Whole-body single-cell atlas of an adult vertebrate in homeostasis and regeneration

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This study generated a whole-body single-cell atlas of *Danionella cerebrum*, revealing distinct neural cell types, paedomorphic features, conserved neural cell types, and neural regeneration dynamics.

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The study generated a whole-body single-cell RNA sequencing atlas in the adult teleost Danionella cerebrum, using regionally stratified sampling and whole-animal spatial transcriptomics to map cell types and gene expression at single-cell resolution across the entire body. It identified spatially distinct neural progenitor and neuronal cell types with regional gene-expression signatures, and the atlas revealed paedomorphic features and constitutive expression of conserved body-region and appendage-specification programs in adult connective tissue. Comparative analyses showed conserved neural cell types across evolutionary distance, and neural regeneration datasets provided temporally resolved expression dynamics in neural progenitors for telencephalon regeneration, with a limitation that the experiments focus on this species’ adult homeostasis and specific regeneration context rather than directly testing broader disease mechanisms. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

A complete transcriptome atlas of every cell type of a vertebrate could promote understanding of animal cell-type composition, organization, and evolution. The miniaturized, transparent, and regenerative teleost Danionella cerebrum brings whole-organism single-cell profiling experiments within experimental reach for adult vertebrate biology. We performed regionally stratified single-cell RNA sequencing experiments in adult Danionella to profile cells across the whole body and mapped cell types and gene expression spatially at single-cell resolution using whole-animal spatial transcriptomics. We delineated spatially distinct neural progenitor and neuronal cell types across the adult nervous system based on their regional gene expression signatures. The body-wide atlas uncovered paedomorphic features, allowed elucidation of cell types likely to harbor adult positional information, and revealed constitutive expression of conserved body region and appendage specification programs in adult connective tissue. Comparative analyses revealed conserved neural cell types over a large evolutionary distance, and neural regeneration datasets uncovered temporally resolved expression dynamics in neural progenitors for telencephalon regeneration. This whole-vertebrate transcriptome atlas yields a comprehensive resource for myriad questions in biology and neuroscience.
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Abstract A complete transcriptome atlas of every cell type of a vertebrate could promote understanding of animal cell-type composition, organization, and evolution. The miniaturized, transparent, and regenerative teleost Danionella cerebrum brings whole-organism single-cell profiling experiments within experimental reach for adult vertebrate biology. We performed regionally stratified single-cell RNA sequencing experiments in adult Danionella to profile cells across the whole body and mapped cell types and gene expression spatially at single-cell resolution using whole-animal spatial transcriptomics. We delineated spatially distinct neural progenitor and neuronal cell types across the adult nervous system based on their regional gene expression signatures. The body-wide atlas uncovered paedomorphic features, allowed elucidation of cell types likely to harbor adult positional information, and revealed constitutive expression of conserved body region and appendage specification programs in adult connective tissue. Comparative analyses revealed conserved neural cell types over a large evolutionary distance, and neural regeneration datasets uncovered temporally resolved expression dynamics in neural progenitors for telencephalon regeneration. This whole-vertebrate transcriptome atlas yields a comprehensive resource for myriad questions in biology and neuroscience. Competing Interest Statement The authors have declared no competing interest.

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europepmc
last seen: 2026-05-20T01:45:00.602351+00:00
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last seen: 2026-05-22T02:00:06.705733+00:00
License: CC-BY-4.0