A high-resolution atlas of the brain predicts lineage and birth order underlying neuronal identity

Gene expression shapes the nervous system at every biological level, from molecular and cellular processes defining neuronal identity and function to systems-level wiring and circuit dynamics underlying behavior. Here, we generate the first high-resolution, single-cell transcriptomic atlas of the adult Drosophila melanogaster central brain by integrating multiple datasets, achieving an unprecedented 10-fold coverage of every neuron in this complex tissue. We show that a neuron's genetic identity overwhelmingly reflects its developmental origin, preserving a genetic address based on both lineage and birth order. We reveal foundational rules linking neurogenesis to transcriptional identity and provide a framework for systematically defining neuronal types. This atlas provides a powerful resource for mapping the cellular substrates of behavior by integrating annotations of hemilineage, cell types/subtypes, and molecular signatures of underlying physiological properties. It lays the groundwork for a long-sought bridge between developmental processes and the functional circuits that give rise to behavior.

Institutions

Publication Details

Journal
Cell Genomics
Published
2025-12-19
DOI
https://doi.org/10.1016/j.xgen.2025.101103
Citations
3
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
2.73
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article

A high-resolution atlas of the brain predicts lineage and birth order underlying neuronal identity

3 citations
Cell Genomics
Neurobiology and Insect Physiology Research
2.73
article

A high-resolution atlas of the brain predicts lineage and birth order underlying neuronal identity

article en
3 citations

Abstract

Gene expression shapes the nervous system at every biological level, from molecular and cellular processes defining neuronal identity and function to systems-level wiring and circuit dynamics underlying behavior. Here, we generate the first high-resolution, single-cell transcriptomic atlas of the adult Drosophila melanogaster central brain by integrating multiple datasets, achieving an unprecedented 10-fold coverage of every neuron in this complex tissue. We show that a neuron's genetic identity overwhelmingly reflects its developmental origin, preserving a genetic address based on both lineage and birth order. We reveal foundational rules linking neurogenesis to transcriptional identity and provide a framework for systematically defining neuronal types. This atlas provides a powerful resource for mapping the cellular substrates of behavior by integrating annotations of hemilineage, cell types/subtypes, and molecular signatures of underlying physiological properties. It lays the groundwork for a long-sought bridge between developmental processes and the functional circuits that give rise to behavior.

Cell GenomicsVol. 6(3)
University of Oxford (GB), MRC Weatherall Institute of Molecular Medicine (GB), MRC Human Immunology Unit (GB), Oxford Centre for Mission Studies (GB)
Openalex Percentile: Top 9%
Neurobiology and Insect Physiology Research
2.73
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