Co-Conservation of synaptic gene expression and circuitry in collicular neurons

The superior colliculus (SC), a midbrain sensorimotor hub, is anatomically and functionally similar across vertebrates, but how its cell types have evolved is unclear. Using single-nucleus transcriptomics, we compared the SC's molecular and cellular organization in mice, tree shrews, and humans. Despite over 96 million years of evolutionary divergence, we identified ~30 consensus neuronal subtypes, including Cbln2+ neurons that form the SC-pulvinar circuit in mice and tree shrews. Synapse-related genes were among the most conserved in the SC, unlike neocortex, suggesting co-conservation of synaptic genes and collicular circuitry. In contrast, cilia-related genes diverged significantly across species, highlighting the potential importance of the neuronal primary cilium in SC evolution. Additionally, we identified an inhibitory SC neuron in tree shrews and humans but not mice. Our findings reveal that the SC has evolved by conserving neuron subtypes, synaptic genes, and circuitry, while diversifying ciliary gene expression and an inhibitory neuron subtype.

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Publication Details

Journal
Nature Communications
Published
2025-10-15
DOI
https://doi.org/10.1038/s41467-025-64204-5
Citations
2
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
1.61

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article

Co-Conservation of synaptic gene expression and circuitry in collicular neurons

John N. Campbell, Jianhua Cang, Alev Erişir, Élise Savier et al.
2 citations
Nature Communications
Retinal Development and Disorders
1.61
article

Co-Conservation of synaptic gene expression and circuitry in collicular neurons

John N. Campbell, Jianhua Cang, Alev Erişir, Élise Savier, Chen Chen, Lü Yang, Yuanming Liu, John A. McDaniel, Arda Kıpçak
article en
2 citations

Abstract

The superior colliculus (SC), a midbrain sensorimotor hub, is anatomically and functionally similar across vertebrates, but how its cell types have evolved is unclear. Using single-nucleus transcriptomics, we compared the SC's molecular and cellular organization in mice, tree shrews, and humans. Despite over 96 million years of evolutionary divergence, we identified ~30 consensus neuronal subtypes, including Cbln2+ neurons that form the SC-pulvinar circuit in mice and tree shrews. Synapse-related genes were among the most conserved in the SC, unlike neocortex, suggesting co-conservation of synaptic genes and collicular circuitry. In contrast, cilia-related genes diverged significantly across species, highlighting the potential importance of the neuronal primary cilium in SC evolution. Additionally, we identified an inhibitory SC neuron in tree shrews and humans but not mice. Our findings reveal that the SC has evolved by conserving neuron subtypes, synaptic genes, and circuitry, while diversifying ciliary gene expression and an inhibitory neuron subtype.

Nature CommunicationsVol. 16(1)
University of Virginia (US)
American Diabetes Association, University of Virginia, Jefferson Scholars Foundation, National Institutes of Health
Openalex Percentile: Top 14%
Retinal Development and Disorders
1.61
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Co-Conservation of synaptic gene expression and circuitry in collicular neurons — John N. Campbell, Jianhua Cang, et al. · Nature Communications (2025) | TGRS Research Map | TGRS