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1
Expression and activation of SH2/PTB-containing ShcA adaptor protein reflects the pattern of neurogenesis in the mammalian brain.含SH2/PTB结构域的ShcA衔接蛋白的表达与激活反映了哺乳动物大脑中的神经发生模式。
Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):8185-90. doi: 10.1073/pnas.94.15.8185.
2
A mammalian adaptor protein with conserved Src homology 2 and phosphotyrosine-binding domains is related to Shc and is specifically expressed in the brain.一种具有保守的Src同源2结构域和磷酸酪氨酸结合结构域的哺乳动物衔接蛋白与Shc相关,且在脑中特异性表达。
Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2729-34. doi: 10.1073/pnas.93.7.2729.
3
Emerging roles for SH2/PTB-containing Shc adaptor proteins in the developing mammalian brain.含SH2/PTB结构域的Shc衔接蛋白在发育中的哺乳动物大脑中的新作用。
Trends Neurosci. 1998 Nov;21(11):476-81. doi: 10.1016/s0166-2236(98)01282-x.
4
Differential utilization of ShcA tyrosine residues and functional domains in the transduction of epidermal growth factor-induced mitogen-activated protein kinase activation in 293T cells and nerve growth factor-induced neurite outgrowth in PC12 cells. Identification of a new Grb2.Sos1 binding site.ShcA酪氨酸残基和功能域在293T细胞中表皮生长因子诱导的丝裂原活化蛋白激酶激活转导以及PC12细胞中神经生长因子诱导的神经突生长转导中的差异利用。一个新的Grb2-Sos1结合位点的鉴定。
J Biol Chem. 1997 Aug 29;272(35):22293-9. doi: 10.1074/jbc.272.35.22293.
5
Signal transduction through tyrosine-phosphorylated carboxy-terminal fragments of APP via an enhanced interaction with Shc/Grb2 adaptor proteins in reactive astrocytes of Alzheimer's disease brain.在阿尔茨海默病大脑的反应性星形胶质细胞中,通过APP酪氨酸磷酸化的羧基末端片段与Shc/Grb2衔接蛋白增强相互作用进行信号转导。
Ann N Y Acad Sci. 2002 Nov;973:323-33. doi: 10.1111/j.1749-6632.2002.tb04660.x.
6
ShcA and Grb2 mediate polyoma middle T antigen-induced endothelial transformation and Gab1 tyrosine phosphorylation.ShcA和Grb2介导多瘤病毒中T抗原诱导的内皮细胞转化以及Gab1酪氨酸磷酸化。
EMBO J. 2001 Nov 15;20(22):6327-36. doi: 10.1093/emboj/20.22.6327.
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Neural-specific inactivation of ShcA results in increased embryonic neural progenitor apoptosis and microencephaly.ShcA在神经细胞中的特异性失活会导致胚胎神经祖细胞凋亡增加和小头畸形。
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8
ShcA tyrosine phosphorylation sites can replace ShcA binding in signalling by middle T-antigen.ShcA酪氨酸磷酸化位点可在中T抗原信号传导中取代ShcA结合。
EMBO J. 2001 Nov 15;20(22):6337-46. doi: 10.1093/emboj/20.22.6337.
9
Signal transduction through tyrosine-phosphorylated C-terminal fragments of amyloid precursor protein via an enhanced interaction with Shc/Grb2 adaptor proteins in reactive astrocytes of Alzheimer's disease brain.在阿尔茨海默病大脑的反应性星形胶质细胞中,通过淀粉样前体蛋白酪氨酸磷酸化的C末端片段与Shc/Grb2衔接蛋白增强相互作用进行信号转导。
J Biol Chem. 2002 Sep 20;277(38):35282-8. doi: 10.1074/jbc.M110785200. Epub 2002 Jun 25.
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Disruption of ShcA signaling halts cell proliferation--characterization of ShcC residues that influence signaling pathways using yeast.ShcA信号通路的破坏会阻止细胞增殖——利用酵母对影响信号通路的ShcC残基进行表征。
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Neurochem Res. 2022 Dec;47(12):3709-3722. doi: 10.1007/s11064-022-03717-7. Epub 2022 Aug 12.
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Localization of phosphotyrosine adaptor protein ShcD/SHC4 in the adult rat central nervous system.磷酸酪氨酸衔接蛋白 ShcD/SHC4 在成年大鼠中枢神经系统中的定位。
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Diurnal oscillations of endogenous HO sustained by p66 regulate circadian clocks.内源性 HO 的昼夜波动由 p66 调控的。
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Neonatal ketamine exposure-induced hippocampal neuroapoptosis in the developing brain impairs adult spatial learning ability.新生儿期氯胺酮暴露诱导发育中大脑的海马神经细胞凋亡,损害成年后的空间学习能力。
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Cellular heterogeneity during embryonic stem cell differentiation to epiblast stem cells is revealed by the ShcD/RaLP adaptor protein.ShcD/RaLP 衔接蛋白揭示了胚胎干细胞向胚外干细胞分化过程中的细胞异质性。
Stem Cells. 2012 Nov;30(11):2423-36. doi: 10.1002/stem.1217.
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Permanent embryo arrest: molecular and cellular concepts.永久性胚胎停滞:分子与细胞概念
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Analysis of a Shc family adaptor protein, ShcD/Shc4, that associates with muscle-specific kinase.与肌肉特异性激酶相关的Shc家族衔接蛋白ShcD/Shc4的分析。
Mol Cell Biol. 2007 Jul;27(13):4759-73. doi: 10.1128/MCB.00184-07. Epub 2007 Apr 23.
10
Neural-specific inactivation of ShcA results in increased embryonic neural progenitor apoptosis and microencephaly.ShcA在神经细胞中的特异性失活会导致胚胎神经祖细胞凋亡增加和小头畸形。
J Neurosci. 2006 Jul 26;26(30):7885-97. doi: 10.1523/JNEUROSCI.3524-05.2006.

本文引用的文献

1
Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse.小鼠大脑皮质组织发生过程中细胞迁移的放射自显影研究。
Nature. 1961 Nov 25;192:766-8. doi: 10.1038/192766b0.
2
Opposite effects of the p52shc/p46shc and p66shc splicing isoforms on the EGF receptor-MAP kinase-fos signalling pathway.p52shc/p46shc和p66shc剪接异构体对表皮生长因子受体-丝裂原活化蛋白激酶-fos信号通路的相反作用。
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Activation of the JAK/STAT pathway leads to proliferation of ST14A central nervous system progenitor cells.
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Vertebrate neural progenitor cells: subtypes and regulation.脊椎动物神经祖细胞:亚型与调控
Curr Opin Neurobiol. 1996 Feb;6(1):11-7. doi: 10.1016/s0959-4388(96)80003-1.
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Role of neurotrophic factors in neuronal development.神经营养因子在神经元发育中的作用。
Curr Opin Neurobiol. 1996 Feb;6(1):64-70. doi: 10.1016/s0959-4388(96)80010-9.
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A family of Shc related proteins with conserved PTB, CH1 and SH2 regions.一个具有保守的PTB、CH1和SH2区域的Shc相关蛋白家族。
Oncogene. 1996 Aug 1;13(3):633-41.
7
Not all Shc's roads lead to Ras.并非所有Shc的通路都通向Ras。
Trends Biochem Sci. 1996 Jul;21(7):257-61.
8
Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse.Emx1和Emx2在小鼠发育中的大脑皮质增殖和分化过程中表现出不同的表达模式。
Eur J Neurosci. 1996 May;8(5):1037-50. doi: 10.1111/j.1460-9568.1996.tb01590.x.
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T cell antigen receptor signal transduction pathways.T细胞抗原受体信号转导途径。
Annu Rev Immunol. 1996;14:259-74. doi: 10.1146/annurev.immunol.14.1.259.
10
Insulin and epidermal growth factor receptors regulate distinct pools of Grb2-SOS in the control of Ras activation.胰岛素和表皮生长因子受体在调控Ras激活过程中调节Grb2-SOS的不同池。
J Biol Chem. 1996 Jul 26;271(30):18224-30. doi: 10.1074/jbc.271.30.18224.

含SH2/PTB结构域的ShcA衔接蛋白的表达与激活反映了哺乳动物大脑中的神经发生模式。

Expression and activation of SH2/PTB-containing ShcA adaptor protein reflects the pattern of neurogenesis in the mammalian brain.

作者信息

Conti L, De Fraja C, Gulisano M, Migliaccio E, Govoni S, Cattaneo E

机构信息

Institute of Pharmacological Sciences, University of Milano, Via Balzaretti 9, Milan 20133, Italy.

出版信息

Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):8185-90. doi: 10.1073/pnas.94.15.8185.

DOI:10.1073/pnas.94.15.8185
PMID:9223336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC21578/
Abstract

The adult mammalian brain comprises many functionally distinct neuronal types, which are generated during development as a result of a coordinated signaling cascade that drives neuroblasts from proliferation into differentiation. We investigated whether and how ShcA adaptor proteins, which are known to function as initiators of the Ras signaling cascade in various nonneuronal systems where they have been considered to be expressed ubiquitously, are involved in the proliferative and differentiative phases of the developing brain. We found that in the forebrain expression and activation of ShcA proteins were strictly regulated during embryonic development, both temporally and spatially. The mRNAs encoded by the ShcA gene were expressed exclusively within an area to which active proliferation of immature neuroblasts was confined, the ventricular zone. In postnatal and adult brain, ShcA mRNAs and proteins were present only faintly. In the adult olfactory epithelium, in which neuronal cell renewal occurs throughout life, ShcA remained strongly expressed. These phenomena were peculiar to ShcA, since Grb2 adaptor protein remained expressed at constant level throughout development. The embryonically expressed ShcA proteins were functionally active, since p52(ShcA) became phosphorylated on tyrosine and associated with Grb2 following intraventricular injection of epidermal growth factor in the embryonic brain. Our data indicate that, through an orderly pattern of expression, ShcA gene products may play a role in the control of the switch between proliferation and differentiation of brain neuroblasts.

摘要

成年哺乳动物的大脑包含许多功能不同的神经元类型,这些神经元类型在发育过程中由协调的信号级联反应产生,该信号级联反应促使神经母细胞从增殖阶段进入分化阶段。我们研究了ShcA衔接蛋白是否以及如何参与发育中大脑的增殖和分化阶段,已知ShcA衔接蛋白在各种非神经元系统中作为Ras信号级联反应的启动子发挥作用,并且在这些系统中被认为是普遍表达的。我们发现,在前脑,ShcA蛋白的表达和激活在胚胎发育过程中在时间和空间上都受到严格调控。ShcA基因编码的mRNA仅在未成熟神经母细胞活跃增殖的区域即脑室区表达。在出生后和成年大脑中,ShcA的mRNA和蛋白仅微弱存在。在成年嗅上皮中,神经元细胞终生更新,ShcA仍强烈表达。这些现象是ShcA特有的,因为Grb2衔接蛋白在整个发育过程中保持恒定水平的表达。胚胎期表达的ShcA蛋白具有功能活性,因为在胚胎脑室内注射表皮生长因子后,p52(ShcA)在酪氨酸上磷酸化并与Grb2结合。我们的数据表明,通过有序的表达模式,ShcA基因产物可能在控制脑成神经细胞增殖和分化之间的转换中发挥作用。