Single-cell analysis of prenatal and postnatal human cortical development

被引:34
|
作者
Velmeshev, Dmitry [1 ,2 ,3 ]
Perez, Yonatan [1 ,2 ]
Yan, Zihan [3 ]
Valencia, Jonathan E. [4 ]
Castaneda-Castellanos, David R. [5 ]
Wang, Li [1 ,2 ]
Schirmer, Lucas [6 ,7 ,8 ,10 ]
Mayer, Simone [1 ,2 ,9 ]
Wick, Brittney [11 ]
Wang, Shaohui [1 ,2 ]
Nowakowski, Tomasz Jan [12 ]
Paredes, Mercedes [2 ]
Huang, Eric J. [1 ,13 ]
Kriegstein, Arnold R. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Eli & Edythe Broad, Ctr Regenerat Med & Stem Cell Res, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[3] Duke Univ, Sch Med, Dept Neurobiol, Durham, NC 27710 USA
[4] Curio Biosci, Palo Alto, CA 94303 USA
[5] Vizgen Inc, Cambridge, MA 02138 USA
[6] Heidelberg Univ, Med Fac Mannheim, Dept Neurol, Div Neuroimmunol, D-68167 Mannheim, Germany
[7] Heidelberg Univ, Mannheim Ctr Translat Neurosci, D-68167 Mannheim, Germany
[8] Heidelberg Univ, Inst Innate Immunosci, Med Fac Mannheim, D-68167 Mannheim, Germany
[9] Univ Tubingen, Hertie Inst Clin Brain Res, D-72076 Tubingen, Germany
[10] Heidelberg Univ, Interdisciplinary Ctr Neurosci, D-68167 Heidelberg, Germany
[11] Univ Calif Santa Cruz, UC Santa Cruz Genom Inst, Santa Cruz, CA 95060 USA
[12] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[13] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94115 USA
关键词
D O I
10.1126/science.adf0834
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We analyzed >700,000 single-nucleus RNA sequencing profiles from 106 donors during prenatal and postnatal developmental stages and identified lineage-specific programs that underlie the development of specific subtypes of excitatory cortical neurons, interneurons, glial cell types, and brain vasculature. By leveraging single-nucleus chromatin accessibility data, we delineated enhancer gene regulatory networks and transcription factors that control commitment of specific cortical lineages. By intersecting our results with genetic risk factors for human brain diseases, we identified the cortical cell types and lineages most vulnerable to genetic insults of different brain disorders, especially autism. We find that lineage-specific gene expression programs up-regulated in female cells are especially enriched for the genetic risk factors of autism. Our study captures the molecular progression of cortical lineages across human development.
引用
收藏
页码:173 / +
页数:9
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