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1 June 2016 Multiple Neuropeptide-Coding Genes Involved in Planarian Pharynx Extension
Seira Shimoyama, Takeshi Inoue, Makoto Kashima, Kiyokazu Agata
Author Affiliations +

Planarian feeding behavior involves three steps: moving toward food, extending the pharynx from their planarian's ventral side after arriving at the food, and ingesting the food through the pharynx. Although pharynx extension is a remarkable behavior, it remains unknown what neuronal cell types are involved in its regulation. To identify neurons involved in regulating pharynx extension, we quantitatively analyzed pharynx extension and sought to identify these neurons by RNA interference (RNAi) and in situ hybridization. This assay, when performed using planarians with amputation of various body parts, clearly showed that the head portion is indispensable for inducing pharynx extension. We thus tested the effects of knockdown of brain neurons such as serotonergic, GABAergic, and dopaminergic neurons by RNAi, but did not observe any effects on pharynx extension behavior. However, animals with RNAi of the Prohormone Convertase 2 (PC2, a neuropeptide processing enzyme) gene did not perform the pharynx extension behavior, suggesting the possible involvement of neuropeptide(s in the regulation of pharynx extension. We screened 24 neuropeptide-coding genes, analyzed their functions by RNAi using the pharynx extension assay system, and identified at least five neuropeptide genes involved in pharynx extension. These was expressed in different cells or neurons, and some of them were expressed in the brain, suggesting complex regulation of planarian feeding behavior by the nervous system.


Observation of the feeding behavior of the freshwater carnivorous planarian Dugesia japonica revealed that this behavior can be divided into three major processes: moving toward the food source (Chemotaxis, Fig. 1A), extension of the pharynx (pharynx extension, Fig. 1B), and ingestion of food through the extended pharynx (ingestion, Fig. 1C) (Pearl, 1903; Inoue et al., 2015). Some amino acids induce Chemotaxis in planarian (Coward and Johannes, 1968; Ash et al., 1973; Miyamoto and Shimozawa, 1985). However, although the structure and regeneration of the pharynx have been studied extensively (Kobayashi et al., 1998, 1999; Adler et al., 2014), planarian feeding behavior has not been analyzed.

The planarian central nervous system (CNS) has been extensively studied in recent years and its regeneration process is also well characterized (Cebrià et al., 2002; Agata et al., 2008; Umesono et al., 2011). The planarian CNS is composed of two morphologically distinct structures: an inverted U-shaped bi-lobed brain with nine lateral branches on each outer side, and a pair of two longitudinal ventral nerve cords (VNCs) ( Supplementary Figure S1 (10.2108.zsj.33.311.s1.pdf); Agata et al., 1998). Combinations of planarian behavior assay systems and RNAi experiments have identified neurons involved in particular behaviors, such as movement, phototaxis and thermotaxis (Inoue et al., 2004; Takano et al., 2007; Nishimura et al., 2008b; Inoue et al., 2014). A negative phototactic behavior assay demonstrated that two neuropeptide-coding genes, 1020HH and eye53, are essential for the recovery of negative phototactic behaviors during regeneration (Inoue et al., 2004). It has also been shown that GABAergic neurons, which may connect with visual center neurons in the brain, are indispensable for negative phototaxis in planarians (Nishimura et al., 2008b; Akiyama et al., unpublished data). A thermosensing behavior assay system revealed that brain serotonergic neurons connected to transient receptor potential (TRP)-positive thermosensing neurons are required for planarian thermotaxis (Inoue et al., 2014). Dopaminergic neurons and serotonergic neurons are likewise essential for regulating normal movement behaviors (Nishimura et al., 2007a; Currie and Pearson, 2013). A combination of RNAi and behavior assays would thus appear to be useful for investigating genes and neural circuits regulating planarian behaviors.

Fig. 1.

Planarian feeding behavior consists of three steps. (A) Chemotaxis: Planarians move to food (chicken liver). (B) Pharynx extension: Planarians extend their pharynx from the ventral side of the body after arriving at food. Pharynx is indicated by a black arrow. (C) Ingestion: Planarians ingest food via the pharynx. The color of the intestinal duct changes to red (the color of the food, black arrow).


Our group previously reported that brain activity is required for the chemotactic behavior in planarian (Inoue et al., 2015), but although pharynx extension is one of the most fundamental planarian behaviors, the mechanisms underlying this behavior are not well elucidated at the cellular and molecular levels. In the present study, we sough to to identify neurons involved in regulating pharynx extension through a quantitative pharynx extension assay and RNAi experiments.



A clonal asexual strain (SSP) of Dugesia japonica was used for all experiments (Asami et al., 2002). Planarians were bred in water containing 0.05 g/L artificial seawater (Instant Ocean, VA, USA) at 24°C. They were fed chicken liver once a week. Six- to 8-mm-long planarians that had been starved for 7–9 days were used for all experiments. For regeneration analysis, planarians were amputated on wet filter paper on ice. All planarians were maintained and manipulated according to a protocol approved by the Animal Care and Use Committee of Kyoto University.

Behavior assay

Liver extract was prepared as previously reported (Inoue et al., 2015). For the novel pharynx extension behavior assay devised here, planarians were put into a small linear chamber (2 mm wide × 0.5 mm deep) filled with their breeding water ( Supplementary Figure S2A (10.2108.zsj.33.311.s1.pdf)), and then 5 µL of 10-fold diluted chicken liver extract was placed in front of them ( Supplementary Figure S2A (10.2108.zsj.33.311.s1.pdf)). To visualize the pharynx extension, planarian behavior was recorded using a video camera from underneath the chamber by using a mirror, as illustrated in  Supplementary Figure S2A (10.2108.zsj.33.311.s1.pdf). Usually, 12 planarians were used in one series of experiments, and the number of planarians extending their pharynx was counted after video recording. We conducted 3–6 repetitions of each experiment to obtain statistically reliable results. The number of individuals that extended their pharynx was counted (number of degrees of freedom = 1). The results were shown as the average pharynx extension rate in the total experiments, and the standard error of the mean (s.e.m.) among experiments.

For the primary feeding behavior assay, 10 planarians were put at the edge of a 90-mm-diameter Petri dish, and a slice of chicken liver was placed in the center of the dish ( Supplementary Figure S2B (10.2108.zsj.33.311.s1.pdf)). At 20 minutes, the planarians which had arrived at the food and started to ingest it were counted.

For evaluation of the planarians' locomotor activity, the distance that planarians moved during a test period (5 min) was recorded while they moved randomly in the chamber (10 × 60 mm), and the distance moved was measured with behavior analysis software (SMART) (Panlab, Spain).

RNA interference

Double-stranded RNA (dsRNA) synthesis and RNAi treatment were performed according to Shibata et al. (2012) and Rouhana et al. (2013). For the pharynx-extension assay, planarians were fed dsRNA-containing food twice and also injected with dsRNA dissolved in H2O to fill their intestinal ducts every three days using a microinjector (Drummond Scientific Nanoject injector, Broomall, PA, USA). Nine days after amputation, planarians were used for behavior assay and real-time RT-PCR. For negative controls, planarians were injected with dsRNA coding for green fluorescent protein (GFP), a gene that is not found in planarians. cDNA sequences for the following genes were obtained from the DDBJ/EMBL/GenBank databases: TH, tyrosine hydroxylase, a gene encoding an enzyme limiting dopamine synthesis, AB266095 (Nishimura et al., 2006); TBH, tyramine ß-hydroxylase, a gene encoding an enzyme limiting serotonin synthesis, AB362394 (Nishimura et al., 2008a); TPH, tryptophan hydroxylase, a gene encoding an enzyme limiting octopamine synthesis, AB288367 (Nishimura et al., 2007b); ChAT, choline acetyltransferase, a gene encoding an enzyme limiting acetylcholine synthesis, AB536929 (Nishimura et al., 2010); GAD, glutamic acid decarboxylase, a gene encoding an enzyme limiting GABA synthesis, AB332029 (Nishimura et al., 2008b); glutaminase, a gene encoding an enzyme limiting glutamic acid synthesis, BAG16389 (Higuchi et al., 2008); synaptotagmin (syt), BAA85622 (Tazaki et al., 1999); and Prohormone convertase 2 (PC2), AK388877 (Agata et al., 1998). To induce effective gene knockdown, we used planarians after head amputation (Sánchez Alvarado and Newmark, 1999; Takano et al., 2007).

Cloning of genes coding for neuropeptide precursors of D. japonica

Partial or full-length sequences of neuropeptide genes, putative orthologs of neuropeptide genes in other planarian species (Collins et al., 2010), were obtained from our EST database (Nishimura et al., 2012) and transcriptome database (Kashima et al., unpublished) of D. japonica. To clone these genes, we performed PCR using specific primers ( Supplementary Table S1 (10.2108.zsj.33.311.s1.pdf)) corresponding to the planarian sequences of interest using cDNA derived from intact planarians (Yazawa et al., 2009). These PCR fragments were cloned using pCR II plasmid (Invitrogen, CA, USA).

In situ hybridization

Digoxigenin-labeled antisense RNA probes were prepared and whole-mount in situ hybridization was performed as described previously (Agata et al., 1998; Tasaki et al., 2011).

To clearly detect signals in the pharynx, the pharynx was amputated from the planarian body on ice, and then fixed and hybridized with the probe of interest. The in situ hybridization of the isolated pharynx was performed using a modification of the protocol for whole-mount in situ hybridization as follows: fixation for 10 min, no decoloring or hydration, treatment with 5 µg/mL proteinase K for 10 min, re-fixation for 10 min and hybridization with probes for 16 hours. Photographs were taken using a Leica M205FA microscope (Leica Microsystems, Germany).

For observation of transverse sections, after detection of in situ hybridization signals of whole-mount planarians or of the isolated pharynx, the samples were fixed with 1% glutaraldehyde in PBS for one hour and subsequently cut transversely.

To distinguish the dorsal- and ventral-side in transverse sections, whole-mount planarians were incubated with 10 µg/ml Hoechst 33342 (Thermo Fisher Scientific) in PBS and then fixed with 1% glutaraldehyde in PBS for one hour, and subsequently these planarian samples were cut transversely. The in situ hybridization signals of the sections were detected using an Olympus BX62 microscope. In these transverse sections, the ventral nerve cords (VNCs) did not show any Hoechst 33342 staining signals because the VNCs consisted only of axons.

Semi-quantitative RT-PCR analysis

Reverse transcription was carried out using total RNA from six planarians at nine days post-amputation using a Quantitect Reverse Transcription kit (Qiagen, Netherlands). Semi-quantitative-PCR (qPCR) was performed as reported previously (Yazawa et al., 2009) using the primers listed in  Supplementary Table S2 (10.2108.zsj.33.311.s1.pdf). The expression level of genes in GFP(RNAi) planarians was taken as = 1. Measurements were performed four times for technical replicates and three times for biological replicates and were normalized by the expression level of DjEF-1, D49924 (Mineta et al., 2003).

Statistical analysis

The statistical significance of differences between pharynx extension rate test results was determined by the chi-square test; p values greater than 0.05 were taken as not significant (NS) when examining the total value obtained from several experiments. The statistical significance of differences was evaluated by comparison with the value in intact animals in amputation assays, and by comparison of the value in GFP(RNAi) planarians with the value in other RNAi planarians in other assays.

The statistical significance of differences between untreated planarians and RNAi planarians in the distance-moved and qPCR assays was determined by the Steel test after F-tests for the equality of variances: p values greater than 0.05 were taken as not significant (NS).

Data deposition

Neuropeptide cDNA sequences were deposited in DDBJ/ EMBL/GenBank databases with the accession numbers listed in Table 4.


Quantitative observation of planarian pharynx-extension

To determine the optional dilution of liver extract for use in the pharynx-extension assay, one of a range of dilutions, including undiluted extract, was put into the chamber in front of a planarian, and the number of pharynx-extending planarians was counted in three experiments and shown as the pharynx extension rate ( Supplementary Table S3 (10.2108.zsj.33.311.s1.pdf)). Dilutions of liver extract in the range between undiluted and 1:10 diluted liver extract induced pharynx extension in more than 85% of planarians on average. However, undiluted liver extract induced not only pharynx extension but also ingestion in some cases (data not shown). We thus used 1:10 diluted liver extract in further analyses of pharynx extension.

Pharynx extension requires the head region

In order to investigate how the pharynx extension is regulated, the pharynx-extension assay was performed using planarians cut into several fragments. It had been thought that the planarian might extend its pharynx in response to liver extract using the nerve ring of the tip of the pharynx ( Supplementary Figure S1 (10.2108.zsj.33.311.s1.pdf) ; Tazaki et al., 1999; Okamoto et al., 2005). We therefore tested pharynx extension using intact, head-less (head amputated) and tail-less (tail amputated) planarians at three hours after amputation. Unexpectedly, the head-less planarians never extended their pharynx at all (Table 1), suggesting that pharynx extension requires the head, and that the pharynx by itself cannot be extended as a reflex movement. Tail-less planarians extended the pharynx normally, like intact planarians, suggesting that simple amputation of the nervous system does not affect pharynx extension.

Next, we closely observed the process of recovery of pharynx-extension ability during regeneration after head amputation. Pharynx-extension ability was gradually recovered in head-less planarians during head regeneration (Fig. 2, open circles). At day 5, half of the head-less planarians undergoing head regeneration had recovered pharynx-extension ability, and most of them had recovered this ability by seven days after amputation.

Monoaminergic and amino acidergic neurons may not be involved in pharynx extension

Previous studies identified six types of monoaminergic neurons (dopaminergic, octopaminergic, serotonergic and cholinergic) and amino acidergic neurons (GABAergic and glutamatergic) in planarian based on their expression of the gene for a rate-limiting enzyme for the respective neurotransmitter (Nishimura et al., 2007a, b, 2008a, b, 2010). To identify the subtype of brain neurons involved in pharynx extension, we analyzed the possible functions of these monoaminergic and amino acidergic neurons by combinatory analysis using the pharynx-extension assay system and RNAi. Unexpectedly, none of these six types of RNAi-treated planarians showed any statistically significant effects on pharynx extension (Table 2). There was almost no difference in the results of three independent experiments. The efficiency of RNAi was tested by qPCR ( Supplementary Figure S3A (10.2108.zsj.33.311.s1.pdf)). Significant reduction of the TPH and ChAT genes was not observed, so we could not exclude the possibility that TPH and ChAT are related pharynx extension. Although the locomotion activity in planarians treated with RNAi against for each of these genes was unaffected (Table 2), GAD(RNAi) planarians did show defects in phototactic behavior, in agreement with previously reported findings (data not shown) (Nishimura et al., 2008b). These results suggested that dopamine-, octopamine-, GABA- and glutamic acid-producing neurons may be not involved in pharynx extension.

Table 1.

Pharynx extension rate of amputated planarians. **, P < 0.005. t = 120 sec; n = 43 or 44.


Fig. 2.

Recovery of pharynx-extension ability during 0–14 days after amputation. The statistical significance of differences of the pharynx-extension rate was determined between the data of intact planarians at Day 0 to Day 14, and the data of head-less fragments of planarians on each of the respective days. *, P < 0.05; **, P < 0.005; NS, not significantly different; t = 120 sec; n (number of animals) = 16–20.


Table 2.

Pharynx extension rate of planarians with RNAi of the genes coding for limiting enzymes for synthesis of monoamine and amino acid neurotransmitters, t = 120 sec; n = 31–72. Distance moved, t = 300 sec; n = 11–24.


Table 3.

Pharynx extension rate of syt(RNAi) and PC2(RNAi) treated planarians. **P < 0.005; t = 120 sec; n = 55–60. Distance moved. **P < 0.005; t = 300 sec; n = 12–60.


Neuropeptide-producing neurons may be involved in pharynx extension

Given this surprising result, what types of neurons are involved in the regulation of pharynx extension? We conducted RNAi experiments of two pan-neural genes, the syt and PC2 genes, and confirmed the reduction of the level of the target mRNAs by qPCR ( Supplementary Figure S3B (10.2108.zsj.33.311.s1.pdf)). Although both of these genes are widely expressed in the CNS and are used as pan-neural markers, it has been reported that syt(RNAi) and PC2(RNAi) respectively do not accumulate in small synaptic vesicles or large neurosecretory vesicles in presynaptic regions (Oosaki and Ishii, 1965; Takeuchi et al., unpublished observation). syt(RNAi) planarians showed almost normal pharynx-extension behavior, and the locomotion activity of syt(RNAi) planarians was unaffected (Table 3). In contrast, pharynx extension was dramatically reduced in PC2(RNAi) planarians (Table 3). The enzyme PC2 is known to be involved in the first step of processing neuropeptide precursors to mature forms in pig and many other species (Seidah et al., 1992; Zhou et al., 1999). The active site sequence of PC2 family proteins is conserved in the predicted planarian PC2 protein, although no direct functional analysis has been reported in planarian. The reduction of pharynx extension of PC2(RNAi) planarians suggested that neuropeptide-producing neurons may be involved in pharynx extension.

Neuropeptide-coding genes in D. japonica

Next, we searched for genes coding for neuropeptides and peptide-hormones in our EST database and in our transcriptome database that was obtained by next-generation sequencing using a Roche 454 system (Nishimura et al., 2012; Kashima et al., unpublished). The DNA sequence data of genes that had been identified as genes coding for neuropeptides and peptide-hormones of another planarian species, Schmidtea mediterranea (Collins et al., 2010), were used as queries for BLAST searches. The amino acid sequences of BLAST hits were compared, and conservation of landmark sequences of neuropeptides, such as GKR and signal peptides, was confirmed (Table 4). We identified 21 neuropeptide and peptide-hormone coding genes from D. japonica as homologs of related genes in S. mediterranea. Two of these cDNA clones (Dj_aH_019_P02 and Dj_aH_401_P19) were found in our EST library (Nishimura et al., 2012). The remaining 19 cDNA clones were obtained by PCR using specific primers ( Supplementary Table S1 (10.2108.zsj.33.311.s1.pdf)). We also added the following genes, which had previously been identified in our laboratory as neuropeptide-coding, to the list of neuropeptide genes: 1020HH (Inoue et al., 2004), eye53 (Inoue et al., 2004) and Dj_aH_308_M24 (Takatsu et al., unpublished data). A total of 24 neuropeptide-coding genes were thus taken to be candidates for further analysis as putative neuropeptide neurons involved in pharynx extension (Table 4).

Candidate genes possibly involved in feeding behavior were narrowed down using a simple assay

In order to select from the above 24 candidates, we utilized a simple feeding-behavior assay using planarians treated with RNAi for each candidate gene. Ten RNAi-treated planarians were placed at the periphery of a Petri dish (90 mm diameter), and a piece of chicken liver was placed at the center of the dish ( Supplementary Figure S2B (10.2108.zsj.33.311.s1.pdf)). The number of planarians that started eating the food was counted after 20 minutes. Of the 24 candidate genes, we selected the 13 genes that caused reduction of feeding activity to < 60% of the control level in this assay as candidates for secondary screening ( Supplementary Figure S4 (10.2108.zsj.33.311.s1.pdf)).

Identification of five genes as genes required for pharynx extension

After thus narrowing the field of D. japonica neuropeptide-coding gene candidates to 13, we used these to conduct a full pharynx-extension assay using RNAi planarians nine days after amputation (Table 5,  Supplementary Figure S3C (10.2108.zsj.33.311.s1.pdf)). The five candidates (Dj_aH_308_M24 (DjNpM24), Dj_aH_019_P02 (DjNpP02), DjNp19, DjNp42 and DjNp47) causing a statistically significant effect (P < 0.005) were selected as genes putatively required for pharynx extension, and subjected to further analyses to identify the cells/neurons in which they are expressed (Table 5). Importantly, there was almost no difference among the results of several independent experiments (Table 5). We did not observe any significant defect in locomotion ability in any of these five RNAi-treated planarians (Table 5).

Table 4.

Neuropeptide-coding genes reported previously and newly identified here in D. japonica.


Table 5.

Identification of genes required for pharynx extension. *P < 0.05; **P < 0.005; t = 120 sec; n = 54–131. Distance moved. **P < 0.005; t = 300 sec; n = 12–108.


Expression patterns of the five neuropeptide-coding genes found to be required for pharynx extension

We then examined the expression patterns of the five neuropeptide-coding genes found to be required for pharynx extension by whole-mount in situ hybridization. To investigate the detailed expression patterns of these genes in the pharynx, we conducted both general whole-mount in situ hybridization and in situ hybridization using the isolated pharynx (see Materials and Methods), since RNA probes sometimes did not soak into the pharynx in whole-body specimens. Ventral views of whole-mount in situ hybridization staining of planarians are shown in Fig. 3A. Figure 3B shows the whole-mount in situ hybridization staining patterns of the corresponding isolated pharynxes.

DjNpM24- and DjNp19-positive in situ hybridization signals were detected in a minor population of CNS cells, including in the brain. Higher-magnification views of DjNpM24 and DjNp19 signals in the head region are shown in Fig. 3C. Expression of DjNp19 was not detected in the pharynx, while DjNpM24-positive cells were detected in the pharynx, in addition to the CNS. The number of DjNpM24-positive cells was larger in the distal part of the pharynx than in the basal part (Fig. 3B, D). In the case of DjNp47, a clear signal was not detected in the whole-mount specimen, but qPCR analysis suggested that DjNp47 may also be expressed in the head and pharynx (Fig. 3E).

In contrast to the expression patterns of the above three genes, DjNpP02-positive cells were detected sparsely in the body surface region (Fig. 3A). Examining the expression pattern of this gene in transverse sections revealed that DjNpP02-expressing cells are present in both the ventral and dorsal sides of the body surface region (Fig. 3D, arrowheads;  Supplementary Figure S5 (10.2108.zsj.33.311.s1.pdf)). DjNp42-expressing cells were detected only in the pre-pharyngeal region of the ventral side, which is defined as the body region between the brain and pharynx, suggesting that DjNp42-positive neurons may be involved in the connection between the brain and pharynx in the ventral side of the body (Fig. 3A, D). The predicted amino acid sequences and the expression patterns of these five genes are summarized in Fig. 4. In conclusion, five genes were identified here as genes involved in regulating pharynx extension, each of which showed a distinct expression pattern, suggesting that the control of pharynx extension may involve a complex neural circuit.

Fig. 3.

Expression pattern analysis of genes encoding neuropeptides involved in pharynx extension. (A) Expression pattern of neuropeptide genes detected by in situ hybridization in the whole body. Ventral views. Scale bar 500 µm. (B) Expression pattern of neuropeptide genes in the pharynx detected by in situ hybridization Scale bar 500 µm. (C) Higher-magnification view of the expression in the head region of the PC2, Dj_aH_308_M24 (DjNpM24) and DjNp19 genes. Scale bar 250 µm. (D) Expression of indicated genes by in situ hybridization in transverse sections of body cut at the pre-pharyngeal region (DjNpM24, DjNpP02 and DjNp42) and in the tip of the pharynx (DjNpM24). Arrowheads indicate DjNpP02-positive cells. Scale bar 250 µm. (E) Relative expression level of DjNp47 measured by qPCR in each indicated portion of the body. Relative expression level of the whole body was taken as = 1. Error bars indicate s.e.m.


Fig. 4.

Predicted amino acid sequences and expression patterns of five putative neuropeptide-coding genes shown in this study to be involved in pharynx extension. (A) Comparison of the predicted peptide(s) between S. mediterranea and D. japonica. Predicted peptide(s) sequence of DjNpM24, DjNpP02, DjNp19, DjNp42 and DjNp47 (each upper line) are aligned with the corresponding predicted peptide sequences (each lower line) of spp-18, spp-19, npp-3, spp-8 and npp-10 in S. mediterranea, respectively (Collins et al., 2010). Amino acid residues in the D. japonica sequence that match those in S. mediterranea are shaded with color. (B) Diagram of expression patterns of four neuropeptide-coding genes in the planarian whole body. Symbols show the expression patterns of the four neuropeptide-coding genes.



In the present study, we focused on pharynx extension behavior in planarian and sought to identify types of neurons involved in the regulation of pharynx extension. Our amputation experiments clearly showed that the head region is indispensable for pharynx extension, suggesting that pharynx extension is regulated by the brain. The time-course of recovery was nearly the same as the reported time-course of recovery of phototactic and thermotactic behaviors from planarian trunk fragments (Inoue et al., 2004, 2014), suggesting that brain function is required for pharynx extension, as it is for other brain-regulated behaviors. Thus, it seems that certain interconnection(s) between the brain and the regenerating pharynx may be necessary for complete recovery of pharynx-extension ability.

To identify neurons in the head region involved in regulating pharynx extension, first we checked the possible involvement of monoaminergic and amino acidergic neurons, since in a previous study we found that certain of these neurons are involved in the regulation of fundamental behaviors, such as negative phototaxis and thermotaxis (Inoue et al., 2004, 2014). However, in the work reported here we did not obtain clear evidence showing that monoaminergic or amino acidergic neurons are involved in pharynx extension. RNAi of syt had almost no effect on pharynx extension in planarians (Table 3), but did inhibit chemotactic behavior (Table 3; Inoue et al., 2015), suggesting that Chemotaxis and pharynx extension might involve different neural regulation.

We found that PC2, an enzyme involved in neuropeptide synthesis in various species (Seidah et al., 1992; Zhoue et al., 1999), is required for pharynx extension, suggesting the possible involvement of neuropeptide-producing neurons in pharynx extension. Fifty-one neuropeptide or peptide hormone-related genes have been reported in another planarian species, S. mediterranea (Collins et al., 2010), and it would thus be very difficult to screen candidate genes from the full set of such genes using our pharynx-extension assay. Thus, we first narrowed down the set of candidate genes by using a simpler “primary feeding behavior assay” that includes chemosensing, pharynx extension, and ingestion. Then we further analyzed 13 of the thus-identified genes using our specific full pharynx-extension assay system. Finally, five candidate genes were identified as involved in pharynx extension, and their expression patterns are summarized in Fig. 4. We concluded that planarian pharynx extension is regulated by a complex system involving a number of different types of neuropeptide-producing cells. Combinatory RNAi of several of these five coding genes may completely suppress pharynx extension in planarian, although we have not yet been able to conduct this experiment due to technical issues.

We cannot exclude the possibility that other neurons contribute the regulation of the pharynx extension in planarians. Recently, nearly the entire genome sequence of the planarian D. japonica was reported (Nishimura et al., 2015), and we expect to discover additional neuropeptide-coding genes using this genome sequence information.

In the case of mammals, several neuropeptides, such as neuropeptide Y (NPY), orexin and galanin, were identified as neuropeptides that promote feeding (Arora and Anubhti, 2006). It is well known that neuropeptide Y (NPY) is a highly conserved neuropeptide that promotes feeding in both invertebrate and vertebrate species (Stanley and Leibowitz, 1985; Blomqvi et al., 1992; Matsuda, 2009; Yokobori et al., 2012; Shimizu et al., 2013). The NPY homolog in invertebrates is called neuropeptide F (Nässel and Wegener, 2011). However, we did not find any contribution of NPY homologs to pharynx extension in planarian in this study. Although DjNp28 encodes an NPY homolog with conservation of all of the consensus amino acid sequences of NPY (Table 4), DjNp28(RNAi) planarians showed normal pharynx-extension ability, suggesting that planarian pharynx extension may not be involved in the promotion of feeding behavior. However, as planarians possess a large number of NPY family genes (Collins et al., 2010; Matsuda et al., 2012) , further study is needed to determine whether NPY is involved in feeding behavior in planarians.

Although the auricles and lateral branches of the brain are thought to be involved in chemosensing in planarian, we did not identify neuropeptide genes expressed in the auricles or the lateral branches of the brain. It has been observed that some G-proteins are expressed in planarian in the tip of the pharynx as well as in lateral branches of the brain (Inoue et al., 2007). We speculate that G-protein coupled receptors may be involved in detecting food by chemosensory neurons located in the head or in the tip of the pharynx. However, one gene (DjNpP02) shown here to be required for pharynx extension had a dispersed expression pattern on the body surface region throughout the body in both the ventral and dorsal margins (Fig. 3A, D), suggesting that DjNpP02-expressing cells might work as one type of food-sensing cells in a short-range manner. The DjNpM24-expressing cells in the tip of the pharynx may also work as sensory neurons in responding to food signals. In addition, the possibility that chemosensory neurons located in the lateral branch region also play a role in pharynx extension has not been ruled out. If these chemosensory neurons are indeed involved in pharynx extension, that may account for the limited reduction of pharynx-extension ability in DjNpP02(RNAi) planarians (Table 5). We need to perform further screening to identify sensory neurons responsive to food at short range from the animal.

DjNpM24- and DjNp19-positive cells were detected in the brain. However, both were also distributed in the CNS in a dispersed pattern, suggesting that a subpopulation of CNS neurons may be involved in the regulation of pharynx extension. Why are brain neurons involved in regulating pharynx extension? Planarian's brain integrates various kinds of sensory information (Inoue et al., 2015). In order to eat, planarians must orient the extension of the pharynx onto the food source in a manner depending on their internal state and/or external stimuli. After ingestion of food, a planarian retracts its pharynx to its original position and detaches from the food, suggesting that the planarian may have a satiety center in the brain. For these reasons, it seems very likely that pharynx extension should be regulated by the brain. Identification of the satiety center in the brain and unraveling the relationship between the regulatory circuit of pharynx extension and the satiety center are goals for future study in our group.

The most interesting expression pattern was obtained with the DjNp42 probe. DjNp42-expressing cells were located just between the brain and pharynx, suggesting that these neurons may work as interneurons connecting brain and pharyngeal neurons. Okamoto et al. have reported the existence of neurons directly connecting the brain and pharynx, as detected by Dil tracing (Okamoto et al., 2005). We thus plan to investigate how neurons connect brain and pharynx neurons by immunostaining using anti DjNp42 antibody in a future study.

We typically use the syt and PC2 genes as pan-neural genes to stain the planarian nervous system. In other species, a subpopulation of CNS neurons produces neuropeptides (Seidah et al., 1992; Zhou et al., 1999). However, in the case of planarian, we found here that all CNS neurons express PC2. In addition, in the synaptic region of another planarian, both small synaptic vesicles and large neurosecretory vesicles were observed (Oosaki and Ishii, 1965). Here we showed that neuropeptide-producing neurons have diverse expression patterns. However, we do not yet know whether each neuropeptide is expressed exclusively in a distinct subset of neurons or whether some neuropeptides are produced in the same neurons. It will be interesting to elucidate the functions of the neuropeptides and neural networks in various behaviors and physiological controls in planarians. For example, knockdown of eight of 13 candidate neuropeptide-coding genes examined here caused defects of feeding behavior, although the knockdown planarians showed normal pharynx extension. Thus, these eight genes appear to be involved in feeding behaviors other than pharynx extension, such as chemotaxis or ingestion. We expect that some may be involved in ingestion of food via the pharynx. To identify the functions of each neuropeptide-coding gene, in the future we will need to perform combinatory experiments using behavior assay systems and RNAi screening, which will enable us to clarify how different kinds of information are integrated to regulate feeding behavior in planarians.


We sincerely thank Dr. Elizabeth Nakajima for critically reading the manuscript. This work was supported by a Grant-in-Aid for JSPS Fellows (14J01042) to SS, a Grant-in-Aid for JSPS Fellows (13J01064) to MK, Grants-in-Aid for Scientific Research (22700336, 15K07148) to TI, The Takeda Science Foundation funds to TI, and Grants-in-Aid for Scientific Research on Innovative Areas (22124001, 22124002) to KA.



Adler CE , Seidel CW , Sánchez Alvarado A (2014) Selective amputation of the pharynx identifies a FoxA-dependent regeneration program in planaria. eLife :e02238 Google Scholar


Agata K , Umesono Y (2008) Brain regeneration from pluripotent stem cells in planarian. Philos Trans R Soc Lond B Biol Sci 363: 2071–2078 Google Scholar


Agata K , Soejima Y , Kato K , Kobayashi C , Umesono Y , Watanabe K (1998) Structure of the planarian central nervous system (CNS) revealed by neuronal cell markers. Zool Sci 15: 433–440 Google Scholar


Arora S , Anubhuti (2006) Role of neuropeptides in appetite regulation and obesity. Neuropeptides 40: 375–401 Google Scholar


Asami M , Nakatsuka T , Hayashi T , Kou K , Kagawa H , Agata K (2002) Cultivation and characterization of planarian neuronal cells isolated by fluorescence activated cell sorting (FACS). Zool Sci 19: 1257–1265 Google Scholar


Ash JF , McClure WO , Hirsch J (1973) Chemical studies of factor which elicits feeding behavior in Dugesia dorocephara. Anim Behav 21: 796–800 Google Scholar


Blomqvist AG , Söderberg C , Lundell I , Milner RJ , Larhammar D (1992) Strong evolutionary conservation of neuropeptide Y: Sequence of chicken, goldfish and Torpedo marmorata DNA clones. Proc Natl Acad Sci USA 89: 2350–2354 Google Scholar


Cebrià F , Nakazawa M , Mineta K , Ikeo K , Gojobori T , Agata K (2002) Dissecting planarian central nervous system regeneration by the expression of neural-specific genes. Dev Growth Differ 44: 135–146 Google Scholar


Collins JJ 3rd, Hou X , Romanova EV , Lambrus BG , Miller CM , Saberi A , et al. (2010) Genome-wide analyses reveal a role for peptide hormones in planarian germline development. PLoS Biol 8: e1000509 Google Scholar


Coward SJ , Johannes RE (1968) Amino acid chemorecereption by the planarian Dugesia dotocephara. Comp Biochem Physiol 29: 475–478 Google Scholar


Currie KW , Pearson BJ (2013) Transcription factors lhx1/5-1 and pitx are required for the maintenance and regeneration of serotonergic neurons in planarians. Development 140: 3577–3588 Google Scholar


Higuchi S , Hayashi T , Tarui H , Nishimura O , Nishimura K , Shibata N , et al. (2008) Expression and functional analysis of musashi-like genes in planarian CNS regeneration. Mech Dev 125: 631–645 Google Scholar


Inoue T , Kumamoto H , Okamoto K , Umesono Y , Sakai M , Sánchez Alvarado A , Agata K (2004) Morphological and functional recovery of the planarian photosensing system during head regeneration. Zool Sci 21: 275–283 Google Scholar


Inoue T , Hayashi T , Takeuchi K , Agata K (2007) Clathrin-mediated endocytic signals are required for the regeneration of, as well as homeostasis in, the planarian CNS. Development 134: 1679–1689 Google Scholar


Inoue T , Yamashita T , Agata K ( 2014) Thermosensory signaling by TRPM is processed by brain serotonergic neurons to produce planarian thermotaxis. J Neurosci 34: 15701–15714 Google Scholar


Inoue T , Hoshino H , Yamashita T , Shimoyama S , Agata K (2015) Planarian shows decision-making behavior in response to multiple stimuli by integrative brain function. Zoological Lett 1: 7 Google Scholar


Kobayashi C , Kobayashi S , Orii H , Watanabe K , Agata K (1998) Identification of two distinct muscles in the planarian Dugesia japonica by their expression of myosin heavy chain genes. Zool Sci 15: 861–869 Google Scholar


Kobayashi C , Watanabe K , Agata K (1999) The process of pharynx regeneration in planarians. Dev Biol 211: 27–38 Google Scholar


Matsuda K (2009) Recent advances in the regulation of feeding behavior by neuropeptides in fish. Ann NY Acad Sci 1163: 241–250 Google Scholar


Matsuda K , Sakashita A , Yokobori E , Azuma M (2012) Neuroendocrine control of feeding behavior and psychomotor activity by neuropeptide Y in fish. Neuropeptide 46: 275–283 Google Scholar


Mineta K , Nakazawa M , Cebrià F , Ikeo K , Agata K , Gojobori T (2003) Origin and evolutionary process of the CNS elucidated by comparative genomics analysis of planarian ESTs. Proc Natl Acad Sci USA 100: 7666–7671 Google Scholar


Miyamoto S , Shimozawa A (1985) Chemotaxis in the Freshwater Planarian, Dugesia japonica. Zool Sci 2: 389–395 Google Scholar


Nässel DR , Wegener C (2011) A comparative review of short and long neuropeptide F signaling in invertebrates: Any similarities to vertebrate neuropeptide Y signaling. Peptides 32: 1335– 1355 Google Scholar


Nishimura K , Kitamura Y , Inoue T , Umesono Y , Sano S , Yoshimoto K , et al. (2007a) Reconstruction of dopaminergic neural network and locomotion function in planarian regenerates. Dev Neurobiol 67: 1059–1078 Google Scholar


Nishimura K , Kitamura Y , Inoue T , Umesono Y , Yoshimoto K , Takeuchi K , et al. ( 2007b) Identification and distribution of tryptophan hydroxylase (TPH)-positive neurons in the planarian Dugesia japonica. Neurosci Res 59: 101–106 Google Scholar


Nishimura K , Kitamura Y , Inoue T , Umesono Y , Yoshimoto K , Taniguchi T , Agata K (2008a) Characterization of tyramine beta-hydroxylase in planarian Dugesia japonica: cloning and expression. Neurochem Int 53: 184–192 Google Scholar


Nishimura K , Kitamura Y , Umesono Y , Takeuchi K , Takata K , Taniguchi T , Agata K (2008b) Identification of glutamic acid decarboxylase gene and distribution of GABAergic nervous system in the planarian Dugesia japonica. Neuroscience 153: 1103–1114 Google Scholar


Nishimura K , Kitamura Y , Taniguchi T , Agata K (2010) Analysis of motor function modulated by cholinergic neurons in planarian Dugesia japonica. Neuroscience 168: 18–30 Google Scholar


Nishimura O , Hirao Y , Tarui H , Agata K (2012) Comparative transcriptome analysis between planarian Dugesia japonica and other platyhelminth species. BMC Genomics 13: 289–306 Google Scholar


Nishimura O , Hosoda K , Kawaguchi E , Yazawa S , Hyashi T , Inoue T , et al. (2015) Unusually Large Number of Mutations in Asexually Reproducing Clonal Planarian Dugesia japonica. PLoS One 10: e0143525 Google Scholar


Okamoto K , Takeuchi K , Agata K (2005) Neural projections in planarian brain revealed by fluorescent dye tracing. Zool Sci 22: 535–546 Google Scholar


Oosaki T , Ishii S (1965) Observations on the ultrastructure of nerve cells in the brain of the planarian, Dugesia gonocephala. Cell Tissue Res 66: 782–793 Google Scholar


Pearl R (1903) The movements and reactions of fresh-water planarians: A study in animal behavior. Q J Microsc Sci 46: 509–714 Google Scholar


Rouhana L , Weiss JA , Forsthoefel DJ , Lee H , King RS , Inoue T (2013) RNA interference by feeding in vitro-synthesized double-stranded RNA to planarians. Dev Dyn 242: 718–730 Google Scholar


Sánchez Alvarado A , Newmark PA (1999) Double-stranded RNA specifically disrupts gene expression during planarian regeneration. Proc Natl Acad Sci USA 96: 5049–5054 Google Scholar


Seidah NG , Fournier H , Boileau G , Benjannet S , Rondeau N , Chretien M (1992) The cDNA structure of the porcine pro-hormone convertase PC2 and the comparative processing by PC1 and PC2 of the N-terminal glycopeptide segment of porcine POMC. FEBS Lett 310: 235–239 Google Scholar


Shibata N , Hayashi T , Fukumura R , Fujii J , Kudome-Takamatsu T , Nishimura O , Agata K (2012) Comprehensive gene expression analyses in pluripotent stem cells of a planarian, Dugesia japonica. Int J Dev Biol 56: 93–102 Google Scholar


Shimizu S , Azuma M , Morimoto N , Kikuyama S , Matsuda K (2013) Effect of neuropeptide Y on food intake in bullfrog larvae. Peptides 46: 102–107 Google Scholar


Stanley BG , Leibowitz SF (1985) Neuropeptide Y injected in the paraventricular hypothalamus: A powerful stimulant of feeding behavior. Proc Natl Acad Sci USA 82: 3940–3943 Google Scholar


Takano T , Pulvers JN , Inoue T , Tarui H , Sakamoto H , Agata K , Umesono Y (2007) Regeneration-dependent conditional gene knockdown (Readyknock) in planarian: demonstration of requirement for Djsnap-25 expression in the brain for negative phototactic behavior. Dev Growth Differ 49: 383–394 Google Scholar


Tasaki J , Shibata N , Nishimura O , Itomi K , Tabata Y , Son F , et al. ( 2011) ERK signaling controls blastema cell differentiation during planarian regeneration. Development 138: 2417–2427 Google Scholar


Tazaki A , Gaudieri S , Ikeo K , Gojobori T , Watanabe K , Agata K (1999) Neural network in planarian revealed by an antibody against planarian synaptotagmin homologue. Biochem Biophys Res Commun 260: 426–432 Google Scholar


Umesono Y , Tasaki J , Nishimura K , Agata K (2011) Regeneration in an evolutionarily primitive brain: the planarian Dugesia japonica model. Eur J Neuro 34: 863–869 Google Scholar


Yazawa S , Umesono Y , Hayashi T , Tarui H , Agata K (2009) Planarian Hedgehog/Patched establishes anterior-posterior polarity by regulating Wnt signaling. Proc Natl Acad Sci USA 106: 22329–22334 Google Scholar


Yokobori E , Azuma M , Nishiguchi R , Kang KS , Kamiji M , Uchiyama M , Matsuda K (2012) Neuropeptide Y stimulates food intake in the zebrafish, Danio rerio. J Neuroendocrinol 24: 766–773 Google Scholar


Zhou A , Webb G , Zhu X , Steiner DF (1999) Proteolytic processing in the secretory pathway. J Bio Chem 274: 20745–20748 Google Scholar


[1] Supplemental material for this article is available online.

© 2016 Zoological Society of Japan
Seira Shimoyama, Takeshi Inoue, Makoto Kashima, and Kiyokazu Agata "Multiple Neuropeptide-Coding Genes Involved in Planarian Pharynx Extension," Zoological Science 33(3), 311-319, (1 June 2016).
Published: 1 June 2016
feeding behavior
pharynx extension
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