E3 Ligase Nedd4 Promotes Axon Branching by Downregulating PTEN

被引:188
作者
Drinjakovic, Jovana [1 ]
Jung, Hosung [1 ]
Campbell, Douglas S. [1 ]
Strochlic, Laure [1 ]
Dwivedy, Asha [1 ]
Holt, Christine E. [1 ]
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3DY, England
基金
英国惠康基金;
关键词
RETINAL GROWTH CONES; RETINOTECTAL SYNAPTIC CONNECTIVITY; UBIQUITIN LIGASE; IN-VIVO; TUMOR-SUPPRESSOR; XENOPUS EMBRYOS; CHEMOTROPIC RESPONSES; PROTEIN-SYNTHESIS; ZEBRAFISH RETINA; VISUAL-SYSTEM;
D O I
10.1016/j.neuron.2010.01.017
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Regulated protein degradation via the ubiquitin-proteasome system (UPS) plays a central role in building synaptic connections, yet little is known about either which specific UPS components are involved or UPS targets in neurons. We report that inhibiting the UPS in developing Xenopus retinal ganglion cells (RGCs) with a dominant-negative ubiquitin mutant decreases terminal branching in the tectum but does not affect long-range navigation to the tectum. We identify Nedd4 as a prominently expressed E3 ligase in RGC axon growth cones and show that disrupting its function severely inhibits terminal branching. We further demonstrate that PTEN, a negative regulator of the PI3K pathway, is a key downstream target of Nedd4: not only does Nedd4 regulate PTEN levels in RGC growth cones, but also, the decrease of PTEN rescues the branching defect caused by Nedd4 inhibition. Together our data suggest that Nedd4-regulated PTEN is a key regulator of terminal arborization in vivo.
引用
收藏
页码:341 / 357
页数:17
相关论文
共 78 条
[1]
The tumour suppressor PTEN mediates a negative regulation of the E3 ubiquitin-protein ligase Nedd4 [J].
Ahn, Younghee ;
Hwang, Chae Young ;
Lee, Seung-Rock ;
Kwon, Ki-Sun ;
Lee, Cheolju .
BIOCHEMICAL JOURNAL, 2008, 412 (02) :331-338
[2]
Visualizing synapse formation in arborizing optic axons in vivo:: dynamics and modulation by BDNF [J].
Alsina, B ;
Vu, T ;
Cohen-Cory, S .
NATURE NEUROSCIENCE, 2001, 4 (11) :1093-1101
[3]
[Anonymous], 1994, Normal table of xenopus laevis (Daudin): A systematical and chronological survey of the development from the fertilized egg till the end of metamorphosis
[4]
Cell survival through Trk neurotrophin receptors is differentially regulated by ubiquitination [J].
Arévalo, Juan Carlos ;
Waite, Janelle ;
Rajagopal, Rithwick ;
Beyna, Mercedes ;
Chen, Zhe-Yu ;
Lee, Francis S. ;
Chao, Moses V. .
NEURON, 2006, 50 (04) :549-559
[5]
The requirement for Phr1 in CNS axon tract formation reveals the corticostriatal boundary as a choice point for cortical axons [J].
Bloom, A. Joseph ;
Miller, Bradley R. ;
Sanes, Joshua R. ;
DiAntonio, Aaron .
GENES & DEVELOPMENT, 2007, 21 (20) :2593-2606
[6]
Slit proteins: key regulators of axon guidance, axonal branching, and cell migration [J].
Brose, K ;
Tessier-Lavigne, M .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (01) :95-102
[7]
Slit1a inhibits retinal ganglion cell arborization and synaptogenesis via Robo2-Dependent and -independent pathways [J].
Campbell, Douglas S. ;
Stringham, Sydney A. ;
Timm, Adam ;
Xiao, Tong ;
Law, Mei-Yee ;
Baier, Herwig ;
Nonet, Michael L. ;
Chien, Chi-Bin .
NEURON, 2007, 55 (02) :231-245
[8]
Apoptotic pathway and MAPKs differentially regulate chemotropic responses of retinal growth cones [J].
Campbell, DS ;
Holt, CE .
NEURON, 2003, 37 (06) :939-952
[9]
Chemotropic responses of retinal growth cones mediated by rapid local protein synthesis and degradation [J].
Campbell, DS ;
Holt, CE .
NEURON, 2001, 32 (06) :1013-1026
[10]
Semaphorin 3A elicits stage-dependent collapse, turning, and branching in Xenopus retinal growth cones [J].
Campbell, DS ;
Regan, AG ;
Lopez, JS ;
Tannahill, D ;
Harris, WA ;
Holt, CE .
JOURNAL OF NEUROSCIENCE, 2001, 21 (21) :8538-8547