Di Nardo Ariel A, Nedelec Stéphane, Trembleau Alain, Volovitch Michel, Prochiantz Alain, Montesinos Maria Luz
CNRS UMR 8542, Développement et Neuropharmacologie, Ecole Normale Supérieure, 46 rue d'Ulm, 75005 Paris, France.
Mol Cell Neurosci. 2007 Jun;35(2):230-6. doi: 10.1016/j.mcn.2007.02.015. Epub 2007 Mar 3.
Engrailed1 (En1) is a homeoprotein transcription factor expressed throughout adulthood in several midbrain cells, including the dopaminergic neurons of the substantia nigra. Here we report the presence of Engrailed protein and En1 mRNA in proximal dendrites of these neurons and of En1 mRNA in ventral midbrain synaptoneurosomes. We show that the 3' untranslated region of En1 mRNA contains a functional cytoplasmic polyadenylation element (CPE), suggesting that its dendritic localization is regulated by CPE binding protein (CPEB). In order to evaluate activity-regulated translation, conditions were developed using primary midbrain neurons. With this in vitro model, En1 mRNA translation is increased by depolarization in a polyadenylation dependent manner. Furthermore, En1 translation is prevented by rapamycin, implicating the mTOR pathway, which is known to regulate dendritic translation. Together, these results suggest an activity-dependent role for Engrailed in midbrain dopaminergic neuron physiology.
Engrailed1(En1)是一种同源结构域蛋白转录因子,在成年期的几个中脑细胞中均有表达,包括黑质中的多巴胺能神经元。在此我们报告,在这些神经元的近端树突中存在Engrailed蛋白和En1 mRNA,并且在腹侧中脑突触神经小体中存在En1 mRNA。我们发现,En1 mRNA的3'非翻译区包含一个功能性细胞质聚腺苷酸化元件(CPE),这表明其树突定位受CPE结合蛋白(CPEB)调控。为了评估活性调节的翻译过程,我们利用原代中脑神经元建立了相关条件。通过这个体外模型,En1 mRNA的翻译在聚腺苷酸化依赖的方式下因去极化而增加。此外,雷帕霉素可阻止En1的翻译,这涉及到已知可调节树突翻译的mTOR途径。这些结果共同表明,Engrailed在中脑多巴胺能神经元生理学中具有活性依赖的作用。