VIB Center for Brain & Disease Research, Leuven, Belgium.
Department of Human Genetics, KU Leuven, Leuven, Belgium.
Nature. 2022 Jan;601(7894):630-636. doi: 10.1038/s41586-021-04262-z. Epub 2022 Jan 5.
The Drosophila brain is a frequently used model in neuroscience. Single-cell transcriptome analysis, three-dimensional morphological classification and electron microscopy mapping of the connectome have revealed an immense diversity of neuronal and glial cell types that underlie an array of functional and behavioural traits in the fly. The identities of these cell types are controlled by gene regulatory networks (GRNs), involving combinations of transcription factors that bind to genomic enhancers to regulate their target genes. Here, to characterize GRNs at the cell-type level in the fly brain, we profiled the chromatin accessibility of 240,919 single cells spanning 9 developmental timepoints and integrated these data with single-cell transcriptomes. We identify more than 95,000 regulatory regions that are used in different neuronal cell types, of which 70,000 are linked to developmental trajectories involving neurogenesis, reprogramming and maturation. For 40 cell types, uniquely accessible regions were associated with their expressed transcription factors and downstream target genes through a combination of motif discovery, network inference and deep learning, creating enhancer GRNs. The enhancer architectures revealed by DeepFlyBrain lead to a better understanding of neuronal regulatory diversity and can be used to design genetic driver lines for cell types at specific timepoints, facilitating their characterization and manipulation.
果蝇大脑是神经科学中常用的模型。单细胞转录组分析、三维形态分类和连接组的电子显微镜图谱揭示了大量的神经元和神经胶质细胞类型,这些类型为果蝇的一系列功能和行为特征提供了基础。这些细胞类型的身份由基因调控网络(GRN)控制,涉及转录因子的组合,这些转录因子与基因组增强子结合,以调节其靶基因。在这里,为了在果蝇大脑的细胞类型水平上表征 GRN,我们对跨越 9 个发育时间点的 240919 个单细胞的染色质可及性进行了分析,并将这些数据与单细胞转录组进行了整合。我们鉴定了超过 95000 个在不同神经元细胞类型中使用的调控区域,其中 70000 个与涉及神经发生、重编程和成熟的发育轨迹有关。对于 40 种细胞类型,通过基序发现、网络推断和深度学习的组合,唯一可及的区域与它们表达的转录因子及其下游靶基因相关联,从而构建了增强子 GRN。DeepFlyBrain 揭示的增强子结构有助于更好地理解神经元调控多样性,并可用于设计特定时间点特定细胞类型的遗传驱动线,从而促进其表征和操作。