A Toolkit for In Vivo Mapping and Modulating Neurotransmission at Single-Cell Resolution

Abstract

Understanding the organization and regulation of neurotransmission at the level of individual neurons and synapses requires tools that can track and manipulate transmitter-specific vesicles in vivo. Here, we present a suite of genetic tools in Caenorhabditis elegans to fluorescently label and conditionally ablate the vesicular transporters for glutamate, GABA, acetylcholine, and monoamines. Using a structure-guided approach informed by protein topology and evolutionary conservation, we engineered endogenously tagged versions for each transporter that maintain their physiological function while allowing for cell-specific, bright, and stable visualization. We also developed conditional knockout strains that enable targeted disruption of neurotransmitter synthesis or packaging in single neurons. We applied this toolkit to map co-expression of vesicular transporters across the C. elegans nervous system, revealing that over 10% of neurons exhibit co-transmission. Using the ADF sensory neuron as a case study, we demonstrate that serotonin and acetylcholine are trafficked in partially distinct vesicle pools. Our approach provides a powerful platform for mapping, monitoring, and manipulating neurotransmitter identity and use in vivo. The molecular strategies described here are likely applicable across species, offering a generalizable approach to dissect synaptic communication in vivo.

INTRODUCTION

Understanding how the nervous system generates behavior requires tools that can resolve the molecular identity, spatial localization, and functional contribution of neurotransmitters in vivo. Neurotransmitters are the primary means by which neurons communicate, and their synthesis, packaging, and release are governed by evolutionarily conserved molecular pathways shared from Caenorhabditis elegans to vertebrates (Südhof, 2021). These transmitters shape the strength, kinetics (tonic vs. phasic), and polarity (excitatory vs inhibitory) of synaptic transmission, thereby influencing how information is processed and how behavior is regulated (Crawford & Kavalali, 2015; Gouwens et al., 2020; Kamalova & Nakagawa, 2021; Liu et al., 2021). Because neurotransmitters are central to defining the functional properties of synapses, understanding their identity and dynamics is essential for interpreting circuit function. Even in organisms with complete connectomes—such as C. elegans (White et al., 1986) and Drosophila melanogaster (Scheffer et al., 2020; Seggewisse & Winding, 2024; Yi et al., 2024)— anatomical connectivity alone cannot explain how neural circuits generate behaviors. To build accurate, testable models of circuit function, it is necessary to also determine which neurotransmitters are used at specific synapses and how their release is spatiotemporally organized and regulated in vivo. Yet, despite the centrality of neurotransmitters to circuit logic, the field still lacks broadly applicable tools to visualize and manipulate transmitter-specific vesicle pools with the precision needed to study their roles in intact, living animals.

Traditional approaches—such as in situ hybridization, immunohistochemistry, and transcriptomics—have been instrumental in mapping neurotransmitter identity. However, these methods often lack cell-specific control, temporal resolution, or the ability to monitor transmitter usage dynamically within intact circuits. Moreover, neurotransmitter identity can change in response to environmental or physiological cues. For example, neurons may co-release multiple transmitters or modulate transmitter usage depending on stress, activity, or developmental stage, and these changes have consequences in animal behavior and circuit function (Li et al., 2020; Maddaloni et al., 2024; Sitko et al., 2025; Wu et al., 2020). Tracking and manipulating these physiological changes require new tools that allow endogenous, live imaging and functional interrogation of neurotransmitters in single neurons (Chen et al., 2023).

Vesicular transporters offer a strategic entry point for such investigations. These multi-pass membrane proteins package specific neurotransmitters—such as glutamate, GABA, acetylcholine, and monoamines—into synaptic vesicles and are necessary and sometimes sufficient for defining a neuron’s transmitter phenotype (Edwards, 2007). Because they are genetically encoded and highly conserved (Alfonso et al., 1993; Bellocchio et al., 1998; Chaudhry et al., 1998; Lee et al., 1999; McIntire, Jorgensen, & Horvitz, 1993; McIntire et al., 1997; Roghani et al., 1994), vesicular transporters provide a powerful molecular handle for developing generalizable tools that probe synaptic identity and function across species (Chen et al., 2023). Tagging these transporters can offer direct, real-time readouts of presynaptic signaling and enable manipulations that dissect the functional contribution of specific neurotransmitters in vivo (Li et al., 2020). Yet for these tools to be broadly useful, it is essential that tagging does not disrupt the localization or function of the transporter. If appropriate insertion sites can be identified and validated functionally, the evolutionary conservation of vesicular transporters suggests that such designs could serve as generalizable platforms across systems and species.

Here, we present a comprehensive toolkit for tracking and manipulating transmitter-specific vesicles in C. elegans. Using a structure-guided approach informed by predicted protein topology and sequence conservation, we engineered endogenously tagged versions of the vesicular transporters for glutamate (EAT-4/VGLUT), GABA (UNC-47/VGAT), acetylcholine (UNC-17/VAChT), and monoamines (CAT-1/VMAT). We validated in vivo that the tagged transporters retain functionality and enables bright, cell-specific imaging. In parallel, we developed conditional knockout strains that enabled spatiotemporal access to the ablation of the packaging or synthesis of specific neurotransmitters in defined neurons, allowing causal tests of neurotransmitter function at the single-cell level within behaving animals.

We applied this toolkit to identify neurons that co-express multiple vesicular transporters, revealing that 10% of C. elegans neurons contain the machinery for co-transmission. Focusing then on the ADF sensory neuron, we validate that ADF expresses the machinery for co-transmission of serotonin and acetylcholine. We demonstrate that serotonin and acetylcholine are packaged in partially distinct vesicle populations. Together, our observations suggest that co-transmission can be spatially organized, offering a refined view of how individual neurons diversify their signaling output in vivo. Our discoveries also highlight co-transmission as a widespread and previously underappreciated feature of nervous system organization, rather than a rare or specialized exception. Co-transmission is not unique to C. elegans; in Drosophila the VAChT protein can be modulated in GABAergic and glutamatergic neurons by microRNAs (Chen et al., 2023); in mammals, serotonergic neurons in the dorsal raphe co-release glutamate or GABA depending on context (Li et al., 2024), while starburst amacrine cells in the retina release both acetylcholine and GABA with distinct calcium sensitivities (Lee et al., 2010; Morrie & Feller, 2015). These examples, along with our findings, underscore the evolutionary conservation of co-transmission as a mechanism for expanding the functional repertoire of single neurons.

By enabling simultaneous visualization of different transmitter-specific vesicle pools within the same neuron, our tools uncover molecular heterogeneity at individual synapses and reveal new layers of synaptic plasticity. More broadly, our findings establish a functional framework for probing neurotransmitter dynamics, synaptic architecture, and co-transmission in vivo. The strategies developed here are generalizable to other model systems and open new avenues for dissecting neural circuit logic with molecular and cellular precision.

RESULTS

A systematic strategy for tagging and manipulating transmitter-specific vesicles in vivo

All synaptic vesicle transporters are multi-pass transmembrane proteins with structural loops facing either the cytosolic or luminal space. To visualize transmitter-specific vesicle pools in vivo, we developed a suite of fluorescently tagged, functional versions of the vesicular transporters for glutamate (EAT-4/VGLUT), GABA (UNC-47/VGAT), acetylcholine (UNC-17/VAChT), and monoamines (CAT-1/VMAT) in C. elegans. We chose these four neurotransmitter classes because they are used by more than 90% of the neurons in C. elegans (Wang et al., 2024). We used a systematic design pipeline that integrated (1) protein topology predictions, (2) evolutionary conservation, and (3) structure-guided fluorophore placement to identify regions of each transporter suitable for tagging without disrupting function. These approaches were used to generate endogenous knock-in alleles with bright, cell-specific labeling through Flippase recombinase systems or self-assembling split-GFP tags (Figure 1). When possible, tools were developed for both green and red-based fluorophores to allow for multi-color imaging. For each transporter, we also created matched conditional knockout strains by inserting FRT-flanked cassettes to disrupt neurotransmitter packaging or synthesis in defined cells, adding to the existing cell-specific knockout tools available in the field (Huang et al., 2023; Lopez-Cruz et al., 2019) (Figure 1). To drive Together, these new tools allow precise labeling and loss-of-function analysis of transmitter-specific vesicles in intact circuits and behaving animals (summarized in Table 1).

Figure 1 -. Endogenous fluorescence labeling of synaptic vesicle transporters.

(Left) FLP-on and (Right) split GFP strategies to endogenously label synaptic vesicle transporters. (A) Cartoon representation of the CRISPR-engineered worm in the endogenous locus of the target synaptic vesicle gene. (B) Cell-specific driver that expresses (Left) Flippase or (Right) GFP1–10. (C) Resulting tagged synaptic vesicle proteins with a (Left) full-length GFP or mRuby3 or (Right) by reconstituting GFP in the cell of interest. (D) Schematic of the resulting toolkit to label and eliminate the endogenous machinery that packages or synthesizes glutamate, GABA, acetylcholine and monoamines.

Table 1.

Cellular, genetic and molecular tools to probe neurotransmission in single cells

Genotype	Purpose
Toolkit for examining Glutamatergic transmission
eat-4::gfp FLP-on(syb8568)	Cell-specific GFP knock-in (C-terminus end)
eat-4::mRuby3 FLP-on(syb9193)	Cell-specific mRuby3 knock-in (C-terminus end)
eat-4 (kySi76 kySi77)	Cell-specific knockout
Toolkit for examining GABAergic transmission
unc-47::gfp (syb6990)	Endogenous full body GFP tagging
unc-47::mKate2 (syb7358)	Endogenous full body mKate2 tagging
unc-47::gfp11 (syb7313)	Endogenous and cell-specific GFP labeling
unc-47::gfp11x3 (syb7849)	Endogenous and cell-specific GFPx3 labeling
unc-25 (syb5949 syb6275)	Cell-specific knockout
Toolkit for examining Cholinergic transmission
unc-17::mKate2 (ot907)	Endogenous full body mKate2 tagging
unc-17::GFP FLP-on (ola503)	Cell-specific GFP knock-in (C-terminus end)
unc-17::mRuby3 FLP-on (syb7882)	Cell-specific mRuby3 knock-in (C-terminus end)
GFP FLP-on::unc-17 (syb7251)	Cell-specific GFP knock-in (N-terminus end)
unc-17 (syb5779 syb5987)	Cell-specific knockout
Toolkit for examining Monoaminergic transmission
cat-1::gfp11x3 (syb7239)	Endogenous and cell-specific GFPx3 labeling
cat-1 (ky1101 ky1118)	Cell-specific knockout
Flippase drivers
unc-47::T2A::Flippase(syb8125)	Flippase expression in GABAergic neurons
unc-17::T2A::Flippase (syb8059)	Flippase expression in Cholinergic neurons
bqSi488 [Ptph-1::Flippase]	Flippase expression in Serotonergic neurons
bqSi614 [Pdat-1::Flippase]	Flippase expression in Dopaminergic neurons

Functional labeling of glutamatergic vesicles via EAT-4/VGLUT

Glutamate functions as a key excitatory neurotransmitter in the nervous system, and its packaging into synaptic vesicles requires the conserved Vesicular Glutamate Transporter (VGLUT) (Bellocchio et al., 1998; Lee et al., 1999), which is sufficient to confer glutamatergic identity to a neuron. In C. elegans, the VGLUT homolog EAT-4 is expressed in 43 of the 118 neuronal classes catalogued (Wang et al., 2024). EAT-4/VGLUT is predicted to have 12 transmembrane domains (Figure 2A), and prior tools have allowed for cell-specific knockout of its full coding sequence (Lopez-Cruz et al., 2019). A previously reported transgene with EAT-4/VGLUT fused to GFP demonstrated localization to synapses (Yu & Chang, 2022); here we extend this approach to an endogenously tagged allele.

Figure 2 – Probing glutamatergic transmission in C. elegans.

(A) Predicted protein structure (using AlphaFold Protein Structure Database) of EAT-4 (cyan) tagged with GFP (green) (Abramson et al., 2024). The last amino acid in the C-terminus end (W576) corresponds to the tagged residue. (B) Schematic of the Vesicular Glutamate Transporter (VGLUT/eat-4) gene structure, loss of function allele (ky5) and endogenously tagged versions built for this study and by others. eat-4 (ky5) mutants lack the first three exons. For cell-specific knock-in (KI) tools, GFP (syb8568) and mRuby (syb9193) FLP-ON cassettes (Schwartz & Jorgensen, 2016) were inserted before the STOP codon. To cell-specifically knock out (KO) eat-4, two FRT sites flank the coding sequence of the eat-4 gene (kySi76 kySi77) (Lopez-Cruz et al., 2019). When recombination takes place, the eat-4 coding sequence is removed and cytosolic mCherry is inserted in-frame to be expressed as a proxy for eat-4 sequence removal. (C) Mutations in the che-1 (prevents ASE development (Uchida et al., 2003)) (17.42 ± 7.7 mm) or eat-4 gene (13.15 ± 4 mm) results in disrupted migration across the salt gradient. Wild-type animals (7.76 ± 5.2 mm) migrate across the salt gradient similarly to EAT-4::GFP FLP-on animals that express (7.6 ± 3.6 mm) or not (4.9 ± 4.3 mm) flippase pan-cellularly. Animals that express flippase in all cells (5.61 ± 3.9 mm) migrate across the salt gradient as a wild-type animals. Results represent the mean distance of each worm from the salt peak, averaged across the final minute of the assay, with each dot representing a single animal. Plots are overlaid with Mean ± Standard Deviation. Kruskal-Wallis test with Dunn’s multiple comparison post hoc test. **** represents p<0.0001; and NS means “not significant”. (D) (Top) Fluorescent image of an adult worm expressing endogenously labeled EAT-4 with GFP in all cells (Peft-3::Flippase). Scale Bar = 50μm. (Bottom) Zoom-in area of the head shows EAT-4 expressed predominantly in the nerve ring. Scale Bar = 10μm. (E) (Left) Electron microscopy rendering of ASE synapses in an L4 wild-type animal (White et al., 1986) (image generated with NeuroSC (Koonce et al., 2025). (Right) Fluorescent image of endogenously tagged EAT-4 protein cell-specifically in the ASE axons (Pflp-6::Flippase). Scale Bar = 10μm.

To generate a bright, functional reporter that reflects endogenous EAT-4/VGLUT localization in vivo, we inserted a GFP tag into the protein C-terminal cytoplasmic domain using a FLP-on cassette (Schwartz & Jorgensen, 2016). The C-terminus was chosen based on conservation analysis and AlphaFold structural predictions (Jumper et al., 2021; Pei & Grishin, 2001), which identified it as a cytosolic and weakly conserved region, minimizing the risk of disrupting conserved protein functions (Figure S1A–B). GFP was inserted just before the STOP codon (Figure 2B). To examine if introduction of GFP into the endogenous EAT-4/VGLUT gene affected function, we assessed NaCl chemotaxis (Figure S1C) —an EAT-4–dependent learning behavior mediated by the ASE neurons (Figure S1C–D) (Bargmann & Horvitz, 1991; Uchida et al., 2003; Sato et al., 2021). EAT-4::GFP FLP-on strains, with or without Flippase expression in all neurons or selectively in ASE neurons, displayed normal chemotaxis behavior (Figure 2C and S1D), in contrast to eat-4(ky5) loss-of-function mutants or mutant animals with defects in chemosensory neurons, including ASE (che-1 mutants; Figure 2C, S1C–D). Our findings suggest that the tagged protein remains functional and capable of sustaining known glutamate-dependent behaviors in the organism.

The insertion of the FLP-on cassette enables expression of EAT-4/VGLUT::GFP upon cell-specific expression on the FLP recombinase. To validate its use, we expressed pan-cellular flippase via the eft-3 promoter (Seydoux & Fire, 1994) in the worms engineered with the EAT-4::GFP FLP-on cassette. We observed bright EAT-4::GFP signal throughout the nervous system, especially in the nerve ring and sensory neurons (Figure 2D), consistent with earlier transcriptional reporters of the eat-4 gene (Lee et al., 1999; Serrano-Saiz et al., 2013). Moreover, when Flippase was driven specifically in ASE neurons (using the ASE-specific promoter, Pflp-6), we observed punctate labeling along ASE axons, matching the distribution of presynaptic sites identified by serial electron microscopy (Figure 2E), and cataloged in NeuroSCAN (Koonce et al., 2024; White et al., 1986).

To expand the utility of this tool for multicolor imaging, we also generated a red-shifted FLP-on reporter for the eat-4/VGLUT gene by inserting mRuby3 (Bajar et al., 2016) at the same C-terminal site (Figure 1B). These spectrally distinct reporters, when combined with the previously developed eat-4 conditional knockout (Lopez-Cruz et al., 2019) provide a comprehensive toolkit for dissecting glutamatergic transmission in a cell-specific manner in vivo.

Cell-specific imaging and silencing of GABAergic neurotransmission

GABAergic neurons package GABA into synaptic vesicles via the conserved vesicular GABA transporter VGAT(Chaudhry et al., 1998; McIntire et al., 1997). In C. elegans, the VGAT homolog UNC-47 is expressed in 11 of the 118 neuronal classes (Gendrel et al., 2016; Wang et al., 2024). Based on in vivo data, the N-terminus of VGAT is cytoplasmic while the C-terminus is luminal (Martens et al., 2008). The N-terminus contains dileucine motifs critical for proper trafficking (Santos et al., 2013), and to preserve transporter function we focused on tagging long cytoplasmic loops. Structural predictions from AlphaFold indicate that UNC-47 has 11 transmembrane domains (Figure 3A), and we identified the cytosolic loop between transmembrane domains 2 and 3— a long (13 amino acids) region (Figure S2A–B)—as an optimal tagging site.

Figure 3 – Probing GABAergic transmission in C. elegans.

(A) UNC-47 predicted protein structure from AlphaFold Protein Structure Database. GFP11 tag (red) was added between amino acids E145 and N146. Complementary GFP1–10 (green) was modeled as bound to GFP11. (B) Schematics of the Vesicular GABA Transporter (VGAT/unc-47) loss of function allele and endogenously tagged versions built for this study. unc-47(e307) mutant animals have a single base pair substitution (G to A in the first nucleotide of exon 6) that results in a splicing acceptor mutant. Fluorescent tags GFP (syb6990) and mKate2 (syb7358) were inserted between amino acids E145 and N146. For cell-specific endogenous labeling, UNC-47 was tagged with one (syb7313) or three copies (syb7849) of GFP11. To silence GABA transmission, we flanked the Glutamic Acid Decarboxylase/unc-25 coding sequence with two FRT sites (syb5949 syb6275). Upon recombination, the unc-25 coding sequence is removed and nuclear (black) mCherry (purple) is designed to be in-frame and expressed as a proxy for unc-25 sequence removal.

(C) (Top) Fluorescent image of an adult worm expressing endogenously labeled UNC-47 with reconstituted split-GFP in all cells (Peft-3::GFP1–10). Scale Bar = 50μm. (Bottom) Zoom-in area of the head shows UNC-47 expressed in the nerve ring and nerve cords. Scale Bar = 10μm.

(D) (Left) Electron microscopy renderings of RIB synapses in an L4 wild-type animal (White et al., 1986) (image generated with NeuroSC (Koonce et al., 2025)). (Right) RIB-specific UNC-47 puncta (green) in-vivo using the UNC-47:GFP11 with reconstituted split-GFP in RIB (Psto-3b::GFP1–10) Scale Bar = 10μm. (E) unc-47(e307) mutant animals thrash significantly less per minute (30.8 ± 17) than wild-type animals (94.5 ± 10). Animals with non-reconstituted UNC-47::GFP11X3 (82.2 ± 9) thrash slightly less than wild-type animals (94.5 ± 10), while animals that express pan-cellular GFP1–10 (100.5 ± 9) are no different than wild-type animals. UNC-47::GFP11x3 animals that express Pan-cellular::Flippase (with reconstituted GFP) (88.6 ± 7) thrash similarly to wild-type animals. FRT-flanked unc-25 animals (syb5949 syb6275) that do not express Flippase (95.8 ± 12) thrash similarly to wild-type animals (91 ± 8). Cell-specific unc-25 knockout animals (syb5949 syb6275) that express Flippase in every cell (Peft-3::Flippase) (49.36 ± 19) thrash to the same extent as unc-25 (e156) mutant animals (40.2 ± 19). Plots are overlaid with Mean ± Standard Deviation. Kruskal-Wallis test with Dunn’s multiple comparison post hoc test. **** represents p<0.0001; *** represents p<0.001; and NS means “not significant”.

Within this loop, AlphaFold predicts two beta-sheet regions with high confidence. We inserted GFP between amino acids E145 and N146, immediately following the first predicted beta sheet, to avoid disrupting secondary structures (Figure 3A, S2A–B). To assess functionality of the newly engineered UNC-47/VGAT::GFP strain, we performed thrashing assays on unc-47 (e307) mutants, which show impaired locomotion due to loss of GABA signaling at neuromuscular junctions (McIntire, Jorgensen, Kaplan, et al., 1993). Expression of UNC-47::GFP from an extrachromosomal array rescued the thrashing defect to wild-type levels (Figure S2C and D), as expected. We next generated endogenous knock-ins of GFP and mKate2 at the same site but in the endogenous unc-47 locus, and observed wild-type locomotion for these strains, consistent with the insertion of the fluorophores not affecting endogenous function of the transporter (Figure S2D). These strains showed bright, punctate fluorescence in the nerve ring and along the dorsal and ventral nerve cords (Figure S2E–F), consistent with previously reported unc-47 expression patterns (McIntire et al., 1997). Together, these results demonstrate that inserting a fluorescent protein at position E145 results in a functionally tagged UNC-47/VGAT reporter that enables endogenous visualization of the protein.

To enable in vivo visualization of GABAergic vesicles in single-cells, we next generated two UNC-47::splitGFP alleles by inserting either one or three tandem copies of GFP11 at the E145 position (Figure 3B). We used the splitGFP approach to avoid disruptions of the protein structures due to the introduction of the FRT-cassettes at an internal sequence site. By leveraging the self-assembling property of the GFP beta barrel, knock-in of the eleventh beta strand (GFP11) results in labeling of a protein that is only visible when the complementary GFP1–10 is expressed in the same cell. This property results in a combinatorial labeling strategy, in which cell-specific labeling is achieved only in those cells that express both the GFP11 and the GFP 1–10 (He et al., 2019). To validate these tools, we first achieved pan-cellular expression of GFP1–10 (eft-3 promoter) (Seydoux & Fire, 1994) in animals carrying the UNC-47::GFP11x3 (syb7849) allele. We observed GABAergic synapses throughout the nerve ring and nerve cords (Figure 3C), similar to full-body knock-in strains (Figure S2E–F). To then visualize GABAergic vesicles in subsets of cells, we expressed GFP1–10 in the GABAergic DD motor neurons using the flp-13 promoter and in animals carrying the GFP11 (syb7313) or UNC-47::GFP11x3 (syb7849) alleles. We observed punctate reconstituted signal in the dorsal nerve cord of both GFP11 and GFP11x3 strains, consistent with the known distribution of DD synapses (Figure S3E). The triple GFP11 version produced significantly brighter signal (Figure S3E–G), in line with reports of enhanced fluorescence from multimerized tags (He et al., 2019).

To then visualize GABAergic synapses in single cells, we expressed GFP1–10 under an RIB-interneuron, cell-specific promoter. We selected RIB because it is a GABAergic interneuron embedded in the nerve ring and proximal to three other GABAergic interneurons with overlapping neurites that impede visualization of RIB-specific synapses in vivo when using traditional approaches (Figure S3A–C). Reconstituted fluorescence using our tools enabled visualization of RIB-specific synapses, and the observed synaptic pattern (Figure 3D, S3D) was consistent with the pattern expected from electron microscopy reconstructions (Koonce et al., 2024; White et al., 1986). These findings underscore the value of the tool in labeling GABAergic synapses in individual cells in vivo.

To functionally dissect GABAergic transmission, we developed a conditional knockout of unc-25, the gene encoding Glutamic Acid Decarboxylase (GAD), which catalyzes GABA synthesis. We decided to target unc-25/GAD because it results in the elimination of GABA from neurons (Gendrel et al., 2016). We flanked the unc-25 coding sequence with FRT sites and inserted a nuclear mCherry reporter downstream to indicate successful recombination (Figure 3B). We then validated the tool by using thrashing assays. Consistent with previous findings, unc-25 null mutants show severely reduced locomotion in the thrashing assays (McIntire, Jorgensen, & Horvitz, 1993; Figure 3E). We observed that animals carrying the conditional knockout allele behaved normally in the absence of Flippase, but that pan-cellular Flippase expression in all GABAergic neurons (unc-47 promoter), which is expected to result in loss of GABAergic neurotransmission, phenocopied the thrashing defect of unc-25 mutants (Figure 3E). These results confirm that this tool effectively eliminates unc-25/GAD activity, with the capacity to be activated in a cell-specific manner and allows investigation of how GABAergic transmission contributes to neural function and behavior.

Functional labeling of cholinergic vesicles via UNC-17/VAChT

The cholinergic identity of neurons is defined by the expression of a conserved gene locus, shared from nematodes to vertebrates, that includes both the acetylcholine synthesis enzyme Choline Acetyltransferase (ChAT) and the Vesicular Acetylcholine Transporter (VAChT) (Eiden, 1998). In C. elegans, the VAChT homolog UNC-17 is expressed in 57 of the 118 neuronal classes (Wang et al., 2024). Based on prior studies, both the N- and C-termini of VAChT face the cytosol and contain regulatory motifs important for trafficking (Fei et al., 2008). AlphaFold predicts UNC-17 has 12 transmembrane domains, but most cytosolic loops are very short (<5 amino acids), except for the third cytoplasmic loop, which contains 28 amino acids and exhibits relatively high sequence conservation (Figure S4A–B).

To determine suitable tagging sites for imaging UNC-17 without disrupting function, we tested three locations: the conserved third cytosolic loop (site 1), the N-terminus (site 2), and the C-terminus (site 3) (Figure S4B–C and S4E). We used a thrashing assay to assess function, as unc-17(e245) null mutants fail to thrash in liquid and are rescued by the re-expression of untagged UNC-17 under its own promoter (Figure S4F). We generated transgenic strains with a rescue array containing the unc-17 gene with GFP inserted into these three sites. We observed that GFP insertion into site 1 failed to rescue the phenotype, suggesting disruption of UNC-17 function. In contrast, tagging either the N-terminus or C-terminus restored normal thrashing (Figure S4E–F), indicating that these positions tolerate modification. Informed by these rescue experiments, we then generated two FLP-on conditional knockout alleles (Schwartz & Jorgensen, 2016) with GFP inserted at either the N-terminus (syb7251) or C-terminus (ola503) (Figure 4A–B). To test whether the FLP-on cassettes affected protein function, we examined behavior before Flippase expression and found that both alleles behaved like wild-type animals (Figure S4F). Because splicing regulatory elements are located near the 5’ end of the unc-17 gene and are required for successful splicing of the cholinergic locus (both unc-17 and cha-1 transcripts) (Mathews et al., 2015), we proceeded with the C-terminally tagged ola503 allele, which leaves the 5’ region intact. We tested whether pan-cellular expression of Flippase in this strain impairs behavior. Animals with global GFP-tagged UNC-17 showed wild-type thrashing in liquid (Figure 4C), confirming that the tagged transporter is functional and validating this approach for cell-specific labeling of cholinergic vesicle pools.

Figure 4 – Probing cholinergic transmission in C. elegans.

(A) Predicted UNC-17 protein structure (magenta) tagged with GFP (green) on the last amino acid in the C-terminus end (W532). (B) Schematics of the Vesicular Acetylcholine Transporter (VACHT/unc-17) loss-of-function allele and endogenously tagged versions tested in this study (and built by others). unc-17(e245) mutant animals have a single base pair substitution in the third exon which leads to an amino acid change (arrowhead). Full-body knock-in animal labels UNC-17 with mKate (ot907). For cell-specific labeling, the N-terminus GFP FLP-ON cassette (syb7251) was inserted between amino acids P6 and V7 (See Methods). Similarly, the C-terminus GFP FLP-ON cassette (ola503) and mRuby FLP-on cassette (syb7882) were inserted before the STOP codon. (C) unc-17(e245) mutant animals (1.9 ± 2) thrash significantly less than wild-type animals (93 ± 10). UNC-17::GFP FLP-on animals that express pan-cellular::Flippase (88 ± 1) or animals that only express pan-cellular::Flippase (94.8 ± 12) are indistinguishable from wild-type animals in their thrashing behavior. UNC-17::GFP FLP-on animals (98.7 ± 8) thrash significantly more than wild-type animals. Mean ± Standard Deviation. Brown-Forsythe ANOVA test with Dunnett’s T3 multiple comparisons post hoc test. **** represents p<0.0001; * represents p<0.05; and NS means “not significant”. (D) (Top) Fluorescent image of an adult worm expressing endogenously labeled UNC-17::GFP in all cells (Peft-3::Flippase). Scale Bar = 50μm. (Bottom) Zoom-in area of the head shows UNC-17 expressed in the nerve ring, nerve cords and sub-lateral cords. DNC = Dorsal Nerve Cord, VNC = Ventral Nerve Cord. Scale Bar = 10μm. (E) (Left) Electron microscopy rendering of ADF synapses in an L4 wild-type animal (White et al., 1986) (image generated with NeuroSC (Koonce et al., 2025). (Right) Fluorescence image of endogenously tagged UNC-17::GFP protein specifically in the ADF neuron. . Scale Bar = 10μm.

At the cellular level, GFP labeling of UNC-17/VAChT using the ola503 allele and pan-cellular Flippase expression (driven by the eft-3 promoter) (Seydoux & Fire, 1994) resulted in fluorescence in the nerve ring, dorsal cord, ventral cord, and sublateral cords (Figure 4D). This expression pattern matched that of a full-body mKate2 knock-in of endogenous UNC-17/VAChT (Figure S4D) and was consistent with prior transcriptional reporters (Pereira et al., 2015) and anti-UNC-17 antibody staining (Duerr et al., 2008). The ola503 allele also enables cell-specific labeling. When Flippase was expressed specifically in ADF neurons using the Psrh-142 promoter (Maicas et al., 2021), we observed UNC-17::GFP puncta along the ADF axon (Figure 4E). This punctate pattern aligned with known ADF presynaptic sites from electron microscopy reconstructions of L4 animals (Koonce et al., 2024; White et al., 1986). Together, these results demonstrate that the UNC-17::GFP FLP-on allele provides a reliable tool to label cholinergic vesicles in individual neurons in vivo, and that this labeling does not affect function in our assays. To enable multicolor imaging, we generated a red fluorescent version of the UNC-17/VAChT tool by replacing GFP with mRuby (Figure 4B). Combined with the previously described cell-specific unc-17 knockout strain (Huang et al., 2023) (Figure 4B), these tools allow precise tracking and manipulation of cholinergic neurotransmission in vivo.

Probing Monoaminergic Transmission

Monoamines such as serotonin, dopamine, norepinephrine, epinephrin, octopamine, and tyramine are transported into vesicles by the conserved Vesicular Monoamine transporter (Duerr et al., 1999; Erickson et al., 1992). In C. elegans, the VMAT homolog CAT-1 is expressed in 16 of the 118 neuronal classes (Wang et al., 2024). Recently, CAT-1 was tagged at its C-terminus with a split GFP11x3 reporter (Figure 5A–B) (Huang et al., 2023). When GFP is reconstituted pan-cellularly, this fusion produces a punctate signal enriched in the nerve ring—including the characteristic and well-known serotonergic neuron NSM—and in serotonergic neurons that are part of the reproductive organs (Figure 5C).

Figure 5 – Probing Monoaminergic transmission in C. elegans.

(A) Predicted CAT-1 protein structure (blue) labeled with GFP11 (red) at C-terminus end (E145). Complementary GFP1–10 (green) was modeled with bound GFP11. (B) Schematic of the Vesicular Monoamine Transporter (VMAT/cat-1) loss-of-function allele and endogenously tagged versions used to monitor monoaminergic transmission. cat-1(ok411) mutant animals have a deletion that spans exons 7 and 8 (black line) of the cat-1 gene. For cell-specific labeling, three copies of GFP11 (syb7239) were inserted before the STOP codon. For cell-specific silencing of cat-1 activity, two FRT sites (ky1101 ky1118) flank the coding sequence of the cat-1 gene. Upon recombination, expression of cytosolic mCherry (magenta) is used as a proxy for deletion of the cat-1 coding sequence. (C) (Top) Fluorescence image of reconstituted CAT-1::GFP11x3 with expression of complementary GFP1–10 in the whole animal (Peft-3::GFP1–10). Scale Bar = 50μm. (Bottom) Zoom-in of the (Left) head and (Right) vulva area of an adult worm shows CAT-1 expressed in the nerve ring and pharyngeal neurons as well as in the vulva. Scale Bar = 10μm. (D) (Top) A well-fed day-1 adult animal is placed on NGM plates covered with a thin layer of bacteria, allowed to roam for 16 hours and the number of squares traveled was recorded. (Bottom) Wild-type animals (43.6 ± 10) roam less than cat-1(ok411) mutants (87.5 ± 12). CAT-1::GFP11x3 animals with GFP reconstituted (43.3 ± 20) (or not (56.8 ± 14)) roam similar to wild-type animals. Animals with pan-cellular expression of GFP1–10 (53.3 ± 20) also roam like wild-type animals. (E) (Top) A well-fed day-1 adult animal is placed on NGM plates covered with a thin layer of E. coli, allowed to roam for 20 hours and the aversion ratio was calculated. (Bottom) Wild-type animals (0.12 ± 0.07) display less aversion to E. coli lawns than ADF-specific cat-1 conditional KO animals (0.4 ± 0.1), consistent with previous reports using serotonin-depletion mutants (Feng et al., 2025). cat-1 conditional KO animals that do not express Flippase in ADF neurons (0.07 ± 0.03) are indistinguishable from wild-type. Mean ± Standard Deviation. Kruskal-Wallis test with Dunn’s multiple comparison post hoc test. **** represents p<0.0001; ** represents p<0.01; * represents p<0.05; and NS means “not significant”.

To determine whether the CAT-1::GFP11x3 fusion maintains protein function, we used a behavioral assay based on the role of serotonin to prevent animal exploration on a lawn of bacteria (Flavell et al., 2013). Since serotonin is packaged into vesicles by CAT-1/VMAT, similar to mutants of serotonin production (Flavell et al., 2013), cat-1 mutants display increased exploration behavior compared to wild-type animals (Figure 5D). We found that animals with reconstituted CAT-1::GFP11x3 explore bacterial lawns at levels comparable to wild-type (Figure 5D), indicating that the GFP11x3 tag nor its reconstitution impair CAT-1 function. To complement this tool, we also developed a cell-specific cat-1 knockout allele in which the full coding sequence is excised upon Flippase expression (Figure 5B). Removal of serotonin production (tph-1) specifically from ADF neurons result in increased aversion from wild type E. coli bacteria lawns (Feng et al., 2025). Consistent with this, cell-specific KO of cat-1 in ADF neurons (via expression of ADF::Flippase) results in increased E. coli aversion (Figure 5E). Together, these tools now enable the cell-specific tracking and silencing of monoaminergic synapses in living animals.

In-Vivo Identification of Co-Transmitter Neurons

Co-transmission is a conserved feature of neurons across the animal kingdom (Granger et al., 2017; Trudeau & El Mestikawy., 2018; Vaaga et al., 2014), including C. elegans (Duerr et al., 2008; Gendrel et al., 2016; Pereira et al., 2015; Pocock & Hobert, 2010; Serrano-Saiz et al., 2017; Serrano-Saiz et al., 2013; Taylor et al., 2021; Wang et al., 2024), but the prevalence of co-transmission in vivo for any given organism is not well understood. To validate the utility of our tools and to map the architecture of co-transmission in C. elegans, we developed an intersectional genetic strategy using Flippase recombinase and FRT-flanked fluorescent reporters (Figure 6A). We focused on identifying neurons that co-transmit glutamate or acetylcholine—the two most abundant excitatory neurotransmitters in C. elegans—in combination with other transmitters (Figure 6B).

Figure 6 – Mapping of co-transmitter neurons in the C. elegans nervous system.

(A) Schematic of the approach used to find co-expression of two vesicular transporters in the same cells. Flippase drivers (Element #1, blue) and Flippase-dependent cassettes that result in fluorescence (Element #2, orange) are used. Magenta cells are seen when both elements are co-expressed (in green box). (B) Strategy to track the co-expression of the vesicular glutamate and acetylcholine transporter in combination with the 4 most common neurotransmitters in C. elegans: Acetylcholine, GABA, Serotonin and Dopamine. “Elements #1” or “Element #2” refers to the genetic elements in the schematic in Fig 6A. (C-D) Specific example of the genetic strategy outlined in Fig 6A, for the vesicular transporters of glutamate (EAT-4) and acetylcholine (UNC-17). (C) We repurposed the eat-4 conditional KO strain (kySi76 kySi77) (Figure 1B) (Lopez-Cruz et al., 2019) in which the eat-4 gene coding sequence is flanked by two FRT sites and followed by cytosolic mCherry (Element #1). We crossed this line with a strain that has an endogenously inserted self-cleaving peptide sequence (T2A) followed by Flippase before the STOP codon in the unc-17 gene locus (Table 1). (D) (Top) Co-expression of EAT-4 and UNC-17 results in cytosolic mCherry. (Bottom) Cytosolic mCherry was detected in the head of three neurons: (i) AFDR, AFDL and M5; and in two neurons in the tail region: (ii) PVN, and DVA. (E) Fluorescence microscopy shows neurons with co-expression of (E) VGLUT/EAT-4 and VGAT/UNC-47; (F) VGLUT/EAT-4 and dopamine synthesis gene DAT-1; (G) VAChT/UNC-17 and VGAT/UNC-47; and (H) VAChT/UNC-17 and the serotonin synthesis gene TPH-1. All scale bars = 10μm.

We reasoned that if two neurotransmitters were co-expressed in the same neuron, driving Flippase under the promoter of one transmitter would activate the conditional reporter—resulting in fluorescence—only in cells also expressing a second neurotransmitter identity (Figure 6A–B). To achieve this, we used the engineered alleles for each vesicular transporter that we developed (Figures 2B, 3B, 4B, and 5B) (Table 1) and developed additional Flippase driver lines based on promoters from genes involved in the packaging of acetylcholine and GABA. Additionally, we used available Flippase driver lines for serotonin and dopamine (Figures S6A–B, Table 1) (Muñoz-Jiménez et al., 2017).

We first used a conditional eat-4/VGLUT reporter strain in which cytosolic mCherry is expressed upon Flippase-mediated recombination (Lopez-Cruz et al., 2019). When Flippase was driven by the unc-17/VAChT promoter (cholinergic), we observed five mCherry-positive neurons in the head and tail, consistent with co-expression of unc-17/VAChT and eat-4/VGLUT. Based on cell position, neurite morphology, transcriptomic data (Taylor et al., 2021), and anatomical maps (Wang et al., 2024), we identified these neurons as AFDL, AFDR, M5, DVA, and PVN (Figure 6C–D).

Flippase expression from the GABAergic unc-47 promoter activated eat-4-driven mCherry expression in a single pharyngeal neuron, identified as I2L (Figure 6E, S6A). Driving Flippase from the dopaminergic dat-1 promoter labeled the PDE neuron (Figure 6F, S6B), while serotonergic tph-1-driven Flippase did not produce any mCherry-positive neurons. These results are summarized in Figure S5C.

We applied a similar strategy by using our Flippase-dependent unc-17::GFP reporter to identify candidate neurons that co-release acetylcholine with other neurotransmitters. In this context, when Flippase was driven from the GABAergic unc-47 locus, we observed GFP expression in the M4, SDQR, and SMD neurons—suggesting these cells co-express acetylcholine and GABA (Figure 6G, S6D). Flippase expression from the serotonergic tph-1 promoter revealed previously described acetylcholine/serotonin co-transmitting neurons, including ADF, HSN, and VC4/VC5 (Figure 6H, S6C), consistent with prior findings (Pereira et al., 2015).

Together, we observe that C. elegans has 35 neurons exhibiting molecular signatures of co-transmission—representing ~ 10% of the C. elegans nervous system (Figure S7). Strikingly, the pharyngeal nervous system—analogous to the vertebrate enteric nervous system (Albertson & Thomson, 1976)—had the highest density of co-transmitter neurons: 30% (6 of 20 neurons) displayed co-expression of multiple vesicular transporters (Table 2). Across the entire nervous system, co-transmission was prevalent among sensory neurons, with 12% (10 of 83), compared to 11% of interneurons (9 of 81) and 7% of motor neurons (8 of 116) (Table 2). All neurons identified through this dual-reporter approach are summarized in Figure S5C. Our findings are consistent with previous atlases of neurotransmission (Taylor et al., 2021; Wang et al., 2024) and now expand them to provide new insights onto co-transmission in C. elegans.

In-vivo visualization of co-transmitter synapses in the ADF chemosensory neuron

We next used our toolkit to investigate the subcellular localization of vesicular transporters in a co-transmitting neuron, ADF. The ADF neurons are a bilaterally symmetric pair of sensory neurons in C. elegans known to regulate food exploration, chemotaxis and entry into the lethargic-like dauer state (Bargmann & Horvitz, 1991). While ADF has long been known to use serotonergic neurotransmission, our findings indicate that it is also capable of acetylcholine synthesis and packaging (Figure 6H, S6C and S8A–B). Our findings are consistent with recent transcriptomic and reporter-based studies (Pereira et al., 2015; Taylor et al., 2021; Wang et al., 2024).

To examine the subcellular distribution of serotonin or acetylcholine vesicular transporters in ADF, we used previously developed tools to endogenously label the serotonin vesicular transporter CAT-1/VMAT (Huang et al., 2023), and the acetylcholine vesicular transporter UNC-17/VAChT with GFP (Figures 4 and 5). To label these vesicular transporters specifically in ADF, we drove Flippase and GFP1–10 expression using the AFD-specific promoter, srh-142 promoter (Maicas et al., 2021). Both UNC-17/VAChT and CAT-1/VMAT displayed punctate fluorescence along the ADF axon, consistent with the location of presynaptic sites expected from electron microscopy-based 3D reconstructions (Figure S8C) (Koonce et al., 2024; White et al., 1986).

To then visualize the spatial relationship between these two vesicular transporters, we generated a strain in which UNC-17/VAChT was tagged with mRuby and CAT-1/VMAT with GFP at their respective endogenous loci, cell-specifically in ADF neurons (Figure 7A). In vivo imaging using a spinning disk confocal microscope revealed that these transporters frequently co-localize within the same synaptic boutons (Figure 7B and 7B’). Interestingly, we also found instances in which the UNC-17/VAChT::mRuby and CAT-1/VMAT::GFP signals partially segregate into separate boutons along the same axon (Figure 7C and 7C’), suggesting that these vesicular transporters can be sorted into distinct vesicle populations.

Figure 7 – Visualizing the distribution of cholinergic and serotonergic vesicles in ADF neurons.

(A) Dual-labeling of the endogenous acetylcholine (UNC-17, magenta) and serotonin (CAT-1, green) vesicular transporters in ADF neurons. (B) UNC-17::mRuby and CAT-1::GFP overlap along the ADF axon. White arrowheads denote overlap of both signals. (B’) UNC-17::mRuby and CAT-1::GFP intensity profile. (C) Example of UNC-17::mRuby and CAT-1::GFP when they partially do not overlap along the ADF axon, green arrowheads point to CAT-1-only puncta. (C’) UNC-17::mRuby and CAT-1::GFP intensity profile. Scale bar = 10μm. (D) Schematic of the dual-labeling of endogenous CAT-1::GFP or UNC-17::GFP with endogenous active zone protein UNC-13::mScarlet along the ADF axon. (E) Live imaging of the ADF axon reveals UNC-13::mScarlet puncta that lack CAT-1::GFP. Scale bar = 10 μm. (E’- E”) Zoom-in region of E. White arrowheads show overlapping vesicular transporter tagged (green) with the active zone protein UNC-13 (magenta) in individual puncta. Magenta arrowhead points to UNC-13::mScarlet puncta that do not overlap with CAT-1::GFP. (F) Live imaging of the ADF axon reveals UNC-13::mScarlet puncta that lack UNC-17::GFP. Scale bar = 10 μm. (F’- F”) Zoom-in region of F. White arrowheads show overlapping vesicular transporter tagged (green) with the active zone protein UNC-13 (magenta) in individual puncta. Magenta arrowhead points to UNC-13::mScarlet puncta that do not overlap with CAT-1::GFP. Scale Bar = 2 μm. (G) AiryScan imaging of dual-labeled UNC-17::mRuby and CAT-1::GFP along the ADF axon show localization in the same synaptic bouton but with distinct enrichment areas. Green arrowhead head points to CAT-1 enrichment and magenta arrowhead points to UNC-17 enrichment. Scale Bar = 2 μm.

To test whether both transporters are present at all ADF synapses, we endogenously tagged the active zone protein UNC-13/Munc13 with mScarlet and examined its spatial relationship to UNC-17/VAChT::GFP and CAT-1/VMAT::GFP (Figure 7D). We observed active zone UNC-13::mScarlet puncta that lacked either CAT-1/VMAT::GFP (Figure 7E) or UNC-17/VAChT::GFP labeling (Figure 7F). These findings are consistent with the idea that, while these two vesicular transporters display co-localization in synaptic varicosities, they also independently localize to distinct subcellular compartments.

Synaptic varicosities in C. elegans can be within the diffraction limits of light microscopy, preventing differentiation of co-localizing vesicular populations. To better understand the relative distribution of these vesicular transporters, we next visualized ADF synapses with increased resolution, using AiryScan imaging, which can achieve differentiation of fluorophores up to 120 nm apart (Wu & Hammer, 2021). We observed that, even in synaptic buttons in which the vesicular transporters were observed to co-localize with traditional light microscopy methods, UNC-17/VAChT::mRuby and CAT-1/VMAT::GFP differentially segregated when imaged using AiryScan microscopy (Figure 7G).

Together these results suggest that acetylcholine and serotonin co-localize to synapses, but might be packaged into distinct vesicles with specific synaptic subcellular localization that is detectable upon super-resolution microscopy. Our findings underscore the importance of endogenous labeling in determining the specific localization of these vesicular transporters and their use with higher-resolution imaging methods, highlighting the value of the tools developed in this study to understand the cell-biological organization of synapses in vivo, particularly for neurons using more than one neurotransmitter.

DISCUSSION

The integration of anatomical connectivity, molecular identity, neural activity, and transmitter usage provides a powerful framework for building models of neural circuit function. The C. elegans community has access to a complete connectome (White et al., 1986); the cellular identity of all neurons (Sulston & Horvitz, 1977; Sulston et al., 1983); whole-brain calcium imaging (Nguyen et al., 2016; Prevedel et al., 2014; Schrödel et al., 2013); single-cell transcriptomic profiles (Taylor et al., 2021); and a full neurotransmitter identity map for all neurons (Wang et al., 2024). These datasets have inspired models describing how specific circuits may give rise to behavior. However, validating these models in vivo requires tools that can precisely manipulate the molecular components of individual synaptic connections (Dag et al., 2023; Hawk et al., 2018; Kumar et al., 2024). The tools developed in this study provide that missing capability (Table 1) for the neurotransmitter systems that cover approximately 90% of the C. elegans nervous system (GABA, glutamate, acetylcholine, and the monoamines). By enabling cell-specific labeling and conditional knockout of vesicular transporters, we can now directly test the contribution of individual neurotransmitters within defined circuits and link those changes to behavioral outcomes. Moreover, due to the evolutionary conservation of vesicular transporters, the in vivo validation of tagging strategies will help identify suitable labeling strategies for other organisms, providing a path toward comparative and cross-species studies of synaptic dynamics based on neurotransmitter identity.

Co-transmission is a conserved feature of neural systems across the animal kingdom (Granger et al., 2017; Lacin et al., 2019; Vaaga et al., 2014), but its preponderance in vivo, its regulation and its functional significance is still an area of active research. Using in-vivo reporters subject to endogenous regulation, we determine that more than 10% of C. elegans neurons have co-transmission potential (Figure S7) (Table 2) (Wang et al., 2024). Our in vivo characterization of co-transmitting neurons confirm and expand findings reported for the neurotransmitter atlas of C. elegans (Wang et al., 2024) and yield three key insights. First, co-transmission occurs throughout the nervous system of C. elegans, including both the pharyngeal (enteric-like) and more central nervous systems, like the nerve ring and nerve cords (Table 2). Second, neurons can co-transmit multiple neurotransmitters in specific combinations that are conserved from nematodes to mammals (Figure 6 and S7) (Granger et al., 2017; Lacin et al., 2019; Trudeau & El Mestikawy., 2018; Vaaga et al., 2014; Wang et al., 2024). Importantly, the same neurons consistently exhibit co-transmission of the same neurotransmitter identities across individual animals, consistent with co-transmitter identity mapping to neuronal identity (Figure 6D–H). Third, co-transmission is part of every layer of a circuit, from sensory neurons to interneurons and motor neurons (Table 2). This is especially interesting in light of recent studies showing that co-transmission in sensory and motor circuits can be modulated by environmental cues such as stress (Bertuzzi et al., 2018; Li et al., 2024; Pocock & Hobert, 2010) or light-dark cycles (Chen et al., 2023; Maddaloni et al., 2024). With the tools developed here - based on endogenously tagged vesicular transporters – it is now possible to monitor the dynamic expression and subcellular distribution of specific vesicle populations in vivo and what molecular mechanisms drive those changes.

We note that the current characterization of co-transmitting neurons might be an under-estimate of the total number of neurons which use co-transmission. For example, it has been proposed that additional neurotransmitters, like betaine, may function in the C. elegans nervous system (Wang et al., 2024). Accounting for neurons that express proteins capable of synthesizing or packaging betaine, the proportion of potential co-transmitter neurons may exceed 20% of the whole nervous system of C. elegans. Our characterization of co-transmission focused on the C. elegans adult hermaphrodite, and co-transmitting neuron identities could be developmentally regulated, or modulated based on prior experience. Consistent with this, it has been observed that the identity of co-transmitting neurons is different between males and hermaphrodites (Serrano-Saiz et al., 2017), underscoring the importance of future examination of the plasticity and developmental regulation (Pereira et al., 2019; Pereira et al., 2015) of co-transmitting capacity for individual neurons.

Expression of a vesicular transporter, while consistent with co-transmitting capacity, is not conclusive for the existence of co-transmission for that neuron. For example, we identified co-expression of the GABA and Glutamate vesicular transporters in the pharyngeal neurons I2 (Figure S6A). Notably, I2 does not express the GABA synthesis enzyme, unc-25/GAD (McIntire, Jorgensen, & Horvitz, 1993) or the GABA re-uptake transporter, snf-11 (Mullen et al., 2006). Thus, it is unlikely that it produces GABA or uptakes it from the extracellular space, at least through the known mechanisms. VGAT/UNC-47 has also been reported to transport neurotransmitters such as glycine (Aubrey et al., 2007) and beta-alanine (Juge et al., 2013), raising the possibility that I2 could co-transmit glutamate with an unconventional neurotransmitter. Thus, we conceptualize the list of co-transmitting neurons as a hypothesis-generating framework to be further examined with the tools developed in this study.

Our observations of the identity of co-transmitting neurons, and the specific combinations represented in the neurons, suggest that there may be transmitter-specific rules of synaptic biology important for circuit function (Silm et al., 2019; Trudeau & El Mestikawy., 2018). This is consistent with findings in vertebrates, in which specific neurotransmitter combinations and their distributions could underpin specific features of circuit function. For example, in Starburst Amacrine cells in the mammalian retina, acetylcholine and GABA (O’Malley et al., 1992) are packaged into distinct vesicle pools that exhibit different calcium sensitivities for release (Lee et al., 2010). The distribution of specific vesicular populations and their release probabilities might constitute an architecture that helps encode the sensory signals processed by Starburst Amacrine cells. We similarly hypothesize that the specific distribution of co-transmitting synapses across the C. elegans connectome, and the identities of the neurotransmitters used, might help encode features important for circuit function and animal behavior. The tools described in this study now allow examination of these cell biological and computational principles, in vivo.

METHODS

Strains

Worms were maintained at 20°C using standard techniques (Brenner, 1973). Strains were maintained on NGM plates seeded with E. coli (OP-50). The wild type (WT) is N2, and only hermaphrodite worms were used for this study. A complete list of strains appears below.

Generation of new alleles

For the strains engineered by Sunybiotech, as described below, strain design was performed in the Colón-Ramos lab by Andrea Cuentas-Condori.

Sunybiotech used CRISPR/Cas9 to insert GFP FLP-on cassettes (Schwartz & Jorgensen, 2016) at either the N-termini of the unc-17 locus (syb7251) or C-termini end of the unc-17 (ola503), or eat-4 (syb8568) locus, according to sequence design. mRuby FLP-on cassettes were inserted similarly at the C-termini end of eat-4 (syb9193) and unc-17 (syb7882) locus. To visualize the fluorescent signal tagged to the protein of interest, Sunybiotech generated single-copy MosCI strains.

Sunybiotech used CRISPR/Cas9 to add full length GFP (syb6990), full length mKate (syb7358) or split GFP (one (syb7313) or three (syb7849) copies of GFP11) to the unc-47 locus at the +893bp position. To visualize the reconstituted GFP signal in RIB neurons, complementary GFP1–10 was driven with the Psto-3b promoter; and to visualize the GFP-reconstituted signal in DD neurons, GFP1–10 was driven with the Pflp-13 promoter.

Sunybiotech used CRISPR/Cas9 to introduce an FRT site before the +1bp in the unc-25 gene locus (syb5949). In a second round of CRISPR editing, they introduced let-858 3’ UTR followed by a second FRT and nuclear mCherry (syb6275).

cat-1 (ky1101 ky1118) cell-specific knock out strain was created using CRISPR/Cas9 to introduce an FRT site immediately before the ATG in the cat-1 gene locus (ky1101). A second round of CRISPR editing in that strain introduced the let-858 3’ UTR followed by a second FRT and the mCherry coding region immediately after the stop codon of cat-1 to generate ky1118.

Sunybiotech used CRISPR/Cas9 to introduce a T2A::Flippase sequence before the STOP codon of unc-47(syb8125) and unc-17(syb8059). All strains generated using CRISPR/Cas9 were outcrossed twice before use.

Molecular Biology

Plasmids were constructed using Gibson cloning. First, Snapgene (Version 7.0.3) software was used to design primers targeting the desired DNA vector backbone and DNA insert. The vector backbone and DNA insert were PCR linearized and amplified using “CloneAmp HiFi PCR Premix.” To assemble the desired plasmid, the purified vector backbone DNA and insert DNA were combined and incubated in solution with “2x Gibson Assembly Enzyme Premix.” Following incubation, the reaction mixture was used to transform Stellar Competent Cells, which were subsequently plated and grown overnight on LB-Amp plates. All plasmids were verified with Sanger sequencing.

Protein alignment and structure visualization

For each gene under study, NCBI BLAST was used to generate a protein sequence alignment of the C. elegans gene with the closest orthologs from the other model organisms M. musculus, D. rerio, D. melanogaster, and H. sapiens. Protein structure models for the C. elegans genes were downloaded from the AlphaFold database (Jumper et al., 2021) and predicted models for the CRISPR-Cas9 modified genes including fluorophores were generated by the Alphafold3 online server (Abramson et al., 2024). Visualization and image generation of protein structures was done using the ChimeraX software (Pettersen et al., 2021). To color the structures by sequence conservation, the alignments per gene were overlaid onto the structures with ChimeraX and colored by resulting sequence conservation Z-scores as calculated by the AL2CO algorithm (Pei & Grishin, 2001) within the software.

Microscopy

Larval or young adult animals were immobilized on 2–10% agarose pads with 10mM levamisole. A Nikon Ti2 microscope equipped with a CSU-W1 spinning disk head, ORCA-Fusion BT SCMOS camera, high-speed piezo stage motor, 60X/1.40 Apo Lambda oil objective lens was used for live imaging. Z-stack images were collected (0.3–0.5 μm/step), spanning the focal depth of the nerve cord and nerve ring synapses. A Zeiss LSM880 microscope equipped with an AiryScan detector and 63X NA 1.4 oil objective was used for AiryScan imaging. FIJI (Schindelin et al., 2012) or NIS Elements AR analysis software (version 6.10.01) were used to create maximum intensity projections and 2D renderings.

Thrashing Assay

C. elegans were raised at 20°C under standard laboratory conditions on agar plates seeded with a lawn of E. coli (OP50). Worms were synchronously grown to L4-stage and placed in individual wells of a Corning^™ PYREX^™ Spot Plate (Catalogue #722085) containing 1000 μl of M9 buffer, ensuring the buffer remained within the well’s borders. After a 30-second acclimation period to M9, thrashes were manually counted for 1 min. A single thrash was defined as a change in the direction of the worm’s midbody bending, counting each time the worm’s body flexed to one side. Following each trial, the worm was removed using a pipette and disposed of, and the M9 buffer was absorbed and discarded. The well was then cleaned with 70% ethanol and wiped dry. To avoid bias, the counter was blinded to each genotype. Each worm was tested only once, with assays conducted on 10 worms per genotype per day, and repeated over 2–3 days to account for potential day-to-day environmental variations.

Chemotaxis Assay

Worms were maintained at 20°C for at least two generations on Nematode Growth Medium (NGM) seeded with OP50 Escherichia coli bacteria. The concentration of our attractant (NaCl) is approximately 50 mM in NGM plates. “Training” plates were produced using NGM with the further addition of 50 mM NaCl to a total concentration of 100 mM, then also seeded with OP50.

Chemotaxis assay was modified from standard procedure (Ward, 1973). All assays were performed on 50 mm diameter plates. Unseeded NGM plates were marked at the center and one point 12.5 mm away from the center. A ~60–85 mM gradient of NaCl was created between the center and outer point by adding 5 M NaCl at the outer point as drops of 4μL (20–24 hours before the assay), 4μL (5 hours before), and 1.6μL (2 hours before); a sham gradient was created using only water. Gradient prediction was determined as previously described (Crank, 1956; Pierce-Shimomura et al., 1999); briefly, for every point some distance $r$ in cm from the salt peak, the concentration $C$ in mM at any point in time was calculated as:

$$C\left(t_i,r\right)=C_o+\sum _{i=1}^{n}c\left(t_i,r\right)$$ (1)

where $C_o$ is the initial concentration of NaCl in the agar (50 mM), $n$ is the drop number, and $t_i$ is the time in seconds since the drop had been applied; the contribution from each drop, in turn, was calculated as:

$$c\left(t_i,r\right)={10}^6\frac{N_i}{\sqrt{4\pi dD\left(t_i\right)}}{e}^{-\left(\frac{r^2}{4D\left(t_i\right)}\right)}$$ (2)

where $N_i$ is the moles of NaCl added per drop; $d$ is the depth (cm) of the agar; and $D$ is 1.590 x 10⁻⁵ cm²/s, the diffusion coefficient for 5 M NaCl through an aqueous medium (Robinson RA, 1959). The resulting gradients were validated by electrical conductivity measurements using an Oakton CON 6+ Handheld Conductivity Meter with a custom conductivity probe with 1 mm insertion depth (Micro-electrodes, Inc, Bedford, NH). The conductivity readings from 50 mM and 100 mM NaCl NGM plates were used for calibration at specific room temperatures.

The day before experiments, L4 animals were transferred to a seeded NGM plate to synchronize worms by developmental stage. At 5 hours before each assay, worms were transferred to a training plate using standard NGM plate recipe adjusted to 100 mM NaCl. After training, 8 worms were picked, with preference to those on the bacterial lawn, washed sequentially in two 100 μL drops of liquid NGM buffer (25 mM potassium phosphate pH 6, 1 mM CaCl2, 1 mM MgSO4, 50 mM NaCl) to remove adherent OP50, and transferred to a single 2 μL drop of NGM buffer at the center of the assay plate with prepared NaCl gradient as described. Data collection began when the water drop was fully absorbed into the assay plate and the first worm began to migrate from its starting point. Six assay plates were imaged for each strain across two separate days, yielding a total of 48 worms imaged per strain.

Images of chemotaxis behavior were acquired at 3.75 fps for 7 minutes using a Basler acA2440–35mm monochromatic sensor with an infrared filter on a commercially available WormLab imaging system and computer running WormLab 2023.1.1 software (MBF Bioscience LLC, Williston, VT USA). Individual worm position data was obtained by constructing tracks in WormLab software, then analyzed using custom scripts in R 4.4.1 (can be accessed through GitHub (https://github.com/colonramoslab/Cuentas-Condori-et-al.-2025-Toolkit-)). The assay outcome was defined as the mean distance from the peak of the salt gradient for each worm, averaged over every available frame in the last minute of the assay. When a worm track was interrupted, e.g. by a worm exiting the camera field of view or by two worms intersecting, the last available position for the worm was repeated until the worm was re-detected.

Roaming Assay

Roaming assay plates were prepared 3–5 days prior to the experiment by seeding NGM agar plates with E. coli (OP50) culture no older than 2 days. Plates were seeded using a sterile glass rod to spread the bacteria evenly across each plate. Plates were left to dry completely between 3–5 days at room temperature to ensure the bacteria layer was fully dry, thereby allowing for visible worm tracks during the assay. C. elegans were raised at 20°C under standard laboratory conditions on agar plates seeded with a lawn of E. coli (OP50). On the day before the assay, worms synchronously grown to L4-stage were transferred to regular seeded plates and stored at 20°C. After approximately 10 hours, worms were transferred to individual assay plates and incubated at 20°C for 16 hours. After this time, worms were removed and a grid overlay (3 mm x 3 mm squares) covering the assay plate was used to count the number of squares the worms had traversed during the incubation period. The number of squares crossed provided a quantifiable measure of roaming activity. To avoid bias, the counter was blinded to each genotype. Each worm was tested only once, with assays conducted on 10 worms per genotype per day and repeated over 2–3 days to account for potential day-to-day environmental variations.

Aversion behavior Assay

Aversion behavior assay were performed as previously described (Feng et al., 2025). Animals were fed on E. coli BW25113 for at least three generations before the behavioral assay. 12.5 μL of overnight BW25113 cultures were seeded onto standard NGM agar plates, grown at 37°C incubator for 24 hours and then left at room temperature for another 24 hours. 15~20 animals at L4 stages from each genotype were transferred onto behavioral assay plate and recorded at 21°C for 20 hours, at a recording rate of 1 frame per minute. Biological replicates across two different days were conducted. Videos were cropped and analyzed using standard MatLab codes (Marquina-Solis et al., 2024). Aversion ratio was defined by the number of worms outside the bacterial lawn over total number of worms on assay plates.

Statistical Analysis

We used the Shapiro-Wilk test to determine sample distribution. For comparisons between 2 normally distributed groups, Student’s T-test was used and p<0.05 was considered significant. ANOVA was used to compare between 3 or more normally distributed groups followed by Dunnett’s multiple-comparison test. If the samples were not normally distributed, we used a Mann-Whitney test to compare two groups and a Kruskal-Wallis test to compare three or more groups. Specific post-hoc statistical tests are listed in the figure legend of each experiment. Prism 10.4.2 was used to graph the data and for all statistical analysis.

List of strains

Strain name	Genotype
PHX8568	eat-4::gfp FLP-on(syb8568) III
DCR9575	eat-4::gfp FLP-on(syb8568) III 2X outcrossed
MT6308	eat-4(ky5) III
DCR9690	Pegl-6::FLP(sybIs9606) II
DCR9814	Pegl-6::FLP(sybIs9606) II 2X outcrossed
DCR9872	eat-4::gfp FLP-on(syb8568) III; Peft-3::FLP (sybIs9614) II
DCR9816	eat-4::gfp FLP-on(syb8568) III; Pegl-6::FLP(sybIs9606) II
DCR9681	eat-4::mRuby FLP-on(syb9193) III 2X outcrossed
DCR9210	unc-47::gfp (syb6990) III 2X outcrossed
DCR9453	unc-47::mKate2 (syb7358) III 2X outcrossed
CB307	unc-47(e307) III
DCR9269	unc-47::gfp (syb6990) III; olaEx5490[Psto-3b::BFP; Punc-122::RFP]
PHX7313	unc-47::gfp11 (syb7313) III
DCR9280	unc-47::gfp11 (syb7313) III 1X outcrossed
DCR9738	unc-47::gfp11 (syb7313) III; olaEx5686[Pflp-13::GFP1-10; Pmyo-2::mCherry]
PHX7849	unc-47::gfp11x3 (syb7849) III
DCR9739	unc-47::gfp11x3 (syb7849) III 2X outcrossed
DCR9740	unc-47::gfp11x3 (syb7849) III; olaEx5686[Pflp-13::GFP1-10; Pmyo-2::mCherry]
DCR9741	unc-47::gfp11x3 (syb7849) III; olaEx5687[Psto-3b::GFP1-10; Punc-122::RFP]
CF4587	muIs253 [Peft-3::GFP1-10::unc-54 3’UTR + Cbr-unc-119(+)] II; unc-119(ed3) III
DCR9838	muIs253 [Peft-3::GFP1-10::unc-54 3’UTR + Cbr-unc-119(+)] II; unc-119(ed3) III unc-47::gfp11x3 (syb7849) III recombinant
PHX6275	unc-25 (syb5949 syb6275) III
DCR9898	unc-25 (syb5949 syb6275) III; bqSi506[Prgef-1::FLP D5 + unc-119(+)] IV
CB933	unc-17(e245) IV
DCR9891	unc-17(e245) IV; olaEx5703[Punc-17::UNC-17cDNA]
DCR9074	unc-17(e245) IV; olaEx5400[Punc-17::GFP::UNC-17 (N-terminal tag)]
DCR9892	unc-17(e245) IV; olaEx5704[Punc-17::UNC-17::GFP (between TM6-7)]
OH15568	unc-17::mKate2 (ot907) IV
DCR9011	unc-17::GFP FLP-on(ola503) IV
DCR9211	unc-17::GFP FLP-on(ola503) IV 1X outcrossed
PHX7251	GFP FLP-on::unc-17 (syb7251) IV
DCR9265	GFP FLP-on::unc-17 (syb7251) IV 1X outcrossed
DCR9720	Peft-3::FLP (sybIs9614) II
DCR9733	Peft-3::FLP (sybIs9614) II 2X outcrossed
DCR9742	unc-17::GFP FLP-on(ola503) IV; Peft-3::FLP (sybIs9614) II
DCR9374	unc-17::mRuby FLP-on(syb7882) II 2X outcrossed
PHX7239	cat-1::gfp11x3(syb7239) X
DCR9370	cat-1::gfp11x3(syb7239) X 2X outcrossed
DCR9338	cat-1::gfp11x3(syb7239) X; olaEx5516[Psrh-142::GFP1-10; Psrh-142::BFP; Punc-122::RFP]
RB681	cat-1(ok411)
DCR9837	muIs253 [Peft-3::GFP1-10::unc-54 3’UTR + Cbr-unc-119(+)] II; unc-119(ed3) III cat-1::GFP11x3(syb7239) X
DCR9414	cat-1(ky1101 ky1118) X 2X outcrossed
DCR9736	Psrh-142::FLP (syb9159) II 2X outcrossed
DCR9912	Psrh-142::FLP (syb9159) II; cat-1(ky1101 ky1118) X
DCR9342	unc-17::GFP FLP-on(ola503) IV; unc-13::mScarlet FLP-on (wy1322) I; vlcSi1[unc-119(+); Psrh-142::Flippase] III
DCR9574	unc-17::mRuby FLP-on(syb7882) II; cat-1::gfp11x3(syb7239) X; olaIs153 [Psrh-142::GFP1-10; Psrh-142::FLP; Punc-122::RFP]
DCR9448	cat-1::gfp11x3(syb7239) X; unc-13::mScarlet FLP-on (wy1322) I; olaEx5550[Psrh-142::Flippase; Psrh 142::GFP1-10; Punc-122::RFP]
DCR9583	bas-1(syb5923[bas-1::SL2::GFP::H2B]) III; olaex5513 [Psrh-142::BFP; Punc-122::RFP]
DCR9590	mod-5(vlc47[mod-5::T2A::mNeonGreen]); olaex5513 [Psrh-142::BFP; Punc-122::RFP]
DCR9577	eat-4(kySi76 kySi77) III [eat-4 cell-specific KO]; unc-17(syb8059) IV [Flippase expression in unc-17 locus]
DCR9584	eat-4(kySi76 kySi77) III [eat-4 cell-specific KO]; unc-47(syb8125) III [Flippase expression in unc-47 locus]
DCR9371	eat-4(kySi76 kySi77) III [eat-4 cell-specific KO]; bqSi614 IV [Pdat-1::Flippase]
DCR9334	eat-4(kySi76 kySi77) III [eat-4 cell-specific KO]; bqSi488 IV [Ptph-1::Flippase]
DCR9576	unc-17::GFP FLP-on(ola503) IV [unc-17 cell-specific GFP knock-in]; unc-47(syb8125) III [Flippase expression in unc-47 locus]
DCR9344	unc-17::GFP FLP-on(ola503) IV [unc-17 cell-specific GFP knock-in]; bqSi488 IV [Ptph-1::Flippase] recombinant
DCR9897	unc-17::GFP FLP-on(ola503) IV [unc-17 cell-specific GFP knock-in]; bqSi614 IV [Pdat-1::Flippase]

List of plasmids

Plasmid name	Genotype
DACR218	Punc-122::RFP
DACR704	Pmyo-2::mCherry
DACR4016	Psto-3b::BFP
DACR4027	Punc-17::UNC-17cDNA
DACR4033	Punc-17::UNC-17cDNA::GFP in TM6-7
DACR4038	Punc-17::GFP::UNC-17cDNA
DACR4064	Psto-3b::GFP1-10
DACR4078	Psrh-142::BFP
DACR4083	Psrh-142::Flippase
DCR4092	Psrh-142::GFP1-10
pSH87	Pflp-13::GFP1-10