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Single-cell analysis of prenatal and postnatal human cortical development

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 vasc...

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Bibliographische Detailangaben
Hauptverfasser: Velmeshev, Dmitry (VerfasserIn) , Perez, Yonatan (VerfasserIn) , Yan, Zihan (VerfasserIn) , Valencia, Jonathan E. (VerfasserIn) , Castaneda-Castellanos, David R. (VerfasserIn) , Wang, Li (VerfasserIn) , Schirmer, Lucas (VerfasserIn) , Mayer, Simone (VerfasserIn) , Wick, Brittney (VerfasserIn) , Wang, Shaohui (VerfasserIn) , Nowakowski, Tomasz Jan (VerfasserIn) , Paredes, Mercedes (VerfasserIn) , Huang, Eric J. (VerfasserIn) , Kriegstein, Arnold R. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: Oct 2023
In: Science
Year: 2023, Jahrgang: 382, Heft: 6667, Pages: 1-8
ISSN:1095-9203
DOI:10.1126/science.adf0834
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1126/science.adf0834
Verlag, lizenzpflichtig, Volltext: https://www.science.org/doi/10.1126/science.adf0834
Volltext
Verfasserangaben:Dmitry Velmeshev, Yonatan Perez, Zihan Yan, Jonathan E. Valencia, David R. Castaneda-Castellanos, Li Wang, Lucas Schirmer, Simone Mayer, Brittney Wick, Shaohui Wang, Tomasz Jan Nowakowski, Mercedes Paredes, Eric J. Huang, Arnold R. Kriegstein
Beschreibung
Zusammenfassung: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.
Beschreibung:Online veröffentlicht: 13. Oktober 2023
Gesehen am 22.07.2024
Beschreibung:Online Resource
ISSN:1095-9203
DOI:10.1126/science.adf0834

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