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Single-cell transcriptomics identifies conserved regulators of neuroglandular lineages
Julia Steger1, Alison G Cole2, Andreas Denner1
1Department of Neurosciences and Developmental Biology, Faculty of Life Sciences, University of Vienna, 1030 Vienna, Austria.
Cell Reports
|September 21, 2022
Summary
Neurons and secretory cells in the sea anemone arise from a shared progenitor, regulated by SoxC. This neuroglandular cell lineage is maintained throughout life, offering insights into nervous system evolution.
Area of Science:
- Evolutionary developmental biology
- Neuroscience
- Cell biology
Background:
- Nervous system evolution remains incompletely understood.
- The relationship between neurons and other secretory cells is unclear.
- Cnidarians represent an early-diverging lineage with a simple nervous system.
Purpose of the Study:
- To investigate the evolutionary origins of neurons and secretory cells.
- To identify molecular regulators of neuroglandular cell development in cnidarians.
- To compare neurogenesis across different life stages in Nematostella vectensis.
Main Methods:
- Developmental single-cell RNA sequencing in Nematostella vectensis.
- Transgenic validation of gene function.
- Knockdown experiments using SoxC.
Main Results:
- Neurons, stinging cells, and gland cells originate from a common multipotent progenitor.
- The transcription factor SoxC is a crucial regulator for neuroglandular lineages.
- SoxC knockdown ablates both neuronal and secretory cell types.
- Neuroglandular cell differentiation persists throughout all life stages in sea anemones, mirroring embryonic trajectories.
Conclusions:
- Cnidarians provide a model for understanding the early evolution of neurosecretory cell lineages.
- SoxC is a conserved regulator of neuroglandular development.
- Lifelong neuroglandular cell homeostasis is maintained through conserved molecular pathways in sea anemones.

