Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex

Author:

Kim Sonia NanORCID,Viswanadham Vinayak V.ORCID,Doan Ryan N.ORCID,Dou YanmeiORCID,Bizzotto SaraORCID,Khoshkhoo SattarORCID,Huang August YueORCID,Yeh Rebecca,Chhouk Brian,Truong Alex,Chappell Kathleen M.,Beaudin Marc,Barton AlisonORCID,Akula Shyam K.ORCID,Rento Lariza,Lodato MichaelORCID,Ganz JavierORCID,Szeto Ryan A.,Li Pengpeng,Tsai Jessica W.,Hill Robert Sean,Park Peter J.ORCID,Walsh Christopher A.ORCID

Abstract

AbstractThe mammalian cerebral cortex shows functional specialization into regions with distinct neuronal compositions, most strikingly in the human brain, but little is known in about how cellular lineages shape cortical regional variation and neuronal cell types during development. Here, we use somatic single nucleotide variants (sSNVs) to map lineages of neuronal sub-types and cortical regions. Early-occurring sSNVs rarely respect Brodmann area (BA) borders, while late-occurring sSNVs mark neuron-generating clones with modest regional restriction, though descendants often dispersed into neighboring BAs. Nevertheless, in visual cortex, BA17 contains 30-70% more sSNVs compared to the neighboring BA18, with clones across the BA17/18 border distributed asymmetrically and thus displaying different cortex-wide dispersion patterns. Moreover, we find that excitatory neuron-generating clones with modest regional restriction consistently share low-mosaic sSNVs with some inhibitory neurons, suggesting significant co-generation of excitatory and some inhibitory neurons in the dorsal cortex. Our analysis reveals human-specific cortical cell lineage patterns, with both regional inhomogeneities in progenitor proliferation and late divergence of excitatory/inhibitory lineages.

Publisher

Cold Spring Harbor Laboratory

Reference105 articles.

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