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Network activity-independent coordinated gene expression program for synapse assembly

机译:突触组装的网络活动无关的协同基因表达程序

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摘要

Global biological datasets generated by genomics, transcriptomics, and proteomics provide new approaches to understanding the relationship between the genome and the synapse. Combined transcriptome analysis and multielectrode recordings of neuronal network activity were used in mouse embryonic primary neuronal cultures to examine synapse formation and activity-dependent gene regulation. Evidence for a coordinated gene expression program for assembly of synapses was observed in the expression of 642 genes encoding postsynaptic and plasticity proteins. This synaptogenesis gene expression program preceded protein expression of synapse markers and onset of spiking activity. Continued expression was followed by maturation of morphology and electrical neuronal networks, which was then followed by the expression of activity-dependent genes. Thus, two distinct sequentially active gene expression programs underlie the genomic programs of synapse function.
机译:由基因组学,转录组学和蛋白质组学生成的全球生物学数据集提供了新的方法来理解基因组和突触之间的关系。组合的转录组分析和神经网络活动的多电极记录被用于小鼠胚胎原代神经元培养物中,以检查突触的形成和活性依赖性基因的调控。在编码突触后和可塑性蛋白的642个基因的表达中观察到了用于突触装配的协调基因表达程序的证据。该突触发生基因表达程序先于突触标记物的蛋白表达和尖峰活性的发作。继续表达后,形态学和电神经元网络成熟,然后表达活性依赖性基因。因此,两个不同的顺序活跃的基因表达程序是突触功能的基因组程序的基础。

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