Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Cell Rep. 2023 May 30;42(5):112430. doi: 10.1016/j.celrep.2023.112430. Epub 2023 Apr 25.
The complex functions of neuronal synapses depend on their tightly interconnected protein network, and their dysregulation is implicated in the pathogenesis of autism spectrum disorders and schizophrenia. However, it remains unclear how synaptic molecular networks are altered biochemically in these disorders. Here, we apply multiplexed imaging to probe the effects of RNAi knockdown of 16 autism- and schizophrenia-associated genes on the simultaneous joint distribution of 10 synaptic proteins, observing several protein composition phenotypes associated with these risk genes. We apply Bayesian network analysis to infer hierarchical dependencies among eight excitatory synaptic proteins, yielding predictive relationships that can only be accessed with single-synapse, multiprotein measurements performed simultaneously in situ. Finally, we find that central features of the network are affected similarly across several distinct gene knockdowns. These results offer insight into the convergent molecular etiology of these widespread disorders and provide a general framework to probe subcellular molecular networks.
神经元突触的复杂功能依赖于其紧密相互连接的蛋白质网络,其失调与自闭症谱系障碍和精神分裂症的发病机制有关。然而,突触分子网络在这些疾病中如何在生化层面上发生改变仍不清楚。在这里,我们应用多重成像技术来探测 RNAi 敲低 16 个自闭症和精神分裂症相关基因对 10 种突触蛋白同时联合分布的影响,观察到与这些风险基因相关的几种蛋白质组成表型。我们应用贝叶斯网络分析来推断八种兴奋性突触蛋白之间的层次依赖关系,得出仅通过在原位同时进行的单突触、多蛋白测量才能获得的预测关系。最后,我们发现,网络的核心特征在几种不同的基因敲低中受到相似的影响。这些结果为这些广泛存在的疾病的趋同分子病因学提供了深入了解,并为探测亚细胞分子网络提供了一个通用框架。