Calcineurin and Protein kinase G regulate C. elegans behavioral quiescence during locomotion in liquid
© Ghosh and Emmons; licensee BioMed Central Ltd. 2010
Received: 6 November 2009
Accepted: 27 January 2010
Published: 27 January 2010
Most rhythmic motor behaviors in nature are episodic i.e. they alternate between different behavioral states, including quiescence. Electrophysiological studies in invertebrate behavioral switching, maintenance and quiescence have elucidated several neuronal mechanisms that generate a temporal pattern in behavior. However, the genetic bases of these processes are less well studied. We have previously uncovered a novel episodic behavior exhibited by C. elegans in liquid media where they alternate between distinct phases of rhythmic swimming and quiescence. Here, we have investigated the effect of several genes and their site of action on the behavioral quiescence exhibited in liquid by the nematode C. elegans.
We have previously reported that high cholinergic signaling promotes quiescence and command interneurons are critical for timing the quiescence bout durations. We have found that in addition to command interneurons, sensory neurons are also critical for quiescence. We show that the protein phosphatase calcineurin homolog tax-6 promotes swimming whereas the protein kinase G homolog egl-4 promotes quiescence. tax-6 expression in the sensory neurons is sufficient to account for its effect. egl-4 also acts in multiple sensory neurons to mediate its effect on quiescence. In addition our data is consistent with regulation of quiescence by egl-4 acting functionally downstream of release of acetylcholine (ACh) by motor neurons.
Our study provides genetic evidence for mechanisms underlying the maintenance of a behavioral state operating at multiple neuronal levels through the activities of a kinase and a phosphatase. These results in a genetically tractable organism establish a framework for further dissection of the mechanism of quiescence during episodic behaviors.
Most natural behaviors are characterized by transitions between distinct behavioral states determined by the internal state of an organism as well as spatial and temporal variance of the environment. Observations of leech long-term behavior in an unstructured environment have resulted in identification of several behavioral states, including stationary states, and transitions between these states that depend only on the most recent prior behavioral state [1, 2]. Invertebrate electrophysiological studies of a given behavioral state such as quiescence and switching between behavioral states e.g. swimming and crawling in Tritonia [3, 4], swallowing and quiescent states in Lymnea  among many others have elucidated several neuronal mechanisms. However the genetic basis of these processes are less well studied.
Despite a single gait underlying locomotion in liquid and solid media , referred to as swimming [7, 8] and crawling respectively, nematodes exhibit distinct behavioral patterns when observed for long periods of time in liquid [9, 10]. We have previously described that in liquid, wild type worms display periods of active swimming alternating with a quiescent state lasting for several minutes . We previously showed that quiescence in liquid results from high cholinergic signaling downstream of motor neurons and that the maintenance of the quiescent state requires command inter-neurons .
In addition to the quiescent state exhibited by worms in liquid , two other behavioral quiescent states have been studied in C. elegans [11–13]. Movement of C. elegans stops when they undergo lethargus, a developmental state that occurs before each of the four molts during its life cycle [11, 12]. This quiescent state exhibits characteristics that resemble sleep in other organisms . On agar plates with high-quality food, movement and feeding of an adult worm is interjected by stops, a behavioral characteristic that has parallels to satiety in mammals . Molecularly, two different signaling systems have been identified to influence these quiescent states. Insulin/TGF-β and EGF signaling induce quiescence on plates with high quality food and during lethargus respectively [11–13]. In both quiescence paradigms, protein kinase G (PKG) activity in sensory neurons is required to promote quiescence. Eventually the activity of PKG at the sensory neuronal level must modulate activities of the motor and/or interneurons to bring about quiescence. How PKG activity in sensory neurons drives quiescence at the motor/interneuron levels is not known. Also it remains to be seen how much overlap exists in the genetics of the three behavioral quiescence states that have been described. The unique features of long term swimming behavior, ease of genetic analysis and the knowledge of the pattern of synaptic connectivity of the entire nervous system  that allow mapping of molecular to neuronal correlates underlying behavior makes C. elegans a suitable model to dissect the molecular mechanisms underlying this long-term behavioral pattern.
To further investigate the underlying mechanism(s) of quiescence in liquid, we examined the cellular site of action of several genes that had important effects on swim/quiescence cycling. Several of these do not act at the motor neuron-muscle circuitry but instead act in sensory neurons. We found that maintenance of swimming requires calcineurin activity in the sensory neurons. The PKG homolog egl-4 promotes quiescence by acting at two levels: in the sensory neurons and also downstream of command interneurons. Our analysis suggests that there may be two mechanisms by which swimming motions may be stopped, one by blocking output of the motor system at the level of motor neurons and muscles, a mechanism that appears to come into play when worms swim in liquid, and one by inhibition of initiation of swimming motions upstream of this block, which is strongly influenced by sensory input.
PKG is required for maintenance of the quiescent state during swimming in liquid
The increased cholinergic activity during quiescence appeared by several criteria to be at the neuromuscular junction . During quiescence in liquid body-wall muscles are uniformly contracted. Quiescence induced by aldicarb was enhanced by mutation in dgk-1, which increases ACh release from motor-neurons [9, 19]. Mutations resulting in reduced synthesis/release of GABA by GABAergic motor neurons, which opposes the action of ACh on muscles, also increased quiescence, whereas the GABA agonist muscimol promoted swimming. Since egl-4 is necessary for ACh- mediated quiescence, we conclude that egl-4 has an activity that promotes quiescence functionally downstream of ACh release by motor neurons.
Further evidence for PKG activity downstream of motor neurons in regulating quiescence
Quiescent Bout Durations
Number of bouts
egl-4(ks60) in 0.6 OD E.coli(OP50)
Wild type in 0.6 OD E.coli(OP50)
egl-4(n479) [odr-3p::egl-4] NQ2
egl-4(n479) [odr-3p::egl-4] NQ5
egl-4(n479) [odr-3p::egl-4] NQ7
egl-4(n479) [odr-1p::egl-4] NQ11
egl-4(n479) [odr-1p::egl-4] NQ13
egl-4(n479) [tax-4p::egl-4] NQ20
egl-4(n479) [tax-4p::egl-4] NQ21
egl-4(n479) [tax-4p::egl-4] NQ22
We previously found that command interneurons regulate the timing of quiescence bouts . Consistent with a role of egl-4 downstream of command interneurons, increased quiescence in transgenic strains expressing a leaky glutamate channel in the command neurons plus 12 classes of additional neurons (akIs9) causing constitutive depolarization of command interneurons , were partially suppressed by egl-4(ks60) (Figure 1A, C). Taken together, these observations suggest a role of egl-4 genetically downstream of command interneurons in sustaining quiescence. We also observed that suppression of the increased quiescence due to akIs9 by egl-4(ks60) was more potent during the first ~90 minutes of the assay (Figure 1C). Thus egl-4 independent mechanisms are required to shape the behavioral pattern beyond that time period. Overall, these results place a site of action for activity of egl-4 required for quiescence during swimming downstream of command interneurons and release of ACh by motor neurons, but upstream of GABA signaling.
Consistent with a role of command interneurons in timing quiescent bout duration, we found that a deletion in nmr-1, encoding NMDA receptor subunit expressed in the ring motor neuron RIM and all command interneurons except AVB , resulted in dramatically increased durations of quiescent bout (Figure 1A). The median quiescent bout durations of nmr-1(ak4); egl-4(ks60) were similar to egl-4(ks60) indicating egl-4 acts downstream of or within command interneurons in maintenance of quiescence (Figure 1A).
PKG acts in sensory neurons to modulate the quiescent state
Consistent with a role of sensory neurons in quiescence, we found that quiescence duration could be increased by defects in sensory physiology due to mutations in osm-6 or osm-3 (critical for proper cilium structure in sensory neurons). Both of these mutations result in abnormal sensory neuron structure  (Figure 2B, Table 1). Increased quiescence in osm-3 and osm-6 mutants was suppressed by egl-4(ks60) mutation (Figure 2B) indicating that egl-4 acts downstream or in sensory neurons. In addition we previously reported that inclusion of food (0.6 O.D. E.coli(OP50)) increased the quiescent bout durations . The increased quiescence bout duration of wild type worms induced by inclusion of E.coli in the assay media was also significantly reduced in egl-4(ks60) mutants (Figure 1A, Table 1).
Since both sensory neurons and command interneurons contribute towards sustaining quiescence and thus there appeared to be two sites of action of egl-4, we asked whether these two pathways were independent. We assayed double mutants of nmr- 1(ak4);osm-6(p811). The quiescence bouts in the nmr-1(ak4);osm-6(p811) mutants were significantly longer than either of the single mutants alone (Figure 2B, Table 1). This additive role of nmr-1 and osm-6 is consistent with two independent pathways of quiescence maintenance.
Calcineurin activity in sensory neurons is essential for swimming in liquid
tax-6 and cnb-1, the C. elegans homologues of subunits of calcineurin phosphatase subunits A and B respectively, are expressed in many tissues, including sensory neurons, interneurons and muscles [25, 26]. C. elegans calcineurin has been implicated in diverse behaviors including locomotion, thermosensation and chemosensation [25, 26]. Calcineurin negatively affects several sensory behaviors. For example, loss of tax-6 results in hyper-activation of sensory neurons in an olfactory adaptation paradigm .
We have previously observed that in a long-term swimming assay , the average fraction of wild type animals in quiescence during the first phase (first 90 minutes) of swimming was low 0.02 +/- 0.004. In the subsequent 90 minutes the average fraction of worms in quiescence increased to 0.23 +/- 0.01. Loss-of-function mutants of either of calcineurin subunit cnb-1(jh300) or tax-6(db60) [25, 26] exhibited a striking temporally changing phenotype in which a spike in fraction of animals in quiescence during the first 90 minutes (0.75 ± 0.2 for cnb-1(jh103)) were followed by a decrease in fraction of animals in quiescence (0.62 ± 0.05 for cnb-1(jh103), p < 0.0001, Mann-Whitney U test) during the subsequent period of the assay. In other words a higher fraction of cnb-1(jh103) and tax- 6(db60) animals went into quiescence in the first 90 minutes of the assay and remained quiescent during the entire assay duration compared to wild type animals. Thus calcineurin activity is required for preventing animals from going into quiescence. Moreover, the increased quiescence duration in calcineurin loss-of-function mutants is indicative of a role of calcineurin in proper termination of quiescence. Interestingly, the decrease in the fraction of worms in quiescence exhibited by cnb-1(jh103) and tax- 6(db60) animals after approximately 90 minutes of the assay (Additional File 2) suggested distinct mechanisms underlying quiescence in the first and second phase of swimming.
PKG and calcineurin genetically interact to regulate quiescence
To investigate whether the quiescence induced due to loss of calcineurin activity was dependent on egl-4, we assayed cnb-1(jh103); egl-4(ks60) double mutants. A significantly lower fraction of worms (0.05 ± 0.04) went into and remained in quiescence compared to the cnb-1 mutant worms (0.62 ± 0.05) throughout the assay suggesting that egl-4 acts genetically downstream of or parallel to cnb-1 in promoting the quiescent state (Figure 3B). Since calcineurin loss-of-function resulted in increased quiescent bout duration, which was dependent on PKG function, our data is consistent with a mechanism where events mediated by unopposed phosphorylation by egl-4 in the cnb-1 loss-of-function mutant increases quiescent bout durations.
We investigated the genetic basis of a striking behavioral pattern displayed by swimming nematodes in liquid in which they undergo alternate bouts of swimming and quiescence. We found that like other calcineurin-modulated behaviors in C elegans, activity of calcineurin in the sensory neurons is critical to maintain swimming in C. elegans in liquid. In analogy with the neuronal properties that change in a calcineurin mutant, namely defect in gain control , it is likely that increased quiescence in the tax- 6/cnb-1 loss-of-function mutants is due to hyperactivation of one or more sensory neurons. In addition, calcineurin mutants displayed a temporally changing phenotype in which there was a significant drop in the fraction of worms in quiescence after 90 minutes. This recovery after 90 minutes from start of assay was more pronounced in case of tax-6(db60) mutants than cnb-1(jh300) mutants, suggesting other phosphatases or autoregulatory mechanisms may play a role in shaping the temporal pattern of swim- quiescence pattern in liquid. It is possible that in tax-6 loss-of-function mutants unopposed phosphorylation of a yet unidentified substrate induces prolonged quiescence. The phosphorylation possibly involves egl-4 activity as the increased quiescence in calcineurin loss of function mutants was suppressed by loss of function muations in egl-4. During the first 90 minutes of the assay, PKG and calcineurin play opposing roles in maintenance of swimming. In the second phase (the subsequent 90 minutes) of the assay, however, the fraction of worms in quiescence in egl-4;cnb-1 double mutants was lower than the egl-4 loss of function mutants, suggesting that additional yet unidentified mechanisms may play a role in shaping the temporal pattern of quiescence during swimming in liquid.
We found that the protein kinase G homolog egl-4 acts in the sensory neurons to enhance the quiescence duration liquid. Similar to other paradigms of behavioral quiescence, we found that PKG activity in sensory neurons expressing the cGMP-gated calcium channel tax-4 is critical for regulating quiescent bout duration. However, beyond the involvement of egl-4 in tax-4 expressing neurons, the pathways for induction of different types of quiescence seem to be different. For instance, in quiescence induced by high quality food, loss-of-function mutants of tax-2, encoding the alpha subunit of the cGMP gated ion channels, exhibited very little quiescence . However quiescence in liquid without food doesn't seem to involve participation of these channels as quiescence bouts of double mutants of alpha and beta subunits, tax-2(p691);tax-4(ky89), were not different from wild type (Table 1), ruling out these channels as phosphorylation targets of egl-4 in modulating quiescence duration in liquid without food. This difference may be attributed to a different target of egl-4 in the sensory neurons or action of egl-4 in additional sites beyond the sensory neurons.
In summary, we have identified parts of a genetic network involving calcineurin and PKG that generate a temporal pattern during swimming in C.elegans. Though egl-4 has been implicated in all paradigms of behavioral quiescence in C. elegans, our results indicate that the target of EGL-4 in regulating quiescence in liquid is distinct from the other forms of quiescence. Based on our results we propose dual function of egl-4: one in the sensory neurons that is inhibited by calcineurin and another in inhibiting GABAergic neurotransmission (Figure 4). Our study also implicates opposite roles of a kinase and a phosphatase in generating temporal pattern in behavior. It is likely that the activity of kinase(s) increases the probability of the motor circuit to switch to a quiescent state. Such a process is opposed by calcineurin phosphatase activity in the sensory neurons. Studies of temporal patterns generated by intermittent motor activities have explored statistical properties of the behavioral state transitions or neuro-physiological properties of neural circuits underlying them [1, 5, 28]. However, very little is known about the genetics of the behavioral intermittencies over time. Our results in a genetically tractable organism establish a framework for further dissection of episodic behaviors.
Nematodes were reared and maintained at 20°C on E. coli OP50 on NGM agar plates according to published procedures . Strains that were used are as follows: tax- 6(db60), tax-6(db60) [myo3::tax-6], tax-6(db60) [tax-6sensory+inter+::tax-6], tax- 6(db60) [tax-6 sensory+inter-::tax-6] were a kind gift from Ikue Mori (see Figure legend 3 for description of the promoters). The egl-4 transgenic rescue strains (egl-4(n479) [odr- 3::egl-4], egl-4(n479) [odr-1::egl-4] and egl-4(n479) [tax-4::egl-4]) were generously provided by David Raizen. akIs9 and tax-2(p691);tax-4(ky89) were kindly provided by A.V. Maricq and Cornelia Bargmann respectively. All other strains were either made during this work or obtained from CGC. Double mutants were generated using standard genetic procedures. osm-6(p811) and osm-3(p802) mutants were monitored by the inability of their sensory neurons to uptake the fluorescent dye DiO . cnb-1(jh103), egl-4(ks60) and nmr-(ak4) deletions were confirmed by the following primer pairs:
Left oligo cnb-1: TCTTCTTGTGCACTTCGGTG
Right oligo cnb-1: CAACACAGCCGATCAAATG
EGL-4(KS60) FD: GAAACCTCCAATTCTGCCGAAGG
EGL-4(KS60) RV: GAATTTCCAGTCAACCAAATTCATAC
Nmr-1 (ak4) left: GGAAGAGTTTGAAAAACGGCG
Nmr-1 (ak4) right: CGTGTTCTTAGCTCACAGTGTCG
Swimming assays were performed essentially as described previously . Briefly, one day old adults were transferred to a fresh unseeded plate at 25°C and allowed to forage for 2 min, after which they were picked singly into wells of a microtiter plate containing 200 μl M9 buffer at 25°C. The assays were carried out in a room where the temperature was maintained at 25 ± 1°C. Quiescence was defined as before . Briefly less than two body bends per 5 seconds of observation were considered as quiescent irrespective of movement of the nose/head.
Aldicarb and dye-filing assays
Statistical analysis on the data was done using the Graphpad Prism version 5.0a software for Macintosh. For most cases the data was not normally distributed as determined by the by the D'Agastino and Pearson method. Unless otherwise mentioned we used the non parametric Mann Whitney U test for the quiescence bout durations for two genotypes or Kruskal-Wallis test followed by Dunn's multiple comparison for more than two genotypes. We also used the non-parametric Wilcoxon signed rank test to compare the medians of any given genotype against a hypothetical median of 4.500, which was not significantly different from the median for wild type worms.
We thank Erik Andersen and Soumen Basak for their comments on the manuscript. We thank J. Di Miele and C. Smith for expert technical assistance. We are grateful to David Raizen for sending us the egl-4 rescue strains, Ikue Mori for the tax-6 rescue strains and constructs, Cornelia Bargmann for tax-2(p691);tax-4(ky89) strain and A. V. Maricq for the akIs9 strain. Additional strains were provided by the Caenorhabditis Genetic Center. This research was supported by NIH grant R01GM066797 to S.W.E. S.W.E. is the Siegfried Ullmann Professor of Genetics.
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