Caenorhabditis elegans G_q Regulates Egg-Laying Behavior via a PLCß-Independent and Serotonin-Dependent Signaling Pathway and Likely Functions Both in the Nervous System and in Muscle

Corresponding author: Paul W. Sternberg, California Institute of Technology, Pasadena, CA 91125., pws{at}its.caltech.edu (E-mail)

Communicating editor: B. J. MEYER

	ABSTRACT

TOP ABSTRACT MATERIALS AND METHODS RESULTS DISCUSSION LITERATURE CITED

egl-30 encodes the single C. elegans ortholog of vertebrate G_q family members. We analyzed the expression pattern of EGL-30 and found that it is broadly expressed, with highest expression in the nervous system and in pharyngeal muscle. We isolated dominant, gain-of-function alleles of egl-30 as intragenic revertants of an egl-30 reduction-of-function mutation. Using these gain-of-function mutants and existing reduction-of-function mutants, we examined the site and mode of action of EGL-30. On the basis of pharmacological analysis, it has been determined that egl-30 functions both in the nervous system and in the vulval muscles for egg-laying behavior. Genetic epistasis over mutations that eliminate detectable levels of serotonin reveals that egl-30 requires serotonin to regulate egg laying. Furthermore, pharmacological response assays strongly suggest that EGL-30 may directly couple to a serotonin receptor to mediate egg laying. We also examined genetic interactions with mutations in the gene that encodes the single C. elegans homolog of PLCß and mutations in genes that encode signaling molecules downstream of PLCß. We conclude that PLCß functions in parallel with egl-30 with respect to egg laying or is not the major effector of EGL-30. In contrast, PLCß-mediated signaling is likely downstream of EGL-30 with respect to pharyngeal-pumping behavior. Our data indicate that there are multiple signaling pathways downstream of EGL-30 and that different pathways could predominate with respect to the regulation of different behaviors.

CAENORHABDITIS elegans G_q is encoded by egl-30 (BRUNDAGE et al. 1996 ). In mammals, on the basis of sequence similarity the G_q family is represented by four members: G_q, G₁₁, G₁₄, and murine G₁₅/human G₁₆ (WILKIE et al. 1991 ). Mutations in egl-30 were originally identified because of their egg-laying-defective phenotype (TRENT et al. 1983 ). Subsequent characterization and identification of additional egl-30 mutant alleles revealed that egl-30 is involved with the regulation of many behaviors, including egg laying (TRENT et al. 1983 ; BRUNDAGE et al. 1996 ), pharyngeal pumping (BRUNDAGE et al. 1996 ), movement (BRUNDAGE et al. 1996 ), viability (BRUNDAGE et al. 1996 ), and spicule protraction (GARCIA et al. 2001 ). The vertebrate G_q family is involved in pertussis-toxin-insensitive regulation of phospholipase Cß (PLCß) isoforms (EXTON 1996 ). Like its vertebrate homolog, EGL-30 can stimulate endogenous phospholipase activity in COS-7 cells (BRUNDAGE et al. 1996 ).

Given the fact that EGL-30 and G_q and G₁₁ share >80% identity at the amino acid level and that EGL-30 can functionally complement G_q (BRUNDAGE et al. 1996 ), it is likely that the biochemistry of signaling is well conserved between C. elegans and mammals. We employed a genetic approach in C. elegans to further characterize EGL-30-mediated signaling pathways. To this end, we screened for mutations that were able to phenotypically suppress a reduction-of-function allele, egl-30(md186). egl-30(md186) mutants are lethargic, exhibit slow pharyngeal pumping, and lay eggs at a later stage of development than do wild type.

From our suppressor screen, two intragenic revertants of egl-30(md186) that increase egl-30 function were isolated. We used these mutants and another strong egl-30 gain-of-function mutant (DOI and IWASAKI 2002 ) as a tool to explore interactions with genes that encode candidate downstream molecules. Double-mutant strains were constructed to analyze interactions with the PLCß-signaling pathway and to analyze interactions with respect to the pathway defined as downstream of EGL-30 with respect to synaptic transmission (LACKNER et al. 1999 ). We focused primarily on egg-laying behavior since this behavior is regulated by neural input to the vulval muscles by only two classes of motor neurons, the hermaphrodite-specific neurons (HSNs) and the ventral type C neurons (VCs) (WHITE et al. 1986 ; WAGGONER et al. 1998 ). We also examined the double mutants with respect to pharyngeal-pumping behavior since egl-30 mutants display strong pumping defects.

Our results suggest that PLCß, the only well-characterized effector for vertebrate G_q family members, is not the only effector for EGL-30. With respect to egg laying, PLCß either acts in parallel to egl-30 or is a minor downstream component of EGL-30-mediated signaling. Consistent with this result, mutations in itr-1, which encodes the single inositol 1,4,5 triphosphate (IP₃) receptor, and in a gene that encodes protein kinase C (PKC) also do not significantly modify egl-30 gain-of-function phenotypes. However, with respect to pharyngeal pumping, each of the mutations in genes that encode components of PLCß signaling do suppress egl-30 gain-of-function phenotypes to a similar extent with respect to pharyngeal pumping.

We conclude that in C. elegans there are other effector(s) for EGL-30 in addition to PLCß and that different downstream pathways predominate to control egg laying and pharyngeal pumping. Expression analyses also indicate that there is not complete overlap with respect to EGL-30 localization and EGL-8 localization (MILLER et al. 1999 ). It is conceivable that different effector pathways are cell-type specific, and we show that EGL-30 does function in, or via, at least one class of motor neurons that activate the vulval muscles and likely in the vulval muscles themselves as well.

	MATERIALS AND METHODS

TOP ABSTRACT MATERIALS AND METHODS RESULTS DISCUSSION LITERATURE CITED

Manipulation of C. elegans:
Maintenance and manipulation of C. elegans were as described (BRENNER 1974 ). The following alleles were used for behavioral analyses and for double-mutant constructions: LGI, egl-30(md186)I (MILLER et al. 1996 ), egl-30(ad805)I (BRUNDAGE et al. 1996 ), and unc-13(e51) unc-122(n2916) I (BRENNER 1974 ); LGII, tph-1(mg280)II (SZE et al. 2000 ); LGIV, dpy-20(e1282)IV (HOSONO et al. 1982 ), itr-1(sa73)IV (IWASAKI et al. 1995 ), dpy-9(e12)IV (BRENNER 1974 ), and tpa-1(k530)IV (TABUSE and MIWA 1983 ); LGV, egl-8(md1971)V (MILLER et al. 1999 ), egl-8(n488)V (TRENT et al. 1983 ), egl-8(sa47)V (THOMAS 1990 ), and egl-1(n487)V (TRENT et al. 1983 ). The unc-13 strain used in this study (CB51) also contains a linked unc-122 mutation. This linked mutation was uncovered in RICHMOND et al. 1999 and was presumably used in all similar studies prior to this discovery (LACKNER et al. 1999 ). In general, mutations were followed in crosses on the basis of their own visible phenotypes. For strains harboring tpa-1, dpy-9(e12) was used as a balancer, and for strains with itr-1, dpy-20(e1282) was used as a balancer in trans. For example, egl-30(gf)/+ males were mated to dpy-9 hermaphrodites. Since egl-30(md186sy676) is semidominant, it was possible to identify heterozygous male progeny. Hyperactive (egl-30(md186sy676)/+; dpy-9/+) F₁ males were mated with tpa-1 mutant hermaphrodites. A total of 10 hyperactive (egl-30(md186sy676)/+) F₁ progeny were selected and picked onto individual plates. A total of 25 candidate egl-30(md186sy676) homozygous animals were selected only from plates that segregated dpy-9. Plates that segregated only hyperactive non-Dpy progeny were examined for progeny that segregated hyperactive animals of which approximately one-fourth had a modified phenotype. In the cases of itr-1 and tpa-1, both mutations slightly modified the movement of egl-30(gf) homozygotes. egl-30(gf); itr-1(sa47) animals were scrawnier than egl-30(gf) homozygotes and in egl-30(gf); tpa-1 double mutants a synthetic phenotype was observed such that a tail spike and vacuolization of some of the nerve ring ganglia was apparent in the double mutant, but not in either single mutant. In all cases, double mutants were backcrossed to N2 and, after picking F₁'s to individual plates, each single mutant was reisolated in the F₂ progeny.

Construction and integration of functional GFP-tagged EGL-30, hsp-16::egl-30(QL), and overexpression and integration of the wild-type egl-30 locus:
Standard molecular biological techniques were performed as described (SAMBROOK et al. 1989 ). For construction of an in-frame green fluorescent protein (GFP) fusion just 5' to the egl-30 initiator ATG, the following primers were used to amplify a GFP S65T mutant from a pRSET vector (kind gift from Roger Tsien): 5'-AATAAAGGCCTAAATGGCCATGAGTAAAGGAGAAGAACTTTTC-3'/5'-TTAGCAGGCCATGGCGGCCAAGCATTTGTATAGTTCATCCATGC-3'. The PCR product was gel purified (QiaexII, QIAGEN, Valencia, CA), digested with SfiI, and cloned into the SfiI site of pLB2 (BRUNDAGE et al. 1996 ). The resulting construct, pCB50, was injected into egl-30(md186); dpy-20(e1282) at a concentration of 5 ng/µl. Animals were microinjected according to standard procedures (MELLO et al. 1991 ; MELLO and FIRE 1995 ). The dpy-20 rescuing plasmid, pMH86, was injected at 20 ng/µl (HAN and STERNBERG 1990 ) and was used as the coinjection marker. pBluescript was included as carrier DNA to bring the total DNA concentration to 200 ng/µl.

A fusion of the egl-30(Q205L) cDNA was cloned into pPD49.78 as a Kpn1-SacI fragment to generate pLB24. pLB24 was at injected at 50 ng/µl as described for pCB50.

Transgenic arrays (pLB24 and pCB50) were chromosomally integrated as described (WAY et al. 1991 ), except that animals were treated with 38 Gy from an X-ray source. The pLB24 integrant was named syIs38, and the pCB50 integrant was named syIs105. Construction of and expression from the extrachromosomal array that was integrated (syEx125) to make syIs36 by the procedures described for other integrated lines (BRUNDAGE et al. 1996 ). The integrated lines were outcrossed a minimum of six times with dpy-20(e1282). The integration of the transgenic arrays generally increased the expressivity of the phenotype observed in the nonintegrated lines. In the case of syIs38, the severity of the phenotype after heat shock also increased.

Expression analysis:
An EGL-30 antibody was generated in rabbits against the C-terminal peptide: KDTILQHNLKEYNLV (Quality Controlled Biochemicals). The antibody was affinity purified with the peptide used for immunization using SulfoLink Coupling Gel (Pierce, Rockford, IL) according to the manufacturer's instructions. Indirect immunofluorescence was done as described (RUVKUN and GIUSTO 1989 ), except 2x fixation buffer contained 50% MeOH and did not contain n-heptane, and Triton X-100 was used at 0.1%. Either a fluorescein-conjugated anti-rabbit antibody was used at 1:1000 (Vector Laboratories, Burlingame, CA) or the Vectastain Elite ABC avidin/biotin blocking kit was used with a biotinylated anti-rabbit antibody (Vector Laboratories). When the biotinylated antibody was used, an avidin/biotin blocking step was included after the collagenase digestion step. Animals were examined with a Zeiss axioskop under a x100 objective. For examination of GFP fluorescence, animals were examined on a Leica DMIRBE confocal microscope.

Isolation of intragenic suppressor mutations:
Ethyl methanesulfonate (EMS) mutagenesis of 60,000 egl-30(md186) gametes was done as described (BRENNER 1974 ) using 50 mM EMS. From this screen, we isolated two intragenic revertants and three strong extragenic suppressor mutations. F₂ progeny were selected on the basis of their ability to suppress egg-laying and/or movement defects of egl-30(md186) mutants. Intragenic suppressor mutants were outcrossed to N2 at least six times.

Sequencing of egl-30 mutations:
Suppressor mutations (sup) were picked as potential intragenic revertants on the basis of the inability to isolate egl-30(md186) homozygous F₁ progeny when sup egl-30(md186)/++ males were mated to egl-30(md186). Fragments of the egl-30 locus were amplified using Takara LA-Taq (PanVera) with the following primer sets: 5'-GCATCGAACTTCTATCCTC-3'/5'-GCTACGAGATATTTGTTGC-3' (exons 1 and 2), 5'-GAGATTAAAATACTCATTTCG-3'/5'-CGAAAAAAGCATCAGAGATTG-3' (exons 3–5), and 5'-CTTTCTGTAAATTGTCAGC-3'/GTGGTGTCTCACTCGACC-3' (exons 6–8). DNA was amplified in 10 50-µl reactions, gel purified using Qiaex II (QIAGEN), and directly sequenced on an automated sequencer (ABI). The DNA was compared with N2 and with the original egl-30(md186) strain. Mutations were confirmed by sequence from the reverse strand. Mutations were mapped onto known crystal structures using Protein Explorer (http://www.umass.edu/microbio/chime/explorer/index.htm). egl-30(tg26) was isolated in a screen for suppressors of unc-31 by L. Khan (DOI and IWASAKI 2002 ) and obtained as a generous gift from the Iwasaki laboratory.

Sequencing of egl-8 mutations:
Primers flanking the n488 deletion were used for PCR: 5'-CTA CTA CCC AAC AAG TGA GAG 3'/5'-CGG AAG TTT TGG GCT GTT TTG G-3'. The deletion was found to extend from 7905–9735 in the unspliced DNA sequence displayed in WormBase (WS62) such that the sequence 5'-GTGTGGGAAAAAATGTGT-3' was fused to 5'-TGTTGATTATCATTTTCT-3'. Primers flanking the md1971 mutation were used for PCR: 5'-CGA AGA CCC GAC AGA ACA TT-3'/5'-CCC GGG TAT TAC CTT CGT CT-3'. PCR products were amplified, purified, and sequenced as above.

Behavioral assays:
To measure pharyngeal pumping rates, 1-day-old adults were placed on nematode growth media (NGM) plates seeded with OP50 and left undisturbed for at least 15 min before counting. Pharyngeal pumps were measured using a counter for a period of 3 min. Response was measured only from animals that remained in food throughout the period of observation.

To characterize egg-laying behavior, animals were examined 24–28 hr after selecting them as L4 larvae. Young adults were placed on fresh plates seeded with OP50 and newly laid eggs were examined every 5 min for their developmental stage using a Wild M420 macroscope and then removed from the plate. In all cases, at least two trials were performed on different days, and at least 10 different adults were assayed per trial. For mutants that never laid eggs past the gastrulation stage of development, at least three trials were performed.

For response to 5-hydroxytryptamine (5-HT; Sigma, St. Louis), levamisole (Sigma), and -methyl 5-hydroxytryptamine (-methyl 5-HT; Sigma), animals were tested singly (except as indicated) as 1-day-old adults in wells of a microtiter plate containing a solution of the indicated drug. Response was measured after 60 or 90 min, as indicated in figure legends. 5-HT was generally used at a concentration of 7.5 mM, levamisole at 6.25 µm, and -methyl 5-HT at 1 mM. For 5-HT and levamisole, we used M9, but sodium phosphate was substituted for potassium phosphate. To test response to -methyl 5-HT, assays were performed in water since M9 inhibited the response for all genotypes tested, except for strains that also contained egl-1 mutations.

Phalloidin staining:
Worms were stained with phalloidin using a modification of a previously described protocol (MYERS et al. 1996 ). Worms were grown on NGM plates, harvested in S-basal medium, and washed once with S basal. Supernatant was removed with a Pasteur pipette and worms were frozen in liquid nitrogen. A few drops of ice-cold acetone were added to worms and worms were incubated on ice for 5 min. Acetone was removed and worms were air dried. A total of 10 µg of fluorescein-conjugated phalloidin was added to the worms in PBS buffer containing 1 mM magnesium chloride and 0.4% SDS. Worms were stained for 1 hr at room temperature, harvested, and washed three times in PBS containing 0.5% Tween-20. Animals were examined for fluorescence on a Zeiss axioscope.

Western analysis:
Worms were harvested from NGM plates in M9 and washed one time with M9. Worm pellets were resuspended in 2x SDS sample buffer (Novex, San Diego) and heated at 70° for 10 min. Worm debris was pelleted at 14 K in a microcentrifuge for 10 min, and the supernatant was promptly loaded on an SDS/PAGE gel (Novex).

For Western analysis of EGL-30, the same number of syIs36 mutants was first picked to separate plates for each time point. Four days later (prior to starvation) worms were heat-shocked for 30 min at 32°. At the indicated time points, worms from each plate were harvested and prepared as described above. Worm extracts were loaded onto a 10% gel.

For analysis of egl-8 expression, worms were harvested in M9 as above. Extracts for analysis of egl-8 expression were loaded onto a 4–12% gradient gel (Novex).

Electrophoretic transfer was carried out for 1.5 hr for EGL-30 Western analysis and overnight for EGL-8 analysis. Following transfer to nitrocellulose membranes, EGL-8 antibody (generously provided by Kenneth Miller) was used at a concentration of 1:1000 (MILLER et al. 1999 ), and affinity-purified EGL-30 antibody generated against the peptide was used at a dilution of 1:50,000. HRP-linked anti-rabbit IgG (Amersham, Buckinghamshire, UK) was added at a concentration of 1:1000, and bands were visualized using enhanced chemiluminescence (Amersham).

	RESULTS

TOP ABSTRACT MATERIALS AND METHODS RESULTS DISCUSSION LITERATURE CITED

Expression of egl-30:
To clarify the site and mode of action for egl-30 with respect to the behaviors that it regulates, to resolve differences in the inferred site-of-action from previous reports (BRUNDAGE et al. 1996 ; LACKNER et al. 1999 ), and to examine the subcellular localization of egl-30, we sought to construct a rescuing GFP fusion transgene. This transgene contains all of the presumptive 5'-transcriptional regulatory sequences, introns, and presumptive 3' regulatory sequences for egl-30, in addition to the coding sequences for GFP just 5' of the egl-30 initiating methionine. We expected that this transgene should be appropriately expressed as well as appropriately localized. This transgene was integrated into the genome of egl-30(md186) animals, and the integrated transgene, syIs105, was found to partially rescue egl-30(md186) with respect to egg laying, movement, pharyngeal pumping, and response to neurotransmitters in egg-laying assays (Table 1 and Table 2). Expression was first observed in early embryos at cell peripheries and in a punctate pattern throughout embryos (Fig 1D). Later, expression was observed in larvae in the nerve ring and many neurons of the nerve ring ganglia, pharyngeal muscle, and ventral cord and many neurons in the tail ganglia and hypodermis (Fig 1). Highest expression levels were observed in L4 larvae and in adult animals. In the nervous system, expression was observed in cell bodies and in neural processes. However, the highest expression was observed in the axons of the nerve ring. Expression in larvae and in adults was also evident in the pharyngeal muscle. Expression was also observed in the dorsal nerve cord and in sublateral processes (Fig 1E). In addition, occasional expression was observed throughout the intestine (particularly in the posterior intestine), vulval muscle, head muscle, in sperm, tonofilaments, and in vulval cells. With the exception of the pharyngeal muscle, expression levels in muscle were generally extremely low such that only rare animals (10%) showed weak expression. The CAN cell bodies and associated canals were observed to express GFP-tagged EGL-30 in most animals (Fig 1C). The HSN cell bodies and the VC4 and VC5 neuronal cell bodies also occasionally expressed EGL-30 (10%), on the basis of proximity to the vulva. Other cell bodies in the ventral nerve cord were also observed to occasionally express GFP.

View larger version (72K): In this window In a new window Download PPT slide   Figure 1. Expression of egl-30, based on an integrated GFP fusion transgene (A–F) and indirect immunofluorescence (G and H). (A) The arrow indicates expression in the nerve ring. The arrowhead indicates expression in the pharyngeal muscle. (B) Arrow indicates expression in the ventral nerve cord. (C) Arrow indicates expression in the CAN neuron. (D) Arrow points to expression in the vulval muscle. (E) Expression in nerve tracts. (F) Expression in the VC4 and VC5 motor neurons, based on their positions, is indicated by the arrow. (G) Expression in the nerve ring, as detected using a biotinylated secondary antibody and HRP-avidin. (H) Expression in the anal sphincter muscle, as visualized with a FITC-labeled secondary antibody. Images in A–F were obtained with a Leica DMIRBE microscope and images in G and H were obtained on a Zeiss axioscope.

Immunolocalization analysis with a polyclonal antibody generated against the carboxyl terminus of EGL-30 generally revealed the areas with highest expression levels. Using an HRP-conjugated secondary antibody and a FITC-conjugated secondary antibody, we observed high expression in axons of the nerve ring. The FITC-conjugated antibody also indicated expression in pharyngeal muscle. Both secondary antibodies revealed expression in sperm, and the FITC-conjugated antibody consistently showed expression in the anal sphincter muscle (Fig 1H). Nonspecific antibody staining was observed in intestinal nuclei using both secondary antibodies and is most likely due to cross-reactivity with an unrelated protein. Western analysis supports this hypothesis since the band that migrates at the position where EGL-30 migrates on an SDS/PAGE gel is present at almost equivalent intensities in protein extracts prepared from egl-30(ad805) mutants compared to wild-type extracts (data not shown), but the levels of this band increase significantly after heat-shock induction of an egl-30 transgene (Fig 2A). When egl-30 was overexpressed from an integrated array (syIs36), an increase in the intensity of staining was observed in the nerve ring and in pharyngeal muscle, but not in intestinal nuclei.

View larger version (78K): In this window In a new window Download PPT slide   Figure 2. Heat-shock induction of EGL-30(Q205L) under the control of the hsp-16-2 promoter element (integrant syls38). (A) Protein levels following a 30-min heat shock at 32°. Times indicated represent the amount of time following the end of the heat-shock regimen. Protein levels did not appear to increase more than threefold above basal levels. (B) Phenotypic effects on adults following heat shock. After 2 hr worms exhibited a hyperactive phenotype, laid early eggs, and moved with exaggerated body bends. Within 4 hr, animals were completely paralyzed. Twenty-four hours later, adults displayed a hypercontracted posture, constitutive pumping of many muscle types, and exhibited vacuolization of many cells.

The broad expression pattern of egl-30 is consistent with its pleiotropic and essential function. Expression levels of egl-30 were clearly higher in the nervous system and in pharyngeal muscle, suggesting that EGL-30 exerts a primary role in these tissues. Weak or occasional expression in other muscle-cell types, sperm, intestine, tonofilaments, and vulval cells indicates the possibility that EGL-30 might have an almost ubiquitous expression pattern.

Dose sensitivity of egl-30:
Haplo-insufficiency of the egl-30 locus, together with phenotypic analysis of gain- and reduction-of-function mutations in egl-30, demonstrates that perturbations in activity levels of egl-30 result in a clear phenotypic readout. Heterozygous reduction-of-function mutants exhibit semidominance with respect to lethargic locomotion and egg-laying defects (BRUNDAGE et al. 1996 ). egl-30(md186) mutants behaved like other reduction-of-function mutations previously described and lay >94% of their eggs after the gastrulation phase of development (Table 1). Wild-type hermaphrodites lay eggs 2–3 hr after fertilization during the gastrulation phase (beginning at the 28-cell stage) of development and always before morphogenesis begins (comma stage; SULSTON et al. 1983 ). For our purposes, late-stage eggs are defined as eggs laid at or after the comma stage of development. egl-30(md186) mutants also exhibited semidominance with respect to pharyngeal-pumping and egg-laying defects (Table 1). Consequently, it is clear that reducing activity levels of EGL-30 by <50% has significant phenotypic consequences.

Similarly, raising both expression or activity levels of EGL-30 has drastic effects on behavior (BRUNDAGE et al. 1996 ). A transgenic strain that overexpresses wild-type egl-30 under its own regulatory regions, syIs36, exhibited hyperactive movement, moved with exaggerated body bends, and laid eggs at an early stage of development (data not shown and Table 3). These animals also exhibited a pale, starved appearance. Heat-shock induction of syIs38, an integrated transgene that contains a gain-of-function cDNA of egl-30 fused to the hsp-16-2 enhancer-promoter element, demonstrated the progressive effects caused by increasing EGL-30 expression and activity levels over time. Approximately 2 hr after a heat-shock induction of 32° for 30 min, worms became hyperactive, started to move with exaggerated body bends, and had laid all of the eggs contained within their uteri (Fig 2B). After 4 hr, worms became paralyzed and hypercontracted. After 24 hr, the hypercontracted phenotype was still apparent, and animals exhibited weak but constitutive pumping of all muscle types and displayed vacuolization of many cell types (Fig 2B). Eventually, these worms died. These effects are evident in spite of the fact that expression levels of egl-30 increased only at most threefold above endogenous levels (Fig 2A). This low induced level of expression is in marked contrast to the high induced levels of expression that were obtained with an analogous GOA-1 construct (C. BASTIANI, W. CHEN, M. I. SIMON and P. W. STERNBERG, unpublished results). The same differences in expression levels are observed when levels of GOA-1 and EGL-30 are compared after transfection of cDNA expression plasmids into HEK293T cell lines (C. BASTIANI, W. CHEN, M. I. SIMON and P. W. STERNBERG, unpublished results).

Gain-of-function mutants of egl-30:
Mutations that do not affect expression levels of egl-30, on the basis of Western blot analysis (data not shown), similarly demonstrate the effects of altered activity levels of EGL-30. Two intragenic revertants of a reduction-of-function allele, egl-30(md186), were obtained in screens for mutations for suppression of the allele's egg-laying-defective and lethargic phenotypes (Table 3 and Table 4 and data not shown). egl-30(md186) encodes a D201E change immediately adjacent to the switch 2 region, suggesting that association with guanine nucleotides is probably altered. The two intragenic revertants differ in their strengths.

The stronger intragenic suppressor mutant, sy676, exhibited semidominant hyperactive movement, movement with exaggerated body bends, and constitutive egg-laying phenotypes (heterozygotes lay 19% of eggs at or before the four-cell stage; N = 224), similar to phenotypes caused by overproduction of wild-type EGL-30 (BRUNDAGE et al. 1996 ). This intragenic revertant encodes a R334W change within the 5 helix. This amino acid change results in a string of eight consecutive hydrophobic residues, of which W334 is the second. Mutations of residues within the ß6/5 loop promote dissociation of GTP and GTP/GDP exchange on several G subunits (THOMAS et al. 1993 ; IIRI et al. 1994 ; POSNER et al. 1998 ). This region also lies very close to the carboxyl terminus of EGL-30, which in G subunits is implicated in interactions with membrane receptors (HAMM et al. 1988 ; GARCIA et al. 1995 ; OSAWA and WEISS 1995 ; KISSELEV et al. 1998 ). On the basis of comparative analysis with the crystal structure of G_i in a complex with RGS4 (TESMER et al. 1997 ), it is likely that the mutated amino acid does not directly interact with the site of the original egl-30(md186) mutation (Fig 3). Also on the basis of comparative analysis with the crystal structure of G_i in a complex with ß/ (WALL et al. 1995 ), we know that this mutation lies in a region that likely does not affect interaction with ß/. In addition, alignments with mammalian G_i indicate that this mutation does not lie in a region important for activation of PLCß (VENKATAKRISHNAN and EXTON 1996 ). Consequently, we speculate that GTP dissociation, GTP/GDP exchange, or interaction with seven-pass membrane receptors is affected by this mutation.

View larger version (39K): In this window In a new window Download PPT slide   Figure 3. Mutations in egl-30 positioned on the crystal structure of rat Gi1 bound to GDP, AIF-4, and Mg2+ in a complex with RGS4 (TESMER et al. 1997 ). Blue and green chains show Gi1 -, ß-, and -subunits. RGS4 chains are shown in red and yellow. Two citrate ions are positioned within the Gi1 dimer interface.

The weaker intragenic suppressor mutation, sy679, encodes an E277K change, a change from an acidic residue to a basic residue, within the G helix. On the crystal structure of G_i (RAW et al. 1997 ), this mutation is in close proximity to the residues involved in guanine ring binding and is diametrically opposite from the original egl-30(md186) mutation (Fig 3). It is possible that this mutation partially compensates for any alterations in guanine nucleotide interactions modified by the original egl-30(md186) mutation. However, E277K did not completely suppress the original D201E change in egl-30(md186) with respect to pharyngeal pumping (data not shown) and egg laying (Table 3). Again, on the basis of comparative crystal structure analysis, ß/ interactions are probably not affected.

Another gain-of-function mutant, egl-30(tg26), was obtained in a screen for suppressors of unc-31 (DOI and IWASAKI 2002 ). tg26 encodes an R243Q change (DOI and IWASAKI 2002 ), and this mutation is contained within the switch III region of the 3 helix, indicating that R243Q probably alters guanine nucleotide binding (Fig 3). tg26 is also semidominant (heterozygotes lay 23% of eggs at or before the four-cell stage; N = 44) and confers the most severe gain-of-function phenotypes compared with the two other mutants. Mutants moved with exaggerated body bends and laid eggs at an earlier stage of development than wild type did (Table 3). In addition, brood sizes were significantly lower than those in egl-30(md186sy676) mutants (77 ± 44 vs. 175 ± 32). Unlike the egl-30(md186sy676) mutant, but like syIs36 that overexpresses wild-type egl-30, the pharyngeal pumping exhibited by these mutants would alternate from a very fast rate to no visibly evident pumping, possibly due to tonic contraction of these muscles.

In summary, haplo-insufficiency of the egl-30 locus, the semidominance of the gain-of-function mutants, and the progressive phenotypes caused by heat-shock-induced overexpression of a gain-of-function transgene demonstrated a clear phenotypic readout when levels of egl-30 expression or activity were altered. Given this result, if there is only one primary downstream effector for egl-30, a knockout or near knockout in a primary downstream effector should strongly suppress egl-30 gain-of-function mutations.

The PLCß-signaling pathway is not the predominant pathway downstream of EGL-30 with respect to egg laying:
Mammalian G_q family members are believed to principally activate isoforms of PLCß (LEE et al. 1992 ). PLC hydrolyzes phosphatidylinositol 4,5-bisphosphate (PIP₂) into the signaling molecules diacylglycerol (DAG) and IP₃. DAG activates PKC while IP₃ activates release of calcium from intracellular stores via activation of the IP₃ receptor, a calcium channel. egl-8 encodes the only recognizable PLCß isoform in the worm and is most closely related to vertebrate PLCß4. egl-8 reduction-of-function mutants exhibit lethargic locomotion and a reduced rate of pharyngeal pumping, and they lay late-stage eggs (TRENT et al. 1983 ; MILLER et al. 1999 ; Table 3 and Table 4), as do egl-30 reduction-of-function mutants. However, a candidate null allele in egl-8 (LACKNER et al. 1999 ) is not as severely impaired as egl-30 reduction-of-function mutants with respect to egg laying and locomotion (Table 3 and data not shown). In addition, egl-8 mutants are fully viable, unlike egl-30 severe loss-of-function alleles (BRUNDAGE et al. 1996 ), suggesting that EGL-8 is not the only downstream effector for EGL-30.

Three alleles of egl-8 have been previously described with respect to their molecular lesions. egl-8(sa47) encodes an early termination codon and is presumed to be a null allele (LACKNER et al. 1999 ). egl-8(md1971) encodes a premature termination codon 3' of the C2 domain (although the mutation was predicted to be contained within the catalytic Y domain as reported; MILLER et al. 1999 ). egl-8(n488) deletes 1.8 kb of sequence including exons 10 and 11 (MILLER et al. 1999 ). Unlike egl-30 reduction-of-function mutants, sa47 and md1971 exhibit a strong induction of egg laying in response to 5-HT (serotonin; Table 2). On the basis of phenotypic similarities with egl-8(sa47), egl-8(md1971) is likely a partial reduction-of-function allele (Table 2). Like egl-30 reduction-of-function mutations, but unlike sa47 and md1971, egl-8(n488) mutants are completely resistant to serotonin in egg-laying assays (TRENT et al. 1983 ). egl-8(n488) is the canonical egl-8 allele and has been the only allele previously tested for pharmacological response in egg-laying assays.

To investigate the interaction between C. elegans G_q and PLCß, we constructed strains defective in egl-30 as well as in genes that encode components of the PLCß-signaling pathway. Interactions were examined with the three alleles of egl-8 described above: egl-8(sa47), egl-8(md1971), and egl-8(n488) (Table 3). We also examined interactions with itr-1, tpa-1, and unc-13 mutations. itr-1 encodes the only IP₃ receptor homolog in the worm (CLANDININ et al. 1998 ; BAYLIS et al. 1999 ; DAL SANTO et al. 1999 ) and loss-of-function mutations were originally isolated because of their defecation defects (IWASAKI et al. 1995 ). tpa-1 encodes a protein most similar to vertebrate PKC and was identified since mutations in the gene that encode TPA-1 confer resistance to TPA (TABUSE and MIWA 1983 ; TABUSE et al. 1989 ). UNC-13 is also implicated in a pathway downstream of DAG since the discovery that its mammalian ortholog, mUNC-13, is a receptor for DAG and enhances neurotransmitter release (BETZ et al. 1998 ). Later, UNC-13 was found to regulate acetylcholine and GABA release from neuromuscular junctions in C. elegans (LACKNER et al. 1999 ; RICHMOND et al. 1999 ) and to be essential for neurotransmitter release in Drosophila melanogaster (ARAVAMUDAN et al. 1999 ).

To analyze epistasis, we constructed all double mutants using egl-30(md186sy676) and confirmed selected interactions using egl-30(tg26), because the egl-30(md186sy676) strain does not exhibit the pale, scrawny, starved appearance of egl-30(tg26) and has a brood size comparable to wild type. egl-30(gf) mutants exhibited a constitutive egg-laying phenotype, defined in these assays as worms that lay eggs at or before the four-cell stage. egl-8(sa47) and egl-8(n488) mutants exhibited an egg-laying-defective phenotype as single mutants; however, these mutations did not significantly suppress egl-30(gf) mutations with respect to egg-laying behavior (Table 3). Some level of mutual suppression appeared to be generally true with respect to movement since egl-30(gf); egl-8 double mutants still moved with exaggerated body bends, but activity levels appeared slightly reduced (data not shown). egl-30(md186sy679); egl-8(sa47) double mutants did display a further reduction in egg-laying behavior, which is expected if these genes act in parallel. The apparent increase in egg-laying activity exhibited by egl-30(md186); egl-8(sa47) mutants, on the basis of hatched larvae observed on the plate, is not absolutely understood at this point. The most likely possibility is that the egl-30(md186); egl-8(sa47) larvae are more seriously impaired with respect to movement and are therefore not as competent to crawl out of the mother. These results indicate either that egl-8 is a minor effector for egl-30 or that egl-8 functions completely in parallel with egl-30 with respect to egg laying and possibly movement.

unc-13 single mutants displayed a severe egg-laying defect, and unc-13(e51) mutations did suppress constitutive egg laying conferred by egl-30(gf) mutants (Table 3). However, double mutants were not nearly as impaired with respect to egg laying as unc-13 single mutants were. The observation that egl-30(md186); unc-13 double mutants are apparently less defective in egg laying than either single mutant may reflect the fact that acetylcholine must exert both a positive and a negative regulatory role in egg laying; cha-1 mutants lay early embryos and are hypersensitive to serotonin (SCHAFER et al. 1996 ).

C. elegans UNC-13 is known to affect evoked neurotransmitter release at both GABAergic and cholinergic synapses, but it has not been shown to affect serotonin release (RICHMOND et al. 1999 ). The unc-13(e51) allele appears to almost fully compromise the function of UNC-13, as assessed by measuring evoked responses in muscle by whole-cell patch clamp recordings in response to stimulation of the ventral nerve cord (RICHMOND et al. 1999 ). Acetylcholine is a known positive regulator of egg-laying behavior (WAGGONER et al. 1998 ), and a role for EGL-30 in the regulation of the release of acetylcholine from motor neurons has previously been reported (LACKNER et al. 1999 ). Our analysis of egg-laying behavior suggests either that the regulation of acetylcholine release is not the only neuronal pathway downstream of EGL-30 or that EGL-30 function in the vulval muscle can partially bypass the requirement for acetylcholine.

tpa-1 is the only PKC in the worm for which mutations have been identified (TABUSE et al. 1995 ). tpa-1 encodes a protein with similarity to PKC. Loss-of-function tpa-1(k501) mutants lay eggs at significantly lower rates than wild type do, and mutants are resistant to the stimulation of egg laying by serotonin (WAGGONER et al. 1998 ). TPA-1 acts in and is expressed in vulval muscle and in the nervous system (WAGGONER et al. 2000 ). Although egg-laying defects are evident in single-worm tracking assays over long periods, the developmental stage of eggs laid by tpa-1 mutants did not differ from wild-type worms (Table 3). Mutations also do not suppress egl-30(gf) mutations with respect to the developmental stage of eggs laid (Table 3). We conclude from these results that tpa-1 either is not downstream of egl-30 or functions redundantly with another gene downstream of egl-30.

egl-30(md186sy676); itr-1 double mutants also did not display significant differences with respect to egg laying compared with egl-30(gf) single mutants. itr-1(sa73) mutants have reduced brood sizes, but the stage of eggs laid by these worms is similar to wild type (Table 3). itr-1(sa73) encodes a C1525Y change in the central modulatory domain (DAL SANTO et al. 1999 ). We did not use a null allele for our analysis since null alleles exhibit a sterile phenotype (DAL SANTO et al. 1999 ). These results indicate that egl-30(gf) can also bypass the requirement for itr-1 with respect to the regulation of egg-laying behavior.

Mutations in the PLCß gene and in genes encoding components described as downstream of PLCß conferred a weak, but insignificant, suppression of the hyperactive egg laying conferred by egl-30(md186sy676) mutations. We conclude that this pathway either is a minor component downstream of EGL-30 or functions completely in parallel to EGL-30 with respect to egg laying.

PLCß is likely a major component downstream of EGL-30 with respect to pharyngeal pumping behavior:
On the basis of defects in pumping exhibited by egl-30(rf) mutants and of expression of egl-30 in the pharyngeal muscle, EGL-30 may act in pharyngeal muscle to regulate pharyngeal pumping behavior (BRUNDAGE et al. 1996 ; Fig 1). Genetic interactions among egl-30 mutations and egl-8(sa47), itr-1(sa73), and unc-13(e51) mutations were also examined with respect to pharyngeal pumping behavior (Table 4). In contrast to the insignificant effect of these mutations on the constitutive egg-laying behavior conferred by egl-30(gf) mutations, the interaction of these mutations on the hyperactive pumping exhibited by egl-30(md186 sy676) mutations is clear.

egl-30(md186sy676); egl-8(sa47) double mutants exhibited a pharyngeal-pumping rate that is similar to egl-8(sa47) single mutants, suggesting that EGL-8 could be a primary effector for EGL-30. unc-13(e51) suppressed pharyngeal pumping to a similar extent as egl-8(sa47), suggesting that these genes function in a common pathway. itr-1(sa73) exhibits the most severe pumping defect and accordingly exhibits the strongest suppression of egl-30(md186sy676). The stronger effect of the itr-1 mutation on pumping rate, compared with egl-8 mutations, may reflect the fact that ITR-1 responds to other receptor pathways, such as the EGF receptor, LET-23 (CLANDININ et al. 1998 ; BUI and STERNBERG 2002 ). We also investigated the genetic interactions between egl-30(md186) and egl-8(sa47) or unc-13(e51) and found that double mutants exhibited a roughly additive decrease in overall pharyngeal pumping rate compared with single mutants. If egl-8(sa47) completely lacks EGL-8 activity, and EGL-8 is the only direct effector for egl-30, then double mutants are expected to exhibit a phenotype not more severe than that of egl-8 single mutants. Consequently, we believe that although EGL-8 could represent the primary effector for EGL-30 with respect to the regulation of pharyngeal pumping, it is likely that there are also other minor downstream effector molecules involved with the regulation of this behavior.

Analysis of egl-8 alleles:
egl-8(sa47) is believed to represent the null allele of egl-8 since it encodes a Q85Term change in exon 2 (LACKNER et al. 1999 ). However, the egg-laying defect exhibited by egl-8(sa7) mutants is not as severe as the defect exhibited by egl-8(n488) mutants (Table 3). Furthermore, egl-8(sa47) responds to the stimulation of egg-laying behavior by 5-HT and egl-8(n488) does not (Table 2). The weaker defects exhibited by egl-8(sa47) mutants might be explained by the presence of alternative downstream transcriptional initiation sites or by readthrough past the termination codon. In this case, egl-8(n488) mutants might better represent the null phenotype of egl-8. The endpoints of the deletion in egl-8(n488) (see Fig 4) predict exons 10 and 11 are deleted, thus disrupting the reading frame (MILLER et al. 1999 ). Exons 10 and 11 correspond to a portion of the region between the catalytic X and Y domains, and it is possible that a protein of altered function is produced. To examine the molecular nature of the egl-8 alleles, we performed Western analysis using the three mutant alleles of EGL-8 that were used in this study.

View larger version (10K): In this window In a new window Download PPT slide   Figure 4. Gene and protein domain structure of EGL-8. (A) Exon/intron structure, starting with the first ATG and ending with the stop codon within a coding region that extends >22,164 bp. Numbered exons are exons that have been shown to be alternatively spliced (MILLER et al. 1999 ). The solid line indicates the region deleted in egl-8(n488). The egl-8(n488) deletion extends from an intron 212 bp after exon 9 to an intron 434 bp after exon 11 (MILLER et al. 1999 ; and see MATERIALS AND METHODS). The catalytic X domain is contained within exons 6–8, and the catalytic Y domain is contained within exons 12–13. (B) Domain structure of EGL-8, encoded by 1431-amino-acid residues. The egl-8(n488) deletion extends between the X and Y catalytic domains, and the deleted region is indicated by the solid line. () The position of mutations encoding early termination codons in sa47 (LACKNER et al. 1999 ) and md1971 (MILLER et al. 1999 ). The position of the md1971 mutation is slightly different within the context of the protein domain structure from what was previously predicted.

Consistent with the hypothesis that egl-8(sa47) represents a null allele, Western analysis using a carboxy-terminal antibody produced against residues 1041–1382 (MILLER et al. 1999 ) indicated that the extracts obtained from the egl-8(sa47) mutants did not contain EGL-8 or contained undetectable amounts of the complete protein (Fig 5). The faint band present in egl-8(sa47) extracts that migrates slightly faster than the EGL-8 band is also present in egl-8(n488) extracts. It is also present, but partially obscured, in N2 and unc-13 extracts. Furthermore, extracts from egl-8(sa47) did not contain any additional smaller bands compared with N2, egl-8(n488), or unc-13 mutant extracts, indicating that egl-8(sa47) mutants do not produce protein from an alternative downstream start site.

View larger version (81K): In this window In a new window Download PPT slide   Figure 5. Western analysis of egl-8 mutant protein extracts. Arrow indicates the band present from N2 and unc-13 mutant extracts but not from egl-8(n488) or egl-8(sa47) mutant extracts.

An extra band also was not present in egl-8(n488), consistent with antibody staining of whole worms described previously (MILLER et al. 1999 ). The differences in response of egl-8(n488) and sa47 and md1971 mutants to 5-HT in egg-laying assays suggested that the egl-8(n488) allele is neomorphic, so we determined the molecular lesion of n488 and inferred the effect on the reading frame in egl-8(n488) mutants on the basis of deletion endpoints. We found that fusion of exons 9–12 would produce a termination codon at amino acid residue 681, just 44 amino acids after the last amino acid encoded in exon 9. Therefore, the hypothesis that egl-8(n488) encodes the truncated protein of altered function, that it contains an X domain but not a Y domain, and that it is not recognized by the EGL-8 antibody to the carboxyl terminus is possible.

Like egl-8 null mutants, unc-13 mutants also exhibit a response to serotonin in egg-laying assays that is comparable to wild type (Table 2). This result lends support to a hypothesis that egl-8 functions in a linear pathway with unc-13 to regulate egg laying. Unlike loss of EGL-30-regulated response pathways, loss of EGL-8- or UNC-13-mediated regulation of egg laying does not interfere with serotonin response. In fact, cha-1 mutants also exhibit increased sensitivity to serotonin (SCHAFER et al. 1996 ), lending support to the notion that acetylcholine response pathways are directly coupled to egl-8 and unc-13 with respect to egg laying.

egl-30 function in vulval muscle:
Our expression analysis revealed only rare expression of egl-30 in the vulval muscles (evident in 10% of adult animals). We sought to determine whether the low expression levels reflected a true site-of-action for egl-30 in the vulval muscles. Vulval muscle expression of egl-8 has not been previously reported and to facilitate the interpretation of our double-mutant analysis, we wanted to determine whether EGL-8 might have a site-of-action in the vulval muscles. The egg-laying system of C. elegans consists of the vulval muscles with direct innervation from two classes of motor neurons, the VCs and the HSNs (WHITE et al. 1986 ; DESAI et al. 1988 ). Dominant mutations in egl-1 cause the cells that would normally be destined to become the HSN motor neurons to undergo programmed cell death (ELLIS and HORVITZ 1986 ). In wild-type hermaphrodites, genetic ablation of the HSNs, via egl-1 mutations, causes worms to lay eggs at a very late stage of development (TRENT et al. 1983 ; ELLIS and HORVITZ 1986 ; DESAI and HORVITZ 1989 ). Ablation of the VC4 and VC5 motor neurons alone does not have a drastic effect on egg-laying behavior (GARRIGA et al. 1993 ; WAGGONER et al. 1998 ). However, laser ablation of the VC4 and VC5 motor neurons of egl-1 hermaphrodites during the L4 larval stage further compromises egg-laying behavior and animals do not respond to the neurotransmitter 5-HT (WAGGONER et al. 1998 ), normally a strong stimulator of egg-laying behavior (HORVITZ et al. 1982 ; TRENT et al. 1983 ). Egg laying can be rescued in egl-1 animals that have ablated VC4 and VC5 motor neurons with the exogenous addition of both serotonin and levamisole (WAGGONER et al. 1998 ).

egl-30 reduction-of-function mutants exhibit a reduced response to serotonin in egg-laying assays (TRENT et al. 1983 ; BRUNDAGE et al. 1996 ). Like other egl-30 reduction-of-function mutants, egl-30(md186) displayed a reduced response to serotonin (Table 2). On the basis of the neuron ablations described above, if nervous system but not muscle function is compromised in egl-30 mutants, then reduction-of-function mutants should respond to serotonin and levamisole in egg-laying assays. In contrast to animals that lack the motor neurons that innervate the vulval muscle, egg laying was not restored in egl-30(md186) mutants or in the stronger reduction-of-function mutant, egl-30(ad805) (data not shown) when treated with exogenous serotonin and levamisole (Table 2). Like egl-30 mutants, egg laying was not rescued in egl-8(n488) mutants with serotonin and levamisole (Table 2), also indicating a previously unsuspected role for EGL-8 in vulval muscle (Table 2).

Two simple possibilities could explain the reduced response of egl-30 and egl-8 mutants to serotonin and levamisole. First, egl-30 and egl-8 might have a cell-autonomous site of action in the vulval muscle. Second, when function of the protein is reduced throughout development, muscle development or function might be compromised. However, the actin structure of egl-30 mutants appears to be intact on the basis of phalloidin staining (Fig 6). Also, the contractile apparatus of the pharyngeal muscle in the putative null mutant, egl-30(ad810), is still functional, on the basis of the ability of the pharyngeal muscle to contract in response to laser stimulation of the plasma membrane (BRUNDAGE et al. 1996 ). We conclude that the function of the muscle is more likely compromised with respect to the ability to transduce a signal.

View larger version (77K): In this window In a new window Download PPT slide   Figure 6. Tetramethyl rhodamine isothiocyanate-phalloidin staining of N2 and egl-30 (ad805) adults to visualize actin filaments. Staining was performed as described in MATERIALS AND METHODS. BM, body-wall muscle; VM, vulval muscle. Bars, 10 µm. (A) The vulval muscle structure of a wild-type hermaphrodite, lateral view. (B) The vulval muscle structure of an egl-30(ad805) mutant, ventral view.

egl-30(md186sy676) cannot bypass the requirement for serotonin with respect to egg laying:
Serotonin is the primary neurotransmitter that potentiates egg laying (DESAI and HORVITZ 1989 ) and egl-30(rf) mutants are resistant to the effects of serotonin in egg-laying assays (Table 2). Thus, egl-30(rf) mutants might be resistant to the effects of serotonin either because EGL-30 couples to a serotonin receptor or because EGL-30 is involved with response or release of serotonin from the motor neurons that innervate the vulval muscles. In mammals, -methyl 5-HT stimulates 5-HT₂ receptor subtypes (RICHARDSON et al. 1985 ; ISMAIEL et al. 1990 ) that can couple to mammalian G_q (SEUWEN et al. 1988 ; LAUNAY et al. 1996 ). On the basis of stimulation by -methyl 5-HT, 5-HT₂ receptors have been shown to mediate tonic firing in pyramidal neurons of the rat prefrontal cortex (ZHANG 2003 ).

To investigate whether a receptor that exhibits a similar pharmacological response exists in C. elegans, we tested the response of worms to -methyl 5-HT in egg-laying assays. We found that wild-type worms exhibited a robust response to -methyl 5-HT (Table 5B). In contrast, egl-30(md186) mutants did not respond to this agonist (Table 5B). egl-30(md186sy676) mutants cannot be accurately tested since they immediately laid eggs when placed in water, and the activity of this agonist is inhibited in M9, similar to dopamine and dopamine antagonists (WEINSHENKER et al. 1995 ). However, egl-30(md186sy676); egl-1 double mutants exhibited a similar or higher response to -methyl 5-HT compared with egl-1 single mutants (Table 5B). We then compared the response to 5-HT and -methyl 5-HT of syIs36, a strain that overexpresses wild-type egl-30. As shown in Table 5A and Table 5C, syIs36 exhibited similar responses to both -methyl 5-HT and 5-HT as egl-30(md186sy676) mutants. These results suggest that EGL-30 mediates response to a 5-HT₂-type receptor to regulate egg laying. Finally, on the basis of the observation that a response was elicited from egl-1 mutants, we conclude that an -methyl 5-HT-responsive receptor functions either in a VC-dependent neuronal pathway or in the vulval muscle.

If, as we propose, serotonin is required for EGL-30-induced egg-laying behavior, then egl-30(md186sy676) mutants that lack endogenous serotonin should not exhibit constitutive egg laying. To further test this hypothesis, we analyzed epistasis between egl-30(gf) and tph-1(lf) mutants. tph-1(mg280) mutants lack detectable serotonin because of a defect in tryptophan hydroxylase, an enzyme involved in serotonin biosynthesis (SZE et al. 2000 ). tph-1 mutants lay late-stage eggs (SZE et al. 2000 ), but tph-1 mutants were not as defective in egg laying as egl-1 mutants (Table 6). egl-30(gf); tph-1 double mutants displayed an egg-laying defect that is similar to tph-1 single mutants. This result suggests a direct linear pathway between serotonin response and EGL-30 function and indicates that egl-30(md186sy676) cannot bypass the requirement for serotonin with respect to egg-laying behavior. However, tph-1 mutants were not as defective in egg laying as egl-30 mutants (Table 1 and Table 6B). Consistent with the partial suppression of egl-30(md186sy676) by unc-13 (Table 3), acetylcholine may represent another minor regulatory pathway associated with egl-30 (see DISCUSSION).

The HSNs are the primary serotonergic motor neurons that regulate egg laying. Accordingly, egl-1 mutants exhibit a severe egg-laying defect. However, egl-1 single mutants exhibit a more severe egg-laying defect than do egl-30(gf); egl-1 double mutants (Table 6A), indicating that EGL-30 can partially bypass the requirement for the HSNs. This result is evident even with the stronger gain-of-function allele, egl-30(tg26), that does not contain the egl-30(md186) mutation in the background. Epistasis with tph-1, but not with egl-1, is likely due to the fact that the VC motor neurons are also known to be weakly serotonergic (DUERR et al. 1999 ). We infer that egl-30 does function in or via the HSN motor neurons. However, since EGL-30 can partially bypass the HSN neurons, a role for egl-30 either in the VC motor neurons or in the muscle is indicated.

	DISCUSSION

TOP ABSTRACT MATERIALS AND METHODS RESULTS DISCUSSION LITERATURE CITED

The expression pattern reported here indicates that egl-30 is broadly expressed, consistent with its pleiotropic function. Similarly, vertebrate G_q and G₁₁, two members of the G_q family that share 88% sequence identity with one another, are coexpressed in almost every cell type (WILKIE et al. 1991 ). The other G_q subunits are expressed in a more restricted pattern (AMATRUDA et al. 1991 ; WILKIE et al. 1991 ). Like C. elegans EGL-30, the vertebrate G_q family is required for viability since targeted disruption of both G_q and G₁₁ results in embryonic lethality at embryonic day 11 (OFFERMANNS and SIMON 1998 ).

The expression pattern of egl-30 suggests that EGL-30 functions in many cell types and likely has a role throughout development. As larval development begins and progresses, we found that expression levels of egl-30 generally increased with the highest expression in L4 larvae and adult animals. Its earliest role in development was previously presumed to be during larval development since mutations that should abort translation at Trp212 or Trp259 (ad810 and ad813) arrest at various stages during larval development (BRUNDAGE et al. 1996 ). However, the rolling movement of embryos during embryonic elongation was found to be indistinguishable from wild type, and some of these animals were also able to develop to semifertile adults (BRUNDAGE et al. 1996 ). We speculate that since embryos express only low levels of egl-30, low levels of translational readthrough (as indicated by the ability of some animals to develop into adults) or maternal rescue from heterozygous mothers is sufficient to rescue embryonic development. We also speculate that the general increase in expression levels of egl-30 during larval development, revealed by the GFP fusion transgene, reflects a requirement for increased activity levels as animals develop. This hypothesis is supported by the larval arrest phenotype exhibited by egl-30(ad810 and ad813) mutants.

Expression and site of action of egl-30:
In L4 larvae and in adult animals, egl-30 is expressed at highest levels in the nervous system and then in the pharyngeal muscle. In spite of the rare expression observed in the vulval muscle, the pharmacological response of egl-30 mutants in egg-laying assays indicates that EGL-30 also functions in the vulval muscle. Antibody staining also revealed consistent expression in the anal sphincter muscle, which is consistent with a weak defect that egl-30 reduction-of-function mutants exhibit with respect to defecation (MILLER et al. 1996 ). Rare expression was also observed in the head muscles and in body wall muscle, and the role for egl-30 in these tissues remains to be explored.

Initial analysis regarding the site of action for EGL-30 indicated that EGL-30 has a general site of action in the muscle, i.e., pharyngeal, vulval, or uterine, and in the body (BRUNDAGE et al. 1996 ). Specifically, ablation of the pharyngeal neurons, with the exception of the essential M4 neuron, suggests that egl-30 functions in the muscle with respect to the suppression of gpb-2-induced arecoline hypersensitivity (BRUNDAGE et al. 1996 ). LACKNER et al. 1999 later found that overexpression of constitutively active EGL-30, EGL-30(QL), in the motor neurons of the ventral cord is sufficient to alter the locomotion of wild-type animals and results in enhanced sensitivity to the acetylcholinesterase inhibitor, aldicarb (LACKNER et al. 1999 ). On the basis of expression pattern, HSN ablations, and pharmacological analysis with egl-30 mutants, we found that egl-30 likely acts in or via neurons and in muscle during egg laying.

However, our unpublished experiments suggest that C. elegans is not tolerant to overproduction of egl-30 in muscle cells, on the