皮质激素生成
新皮层
生物
神经科学
谱系(遗传)
大脑皮层
电池类型
进化生物学
染色质
胚胎干细胞
计算生物学
遗传学
细胞
基因
作者
Daniela J. Di Bella,Ehsan Habibi,Robert R. Stickels,Gabriele Scalia,Juliana Brown,Payman Yadollahpour,Sung Min Yang,Catherine Abbate,Tommaso Biancalani,Evan Z. Macosko,Fei Chen,Aviv Regev,Paola Arlotta
出处
期刊:Nature
[Springer Nature]
日期:2021-06-23
卷期号:595 (7868): 554-559
被引量:247
标识
DOI:10.1038/s41586-021-03670-5
摘要
The mammalian cerebral cortex has an unparalleled diversity of cell types, which are generated during development through a series of temporally orchestrated events that are under tight evolutionary constraint and are critical for proper cortical assembly and function1,2. However, the molecular logic that governs the establishment and organization of cortical cell types remains unknown, largely due to the large number of cell classes that undergo dynamic cell-state transitions over extended developmental timelines. Here we generate a comprehensive atlas of the developing mouse neocortex, using single-cell RNA sequencing and single-cell assay for transposase-accessible chromatin using sequencing. We sampled the neocortex every day throughout embryonic corticogenesis and at early postnatal ages, and complemented the sequencing data with a spatial transcriptomics time course. We computationally reconstruct developmental trajectories across the diversity of cortical cell classes, and infer their spatial organization and the gene regulatory programs that accompany their lineage bifurcation decisions and differentiation trajectories. Finally, we demonstrate how this developmental map pinpoints the origin of lineage-specific developmental abnormalities that are linked to aberrant corticogenesis in mutant mice. The data provide a global picture of the regulatory mechanisms that govern cellular diversification in the neocortex.
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