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. 2017 Jan 24;6:e21166. doi: 10.7554/eLife.21166

Sexually dimorphic control of gene expression in sensory neurons regulates decision-making behavior in C. elegans

Zoë A Hilbert 1, Dennis H Kim 1,*
Editor: Oliver Hobert2
PMCID: PMC5262377  PMID: 28117661

Abstract

Animal behavior is directed by the integration of sensory information from internal states and the environment. Neuroendocrine regulation of diverse behaviors of Caenorhabditis elegans is under the control of the DAF-7/TGF-β ligand that is secreted from sensory neurons. Here, we show that C. elegans males exhibit an altered, male-specific expression pattern of daf-7 in the ASJ sensory neuron pair with the onset of reproductive maturity, which functions to promote male-specific mate-searching behavior. Molecular genetic analysis of the switch-like regulation of daf-7 expression in the ASJ neuron pair reveals a hierarchy of regulation among multiple inputs—sex, age, nutritional status, and microbial environment—which function in the modulation of behavior. Our results suggest that regulation of gene expression in sensory neurons can function in the integration of a wide array of sensory information and facilitate decision-making behaviors in C. elegans.

DOI: http://dx.doi.org/10.7554/eLife.21166.001

Research Organism: C. elegans

eLife digest

For almost all species of animal, males and females will often behave differently in similar situations. Little is known about how these sex-specific differences are generated or, for example, how different the nervous system of a male is to that of a female. Moreover, it is also poorly understood how these underlying differences based on the biological sex of an animal are integrated with and influenced by its experiences and environment.

The roundworm Caenorhabditis elegans has two sexes, hermaphrodites and males. The male worms behave differently to the hermaphrodites in a number of situations. This means that these animals offer the opportunity to explore and understand sex-specific differences in behavior. It is also possible to analyze the underlying factors that contribute to behavior in C. elegans, because it has a relatively simple and well-defined nervous system.

Now, Hilbert and Kim show that a signal that influences how C. elegans explores in response to chemicals in its environment is expressed differently in male and hermaphrodite worms. The signal in question is molecule called DAF-7, which is released by several sensory neurons—nerve cells that are used for detecting cues from the environment. The sensory neurons that release DAF-7 are found in both sexes of C. elegans but the specific way that the male worms express this signal encourages them to search for mates. Hermaphrodites, on the other hand, do not need to search for mates because they can fertilize their own eggs.

Hilbert and Kim showed that the biological sex in combination with multiple other inputs – including the animal’s past diet and age – regulate how the DAF-7 signal is expressed in C. elegans. These inputs all converge onto a single pair of sensory neurons, which integrate the inputs and enable the worm to assess its current and past experiences and alter its behavior accordingly.

Moving forward the next challenge is to understand how information about both external environment and internal states, such as hunger, are communicated to and integrated by these sensory neurons. Decoding the signals behind this process may illuminate how biological sex and internal states influence behavior in other species of animals.

DOI: http://dx.doi.org/10.7554/eLife.21166.002

Introduction

In order to effectively adapt to an environment, organisms need to be able to analyze both their internal state and external surroundings to make behavioral decisions that will maximize their chances of survival. It has been hypothesized that decision making in animals is controlled primarily at the level of command interneurons or decision centers in the central nervous system, which receive input from an array of sensory neurons and integrate the information conveyed to inform behavioral decisions (Kristan, 2008). However, recent work in a number of animal species has demonstrated that modulation of gene expression and neuronal activity by both environmental cues and internal state can occur at the level of sensory neurons, suggesting that aspects of behavioral decision making may also occur in the peripheral nervous system (Dey et al., 2015; Farhadian et al., 2012; Ryan et al., 2014).

Two pervasive internally derived modifiers of decision making in animals are the nutritional state of the animal and biological sex. Feeding status and satiety levels have long been known to have dramatic effects on the behaviors and decisions of species across the animal kingdom (Pool and Scott, 2014; Sengupta, 2013). In many cases, the nutritional state of the animal will serve as a source of regulation directly on feeding and other food-related behaviors. For instance, in the medicinal leech, periods of food deprivation can lead to a heightened response to appetitive stimuli in its environment, a response that has been shown to be carried out via a correlation between serotonin production and time of last meal (Gaudry and Kristan, 2012; Groome et al., 1993; Lent et al., 1991). Starvation or nutritional deprivation can also have less direct effects on feeding behaviors as in Drosophila, where periods of starvation have been demonstrated to both enhance odor sensitivity and attraction as well as abrogate avoidance responses to normally aversive stimuli (Bräcker et al., 2013; Inagaki et al., 2014; Ko et al., 2015; Root et al., 2011). Similarly, the biological sex of an animal is a potent modifier of decision-making. Not only does the sex of the animal lead to differences in mating behaviors and pheromone attraction, but studies in several systems have suggested that biological sex can also alter olfactory and gustatory preferences, perhaps to guide decision-making in the context of mating and reproduction (Dey et al., 2015; Kimchi et al., 2007; Kurtovic et al., 2007; Lebreton et al., 2015; Lee and Portman, 2007; Meunier et al., 2000; Nakagawa et al., 2005; Ribeiro and Dickson, 2010; Ryan et al., 2014; Stowers and Logan, 2010; Stowers et al., 2002; Vargas et al., 2010).

The roundworm, Caenorhabditis elegans, and its well-defined nervous system provide a simple experimental system well suited to investigate how internal states and environmental cues can be integrated to modulate animal behavior. C. elegans exist as one of two sexes: hermaphrodite or male. Hermaphrodites produce a limited amount of sperm during larval development making them capable of self-fertilization in addition to cross-fertilization. In contrast, males are only cross-fertile and must find mating partners for reproduction. As such, the male displays a large behavioral repertoire primarily aimed at facilitating mate finding and successful mating encounters. These behaviors include complex mating rituals (Liu and Sternberg, 1995), differential sensitivity to hermaphrodite pheromone (Srinivasan et al., 2008), and a mate-searching behavior in adult male animals that is driven by the prioritization of mating over feeding (Lipton et al., 2004). Mate-searching behavior of C. elegans has thus emerged as an interesting case study of decision making in a simple animal, which is subject to regulation by multiple features of internal state—sex, age, and nutritional status—as well as by external sensory experiences such as the presence of food or hermaphrodites in the environment (Barrios et al., 2008; Lipton et al., 2004; Ryan et al., 2014).

Here, we focus on the DAF-7/TGF-β signaling pathway, which plays a pivotal role in the regulation of diverse aspects of C. elegans physiology and behavior including the dauer developmental decision, reproductive egg laying, feeding and foraging, fat storage, satiety quiescence, longevity, aggregation, aerotaxis and avoidance of pathogenic bacteria (Chang et al., 2006; Gallagher et al., 2013; Greer et al., 2008; Meisel et al., 2014; Milward et al., 2011; Ren et al., 1996; Shaw et al., 2007; White and Jorgensen, 2012; You et al., 2008). The expression pattern of daf-7 was originally identified as being restricted to a single bilaterally symmetric pair of neurons in the head of the worm, the ASI chemosensory neurons, but it is also expressed in the ADE and OLQ neurons under normal laboratory growth conditions (Meisel et al., 2014; Ren et al., 1996; Schackwitz et al., 1996). We recently defined an altered expression pattern for daf-7 in hermaphrodites in response to exposure to bacterial metabolites produced by the pathogenic bacteria Pseudomonas aeruginosa (Meisel et al., 2014). Within minutes of being exposed to P. aeruginosa, daf-7 expression is induced in an additional pair of chemosensory neurons, the ASJ neurons, which in turn promotes behavioral avoidance of the pathogenic bacterial lawn (Meisel et al., 2014). Here, we show that in male C. elegans, daf-7 expression in the ASJ neuron pair is not only induced in response to environmental cues such as Pseudomonas aeruginosa, but can be switched ‘on’ or ‘off’ depending on multiple internal states such as sex, age, and experience. The differential effects of internal states and environmental experience on the DAF-7 transcriptional switch in the two ASJ sensory neurons reveal a hierarchy among different inputs that can function to modulate behavior.

Results

Male-specific expression of daf-7/TGF-β in the ASJ neurons

While expression of the DAF-7/TGF-β ligand was long thought to be confined to the ASI chemosensory neurons (Ren et al., 1996; Schackwitz et al., 1996), we recently reported that a change in the microbial environment of the worm—namely, the introduction of the pathogen P. aeruginosa—can alter the neuronal expression pattern of daf-7, inducing expression in the ASJ neuron pair of hermaphrodite animals (Meisel et al., 2014). In the current study, we observed that adult males exhibit daf-7 expression in both the ASI and the ASJ neuron pairs in the absence of P. aeruginosa (Figure 1A and B). This expression pattern difference in adult C. elegans, can be observed both through the use of a pdaf-7::gfp transcriptional reporter (Figure 1A and B) as well as by fluorescence in situ hybridization (FISH) that directly probes for endogenous daf-7 mRNA (Figure 1—figure supplement 1A–C).

Figure 1. Sex-specific expression of daf-7 in the ASJ neurons of adult males.

(A) pdaf-7::gfp expression pattern in hermaphrodites (left) and males (right). Filled triangles indicate the ASI neurons; dashed triangles indicate the ASJ neurons. Scale bar indicates 50 µm. (B) Maximum fluorescence values of pdaf-7::gfp in the ASI (left) and ASJ (right) neurons of age-matched adult hermaphrodites (grey) and males (black). *p<0.05 as determined by an unpaired t-test with Welch’s correction. Error bars indicate standard deviation (SD). n.s., not significant. (C) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons of males through larval development and early adulthood. The developmental timeline of C. elegans is shown to scale on top. Time values indicate hours after an egg is laid. Error bars indicate SD. (D) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons of both males and hermaphrodites on E. coli (yellow) or P.aeruginosa (green). ***p<0.001 as determined by unpaired t-tests with Welch’s correction. Error bars indicate SD.

DOI: http://dx.doi.org/10.7554/eLife.21166.003

Figure 1.

Figure 1—figure supplement 1. daf-7 expression in the ASJ neuron pair is specific to adult males.

Figure 1—figure supplement 1.

(A–B) FISH images of endogenous daf-7 mRNA in adult hermaphrodite (A) and adult male (B). White dotted lines indicate outline of the ASJ neuron(s). Both images are a single slice through the animal where ptrx-1::gfp was visible and in focus in one or both ASJ neurons. Other neurons visible anterior to the ASI neurons are likely the OLQ neurons, and the cells posterior to the ASJ neurons that express daf-7 mRNA are likely the ADE neurons. Scale bar represents 25 µm. Orientation provided in (A) applies to both images. (C) Fluorescence quantification for daf-7-Cy5 probe in the ASJ neurons (as localized by ptrx-1::gfp) in males and hermaphrodites. ***p<0.001 as determined by unpaired t-test with Welch’s correction. Error bars represent SD. (D) pdaf-7::gfp expression pattern in an L4 larval male. Filled triangles indicate the ASI neurons. Scale bar (shown in C) indicates 50 µm. (E–F) Maximum fluorescence values of pdaf-7::gfp in the ASI (E) and ASJ (F) neurons of developing males. **p<0.01, ***p<0.001, as determined by unpaired t-test with Welch’s correction. Error bars represent SD. n.s., not significant.
DOI: http://dx.doi.org/10.7554/eLife.21166.004
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Recent studies have suggested that, in addition to the generation of sex-specific neurons late in larval development, both male-specific and sex-shared neurons exhibit changes in gene expression as well as synaptic remodeling as the male undergoes the sexual maturation process (Oren-Suissa et al., 2016; Pereira et al., 2015; Ryan et al., 2014; Sammut et al., 2015). This predicts that a number of additional unidentified changes may occur in the anatomy, connectivity and gene expression profiles of the male nervous system as the animal transitions from larva to adult. Given this, we asked if daf-7 expression in males was correlated with the developmental stage of the animal. We observed that in populations of early larval animals carrying the pdaf-7::gfp transcriptional reporter, males and hermaphrodites were indistinguishable, with fluorescence observed only in the ASI neurons (Figure 1—figure supplement 1D). To determine the onset of daf-7 expression in males, we imaged animals carrying the fluorescent reporter at multiple time points during development beginning in the L4 larval stage and extending into reproductive maturity. We found that daf-7 expression remains off in the ASJ of males through the end of the last (L4) larval stage, but is switched on during young adulthood as the animals reach reproductive maturity (Figure 1C). In addition, we examined expression of daf-7 in the ASI neuron pair at several matched timepoints during development and observed a significant drop in the expression of daf-7 in the ASI neurons from L4 to young adulthood (Figure 1—figure supplements 1E and F, 52 hr and 64.5 hr timepoints). At subsequent timepoints during adulthood, however, expression levels in the ASI neurons remained constant as expression in the ASJ neurons increased (Figure 1—figure supplements 1E,3F 64.5 hr and 71.5 hr timepoints).

Genetic sex of the nervous system modulates daf-7 expression in adult males

We asked what the role of the genetic sex of the animal is in regulating daf-7 expression in the ASJ neurons. The C. elegans sex determination pathway terminates on the master regulator GLI-family transcription factor, TRA-1 (Zarkower and Hodgkin, 1992; Zarkower, 2006). TRA-1 activity functions to promote hermaphrodite cell fates and inhibit male development. We first looked at tra-1(e1099) mutants which are karyotypically XX, but develop as fertile pseudomales due to the lack of active TRA-1 (Hodgkin and Brenner, 1977). In these mutant XX males, daf-7 expression could be seen in both the ASI and ASJ neurons, suggesting that daf-7 is regulated by the genetic sex determination pathway either directly or indirectly (Figure 2—figure supplement 1A).

We next looked at the role of genetic sex specifically in the nervous system using transgenic sexual mosaics. TRA-1 is negatively regulated by the FEM proteins—FEM-1, FEM-2, and FEM-3—and it has been demonstrated by many groups that overexpression of FEM-3 cDNA is sufficient to lead to ‘masculinization’ in otherwise hermaphrodite animals (Mehra et al., 1999; Oren-Suissa et al., 2016; Pereira et al., 2015; Sammut et al., 2015; White et al., 2007). We expressed the FEM-3 cDNA under the control of the pan-neural promoter, rab-3, and found that daf-7 expression was up-regulated in the ASJ neurons of adult hermaphrodites, suggesting that a genetically ‘male’ nervous system is sufficient for daf-7 expression in ASJ (Figure 2A, C and E). Although we observed an increase in daf-7 expression in these genetically masculinized animals, the overall expression of daf-7 in the ASJ of masculinized hermaphrodites was still notably lower than what we observe in wild-type males (e.g. Figure 1B). This could possibly be explained by the lack of male-specific neurons in these transgenic animals. While genetic masculinization is effective in sexualizing neurons of the sex-shared nervous system, this technique fails to reliably retain the male-specific CEM neurons and produces hermaphrodites which also lack other male-specific neurons found in the tail (White et al., 2007). To assess the importance of these male-specific neurons for daf-7 expression in ASJ, we examined pdaf-7::gfp fluorescence in ceh-30(n4289), mab-3(e1240), and pkd-2(sy606);lov-1(sy582) mutant males. While ceh-30(n4289) males lack the male-specific CEM neurons in the head (Schwartz and Horvitz, 2007), mab-3(e1240) mutants display marked defects in male-tail formation including ray differentiation as well as in male specific circuitry in the head of the animal (Yi et al., 2000). Similarly, PKD-2 and LOV-1 constitute a TRP channel necessary for the function of the B-type ray neurons—another set of male-specific neurons in the tail of the animal (Barr et al., 2001; Barr and Sternberg, 1999; Barrios et al., 2008). Males of all mutant strains retained wild-type expression levels of daf-7 in ASJ, suggesting that the male-specific neural circuitry is not required for daf-7 expression and is unlikely to underlie the lower daf-7 expression we see in genetically masculinized hermaphrodites (Figure 2—figure supplement 1B).

Figure 2. Genetic sex regulates male-specific expression of daf-7 in the ASJ neuron pair.

(A–D) Representative images of pdaf-7::gfp expression in: wild-type (WT) hermaphrodites (A) and males (B), nervous-system-masculinized hermaphrodites (C) and nervous-system-feminized males (D). Closed triangles indicate the ASI neurons; dashed triangles indicate the ASJ neurons. Scale bar indicates 50 µm. (E) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons of control (black) and partially masculinized hermaphrodites (purple). Masculinization was effected by driving expression of fem-3 cDNA under pan-neural (left) and ASJ-specific (right) promoters. ***p<0.001 as determined by unpaired t-test with Welch’s correction. n.s., not significant. Error bars represent SD. (F) Maximum fluorescence values of pdaf-7::gfp in ASJ of control (black) and partially feminized males (orange). Feminization was effected by driving expression of tra-2IC under pan-neural (left), ciliated neuron (middle), and ASJ-specific (right) promoters. ***p<0.001 as determined by unpaired t-test with Welch’s correction. Error bars indicate SD.

DOI: http://dx.doi.org/10.7554/eLife.21166.005

Figure 2.

Figure 2—figure supplement 1. daf-7 expression in the ASJ neuron pair is regulated by TRA-1 but not by male-specific neurons.

Figure 2—figure supplement 1.

(A) Representative image of pdaf-7::gfp expression pattern in tra-1(e1099) pseudomale. Filled triangles indicate the ASI neurons; dashed triangles indicate the ASJ neurons. Scale bar represents 50 µm. (B) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons of WT, ceh-30(n4289), mab-3(e1240), and pkd-2(sy606);lov-1(sy582) mutant animals. Significance determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. Error bars represent SD. n.s., not significant.
DOI: http://dx.doi.org/10.7554/eLife.21166.006
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Complementary to masculinization, genetic ‘feminization’ of XO male animals can be achieved via the overexpression of the intracellular domain of the TRA-2 protein, which negatively interacts with FEM-3 to prevent TRA-1 degradation (Mehra et al., 1999). Overexpression of TRA-2IC under the control of the rab-3 promoter led to complete loss of daf-7 expression in the ASJ of otherwise male animals (Figure 2B, D and F). These results suggest that a genetically male nervous system is both necessary and sufficient for the sex-specific expression pattern of daf-7.

We next asked whether the sex determination pathway acts cell-autonomously in ASJ to regulate daf-7 expression. Using the trx-1 ASJ-specific promoter, we masculinized the ASJ neuron pair alone and saw no daf-7 expression in the resulting adult hermaphrodites (Figure 2E). Similarly, no daf-7 expression could be observed when only the ciliated neurons (of which ASJ is a member) were masculinized (data not shown). These data suggest the requirement that an additional neuron (or neurons) or other tissues have a male cell identity for daf-7 to be expressed in the ASJ neurons, although differences in the strength of the heterologous promoters used in the masculinization constructs may also account for these observations. In contrast, both ciliated neuron-specific and ASJ-specific feminization in males led to down-regulation of daf-7 expression, confirming that a male cell identity in ASJ is necessary, though not sufficient, for proper daf-7 expression (Figure 2F).

DAF-7 is required for male-specific mate-searching behavior

We next sought to determine the functional significance of the sex-specific changes in daf-7 expression that we observe in males. Mate-searching behavior is a behavioral program specific to adult male C. elegans, which features the prioritization of mating over feeding in these animals. While hermaphrodite animals prefer to remain in a patch of bacterial food indefinitely and exhibit limited exploratory behavior, males will wander away from a food source at a predictable and constant rate (Lipton et al., 2004). This can be examined in an assay in which the movement of the animal is tracked over time to determine the leaving probability of any given genotype (Figure 3A; Lipton et al., 2004). We observed that mutants in both the DAF-7/TGF-β ligand and its Type I receptor, DAF-1, showed defects in the mate-searching assay (Figure 3A and B, and Figure 3—figure supplement 1). This behavioral defect in the daf-7 mutant can be fully suppressed by mutation of the downstream antagonistic co-SMAD, DAF-3, suggesting that DAF-7 functions through its canonical TGF-β signaling pathway to regulate mate-searching behavior (Figure 3B, and Figure 3—figure supplement 1B). Given the change in expression of daf-7 in the ASJ neurons of males at the transition to adulthood when this behavior is first displayed, we used genetic ablations of the ASJ neuron pair to ask what their contribution to this behavior might be. We observed that the ASJ-ablated animals were defective in mate-searching behavior, establishing a role for the ASJ neuron pair in promoting this behavior (Figure 3C and Figure 3—figure supplement 1A). Importantly, the defects that we see in daf-7 mutant and ASJ-ablated male behavior are not accounted for by global defects in locomotion. When mutant animals are tested on leaving assay plates on which the bacterial food has been fully spread, these males reach the scoring distance at equivalent rates to WT controls (Figure 3—figure supplement 2; Barrios et al., 2012). This suggests that the reduced leaving behavior we observe in these animals isspecific to the decision to leave the food source in search of a mate.

Figure 3. DAF-7/TGF-β is required for male mate-searching behavior.

(A) Schematic of mate-searching assay (top). Animals are placed individually into the center of a lawn of bacteria. The tracks of the animal are followed over time and scored for movement beyond 3 cm away from the food source. A representative data curve is shown on the bottom depicting hermaphrodites (solid black), males (dashed black), and daf-7(e1372) mutant males (blue). (B) Probability of leaving values for WT, daf-7 mutant, and daf-7;daf-3 double mutant males. Values plotted are the average + SEM for two independent experiments, n = 40 animals for all strains except daf-7(ok3125) where n = 29. *p<0.05, **p<0.01 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. n.s., not significant. (C) Probability of leaving values for two independent lines of male animals with genetic ablation of the ASJ neurons, compared with corresponding values for WT and daf-7 mutant males. Values plotted are the average + SEM for two independent experiments for daf-7 mutant animals and three independent experiments for WT control and ASJ ablation strains. n = 60 animals for all strains except daf-7(ok3125) where n = 29 animals. **p<0.01 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. One replicate was performed with the daf-7;daf-3 double mutant strains in 1B and controls (WT and daf-7) are identical, so probability values for that experiment were used in the averages shown in both B and C of this figure. (D) Probability of leaving values for daf-7(ok3125) mutant animals carrying transgenes expressing daf-7 cDNA specifically under the control of the indicated promoters. Values on graph are the average + SEM of two independent experiments with an n = 40 total animals for each strain. **p<0.01 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. n.s., not significant.

DOI: http://dx.doi.org/10.7554/eLife.21166.007

Figure 3.

Figure 3—figure supplement 1. daf-7 regulates mate-searching behavior in males.

Figure 3—figure supplement 1.

(A) Representative mate-searching data for strains with genetic ablation of the ASJ neurons (shown in shades of orange). WT hermaphrodites (solid black), WT males (dashed black), and daf-7 mutant (blue) animals are included in each assay as controls. (B) Representative data for daf-7;daf-3 double mutant (green) in the mate-searching assay. (C) Representative data for daf-7 rescue strains (shown in shades of red). (D) Representative mate-searching curves for daf-1 mutants (purple). (E) Probability of leaving values for WT, daf-7, and daf-1 mutant animals. Values shown are the average + SEM of two independent experiments. n = 40 for WT and daf-7 mutants, n = 32 for daf-1(e1287) and n = 36 for daf-1(m402). *p<0.05 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test.
DOI: http://dx.doi.org/10.7554/eLife.21166.008
Figure 3—figure supplement 2. daf-7 mutant animals and strains carrying genetic ablation of the ASJ neurons exhibit no locomotion defect.

Figure 3—figure supplement 2.

(A) Schematic of locomotion assay. E. coli food (shown in yellow) was spread to the edges of the plate and a standard mate searching assay performed to determine animal movement on a full lawn of bacteria. (B–C) Raw data curves for daf-7 (blue) and ASJ-ablation (orange) males in locomotion assay. WT males shown in black for reference.
DOI: http://dx.doi.org/10.7554/eLife.21166.009
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Since DAF-7 is a secreted ligand, we anticipated that overexpression of DAF-7 from either the ASI or ASJ neurons would be sufficient to rescue daf-7-associated mutant phenotypes. As expected, we saw that transgenic rescue from the endogenous promoter as well as from ASI- and ASJ-specific promoters were sufficient to restore mate-searching behavior in the daf-7(ok3125) mutant background (Figure 3D and Figure 3—figure supplement 1C). Taken together, these data imply that the dynamic expression of daf-7 in the ASJ neurons of adult males regulates mate-searching behavior.

Nutritional state dynamically regulates daf-7 expression in the ASJ neurons of males

Mate-searching behavior has been demonstrated to be dependent on the feeding state of the animal—starved male animals will re-prioritize feeding over mate searching for a limited period of time until the animal has had sufficient opportunity to re-feed (Figure 4C; Lipton et al., 2004). We asked whether daf-7 expression in the male ASJ neurons might be dependent on the nutritional state of the animal or the bacterial availability in its environment. We found that males subjected to starvation beginning early in the L4 larval stage failed to express daf-7 in the ASJ neurons as adults (Figure 4A, conditions i and ii, and Figure 4B). This lack of daf-7 in the ASJ neuron pair was apparent both by GFP visualization as well as by FISH, with daf-7 mRNA entirely absent from the ASJ neurons (Figure 4A and B). We noticed that daf-7 mRNA was still apparent in the ASI, OLQ, and ADE neurons of these starved animals, suggesting that the loss of daf-7 expression in the ASJ neurons is specific and not representative of a global down-regulation of transcription in these animals (Figure 4—figure supplement 1).

Figure 4. Nutritional state regulates daf-7 expression in the ASJ neurons of males.

(A) Schematic of experiment design indicating timing and duration of starvation periods (left). FISH images of endogenous daf-7 mRNA in the ASJ neurons for each experimental condition (right). White dotted lines indicate outline of ASJ cell body as localized by ptrx-1::gfp. Scale bar represents 5 µm. (B) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons during re-feeding experiment. Re-fed animals were starved for a period of 24 hr before being reintroduced to E. coli for the indicated amount of time. ***p<0.001 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. Error bars indicate SD. n.s., not significant. (C) Representative curves of mate-searching data in fed and post-starvation WT males. Animals were starved for a period of 24 hr as in previous experiments before being assayed for mate-searching behavior.

DOI: http://dx.doi.org/10.7554/eLife.21166.010

Figure 4.

Figure 4—figure supplement 1. daf-7 expression is down-regulated by starvation specifically in the ASJ neurons.

Figure 4—figure supplement 1.

(A) Representative FISH image of endogenous daf-7 mRNA in a starved adult male. White dotted line indicates outline of an ASJ neuron. Closed triangle indicates an ASI neuron. Other neurons visible anterior to the ASI neuron are likely the OLQ neurons, and posterior to the ASJ neuron are likely the ADE neurons. Scale bar represents 25 µm. (B) Fluorescence quantification for daf-7-Cy5 probe in the ASJ neurons (as localized by ptrx-1::gfp) of males fed and starved at various different points in their lives. ***p<0.001 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. Error bars represent SD. n.s., not significant. (C) Fluorescence quantification for daf-7-Cy5 probe in the ASI neurons of starved and fed males. Significance determined by unpaired t-test with Welch’s correction. Error bars represent SD. n.s., not significant.
DOI: http://dx.doi.org/10.7554/eLife.21166.011
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We next asked if daf-7 expression could be dynamically modulated by removal and re-introduction of food at various points during the life of the male. We first looked at daf-7 expression in animals that had experienced starvation during the L4-to-adulthood period before being returned to an E. coli food source as adults. In these animals, daf-7 expression could be detected both by the GFP reporter as well as by FISH (Figure 4A, condition iii, and 4B). We asked whether fully mature adult animals would turn off daf-7 expression in response to starvation after having already induced expression of daf-7 in the ASJ neuron pair. For these experiments, we utilized FISH of the endogenous daf-7 mRNA because perdurance of the GFP reporter might complicate analysis. When males were allowed to develop into adulthood unperturbed and then subjected to a period of food deprivation, we observed a complete loss of daf-7 mRNA in the ASJ neurons (Figure 4A, condition iv). Together this data demonstrates that daf-7 expression in the ASJ neurons is subject to dynamic regulation by periods of starvation and re-feeding.

These data suggest two distinct possibilities for how bacterial food levels in the environment modulate daf-7 transcriptional regulation in the ASJ neuron pair of males. First, daf-7 transcription could be regulated by the internal nutritional state of the animal (starved or fed). Alternatively, daf-7 transcription could be activated by the chemosensation (smell or taste) of bacterial food. To distinguish between these two possibilities, we measured the kinetics of daf-7 expression in response to re-feeding in starved animals. We observed that daf-7 expression in the ASJ neuron pair is not significantly increased compared to starved controls until 9 hr after the re-introduction of an E. coli food source (Figure 4B). Although some animals could be observed expressing daf-7 weakly in the ASJ neuron pair at 4 hr of re-feeding, the majority of animals still exhibited no pdaf-7::gfp expression in the ASJ neuron pair until later time points. The extended period of time required to restore daf-7 expression in the ASJ neuron pair suggests that internal nutritional state, not the chemosensation of bacterial food, exerts control over daf-7 transcription in the ASJ neuron pair. Moreover, we observed that the onset of daf-7 expression in the ASJ neurons of males following the re-introduction of food are consistent with the previously noted kinetics of resumption of mate-searching behavior after males have been starved (Figure 4C; Lipton et al., 2004).

Differential regulation of daf-7 expression in the ASJ neurons establishes a hierarchy of behaviors in male C. elegans

We recently showed that the microbial environment is an important regulator of daf-7 expression in the ASJ neurons in hermaphrodite animals (Figure 1D; Meisel et al., 2014). Given that males induce expression of daf-7 in the same ASJ neuron pair independently of the bacterial food source, we sought to determine if they would be capable of responding to exposure to P. aeruginosa in the same way as their hermaphrodite siblings—namely, through additional up-regulation of daf-7 expression in the ASJ neurons. We observe that, when transferred to P. aeruginosa, males carrying the pdaf-7::gfp transcriptional reporter exhibited an increase in daf-7 expression in the ASJ neurons compared to E. coli-fed controls (Figure 1D). The additive nature of DAF-7 levels in males suggests that the ASJ neuron pair of males retain the ability to respond to P. aeruginosa that we observe in hermaphrodites.

Our data suggest that daf-7 expression in the ASJ neurons is subject to regulation by both sensory cues from the microbial environment as well as by internal state sensing mechanisms. Because daf-7 expression in the ASJ neuron pair and mate-searching behavior in males are dependent on nutritional state during feeding on the non-pathogenic bacterial food, E. coli, we sought to determine if expression of daf-7 in response to P. aeruginosa might also be dependent on the nutritional state in males. We tested this by challenging starved animals with E. coli or P. aeruginosa to see how daf-7 expression would be affected and to observe any behavioral differences. Looking at animals carrying the pdaf-7::gfp reporter during post-starvation re-feeding, we observed a rapid up-regulation of daf-7 expression in the ASJ neurons of starved males returned to P. aeruginosa as a food source (Figure 5A and B, and Figure 5—figure supplement 1E). This increase in daf-7 expression in the ASJ neuron pair could be seen as early as 2 hr after first exposure to the pathogenic bacteria (Figure 5—figure supplement 1E). In contrast, starved males that were returned to the non-pathogenic E. coli showed little to no daf-7 expression in the ASJ neurons until much later time points (Figure 5A,B and 4B). The kinetics of the increase in fluorescence of the pdaf-7::gfp reporter in response to P. aeruginosa secondary metabolites, which lags behind the immediate response observed by FISH is consistent with what we observed previously for hermaphrodite animals (Meisel et al., 2014), and notably faster than the slower increase in pdaf-7::gfp reporter fluorescence in response to repletion of the non-pathogenic E. coli bacterial food.

Figure 5. Prioritization of multiple inputs through the regulation of daf-7 expression in the ASJ neurons of males.

(A) Schematic of refeeding experimental design indicating timing and duration of each starving and feeding period (left). On right, representative images of daf-7 expression following 4 hr of post-starvation refeeding on E.coli (left) or P.aeruginosa (right). Closed triangles indicate the ASI neurons; dashed triangles indicate the ASJ neurons. Scale bar represents 50 µm. (B) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons of fed and starved animals and animals that were starved for a period of 24 hr and then reintroduced either to the normal E. coli food source or to pathogenic P. aeruginosa. Images were taken for quantification after 4 hr of re-feeding. ***p<0.001 as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. Error bars indicate SD. n.s., not significant. (C) Representative curve of food-leaving data in starved animals on E. coli (yellow) and P. aeruginosa (green). Animals were starved as in previous experiments before being run in the assay.

DOI: http://dx.doi.org/10.7554/eLife.21166.012

Figure 5.

Figure 5—figure supplement 1. P. aeruginosa influences exploratory behavior and daf-7 expression in both males and hermaphrodites.

Figure 5—figure supplement 1.

(A) Representative leaving curves for males (dashed) and hermaphrodites (solid) on E. coli (shades of grey) and P. aeruginosa (shades of green). All strains were fed in this experiment. (B) Probability of leaving values for males and hermaphrodites on E. coli and P. aeruginosa. All strains were fed in these experiments. Values plotted are the mean + SEM for two independent experiments, n = 40 animals for all conditions. *p<0.05 as determined by unpaired t-test with Welch’s correction. n.s., not significant. (C) Representative raw data curves for starved hermaphrodites on E. coli and P. aeruginosa. Fed hermaphrodites shown as control. (D) Maximum fluorescence of pdaf-7::gfp in the ASJ neurons of starved hermaphrodites re-fed E. coli or P. aeruginosa for four hours (compare to Figure 5B). Error bars indicate SD. (E) Maximum fluorescence values of pdaf-7::gfp in the ASJ neurons of fed and starved animals and animals that were starved for a period of 24 hr and then reintroduced to P. aeruginosa for the indicated amount of time. The experiment in Figure 4B was run in parallel, controls (fed and starved) were shared between conditions. These controls are shown in both figures for comparison purposes. *p<0.05 and ***p<0.001, as determined by ordinary one-way ANOVA followed by Dunnett’s multiple comparisons test. Error bars indicate S.D.
DOI: http://dx.doi.org/10.7554/eLife.21166.013
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We followed up by asking if this difference in expression after starvation is also reflected in behavioral differences of post-starvation animals experiencing different microbial environments. Normally, following a period of starvation, a male prefers feeding over leaving a lawn of bacteria in search of a mate (Figure 4C; Lipton et al., 2004), but we reasoned that these priorities might be re-set if the only available food is pathogenic to the starved animal. Indeed, whereas starved males will remain on the E. coli lawn for several hours, starved males who are instead returned to a lawn of P. aeruginosa will readily leave the bacterial lawn at a rate similar to non-starved animals on the normal E. coli food source (Figures 4C and 5C). This lawn-leaving behavior is not male-specific, as both fed and starved hermaphrodites will also readily leave a lawn of P. aeruginosa and starved hermaphrodites are also capable of responding to P. aeruginosa through an upregulation of daf-7 in the ASJ neurons (Figure 5—figure supplement 1A–1D). In this regard, one might consider that lawn-leaving under these conditions is driven by the presence of pathogenic P. aeruginosa, and not mate-searching. Our data suggest that daf-7 expression in the ASJ neurons is one way through which animals are both able to interpret internal and external cues and prioritize their behaviors accordingly.

Discussion

We have presented a set of experiments that suggest that behavioral prioritization and decision-making may be effected through the transcriptional control of a key neuroendocrine regulator, the TGF-β ligand, DAF-7, in a pair of chemosensory neurons, the ASJ neurons. Our data suggest that daf-7 expression in the ASJ neuron pair is utilized to promote exploratory behaviors in different physiological and ecological contexts. In hermaphrodites, expression of daf-7 is induced by the detection of secondary metabolites and functions to allow animals to discriminate between microbial species and promote avoidance of pathogenic bacteria (Meisel et al., 2014). In essence, pathogen avoidance represents the behavioral choice an animal makes when confronted with two competing needs—the need to eat and remain well fed and the need to avoid danger and infection. Mate searching presents a paralagous but sex-specific behavior, where the decision instead is between food and mating. Our data suggest that modulation of daf-7 expression provides a striking example of how a neuroendocrine signaling pathway may be coopted to guide behavioral decisions in entirely different contexts.

Our study suggests that internal states and environmental cues that converge on the transcriptional control of DAF-7 in the ASJ neuron pair are processed in a hierarchical manner that, in turn, serves to modulate the exploratory mate-searching behavior in the male (Figure 6). The work presented here suggests that the transcriptional regulation of daf-7 in the ASJ neurons functions as an ON/OFF switch, where each input holds the switch—and thus, daf-7 expression—in one of two states. However, the various regulatory inputs into this switch exert differential control, with environmental cues being prioritized over all others. This differential control of the transcriptional switch, in turn allows for re-adjustments of behavioral priorities in the worm based on its current and past experience.

Figure 6. A hierarchy of inputs regulates daf-7 expression in the ASJ neurons to modulate exploratory behaviors.

Figure 6.

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We show that the information from many different sources both internal and external is integrated hierarchically in the regulation of daf-7 expression in the ASJ neuron pair. This hierarchical regulation of daf-7 in turn leads to a distinct prioritization of exploratory behaviors in the male worm.

DOI: http://dx.doi.org/10.7554/eLife.21166.014

Interestingly, dynamic transcriptional regulation has previously been implicated in the regulation of sex-specific decision-making behavior in C. elegans. Expression of the chemoreceptor, ODR-10, in the sex-shared sensory AWA neurons has also been shown to be dependent on both internal and external cues to regulate food-related decision making in male C. elegans (Ryan et al., 2014). Given the similarities in the regulation of these two genes by both sex and satiety, it is possible that DAF-7 and ODR-10 function in a single pathway to regulate decision-making behaviors in the male. Previous studies of daf-7 have suggested that it is involved in regulating the expression of numerous chemoreceptors in many different neuron types (Nolan et al., 2002). While no interaction has been identified between daf-7 and odr-10 in the hermaphrodite nervous system, there has been no examination as yet of the effects of daf-7 mutation on odr-10 in the relevant cell types, sex, or under different food conditions, which may be an interesting line of future research.

DAF-7/TGF-β has previously been found to be involved in the regulation of other satiety-regulated behaviors such as quiescence and foraging (Gallagher et al., 2013; Milward et al., 2011; You et al., 2008). daf-7 mutants show marked defects in the ability to respond to fasting through an increase in quiescence, suggesting that DAF-7 may serve as a critical signal of food availability in the worm (You et al., 2008). Similarly, DAF-7 signaling has also been implicated in promoting food-leaving (or foraging) in the context of a rapidly depleting food source, further underscoring the importance of this pathway for communicating nutritional availability (Milward et al., 2011). While DAF-7 from the ASI neurons, and not the ASJ neurons, contributes to these other possibly related phenotypes, similar mechanisms may be involved in regulating daf-7 expression and release in these three distinct food/satiety-dependent assay contexts. Taken together with our data, the important role of daf-7 in these different behavioral paradigms suggests that the daf-7 pathway may act as a more global food signal that is critical for allowing the animal to sense food and satiety and modulate its behaviors accordingly.

Finally, our results support a model where integration of internal and external sensory information can occur at the level of the sensory neuron itself to regulate behavioral prioritization. Our data on the role of the ASJ sensory neurons in male mate-searching behavior are consistent with emerging evidence from studies in several species to suggest that the regulatory control of sensory neurons contributes to information processing and decision making behavior (Dey et al., 2015; Lebreton et al., 2015; Peckol et al., 2001; Ryan et al., 2014).

Materials and methods

C. elegans strains

C. elegans were grown on E. coli OP50 as a food source as previously described (Brenner, 1974). Strains were grown at 20°C except for assays containing dauer-constitutive mutants, in which case, all strains were grown at 16°C until they passed the dauer developmental decision. Unless otherwise indicated, all strains carry the him-5(e1490) mutation to increase the number of spontaneous males available. For a complete list of strains used in this study, please see Supplementary file 1.

Measurement of gene expression in the ASJ neurons

For quantification of daf-7 expression in mutants and developing animals, animals were egg laid for 2 hr on OP50 to obtain synchronized populations of animals. The animals were then mounted and anesthetized in 50 mM sodium azide at the indicated hour of development or at 72 hr if not indicated. The animals were imaged at 40x using a Zeiss Axioimager Z1 microscope. 15–20 animals were imaged for each condition or strain. For quantification, maximum intensity values of GFP within the ASJ neurons was calculated using FIJI software (Schindelin et al., 2012); Fiji, RRID:SCR_002285).

For P. aeruginosa experiments, the P. aeruginosa PA14 strain was grown overnight at 37°C in 3 mL of LB as previously described and the next day 7 µL of culture was seeded onto SKA plates (Tan et al., 1999). Plates were incubated at 37°C overnight and then allowed to grow for an additional two days at room temperature before being used for experiments. Animals for P.aeruginosa experiments were synchronized by treatment with bleach and then allowed to hatch and arrest as L1 larvae in M9 media overnight. This provided synchronized populations free from any possible bacterial contamination. Animals were transferred to PA14 plates or OP50 controls at the L4 larval stage. Imaging and quantification were performed as described above at 16 hr after transfer to PA14 plates.

Generation of transgenic animals

To generate the neural feminization and masculinization transgenes, the pGH8 plasmid containing the pan-neural rab-3 promoter along with mCherry::unc-54 3’UTR was linearized by PCR. The fem-3 and intracellular tra-2 cDNAs were amplified from cDNA generated with an Ambion RETROScript kit. The unc-54 3’UTR was amplified from the pPD95.75 vector and the SL2 trans-splicing sequence leader (Huang et al., 2001; Spieth et al., 1993) was amplified from genomic DNA. The fem-3 or tra-2 cDNA along with the unc-54 3’UTR and SL2 sequence were cloned into the linearized pGH8 vector by Gibson assembly (Gibson et al., 2009). For cell specific manipulations, the ciliated neuron bbs-1 promoter (1.9 kb) and ASJ specific trx-1 promoter (1.1 kb; Fierro-González et al., 2011) were amplified from genomic DNA and inserted in the place of the rab-3 promoter by Gibson assembly. All plasmids were sequenced to confirm identity and injected into ksIs2;him-5(e1490) animals at a concentration of 50 ng/µL, along with a plasmid carrying ofm-1::gfp (50 ng/µL). At least three independent transgenic lines were obtained and analyzed for each construct and one representative line is shown. For a complete list of primers used in this paper, please see Supplementary file 2.

Mate-searching assays

Mate-searching behavior was assessed in animals through a food leaving assay as previously described (See diagram in Figure 3A; Lipton et al., 2004). Briefly, animals were placed individually onto a 1 cm lawn (~20 µL of culture) of E. coli OP50 in the center of a 10 cm plate. Movement of each animal was tracked at hourly time points. When an animal’s tracks extended a distance of 3 cm away from the starting lawn, the animal was scored as a ‘leaver’. It has been previously demonstrated that male leaving behavior can be modeled by the single exponential decay function N(t)/N(0)=exp(-λt), where N(t) refers to the number of non-leavers at a given time and the hazard value (λ) gives an estimate for the probability of leaving, which remains constant over the course of an assay (Lipton et al., 2004). Hazard values were calculated by fitting data using the R survival package with an exponential parametric survival model using maximum likelihood (R Project for Statistical Computing, RRID:SCR_001905). These values were pooled across replicates. At least two independent experiments were performed for each genotype (~40 animals per genotype). For leaving assays with P. aeruginosa, plates were supplemented with additional peptone and were seeded with 15 µL of bacterial culture. In addition, all plates for PA14 assays were incubated overnight at 37°C after being seeded with bacteria and then for an additional 2 days at room temperature before being used for the assay.

For locomotion assays, 10 cm mate-searching plates were seeded with ~400 µL of E. coli OP50 culture spread to the edge of the plate. Plates were allowed to dry and remained at room temperature for ~16 hr before being used in the assay. Males were placed individually on these plates and their movement tracked over time as in the standard mate-searching assay. The same scoring distance was used for locomotion assays as for the mate-searching assay.

Fluorescence In Situ hybridization

FISH was performed as described previously (Raj et al., 2008). Animals were fixed in 4% formaldehyde for 45 min at 20°C. Following washing in PBS, animals were resuspended in 70% ethanol and incubated overnight at 4°C. Samples were then hybridized with probes to the endogenous daf-7 mRNA as previously published (Meisel et al., 2014). Hybridization was carried out at 30°C overnight. Imaging was performed using a Nikon Eclipse Ti Inverted microscope with a Princeton Instruments PIXIS 1024 camera. All data were analyzed in FIJI. For quantifications of FISH data, fluorescence values were calculated within the ASJ (or ASI) neurons for the indicated conditions. All samples were hybridized using daf-7-Cy5 probes and imaged at an exposure time of 1500 ms. For all FISH experiments, animals carrying the ofEx4[ptrx-1::gfp] transgene were used in order to localize the ASJ neurons.

Starvation experiments

For all starvation experiments, animals were synchronized by treatment with bleach and then were allowed to hatch and arrest as L1s in M9 media for 14 hr. After 14 hr, animals were dropped onto plates containing abundant OP50 E. coli and were allowed to develop for 34–36 hr at 20°C. At this time point, animals had already entered the L4 larval stage. All animals were washed from the plates and subjected to an additional 4–5 washes with M9 media to remove any remaining bacteria. Animals were placed either back onto plates seeded with E. coli or were dropped onto plates lacking peptone to inhibit any bacterial growth.

For re-feeding experiments, animals were starved on peptone free plates for 24 hr at 20°C. After 24 hr of starvation, nearly all of the male animals had molted into adults as evident by tail and gonadal morphology. Only animals with adult morphology were used for experiments and imaging. They were subsequently collected and placed onto plates seeded with either E. coli or P. aeruginosa for the designated amount of time. For the FISH experiment shown in Figure 3, animals were re-fed on E. coli OP50 for 16 hr at 20°C before being fixed for imaging.

For the late starve experiments, animals dropped back onto E. coli after the washing step were allowed to grow for an additional 24 hr at 20°C before being collected and washed 4–5 times in M9 media. These animals were then placed onto peptone-free plates and starved for 16 hr at 20°C before being fixed for imaging.

Statistical analyses

All statistical analysis was performed using the GraphPad Prism software (Graphpad Prism, RRID:SCR_002798). Statistical tests used are indicated in each figure legend.

Acknowledgements

We thank HR Horvitz and the Caenorhabditis Genetics Center, which is funded by the NIH Office of Research Infrastructure Programs (P40 OD010440), for strains. We thank members of the Kim and Horvitz labs for helpful conversation and feedback on the manuscript and figures.

Funding Statement

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Funding Information

This paper was supported by the following grant:

  • National Institutes of Health GM084477 to Dennis H Kim.

Additional information

Competing interests

The authors declare that no competing interests exist.

Author contributions

ZAH, Conceptualization, Formal analysis, Validation, Investigation, Visualization, Methodology, Writing—original draft, Writing—review and editing.

DHK, Conceptualization, Supervision, Funding acquisition, Visualization, Methodology, Writing—original draft, Writing—review and editing.

Additional files

Supplementary file 1. C. elegans strains used in this study.

A comprehensive list of the strains used in this study. With the exception of CB1490, all strains are previously unpublished and were constructed for this study.

DOI: http://dx.doi.org/10.7554/eLife.21166.015

elife-21166-supp1.docx (90.3KB, docx)
DOI: 10.7554/eLife.21166.015
Supplementary file 2. Oligos used for transgenic strain generation.

A comprehensive list of the oligos used for constructing the transgenic strains created for this study. All sequences are listed in the 5’ to 3’ direction.

DOI: http://dx.doi.org/10.7554/eLife.21166.016

elife-21166-supp2.docx (114.1KB, docx)
DOI: 10.7554/eLife.21166.016

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eLife. 2017 Jan 24;6:e21166. doi: 10.7554/eLife.21166.017

Decision letter

Editor: Oliver Hobert1

In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.

Thank you for submitting your article "Sexually Dimorphic Expression of daf-7/TGF-β in Sensory Neurons Regulates Behavior of C. elegans" for consideration by eLife. Your article has been reviewed by three peer reviewers, one of whom, Oliver Hobert, is a member of our Board of Reviewing Editors, and the evaluation has been overseen by a Senior Editor. The following individual involved in review of your submission has agreed to reveal her identity: Arantza Barrios (Reviewer #3).

The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.

All reviewers appreciated the overall importance of this work. Dynamic regulation of sensory neuron functions by external conditions and internal state is now appreciated as a major mechanism underlying behavioral plasticity. The ability to monitor the expression of single genes with defined functions in individual identified neurons in C. elegans, together with the ability to precisely manipulate external and internal conditions, has made this organism an excellent choice for exploring sensory neuron contributions to behavioral changes.

In this paper, the authors have followed up on their previous finding that the spatial expression pattern of the daf-7 TGF-β ligand is dynamically regulated by perception of specific bacterial metabolites. You demonstrate that daf-7 expression in the ASJ sensory neurons is also regulated by genetic sex, and that this sexually dimorphic expression contributes to male mate-searching behavior. Further regulation of expression by nutritional state allows reprioritization of feeding over mate-searching, a behavioral change previously reported by others. Overall, the experiments are nicely done, and the observation is novel. However, a number of concerns need to be addressed before this manuscript becomes acceptable for publication in eLife:

Major comments:

– One major concern is that this work is not well integrated with previously reported related work (Young-Jai You, Birgitte Olofsson) that implicated DAF-7 in regulating foraging behaviors in response to satiety state. Such integration would provide a more nuanced view that would make this work appropriate for publication in eLife. Several experiments are possible to integrate previous results on the roles of DAF-7 and ODR-10 in exploratory vs feeding behaviors. We suggest some specific ones here although other approaches may also be appropriate: (a) Compare time course of changes in daf-7 vs odr-10 expression upon starvation; (b) test if the changes in daf-7 and odr-10 are interdependent or independent of each other (i.e. analyze reporters in respective mutant backgrounds); (c) test if NPR-5 is involved in regulation of daf-7 expression in ASJ in males as a function of satiety; (d) Do males raised on P. aeruginosa also exhibit increased food leaving?

– In Figure 5C, starved males are shown to leave a lawn of P. aeruginosa at a higher rate than E. coli, and this is interpreted as mate-searching behavior. However, the leaving assay does not discriminate mate-searching behavior from what could be pathogen avoidance in this context. Either this assay needs to be performed on hermaphrodites to distinguish it as a male-specific behavior, or an additional assay (i.e. retention assay, as in Barrios et al. 2008) performed to distinguish between these two possibilities.

– Exploratory behaviors rely on the ability of worms to locomote properly. The authors need to show that ASJ-ablated and daf-7 mutant males have no general defects in locomotion before they can conclude that these manipulations specifically affect the decision to explore within or away from the patch of food. One way by which this could be addressed is by measuring and comparing the rate at which wild-type and experimental males reach the scoring distance in a leaving-assay plate when the area is completely covered with food (as in Barrios et al. 2012, Nat. Neurosc. for example).

eLife. 2017 Jan 24;6:e21166. doi: 10.7554/eLife.21166.018

Author response

Major comments:

– One major concern is that this work is not well integrated with previously reported related work (Young-Jai You, Birgitte Olofsson) that implicated DAF-7 in regulating foraging behaviors in response to satiety state. Such integration would provide a more nuanced view that would make this work appropriate for publication in eLife.

We have included a more complete description of prior studies that have implicated a role for DAF-7 in behaviors modulated by satiety. In addition, we have investigated how genes previously implicated by the work of You and Olofsson in satiety-influenced behaviors affect the expression of DAF-7 in the ASJ neurons of males that promotes mate-searching behavior. Our studies in the development of the revised manuscript suggest that there is not a straightforward correlation that can be applied in the genetic analysis of the three distinct DAF-7-involved behavioral phenotypes of quiescence, foraging, and male mate-searching behavior.

Several experiments are possible to integrate previous results on the roles of DAF-7 and ODR-10 in exploratory vs feeding behaviors. We suggest some specific ones here although other approaches may also be appropriate: (a) Compare time course of changes in daf-7 vs odr-10 expression upon starvation; (b) test if the changes in daf-7 and odr-10 are interdependent or independent of each other (i.e. analyze reporters in respective mutant backgrounds); (c) test if NPR-5 is involved in regulation of daf-7 expression in ASJ in males as a function of satiety; (d) Do males raised on P. aeruginosa also exhibit increased food leaving?

We agree that suggested experiments linking daf-7 and odr-10 might be illuminating given prior work that implicates dynamic changes in odr-10 expression in the sensory neurons of males. Because the reported changes in odr-10 expression show a variable qualitative increase during starvation compared with the switch-like behavior of changes in daf-7 expression in the ASJ neuron, we anticipate that DAF-7 may function upstream of the regulation of odr-10 expression. We provide further discussion of possible connections between DAF-7 and the prior work of Ryan et al. on ODR-10 in the Discussion of our revised manuscript.

We tested whether npr-5 mutants exhibited altered expression of daf-7 in the ASJ neurons of males but did not observe any appreciable change under fed or starved conditions.

The reviewers suggest an experiment involving raising males on P. aeruginosa, but unfortunately, the pathogenicity of P. aeruginosa precludes such an analysis, as male and hermaphrodite animals raised in such a manner are sick and dying.

– In Figure 5C, starved males are shown to leave a lawn of P. aeruginosa at a higher rate than E. coli, and this is interpreted as mate-searching behavior. However, the leaving assay does not discriminate mate-searching behavior from what could be pathogen avoidance in this context. Either this assay needs to be performed on hermaphrodites to distinguish it as a male-specific behavior, or an additional assay (i.e. retention assay, as in Barrios et al. 2008) performed to distinguish between these two possibilities.

We regret not providing a clear explanation of our rationale and interpretation of this experiment. Given our observation that starvation could abrogate the expression of daf-7 expression in the ASJ neurons in males that would promote mate-searching under fed conditions, we sought to test whether starvation could also override our previously described induction of daf-7 expression in the ASJ neurons in animals exposed to P. aeruginosa. We observe that males that have been starved maintain expression of daf-7 in the ASJ neuron pair on P. aeruginosa and correspondingly exhibit food-leaving behavior—indeed, as the reviewer suggests, we interpret this as primarily driven by pathogen avoidance. We provide several additional panels (Figure 5—figure supplement 1A-D), which show that this P. aeruginosa leaving behavior is executed by both males and hermaphrodites, fed and starved. Additionally, we did perform a retention assay, and saw that while hermaphrodites suppressed the leaving behavior of starved males on E. coli, their presence was not sufficient to suppress P. aeruginosa leaving behaviors. We have provided further clarification and discussion in the text to clarify the rationale and interpretation of this important experiment.

– Exploratory behaviors rely on the ability of worms to locomote properly. The authors need to show that ASJ-ablated and daf-7 mutant males have no general defects in locomotion before they can conclude that these manipulations specifically affect the decision to explore within or away from the patch of food. One way by which this could be addressed is by measuring and comparing the rate at which wild-type and experimental males reach the scoring distance in a leaving-assay plate when the area is completely covered with food (as in Barrios et al. 2012, Nat. Neurosc. for example).

We thank the reviewers for this suggestion. We performed leaving assays with the daf-7 mutant and ASJ ablated strains in which the plate was covered with bacteria, and observed no difference in the ability of mutant animals to reach the scoring distance. These data are provided as Figure 3—figure supplement 2.

Associated Data

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

    Supplementary Materials

    Supplementary file 1. C. elegans strains used in this study.

    A comprehensive list of the strains used in this study. With the exception of CB1490, all strains are previously unpublished and were constructed for this study.

    DOI: http://dx.doi.org/10.7554/eLife.21166.015

    elife-21166-supp1.docx (90.3KB, docx)
    DOI: 10.7554/eLife.21166.015
    Supplementary file 2. Oligos used for transgenic strain generation.

    A comprehensive list of the oligos used for constructing the transgenic strains created for this study. All sequences are listed in the 5’ to 3’ direction.

    DOI: http://dx.doi.org/10.7554/eLife.21166.016

    elife-21166-supp2.docx (114.1KB, docx)
    DOI: 10.7554/eLife.21166.016

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