4.8 Article

Molecular logic of cellular diversification in the mouse cerebral cortex

Journal

NATURE
Volume 595, Issue 7868, Pages 554-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03670-5

Keywords

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Funding

  1. Stanley Center for Psychiatric Research
  2. Broad Institute of MIT and Harvard
  3. National Institutes of Health [P50MH094271, U19MH114821, R01NS103758, DP5OD024583]
  4. Klarman Cell Observatory
  5. NHGRI Center for Cell Circuits CEGS
  6. Pew Latin American Postdoctoral Fellowship
  7. HHMI

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Researchers generated a comprehensive atlas of the developing mouse neocortex, reconstructing developmental trajectories across cortical cell classes and inferring spatial organization and gene regulatory programs. They also demonstrated how this developmental map can pinpoint lineage-specific developmental abnormalities in mutant mice, providing a global picture of the regulatory mechanisms governing cellular diversification in the neocortex.
The mammalian cerebral cortex has an unparalleled diversity of cell types, which are generated during development through a series of temporally orchestrated events that are under tight evolutionary constraint and are critical for proper cortical assembly and function(1,2). However, the molecular logic that governs the establishment and organization of cortical cell types remains unknown, largely due to the large number of cell classes that undergo dynamic cell-state transitions over extended developmental timelines. Here we generate a comprehensive atlas of the developing mouse neocortex, using single-cell RNA sequencing and single-cell assay for transposase-accessible chromatin using sequencing. We sampled the neocortex every day throughout embryonic corticogenesis and at early postnatal ages, and complemented the sequencing data with a spatial transcriptomics time course. We computationally reconstruct developmental trajectories across the diversity of cortical cell classes, and infer their spatial organization and the gene regulatory programs that accompany their lineage bifurcation decisions and differentiation trajectories. Finally, we demonstrate how this developmental map pinpoints the origin of lineage-specific developmental abnormalities that are linked to aberrant corticogenesis in mutant mice. The data provide a global picture of the regulatory mechanisms that govern cellular diversification in the neocortex.

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