Biever Anne, Valjent Emmanuel, Puighermanal Emma
Centre National de la Recherche Scientifique, UMR5203, Institut de Génomique FonctionnelleMontpellier, France; Institut National de la Santé et de la Recherche Médicale, U1191Montpellier, France; Université de Montpellier, UMR-5203Montpellier, France.
Front Mol Neurosci. 2015 Dec 16;8:75. doi: 10.3389/fnmol.2015.00075. eCollection 2015.
Since the discovery of the phosphorylation of the 40S ribosomal protein S6 (rpS6) about four decades ago, much effort has been made to uncover the molecular mechanisms underlying the regulation of this post-translational modification. In the field of neuroscience, rpS6 phosphorylation is commonly used as a readout of the mammalian target of rapamycin complex 1 signaling activation or as a marker for neuronal activity. Nevertheless, its biological role in neurons still remains puzzling. Here we review the pharmacological and physiological stimuli regulating this modification in the nervous system as well as the pathways that transduce these signals into rpS6 phosphorylation. Altered rpS6 phosphorylation observed in various genetic and pathophysiological mouse models is also discussed. Finally, we examine the current state of knowledge on the physiological role of this post-translational modification and highlight the questions that remain to be addressed.
大约四十年前发现40S核糖体蛋白S6(rpS6)磷酸化以来,人们付出了巨大努力来揭示这种翻译后修饰调控背后的分子机制。在神经科学领域,rpS6磷酸化通常用作雷帕霉素复合物1信号激活的哺乳动物靶点的读数或神经元活动的标志物。然而,其在神经元中的生物学作用仍然令人困惑。在这里,我们综述了调节神经系统中这种修饰的药理学和生理学刺激,以及将这些信号转导为rpS6磷酸化的途径。还讨论了在各种遗传和病理生理小鼠模型中观察到的rpS6磷酸化改变。最后,我们研究了关于这种翻译后修饰生理作用的当前知识状态,并突出了有待解决的问题。