Combined somatic mutation and transcriptome analysis reveals region-specific differences in clonal architecture in human cortex
Vinay Viswanadham, Sonia N. Kim, Emre Caglayan, Ryan N. Doan, Yanmei Dou, Sara Bizzotto, Sattar Khoshkhoo, August Yue Huang, Rebecca C. Yeh, Brian H. Chhouk, Alex Truong, Kathleen M. Chappell, Marc Beaudin, Alison R. Barton, Shyam K. Akula, Yifan Zhao, Lariza M. Rento, Michael A. Lodato, Ryan A. Szeto, Javier Ganz, Pengpeng Li, Jessica W. Tsai, Robert Hill, Peter J. Park, Christopher A. Walsh
Abstract
The human cerebral cortex is specialized into regions, but little is known about how human cellular lineages shape cortical regional variation and neuronal cell-type distribution during development. Here, we map single-cell lineages of human cortical regions and neuronal subtypes using >1,000 somatic single-nucleotide variants (sSNVs) identified from deep bulk whole-genome sequencing and analyzed over 25 regions and >72,000 single cells. In the fronto-parietal cortex, sSNVs are rarely restricted, marking neuron-generating clones that disperse into neighboring regions. In contrast, the primary visual cortex harbors 30%-70% more sSNVs than the neighboring secondary visual cortex. Clones at this border exhibit more restricted dispersion, suggesting late developmental lineage segregation. Single-nucleus sSNV and whole-transcriptome analysis reveal glutamatergic neuron clones with modest regional restrictions that share low-mosaic sSNVs with some GABAergic neurons, suggesting a recent dorsal cortical progenitor. Our analysis reveals human-specific cortical lineage patterns, regional differences in clonal patterns, and late divergence of some glutamatergic/GABAergic lineages.