Department of Genetics and Genome Sciences, School of Medicine, University of Connecticut, Farmington, United States.
University of Connecticut, Storrs, United States.
Elife. 2019 Feb 8;8:e42388. doi: 10.7554/eLife.42388.
We applied single-cell RNA sequencing to profile genome-wide gene expression in about 9400 individual cerebellar cells from the mouse embryo at embryonic day 13.5. Reiterative clustering identified the major cerebellar cell types and subpopulations of different lineages. Through pseudotemporal ordering to reconstruct developmental trajectories, we identified novel transcriptional programs controlling cell fate specification of populations arising from the ventricular zone and the rhombic lip, two distinct germinal zones of the embryonic cerebellum. Together, our data revealed cell-specific markers for studying the cerebellum, gene-expression cascades underlying cell fate specification, and a number of previously unknown subpopulations that may play an integral role in the formation and function of the cerebellum. Our findings will facilitate new discovery by providing insights into the molecular and cell type diversity in the developing cerebellum.
我们应用单细胞 RNA 测序技术,对胚胎期第 13.5 天的小鼠胚胎中约 9400 个单个小脑细胞进行了全基因组基因表达谱分析。反复聚类鉴定出了主要的小脑细胞类型和不同谱系的亚群。通过拟时排序来重建发育轨迹,我们确定了控制来自脑室区和菱唇的种群的细胞命运特化的新的转录程序,这两个区域是胚胎小脑的两个不同的生发区。总之,我们的数据为研究小脑提供了细胞特异性标记物、细胞命运特化的基因表达级联,以及一些以前未知的亚群,它们可能在小脑的形成和功能中发挥重要作用。我们的研究结果将为探索发育中小脑的分子和细胞类型多样性提供新的思路,从而促进新的发现。