Single-cell analysis of prenatal and postnatal human cortical development

Velmeshev, D.; Perez, Y.; Yan, Z.; Valencia, J. E.; Castaneda-Castellanos, D. R.; Schirmer, L.; Mayer, S.; Wick, B.; Wang, S.; Nowakowski, T. J.; Paredes, M.; Huang, E. J. J.; Kriegstein, A.

doi:10.1101/2022.10.24.513555

bioRxiv · 10.1101/2022.10.24.513555

Single-cell analysis of prenatal and postnatal human cortical development

Velmeshev, D.·Perez, Y.·Yan, Z.·Valencia, J. E.·Castaneda-Castellanos, D. R.·Schirmer, L.·Mayer, S.·Wick, B.·Wang, S.·Nowakowski, T. J.·Paredes, M.·Huang, E. J. J.·Kriegstein, A.

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Abstract

We analyze more than 700,000 single-nucleus RNA-seq profiles from 106 donors during prenatal and postnatal developmental stages and identify 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 delineate 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 identify 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 upregulated 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. One Sentence SummarySingle-cell transcriptomic atlas of human cortical development identifies lineage and sex-specific programs and their implication in brain disorders.

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Velmeshev, D., Perez, Y., Yan, Z., Valencia, J. E., Castaneda-Castellanos, D. R., Schirmer, L., Mayer, S., Wick, B., Wang, S., Nowakowski, T. J., Paredes, M., Huang, E. J. J., Kriegstein, A.. 2022-10-25. Single-cell analysis of prenatal and postnatal human cortical development. https://doi.org/10.1101/2022.10.24.513555

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