Department of Biological Chemistry, Howard Hughes Medical Institute, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, United States.
Neuroscience Interdepartmental Program, University of California, Los Angeles, Los Angeles, United States.
Elife. 2019 Nov 5;8:e50822. doi: 10.7554/eLife.50822.
Patterns of synaptic connectivity are remarkably precise and complex. Single-cell RNA sequencing has revealed a vast transcriptional diversity of neurons. Nevertheless, a clear logic underlying the transcriptional control of neuronal connectivity has yet to emerge. Here, we focused on T4/T5 neurons, a class of closely related neuronal subtypes with different wiring patterns. Eight subtypes of T4/T5 neurons are defined by combinations of two patterns of dendritic inputs and four patterns of axonal outputs. Single-cell profiling during development revealed distinct transcriptional programs defining each dendrite and axon wiring pattern. These programs were defined by the expression of a few transcription factors and different combinations of cell surface proteins. Gain and loss of function studies provide evidence for independent control of different wiring features. We propose that modular transcriptional programs for distinct wiring features are assembled in different combinations to generate diverse patterns of neuronal connectivity.
突触连接的模式非常精确和复杂。单细胞 RNA 测序揭示了神经元转录的巨大多样性。然而,神经元连接的转录控制背后的明确逻辑尚未显现。在这里,我们关注 T4/T5 神经元,这是一类具有不同连接模式的密切相关的神经元亚型。八种 T4/T5 神经元亚型是由两种树突输入模式和四种轴突输出模式的组合定义的。在发育过程中的单细胞分析揭示了每个树突和轴突连接模式的不同转录程序。这些程序由少数转录因子的表达和不同的细胞表面蛋白组合定义。功能获得和丧失研究为不同连接特征的独立控制提供了证据。我们提出,用于不同连接特征的模块化转录程序以不同的组合组装,以产生不同的神经元连接模式。