Specification of diverse cell types during early neurogenesis of the mouse cerebellum

被引:65
作者
Wizeman, John W. [1 ]
Guo, Qiuxia [1 ]
Wilion, Elliott M. [2 ]
Li, James Y. H. [1 ,3 ]
机构
[1] Univ Connecticut, Sch Med, Dept Genet & Genome Sci, Farmington, CT 06032 USA
[2] Univ Connecticut, Storrs, CT USA
[3] Univ Connecticut, Inst Syst Genom, Farmington, CT 06030 USA
来源
ELIFE | 2019年 / 8卷
关键词
GENE-EXPRESSION; RHOMBIC-LIP; GRANULE CELLS; TRANSCRIPTION FACTORS; PARASAGITTAL STRIPES; PROGENITORS; DIFFERENTIATION; PROLIFERATION; MIDBRAIN; MATH1;
D O I
10.7554/eLife.42388
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:24
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