Single-cell multiomic human brain atlas reveals regulatory drivers of cortical regionality

Distinct regional functionality of the human cortex is orchestrated by diverse cellular and molecular processes, yet the underlying regulatory mechanisms remain poorly understood. We performed multiomic single-cell and spatial characterization of nine regions of the human cortex to define the gene regulatory networks and transcription factors that govern cell-type and region specificity. With the combined data of over three million cells, two striking patterns of cortical neuron specialization were uncovered: a rostral-caudal spatial pattern of calcium regulatory machinery, and subunit switching of multiple signaling receptor families across the transmodal-sensory axis. Gene regulatory network analysis revealed putative transcriptional regulators of cortical neuron specialization with cell-type- and region-specific gene regulation patterns. While regionalization was observed in gene expression, chromatin accessibility, and spatial distributions, these modalities exhibited distinct cortical patterns. Our findings illuminate critical neuronal pathways that vary throughout the cortex and the gene regulatory networks that establish cortical regionalization in the human brain.

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Publication Details

Journal
Nature Communications
Published
2026-02-21
DOI
https://doi.org/10.1038/s41467-026-69368-2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

Single-cell multiomic human brain atlas reveals regulatory drivers of cortical regionality

Jerold Chun, Jingwei Han, Nathan R. Zemke, Joshua S. Kurtz et al.
Nature Communications
Single-cell and spatial transcriptomics
article

Single-cell multiomic human brain atlas reveals regulatory drivers of cortical regionality

Jerold Chun, Jingwei Han, Nathan R. Zemke, Joshua S. Kurtz, Kimberly Y. Conklin, Dinh Diep, Linnea Ransom, Carter R. Palmer, Hannah S. Indralingam, Annie Hiniker, Peter Kharchenko, Christine S. Liu, Bing Yang, Anis Shahnaee, Qiwen Hu, Nongluk Plongthongkum, Chien-Ju Chen, Kun Zhang, Bing Ren, C. Dirk Keene, Rebecca D. Hodge, Ed Lein
article en

Abstract

Distinct regional functionality of the human cortex is orchestrated by diverse cellular and molecular processes, yet the underlying regulatory mechanisms remain poorly understood. We performed multiomic single-cell and spatial characterization of nine regions of the human cortex to define the gene regulatory networks and transcription factors that govern cell-type and region specificity. With the combined data of over three million cells, two striking patterns of cortical neuron specialization were uncovered: a rostral-caudal spatial pattern of calcium regulatory machinery, and subunit switching of multiple signaling receptor families across the transmodal-sensory axis. Gene regulatory network analysis revealed putative transcriptional regulators of cortical neuron specialization with cell-type- and region-specific gene regulation patterns. While regionalization was observed in gene expression, chromatin accessibility, and spatial distributions, these modalities exhibited distinct cortical patterns. Our findings illuminate critical neuronal pathways that vary throughout the cortex and the gene regulatory networks that establish cortical regionalization in the human brain.

Nature Communications
University of Southern California (US), Fleet Science Center (US), Allen Institute for Brain Science (US), Harvard University (US), University of Washington (US), Discovery Institute (US), University of California San Diego (US), La Jolla Bioengineering Institute (US), Allen Institute (US), New York Genome Center (US), Altos Labs, Epigenomics (Germany) (DE)
Openalex Percentile: Top 46%
Single-cell and spatial transcriptomics
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