DA is required for efficient spicule insertion during mating

Male copulation requires monitoring mechanisms to initiate and terminate multiple sub-steps under the proper context. Mating begins when the male presses his tail against the hermaphrodite and moves backwards, scanning for the vulva [25], [34]. After he locates the vulva, he initiates repetitive 7-11 Hz spicule thrusts to breach the vulval slit. During this sub-behavior, the male progressively adopts an arched body posture, which persists throughout spicule insertion and sperm transfer (Figure S1A). In rare events, this arched posture is adopted during scanning. Successful ejaculation occurs after repeated attempts of these motor sub-behaviors [27], [28]. Molecules that promote mating execution have been identified, but few modulators that regulate and refine the behavior have been described [24], [26], [30], [35]–[41].

DA signaling is known to modulate general C. elegans locomotor behaviors. Since 3 pairs of sex-specific sensory ray neurons secrete the neurotransmitter, DA is a candidate for modulating mating [16], [22]. Tyrosine hydroxylase is a key enzyme in the biosynthesis of DA. We first asked how well tyrosine hydroxylase deficient cat-2(lf) males mate [16], [22]. Initially we noticed that in cat-2 male populations, a higher percentage displayed spontaneously protracted spicules (44%; n = 67) relative to wild type (10%; n = 62) (p = 0.0018, Fisher's exact test). This suggested that DA might down-modulate the spicule protraction circuit. When we paired a non-protracted virgin mutant or wild-type 1-day-old adult male with a 1-day-old moving hermaphrodite for 24 hrs, we found that 56% of cat-2 males could sire progeny compared to the 88% of wild type (Figure 1A). To confirm that cat-2 mating deficits were caused by DA depletion and not due to unknown background mutations, we attempted to phenocopy the cat-2 behavioral defect in a different manner. Dopaminergic neurons were artificially hyperpolarized by expressing a hyperpolarizing UNC-103 ERG-like K+ channel (unc-103(gf)) [42] from the dat-1 dopamine transporter promoter [43]. The dat-1 promoter drives expression of this potassium channel exclusively in all DA neurons: CEP, ADE, PDE and rays 5,7,9A [26], [43]. Similar to cat-2 mutants, males containing the unc-103(gf) transgene had increased number of spontaneously protracted spicules (28%; n = 46 vs. 4%; n = 27) (p-value = 0.04, Fisher's exact test), and had decreased ability to sire progeny (40%; n = 49 vs. 69%; n = 50) when compared to the transgenic control strain (Figure 1A). Since the behavior of unc-103(gf) transgenic males mimics the cat-2 mating phenotype, this suggest that secretions from dat-1 and cat-2 expressing cells, likely DA, is necessary for efficient mating.

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Figure 1. DA is required for spicule insertion during mating.

The number of males tested and the percentage of potent males is listed at the bottom and top of the bars, respectively. (A) Mating potency. (B–D) Males were mated with paralyzed mates. (B) Percent of males displaying spicule related behaviors. (C) The duration in contact with a mate between insertion attempts. (D) The spicule efficiency index. Symbols represent an individual male performance. Open symbols represent unsuccessful insertions. Line and error bars represent mean and SEM.

https://doi.org/10.1371/journal.pgen.1003015.g001

To ask how the cat-2 mutation compromised mating, for 2 min we observed copulations between cat-2 males and 2-day-old paralyzed hermaphrodites. We assayed mating initiation time, vulva contact duration and the number of vulva contacts (Figure S2), and found no difference between wild type and cat-2 males. However, when we measured the average duration a male spent between vulval insertions attempts, we found that cat-2 males had longer intervals than wild type (Figure 1B). This was because cat-2 males displayed abnormal arched postures and precocious spicule thrusts at random areas on the hermaphrodite (Figure 1C). This defect also accounted for the mutant's reduced spicule penetration ability compared to wild type (36% vs. 73%, respectively). To quantify the variability of spicule insertion behavior, we calculated the efficiency of spicule insertion (E_SI) in both groups. This metric combines how fast males initiate, sustain, re-attempt and complete spicule insertion. We found that cat-2 males had a lower E_SI than wild type (0.19 vs. 0.075, Figure 1D). Thus, DA signaling promotes spicule insertion by lowering the probability of displaying non-productive ectopic spicule thrusts.

Exposure to DA inhibits ACh-induced spicule protraction

We used pharmacology to address whether DA modulates the cholinergic spicule circuit by pre- or co-regulating the ACh response. ACh agonists artificially stimulate receptors on the spicule neurons and muscles to induce spicule protraction. These agonists include levamisole (LEV) and nicotine (NIC), which activate ionotropic ACh receptors (AChR), and oxotremorine-M (OXOM), which activates G_αq -coupled muscarinic AChRs (mAChR) [25], [28]. Arecoline (ARE) has been reported to stimulate mAChRs in the pharynx [44]; however, we found that in the spicule circuit, ARE is a non-selective agonist. For the spicule protraction circuit to be ARE-insensitive, a male must contain mutations in the NIC receptor (acr-16 (ok789)), LEV receptor (unc-29(e193)) and the OXOM receptor (gar-3(gk305)) (Table S1).

To test whether DA can attenuate the spicule protraction circuit, we exposed males to DA and ACh agonists simultaneously for 5 min and assayed males with protracted spicules. The effective concentrations inducing spicule protraction for 90% of the males (EC90) were 5 µM for LEV, 1 mM for both NIC and ARE and 50 mM for OXOM. The EC90 concentration for DA, inducing paralysis in 90% of the animals, was previously reported to be between 20–30 mM [21]. Therefore, we exposed one-day-old virgin males to 30 mM of DA combined with individual AChR agonists at their respective EC90 concentration (Figure 2A–2C). We found that DA reduced ACh-agonist induced protraction (Figure 2A), supporting our hypothesis that DA antagonizes ACh signaling.

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Figure 2. DA inhibits ACh-agonist-induced spicule protraction.

The number of males tested and the percentage of spicule protracted males is listed at the bottom and top of the bars, respectively. (A&B) One-day-old virgin males were exposed to 30 mM DA and either LEV, NIC, OXOM or ARE. (A) DA simultaneous exposure with or (B) followed by (fb) ACh agonists. (C) Males were bathed in each drug combination for increasing duration. p-values determined with Fisher's exact test comparing mutants to wild type. MIX = LEV,NIC, OXO.

https://doi.org/10.1371/journal.pgen.1003015.g002

To address if DA also preconditions the spicule protraction circuit to be less responsive to ACh stimulation, we bathed males in 30 mM of DA or water for 1 min, followed by (f.b) exposure to the EC90 ACh-agonist concentration. Exposure to DA or water did not induced spicule protraction in any male during a 2 min observation (Figure S1B). We found that DA pre-application still inhibited LEV- and NIC- and to a lesser extent OXOM-induced protraction (Figure 2B). Interestingly, DA pre-exposure didn't inhibit ARE-induced spicule protraction. To rule out the possibility that after DA exposure, ARE induces protraction independently of AChR stimulation, males were exposed to DA followed by an ACh-agonists mixture (MIX). This MIX contained LEV, NIC and OXOM at the EC90 concentrations. Similar to the ARE responses, we found that pre-exposure to DA did not inhibit the MIX-induced protraction, and when treating males with the MIX and DA simultaneously, spicule protraction was down-regulated (Figure 2A and 2B). These results suggest that DA down-modulation occurs simultaneously with ionotropic and muscarinic ACh signaling.

Since 1 min DA pre-exposure didn't antagonize ARE-induced protraction, we tested if the inhibition, which occurred with simultaneous exposure to both compounds, would also dissipate rapidly. Instead, we found that antagonism of sex muscle contractions dissipated by 30 min with DA+ARE treatment; for other agonist combinations, the inhibition remained up to 1 hr (Figure 2C). These results suggest that simultaneous DA and ACh secretion down-regulates spicule circuit excitability for a limited period.

Since ARE's non- selectivity approximates more native ACh signaling (Table S1), DA+ARE co-treatment was used to characterize the mechanism of DA down-modulation. First, we tested males containing the G-protein coupled receptor loss-of-function (lf) mutations dop-1(vs100), dop-2(vs105), dop-3(vs106) or dop-4(tm1392) [17], [21]. In the dop-1 and dop-4 mutants DA suppressed ARE-induced protraction to wild type levels, in accordance with previous studies where these receptors are found to enhance cellular excitability via Gα_q pathways [21], [45]. However, in the dop-2(lf) or dop-3(lf) single mutants and dop-2; dop-3 double mutants DA did not decrease ARE-induced protraction to wild type levels (Table 1). An additional candidate that could mediate DA signaling is the chloride ligand gated channel LGC-53 [46]. We measured the DA+ARE response of a loss-of-function mutant for this channel, lgc-53(n4330) and found that these mutants had wild type DA+ARE sensitivity (Table 1). Although our results indicate that the DOP-2 and DOP-3 receptors partially mediate the DA modulatory response, we cannot rule out that DOP-1, DOP-4, LGC-53 and other yet-to-be identified DA receptors might act in specific combinations and in other cells to further attenuate ACh-induced spicule protraction.

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Table 1. Dopamine receptors DOP-2 and DOP-3 mediate DA inhibition of ARE-induced protraction.

https://doi.org/10.1371/journal.pgen.1003015.t001

Since these D2-like receptors signal via Gα_o/i –pathways, the alleles goa-1(n363), gpa-7(pk610), gpa-14(pk347) and gpa-16(it143), which impair Gα_o/i- like molecules were also tested [47]. In all the single mutant males treated with DA and ARE, spicule protraction was still inhibited. Thus suggesting that these molecules acted in a redundant manner as published in other pathways [48]. We therefore tested the DA/ARE sensitivity in different combinations of loss-of-function mutations in these Gα_o/i- like molecules (Table 2).We found that the double mutant goa-1(lf); gpa-7(lf) males were insensitive to the DA inhibition (Table 2). This is consistent with DOP-2, DOP-3, GOA-1 and GPA-7 expression in the spicule associated muscles and the neurons that innervate them (Figure S3) [47]. In contrast, DOP-1 and DOP-4 are not expressed in these cells, but only in a few ray neurons (data not shown and in [20]). Additionally, when DOP-2 and DOP-3 were transgenically expressed pan-neuronally from the aex-3 promoter or in sex-muscles from the unc-103E promoter, restored DA down-modulation in dop-2 and dop-3 males was observed with DOP-2 and DOP-3 sex muscles expression (Table 1). These data suggest that DA antagonizes ACh signaling via DOP-2 and DOP-3 coupled to GOA-1 and GPA-7.

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Table 2. Effect of mutant Gα alleles on DA inhibition of ARE-induced protraction.

https://doi.org/10.1371/journal.pgen.1003015.t002

Dynamic changes in DA ray neuron activities during arched body postures during spicule insertion attempts

In the hermaphrodite, broad D2-like receptor expression indicates that humoral DA secretions might activate these receptors [20]–[22], [49]. The 3 sex-specific sensory dopaminergic ray neurons (left/right Rn5A, Rn7A and Rn9A) located in the male tail might provide humoral or synaptic DA necessary to antagonize ACh signaling [26]. These ray neurons synapse to other ray neurons, inter- and motor neurons, post-cloacal sensilla neurons (p.c.s.) and sex muscles (Male Wiring Project, http://worms.aecom.yu.edu/pages/male_wiring_project.htm, [50]).

To measure the Ca⁺² transients in DA ray neurons during mating, we compared the changes in fluorescence emissions of the G-CaMP Ca⁺² sensor to a mDSred internal standard, both co-expressed from the DA reuptake transporter promoter (Pdat-1). The G-CaMP transgene slightly reduces the mating potency of the males, but not statistically significant from wild-type males (Figure 1A). This indicates that the calcium binding property of the sensor does not interfere too greatly with dopaminergic cell function. To distinguish fluorescent changes caused by focusing artifacts when the male is performing scanning behavior, from fluorescent changes caused by neural activity, we imaged males in which Rn5,7,9A were additionally hyper-polarized via a dat-1 promoter-expressing unc-103(gf) transgene. The mutant K+ channel should attenuate the ability of neurons to depolarize, and thus allow one to determine the fluorescence ranges that can confidently be attributed to cell activity. We found that throughout matings of unc-103(gf)-containing males, measurements in Rn5,7,9A fluorescence can range between 0 to a approximately 20% change (Figure 3D, Figure S4). These results suggest that focusing/motion artifacts can affect G-CaMP fluorescence measurements within this range.

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Figure 3. Ca⁺² transients in DA ray neurons increase during arched postures.

% ΔF/F0 trace for 5 seconds. Representative recordings for individual wild-type males with (A) an arched posture during spicule insertion attempts (left), (B) with non-arched posture during spicule insertion attempts (left), and (C) arched scanning posture (left). Non-arched scanning recordings for each male are displayed on the right (A–C). A Pdat-1:unc-103(gf) transgenic male displaying an arched posture at the vulva (left) and during scanning (right) (D). The In-Contact Length % (ICL%) are the numbers located at the top of each bar taken from a representative frame for each 1 sec intervals.

https://doi.org/10.1371/journal.pgen.1003015.g003

In contrast, we sometimes observed 30–80% Ca⁺² transient changes in the DA neurons when the male located the vulva (Figure 3A, Figure S4, Video S1). Occasionally, we also noticed up to 30% Ca⁺² transient changes in DA ray neurons during arch scanning postures (Figure 3 and Figure S4). This observation led us to hypothesize that posture was correlated with DA ray neuron activity. To further correlate neuronal dynamics with copulatory postures, we measured In Contact Length percent (%ICL) between the male's body and the hermaphrodite, as a proxy for the adopted posture (arch vs. non-arch). The %ICL was higher when a male was engaged in non-arched vs. arched postures either during scanning or at the vulva (Figure 3). Lower %ICLs, indicating progressive arched postures, coincided with higher Ca⁺² transient dynamics in DA ray neurons occurring while the male pressed his tail sternly against the vulva and with milder Ca⁺² transient dynamics during scanning. However, if the male reached the vulva in a non-arched posture and proceeded to attempt spicule insertion in this posture, the observed Ca⁺² changes were within baseline levels (10–20%) (Figure 3B, Figure 3S). This suggests that during arched postures, DA ray neurons might be more active to down-modulate possible spicule circuit cholinergic activity. To confirm that DA and ACh systems were active simultaneously when the male's cloacal region contacted the vulva, we additionally measured Ca⁺² transients in the male sex muscles: the gubernacular erector, the protractor and the anal depressor muscles (Figure S5). The contractile activities of these muscle cells are responsive to the ACh secretions of the PCB/PCC post-cloacal sensory neurons and the SPC motor neuron. In all of these muscles, Ca⁺² transients increased when the male contacted the vulva (Figure S5) [24], [25]. Thus DA ray neurons likely down-modulate the simultaneously active cholinergic spicule protraction circuit during insertion attempts.

Cholinergic spicule neuron stimulation causes Ca⁺² transients in Rn7A

DA sensory ray neuron activity might be increased at the vulva because of direct vulval chemosensory stimulation, mechanical stimulation from pressing against the vulva or from humoral or synaptic stimulation from other cells. Since the increased activities of DA ray neurons and the spicule protraction neurons coincide during the insertion step of mating, we asked if ray neuronal activity could change as a direct or indirect response to PCB and SPC stimulation (Figure 4A). Therefore, we photo-stimulated PCB and SPC using channelrhodopsin-2 (ChR2), a light sensitive cation channel expressed from the gar-3 mAChR promoter, while simultaneously recording DA ray neurons G-CaMP fluorescence (Figure 4B). The immobilized males were grown with or without all-trans retinol (ATR), a cofactor for ChR2. A microscope fitted with the mosaic imaging and illumination targeting system localized the blue light to the area of the G-CaMP-expressing ray neurons and then concurrently to the ChR2-expressing PCB, SPC neurons. We noticed that in ATR-grown males, the Ca⁺² transients in Rn7A exclusively increased after PCB, SPC stimulation (n = 14 males) (Figure 4B and 4C, Figure S6, Video S2). However, no obvious dynamic Ca⁺² changes were observed in Rn5A and Rn9A. These data suggest that Rn7A can respond, directly or indirectly to spicule circuit activity, whereas Rn5A and Rn9A likely respond to other signals.

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Figure 4. Activation of cloacal neurons increase Ca⁺² transients in Rn7A, and activation of DA neurons attenuate ARE-induced muscle contraction via D2-like receptors.

(A) Abridged schema of synapses between Rn5A, 7A, 9A and spicule circuit components. Arrows embedded in bars indicate reciprocal electrical and chemical synapses. Connections relevant to this work are depicted. For the complete wiring, refer to the male wiring project (S.W. Emmons, D.H. Hall, M. Xu, Y. Wang and T. Jerrel, Male Wiring Project, Albert Einstein College of Medicine, http://worms.aecom.yu.edu/pages/male_wiring_project.htm, [50]). Gubernacular erector (GER), gubernacular retractor (GRT), anterior oblique (AOB), posterior oblique (POB), dorsal spicule protractor (DSP), ventral spicule protractor (VSP) and anal depressor (ADP). (B) Video montage depicting changes in G-CaMP fluorescence in Rn7A. (C) The average %ΔF/F0 determined from all tested males used in both samples (top) with (n = 14) or (bottom) without (n = 11) ATR treatment representing Rn7A neuron Ca⁺² transients before, during and after PCB, SPC stimulation. The dark and light blue lines represent the average and standard deviation values, respectively. (D) Males that protracted their spicules during simultaneous blue light stimulation of DA neurons and ARE exposure. The genotypes are written below each bar. The number of males tested and the percentage of spicule protracted males are listed at the bottom and top of the bars, respectively.

https://doi.org/10.1371/journal.pgen.1003015.g004

Although the activity of the dopaminergic ray neurons is more dynamic when the male contacts the vulva, and D2-like receptors are expressed in the PCB neurons and sex-muscles (Figure S3), these ray neurons might attenuate the excitability of the spicule protraction circuits, not through endogenous DA and D2-like receptors, but through circuitous electrical signaling or other secreted neuropeptides. To address this, we photo-stimulated DA neurons by expressing ChR2 from the Pdat-1 promoter, while simultaneously exposing the males to agar pads soaked with a concentration of ARE that causes ∼80% of males to protract their spicules within 5 minutes (Figure S1C). In a heterozygous dop-2; dop-3/+; Pdat-1:ChR2 background, 32% of the males protracted their spicules when photo-stimulated; however, in the homozygous dop-2;dop-3(lf) background, 71% of the photo-stimulated males protracted their spicules (Figure 4D). This suggests that endogenously evoked DA can attenuate ACh signaling in the spicule circuit via D2-like receptors.

D2-like receptors promote spicule muscle contractile rhythmicity

To ask how DOP-2 and DOP-3 regulate mating, we determined the mating potency of dop-2; dop-3 mutant males with moving hermaphrodites. The mutant and wild type potencies were similar, 92% (n = 38) vs. 88% (n = 40), respectively. Thus, the functions of DOP-2 and DOP-3 are subtle. We then quantified dop-2; dop-3 males' mating performance with paralyzed hermaphrodites and found that wild type, the double and single mutants behaved similarly during various mating steps (Figure S7). However, the double mutants can insert their spicules faster, into the paralyzed and easy-to-penetrate hermaphrodites, than wild type (Figure 5A). This paradoxical result suggests that having a wild-type version of D2-like receptors reduces reproductive fitness. However, males that lack D2-like receptors might not be at a behavioral advantage when paired with a more challenging mate. Therefore, we coupled dop-2; dop-3 or a wild-type male with a moving hermaphrodite and directly measured the first vulval contact duration. We found that dop-2; dop-3 males are displaced from the vulva faster than wild type (Figure 5B). Unlike wild type mating events, most hermaphrodites coupled with mutant males would abruptly move during spicule insertion attempts, causing the males to move off the vulva and thrust their spicules at areas adjacent to the vulva.

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Figure 5. D2-like signaling promotes spicule insertion attempts.

(A) Duration of vulval contact until spicule insertion or 120 sec. Symbols represent individual male performance. Open symbols represent unsuccessful insertions. (B) Duration over the vulval slit during the 1^st spicule insertion attempt. For A&B, line and error bars represent mean and SEM. (C) Spicule movement frequency calculated for 6 sec during spicule thrust against vulval slit. Symbols represent an individual frequency interval. Line and error bars represent mean and SD.

https://doi.org/10.1371/journal.pgen.1003015.g005

We previously showed that a K+ channel mutation disrupts the frequency and amplitude of sex muscle contractions during spicule insertion attempts; the arrhythmic spicule thrusts will startle the hermaphrodite and increase the probability of the male losing contact [29]. We reasoned that a similar phenomenon is occurring with dop-2; dop-3 males. Thus, we measured spicule movement frequency when a male attempted insertion at a paralyzed hermaphrodite vulval slit. We found that relative to wild type, dop-2;dop-3 spicule insertion attempts were less rhythmic. Among the assayed dop-2; dop-3 males, the variability of durations between spicule thrusts was greater than compared to wild-type males, indicating that the mutants displayed more random sustained thrusts in runs of rapid shallow thrusts (Figure 5C, Figure S8).

Restriction of non-productive mating behaviors requires D2-like signaling

Since dop-2; dop-3 and wild-type males behave differently during copulation with moving mates, we identified conditions where that difference would result in reduced mating fitness for the mutants. We paired either one wild type or one mutant male for 4 hrs with increasing numbers of moving fog-2(lf) virgin females (which contain a mutation disrupting self-sperm generation), and counted the number of impregnated females. Since mates with variable mating receptiveness exist in a population, the subtle defects of dop-2; dop-3 males might be more evident in a competition to impregnate the most partners. Although wild type and mutant males' refractory periods between ejaculations are similar (Figure S9A), we found that when the female numbers increased, wild type impregnated more females than dop-2; dop-3 males (Figure 6A). This difference was obvious when dop-2; dop-3 males were exposed to 20 females. The lower serial mating potency is likely attributed to behavioral differences; however it could also be due to subtle germ line variations between the wild type and mutant males.

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Figure 6. D2-like signaling promotes mating fitness.

(A) Y-axis depicts the number of pregnant females amongst 1, 5 or 20 potential mates. Symbols represent individual male's sexual prowess. (B) Mating competition test pairing a wild type and a mutant male with one fog-2 female +/−10 paralyzed males (first 4 columns), and number of fog-2 females impregnated when wild type and dop-2; dop-3 males were paired individually with 10 C. briggsae hermaphrodites ( last 2 columns). The top and bottom of each column indicates the % of pregnant females and the number of males that copulated or number of males assayed (last 2 columns). (C) The cumulative time in contact with males that a wild type and dop-2; dop-3 male, represented by each symbol, spent when surrounded by 40–50 paralyzed males. Each data subset represents non-ablated animals (mock), PCB or PCS ablated animals. p-values calculated using the Mann-Whitney test. For A&C, line and error bars represent mean and SEM. (D) Top shows coincident D2-like and ACh signaling during spicule insertion attempts. Bottom depicts residual DA signaling when a male moves off the vulva. Blue and green color represents DA and ACh signaling components, respectively.

https://doi.org/10.1371/journal.pgen.1003015.g006

To address if behavioral differences caused the double mutants to impregnate fewer females, we simultaneously paired a mutant and a wild-type male with a single 1-day-old fog-2 female and asked which male mated first. We found that dop-2; dop-3 and wild type males impregnated a similar percentage of females (56% vs. 44%) (Figure 6B). Similar to Figure 6A data, this indicates that with a single mate, mutant males are similar to wild type in copulation. However, when we challenged the double mutant and a wild type male with a single fog-2 female and 10 paralyzed males, as unproductive mating distractions, we found that wild type impregnated 80% of the females (Figure 6B). We observed that wild type and the mutant males contacted both sexes with equivalent frequency in this assay, and in a male-female mate choice assay, we did not find any indication that the mutant males had a greater chemotaxic preference to males (Figure S9B, S9C, and S9D). However wild-type males immediately terminated mating attempts with paralyzed males, whereas mutant males would abnormally scan and attempt spicule insertion into these inappropriate mates (Figure S9C). To rule out the possibility that dop-2; dop-3 males displayed general locomotor hyper-exploratory behaviors, which could lead the mutant males to contact another animal before wild-type males, we compared the velocity and distance travelled of mutant and wild-type males during crawling. We found that there were no gross differences in these parameters between wild type and mutant males (Figure S10). Therefore, this indicates that during mating, D2-like signaling dampens ACh-induced behaviors with uncooperative/inappropriate mates.

Next, we addressed, in a more natural scenario, the importance of D2-like receptors in decreasing fruitless mating attempts with nematodes of other species. We paired one fog-2 female and 10 C. briggsae hermaphrodites or 10 C. remanei females, with one wild type or a dop-2; dop-3 male and counted how efficiently the fog-2 female became impregnated. We found that after 4 hrs, wild type impregnated 65% more females than mutant males, when challenged with 10 C. briggsae hermaphrodites (Figure 6B and Figure S9E). In contrast, we found both wild type and mutant males' ability to impregnate a C. elegans mate is severely reduced when challenged with C. remanei females (Figure S9E), consistent with the published report that C. remanei females are more attractive than C. elegans hermaphrodites [51].This indicates that D2-like signaling might limit unproductive mating attempts with other hermaphroditic nematode species.

Finally we addressed whether D2-like signals specifically dampened spicule circuit excitability and/or other mating circuits, to restrict aberrant mating attempts. The male's response to contacting a mate is primarily facilitated by the ray sensilla. However, published reports have demonstrated that other male sensilla, such as the post-cloacal sensilla (p.c.s), spicule tips and possibly the hook sensillum can feebly substitute for ray function; therefore the activity of these sensilla might be increased in the dop-2; dop-3 males [26], [27]. Since driving expression of DOP-2/DOP-3 exclusively in cells of the spicule circuit is not technically possible, we opted for an alternative approach of laser ablating the dop-2-expressing PCB neuron or all of the p.c.s neurons (PCA, PCB and PCC), and asking if mating with a non-hermaphrodite is reduced. First we quantified in wild-type males lacking PCB or all 3 p.c.s. neurons, the cumulative and average duration in contact with another male during a 10 min assay period, when surrounded by 40–50 paralyzed males. We found that the cumulative time that operated males spent with other males was reduced (Figure 6C). This result is consistent with the idea that the post-cloacal sensilla play a minor role in contact response and scanning behavior. However if an operated male does initiate scanning with another male, the average time was not significantly different amongst these groups (Figure S9F). We then tested if PCB or p.c.s ablations in dop-2; dop-3 males would reduce abnormal mating attempts. We found that dop-2; dop-3 males on average spent longer amount of times scanning other males than wild type (Figure S9F); however, neither PCB nor p.c.s ablations reduced this phenotype. In addition, the cumulative time in contact with another male was similar between operated and intact males (Figure 6C). This indicates that D2-like signaling must be modulating other circuits in addition to the post-cloacal sensilla to attenuate contact response and scanning behavior.

Strains and culture methods

Strains were maintained at 20°C on NGM agar plates and fed with E. coli OP50. All C. elegans males contain the allele him-5(e1490). Additional alleles used were: cat-2(e1112), dop-1(vs100), dop-2(vs105), dop-3(vs106), dop-4(tm1392), goa-1(n363), gpa-7(pk610), gpa-14(pk347), gpa-16(it143), pha-1 (e2123), unc-64(e246), fog-2(q71), unc-29(e193), gar-3(gk305) and acr-16(ok789).

Transgenic strains include: pha-1(lf); lite-1(lf); rgEx197[ Punc-103E:G-CaMP1.3, Punc-103E:mDsRed, pha-1(+)], pha-1(lf); lite-1(lf); rgEx317[Pdop-2:ChR2::YFP; pha-1(+)], pha-1(lf); lite-1(lf); rgEx326[Ptph-1:CFP; pha-1(+)], pha-1(lf); lite-1(lf); rgEx431[Phsp-16:egl-2(n693gf)cDNA; Punc-103E:mDsRed; pha-1(+)], dop-2(lf); pha-1(lf); lite-1(lf) rgEx462 [Paex-3:dop-2::CFP], dop-2; pha-1(lf); lite-1(lf); rgEX467 [Punc103E:dop-2::CFP], dop-3; pha-1(lf); rgEx482 [Punc103E:dop-3::YFP]; dop-3; pha-1(lf); rgEx490 [Paex3:dop-3::YFP], pha-1(lf); lite-1(lf); rgEx491[Pgpa-7:YFP; pha-1(+)], pha-1(lf); lite-1(lf); rgEx512[Pgar-3B:GCaMP3::SL2:::mDsRed; pha-1(+)], dop-2(lf); dop-3(lf); rgEx515[Ptph-1:YFP], pha-1(lf); lite-1(lf); rgEx517[Pdat-1:GCaMP3::SL2:::mDsRed; pha-1], pha-1(lf); lite-1(lf); rgEx519[Pgpa-16: gpa-16 exon1::YFP; pha-1(+)], pha-1(lf); lite-1(lf); rgEx523[Pdat-1:G-CaMP3::SL2:::mDsRed, Pgar-3B:ChR2::YFP, pha-1(+)], pha-1(lf); lite-1(lf); rgEx549[Pdat-1:G-CaMP3::SL2:::mDsRed, Pdat-1:unc-103(gf), pha-1(+)], dop-2(lf); dop-3(lf); pha-1(lf); rgEx550[Pdat-1:ChR2::YFP, pha-1(+)]

Plasmids

Transgenics

Plasmids were co-injected with pBX1(50 ng/µl) [65] into strains that contained the pha-1(e2123) allele. Transgenic lines that could stably propagate at 20°C were kept for further analysis. For strains that did not have the pha-1 allele, CFP or YFP expressed from one of the injected plasmids was used to identify transgenic animals. For all injections, pUC18 was used to make the final DNA concentration 200 ng/µl. The expression constructs pPC2 and pPC39 were injected at 100 ng/µL into pha-1 him-5 lite-1 hermaphrodites. To rescue the dop-2(lf) and dop-3(lf) DA+ARE sensitivity, pPC21, pPC19, pPC18 (25 ng/µL) and pPC36, pPC37 (50 ng/µL) were injected into dop-2; pha-1 and dop-3; pha-1 hermaphrodites, respectively. To fluorescently label males for mating competition tests, pTG10 [Ptph-1:CFP](100 ng/µL) and pTG11[Ptph-1:YFP ](100 ng/µL) [30] were injected into him-5 and dop-2(lf); dop-3(lf) hermaphrodites, respectively. The goa-1(lf); gpa-7(lf) strain was injected with pPC41 [Pgpa-16:gpa-16::YFP] (100 ng/µL) to test for RNAi effectiveness. To label separately the dopamine-expressing cells, the male cloacal neurons and the male sex muscles with G-CaMP3::SL2:::mDsRed, pha-1; him-5; lite-1 hermaphrodites were injected with pLR286[Pdat-1:G-CaMP3::SL2:::mDsRed](30 ng/µl), pLR283[Pgar-3B:G-CaMP3::SL2:::mDsRed] (30 ng/µl) or pLR289[Punc-103E:G-CaMP3::SL2:::mDsRed](30 ng/µl), respectively. To co-express G-CaMP3 in dopamine-expressing cells and Channel Rhodopsin in the male cloacal cells, pha-1; him-5; lite-1 hermaphrodites were injected with a mixture of pLR286[Pdat-1:G-CaMP3::SL2:::mDsRed](30 ng/µl), and pLR183[Pgar-3B:ChR2::YFP](100 ng/µl) [24]. To co-express G-CaMP3 and unc-103(gf) in dopamine-expressing cells, pha-1; him-5; lite-1 hermaphrodites were injected with a mixture of pLR286[Pdat-1:G-CaMP3::SL2:::mDsRed](30 ng/µl), and pPC47[Pdat-1:unc-103 (gf)](70 ng/µl). The dop-2; dop-3; pha-1 strain was injected with pPC48 [Pdat-1:ChR2::YFP](70 ng/µl) and then crossed into pha-1; him-5; lite-1 to obtained the heterozygous strain carrying the same transgene for optogenetic experiments. To obtain a strain for behavioral comparisons with transgenic males [Pdat-1:G-CaMP3::SL2:::mDsRed], the pha-1; him-5; lite-1 hermaphrodites were injected with pPC46 [Pdat-1:YFP].

Behavioral assays and drug test

For behavioral and pharmacology assays, virgin males were isolated from non-crowded plates, either at the late L4 stage (when cells in the male tail spike have completely migrated anteriorly) or after they newly crawled out of their L4 cuticle. They were kept solitary or in groups of 10–20. All drug tests scored the number of males that protracted their spicules by directly observing spicule protraction for at least 10 seconds in a 5 min observation window; these behavioral assays were not videotaped. If multiple mating parameters were measured for individual males, we videotaped the mating event from the time a male contacted a hermaphrodite until spicule insertion. Because all of the sensory-motor metrics were objective (% fluorescent changes, motor duration, contact duration, number of contacts, locomoter velocity, sex muscle contraction frequency), and not subjectively defined, it was not necessary to collect data blinded to the genotype of the animals. For populations of objective metrics that were statistically different, but less than twofold between the experimental and control animals, two observers, Paola Correa and L. Rene Garcia, re-analyzed the movies independently to re-verify or amend the results. Graphpad Prism 5 software was used to perform all statistics. Fisher's exact test was used when comparing categorical variables (protracted vs. non-protracted, potent vs. non-potent). The Mann-Whitney nonparametric test was used to compare the metrics of an experimental group with a control group, when the data did not fall under a normal Gaussian distribution. When the data fitted a Gaussian distribution, 1-way ANOVA and Tukey's post-test were used to compare the means and standard deviations of more than two groups.

To assay agonist-induced spicule protraction, we dissolved levamisole (LEV) (ICN Biomedicals, OH), arecoline (ARE) (Acrose organics, NJ) , nicotine (NIC) (EM, NJ), oxotremorine M (OXOM) (Sigma, MO) and dopamine (DA) (Sigma) in water to make a stock solution of 10 mM, 10 mM, 100 mM , 50 mM and 30 mM, respectively. We added between 400–1000 µL of the drug to a three well round-bottom Pyrex titer dish. Five to ten males were then transferred to the drug bath and observed for five minutes at 20°C. Males were considered drug responsive if their spicules remained protracted for ≥5 sec. For simultaneous exposure, DA and ACh-agonists were pre-mixed. For sequential exposure, worms were bathed in DA for 1 min and then ACh-agonists were added at a concentration, such that the final DA concentration was not significantly changed and the ACh-agonists were at the EC90 concentration.

For mating potency tests, 10 µl of a saturated E. coli culture was spotted onto a NGM agar plate, to make a 3.5 mm lawn. ∼20 hr later, a single male and a single adult virgin pha-1(lf) hermaphrodite were put onto the mating lawn and incubated at 20°C for 4 days. A male was considered potent if the plate contained cross-progeny. For mating behavioral assays, we spaced ten 48 hr-old unc-64(lf) adult hermaphrodites on a 5 mm diameter bacterial lawn and placed a male in the lawn's center. Movies were recorded using a stereomicroscope mounted with a Hamamatsu ImagEM CCD camera (Hamamatsu, USA); recordings were taken from the time a male contacted a hermaphrodite until spicule insertion or 5 min. Different mating performances were scored from observations of these recordings to address: the number of times a male contacted the vulva, total duration of vulval contact and the time a male spent scanning a hermaphrodite. The same population of males was used to obtain these data sets for each behavioral metric. Wild type and mutant males were tested in parallel for statistical comparisons. Through direct observation and using a hand-held timer, we measured the time it took wild type and cat-2(lf) males to contact and start scanning a hermaphrodite. Moving hermaphrodites were used to measure the duration over the vulval slit after the 1^st contact for wild type and dop-2(lf); dop-3(lf) males.

To determine if dop-2; dop-3(lf) males differ from wild type in their chemotactic or locomoter behaviors toward paralyzed pha-1; lite-1;him-5; rgEx431[Phsp-16:egl-2(n693gf)cDNA; Punc-103E:mDsRed; pha-1(+)] hermaphrodites or males, 6 paralyzed hermaphrodites and 6 paralyzed males were alternately and equally positioned at the periphery of a 1.5 cm diameter OP50 lawn. One wild type or dop-2; dop-3(lf) male was placed at the center of the lawn and allowed to crawl around for up to 5 minutes. The males were timed when they first placed the ventral side of their tail against the cuticle of a paralyzed worm (either male or hermaphrodite) for greater than 1 second.

To determine the male's movement velocity, an 18–24 hr adult virgin male was placed in the center of a thin 3 mm OP50 lawn. The forward crawling animal was digitally recorded for 1 minute at 30 frames per second using a stereomicroscope mounted with a Hamamatsu ImagEM CCD camera (Hamamatsu, USA). The lighting of the sample was adjusted to maximize the contrast of the male against the bacterial lawn. Recordings were then analyzed using the Hamamatsu SimplePCI (version 6.6.0.0) software to determine the centroid of the male in each frame, and track the changes in the X and Y coordinates of the centroid as the male crawls forward. Microsoft Excel was then used to convert changes in the X and Y coordinates into the velocity and distance traveled during the 1 minute recordings.

For mating assays with multiple mates, a one-day-old wild type or dop-2; dop-3(lf) male was paired with 1, 5, or 20 two-day-old fog-2(lf) females in a plate containing a small bacterial lawn. After 4 hrs, the male was removed. The number of females that laid eggs were determined 4 hours later and then subsequently monitored for an additional 18 hrs. In experiments where wild type or dop-2; dop-3 males must discriminate between C. elegans and either C. remanei or C. briggsae, L4 fog-2(lf) females were grown to adulthood on OP50-seeded NGM agar plates containing 50 µM red fluorescent dye SYTO-17 (Invitrogen, Eugene OR); the dye allowed the fog-2(lf) females to be identified from C. remanei or C. briggsae animals. One stained virgin 18–24 hrs adult fog-2(lf) female was placed with ten 18–24 hrs adult C. briggsae hermaphrodites or 10 virgin C. remanei females on a 3.5 mm diameter lawn of OP50. The animals were allowed to acclimate to the lawn for one to two hours before a single virgin wild type or dop-2; dop-3 male was introduced. Males were kept continuously with their mates for 18 hrs. Four and 18 hours later after the male was first introduce with his mates, using an epi-fluorescence-equipped stereomicroscope, we determined if SYTO-17 stained fog-2(lf) females contained eggs in the uterus or sperm in the spermatheca.

To observed how post-cloacal sensilla-ablated wild type and dop-2; dop-3(lf) males behave with paralyzed males, the cells PCA, PCB and PCC were laser ablated (using a Spectra-Physics VSL-337ND-S nitrogen laser attached to an Olympus BX51 microscope via the MicroPoint laser focusing system) in L4 males prior to tail spike retraction. During the operation, the laser-ablated and mock-ablated males were immobilized between a microscope coverslip and an 8% noble agar pad (a higher % pad caused the males to rupture through their anus) containing Polybead polystyrene 0.1 µm microspheres (Polysciences, Inc., WA). Eighteen to 24 hrs later, 3–4 laser-ablated or mock-ablated adult males were added to a 3 mm diameter OP50 lawn that contained 40–50 paralyzed pha-1; lite-1; him-5; rgEx431[Phsp-16:egl-2(n693gf)cDNA; Punc-103E:mDsRed; pha-1(+)] males. The animals were digitally recorded at 1 frame per second for 10 minutes. The recordings were then reviewed, and time and duration that the moving male placed the ventral side of his tail against the cuticle of a paralyzed worm or another moving worm for greater than 1 second was determined for the whole 10 min recording. Cumulative time was calculated by adding up the total time a male was in ventral contact with other males. The average time was calculated by dividing the total time in contact by the number of mating contacts.

Because the mating behavioral steps that lead up to sperm transfer can be highly variable, we required a metric to score/rank a spectrum of behavioral responses that result in successful spicule insertion. We wanted that metric to differentiate a male that instantly found the vulva and inserted within a second or two of contact, from a male that meandered around the hermaphrodite for 110 secs, but eventually contacts the vulva, and inserts. However, this metric must be able to rank the spectrum of males that immediately undergo spicule insertion attempts and are persistent, but are unsuccessful in penetration, with males that were erratic in prodding behavior (and other steps of mating behavior), but fully inserted their spicules. To achieve this, the metric had to measure the period between vulval contact and full insertion, but it also had to incorporate a penalty for not being diligent at immediately initiating vulval spicule insertion behavior after contacting with a mate, and a bonus if successful penetration occurred, even after erratic performance of other mating behavioral steps. The efficiency of spicule insertion, E_SI, was calculated from recordings made during the first 120 seconds of contact between the male and a paralyzed 2-day-old hermaphrodite. The metrics recorded were: (1) duration of prodding at the vulva; (2) duration in contact with the hermaphrodite at areas outside the vulva. If the male successfully inserted his spicules before the 120 seconds were over, then the observation was stopped. E_SI = (time (sec) spent at spicule insertion attempts/total time (sec) in contact with hermaphrodite, up to 120 sec) X (1/time (sec) in contact with the hermaphrodite, such scanning, but not attempting insertion (penalty)) X (1+ (0 if no penetration, otherwise time (sec) remaining after a successful penetration, /120 sec)(bonus)). A hypothetical E_SI of 1.99 would mean that the male located the vulva and inserted his spicules approximately 1 sec after contact with the hermaphrodite; whereas a hypothetical E_SI of 0.0 meant that the males spent their first 120 seconds of contact not attempting spicule insertion at the vulva [66].

For mating competition tests, transgenic males contained expressed YFP or CFP from the tph-1 promoter [30]. Mid to late L4 fog-2 females were separated from males; 48 hrs later, a single female was added to 5 mm diameter lawns of bacteria. One 18–20 hrs virgin CFP-expressing wild type and one YFP-expressing dop-2(lf);dop-3(lf) male were added simultaneously to the lawn. The plates were incubated at 20°C for one hour. If the female had sperm in the spermatheca (determined via standard bright field microscopy), then both males were removed, otherwise the animals were allowed to mate for another hour. Majority of the females were mated within 1 hour; by 2 or 3 hours, all females were impregnated. The next day, the fluorescence color of serotonergic neurons in the L1 cross-progeny was determined.

For the mating competition test with paralyzed males, rgEx431 males containing a heat shock promoter-driven egl-2(gf) construct were incubated for 30 min at 30°C. After 3 hrs, the heat shocked-expressed EGL-2(gf) K+ channels caused complete paralysis. Ten paralyzed males were placed onto a mating lawn with a single fog-2(lf) female. One CFP-expressing wild type and one YFP-expressing mutant male were simultaneously placed in the middle of the plate. The first male to insert was determined via observations and subsequently identified using fluorescent microscopy.

For mating assays with multiple hermaphrodites, a one-day-old wild-type or a dop-2; dop-3(lf) male was paired with 1, 5, or 20 two-day–old fog-2(lf) females in a plate containing a small bacterial lawn. After 4 hrs, the male was removed. The number of egg-gravid females were determined 4 hours later and then subsequently monitored for an additional 18 hrs.

Ca²⁺ imaging and optogenetics

The genetically encoded Ca²⁺ indicator G-CaMP1.3 was used to visualize calcium transients in the sex muscles, and G-CaMP3 was used to visualize Ca²⁺ transients in neurons. A 2 cm square chunk from an NGM plate containing a 3 mm diameter OP50 lawn was placed on a microscope slide. 10–15 heat shocked paralyzed pha-1; lite-1; him-5; rgEx431[Phsp-16:egl-2(n693gf)cDNA; Punc-103E:mDsRed; pha-1(+)] hermaphrodites were then evenly spaced on the lawn. The hermaphrodites were allowed to condition the lawn for ∼20 min before a male was added. One 18–20 hrs adult virgin transgenic male was placed on the lawn without a microscope coverslip and immediately placed on an epifluorescence–equipped Olympus BX51 microscope (Olympus, USA). Matings were visualized using a 10×, or 20× long working distance objective. Males were not exposed to high intensity filtered blue and green light until they initiated mating behavior. Exposure to the high intensity blue light, even though the males contain the lite-1 mutation, interferes with the contact response step of mating. As the males were being recorded, the stage position and focusing were actively manipulated to keep the fluorescent cells in focus and in the center of the viewing field. New mating lawns were used after every two observations; long exposures to high intensity light affect the E.coli lawn in an unknown way that reduces the males' mating response.

The G-CaMP and DsRed fluorescence signals at the male tail were recorded simultaneously using a Dual View Simultaneous Image splitter (Photometrics, AZ) and a Hamamatsu ImagEM Electron multiplier (EM) CCD camera, at the speed of ∼30 frames per second. The Ca²⁺ data was analyzed using the Hamamatsu SimplePCI (version 6.6.0.0) software and Microsoft Excel, as described previously [24], [30].

The recordings were reviewed to find the first instance of an uninterrupted behavioral step (either moving forwards or backwards along the hermaphrodite cuticle, or attempting spicule insertion at the vulva) with a duration of 6 seconds or greater. Region-of-interests (ROIs), of equal areas, were generated in the Simple PCI software. The individual ray 5,7,9A neurons were too close to one another to separate with different ROIs, and thus their composite fluorescence was measured with a single ROI. The male gubernacular erector muscle, anal depressor and ventral protractor muscles were far enough so that separate ROIs could be drawn for each muscle. ROIs were used to measure the background and cellular fluorescence signals in both the green and red emission channels. The positions of the ROIs were manually adjusted for every frame in the movies. The mean pixel intensity (MPI) was measured for every ROI in every frame, in each recording (Figure S11B and S11C). The data was then transferred from Simple PCI to Microsoft Excel. For each recording frame, background ROIs values were then subtracted from their respective ROIs that quantified neuronal or muscular fluorescence (Figure S11D).

Focusing/gross movement/muscle contraction/mercury arc lamp flicking and photobleaching artifacts caused non-interesting fluorescence changes in both channels and in every frame. In some cases, a higher rate of mDsRed photobleaching, relative to the minimal G-CaMP photobleaching, made a simple green-to-red fluorescence ratio-metric analysis not appropriate to use. To correct this, the red channel was used as a reference to analyze the green channel. In each frame, the red channel background-subtracted MPI for each ROI was plotted with respect to time, and an average line (Figure S11E) or a one-phase decay curve (to correct for mDsRed specific photobleaching) was fitted over the data points using GraphPad Prism (version 4.03). The fitted curve serves as an arbitrary reference to quantify the magnitude of non-interesting fluorescence changes that occurred in each frame. For each frame, the measured background subtracted red channel MPI value was divided by the average or fitted red value to give a correction value. The corrected inverse value for each frame was then multiplied to the subtracted green channel MPI of the respective frame (Figure S11F). This corrects the values for the green channel, so that the fluorescence changes reflect calcium transients rather than gross experimental artifacts. The values for each recorded frame was then calculated as ΔF/F0 = (((corrected MPI (frame n)-corrected MPI (frame 0(initial frame)))/corrected MPI (frame 0(initial frame))) ×100) (Figure S11G). The arbitrary F0 value was determined as the fluorescence value in the first frame of the recordings. The values were then plotted with respect to time.

To determine whether the G-CaMP3 transgene might severely interfere with the behaviors displayed by the males, we quantified the mating behavior of the Pdat-1:G-CaMP3 strain. In a mating potency test, these males sire progeny similar to wild type (Figure 1A). During mating, the vulval contact duration, number of vulval contacts and time in contact between insertion attempts in these males were also similar to males carrying the Pdat-1:YFP transgene (Figure S2D–S2F). This indicates that any observed changes occurring in ray neurons of the Pdat-1:G-CaMP3 strain portray a biological relevant phenomenon possibly occurring during wild type mating.

For the optogenetic analyses, rgEx523[Pdat-1:G-CaMP3::SL2:::mDsRed, Pgar-3B:ChR2::YFP, pha-1(+)] males, incubated +/− with all-trans-retinal, were immobilized between a microscope coverslip and a 10% noble agar pad containing Polybead polystyrene 0.1 µm microspheres (Polysciences, Inc., WA). In the cloacal region, we previously reported that the gar-3B promoter is expressed in PCA, PCB, SPC and the spicule muscles; however, in rgEx523, expression in PCA and the spicule muscles were extremely variable, but expression in PCB and SPC were consistent. The mosaic nature of rgEx523 does not affect the experiments, since PCA, PCB and SPC are highly wired together. Stimulation of any one would result in increased activity of the set. The males were then put on an Olympus IX81microscope scope fitted with the Mosaic illumination targeting system (Andor Technology, USA). Using the Metamorph microscopy automation and imaging analysis software (Molecular Devices, PA), illumination regions were specified over the areas of the cloacal ganglia and dopaminergic ray neurons. The software then controlled the Mosaic targeted illumination system mirrors to reflect the filtered blue and green excitation light to the G-CaMP3/mDsRed expressing dopaminergic rays for ∼4.2 sec, followed by directing the illumination to both the ChR2-expressing cloacal ganglia and G-CaMP3-expressing dopaminergic rays for ∼5.7 sec, and then redirect the illumination to only the dopaminergic rays for ∼4.2 sec. The time between illumination protocols varied from 0.1 to 0.5 sec. The G-CaMP and mDsRed fluorescence signals were recorded simultaneously using an Optosplit II simultaneous image splitter (Cairn Research, UK) and an Andor iXon EM CCD camera, at the speed of ∼35 frames per second. After the males were recorded, the coverslip of the immobilized male was removed. If the male did not immediately crawl around the slide, the data was discarded. The fluorescence data was analyzed using the SimplePCI software and Microsoft Excel, as described earlier.

For ChR2 activation of ray neurons, L4 dop-2; dop-3; rgEx550[Pdat-1:Chr2::YFP] and heterozygous males were incubated overnight with +/− all-trans-retinal. The adult males were then placed in a 2% noble agar pad containing 5 mM ARE on a slide and covered with a cover slip, while simultaneously being exposed to 4.2 mW/mm² blue light illuminated through a 10× objective fitted to a Zeiss Stemi SV 11 stereomicroscope. To determine the working ARE concentration in 2% agar pads, a dose response curved was done with wild-type males (Figure S1C).

Spicule prodding rate measurements

The spicule movements of wild-type or dop-2(lf); dop-3(lf) males copulating with heat-shocked paralyzed pha-1; lite-1; him-5; rgEx431[Phsp-16:egl-2(n693gf)cDNA; Punc-103E:mDsRed; pha-1(+)] hermaphrodites were digitally recorded with Hamamatsu ImagEM camera at a rate of ∼35 frames per second. The grey-scale recordings were analyzed using the SimplePCI software. The recordings were reviewed to find the first instance where the male repetitively prods the vulva with his spicules for an uninterrupted duration of 6 to 10 seconds. In those frames of the recording, a rectangular ROI was drawn over the region of the male spicule. In the ROI of each frame, the standard deviation of the mean pixel intensity was calculated. The data was transferred to Microsoft Excel and plotted against time. Oscillation amplitudes greater than 5% were considered to be due to a spicule deflection. The durations between oscillations were graphed in Figure 5C.

Length measurements

The In-Contact Length (ICL) was calculated by using the SimplePCI imaging software skeletonized tool to measure the length of the male outline that contacted the hermaphrodite cuticle of a representative frame. This measurement was then divided by the total male body length and converted to percentage values.

RNAi

To monitor gpa-16 RNAi effectiveness, pPC41[Pgpa-16:gpa-16::YFP] was injected into goa-1(lf); gpa-7(lf) strain. RNAi was induced by feeding worms bacteria producing double stranded RNA (dsRNA) to the target gpa-16 ORF. Bacteria with the L4440 double-T7 vector including gpa-16 fourth and fifth exons were grown and induced by IPTG using a standard protocol [67]. L4 males expressing the pPC41 transgene were transferred to plates spotted with the dsRNA bacteria or OP50, as a control, and incubated for 20 hours. In a subset of these males, fluorescence of pharyngeal muscles and PDE neurons was checked. We found a similar percentage of males glowing in both tissues when fed with OP50 (80% vs. 75%, n = 20); however when males were fed with dsRNA there was a reduction in fluorescence of pharyngeal muscles when compared to PDE (78% vs. 4%, n = 23). The adult males then were assayed for their response to DA+ARE drug baths (Table 2).