• 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
Dyrk1A overexpression inhibits proliferation and induces premature neuronal differentiation of neural progenitor cells.Dyrk1A 过表达抑制神经祖细胞的增殖并诱导其过早神经元分化。
J Neurosci. 2010 Mar 17;30(11):4004-14. doi: 10.1523/JNEUROSCI.4711-09.2010.
2
Overexpression of DYRK1A inhibits choline acetyltransferase induction by oleic acid in cellular models of Down syndrome.DYRK1A 的过表达抑制唐氏综合征细胞模型中油酸诱导的胆碱乙酰转移酶的诱导。
Exp Neurol. 2013 Jan;239:229-34. doi: 10.1016/j.expneurol.2012.10.016. Epub 2012 Nov 1.
3
Effect of DYRK1A activity inhibition on development of neuronal progenitors isolated from Ts65Dn mice.DYRK1A 活性抑制对 Ts65Dn 小鼠分离的神经元祖细胞发育的影响。
J Neurosci Res. 2012 May;90(5):999-1010. doi: 10.1002/jnr.23007. Epub 2012 Jan 18.
4
Engineering DYRK1A overdosage yields Down syndrome-characteristic cortical splicing aberrations.工程过度表达 DYRK1A 可导致唐氏综合征特征性皮质剪接异常。
Neurobiol Dis. 2010 Oct;40(1):348-59. doi: 10.1016/j.nbd.2010.06.011. Epub 2010 Jun 30.
5
The Down syndrome-related protein kinase DYRK1A phosphorylates p27(Kip1) and Cyclin D1 and induces cell cycle exit and neuronal differentiation.唐氏综合征相关蛋白激酶DYRK1A使p27(Kip1)和细胞周期蛋白D1磷酸化,并诱导细胞周期退出和神经元分化。
Cell Cycle. 2014;13(13):2084-100. doi: 10.4161/cc.29104. Epub 2014 May 7.
6
The spatio-temporal and subcellular expression of the candidate Down syndrome gene Mnb/Dyrk1A in the developing mouse brain suggests distinct sequential roles in neuronal development.候选唐氏综合征基因Mnb/Dyrk1A在发育中的小鼠大脑中的时空及亚细胞表达表明其在神经元发育中具有不同的连续作用。
Eur J Neurosci. 2008 Mar;27(5):1061-74. doi: 10.1111/j.1460-9568.2008.06092.x.
7
Restrained Phosphatidylcholine Synthesis in a Cellular Model of Down's Syndrome is Associated with the Overexpression of Dyrk1A.唐氏综合征细胞模型中磷脂酰胆碱合成受限与Dyrk1A的过表达有关。
Mol Neurobiol. 2017 Mar;54(2):1092-1100. doi: 10.1007/s12035-016-9728-2. Epub 2016 Jan 23.
8
DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome.DYRK1A剂量失衡扰乱NRSF/REST水平,导致唐氏综合征中多能性和胚胎干细胞命运失调。
Am J Hum Genet. 2008 Sep;83(3):388-400. doi: 10.1016/j.ajhg.2008.08.012. Epub 2008 Sep 4.
9
[Molecular Mechanism Underlying Abnormal Differentiation of Neural Progenitor Cells in the Developing Down Syndrome Brain].[唐氏综合征患儿发育中大脑神经祖细胞异常分化的分子机制]
Yakugaku Zasshi. 2017;137(7):795-800. doi: 10.1248/yakushi.16-00236-1.
10
Dyrk1A phosphorylates p53 and inhibits proliferation of embryonic neuronal cells.Dyrk1A 磷酸化 p53 并抑制胚胎神经元细胞的增殖。
J Biol Chem. 2010 Oct 8;285(41):31895-906. doi: 10.1074/jbc.M110.147520. Epub 2010 Aug 9.

引用本文的文献

1
Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis.皮质发生过程中的中间神经元迁移缺陷导致双特异性酪氨酸磷酸化调节激酶1A单倍剂量不足综合征的发病机制。
Mol Psychiatry. 2025 Jul 10. doi: 10.1038/s41380-025-03109-7.
2
Unlocking the Therapeutic Potential of the Dual-Specificity Tyrosine Phosphorylation-Regulated Kinase 1A Inhibitors in Alzheimer's Diseases.揭示双特异性酪氨酸磷酸化调节激酶1A抑制剂在阿尔茨海默病中的治疗潜力
Mol Neurobiol. 2025 Mar 5. doi: 10.1007/s12035-025-04806-8.
3
Total cell N-glycosylation is altered during differentiation of induced pluripotent stem cells to neural stem cells and is disturbed by trisomy 21.在诱导多能干细胞向神经干细胞分化的过程中,细胞的总N-糖基化会发生改变,并且会受到21三体的干扰。
BBA Adv. 2024 Dec 29;7:100137. doi: 10.1016/j.bbadva.2024.100137. eCollection 2025.
4
The role of prenatal choline and its impact on neurodevelopmental disorders.产前胆碱的作用及其对神经发育障碍的影响。
Front Nutr. 2024 Nov 18;11:1463983. doi: 10.3389/fnut.2024.1463983. eCollection 2024.
5
Regulation of Drosophila brain development and organ growth by the Minibrain/Rala signaling network.果蝇大脑发育和器官生长的调控由 Minibrain/Rala 信号网络。
G3 (Bethesda). 2024 Nov 6;14(11). doi: 10.1093/g3journal/jkae219.
6
Sex-specific developmental alterations in DYRK1A expression in the brain of a Down syndrome mouse model.唐氏综合征小鼠模型大脑中 DYRK1A 表达的性别特异性发育变化。
Neurobiol Dis. 2024 Jan;190:106359. doi: 10.1016/j.nbd.2023.106359. Epub 2023 Nov 20.
7
Regulation of CMGC kinases by hypoxia.缺氧对 CMGC 激酶的调节。
BMB Rep. 2023 Nov;56(11):584-593. doi: 10.5483/BMBRep.2023-0165.
8
Functions of SRPK, CLK and DYRK kinases in stem cells, development, and human developmental disorders.SRPK、CLK 和 DYRK 激酶在干细胞、发育和人类发育障碍中的功能。
FEBS Lett. 2023 Oct;597(19):2375-2415. doi: 10.1002/1873-3468.14723. Epub 2023 Sep 4.
9
DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner.DYRK1A 通过激酶非依赖方式促进高致病性人冠状病毒的进入。
PLoS Biol. 2023 Jun 13;21(6):e3002097. doi: 10.1371/journal.pbio.3002097. eCollection 2023 Jun.
10
Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder.出线或改变状态?多基因神经发育障碍中的神经祖细胞作为靶点。
Dev Neurosci. 2024;46(1):1-21. doi: 10.1159/000530898. Epub 2023 May 10.

本文引用的文献

1
Function and regulation of Dyrk1A: towards understanding Down syndrome.Dyrk1A的功能与调控:迈向对唐氏综合征的理解
Cell Mol Life Sci. 2009 Oct;66(20):3235-40. doi: 10.1007/s00018-009-0123-2. Epub 2009 Aug 14.
2
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.两名无关的小头畸形患者中唐氏综合征候选基因DYRK1A的截断。
Am J Hum Genet. 2008 May;82(5):1165-70. doi: 10.1016/j.ajhg.2008.03.001. Epub 2008 Apr 10.
3
The spatio-temporal and subcellular expression of the candidate Down syndrome gene Mnb/Dyrk1A in the developing mouse brain suggests distinct sequential roles in neuronal development.候选唐氏综合征基因Mnb/Dyrk1A在发育中的小鼠大脑中的时空及亚细胞表达表明其在神经元发育中具有不同的连续作用。
Eur J Neurosci. 2008 Mar;27(5):1061-74. doi: 10.1111/j.1460-9568.2008.06092.x.
4
Neurogenesis impairment and increased cell death reduce total neuron number in the hippocampal region of fetuses with Down syndrome.神经发生受损和细胞死亡增加会减少唐氏综合征胎儿海马区的神经元总数。
Brain Pathol. 2008 Apr;18(2):180-97. doi: 10.1111/j.1750-3639.2007.00113.x. Epub 2007 Dec 17.
5
Defects in embryonic neurogenesis and initial synapse formation in the forebrain of the Ts65Dn mouse model of Down syndrome.唐氏综合征Ts65Dn小鼠模型前脑胚胎神经发生和初始突触形成的缺陷。
J Neurosci. 2007 Oct 24;27(43):11483-95. doi: 10.1523/JNEUROSCI.3406-07.2007.
6
Cell cycle alteration and decreased cell proliferation in the hippocampal dentate gyrus and in the neocortical germinal matrix of fetuses with Down syndrome and in Ts65Dn mice.唐氏综合征胎儿以及 Ts65Dn 小鼠的海马齿状回和新皮质生发基质中的细胞周期改变与细胞增殖减少。
Hippocampus. 2007;17(8):665-78. doi: 10.1002/hipo.20308.
7
The regulation of cyclin D1 degradation: roles in cancer development and the potential for therapeutic invention.细胞周期蛋白D1降解的调控:在癌症发展中的作用及治疗干预潜力
Mol Cancer. 2007 Apr 2;6:24. doi: 10.1186/1476-4598-6-24.
8
Mirk/Dyrk1B: a multifunctional dual-specificity kinase involved in growth arrest, differentiation, and cell survival.Mirk/Dyrk1B:一种参与生长停滞、分化和细胞存活的多功能双特异性激酶。
Cell Biochem Biophys. 2006;45(3):303-15. doi: 10.1385/CBB:45:3:303.
9
Identification of mutations that disrupt phosphorylation-dependent nuclear export of cyclin D1.鉴定破坏细胞周期蛋白D1磷酸化依赖性核输出的突变。
Oncogene. 2006 Oct 12;25(47):6291-303. doi: 10.1038/sj.onc.1209644. Epub 2006 May 29.
10
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21.21号染色体上DSCR1和DYRK1A剂量增加导致的NFAT失调。
Nature. 2006 Jun 1;441(7093):595-600. doi: 10.1038/nature04678. Epub 2006 Mar 22.

Dyrk1A 过表达抑制神经祖细胞的增殖并诱导其过早神经元分化。

Dyrk1A overexpression inhibits proliferation and induces premature neuronal differentiation of neural progenitor cells.

机构信息

Department of Cell Biology and Neuroscience, Rutgers, The State University of New Jersey, Piscataway, New Jersey 08854, USA.

出版信息

J Neurosci. 2010 Mar 17;30(11):4004-14. doi: 10.1523/JNEUROSCI.4711-09.2010.

DOI:10.1523/JNEUROSCI.4711-09.2010
PMID:20237271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3842457/
Abstract

Dyrk1A is a member of the mammalian Dyrk [dual-specificity tyrosine-(Y)-phosphorylation regulated kinase] family of protein kinases that is expressed at high levels in the brain, but its role in the development and function of this organ is not well understood. The human DYRK1A gene is located on trisomic chromosome 21 in Down syndrome (DS) patients, leading to its overexpression. Dyrk1A is also overexpressed in animal models of DS and in gene-specific transgenic mice that consistently exhibit cognitive impairment. To elucidate the cellular and molecular mechanisms that are affected by increased levels of Dyrk1A in the developing brain, we overexpressed this kinase in the embryonic mouse neocortex using the in utero electroporation technique. We found that Dyrk1A overexpression inhibits neural cell proliferation and promotes premature neuronal differentiation in the developing cerebral cortex without affecting cell fate and layer positioning. These effects are dependent on the Dyrk1A kinase activity and are mediated by the nuclear export and degradation of cyclin D1. This study identifies specific Dyrk1A-induced mechanisms that disrupt the normal process of corticogenesis and possibly contribute to cognitive impairment observed in DS patients and animal models.

摘要

DYRK1A 是哺乳动物双特异性酪氨酸-(Y)-磷酸化调节激酶家族的一员,在大脑中高表达,但它在该器官的发育和功能中的作用尚未完全了解。人类 DYRK1A 基因位于唐氏综合征(DS)患者的三体 21 号染色体上,导致其过度表达。DS 的动物模型和基因特异性转基因小鼠中也过度表达 Dyrk1A,这些小鼠始终表现出认知障碍。为了阐明 Dyrk1A 在发育中的大脑中水平升高所影响的细胞和分子机制,我们使用体内电穿孔技术在胚胎小鼠新皮层中过表达这种激酶。我们发现 Dyrk1A 过表达抑制神经细胞增殖,并促进发育中的大脑皮层中过早的神经元分化,而不影响细胞命运和层定位。这些效应依赖于 Dyrk1A 激酶活性,并通过细胞周期蛋白 D1 的核输出和降解来介导。这项研究确定了特定的 Dyrk1A 诱导机制,这些机制破坏了皮质发生的正常过程,并可能导致 DS 患者和动物模型中观察到的认知障碍。