sunghwan, Lee Kwanwoo, Rhee Kunsoo

机构信息

Department of Biological Sciences and Research Center for Functional Cellulomics, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2007 Aug 17;360(1):56-62. doi: 10.1016/j.bbrc.2007.05.206. Epub 2007 Jun 8.

DOI:10.1016/j.bbrc.2007.05.206
PMID:17586473
Abstract

NIMA in Aspergillus nidulans is a mitotic kinase for chromosome condensation and segregation. We characterized NEK7, a human homologue of Aspergillus NIMA. NEK7 was located at the centrosome throughout the cell cycle. Temporal localization of NEK7 at midbody of the cytokinetic cell was also observed. NEK7 knockdown by RNAi caused a prometaphase arrest of the cell cycle with monopolar or disorganized spindle. We propose that such defects in spindle assembly are resulted from reduction in microtubule nucleation activity at the centrosome. In consistent to the proposal, we observed a decrease in the centrosomal gamma-tubulin levels and reduction of the microtubule re-growth activity in the NEK7-suppressed cells. In addition, it was evident that NEK7 was directly involved in cytokinesis.

摘要

构巢曲霉中的NIMA是一种用于染色体凝聚和分离的有丝分裂激酶。我们对曲霉NIMA的人类同源物NEK7进行了表征。NEK7在整个细胞周期中都位于中心体。还观察到NEK7在细胞分裂细胞的中体处的时间定位。RNAi介导的NEK7敲低导致细胞周期前中期停滞,纺锤体呈单极或紊乱状态。我们认为,纺锤体组装中的此类缺陷是由于中心体微管成核活性降低所致。与该提议一致,我们观察到NEK7抑制细胞中中心体γ-微管蛋白水平降低,微管重新生长活性降低。此外,很明显NEK7直接参与胞质分裂。

相似文献

1
NEK7 is a centrosomal kinase critical for microtubule nucleation.NEK7是一种对微管成核至关重要的中心体激酶。
Biochem Biophys Res Commun. 2007 Aug 17;360(1):56-62. doi: 10.1016/j.bbrc.2007.05.206. Epub 2007 Jun 8.
2
Nek7 kinase is enriched at the centrosome, and is required for proper spindle assembly and mitotic progression.Nek7激酶在中心体中富集,是正确的纺锤体组装和有丝分裂进程所必需的。
FEBS Lett. 2006 Nov 27;580(27):6489-95. doi: 10.1016/j.febslet.2006.10.069. Epub 2006 Nov 7.
3
NEK7 is essential for centriole duplication and centrosomal accumulation of pericentriolar material proteins in interphase cells.NEK7 对于中心粒复制和间期细胞中中心粒周围物质蛋白的中心体积累是必需的。
J Cell Sci. 2011 Nov 15;124(Pt 22):3760-70. doi: 10.1242/jcs.078089. Epub 2011 Nov 18.
4
The Nek6 and Nek7 protein kinases are required for robust mitotic spindle formation and cytokinesis.Nek6和Nek7蛋白激酶是强大的有丝分裂纺锤体形成和胞质分裂所必需的。
Mol Cell Biol. 2009 Jul;29(14):3975-90. doi: 10.1128/MCB.01867-08. Epub 2009 May 4.
5
A centrosomal function for the human Nek2 protein kinase, a member of the NIMA family of cell cycle regulators.人Nek2蛋白激酶的中心体功能,Nek2蛋白激酶是细胞周期调节因子NIMA家族的成员之一。
EMBO J. 1998 Jan 15;17(2):470-81. doi: 10.1093/emboj/17.2.470.
6
Nek9 phosphorylation of NEDD1/GCP-WD contributes to Plk1 control of γ-tubulin recruitment to the mitotic centrosome.Nek9 对 NEDD1/GCP-WD 的磷酸化作用有助于 Plk1 控制 γ-微管蛋白向有丝分裂中心体的募集。
Curr Biol. 2012 Aug 21;22(16):1516-23. doi: 10.1016/j.cub.2012.06.027. Epub 2012 Jul 19.
7
Nek7 kinase accelerates microtubule dynamic instability.Nek7激酶加速微管动态不稳定性。
Biochim Biophys Acta. 2013 May;1833(5):1104-13. doi: 10.1016/j.bbamcr.2012.12.021. Epub 2013 Jan 8.
8
Human Nek7-interactor RGS2 is required for mitotic spindle organization.有丝分裂纺锤体组织需要人Nek7相互作用蛋白RGS2。
Cell Cycle. 2015;14(4):656-67. doi: 10.4161/15384101.2014.994988.
9
Characterization of NIP2/centrobin, a novel substrate of Nek2, and its potential role in microtubule stabilization.NIP2/中心体蛋白(centrobin)的特性鉴定,Nek2的一种新型底物及其在微管稳定中的潜在作用
J Cell Sci. 2007 Jun 15;120(Pt 12):2106-16. doi: 10.1242/jcs.03458. Epub 2007 May 29.
10
Mitotic kinases: the key to duplication, segregation, and cytokinesis errors, chromosomal instability, and oncogenesis.有丝分裂激酶:复制、分离、胞质分裂错误、染色体不稳定及肿瘤发生的关键因素。
Pharmacol Ther. 2006 Sep;111(3):974-84. doi: 10.1016/j.pharmthera.2006.02.006. Epub 2006 Apr 17.

引用本文的文献

1
The role of MKI67 in the regulation of 60S pre-ribosome nucleolar export, transcripts, energy supply, and apoptosis.MKI67在60S核糖体前体核仁输出、转录本、能量供应及细胞凋亡调控中的作用。
bioRxiv. 2025 Feb 25:2025.02.13.638155. doi: 10.1101/2025.02.13.638155.
2
The dynamic role of nucleoprotein SHCBP1 in the cancer cell cycle and its potential as a synergistic target for DNA-damaging agents in cancer therapy.核蛋白 SHCBP1 在癌细胞周期中的动态作用及其作为癌症治疗中 DNA 损伤剂协同靶标的潜力。
Cell Commun Signal. 2024 Feb 16;22(1):131. doi: 10.1186/s12964-024-01513-0.
3
A detailed molecular network map and model of the NLRP3 inflammasome.
NLRP3 炎症小体的详细分子网络图谱和模型。
Front Immunol. 2023 Nov 15;14:1233680. doi: 10.3389/fimmu.2023.1233680. eCollection 2023.
4
UNC-116 and UNC-16 function with the NEKL-3 kinase to promote axon targeting.UNC-116 和 UNC-16 与 NEKL-3 激酶一起发挥作用,促进轴突靶向。
Development. 2023 Sep 15;150(18). doi: 10.1242/dev.201654. Epub 2023 Sep 27.
5
Structural Mechanisms of NLRP3 Inflammasome Assembly and Activation.NLRP3 炎性小体组装和激活的结构机制。
Annu Rev Immunol. 2023 Apr 26;41:301-316. doi: 10.1146/annurev-immunol-081022-021207. Epub 2023 Feb 7.
6
Activation and regulation mechanisms of NOD-like receptors based on structural biology.基于结构生物学的 NOD 样受体的激活和调控机制。
Front Immunol. 2022 Sep 15;13:953530. doi: 10.3389/fimmu.2022.953530. eCollection 2022.
7
Acetaminophen-induced reduction of NIMA-related kinase 7 expression exacerbates acute liver injury.对乙酰氨基酚诱导的NIMA相关激酶7表达降低会加剧急性肝损伤。
JHEP Rep. 2022 Jul 20;4(10):100545. doi: 10.1016/j.jhepr.2022.100545. eCollection 2022 Oct.
8
NEK7: a new target for the treatment of multiple tumors and chronic inflammatory diseases.NEK7:一种用于治疗多种肿瘤和慢性炎症性疾病的新靶点。
Inflammopharmacology. 2022 Aug;30(4):1179-1187. doi: 10.1007/s10787-022-01026-7. Epub 2022 Jul 13.
9
A Single Amino Acid Residue Defines the Difference in NLRP3 Inflammasome Activation between NEK7 and NEK6.单一氨基酸残基定义了 NEK7 和 NEK6 之间 NLRP3 炎性小体激活的差异。
J Immunol. 2022 Apr 15;208(8):2029-2036. doi: 10.4049/jimmunol.2101154. Epub 2022 Mar 30.
10
Inflammasome Meets Centrosome: Understanding the Emerging Role of Centrosome in Controlling Inflammasome Activation.炎症小体与中心体相遇:了解中心体在控制炎症小体激活中的新作用。
Front Immunol. 2022 Feb 24;13:826106. doi: 10.3389/fimmu.2022.826106. eCollection 2022.