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. 2019 Nov 18;214(1):135–145. doi: 10.1534/genetics.119.302872

Control of Locomotory Behavior of Caenorhabditis elegans by the Immunoglobulin Superfamily Protein RIG-3

Ashwani Bhardwaj *, Pratima Pandey *, Kavita Babu *,†,2
PMCID: PMC6944407  EMSID: EMS124137  PMID: 31740450

Abstract

Cell surface immunoglobulin superfamily (IgSF) proteins play important roles in the development and function of the nervous system . Here we define the role of a Caenorhabditis elegans IgSF protein, RIG-3, in the function of the AVA command interneuron. This study reveals that RIG-3 regulates the abundance of the glutamate receptor subunit, GLR-1, in the AVA command interneuron and also regulates reversal behavior in C. elegans. The mutant strain lacking rig-3 (rig-3 (ok2156)) shows increased reversal frequency during local search behaviors. Genetic and behavioral experiments suggest that RIG-3 functions through GLR-1 to regulate reversal behavior. We also show that the increased reversal frequency seen in rig-3 mutants is dependent on the increase in GLR-1 abundance at synaptic inputs to AVA, suggesting that RIG-3 alters the synaptic strength of incoming synapses through GLR-1. Consistent with the imaging experiments, altered synaptic strength was also reflected in increased calcium transients in rig-3 mutants when compared to wild-type control animals. Our results further suggest that animals lacking rig-3 show increased AVA activity, allowing the release of FLP-18 neuropeptide from AVA, which is an activity-dependent signaling molecule. Finally, we show that FLP-18 functions through the neuropeptide receptor, NPR-5, to modulate reversal behavior in C. elegans.

Keywords: RIG-3, AVA, GLR-1, neuropeptide, Caenorhabditis elegans


IN Caenorhabditis elegans, reversals play a vital role in defining locomotion-based behaviors (Zhao et al. 2003). Local search behavior is a locomotion-based behavior that is executed by C. elegans in the absence of food where they search for food locally (Zhao et al. 2003; Gray et al. 2005). Reverse movements have been studied in detail because reversals are critical factors that define the extent of local search (Zhao et al. 2003; Gray et al. 2005). Although the neural circuit that controls reversals is well defined, how this circuit is tuned during variable environmental conditions remains largely unknown. In the circuitry that controls reversals, the command interneurons, AVA, AVD, and AVE, are the control centers of reverse movement (Chalfie et al. 1985; Gray et al. 2005; Piggott et al. 2011). Hence, signaling through these sets of interneurons needs to be tightly regulated.

Glutamatergic transmission is predominant in the reversal circuitry where most of the sensory neurons that make either direct or indirect connection with reversal controlling command interneurons have been reported to release glutamate as a neurotransmitter (Choi et al. 2015). The command interneurons AVA, AVD, and AVE that are postsynaptic to these glutamatergic sensory neurons are known to express glutamate receptor subunits that include four non-NMDA (N-methyl-D-aspartate)-type glutamate receptors (GLR-1, GLR-2, GLR-4, and GLR-5) and two NMDA-type glutamate receptors (NMR-1 and NMR-2) (White et al. 1986; Brockie et al. 2001; Aronoff et al. 2004). Previous studies have reported several molecules in the reversal circuit that affect the abundance of glutamate receptors and hence control signaling via modulating synaptic strength to generate diverse reversal dependent behaviors. For example, the PDZ-domain containing protein LIN-10 regulates the synaptic localization of the GLR-1 receptors (Rongo et al. 1998). UNC-43, a calcium and calmodulin-dependent protein kinase II, is required to maintain the synaptic GLR-1 density, and SOL-1, a CUB domain protein, affects GLR-1 receptor function (Rongo and Kaplan 1999; Zheng et al. 2004, 2006).

In the nervous system, cell adhesion molecules are known to play essential roles in regulating synaptic structure and coordinating synaptic strength at neuronal junctions (Biederer et al. 2002; Rougon and Hobert 2003; Togashi et al. 2009). The immunoglobulin superfamily (IgSF) class of proteins is one of the most diverse classes of cell adhesion molecules that are known to play important roles in nervous system development and function, including synapse formation and function (Rougon and Hobert 2003). One such IgSF member, RIG-3, is expressed in the reversal circuitry neuron AVA, pharyngeal neurons I1, I4, M4 and NSM, and cholinergic motor neurons (Schwarz et al. 2009; Babu et al. 2011). Previous work has described the role of RIG-3 at the neuromuscular junction, where it has been shown to maintain the acetylcholine receptor ACR-16 (Babu et al. 2011; Pandey et al. 2017). However, although RIG-3 shows expression in the AVA command interneuron, its function in AVA remains largely unknown.

Here we show that RIG-3 functions to maintain the abundance of GLR-1 receptors in the AVA command interneuron and hence regulates the synaptic strength of AVA. This regulation of AVA function modulates AVA-dependent reversal behavior in C. elegans.

Materials and Methods

C. elegans strain maintenance

Strains were maintained on nematode growth medium (NGM) agar plates seeded with OP50 Escherichia coli at 20° under standard conditions (Brenner 1974). The C. elegans N2 Bristol strain was used as the wild-type (WT) control. All experiments were carried out with young adult hermaphrodites at ∼ 23°. A complete list of strains utilized in this study is given in Supplemental Material, Table S1. The primers used for genotyping different mutant strains are tabulated in Table S2. The N2 C. elegans and the OP50 E. coli ware obtained from the Caenorhabditis Genetics Center (CGC) (University of Minnesota, MN).

Transgenic strains and constructs

Table S3 lists all the plasmids and constructs used in this study, Table S2 lists the primers used for constructing various plasmids. Plasmids were generated using a standard restriction digestion-based cloning strategy and sequenced before use in experiments. Briefly, promoters used in this study were cloned into pPD49.26 or pPD95.75, which includes Pflp-18 (4.1 kb), Prig-3 (3 kb), Pgcy-5, and Pgpa-3. The complementary (cDNA) of the gene of interest was cloned downstream of these promoters in the same plasmid backbone. In the case of NPR-5, a 1.2-kb cDNA encoding sequence was custom synthesized (GeneArt, Thermo Fisher Scientific GENEART GmbH, Germany) and cloned in pPD95.75 utilizing KpnI and XhoI restriction sites. The vector backbones used were obtained from Addgene and the Prig-3::GCaMP5 plasmid was a gift from Cori Bargmann’s laboratory. The co-injection markers used were Punc-122::GFP and Pmyo-2::mCherry (pCFJ90) from Addgene and were injected at a concentration of 10–15 ng/μl. Transgenic strains were generated by previously described microinjection techniques using 25–30 ng/μl of the plasmid to generate stable transgenic array lines of C. elegans (Mello and Fire 1995).

Reversal assays

Reversal assays were performed using well-fed young adult hermaphrodite animals. The animals were scored for off food reversal frequency conditions on NGM plates without food. C. elegans were transferred from seeded plates to unseeded ones using an eyelash pick and halocarbon oil. They were allowed to crawl on the unseeded plate for 30 sec and transferred to another unseeded plate that served as the final assay plate (90-mm NGM plate). Following a 1-min unscored acclimation period, animals were scored for the number of reversals over the next 5 min (Zhao et al. 2003). We defined a reversal by an animal as a backward motion greater than or equal to its pharynx length. At least 12 animals were assayed for each genotype. The number of body bends per reversal was calculated and plotted as previously described in Bhardwaj et al. (2018).

Fluorescence imaging and image quantification

Imaging of neuron-specific GLR-1::GFP puncta was performed using the Prig-3::HA::GLR-1::GFP line (Hoerndli et al. 2013). The imaging was performed using the Leica (Leica Microsystems, Wetzlar, Germany) TCS SP8 confocal microscope and the Zeiss (Carl Zeiss AG, Oberkochen, Germany) fluorescence microscope Axio Imager Z2 with an Axiocam MRm camera. All the imaging experiments were performed on young adult animals. The animals were placed on 2% agarose pads and paralyzed using 2,3 butanedione monoxime (BDM) (30 mg/ml) as previously described (Sieburth et al. 2005). The AVA cell body was located and GLR-1::GFP was imaged in the region of the AVA cell body. Images of the C. elegans ventral nerve cord were captured just posterior to the nerve ring using a 63× objective. A fixed region of interest (ROI) was used for all the images and fluorescence intensities along the axons or the cell bodies were calculated using Image J Fiji [National Institutes of Health (NIH), Bethesda] (Schindelin et al. 2012). The threshold was specified such that the puncta of specific size were visible, and it was set using the control sample. The same threshold was applied for all the images. The mean fluorescence intensity was plotted for each sample.

Calcium imaging

Calcium imaging was performed using GCaMP5 expressed in AVA command interneurons (Prig-3::GCaMP5). Calcium transients were recorded in freely navigating young adult animals on a slide with an agarose pad as previously described (Faumont et al. 2011). We used an Olympus (Olympus Corporation, Shinjuku, Tokyo, Japan) IX73 inverted microscope (40× objective with 0.6 NA) fitted with a worm tracker (Applied Scientific Instruments, Eugene, OR), and a Rolera Thunder EMCCD camera (QImaging, Surrey, Canada). Videos were acquired at 10 frames per second with 100-msec exposure using ImageJ software. The analysis of AVA activity was performed as described previously (Kerr 2006). The videos were analyzed using Fiji ImageJ software. The ROI was drawn as a 25 × 25 pixel circle over the AVA cell body that was expressing GCaMP5. The measured value of fluorescence from the ROI was taken as Fmeas, which included fluorescence from sample as well as background fluorescence (Fbkg). The background fluorescence was estimated by repositioning the same ROI at a nonfluorescing region of the video. Then the fluorescence (F) from the given ROI was estimated by subtracting the background fluorescence from the measured fluorescence value (i.e., F= FmeasFbkg). The fluorescence value was estimated for each frame after 100 msec by manual repositioning of the ROI. Calcium transients during reversals were plotted as ΔF/F0, where ΔF is the change in fluorescence (F) from the baseline value (F0). Baseline fluorescence (F0) was the fluorescence value calculated from the same ROI when C. elegans moved in the forward direction. Calcium transients represent a general trend of activity change during reversals for each genotype. Calcium levels were measured as ΔF/F0 max, which represents the maximum change in ΔF/F0 during each event.

Statistical analyses

All statistical analyses were performed and P values determined using GraphPad Prism V6. Experimental data are shown as mean ± SEM. The data sets were analyzed using one-way ANOVA and the post hoc Bonferroni’s multiple comparison test in Graph Pad Prism V6. The level of significance was set at P < 0.05.

Data availability

Strains and plasmids are available upon request. Supplemental Tables S1 and S3 contain the information for all strains and plasmids used in this study. All videos used in this work are also available upon request. Supplemental material available at figshare: https://doi.org/10.25386/genetics.10247969.

Results

Mutants in rig-3 show increased reversals

Studies have shown that RIG-3 plays an important role in maintaining acetylcholine receptor levels at the neuromuscular junction (Babu et al. 2011; Pandey et al. 2017). Apart from showing expression in cholinergic motor neurons, RIG-3 also shows expression in the anterior region that is thought to be restricted to the command interneuron AVA and pharyngeal neurons (Schwarz et al. 2009). Based on these previous reports, we hypothesized that RIG-3 could be affecting synaptic receptors in the AVA command interneuron to regulate signaling through the neural circuit that controls the reverse movement in C. elegans. We observed the reversal behavior of rig-3 (ok2156) mutant animals and found a significant increase in the reversal frequency of rig-3 mutant animals when compared to WT control animals (Figure 1 and Videos 1 and 2). This observation indicated that RIG-3 could be modulating signaling through the reversal circuitry. We next went on to rescue this hyper-reversal phenotype using a construct containing the full-length rig-3 genomic region, expressed in pharyngeal interneurons, AVA command interneuron, and cholinergic motor neurons (Babu et al. 2011). We found that this construct could rescue the increased reversal phenotype seen in the rig-3 mutants (Figure 1). We further performed rescue experiments to pinpoint the site of action of RIG-3 function in the reversal circuitry. The neural circuit that controls the backward (reversal) movement in C. elegans has been well studied, and the role of three command interneurons, AVA, AVD, and AVE, has been established in this process (Chalfie et al. 1985; Gray et al. 2005; Piggott et al. 2011). RIG-3 expression has been shown in the cholinergic motor neurons along the body of the animals and in the AVA command interneurons in the head of the animal (Schwarz et al. 2009; Babu et al. 2011). We decided to attempt rescue of the rig-3 hyper-reversal phenotype using rig-3 cDNA expressed under the cholinergic promoter unc-17 and the interneuron-specific promoter flp-18 that is expressed in AVA, AIY, RIG, and RIM interneurons (Rogers et al. 2003; Kim and Li 2004; Williams et al. 2007). Previously, it has been shown that the expression of RIG-3 under the unc-17 promoter was sufficient to rescue the increased acetylcholine receptor phenotype seen in the mutants (Babu et al. 2011). However, we found that RIG-3 expression using the unc-17 promoter could not rescue the increased reversal phenotype seen in the mutants, while expressing RIG-3 under the flp-18 promoter could largely rescue the hyper-reversal phenotype seen in the rig-3 mutants (Figure 1). These results indicate that RIG-3 could be functioning at the level of interneurons to modulate reversal frequency in C. elegans. To further delineate the neurons through which RIG-3 could be functioning, we decided to rescue RIG-3 specifically using a 3-kb promoter upstream of RIG-3 that has previously been shown to express largely in AVA interneurons (Feinberg et al. 2008). Apart from the AVA interneuron, this promoter has been shown to have expression in the pharyngeal interneurons I1, I4, M4, and NSM (Schwarz et al. 2009; Bhardwaj et al. 2018). However, to our knowledge none of these pharyngeal interneurons has been shown to be involved in reversal behavior or have any direct synaptic connections with AVA, making rescue of reversal frequency using this promoter AVA dependent. Expressing RIG-3 using this promoter also appeared to bring reversal frequencies similar to WT levels in this line (Figure 1 and Video 3). It has been recently shown that AVA could be a cholinergic interneuron (Pereira et al. 2015). However, we found that expression of RIG-3 under the unc-17 promoter could not rescue the increased reversal phenotype seen in the rig-3 mutants giving rise to the possibility that the expression in AVA under the unc-17 promoter could be lower or more variable in our array line and hence unable to rescue the reversal phenotype in the mutants. Together, these results suggest that RIG-3 functions in the AVA command interneuron to regulate reversal frequency in C. elegans.

Figure 1.

Figure 1

rig-3 mutants show increased spontaneous reversal frequency. A dot plot indicating the results of reversal assays from wild-type (WT) control animals, rig-3 mutants, and rescue lines expressing RIG-3 under its own promoter (genomic region of rig-3), in cholinergic neurons (Punc-17 promoter), under the flp-18 promoter expressed in multiple head neurons including the AVA interneuron, and under the rig-3 promoter (Prig-3 contains a 3-kb promoter region of rig-3 and has been shown to largely express in the AVA interneuron and pharyngeal neurons). Reversals were counted manually from videos. In this dot plot, the number of dots represents the number of animals scored for the reversal assay. Each dot represents the number of spontaneous reversals per 5 min from one animal. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA using Bonferroni’s multiple comparison test. Significance is represented as *** P < 0.001 and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot. The number of animals tested for each genotype is: WT (n = 34), rig-3 (n = 36), rig-3; rig-3 gDNA rescue (n = 15), rig-3; Punc-17::RIG-3 (n = 15), rig-3; Pflp-18::RIG-3 (n = 15), and rig-3; Prig-3::RIG-3 (n = 14).

RIG-3 is required for maintaining GLR-1 receptor levels in the AVA command interneuron

Reversal behavior in C. elegans is dependent on the glutamate receptor GLR-1 (Hart et al. 1995; Zheng et al. 1999). Previous reports have suggested that reversal frequency is affected by changes in glutamatergic signaling. There are reports indicating that mutants showing decreased glutamatergic signaling, like glr-1 and eat-4, show a significant reduction in reversal frequency (Zheng et al. 1999; Burbea et al. 2002). On the other hand, mutants with increased glutamatergic signaling show a significant increase in reversal frequency when compared with WT animals (Zheng et al. 1999; Burbea et al. 2002; Juo and Kaplan 2004; Schaefer and Rongo 2006; Juo et al. 2007). Based upon these studies, and the increased reversal frequency of rig-3 mutants, we postulated that RIG-3 could be affecting glutamatergic signaling through GLR-1 receptors in the AVA command interneuron. If RIG-3 were to function through GLR-1, we hypothesized that the reversal frequency of glr-1; rig-3 double mutants would be comparable to that seen in glr-1 mutants. Upon testing the mutants, we found that those with mutations in glr-1 (glr-1 (n2461)) showed a significant decrease in reversal frequency when compared to WT animals as was previously reported (Juo et al. 2007; Figure 2A). Further, glr-1; rig-3 double mutant animals showed similar reversal frequencies as were observed in glr-1 mutants (Figure 2A). These data indicate that RIG-3-based regulation of reversal behavior could occur through GLR-1 receptors.

Figure 2.

Figure 2

rig-3 genetically functions through glr-1. (A) Reversal frequency represented as a dot plot from WT (n = 34), rig-3 (n = 36), glr-1 (n = 31), and glr-1; rig-3 (n = 29) mutant animals. In this dot plot, the number of dots represents the number of animals scored for reversal assays. Each dot represents the number of spontaneous reversals per 5 min from one animal. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA with Bonferroni’s multiple comparison test. Significance is represented as *** P < 0.001 and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot. (B) GLR-1::GFP puncta were imaged from the cord at the anterior region of AVA, just posterior to the nerve ring. The images on the top panel show GLR-1::GFP expression in WT (n = 25), rig-3 mutants (n = 28), and rig-3; Prig-3::RIG-3 rescue line (n = 19). The dot plot in the bottom panel shows the quantitative measure of fluorescence intensity as an arbitrary fluorescence unit (AFU). Number of dots in the dot plot shows the number of animals imaged, where each dot represents the fluorescent intensity from a single animal. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA, Bonferroni’s multiple comparison test. Significance is represented as *** P < 0.001 and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot.

The possible requirement of RIG-3 in the AVA neuron to maintain reversal levels prompted us to look at the abundance of GLR-1 levels in this particular neuron. The AVA neuron is postsynaptic to 40 neurons, and it receives synaptic input from many of the sensory neurons, i.e., ASH, AWC, ASE, AFD, ALM, and interneurons AIB and RIG, many of which are reported to be glutamatergic (White et al. 1986; Choi et al. 2015). Most of these postsynaptic connections are found near the nerve ring (White et al. 1986). The synaptic strength of these postsynaptic connections would depend upon the abundance of GLR-1 levels in the synapse near the nerve ring, which could further affect signaling through AVA. To determine whether RIG-3 regulates GLR-1 specifically in AVA, we used a previously described line where GLR-1 tagged with GFP (GLR-1::GFP) was expressed in the AVA interneuron using the rig-3 promoter (Hoerndli et al. 2013). We analyzed the abundance of GLR-1::GFP puncta along the axon of the AVA neuron and at the cell body near the nerve ring in WT and rig-3 mutants and found a significant increase in GLR-1::GFP levels along the axon and near the nerve ring in rig-3 mutant animals when compared with WT controls (Figure 2B and Figure S1). We performed rescue for this increase in GLR-1::GFP of rig-3 mutants by expressing RIG-3 under the AVA promoter rig-3 and interneuron-specific promoter flp-18 (Figure 2B and Figure S1).

Together these results suggest that RIG-3 functions through GLR-1 in the AVA command interneuron, where it could be regulating the abundance of GLR-1 receptors to maintain normal signaling across the reversal circuitry.

Mutants in rig-3 show increased AVA activity

The AVA command interneuron has been reported to be involved in reversal initiation, thus tracking the activity of the AVA neuron through in vivo calcium imaging during reversals could allow us to further understand changes in the phenotypes seen in rig-3 mutants (Gray et al. 2005; Piggott et al. 2011). Previous studies suggest that there is an increase in the calcium levels in AVA during reversals (Piggott et al. 2011; Bhardwaj et al. 2018). This information along with our results showing increased abundance of GLR-1 levels in rig-3 mutant animals suggest a possible increase in the synaptic strength of the AVA command interneurons in rig-3 mutants (Figure 2B). These data prompted us to analyze the activity of AVA by tracking AVA activity in freely moving rig-3 mutant animals. To determine the activity of AVA, we used a line expressing GCaMP5, a calcium sensor, under the 3-kb rig-3 promoter (Larsch et al. 2013). Upon testing the activity of AVA, we found that rig-3 mutants show a significant increase in AVA activity when compared with WT control animals (Figure 3, A and B, Figure S2A, and Videos 4 and 5). This result suggests that this increase in AVA activity could be the result of increased synaptic strength at AVA synaptic inputs, due to increased GLR-1 levels. A previous study suggested that glutamate-gated currents in AVA are largely dependent upon GLR-1 (Mellem et al. 2002). To further elaborate on the role of GLR-1 in this process, we decided to perform the calcium imaging experiments in glr-1 mutants. We found significantly lower AVA activity in glr-1 mutants when compared with WT animals (Figure 3, A and B, Figure S2A, and Video 6). This suggests that AVA activity is primarily determined by GLR-1 receptors. To further confirm that RIG-3 functions through GLR-1 to modulate the AVA activity, we did the calcium imaging of AVA in glr-1; rig-3 double mutant animals. We found that the AVA activity in glr-1; rig-3 mutants was comparable to that seen in glr-1 mutants, and significantly less than WT control animals (Figure 3, A and B, Figure S2A, and Videos 6 and 7). These data support our previous results that RIG-3 functions through GLR-1 to modulate reversal behavior in C. elegans.

Figure 3.

Figure 3

rig-3 mutants show increased AVA activity during spontaneous reversals. (A) Average traces of calcium activity from freely reversing animals recorded using GCaMP5 expressed in the AVA command interneuron. The genotypes used include WT and mutant strains (rig-3, glr-1, and glr-1; rig-3). The arrow indicates the initiation of reversals at t = 0. Since reversals have variable durations, we have plotted here the shortest reversal for each genotype. The complete traces for all animals are shown in Figure S2A. (B) AVA activity represented as ΔF/F0 max that denotes the maximum transients in calcium levels during each reversal event. The number of dots in the dot plot represents the number of animals observed for calcium change, with each dot representing the maximum change in fluorescence from each C. elegans. Fourteen animals were imaged per genotype. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA with Bonferroni’s multiple comparison test. Significance is represented as ** P < 0.01, *** P < 0.001, and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot.

Our previous work has elaborated on the role of AVA activity and reversal length (Bhardwaj et al. 2018). Since rig-3 mutants showed a significant increase in AVA activity in comparison with WT control animals, we went on to test for reversal length in these mutant animals. We have previously shown that mutants in flp-18 show increased AVA activity and increased reversal length. We used flp-18 animals as controls and found that unlike in flp-18 mutants, rig-3 mutant animals did not show increased reversal lengths (Bhardwaj et al. 2018; Figure S2B). This observation indicates that AVA activation may not be the only factor to control the length of the reverse movement. In our previous study, we reasoned that calcium-raising duration was also an essential factor to control the reversal length; in flp-18 mutant C. elegans, we observed increased calcium-raising duration when compared to WT control animals (Bhardwaj et al. 2018). This calcium-raising duration was substantially lower in rig-3 mutant animals when compared to flp-18 C. elegans (data not shown). This could be a possible reason for rig-3 mutant animals showing early reversal termination that is comparable to that seen in WT C. elegans. We next wanted to understand the mechanism of increased reversals in AVA and tested the role of the FLP-18 neuropeptide that is released from AVA in this process.

FLP-18 and NPR-5 signaling modulates reversal frequency

Neuropeptides are small peptides that act as signaling molecules to allow communication between neurons; this communication can either be synaptic or extrasynaptic. Their extrasynaptic functioning allows them to modulate the activity of the entire neural circuit, which could ultimately modulate the behavioral output of the circuit (Li and Kim 2008). Thus, neuropeptides related to any circuit are of immense importance to study modulation of related behaviors. Our results so far suggest that the increased reversal frequency of rig-3 mutants could be attributed to higher AVA signaling. These data led us to look at the signaling molecules released from AVA, which could be responsible for RIG-3 dependent modulation of reversal frequency. Neuropeptides FLP-1 and FLP-18 are two important signaling molecules released by the AVA command interneuron (Nelson et al. 1998; Rogers et al. 2003). These neuropeptides belong to the FMRFamide-like family that is reported to modulate several locomotion-dependent behaviors in C. elegans (Kim and Li 2004; Peymen et al. 2014; Chang et al. 2015). In previous reports, FLP-1 has been known to regulate coordinated sinusoidal movement of C. elegans, while FLP-18 has been shown to modulate reversal behavior in C. elegans (Nelson et al. 1998; Cohen et al. 2009; Bhardwaj et al. 2018). Based on previous work, we analyzed the reversal behavior in mutants of flp-18 (flp-18 (gk3063)) and found that they showed a small decrease in reversal frequency (Cohen et al. 2009; Bhardwaj et al. 2018; Figure 4A). This allowed us to postulate that FLP-18 could be an important molecule that could regulate reversal initiation based on the activity of AVA. To test this hypothesis, we tested the FLP-18 overexpression line, i.e., Pflp-18::FLP-18::SL2::GFP (Cohen et al. 2009), and found that these animals showed a significant increase in reversal frequency when compared to WT control animals (Figure 4A).

Figure 4.

Figure 4

FLP-18 peptide regulates the spontaneous reversal initiation through the NPR-5 receptor. (A) Quantitation of reversal frequency from WT, flp-18, FLP-18++ (FLP-18 overexpression line), npr-1, npr-4, npr-5, and the three npr mutant lines with FLP-18++. The number of dots represents the number of animals scored, and each dot represents the number of reversals per 5 min in each animal of the same genotype in all graphs. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA with Bonferroni’s multiple comparison test. Significance is represented as * P < 0.05, ** P < 0.01, *** P < 0.001, and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot. The number of animals tested for each genotype is: WT (n = 29), flp-18 (n = 20), FLP-18++ (n = 15), npr-1 (n = 20), npr-4 (n = 20), npr-5 (n = 35), FLP-18++; npr-1 (n = 15), FLP-18++; npr-4 (n = 15), and FLP-18++; npr-5 (n = 14). (B) Results of reversal assays depicted as a dot plot. The animals assayed were WT (n = 39), FLP-18++ (n = 25), npr-5 (n = 45), FLP-18++; npr-5 (n = 24), FLP-18++; npr-5; Pgpa-3::NPR-5 (n = 25), and FLP-18++; npr-5; Pgcy-5::NPR-5 (n = 24). The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA with Bonferroni’s multiple comparison test. Significance is represented as * P < 0.05, ** P < 0.01, *** P < 0.001, and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot. (C) Dot plot of reversals from WT (n = 43), rig-3 (n = 31), flp-18 (n = 35), and rig-3 flp-18 (n = 30) animals. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA with Bonferroni’s multiple comparison test. Significance is represented as * P < 0.05, ** P < 0.01, *** P < 0.001, and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot. (D) A dot plot showing reversal frequency in WT (n = 29), rig-3 (n = 31), npr-5 (n = 35), and npr-5; rig-3 (n = 17) mutants. The error bars represent ± SEM. Statistical significance was determined with one-way ANOVA with Bonferroni’s multiple comparison test. Significance is represented as ** P < 0.01, *** P < 0.001, and “ns” for not significant. The statistics above each plot indicate significance with respect to the WT plot.

We next decided to identify the receptor through which FLP-18 could be functioning to modulate the reversal frequency. Previous work has shown that NPR-1, NPR-4, NPR-5, NPR-10, and NPR-11 could act as receptors for FLP-18 (Li and Kim 2014). The expression patterns for these receptors except that of NPR-10 have been well documented. NPR-1 is expressed in sensory and motor neurons, NPR-4 is largely expressed in the AVA interneuron, and NPR-5 and NPR-11 expression is reported to be mainly in sensory neurons (de Bono and Bargmann 1998; Wang and Wadsworth 2002; Cohen et al. 2009; Chalasani et al. 2010). To delineate the receptor through which FLP-18 modulates the reversal frequency, we started observing the reversal frequencies in mutants of the FLP-18 receptor genes: npr-1 (ok1447), npr-4 (tm1782), and npr-5 (ok1583). We found that the reversal frequency in npr-1 mutants was comparable to WT control animals, whereas npr-4 and npr-5 mutant animals showed a decrease in reversal frequency in comparison to WT animals (Figure 4A). These results suggested that NPR-4 and/or NPR-5 could be receptors for FLP-18 that allow for regulation of reversal frequency in C. elegans. To further elucidate the candidate receptor for FLP-18, we generated double mutants of the FLP-18 overexpression (FLP-18++) line with each receptor mutant, i.e., npr-1, npr-4, and npr-5. We found that the FLP-18++ line with npr-5 mutants showed a significant decrease in reversal frequency when compared with the FLP-18++ line alone (Figure 4A). Moreover, the FLP-18++ line with npr-1 and npr-4 mutants showed a phenotype similar to what was observed in the FLP-18 overexpression line by itself (Figure 4A). These results suggest that FLP-18/NPR-5 signaling could be important in the modulation of reversal initiation behavior.

We then tried to identify the neurons in which NPR-5 could be functioning by performing rescue experiments. We initially rescued the FLP-18++; npr-5 phenotype by expressed NPR-5 largely in sensory neurons and in the AIZ and PVT interneurons using the gpa-3 promoter (Zwaal et al. 1997 and wormbase.org). This experiment indicated that expression of NPR-5 largely in sensory neurons completely rescued the suppression of reversals seen in the FLP-18++; npr-5 mutant animals (Figure 4B). We next expressed NPR-5 in the ASER sensory neurons using the gcy-5 promoter (Yu et al. 1997; Chang et al. 2003). We again found that expression of NPR-5 in the ASER sensory neuron could also rescue the suppressed reversals seen in the FLP-18++; npr-5 strain of C. elegans (Figure 4B). To rule out the possibility that overexpression of NPR-5 in the rescue lines could cause changes in basal reversal frequency, we went on to use these rescue lines to rescue the reversal frequency defects seen in npr-5 mutants and found that both lines could rescue the decreased reversals seen in the npr-5 mutants, and neither rescue lines showed the increase in reversal frequency that was comparable to the FLP-18++ strain (Figure S3, A and B). These data indicate that NPR-5 could be functioning in ASER to maintain reversal frequency in C. elegans. However, these data do not preclude the functioning of NPR-5 in other neurons to maintain reversal initiation.

We next went on to test if RIG-3 could be functioning through the FLP-18/NPR-5 signaling pathway to modulate reversal frequency. To perform this experiment, we decided to test the reversal frequency rig-3 flp-18 and npr-5; rig-3 double mutant animals. We found a significant decrease in reversal frequency in both the rig-3 flp-18 and the npr-5; rig-3 double mutant animals when compared with rig-3 mutant animals (Figure 4, C and D). Finally, to test if the increased reversals in the FLP-18 overexpression line is dependent on GLR-1 levels we tested the reversals in the FLP-18++; glr-1 line and found a significant reduction in reversal frequency in this line in comparison with the FLP-18++ line (Figure S3C). Together, our results suggest that RIG-3/FLP-18/NPR-5 could play a role in maintaining reversal initiations in C. elegans.

Discussion

C. elegans initially search for food locally in a process that is dependent upon local search/exploratory behaviors. The extent of this local search is largely indicated by the frequency of reverse movements (Zhao et al. 2003; Gray et al. 2005). Multiple genetic screens have found mutants that alter the reversal frequency in C. elegans (Rongo et al. 1998; Rongo and Kaplan 1999; Zheng et al. 2004, 2006). In this study we have identified RIG-3, an IgSF protein, as an important regulator of reversal behavior in C. elegans.

RIG-3 is expressed in AVA command interneurons and a small number of pharyngeal interneurons as well as in cholinergic motor neurons (Schwarz et al. 2009; Babu et al. 2011). Previous studies have also shown that RIG-3 functions at the neuromuscular junction, where it has been reported to regulate the acetylcholine receptor delivery (Babu et al. 2011; Pandey et al. 2017). Our results suggest that animals lacking rig-3 show more frequent spontaneous reversals in comparison to WT control animals (Figure 1). Previous work has shown that the AVA command interneuron acts as a master controller of reversal movement (Piggott et al. 2011). Any signaling defect through AVA could result in defects in reversal response. Our results further elaborate the fact that RIG-3 functions in the reversal circuitry to allow for normal reversal initiation.

In C. elegans, increased reversal frequency can be directly related to the extent of glutamatergic signaling through the reversal circuitry. Increased GLR-1 receptors allow the animals to reverse more while mutants in glr-1 showed a significant decrease in reversal frequency (Zheng et al. 1999; Burbea et al. 2002; Juo and Kaplan 2004; Schaefer and Rongo 2006; Juo et al. 2007). Increased reversal frequency in rig-3 mutant animals allowed us to hypothesize that RIG-3 could be functioning through GLR-1 receptors to modulate reversal behavior. We found that rig-3 mutants showed increased GLR-1 levels in the AVA command interneuron (Figure 2). In the AVA command interneuron, most of the synaptic inputs are near the nerve ring (White et al. 1986). Hence, increased GLR-1::GFP levels in this region suggest increased strength of AVA synaptic inputs, which could be responsible for increased signaling through AVA.

To confirm the increased signaling through AVA, we carried out calcium imaging in the AVA command interneuron in freely moving animals and found a significant increase in AVA calcium transients in rig-3 mutants as compared to WT control animals (Figure 3). These results suggest increased AVA activity in rig-3 mutants, which further supports our hypothesis that there could be increased synaptic strength of inputs to AVA in rig-3 mutants. In a previous study by us we have characterized the calcium transients of AVA with respect to reversal length, where we showed changes in calcium levels with reversal length and duration of AVA activation. That study suggested that prolonged activation of AVA interneurons could be allowing the animal to execute longer reversals by minimizing the chance of execution of a second reversal event (Bhardwaj et al. 2018). In this study the change in AVA calcium levels is significantly more than that in WT for a very short duration at the start of reversals. However, this change in calcium levels in rig-3 mutants is considerably less than that seen in flp-18 mutants. Our data suggest that rig-3 affects signaling of AVA in a short duration, which could be sufficient to initiate its motor output (reversal), but there is no prolonged activation of AVA in rig-3 mutants as seen in flp-18 mutants. The other important outcome of the calcium imaging experiments was noting a significant decrease in calcium transients of AVA in glr-1 mutants (Figure 3). This further supports previous work that has reported decreased GLR-1-dependent AVA currents in glr-1 mutants (Mellem et al. 2002). Further, double mutants of glr-1; rig-3 also showed similar calcium transients as was observed in glr-1 mutants validating our finding that RIG-3 likely functions through GLR-1 to modulate AVA activity, which could in turn result in altered reversal behavior in C. elegans.

Taken together our data suggest a model wherein RIG-3 appears to function in AVA to regulate both glutamate receptor levels in AVA and as a consequence the activity of AVA (illustrated in Figure 5). This work has not uncovered the mechanism of how RIG-3 might affect GLR-1 levels in AVA. A possible mechanism could involve maintaining receptor levels by affecting the delivery or anchoring of receptors, as RIG-3 is a cell surface IgSF molecule. This is in contrast to previous work on RIG-3 that has shown that RIG-3 in cholinergic neurons affects receptor levels in the body-wall muscle in a non-cell-autonomous manner through the WNT signaling pathway (Babu et al. 2011; Pandey et al. 2017). It will be interesting to test if RIG-3 functions through the WNT signaling pathway to maintain GLR-1 levels in AVA.

Figure 5.

Figure 5

Possible model of RIG-3 modulating AVA function. The model indicates the function of RIG-3 in the AVA interneuron. Loss of RIG-3 shows increased GLR-1 levels; however, the mechanism of how RIG-3 affects GLR-1 is still unknown. Upon activation of AVA, FLP-18 is released and functions through NPR-5 in sensory neurons, which in turn affect reversals. How NPR-5 affects reversal frequency is another unknown in the model.

These results prompted us to delve further into the molecular basis of RIG-3-dependent modulation of reversal frequency. In previous studies, neuropeptides have been reported to be involved in modulation of locomotory circuits in C. elegans (Li and Kim 2014). FLP-1 and FLP-18 are two main neuropeptides that are released from AVA and are known to affect the locomotory circuit in C. elegans. FLP-1 has been reported to affect locomotory circuits to modulate normal sinusoidal movement in C. elegans and mutants of flp-1 show movement defects, while FLP-18 has been shown to affect the reversal behavior of C. elegans (Nelson et al. 1998; Cohen et al. 2009; Bhardwaj et al. 2018). Mutations in flp-18 show decreased reversal frequency when compared with WT control animals (Cohen et al. 2009; Bhardwaj et al. 2018). We also observed a significant increase in reversal frequency in a FLP-18 overexpression line, and this phenotype was suppressed by the npr-5 mutation (Figure 4, A and B). Together, these data provide strong evidence that FLP-18 acts through NPR-5 to regulate reversal frequency. The data also suggest that NPR-5 could be functioning in sensory neurons to mediate the role of FLP-18 from interneurons. How NPR-5 could be working to modulate reversals from sensory neurons would be an interesting question. Finally, to test if there is a connection between RIG-3/GLR-1 and the FLP-18/NPR-5 signaling pathways we studied the suppression of the rig-3 mutant phenotype with the flp-18 and npr-5 mutations as well as the suppression of the FLP-18 overexpression phenotype with the glr-1 mutation. In all three cases we found suppression of the increased reversals phenotype (Figure 4, C and D). These data allow us to speculate that RIG-3 could be acting through FLP-18/NPR-5 (illustrated in Figure 5). However, these data do not preclude the possibility that RIG-3 and NPR-5 act in separate parallel pathways or that RIG-3 acts through NPR-5 as well as through other molecules to maintain normal reversal frequency during local search behavior in C. elegans.

Acknowledgments

The authors are especially grateful to Yogesh Dahiya for discussions and salary support of A.B. We thank Cori Bargmann and Hernan Jaramillo for the Prig-3::GCCaMP5.0 plasmid, Mario de Bono and Geoff Nelson for the Pflp-18::FLP-18::sl2::GFP strain, Villu Maricq and Fred Horndli for the Prig-3::HA::GLR-1::GFP line, and Josh Kaplan for the glr-1; rig-3 strain. The rig-3, glr-1, flp-18, npr-1, and npr-5 mutant strains were provided by Caenorhabditis Genetics Center, which is funded by National Institutes of Health Office of Research Infrastructure Programs (P40 OD010440). The npr-4 mutant line was provided by National BioResource Project (NBRP), Japan. The authors thank Ankit Negi for routine help, Umer Saleem Bhat for help with counting reversals, and the Institute of Science Education and Research (IISER) Mohali Confocal facility for use of the confocal microscope.A.B. thanks the Indian Council of Medical Research (ICMR) for a graduate fellowship and an India Alliance (IA) grant awarded to Yogesh Dahiya (IA/E/13/1/501257) for salary support. P.P. acknowledges support from a Department of Science and Technology (DST) – Woman of Science (WOS-A) grant as well as past funding from the Department of Biotechnology (DBT) Bio-CARe, IISER Mohali and an IA grant awarded to K.B. K.B. was an Intermediate Fellow of the IA and thanks the Alliance for funding support. K.B. also thanks DBT and DST – Science and Engineering Research Board (SERB) for funding support. This work was supported by the Wellcome Trust/DBT India Alliance Fellowship (grant number IA/I/12/1/500516) and a DBT research grant (grant number BT/PR24038/BRB/10/1693/2018) awarded to K.B. and partially supported by a DST – SERB grant (SERB/F/7047) to K.B. P.P. is supported by a DST WOS-A grant (SR/WOS-A/LS-285/2018) and was earlier supported by a DBT Bio-CARe grant (BioCARe/01/10167). The authors declare no conflict of interest.

Author contributions: A.B. and P.P. designed, performed, and analyzed the experiments. K.B. supervised the experiments, helped with experimental design, and data interpretation, and wrote the manuscript with A.B. and P.P.

Footnotes

Supplemental material available at figshare: https://doi.org/10.25386/genetics.10247969.

1

These authors are co-first authors.

Communicating editor: K. O’ Connor-Giles

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Strains and plasmids are available upon request. Supplemental Tables S1 and S3 contain the information for all strains and plasmids used in this study. All videos used in this work are also available upon request. Supplemental material available at figshare: https://doi.org/10.25386/genetics.10247969.


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