Duan Qichen, Okuwa Sumie, Estrella Rachel, Yeung Chun, Chen Yu-Chieh David, Rio Laura Quintana, Vien Khanh M, Volkan Pelin C
Department of Biology, Duke University, Durham, NC 27708, USA.
Department of Biology, New York University, New York, NY 10003, USA.
bioRxiv. 2025 Jun 3:2025.05.31.657193. doi: 10.1101/2025.05.31.657193.
Over the past decades, many critical molecular players have been uncovered to control distinct steps in olfactory circuit assembly in Drosophila. Among these, multi-member gene families of cell surface proteins are of interest because they can act as neuron-specific identification/recognition tags in combinations and contribute to circuit assembly in complex brains through their heterophilic or homophilic interactions. Recently, a multi-protein interactome has been described between the Beat and Side families of IgSF proteins. Here, we use the publicly available single-cell RNA-seq datasets and newly generated gene trap transgenic driver lines to probe the spatial expression pattern of the gene families in odorant receptor neurons (ORNs) and their synaptic target projection neurons (PNs). Our results revealed that each ORN and its synaptic target PN class expresses a class-specific combination of genes, hierarchically regulated by lineage-specific genetic programs. Though ORNs or PNs from closer lineages tend to possess more similar profiles, we also found many examples of divergence from this pattern among closely related ORNs and closely related PNs. To explore whether the class-specific combination of defines ORN-PN matching specificity, we perturbed presynaptic and postsynaptic in two ORN-PN partners. However, disruption of Beat-IIa-Side-IV interaction did not produce any significant mistargeting in these two examined glomeruli. Though without adecting general glomerular targeting, knockdown of in ORNs leads to the reduction of synaptic development. Interestingly, we found conserved expression patterns of orthologs across ORNs in ants and mosquitoes, indicating the shared regulatory strategies specifying the expression of these duplicated paralogs in insect evolution. Overall, this comprehensive analysis of expression patterns lays a foundation for indepth functional investigations into how Beat/Side combinatorial expression contributes to olfactory circuit assembly.
在过去几十年里,人们发现了许多关键分子在果蝇嗅觉回路组装过程中控制不同步骤。其中,细胞表面蛋白的多成员基因家族备受关注,因为它们可以组合充当神经元特异性识别标签,并通过其异嗜性或同嗜性相互作用,在复杂大脑的回路组装中发挥作用。最近,有人描述了免疫球蛋白超家族(IgSF)蛋白的Beat家族和Side家族之间的多蛋白相互作用组。在这里,我们使用公开可用的单细胞RNA测序数据集和新生成的基因陷阱转基因驱动系,来探究这些基因家族在嗅觉受体神经元(ORN)及其突触靶投射神经元(PN)中的空间表达模式。我们的结果显示,每个ORN及其突触靶PN类均表达由谱系特异性遗传程序分层调控的基因类特异性组合。虽然来自较近谱系的ORN或PN往往具有更相似的表达谱,但我们也在密切相关的ORN和密切相关的PN中发现了许多与这种模式不同的例子。为了探究基因的类特异性组合是否定义了ORN-PN匹配特异性,我们在两个ORN-PN伙伴中干扰了突触前和突触后。然而,Beat-IIa-Side-IV相互作用的破坏在这两个被检测的肾小球中并未产生任何明显的靶向错误。虽然不影响一般的肾小球靶向,但ORN中基因的敲低会导致突触发育减少。有趣的是,我们在蚂蚁和蚊子的ORN中发现了直系同源物的保守表达模式,这表明在昆虫进化中指定这些重复旁系同源物表达的调控策略是共享的。总的来说,这种对表达模式的全面分析为深入功能研究Beat/Side组合表达如何促进嗅觉回路组装奠定了基础。