Mammalian Pumilio 2 regulates dendrite morphogenesis and synaptic function

被引:101
作者
Vessey, John P. [1 ]
Schoderboeck, Lucia [1 ]
Gingl, Ewald [2 ]
Luzi, Ettore [3 ]
Riefler, Julia [1 ]
Di Leva, Francesca [4 ]
Karra, Daniela [1 ]
Thomas, Sabine [1 ]
Kiebler, Michael A. [1 ]
Macchi, Paolo [1 ,4 ]
机构
[1] Med Univ Vienna, Dept Neuronal Cell Biol, Ctr Brain Res, A-1090 Vienna, Austria
[2] Med Univ Vienna, Dept Neurophysiol, Ctr Brain Res, A-1090 Vienna, Austria
[3] Univ Florence, Dept Internal Med, Azienda Osped Univ Careggi, Ctr Endocrine Hereditary Tumors,Lab Mol Genet, I-50139 Florence, Italy
[4] Univ Trent, Mol & Cellular Neurobiol Lab, Ctr Integrat Biol, I-38060 Trento, Italy
基金
奥地利科学基金会;
关键词
dendritic spines; eIF4E; ribonucleoparticles; neuronal development; translational control; HIGH-EFFICIENCY TRANSFECTION; NEURONAL EXCITABILITY; HIPPOCAMPAL-NEURONS; PROTEIN; MORPHOLOGY; GRANULES; SPINES; NANOS; PUM2;
D O I
10.1073/pnas.0907128107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In Drosophila, Pumilio (Pum) is important for neuronal homeostasis as well as learning and memory. We have recently characterized a mammalian homolog of Pum, Pum2, which is found in discrete RNA-containing particles in the somatodendritic compartment of polarized neurons. In this study, we investigated the role of Pum2 in developing and mature neurons by RNA interference. In immature neurons, loss of Pum2 led to enhanced dendritic outgrowth and arborization. In mature neurons, Pum2 down-regulation resulted in a significant reduction in dendritic spines and an increase in elongated dendritic filopodia. Furthermore, we observed an increase in excitatory synapse markers along dendritic shafts. Electrophysiological analysis of synaptic function of neurons lacking Pum2 revealed an increased miniature excitatory postsynaptic current frequency. We then identified two specific mRNAs coding for a known translational regulator, eIF4E, and for a voltage-gated sodium channel, Scn1a, which interacts with Pum2 in immunoprecipitations from brain lysates. Finally, we show that Pum2 regulates translation of the eIF4E mRNA. Taken together, our data reveal a previously undescribed role for Pum2 in dendrite morphogenesis, synapse function, and translational control.
引用
收藏
页码:3222 / 3227
页数:6
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