Department of Molecular Biology, Semmelweis University, Budapest, Hungary.
Department of Emergency Medicine, Semmelweis University, Budapest, Hungary.
PLoS Comput Biol. 2020 Dec 21;16(12):e1007974. doi: 10.1371/journal.pcbi.1007974. eCollection 2020 Dec.
Graph theoretical analyses of nervous systems usually omit the aspect of connection polarity, due to data insufficiency. The chemical synapse network of Caenorhabditis elegans is a well-reconstructed directed network, but the signs of its connections are yet to be elucidated. Here, we present the gene expression-based sign prediction of the ionotropic chemical synapse connectome of C. elegans (3,638 connections and 20,589 synapses total), incorporating available presynaptic neurotransmitter and postsynaptic receptor gene expression data for three major neurotransmitter systems. We made predictions for more than two-thirds of these chemical synapses and observed an excitatory-inhibitory (E:I) ratio close to 4:1 which was found similar to that observed in many real-world networks. Our open source tool (http://EleganSign.linkgroup.hu) is simple but efficient in predicting polarities by integrating neuronal connectome and gene expression data.
神经系统的图论分析通常由于数据不足而忽略连接极性的方面。秀丽隐杆线虫的化学突触网络是一个经过良好重建的有向网络,但它的连接符号尚未阐明。在这里,我们提出了秀丽隐杆线虫离子型化学突触连接组(3638 个连接和总共 20589 个突触)的基于基因表达的符号预测,整合了三个主要神经递质系统的可用突触前神经递质和突触后受体基因表达数据。我们对这些化学突触中的三分之二以上进行了预测,并观察到兴奋性抑制性 (E:I) 比值接近 4:1,这与许多真实世界网络中观察到的相似。我们的开源工具 (http://EleganSign.linkgroup.hu) 通过整合神经元连接组和基因表达数据,在预测极性方面简单而高效。