# Genome-wide analysis reveals pathways important for the development and maturation of excitatory synaptic connections to GABAergic neurons

**Authors:** Devyn B Oliver, Shankar Ramachandran, Kasturi Biswas, Claire Y Bénard, Maria Doitsidou, Hailey McKillop, Noelia Genao, Michele L Lemons, Michael M Francis

PMC · DOI: 10.1093/g3journal/jkag028 · G3: Genes | Genomes | Genetics · 2026-02-08

## TL;DR

This study identifies genes crucial for forming and maturing synapses connecting excitatory neurons to GABAergic neurons in C. elegans.

## Contribution

The research uncovers three novel genes involved in synapse maturation through an unbiased genetic screen in C. elegans.

## Key findings

- Mutation of unc-14 affects GABAergic neuron morphology and dendritic spines.
- Mutation of unc-63 disrupts AChR assembly without affecting dendritic spine structure.
- Mutation of syd-2 impairs both dendritic spines and AChR localization.

## Abstract

A high degree of cell and circuit-specific regulation has presented challenges for efforts to precisely define molecular mechanisms controlling synapse formation and maturation. Here, we pursue an unbiased forward genetic approach to identify Caenorhabditis elegans genes involved in the formation and maturation of cholinergic synaptic connections with GABAergic motor neurons as indicated by the distribution of GFP-tagged postsynaptic acetylcholine receptors (AChR) on GABAergic dendrites. We identified mutations in 3 genes that identify key processes in synapse/circuit maturation. Mutation of the RUN domain (RPIP8, UNC-14, and NESCA) cargo adaptor gene unc-14 dramatically impacts overall GABAergic neuron morphology and dendritic spines. Mutation of the nicotinic acetylcholine alpha subunit gene unc-63 causes a failure in AChR assembly in GABAergic neurons but does not significantly alter dendritic spine structure or abundance. Finally, a mutation in the Liprin-α synaptic scaffold gene syd-2 severely disrupts both dendritic spines and AChR localization. The identification of these 3 genes from our screen highlights how mechanisms for cargo trafficking, receptor assembly, and synapse structural organization each make distinct contributions to synapse assembly and circuit connectivity.

Graphical AbstractFor image description, please refer to the figure legend and surrounding text.

## Linked entities

- **Genes:** unc-14 (RUN domain-containing protein) [NCBI Gene 172450], unc-63 (Acetylcholine receptor subunit alpha-type unc-63) [NCBI Gene 172150], MAPK8IP3 (mitogen-activated protein kinase 8 interacting protein 3) [NCBI Gene 23162]
- **Proteins:** nAChRbeta1 (nicotinic Acetylcholine Receptor beta1)
- **Species:** Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Genes:** unc-14 (RUN domain-containing protein) [NCBI Gene 172450], unc-63 (Acetylcholine receptor subunit alpha-type unc-63) [NCBI Gene 172150], syd-2 (Liprin-alpha) [NCBI Gene 181255]
- **Species:** Caenorhabditis elegans (species) [taxon 6239]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13042287/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC13042287/full.md

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Source: https://tomesphere.com/paper/PMC13042287