Department of Neuro- and Sensory Physiology, University Medical Center Göttingen, Excellence Cluster Multiscale Bioimaging, 37073 Göttingen, Germany.
Department of Clinical Chemistry, University Medical Center Göttingen, 37077 Göttingen, Germany.
Sci Adv. 2019 Dec 18;5(12):eaay2670. doi: 10.1126/sciadv.aay2670. eCollection 2019 Dec.
The cellular and the molecular mechanisms by which long noncoding RNAs (lncRNAs) may regulate presynaptic function and neuronal activity are largely unexplored. Here, we established an integrated screening strategy to discover lncRNAs implicated in neurotransmitter and synaptic vesicle release. With this approach, we identified , a neuron-specific nuclear lncRNA conserved from rodents to humans. is tuned by synaptic activity and influences several other essential aspects of neuronal development including calcium influx, neuritogenesis, and neuronal migration in vivo. We defined the molecular interactors of in detail using chromatin isolation by RNA purification, RNA interactome analysis, and protein mass spectrometry. We found that the effects of on synaptic vesicle release require interaction with the RNA-binding protein TDP-43 (TAR DNA binding protein-43) and the selective stabilization of mRNAs encoding for presynaptic proteins. These results provide the first proof of an lncRNA that orchestrates neuronal excitability by influencing presynaptic function.
长链非编码 RNA(lncRNA)调控突触前功能和神经元活动的细胞和分子机制在很大程度上尚未被探索。在这里,我们建立了一个综合的筛选策略,以发现参与神经递质和突触囊泡释放的 lncRNA。通过这种方法,我们鉴定了一种从啮齿动物到人类都保守的神经元特异性核 lncRNA 。 受突触活动调控,并影响神经元发育的其他几个重要方面,包括体内钙内流、神经突生成和神经元迁移。我们使用 RNA 纯化的染色质分离、RNA 相互作用组分析和蛋白质质谱来详细定义 的分子相互作用体。我们发现, 对突触囊泡释放的影响需要与 RNA 结合蛋白 TDP-43(TAR DNA 结合蛋白 43)相互作用,并选择性稳定编码突触前蛋白的 mRNAs。这些结果首次证明了一种 lncRNA 通过影响突触前功能来协调神经元兴奋性。