Katherine Shaw
Chunyu Lu1
Xiaochun Liu
Vance L. Trudeau- 1Department of Biology, University of Ottawa, Ottawa, ON, Canada
- 2State Key Laboratory of Biocontrol, Institute of Aquatic Economic Animals and Guangdong Province Key Laboratory for Aquatic Economic Animals, School of Life Sciences, Sun Yat-Sen University, Guangzhou, China
In zebrafish, estrogens produced in the ovaries via Cyp19a1a activity are required for both sexual differentiation of the ovary during early development as well as maintenance of the ovarian state during adulthood. The importance of Cyp19a1b that is highly expressed in the brain for female reproduction is still under study. We previously reported that female cyp19a1b-/- mutant zebrafish have significantly lower brain estradiol levels and impaired spawning behavior characterized by an increased latency to oviposition during dyadic sexual behavior encounters. In the current study, we provide evidence that the delayed oviposition in female cyp19a1b-/- mutants is linked to impaired arginine vasopressin (Avp) signaling. Droplet digital PCR experiments revealed that levels of the estrogen receptors, avp, and oxytocin (oxt) are lower in the hypothalamus of mutant females compared to wildtype fish. We then used acute intraperitoneal injections of Avp and Oxt, along with mixtures of their respective receptor antagonists, to determine that Avp can uniquely rescue the delayed oviposition in female cyp19a1b-/- mutants. Using immunohistochemistry, we demonstrated that Cyp19a1b-expressing radial glial cell (RGC) fibers surround and are in contact with Avp-immunopositive neurons in the preoptic areas of the brain. This could provide the neuroanatomical proximity for RGC-derived estrogens to diffuse to and activate estrogen receptors and regulate avp expression levels. Together these findings identify a positive link between Cyp19a1b and Avp for female zebrafish sexual behavior. They also suggest that the female cyp19a1b-/- mutant behavioral phenotype is likely a consequence of impaired processing of Avp-dependent social cues important for mate identification and assessment.
1 Introduction
Estrogens are critical for female reproduction (1). The final and rate limiting step for bioactive estrogen production involves the aromatase (Cyp19a1) enzyme that converts the aromatizable androgens, testosterone and androstenedione, into the bioactive estrogens, estradiol (E2) and estrone, respectively (2). Teleosts have two paralogs encoding aromatase, cyp19a1a and cyp19a1b, that are highly expressed in the ovaries and brain, respectively, due to distinct regulatory elements in their promoter regions (3, 4). Estrogens can exert diverse effects in the body by binding to different estrogen receptors (Esrs) that initiate various signalling pathways with tissue- and cell-specific effects (5). Gene expression can be regulated directly by nuclear Esrs (nEsrs) binding to estrogen response elements (EREs) in gene promoter regions or through indirect pathways involving protein-protein interactions with transcription factors such as the Activator protein 1 (Ap1) and the Specificity protein 1 (Sp1), when bound to their respective promoter elements (6). Though comparatively less studied, membrane-bound Esrs (mEsrs) have also been shown to affect the expression levels of estrogen-regulated genes through second messenger signalling pathways (7). Teleosts have three nEsrs named estrogen receptor 1 (esr1), estrogen receptor 2a (esr2a), and estrogen receptor 2b (esr2b; 8), and the mEsr, g-protein coupled estrogen receptor (gper; 9).
A recent report indicated that cyp19a1b-/- mutant female zebrafish that have significantly lower brain E2 levels compared to wildtype (WT) females have altered female sexual behavior (10). Mutant cyp19a1b-/- females had delayed spawning behavior with WT males in sexual behavior assays compared to WT females. This delayed initiation of sexual behavior is reminiscent of the phenotype observed in aromatase knockout (Aro KO) mice that have reduced sexual behavior (11–15). The behavioral impairments in Aro KO mice are hypothesized to be linked to disrupted olfactory discrimination that reduces social recognition through effects on nEsrs and the nonapeptides, oxytocin (oxt) and arginine vasopressin (avp; 16–18). The overlapping behavioral impairments of the Aro KO mice and cyp19a1b-/- mutant zebrafish suggest potential similarities in the disruption of the signalling pathways underlying the behavioral phenotypes despite differences in cellular localization of brain aromatase. In mice, under normal conditions, aromatase is constitutively expressed in neurons (19). However, in teleosts, due to the presence of a cis-acting regulatory glial x responsive element in the cyp19a1b promoter region, aromatase is exclusively expressed in radial glial cells (RGCs; 3). Thus, the effects of RGC-derived estrogens on female sexual behavior are most likely to occur through E2 diffusing to bind Esrs in nearby neurons to affect signalling pathways involving estrogen-regulated genes important for behavior. There are several candidate genes known to affect zebrafish sexual behavior that could be linked to the female cyp19a1b-/- mutant behavioral phenotype.
An involvement of the nonapeptides in female teleost sexual behavior is strongly suggested by the findings of changes in brain nonapeptide levels across female reproductive states (20–27) and observations that exogenous E2 administration upregulates brain nonapeptide levels (28–31). The nonapeptides exert effects on reproduction through two main signalling pathways in the brain. Firstly, through a hypophysiotropic pathway involving magnocellular neurons in the preoptic area (POA) that project towards the pituitary gland for nonapeptide release into the circulatory system to regulate processes including osmoregulation, gonadal steroidogenesis, gametogenesis and parturition, amongst others (32–34). Secondly, through an encephalotropic pathway involving parvocellular and gigantocellular neurons that project to other brain regions including the telencephalon, prethalamus, hypothalamus, optic tectum, and the hindbrain (32, 33). The encephalotropic pathway is hypothesized to underly the neuromodulatory roles of the nonapeptides in affecting the salience of social information processing in the brain that can affect social recognition and behaviors (35). Indeed, recent findings from teleost studies have identified impairments in social recognition and behavior in avp-/- and oxt-/- mutant females that indicate important roles of these nonapeptides in female sexual behavior. For example, female avp-/- mutant zebrafish displayed reduced sexual behavior characterized by fewer quiver events produced, a measure of female sexual receptivity, when paired with WT males in sexual interactions (36). In another study, the mate preference of female Japanese medaka (Oryzias latipes) for familiar males was absent in oxt-/- and oxytocin receptor 1-/- (oxtr1-/-) mutants suggesting reduced social recognition of mates compared to WT females during pairwise mating trials (37). Given the well conserved expression pattern of cyp19a1b in RGCs lining the teleost diencephalic ventricle (38), which is in close neuroanatomical proximity to the POA where high nonapeptide expression is observed (39), further study to characterize the interactions of cyp19a1b and nonapeptides in the female teleost brain in association with sexual behavior are well warranted.
Other important neuropeptides for female zebrafish sexual behavior are secretoneurin A (SNa) and secretoneurin B (SNb) that are derived from proteolytic processing of the precursor secretogranin 2a (Scg2a) and secretogranin 2b (Scg2b) proteins, respectively. Analysis of scg2a-/- and scg2b-/- frameshift mutant zebrafish lines demonstrated their critical importance for female sexual behavior, ovulation, oviposition, and fertility (40). Interactions between the secretogranergic system and Cyp19a1b have been previously identified in the teleost brain in regions important for sexual behavior. For example, scg2a and scg2b transcripts are expressed in numerous brain regions important for reproduction that lie close to the diencephalic ventricle (41) where cyp19a1b is highly expressed (38). A close neuroanatomical proximity between the soma of Scg2a-immunoreactive neurons and RGC fibres where Cyp19a1b is expressed was also identified in the POA of female goldfish (42). Intracerebroventricular injection of SNa downregulated cyp19a1b levels in the female goldfish telencephalon and hypothalamus, suggesting a regulatory pathway between SNa and neuroestrogen production (42). Together, these findings suggest potential interactions between the SNs and cyp19a1b that might be important for the regulation of female sexual behavior.
The purpose of this study was to investigate the mechanistic pathways through which cyp19a1b mutation in female zebrafish disrupts sexual behavior. Based on the findings from the various studies of Aro KO mice and the recent discoveries of the importance of the nonapeptides and secretoneurins for female zebrafish sexual behavior, we focused the study on identifying the potential interactions between cyp19a1b, the nEsrs and these neuropeptides. We first used droplet digital polymerase chain reaction (ddPCR) experiments to identify significantly lower levels of avp and oxt in the hypothalamus of female cyp19a1b-/- mutants. We then conducted acute injections of the nonapeptides and observed that Avp uniquely rescued the delayed oviposition in female cyp19a1b-/- mutants and this effect was blocked with administration of an arginine vasopressin receptor 1a (Avpr1a) antagonist. Using immunohistochemistry, the preoptic areas were identified as regions with close neuroanatomical proximity between Cyp19a1b-expressing RGCs and Avp-immunopositive neurons in the female zebrafish brain. Together, our findings demonstrate that the impaired sexual behavior in female cyp19a1b-/- mutant zebrafish is likely a consequence of disrupted estrogenic regulation of avp in preoptic areas and that these behavioral effects can be rescued by acute Avp administration in adult fish.
We have adopted the guidelines of the Zebrafish Information Network (ZFIN, www.zfin.org) for nomenclature to designate teleost genes and their protein counterparts. Of note, the recently determined zebrafish nomenclature for avp/Avp and oxt/Oxt contrasts the historically used nomenclature of avt/Avt and ist/Ist. This change highlights the homologous nature of the nonapeptide genes and their protein counterparts rather than the differences in the teleost and mammalian amino acid compositions.
2 Materials and methods
2.1 Experimental animals
Wildtype, cyp19a1b-/- mutant female (43), and cyp19a1b-GFP transgenic (Tg(cyp19a1b-GFP); 44) zebrafish were raised in the University of Ottawa Aquatics Facility. Fish were housed in 10-L tanks of dechloraminated recirculating water maintained at 28°C on a 14:10 light:dark cycle, and fed twice daily at 11h00 and 15h00. All fish tested in this experiment were between the ages of 5-11 months post-fertilization and had no previous experience in the sexual behavior assay; with males and females separated for at least two weeks prior to testing.
2.2 Total RNA extraction and cDNA synthesis
For gene expression measurements, the telencephalon and hypothalamus were selected for study because they contain many key brain areas for regulating sexual behavior and reproduction (45). Female WT and cyp19a1b-/- mutant fish (n=6-9 per group) were euthanized in an ice water bath at two time points corresponding to during (10h00) and outside (14h00) the timing of zebrafish reproductive behavior. The brains were immediately removed, and the telencephalon was dissected at its connections to the olfactory bulb and hypothalamus and placed into a 1.5 mL RNase-free Eppendorf tubes on dry ice. The brains were then inverted to dissect the hypothalamus region including the ventrolateral extending hypothalamic lobes and diencephalon tissue ventral to the optic tectum and placed into separate 1.5 mL RNase-free Eppendorf tubes on dry ice. This dissection method produces telencephalon samples containing the dorsal and ventral telencephalon regions as well as the anterior preoptic area encompassing the parvocellular preoptic neurons, whilst the hypothalamus samples contain the posterior preoptic area including the magnocellular and gigantocellular neurons and surrounding hypothalamic regions. Total ribonucleic acid (RNA) was isolated from samples using Trizol (Thermo Fisher Scientific, Waltham, MA, USA, cat# 15596018) according to the manufacturer’s instructions with a few modifications. Briefly, 50 µL Trizol was added to each tube and tissues were homogenized using a pestle with intermittent vortexing. Samples were incubated for 5 mins at room temperature and then 10 µL chloroform was added to each tube, vortexed, and allowed to incubate for 3 mins. Following incubation, samples were centrifuged for 5 mins at 12,600 rpm at 4°C, the supernatant was carefully transferred to a new labelled RNase-free 1.5 mL tube and 25 µL isopropanol was added to each tube, and samples were vortexed. The tubes were incubated for 10 mins at room temperature and then centrifuged for 30 mins at 12,600 rpm at 4°C. The isopropanol was removed, and pellets were rinsed with 50 µL of 75% ethanol (EtOH) followed by centrifugation for 5 mins at 12,600 rpm at 4°C. The EtOH was then removed from tubes and the rinse step was repeated. The tubes were then left open for 2 mins in a fumehood to dry the samples. Samples were resuspended in 20 µL RNase-free ddH2O and incubated for 10 mins at 60°C on a heat block. The samples were then vortexed and placed on ice before quality assessment. Total RNA concentration as well as 260/280 and 260/230 absorbance measurements were assessed using a spectrophotometer (Thermo Fisher Scientific, NanoDrop 2000). RNA integrity was verified using gel electrophoresis (1% weight/volume agarose). RNA was stored at -80°C until further usage. Total complementary DNA (cDNA) was synthesized using the iScript Reverse Transcription Supermix (Bio-Rad, Hercules, CA, USA, cat# 1708841), according to the manufacturer’s instructions. Synthesis of cDNA used 600 ng of total RNA from telencephalon and hypothalamus samples and cDNA was stored at -20°C.
2.3 Primer design
Primers for gene expression analysis were designed using either NCBI Primer Blast Software (https://www.ncbi.nlm.nih.gov/tools/primer-blast/) or obtained from previous gene expression analysis studies (40, 41, 46). All primers were supplied by Integrated DNA Technologies (Coralville, IA, USA) and the specificity of primers for the genes of interest were confirmed by sanger sequencing of PCR products (Génome Québec, Montréal, QC, Canada) and sequences were matched to the zebrafish genome using the NIH Basic Local Alignment Search Tool (https://blast.ncbi.nlm.nih.gov/Blast.cgi). Appropriate annealing temperatures and cDNA dilutions for ddPCR analysis were identified by performing thermal gradients (51-63°C) with cDNA collected from telencephalon and hypothalamus (1:2 – 1:320 dilution) samples. Primer sequences, annealing temperatures, and amplicon sizes are presented in Table 1.
Table 1 Primer pairs and experimental conditions for gene expression analyses of telencephalon and hypothalamus samples.
2.4 Droplet digital PCR protocol
The ddPCR procedures including experiment set-up, droplet generation, and transfer of emulsified samples to PCR plates, were performed according to the manufacturer’s protocols (Bio-Rad, QX200 Droplet Digital PCR system). In brief, at the start of the experiment, telencephalon or hypothalamus cDNA samples were diluted to the appropriate concentration determined for each primer pair. The reaction mixtures were prepared, each containing 11.5 µL EvaGreen ddPCR Supermix (Bio-Rad, cat# 1864034), 0.23 µL of 10 µM gene-specific forward and revere primers, 6.04 µL nuclease-free water, and 5 µL of template cDNA at primer-specific dilution. 20 µL of the sample reactions were then carefully transferred into the wells of a droplet generation cartridge (Bio-Rad, cat# 1864008) along with droplet generation oil (Bio-Rad, cat# 1864006) to the corresponding oil wells. The cartridge was sealed with a gasket (Bio-Rad, cat# 1863009) and then inserted into a droplet generator (Bio-Rad, model# QX200 Droplet Generator) for droplet generation. The emulsified samples were then carefully transferred to the wells of a 96-well ddPCR plate (Bio-Rad, cat# 12001925) and sealed with a heat foil (Bio-Rad, cat# 1814040). The PCR reactions were performed using a thermal cycler (Bio-Rad, model# C1000 Touch Thermal Cycler) with the cycle conditions: (95°C for 5 mins), 49 cycles of ((95°C for 30 secs), (annealing temperature for 1 min), (72°C for 30 secs), with a ramp rate of -2°C/sec), followed by (4°C for 5 mins), (90°C for 5 mins), and finally (12°C for 5 mins). The fluorescence of droplets was measured using a droplet reader (Bio-Rad, model# QX200 Droplet Reader) and data were analyzed using QuantaSoft Analysis Pro software (Bio-Rad, v1.0.596).
2.5 Brain estradiol enzyme-linked immunosorbent assays
Validated brain steroid extraction (47) and E2 quantification (10) using ELISA test kits (Cayman Chemical, cat# 501890) have been described previously. In brief, brains were collected at two time points corresponding to the morning at the time of lights on when zebrafish are sexually active (10h00) and at a later midpoint time in the light cycle when fish are not sexually active (14h00; n=4-5 per group). At each time point, both WT and cyp19a1b-/- mutant female fish were euthanized in an ice water bath, and brains were immediately dissected and placed into individual labelled 1.5 mL Eppendorf tubes. Homogenization buffer (150 µL per brain) was added to each tube and tissues were then individually sonicated for steroid release into solution. Tubes were centrifuged (4°C, 13,200 rpm, 10 mins) and the supernatant was then carefully removed and transferred to a new labelled tube and evaporated to dryness (Labconco Centrivap Centrifugal Vacuum Concentrator, model# 7810014, 45°C, 1 hr), then stored at 4°C overnight. The next day, samples were resuspended with 100 µL resuspension buffer added to each tube, vortexed, and tubes were sonicated in a water bath for 15 mins. Following resuspension, samples were run on C-18 solid-phase extraction columns (47) with a final elution volume of 120 µL. The eluted samples were then evaporated to dryness (45°C, 3 hrs). The evaporated residue was then resuspended in 200 µL ELISA buffer for 24 hrs at 4°C with intermittent vortexing prior to testing. Samples were run in duplicate and only samples with intra-assay coefficient of variations < 10% were used in analyses.
2.6 Characterizing female cyp19a1b-/- mutant sexual behavior following peptide injection
The methods used in this experiment are similar to those previously described (10, 47). For all trials, a cyp19a1b-/- mutant female was size-matched with a male WT fish (within 2 mm BL, < 10% BL difference). All cyp19a1b-/- mutant females tested were derived from a parental strain to ensure identical genetic backgrounds and raised in the same environmental conditions for assessing the effects of treatment on spawning behavior. The WT males tested were similarly derived from a parental strain and raised in the same environmental conditions. The evening before each experiment, paired fish were transferred to a 1-L testing tank containing an insert at the bottom for egg collection and a divider in the middle of the tank to keep the male and female separate before testing. The testing pair was allowed to acclimate overnight in the Zebracube (Viewpoint Behavior Technology, Inc.) with the camera present (either a Panasonic 16GB HC-V700M Full HD camcorder or a Canon VIXIA HF R800 camcorder). The following morning at 9h00, the pair was transferred to a new 1-L testing tank containing clean system water. The female was immediately removed and anesthetized with Tricaine (Syndel, cat# 02168510) according to University of Ottawa zebrafish husbandry procedures, then weighed on an analytical balance, and transferred to a moist sponge with an insert cut for positioning the female for injection. Females (n=15 per group) were intraperitoneally injected with dosages based on bodyweight (bw) using a 32-gauge syringe (Hamilton Company, Reno, NV, USA, cat# CAL80308) with either 1) Ringer’s solution (pH 7), 2) Oxt (0.5 µg/g bw), 3) Avp (0.5 µg/g bw), 4) mix of 0.5 µg/g bw Avp + 5 µg/g bw Manning Compound (an Avpr1a antagonist), or 5) mix of 0.5 µg/g bw Avp + 5 µg/g bw L-368,899 (an Oxtr antagonist). The zebrafish Oxt and Avp peptides were prepared in house by Fmoc/tBu solid-phase peptide synthesis, and sequences were confirmed by mass spectrometry. The peptide receptor antagonists, Manning Compound (Bio-Techne Canada, Toronto, ON, Canada, cat# 3377) and L-368,899 (Bio-Techne Canada, cat# 2641) were dissolved in water according to manufacturer’s instructions. Following injection, the female was immediately transferred to a new housing tank containing clean system water to recover for 5 mins before being transferred back to the testing tank. The divider was then removed, and video recording started. All filming began within 15 mins of lights on (9h00). The pairs were allowed to interact for 60 mins to determine whether the peptide injections could rescue the delayed time to the first oviposition event observed in the female cyp19a1b-/- mutants (10). Videos were coded by date and viewed by an observer blind to the treatment groups using VLC media player (https://www.videolan.org/) to record the time to the first oviposition event.
2.7 Immunohistochemistry
Fish (n=20) from the Tg(cyp19a1b-GFP) line were euthanized using an ice water bath and carefully positioned under a dissection microscope for the careful removal of scales on the skull cap using dissecting tweezers to expose the brain. Fish heads were then dissected away from the body and placed immediately in a falcon tube containing 4% paraformaldehyde in phosphate-buffered saline (PBS; pH 7.4) for 24 hrs fixation on an orbital shaker at room temperature. Fixed samples were then washed with PBS (3 x 20 mins), following which the heads were placed in 0.5 M ethylenediaminetetraacetic acid for 7 days for decalcification. Following decalcification, the samples were then successively dehydrated for 30 mins each in 30%, 50%, 70%, 80% and finally 99% EtOH. Samples were cleared by 2 x 1 hr incubations in 100% xylene, incubated for 1 hr in melted paraffin at 60°C, and then transferred to new melted paraffin and left overnight at 60°C. The next day, the samples were embedded in a cassette containing newly melted paraffin with heads oriented for transverse sectioning and allowed to cool. The embedded heads were sectioned at 15 µm thickness using a motorized microtome (Leica Biosystems, model# RM2255). Sample sections were spread on a 40°C water bath to remove wrinkles and then mounted on Superfrost Plus slides (Thermo Fisher Scientific, cat# 22-037-246). Slides were allowed to air dry and then stored in a slide box at 4°C prior to use.
All wash steps were conducted using glass Coplin jars (Ted Pella, Inc., Redding, CA, USA, cat# 432-1). Slides were first heated for 1 hr at 60°C on a slide warmer to improve tissue adherence to the slides during wash steps. The slides were then deparaffinized by xylene washes (2 x 20 mins) and rehydrated using a series of washes including 2 x 100% EtOH, 2 x 95% EtOH, 1 x 70% EtOH, 1 x PBS, each for 10 mins. The slides were then transferred to Coplin jars containing 0.01 M sodium citrate (pH 6.0) and placed in a 90°C water bath for 30 mins for antigen retrieval. Following this, slides were allowed to cool and washed in PBS (2 x 5 mins), then incubated in blocking buffer (1% bovine serum albumin in 0.3% Triton PBS) for 30 mins. Slides were then placed in a humid chamber at 4°C to incubate overnight with the primary antibodies: anti-Avp (rabbit, Immunostar, Hudson, WI, USA, cat# 20069) and anti-GFP (chicken, Abcam, Cambridge, UK, cat# ab13970), diluted 1:500 in blocking buffer. The anti-Avp antibody was validated and found to be specific for teleost Avp previously in an electric fish (48) and confirmed for zebrafish in this study (see below). The following day, the slides were washed in PBS (2 x 10 mins), and subsequently incubated for 2 hrs in a dark humid chamber at room temperature with the secondary antibodies: donkey anti-rabbit IgG (H+L) Alexa Fluor 680 (Invitrogen, Waltham, MA, USA, cat# A10043) and goat anti-chicken IgY (H+L) Alexa Fluor 594 (Invitrogen, cat# A11042), diluted 1:500 in PBS. The next day, slides were washed in the dark in PBS (2 x 10 mins), then incubated in 200 µL Hoechst solution (1:10,000, Invitrogen, cat# H3570) in a dark chamber for 8 mins, followed by PBS washes (3 x 5 mins) in the dark, and mounted with SlowFade Diamond Antifade Mountant (Invitrogen, cat# S36963) and a cover slip (VWR, Radnor, PA, USA, cat# 48393-221). Slides were stored in the dark until visualization. Slides were imaged using an Olympus confocal microscope (Olympus, Richmond Hill, ON, Canada, model #FV1000) and FV10-ASW-4.2 Viewer software.
2.8 Antibody characterization
The Avp antibody has been previously validated for use in the teleost Brachyhypopomus gauderio (48). To validate the antibody for use in zebrafish, sections were incubated with anti-Avp (1:500) pre-adsorbed for 24 hrs with an excess of zebrafish Avp (10 µM). No Avp labelling was observed in the sections demonstrating primary antiserum specificity. Separate sections were incubated with anti-Avp (1:500) pre-adsorbed for 24 hrs with an excess of zebrafish Oxt (10 µM). Avp labelling was unaffected by pre-adsorption with Oxt, demonstrating antibody specificity for the Avp antigen. Control sections where the primary or secondary antibodies were omitted did not display any labelling.
2.9 Statistical analyses
Statistical analyses were conducted using Graphpad Prism v9 (GraphPad Software, Inc.). For both gene expression data and E2 measurements, normality of residuals and homoscedasticity were assessed using Shapiro-Wilk tests and Spearman’s tests for heteroscedasticity, respectively. Data were then analyzed in Two-Way ANOVA tests followed by Tukey’s multiple comparisons tests with the Holm-Šídák method used to correct for multiple comparisons. Gene expression data that were non-normally distributed were either log- or square root-transformed, and data that could not be normalized through transformation were grouped by genotype and assessed using Mann Whitney tests with the Holm-Šídák method to correct for multiple comparisons. The absolute transcript levels of target genes in the telencephalon and hypothalamus were normalized to tata-binding protein (tbp), an internal housekeeping gene that is not estrogen-regulated (49). There were no significant differences observed in tbp levels across genotype groups or time points in the study confirming the appropriate usage of tbp as a housekeeping gene. Gene expression levels are presented as fold change relative to WT female levels at 10h00 with individual points and means or median values displayed. For the behavioral rescue experiments, normality and homoscedasticity were assessed using Shapiro-Wilk and Levene’s tests, respectively. If a pair did not spawn eggs in the 60-min test period, a maximum latency of 60 mins was assigned. Data were analyzed using a Kruskal-Wallis test followed by Dunn’s multiple comparisons tests for pairwise comparisons. Data are presented as medians, with values for individual pairs displayed. For all data, significance was defined at p < 0.05 and all significance tests were assessed as two-tailed.
3 Results
3.1 Decreased expression levels of reproductive neuroendocrine genes in the telencephalon and hypothalamus of cyp19a1b-/- mutant females
3.1.1 Telencephalon
Two-Way ANOVA was used to assess the effects of time (10h00 and 14h00) and genotype (cyp19a1b-/- mutant and WT) on gene expression levels in the telencephalon.
There were small differences in the expression levels of the Esrs between the telencephalon of female WT and cyp19a1b-/- mutants. While there were no significant main effects of time (F(1,25)=0.9293, p=0.3443) or genotype (F(1,25)=2.668, p=0.1149) on esr1 levels, there was a statistically significant time X genotype interaction (F(1,25)=5.554, p=0.0266). Post-hoc tests revealed that the telencephalon of WT females had 1.9 times higher esr1 levels compared to cyp19a1b-/- mutant females at 10h00 (p=0.0217; Figure 1A). There were no other significant interactions. A significant main effect of genotype (F(1,25)=8.662, p=0.0069), but not of time (F(1,25)=3.400, p=0.0771) or time X genotype interaction (F(1,25)=2.375, p=0.1358), on esr2a levels was observed. The telencephalon of WT females had 1.7 times higher esr2a levels compared to cyp19a1b-/- mutant females (Figure 1B). For esr2b levels, there were no significant differences in esr2b levels at either 10h00 (U(6,8)=21.00, p=0.2991) or 14h00 (U(5,6)=9.00, p=0.1925; Figure 1C).
Figure 1 Gene expression in the telencephalon of adult wildtype (A++B++) and cyp19a1b-/- mutant (A++B–) female zebrafish in the morning (10h00) and afternoon (14h00). The abundance of mRNAs (copies/µL) for all genes measured was normalized by tata-binding protein levels within the sample and data are plotted as fold change relative to the wildtype female levels at 10h00. Parametric data were analyzed by Two-Way ANOVA tests followed by Tukey’s multiple comparisons tests and individual values are plotted with bars representing mean values (A, B, D, F, G), whilst non-parametric data were analyzed using multiple Mann-Whitney U tests with a Holm-Šídák correction for multiple comparisons and plotted as individual points with bars representing median values (C, E). Error bars are not displayed for clarity. Significant main effects of time (horizontal bars) and genotype (arrows) are indicated by asterisks (** p<0.01; *** p<0.001). When there is a statistically significant interaction effect, means with different letters a-b represent statistically significant differences (p<0.05).
No significant main effects were observed of time (F(1,24)=0.2294, p=0.6363), genotype (F(1,24)=0.5074, p=0.4831), or time X genotype interaction (F(1,24)=0.3781, p=0.5444) on oxt levels (Figure 1D). There were no significant differences in avp levels at either 10h00 (U(7,8)=34.00, p=0.8884) or 14h00 (U(5,6)=17.00, p=0.8618; Figure 1E).
There were statistically significant main effects of time for both scg2a (F(1,26)=7.717, p=0.0100) and scg2b (F(1,25)=14.21, p=0.0009) levels in the telencephalon. Levels of scg2a and scg2b were 1.4 and 1.3 times higher, respectively, at 10h00 compared to 14h00 (Figures 1F, G). There was also a significant main effect of genotype (F(1,25)=8.833, p=0.0065) on scg2b levels. The telencephalon of WT females had 1.2 times higher scg2b levels compared to cyp19a1b-/- mutant females (Figure 1G). There was no significant main effect of genotype on scg2a levels (F(1,26)=2.501, p=0.1258) or time X genotype interaction on scg2a levels (F(1,26)=0.4523, p=0.5072) or scg2b levels (F(1,25)=2.835, p=0.1047).
3.1.2 Hypothalamus
Two-way ANOVA was performed to assess the effects of time (10h00 and 14h00) and genotype (cyp19a1b-/- mutant and WT) on gene expression levels in the hypothalamus.
There were significant differences in esr levels between the hypothalamus of WT and cyp19a1b-/- mutants. There were significant main effects of time (F(1,26)=8.967, p=0.0060) and genotype (F(1,26)=5.475, p=0.0272) on esr1 levels. Levels of esr1 were 1.6 times higher at 14h00 compared to 10h00 (Figure 2A), and WT females had 1.5 times higher esr1 levels compared to cyp19a1b-/- mutant females (Figure 2A). There was no significant time X genotype interaction (F(1,26)=3.758, p=0.0635). No significant main effects of time on esr2a (F(1,25)=2.139, p=0.1560) or esr2b (F(1,27)=0.4068, p=0.5290) levels, or main effects of genotype on esr2a (F(1,25)=0.6108, p=0.4418) or esr2b (F(1,27)=3.782, p=0.0623) levels were observed. However, there were significant time X genotype interactions for esr2a (F(1,25)=10.65, p=0.0032) and esr2b (F(1,27)=9.103, p=0.0055) levels. Post-hoc tests revealed that the hypothalamus of WT females had 3.1 times higher esr2a levels compared to cyp19a1b-/- mutant females at 14h00 (p=0.0076; Figure 2B). Levels of esr2b were 2.4 times higher in the hypothalamus of WT females compared cyp19a1b-/- mutant females at 14h00 (p=0.0120; Figure 2C). No other significant interactions were evident.
Figure 2 Gene expression in the hypothalamus of adult wildtype (A++B++) and cyp19a1b-/- mutant (A++B–) female zebrafish in the morning (10h00) and afternoon (14h00). The abundance of mRNAs (copies/µL) for all genes measured were normalized by tata-binding protein levels within the sample and data are plotted as fold change relative to the wildtype female levels at 10h00. Parametric data were analyzed by Two-Way ANOVA tests followed by Tukey’s multiple comparisons tests and individual values are plotted with bars representing mean values (A–E, G), whilst non-parametric data were analyzed using multiple Mann-Whitney U tests with a Holm-Šídák correction for multiple comparisons and plotted as individual points with bars representing median values (F). Error bars are not displayed for clarity. Significant main effects of time (horizontal bars) and genotype (arrows) are indicated by asterisks (* p<0.05; ** p<0.01). When there is a statistically significant interaction effect, means with different letters a-b represent statistically significant differences (p<0.05).
There were large differences in oxt and avp levels in the hypothalamus of WT and cyp19a1b-/- mutant females. Significant main effects of genotype on both oxt (F(1,27)=7.300, p=0.0118) and avp (F(1,27)=6.848, p=0.0144) levels were observed. The hypothalamus of WT females had 3.2 and 1.8 times higher oxt and avp levels, respectively, compared to cyp19a1b-/- mutant females (Figures 2D, E). There were no significant main effects of time on oxt (F(1,27)=0.0019, p=0.9656) or avp (F(1,27)=0.0848, p=0.7731) levels, or time X genotype interactions on oxt (F(1,27)=1.373, p=0.2515) or avp (F(1,27)=0.0083, p=0.9281) levels.
No significant differences in scg2a levels at either 10h00 (U(6,7)=22.00, p=0.3282) or 14h00 (U(6,7)=11.00, p=0.1852; Figure 2F) were observed. There was a significant time X genotype interaction on scg2b levels (F(1,26)=6.704, p=0.0156), with post-hoc tests revealing that cyp19a1b-/- mutant females had 1.7 times higher scg2b levels at 10h00 compared to 14h00 (p=0.0153; Figure 2G). There were no other significant interactions and no main effects of time (F(1,26)=4.097, p=0.0537) or genotype (F(1,26)=0.8427, p=0.3671) on hypothalamic scg2b levels.
3.2 Brain estradiol content fluctuates between the morning and afternoon
There was a significant main effect of time on brain E2 levels (F(1,13)=10.14, p=0.0072). Brain E2 levels were 1.4 times higher at 14h00 compared to 10h00 (Figure 3). There was also a significant main effect of genotype (F(1,13)=23.04, p=0.0003). WT brains had 1.7 times higher E2 levels compared to cyp19a1b-/- mutant brains (Figure 3). There was no significant time X genotype interaction (F(1,13)=2.291, p=0.1541).
Figure 3 Estradiol (E2) levels in the brains of adult wildtype (A++B++) and cyp19a1b-/- mutant (A++B–) female zebrafish in the morning (10h00) and afternoon (14h00). Data were analyzed using a Two-Way ANOVA followed by Tukey’s multiple comparisons tests. Significant main effects of time (**, p=0.0072) and genotype (*** with arrow; p=0.0003) are indicated. There was no significant interaction effect. Data are plotted as means + standard error of the mean (n=4-5 per group).
3.3 Arginine vasopressin injection rescues the behavioral phenotype in cyp19a1b-/- mutant females
There was a significant difference in the time to the first oviposition event amongst the cyp19a1b-/- mutant female groups (H(4)=14.87, p=0.005; Figure 4). Pairwise comparisons revealed that both Avp (p=0.0221) and Avp + L-368,899 (p=0.0155) groups took significantly less time to the first oviposition event compared to the saline-injected group. Saline-injected cyp19a1b-/- mutant females took 5.5 and 4.3 times longer to the first oviposition event compared to Avp- and Avp + L-368,899-injected cyp19a1b-/- mutant females, respectively. There were no significant differences in the time to the first oviposition event in the Avp + Manning Compound (p=0.7986) or Oxt (p>0.9999) groups compared to saline-injected fish.
Figure 4 Time to first oviposition event during zebrafish pairwise mating trials with female cyp19a1b-/- mutant fish intraperitoneally injected with nonapeptides and mixed nonapeptides with receptor antagonists (n=15 per group). Significant differences were assessed using a Kruskal-Wallis test followed by a Dunn’s multiple comparisons test. Individual data points are displayed with red bars representing median values. Different letters a-b represent statistically significant differences. Statistical significance is defined at p<0.05.
3.4 Cyp19a1b-immunopositive radial glial cell fibres contact arginine vasopressin cells in preoptic areas
Avp immunolabelling in POA neurons (Figure 5) was absent in sections pre-adsorbed with Avp (Figure 5B), but not when pre-adsorbed with Oxt (Figure 5C). Subpopulations of POA neurons were identified based on their neuroanatomical positions in the rostral-caudal and ventral-dorsal axes as previously described (50). Avp-immunopositive neurons were found exclusively in the POA in periventricular locations. In the anterior POA, Cyp19a1b-expressing RGCs in the peripheral layer of the ventral telencephalon were observed in contact with the soma of parvocellular Avp-immunopositive cell bodies (Figure 6). In the posterior POA, probable contact points between Cyp19a1b-expressing RGC fibres lining the diencephalic ventricle and cell bodies of magnocellular and gigantocellular Avp-immunopositive neurons were observable indicating potential functional relationships (Figure 7).
Figure 5 Arginine vasopressin (Avp) immunolabelling in pre-adsorption tests with Avp and Oxytocin (Oxt) in a transverse section of a female wildtype zebrafish preoptic area. The confocal images show Avp-immunopositive cell bodies surrounding the diencephalic ventricle (A). No Avp-immunopositive neurons were present in sections pre-adsorbed with Avp (B). Avp immunolabelling was unaffected in sections pre-adsorbed with Oxt (C). Scale bar=20 µm.
Figure 6 Double immunofluorescence against Cyp19a1b (green) and Arginine vasopressin (Avp; red) in a female Tg(cyp19a1b-GFP) zebrafish anterior preoptic area. In this transverse brain section, Cyp19a1b-positive radial glial cells fibres lining the peripheral layer of the ventral telencephalon (A) surround an Avp-immunopositive parvocellular cell body (B). The nuclear stain Hoescht (blue) is also shown (C). Single slice scanning view of the boxed area in panel D shows Cyp19a1b-positive fibres in contact with the Avp-immunopositive cell body (E). Scale bar=20 µm.
Figure 7 Double immunofluorescence against Cyp19a1b (green) and Arginine vasopressin (Avp; red) in a female Tg(cyp19a1b-GFP) zebrafish posterior preoptic area. In this transverse brain section, Cyp19a1b-positive radial glial cell fibres (A, F) surround Avp-immunoreactive magnocellular (B) and gigantocellular (G) cell bodies. The nuclear stain Hoescht (blue) is also shown (C, H). Single slice scanning view of the boxed areas in (D, I) show Cyp19a1b-positive fibres in contact with the Avp-immunopositive cell bodies (E, J). Scale bar=20 µm.
4 Discussion
It was previously reported that female cyp19a1b-/- mutant zebrafish paired with WT males have a significantly longer latency to initiate spawning compared to WT females during dyadic sexual behavior assays (10). This is suggestive of an impairment in the ability of a female mutant to identify and/or assess a potential mate. Since cyp19a1b is exclusively expressed in RGCs in the teleost brain (38), these findings indicate that locally produced E2 in RGCs is likely diffusing to activate Esrs in nearby neurons to affect the expression of behaviorally relevant estrogen-regulated genes. Indeed, teleost RGCs have been previously shown to have the full complement of steroidogenic enzymes necessary for de novo steroidogenesis and the importance of RGC-derived steroids in the teleost brain for diverse functions, from regulating neurogenesis to various aspects of social behavior has been previously proposed (51). To identify the potential neuroendocrine mechanism underlying the behavioral impairment observed in the cyp19a1b-/- mutant females, we used ddPCR experiments to first quantify changes in the Esrs (esr1, esr2a, esr2b), the nonapeptides (avp, oxt), and the secretogranin 2s (scg2a, scg2b). Telencephalon and hypothalamus samples were analyzed separately at two time points corresponding to during (10h00) and outside (14h00) the time of zebrafish reproductive activity. The findings from the ddPCR experiments revealed significant effects of cyp19a1b mutation on the expression levels of esrs, avp, and oxt in the hypothalamus.
The telencephalon and hypothalamus of cyp19a1b-/- mutant females had significantly lower Esr levels compared to WT females. Levels of esr1 were 1.5 times higher in the hypothalamus of WT fish compared to cyp19a1b-/- mutants. This finding is supported by the previously observed lower brain E2 levels in mutant females (10) and the known positive estrogenic regulation of esr1 due to the presence of an ERE in its promoter region. Time-dependent expression profiles of esr1 were also observed. Levels were 1.6 times higher in the hypothalamus at 14h00 compared to 10h00, and 1.9 times higher levels specifically at 10h00 in the telencephalon of WT females compared to cyp19a1b-/- mutants. Lower levels of esr2a and esr2b were also identified in female cyp19a1b-/- mutants compared to WT females with region- and time-specific effects. Levels of esr2a were 1.7 times higher in the telencephalon of WT females compared to cyp19a1b-/- mutant females, whilst in the hypothalamus both esr2a and esr2b levels were 3.1 and 2.4 times higher, respectively, in WT females compared to mutants specifically at 14h00.
There has been surprisingly little study of the importance of brain Esr signalling for female teleost sexual behavior, outside of fertility assessments. Of the few studies conducted, no effects of esr2a mutation were observed on female medaka sexual behavior (52); however, esr2b mutation affected female sexual receptivity. In pairwise mating trials of medaka, female esr2b-/- mutants were unreceptive to males and therefore did not spawn eggs despite normal ovarian function (53). The study revealed that the female-biased sexual dimorphism in esr2b-expressing neurons in the ventral telencephalic area and the magnocellular/gigantocellular portion of the posterior POA decreased following water-borne aromatase inhibitor treatment, indicating that aromatase activity positively regulates brain esr2b levels. Medaka esr2b was shown to be positively estrogen-regulated using a luciferase reporter cell line in combination with E2 treatment. Together, these findings demonstrate that aromatase activity positively regulates Esr2b signalling levels in female medaka in brain regions important for sexual behavior. Our study findings suggest that brain aromatase activity likely regulates esr2b levels in the female zebrafish brain and that these effects may be linked to female sexual behavior. While in-depth study of esr1-/- mutant effects on female teleost sexual behavior have not been investigated, we observed that esr1 levels were lower in the hypothalamus of cyp19a1b-/- mutants compared to WT females at the time of reproductive activity. Further study of Esr1 involvement in female zebrafish sexual behavior seem particularly well warranted given the similar behavioral phenotypes of female Aro KO and Esr1 KO mice that display increased rejection of male stud mice during sexual behavior assays (11, 13; 54). In zebrafish, all three nEsrs are expressed in neuroendocrine regions controlling female sexual behavior, paralleling cyp19a1b expression (55, 56). Our findings of lower esr levels in the telencephalon and hypothalamus of female cyp19a1b-/- mutants that have abnormal spawning behavior draws attention to the need for further study of esr-/- mutant effects on female sexual behavior.
Both avp and oxt were expressed at significantly lower levels in the hypothalamus of cyp19a1b-/- mutant females compared to WT fish. The hypothalamus of WT females had 1.8 times and 3.2 times higher levels of avp and oxt, respectively, compared to cyp19a1b-/- mutants. These findings are supported by other teleost studies demonstrating that E2 administration increases brain avp and/or oxt levels (28–31, 57, 58). The lower nonapeptides levels in the hypothalamus of female cyp19a1b-/- mutants is particularly interesting considering the important role of Avp and Oxt signalling in modifying the salience of social information processing in the brain to affect behavior (35). Recent studies of nonapeptide mutant lines have identified important roles of Avp and Oxt signalling for mate assessment. Female avp-/- mutant zebrafish displayed significantly reduced sexual receptivity compared to WT females during sexual interactions with WT males (36). In another study, oxt-/- and oxtr1-/- mutant Japanese medaka showed reduced social recognition of familiar males compared to WT females during sexual behavior assays (37). An impairment of sensory information processing that functions in mate identification and assessment, such as might occur by reduced avp and/or oxt levels, could represent a link to the behavioral phenotype observed in the cyp19a1b-/- mutant females during sexual behavior assays (10). Together, these findings suggest that the longer latency to initiate spawning behavior in the cyp19a1b-/- mutant females could be a consequence of impaired processing of sensory information due to reduced positive estrogenic regulation of Avp and/or Oxt signalling in the brain.
There were significant main effects of time on scg2a and scg2b levels in the telencephalon that confirm their high expression levels in the morning during the time at which zebrafish are sexually active. However, there were only minor differences in expression levels between the brains of cyp19a1b-/- mutant and WT females. For example, scg2b levels in the telencephalon of WT females were 1.2 times higher than those observed in cyp19a1b-/- mutants. Though these data indicate some change in scg2b levels, they are unlikely to explain the significant behavioral phenotype of the cyp19a1b-/- mutant females. Of note, scg2a-/- and scg2b-/- mutant female zebrafish are characterized by an ovulatory rather than behavioral dysfunction that underlies their impaired reproductive capacity (40). Therefore, the behavioral dysfunction in the cyp19a1b-/- mutant females seems unlikely to be directly associated with impaired SN signalling.
Based on the differences observed in the expression levels of genes between the morning and afternoon sampling times, we then assessed E2 brain content in cyp19a1b-/- mutants and WT females to determine if there were significant differences at the sampling time points. Female WT brains had 1.7 times higher E2 content compared to cyp19a1b-/- mutant brains confirming our previous study (10). Brain E2 content was 1.4 times higher in the afternoon compared to the morning. This difference in brain E2 content most likely represents E2 that crosses the blood-brain barrier from systemic circulation due to increased Cyp19a1a activity in the ovary at this time. Since no significant differences in ovarian E2 content (10) or serum E2 levels (43) were previously observed between cyp19a1b-/- mutants and WT females, the larger increase in brain E2 content from 10h00 to 14h00 in WT females compared to cyp19a1b-/- mutant females could represent the onset of brain cyp19a1b upregulation in WT females that does not occur in the cyp19a1b-/- mutants. Support for this hypothesis is provided by a previous gene expression study that identified a peak in ovarian cyp19a1a levels at the mid-point of the light phase that was followed by later increased brain cyp19a1b levels (59). This daily rhythm of gene expression is hypothesized to serve important functions in regulating reproductive activity in diurnal spawners like that observed in seasonally breeding species. In seasonally breeding teleosts, increased circulating E2 levels in females, driven by ovarian recrudescence and increased Cyp19a1a activity in the ovary, peak prior to the breeding season. This increases brain cyp19a1b levels and Cyp19a1b activity in the breeding months, due to the positive estrogenic regulation of cyp19a1b (60–63). The expected increase in brain esr1 levels and E2 content in the afternoon was absent in female cyp19a1b-/- mutants. While speculative, it is possible that this altered expression profile is part of the mechanism underlying the behavioral impairment in female cyp19a1b-/- mutants.
We conducted acute intraperitoneal injections of teleost Avp and Oxt to see if either nonapeptide could rescue the behavioral phenotype in the cyp19a1b-/- mutant females. The nonapeptides were selected for study in the rescue experiment based on their known effects on social recognition and the findings that avp and oxt levels were ~45% and ~68% lower, respectively, in the hypothalamus of cyp19a1b-/- mutants compared to WT fish. Acute intraperitoneal Avp injections could rescue the time to the first oviposition event in female cyp19a1b-/- mutants. This behavioral rescue was receptor-dependent because antagonism of Avpr1a receptor signalling by co-administration of Manning Compound blocked the effect of Avp to advance oviposition in female mutants. In marked contrast, coadministration of the Oxtr antagonist L-368,899 had no effect on Avp action. This demonstrates that the rescue effects observed are specific to Avp signalling pathways.
These findings are supported by a previous study in female Asian stinging catfish (Heteropneustes fossilis), whereby low dosage 0.1 µg/g bw E2 intraperitoneal injections given daily for three days in ovariectomized females increased brain Avp levels (29). A functional relationship between E2 and Avp has also been previously observed in female round gobies (Neogobius melanostomus) during the spawning-capable phase whereby brain explants perfused in vitro with E2 released higher concentrations of Avp into the surrounding medium (31). Perfusion of brain explants with E2 increased Oxt release in vitro. Nonapeptide release induced by E2 could be blocked by administration of actinomycin D, demonstrating the dependence of E2 action on de novo RNA synthesis. It is interesting to note that Avp release also occurred rapidly, within 20 mins of E2 administration, suggesting an additional non-genomic pathway of estrogenic regulation. It would be interesting in a future study to measure the levels of bioactive nonapeptides in the brains of cyp19a1b-/- mutants to complement the findings in the current study. Indeed, previous studies in other teleosts have demonstrated links between oviposition and bioactive brain nonapeptide levels in the females (25, 64). It will also be important in future study to identify the potential additional contributions of Gper (the teleost mEsr) signalling to the observed behavioral phenotype in the cyp19a1b-/- mutants. Since significantly lower levels of nuclear esrs were identified in addition to avp in the hypothalamus of cyp19a1b-/- mutants compared to WT females, the current findings suggest at least a genomic regulatory mechanism underlying the behavioral phenotype observed in the mutant fish.
Since acute Avp injection uniquely rescued the delayed oviposition in cyp19a1b-/- mutants, we wanted to establish the neuroanatomical basis for Cyp19a1b-derived estrogenic communication with Avp neurons. To investigate the neuroanatomical proximity for brain-derived E2 induction of avp levels, we used immunohistochemistry with a teleost-validated Avp antibody and the Tg(cyp19a1b-GFP) zebrafish line (44). Close neuroanatomical proximities between Cyp19a1b-positive RGC fibres and Avp-immunopositive cell bodies were identified in the anterior and posterior parts of the POA. This could allow RGC-derived E2 to diffuse into nearby Avp-immunopositive neurons to regulate avp levels in the female zebrafish brain. A close association between Cyp19a1b-immunopositive RGC fibres and avp/Avp-expressing neurons in the POA has also been previously demonstrated in the orange-spotted grouper (Epinephelus coioides; 30) and the bluehead wrasse (Thalassoma bifasciatum; 65). In the orange-spotted grouper, avp colocalized with esr1, esr2b and gper in all three preoptic neuron populations- the parvocellular, magnocellular, and gigantocellular neurons, indicating the potential for direct estrogenic regulation of avp levels (30). In the bluehead wrasse, Cyp19a1b-positive RGC fibres were observed in close association to Avp-immunopositive cell bodies in the POA, indicating a potential functional relationship (65). Though the functional importance of the individual Avp subpopulations in teleost social behavior is currently unknown, evidence has suggested a potential role of gigantocellular neurons in female reproduction. A previous study in the half-spotted goby (Asterropteryx semipunctata) identified significantly high numbers of gigantocellular neurons in the peak-spawning period compared to the pre- and post-spawning periods, which was not seen similarly in the parvocellular or magnocellular neurons (22). These differences were also observed, however, in the non-spawning season and thus it is unclear whether the gigantocellular Avp-immunopositive neurons contribute to female reproduction. It will be important in future to identify if nEsrs colocalize with Avp in the female zebrafish brain to determine if there is a direct pathway for estrogenic regulation of avp. Future study should also identify which Avp-immunopositive subpopulations in the POA are important for the observed effects on female sexual behavior.
5 Conclusions
We have demonstrated that Avp rescues the behavioral phenotype of female cyp19a1b-/- mutant zebrafish. Our data indicate that lower brain E2 levels in the cyp19a1b-/- mutant females reduces Avp signalling in the hypothalamus leading to an increased latency to the first oviposition event during pairwise mating trials. Contact points between Cyp19a1b-expressing RGCs and Avp-immunopositive cell bodies in the POA identify the neuroanatomical proximity and region of interest for locally produced E2 to regulate avp levels. Rescue of delayed oviposition with a single injection of Avp indicates the importance of the RGC-Avp network in the regulation of female behavior. Further study will be needed to identify nEsr and Avp colocalization and the neuronal subpopulations in the POA responsible for the observed effects on female spawning behavior.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The animal study was approved by University of Ottawa Protocol Review Committee. The study was conducted in accordance with the local legislation and institutional requirements.
Author contributions
KS: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Visualization, Writing – original draft, Writing – review & editing. CL: Methodology, Writing – review & editing. XL: Methodology, Writing – review & editing. VT: Conceptualization, Funding acquisition, Resources, Supervision, Writing – review & editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by an Ontario Graduate Scholarship (KS), University of Ottawa Research Chair in Neuroendocrinology (VT), and the Natural Sciences and Engineering Research Council of Canada Graduate Scholarship (KS) and Discovery Grant (VT) Programs.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Findlay JK, Liew SH, Simpson ER, Korach KS. Estrogen signaling in the regulation of female reproductive functions. Fertil Control (2010) 198:29–35. doi: 10.1007/978-3-642-02062-9_2
2. Simpson ER, Mahendroo MS, Means GD, Kilgore MW, Hinshelwood MM, Graham-Lorence S, et al. Aromatase cytochrome P450, the enzyme responsible for estrogen biosynthesis. Endocr Rev (1994) 15(3):342–55. doi: 10.1210/edrv-15-3-342
3. Le Page Y, Menuet A, Kah O, Pakdel F. Characterization of a cis-acting element involved in cell-specific expression of the zebrafish brain aromatase gene. Mol Reprod Development: Incorporating Gamete Res (2008) 75(10):1549–57. doi: 10.1002/mrd.20892
4. Diotel N, Le Page Y, Mouriec K, Tong SK, Pellegrini E, Vaillant C, et al. Aromatase in the brain of teleost fish: expression, regulation and putative functions. Front Neuroendocrinol (2010) 31(2):172–92. doi: 10.1016/j.yfrne.2010.01.003
5. Heldring N, Pike A, Andersson S, Matthews J, Cheng G, Hartman J, et al. Estrogen receptors: how do they signal and what are their targets. Physiol Rev (2007) 87(3):905–31. doi: 10.1152/physrev.00026.2006
6. Klinge CM. Estrogen receptor interaction with estrogen response elements. Nucleic Acids Res (2001) 29(14):2905–19. doi: 10.1093/nar/29.14.2905
7. Maggiolini M, Picard D. The unfolding stories of GPR30, a new membrane-bound estrogen receptor. J Endocrinol (2010) 204(2):105–14. doi: 10.1677/JOE-09-0242
8. Nelson ER, Habibi HR. Estrogen receptor function and regulation in fish and other vertebrates. Gen Comp Endocrinol (2013) 192:15–24. doi: 10.1016/j.ygcen.2013.03.032
9. Thomas P. Rapid steroid hormone actions initiated at the cell surface and the receptors that mediate them with an emphasis on recent progress in fish models. Gen Comp Endocrinol (2012) 175(3):367–83. doi: 10.1016/j.ygcen.2011.11.032
10. Shaw K, Therrien M, Lu C, Liu X, Trudeau VL. Mutation of brain aromatase disrupts spawning behavior and reproductive health in female zebrafish. Front Endocrinol (2023) 14:1225199. doi: 10.3389/fendo.2023.1225199
11. Bakker J, Honda SI, Harada N, Balthazart J. The aromatase knock-out mouse provides new evidence that estradiol is required during development in the female for the expression of sociosexual behaviors in adulthood. J Neurosci (2002) 22(20):9104–12. doi: 10.1523/JNEUROSCI.22-20-09104.2002
12. Bakker J, Honda S, Harada N, Balthazart J. Sexual partner preference requires a functional aromatase (cyp19) gene in male mice. Hormones Behav (2002) 42(2):158–71. doi: 10.1006/hbeh.2002.1805
13. Bakker J, Honda S, Harada N, Balthazart J. The aromatase knockout (ArKO) mouse provides new evidence that estrogens are required for the development of the female brain. Ann New York Acad Sci (2003) 1007(1):251–62. doi: 10.1196/annals.1286.024
14. Honda SI, Harada N, Ito S, Takagi Y, Maeda S. Disruption of sexual behavior in male aromatase-deficient mice lacking exons 1 and 2 of the cyp19 gene. Biochem Biophys Res Commun (1998) 252(2):445–9. doi: 10.1006/bbrc.1998.9672
15. Matsumoto T, Honda SI, Harada N. Alteration in sex-specific behaviors in male mice lacking the aromatase gene. Neuroendocrinology (2003) 77(6):416–24. doi: 10.1159/000071313
16. Choleris E, Gustafsson JÅ, Korach KS, Muglia LJ, Pfaff DW, Ogawa S. An estrogen-dependent four-gene micronet regulating social recognition: a study with oxytocin and estrogen receptor-α and-β knockout mice. Proc Natl Acad Sci (2003) 100(10):6192–7. doi: 10.1073/pnas.0631699100
17. Choleris E, Ogawa S, Kavaliers M, Gustafsson JÅ, Korach KS, Muglia LJ, et al. Involvement of estrogen receptor α, β and oxytocin in social discrimination: a detailed behavioral analysis with knockout female mice. Genes Brain Behav (2006) 5(7):528–39. doi: 10.1111/j.1601-183X.2006.00203.x
18. Pierman S, Sica M, Allieri F, Viglietti-Panzica C, Panzica GC, Bakker J. Activational effects of estradiol and dihydrotestosterone on social recognition and the arginine-vasopressin immunoreactive system in male mice lacking a functional aromatase gene. Hormones Behav (2008) 54(1):98–106. doi: 10.1016/j.yhbeh.2008.02.001
19. Honda SI, Harada N, Abe-Dohmae S, Takagi Y. Identification of cis-acting elements in the proximal promoter region for brain-specific exon 1 of the mouse aromatase gene. Mol Brain Res (1999) 66(1-2):122–32. doi: 10.1016/S0169-328X(99)00017-0
20. Gozdowska M, Kleszczyńska A, Sokołowska E, Kulczykowska E. Arginine vasotocin (Avt) and isotocin (It) in fish brain: diurnal and seasonal variations. Comp Biochem Physiol Part B: Biochem Mol Biol (2006) 143(3):330–4. doi: 10.1016/j.cbpb.2005.12.004
21. Ohya T, Hayashi S. Vasotocin/isotocin-immunoreactive neurons in the medaka fish brain are sexually dimorphic and their numbers decrease after spawning in the female. Zoological Sci (2006) 23(1):23–9. doi: 10.2108/zsj.23.23
22. Maruska KP, Mizobe MH, Tricas TC. Sex and seasonal co-variation of arginine vasotocin (AVT) and gonadotropin-releasing hormone (GnRH) neurons in the brain of the halfspotted goby. Comp Biochem Physiol Part A: Mol Integr Physiol (2007) 147(1):129–44. doi: 10.1016/j.cbpa.2006.12.019
23. Singh V, Joy KP. Immunocytochemical localization, HPLC characterization, and seasonal dynamics of vasotocin in the brain, blood plasma and gonads of the catfish Heteropneustes fossilis. Gen Comp Endocrinol (2008) 159(2-3):214–25. doi: 10.1016/j.ygcen.2008.09.003
24. Zhang D, Xiong H, Mennigen JA, Popesku JT, Marlatt VL, Martyniuk CJ, et al. Defining global neuroendocrine gene expression patterns associated with reproductive seasonality in fish. PloS One (2009) 4(6):e5816. doi: 10.1371/journal.pone.0005816
25. Kulczykowska E, Kleszczyńska A. Brain arginine vasotocin and isotocin in breeding female three-spined sticklebacks (Gasterosteus aculeatus): the presence of male and egg deposition. Gen Comp Endocrinol (2014) 204:8–12. doi: 10.1016/j.ygcen.2014.04.039
26. Sokołowska E, Kleszczyńska A, Nietrzeba M, Kulczykowska E. Annual changes in brain concentration of arginine vasotocin and isotocin correspond with phases of reproductive cycle in round goby, Neogobius melanostomus. Chronobiol Int (2015) 32(7):917–24. doi: 10.3109/07420528.2015.1052142
27. Butler JM, Anselmo CM, Maruska KP. Female reproductive state is associated with changes in distinct arginine vasotocin cell types in the preoptic area of Astatotilapia burtoni. J Comp Neurol (2021) 529(5):987–1003. doi: 10.1002/cne.24995
28. Singh V, Joy KP. Effects of hCG and ovarian steroid hormones on vasotocin levels in the female catfish Heteropneustes fossilis. Gen Comp Endocrinol (2009) 162(2):172–8. doi: 10.1016/j.ygcen.2009.03.016
29. Chaube R, Singh RK, Joy KP. Estrogen regulation of brain vasotocin secretion in the catfish Heteropneustes fossilis: an interaction with catecholaminergic system. Gen Comp Endocrinol (2012) 175(1):206–13. doi: 10.1016/j.ygcen.2011.11.012
30. Nagarajan G, Aruna A, Chang CF. Neuropeptide arginine vasotocin positively affects neurosteroidogenesis in the early brain of grouper, Epinephelus coioides. J Neuroendocrinol (2015) 27(9):.718–736. doi: 10.1111/jne.12298
31. Kalamarz-Kubiak H, Gozdowska M, Guellard T, Kulczykowska E. How does oestradiol influence the AVT/IT system in female round gobies during different reproductive phases? Biol Open (2017) 6(10):1493–501. doi: 10.1242/bio.024844
32. Herget U, Wolf A, Wullimann MF, Ryu S. Molecular neuroanatomy and chemoarchitecture of the neurosecretory preoptic-hypothalamic area in zebrafish larvae. J Comp Neurol (2014) 522(7):1542–64. doi: 10.1002/cne.23480
33. Herget U, Gutierrez-Triana JA, Thula OS, Knerr B, Ryu S. Single-cell reconstruction of oxytocinergic neurons reveals separate hypophysiotropic and encephalotropic subtypes in larval zebrafish. ENeuro (2017) 4(1):1–16. doi: 10.1523/ENEURO.0278-16.2016
34. Mennigen JA, Ramachandran D, Shaw K, Chaube R, Joy KP, Trudeau VL. Reproductive roles of the vasopressin/oxytocin neuropeptide family in teleost fishes. Front Endocrinol (2022) 13:1005863. doi: 10.3389/fendo.2022.1005863
35. Wacker DW, Ludwig M. Vasopressin, oxytocin, and social odor recognition. Hormones Behav (2012) 61(3):259–65. doi: 10.1016/j.yhbeh.2011.08.014
36. Ramachandran D., Sharma K., Saxena V., Nipu N., Rajapaksha D. C., Mennigen J. A. (2023). Knock-out of vasotocin reduces reproductive success in female zebrafish, Danio rerio. Frontiers in Endocrinol 14, 1151299. doi: 10.3389/fendo.2023.1151299
37. Yokoi S, Naruse K, Kamei Y, Ansai S, Kinoshita M, Mito M, et al. Sexually dimorphic role of oxytocin in medaka mate choice. Proc Natl Acad Sci (2020) 117:4802–8. doi: 10.1073/pnas.1921446117
38. Shaw K. Aromatase expression and function in the brain and behavior: A comparison across communication systems in teleosts. J Chem Neuroanat (2018) 94:139–53. doi: 10.1016/j.jchemneu.2018.10.004
39. Banerjee P, Joy KP, Chaube R. Structural and functional diversity of nonapeptide hormones from an evolutionary perspective: a review. Gen Comp Endocrinol (2017) 241:4–23. doi: 10.1016/j.ygcen.2016.04.025
40. Mitchell K, Zhang WS, Lu C, Tao B, Chen L, Hu W, et al. Targeted mutation of secretogranin-2 disrupts sexual behavior and reproduction in zebrafish. Proc Natl Acad Sci (2020) 117(23):12772–83. doi: 10.1073/pnas.2002004117
41. Mitchell K. Characterization and Role of Secretogranin-II/Secretoneurin in Zebrafish Reproduction. Université d'Ottawa/University of Ottawa (2018) p. 1–165. Doctoral dissertation. doi: 10.20381/ruor-22857
42. Da Fonte DF, Xing L, Mikwar M, Trudeau VL. Secretoneurin-A inhibits aromatase B (cyp19a1b) expression in female goldfish (Carassius auratus) radial glial cells. Gen Comp Endocrinol (2018) 257:106–12. doi: 10.1016/j.ygcen.2017.04.014
43. Yin Y, Tang H, Liu Y, Chen Y, Li G, Liu X, et al. Targeted disruption of aromatase reveals dual functions of cyp19a1a during sex differentiation in zebrafish. Endocrinology (2017) 158(9):3030–41. doi: 10.1210/en.2016-1865
44. Tong SK, Mouriec K, Kuo MW, Pellegrini E, Gueguen MM, Brion F, et al. A cyp19a1b-gfp (aromatase B) transgenic zebrafish line that expresses GFP in radial glial cells. Genesis (2009) 47(2):67–73. doi: 10.1002/dvg.20459
45. Gonçalves DM, Oliveira RF. Hormones and sexual behavior of teleost fishes. In: Hormones and reproduction of vertebrates. Volume 1- Fishes. Elsevier Inc. (2010). p. 119–47.
46. Griffin LB, January KE, Ho KW, Cotter KA, Callard GV. Morpholino-mediated knockdown of ERα, ERβa, and ERβb mRNAs in zebrafish (Danio rerio) embryos reveals differential regulation of estrogen-inducible genes. Endocrinology (2013) 154(11):4158–69. doi: 10.1210/en.2013-1446
47. Lu C, Peng D, Erandani U, Mitchell K, Martyniuk CJ, Trudeau VL. Simultaneous extraction and detection of peptides, steroids, and proteins in small tissue samples. Front Endocrinol (2023) 14:1266985. doi: 10.3389/fendo.2023.1266985
48. Pouso P, Cabana Á, Goodson JL, Silva A. Preoptic area activation and vasotocin involvement in the reproductive behavior of a weakly pulse-type electric fish, Brachyhypopomus gauderio. Front Integr Neurosci (2019) 13:37. doi: 10.3389/fnint.2019.00037
49. Filby AL, Tyler CR. Appropriate 'housekeeping' genes for use in expression profiling the effects of environmental estrogens in fish. BMC Mol Biol (2007) 8(1):1–13. doi: 10.1186/1471-2199-8-10
50. Pouso P, Radmilovich M, Silva A. An immunohistochemical study on the distribution of vasotocin neurons in the brain of two weakly electric fish, Gymnotus omarorum and Brachyhypopomus gauderio. Tissue and Cell (2017) 49(2):257–69. doi: 10.1016/j.tice.2017.02.003
51. Diotel N, Charlier TD, Lefebvre d'Hellencourt C, Couret D, Trudeau VL, Nicolau JC, et al. Steroid transport, local synthesis, and signaling within the brain: roles in neurogenesis, neuroprotection, and sexual behaviors. Front Neurosci (2018) 12:84. doi: 10.3389/fnins.2018.00084
52. Kayo D, Zempo B, Tomihara S, Oka Y, Kanda S. Gene knockout analysis reveals essentiality of estrogen receptor β1 (Esr2a) for female reproduction in medaka. Sci Rep (2019) 9(1):8868. doi: 10.1038/s41598-019-45373-y
53. Nishiike Y, Miyazoe D, Togawa R, Yokoyama K, Nakasone K, Miyata M, et al. Estrogen receptor 2b is the major determinant of sex-typical mating behavior and sexual preference in medaka. Curr Biol (2021) 31(8):1699–710. doi: 10.1016/j.cub.2021.01.089
54. Ogawa S, Eng V, Taylor J, Lubahn DB, Korach KS, Pfaff DW. Roles of estrogen receptor-α gene expression in reproduction-related behaviors in female mice. Endocrinology (1998) 139(12):5070–81. doi: 10.1210/endo.139.12.6357
55. Menuet A, Pellegrini E, Anglade I, Blaise O, Laudet V, Kah O, et al. Molecular characterization of three estrogen receptor forms in zebrafish: binding characteristics, transactivation properties, and tissue distributions. Biol Reprod (2002) 66(6):1881–92. doi: 10.1095/biolreprod66.6.1881
56. Pellegrini E, Menuet A, Lethimonier C, Adrio F, Gueguen MM, Tascon C, et al. Relationships between aromatase and estrogen receptors in the brain of teleost fish. Gen Comp Endocrinol (2005) 142(1-2):60–6. doi: 10.1016/j.ygcen.2004.12.003
57. Wang H, Ward AR, Morris JF. Oestradiol acutely stimulates exocytosis of oxytocin and vasopressin from dendrites and somata of hypothalamic magnocellular neurons. Neuroscience (1995) 68(4):1179–88. doi: 10.1016/0306-4522(95)00186-M
58. Ayoub F. Estradiol regulation of the neurohypophysial hormones in the goldfish, Carassius auratus. Université d'Ottawa/University of Ottawa (1998) p. 1–96. Master of Science thesis. doi: 10.20381/ruor-10197
59. Di Rosa V, López-Olmeda JF, Burguillo A, Frigato E, Bertolucci C, Piferrer F, et al. Daily rhythms of the expression of key genes involved in steroidogenesis and gonadal function in zebrafish. PloS One (2016) 11(6):e0157716. doi: 10.1371/journal.pone.0157716
60. Pasmanik M, Callard GV. Changes in brain aromatase and 5α-reductase activities correlate significantly with seasonal reproductive cycles in goldfish (Carassius auratus). Endocrinology (1988) 122(4):1349–56. doi: 10.1210/endo-122-4-1349
61. Gelinas D, Pitoc GA, Callard GV. Isolation of a goldfish brain cytochrome P450 aromatase cDNA:: mRNA expression during the seasonal cycle and after steroid treatment. Mol Cell Endocrinol (1998) 138(1-2):81–93. doi: 10.1016/S0303-7207(98)00015-X
62. Chaube R, Rawat A, Joy KP. Molecular cloning and characterization of brain and ovarian cytochrome P450 aromatase genes in the catfish Heteropneustes fossilis: Sex, tissue and seasonal variation in, and effects of gonadotropin on gene expression. Gen Comp Endocrinol (2015) 221:120–33. doi: 10.1016/j.ygcen.2015.06.004
63. Pal P, Moulik SR, Gupta S, Guha P, Majumder S, Kundu S, et al. Estrogen-regulated expression of P450arom genes in the brain and ovaries of adult female Indian climbing perch, Anabas testudineus. J Exp Zool Part A: Ecol Integr Physiol (2018) 329(1):29–42. doi: 10.1002/jez.2158
64. Kulczykowska E, Kalamarz-Kubiak H, Nietrzeba M, Gozdowska M. Brain nonapeptide and gonadal steroid responses to deprivation of heterosexual contact in the black molly. Biol Open (2014) 4(1):69–78. doi: 10.1242/bio.20149597
Keywords: aromatase, brain, estrogen, neuropeptide, hormone, arginine vasopressin, sexual behavior, zebrafish
Citation: Shaw K, Lu C, Liu X and Trudeau VL (2023) Arginine vasopressin injection rescues delayed oviposition in cyp19a1b-/- mutant female zebrafish. Front. Endocrinol. 14:1308675. doi: 10.3389/fendo.2023.1308675
Received: 06 October 2023; Accepted: 23 November 2023;
Published: 08 December 2023.
Edited by:
Nicholas J. Bernier, University of Guelph, CanadaReviewed by:
Ewa Zofia Kulczykowska, Polish Academy of Sciences, PolandHironori Ando, Niigata University, Japan
Copyright © 2023 Shaw, Lu, Liu and Trudeau. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Katherine Shaw, kshaw032@uottawa.ca; Vance L. Trudeau, trudeauv@uottawa.ca