• 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

Molecular cloning and biological activity of a novel developmentally regulated gene encoding a protein with beta-transducin-like structure.

作者信息

Kumar S, Matsuzaki T, Yoshida Y, Noda M

机构信息

Cancer Institute, Japanese Foundation for Cancer Research, Tokyo.

出版信息

J Biol Chem. 1994 Apr 15;269(15):11318-26.

PMID:8157664
Abstract

In the developing mammalian central nervous system, neural precursor cells show a tightly regulated inverse relationship between cell proliferation and differentiation. The molecular mechanisms which control the inter-relationship between these two events are poorly understood. To approach this problem, we previously identified several novel genes which are most prominently expressed in the early embryonic brain. Further cloning and sequencing of one such gene, Nedd1, revealed that it can encode a protein with a M(r) of 71,000, the amino-terminal half of which shares significant structural similarity with the beta-subunit of heterotrimeric GTP-binding proteins. Nedd1 mRNA is strongly expressed in early embryonic brain, but it can be detected at low levels in a number of adult tissues as well as cell lines and is up-regulated in an embryonal carcinoma cell line upon retinoic acid-induced differentiation. Ectopic expression of Nedd1 gene by means of eukaryotic vectors in various cell lines resulted in varying degrees of growth suppression. The strongest effects were evident in differentiation-competent neuroblastoma-derived cell lines. Our results suggest that the Nedd1 gene may play a role in the differentiation-coupled growth arrest in neuronal cells.

摘要

相似文献

1
Molecular cloning and biological activity of a novel developmentally regulated gene encoding a protein with beta-transducin-like structure.
J Biol Chem. 1994 Apr 15;269(15):11318-26.
2
Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridization.
Hum Genet. 1995 Jan;95(1):96-8. doi: 10.1007/BF00225082.
3
The Gnb5 gene is a novel beta-transducin homolog transcribed from a divergent promoter located immediately upstream of the Syrian hamster p53 P1 promoter.
Mamm Genome. 1995 Apr;6(4):236-41. doi: 10.1007/BF00352407.
4
A novel form of the G protein beta subunit Gbeta5 is specifically expressed in the vertebrate retina.一种新型的G蛋白β亚基Gbeta5特异性地在脊椎动物视网膜中表达。
J Biol Chem. 1996 Nov 8;271(45):28154-60. doi: 10.1074/jbc.271.45.28154.
5
A fifth member of the mammalian G-protein beta-subunit family. Expression in brain and activation of the beta 2 isotype of phospholipase C.哺乳动物G蛋白β亚基家族的第五个成员。在大脑中的表达及对磷脂酶C的β2亚型的激活作用。
J Biol Chem. 1994 Sep 2;269(35):22150-6.
6
Cloning and characterization of a G protein alpha-subunit-encoding gene from the basidiomycete, Coprinus congregatus.担子菌簇生鬼伞中一个G蛋白α亚基编码基因的克隆与特性分析
Gene. 1995 Sep 22;163(1):133-7. doi: 10.1016/0378-1119(95)00378-j.
7
Differential distribution of the G protein gamma3 subunit in the developing zebrafish nervous system.
Int J Dev Neurosci. 2001 Jul;19(4):455-67. doi: 10.1016/s0736-5748(01)00002-8.
8
Truncated forms of a novel yeast protein suppress the lethality of a G protein alpha subunit deficiency by interacting with the beta subunit.一种新型酵母蛋白的截短形式通过与β亚基相互作用来抑制G蛋白α亚基缺陷的致死性。
J Biol Chem. 1995 Oct 27;270(43):25435-44. doi: 10.1074/jbc.270.43.25435.
9
Involvement of the mouse Prp19 gene in neuronal/astroglial cell fate decisions.
J Biol Chem. 2006 Mar 17;281(11):7498-514. doi: 10.1074/jbc.M510881200. Epub 2005 Dec 13.
10
A brain-specific G protein gamma subunit.一种脑特异性G蛋白γ亚基。
Biochem Biophys Res Commun. 1995 Nov 2;216(1):126-32. doi: 10.1006/bbrc.1995.2600.

引用本文的文献

1
Cryo-EM structures of the Plant Augmin reveal its intertwined coiled-coil assembly, antiparallel dimerization and NEDD1 binding mechanisms.植物γ-微管蛋白环状复合物的冷冻电镜结构揭示了其相互缠绕的卷曲螺旋组装、反平行二聚化及NEDD1结合机制。
bioRxiv. 2025 Feb 27:2025.02.25.640204. doi: 10.1101/2025.02.25.640204.
2
Understanding the Genetic Landscape of Gestational Diabetes: Insights into the Causes and Consequences of Elevated Glucose Levels in Pregnancy.了解妊娠期糖尿病的遗传图谱:洞悉孕期血糖升高的原因及后果。
Metabolites. 2024 Sep 20;14(9):508. doi: 10.3390/metabo14090508.
3
Muscle growth differences in Lijiang pigs revealed by ATAC-seq multi-omics.
通过ATAC-seq多组学揭示丽江猪的肌肉生长差异
Front Vet Sci. 2024 Aug 26;11:1431248. doi: 10.3389/fvets.2024.1431248. eCollection 2024.
4
NEDD1 Promotes the Development of Lung Adenocarcinoma and Can be Used as a Prognostic Marker.NEDD1促进肺腺癌的发展并可作为一种预后标志物。
J Cancer. 2024 Aug 13;15(16):5149-5164. doi: 10.7150/jca.98238. eCollection 2024.
5
PLK4-phosphorylated NEDD1 facilitates cartwheel assembly and centriole biogenesis initiations.PLK4 磷酸化的 NEDD1 促进轮辐装配和中心体发生起始。
J Cell Biol. 2021 Jan 4;220(1). doi: 10.1083/jcb.202002151.
6
A direct interaction with NEDD1 regulates gamma-tubulin recruitment to the centrosome.NEDD1 与 γ-微管蛋白的直接相互作用调控其向中心体的募集。
PLoS One. 2010 Mar 10;5(3):e9618. doi: 10.1371/journal.pone.0009618.
7
The WD40 repeat protein NEDD1 functions in microtubule organization during cell division in Arabidopsis thaliana.WD40重复蛋白NEDD1在拟南芥细胞分裂过程中的微管组织中发挥作用。
Plant Cell. 2009 Apr;21(4):1129-40. doi: 10.1105/tpc.109.065953. Epub 2009 Apr 21.
8
Nedd1 expression as a marker of dynamic centrosomal localization during mouse embryonic development.Nedd1表达作为小鼠胚胎发育过程中动态中心体定位的标志物。
Histochem Cell Biol. 2008 Jun;129(6):751-64. doi: 10.1007/s00418-008-0392-0. Epub 2008 Feb 1.
9
NEDD1-dependent recruitment of the gamma-tubulin ring complex to the centrosome is necessary for centriole duplication and spindle assembly.NEDD1 依赖的 γ-微管蛋白环复合物向中心体的募集对于中心粒复制和纺锤体组装是必需的。
J Cell Biol. 2006 Feb 13;172(4):505-15. doi: 10.1083/jcb.200510028. Epub 2006 Feb 6.
10
Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis.人类BM88的克隆、表达及定位表明,它定位于11号染色体p15.5区域,该区域与贝克威思-维德曼综合征及肿瘤发生有关。
Biochem J. 2001 May 1;355(Pt 3):715-24. doi: 10.1042/bj3550715.