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# Assessing olfactory, memory, social and circadian phenotypes associated with schizophrenia in a genetic model based on Rim

## Abstract

Schizophrenia shows high heritability and several of the genes associated with this disorder are involved in calcium (Ca2+) signalling and synaptic function. One of these is the Rab-3 interacting molecule-1 (RIM1), which has recently been associated with schizophrenia by Genome Wide Association Studies (GWAS). However, its contribution to the pathophysiology of this disorder remains unexplored. In this work, we use Drosophila mutants of the orthologue of RIM1, Rim, to model some aspects of the classical and non-classical symptoms of schizophrenia. Rim mutants showed several behavioural features relevant to schizophrenia including social distancing and altered olfactory processing. These defects were accompanied by reduced evoked Ca2+ influx and structural changes in the presynaptic terminals sent by the primary olfactory neurons to higher processing centres. In contrast, expression of Rim-RNAi in the mushroom bodies (MBs), the main memory centre in flies, spared learning and memory suggesting a differential role of Rim in different synapses. Circadian deficits have been reported in schizophrenia. We observed circadian locomotor activity deficits in Rim mutants, revealing a role of Rim in the pacemaker ventral lateral clock neurons (LNvs). These changes were accompanied by impaired day/night remodelling of dorsal terminal synapses from a subpopulation of LNvs and impaired day/night release of the circadian neuropeptide pigment dispersing factor (PDF) from these terminals. Lastly, treatment with the commonly used antipsychotic haloperidol rescued Rim locomotor deficits to wildtype. This work characterises the role of Rim in synaptic functions underlying behaviours disrupted in schizophrenia.

## Introduction

Schizophrenia is a common and debilitating mental illness that severely affects the quality of life of patients and their families. Due to the diversity, intensity and complexity of its symptoms, this disorder is poorly understood, diagnosed and treated1,2. This psychiatric disease is characterized by the presence of a number of behavioural manifestations classified as positive symptoms, a set of conducts that are considered to be exacerbated in schizophrenia patients (e.g. delusions and hallucinations), and negative symptoms, a group of behaviours that are reduced or absent (e.g. social impairments, anhedonia and blunted affect)3,4,5. Further, impairments in cognition, sleep, circadian rhythms and sensory processing, including olfaction, are also observed in this disorder6,7,8. However, the molecular and physiological mechanisms underlying these deficits remain poorly understood5.

The heritability of schizophrenia is one of the highest among complex disorders, ranging from 60% to 80%9. Substantial efforts are focused on understanding its genetic basis. Recent GWAS studies have replicated findings from previous studies, identifying genes associated with a higher incidence for schizophrenia, like CACNA1C, which encodes the pore-forming α-subunit of the L-type Cav1.2 voltage-gated calcium channel (VGCC)10,11. New associations have also been recognized, including the RIM1 gene, which encodes the presynaptic proteins RIM1α and RIM1β12. Although detailed information about the RIM1 alleles associated with schizophrenia is limited, several reports have linked this gene to other neuropsychiatric disorders, such as autism, in which disruptive mutations (e.g. open-reading frameshifts and insertions) are associated with the disorder13,14. RIM1 proteins act as scaffolding molecules in the active zone of presynaptic terminals, clustering VGCCs at the neurotransmitter release sites. They also dock presynaptic vesicles through their interaction with the vesicular protein Rab-315,16. Recent studies have shown impaired sensorimotor gating, increased reactivity to psychotomimetic drugs and reduced social interactions in RIM1α homozygotic knock-out mice (RIM1α−/−), all considered schizophrenia-relevant features17,18,19. Loss of RIM also decreases vesicle tethering at the presynaptic active zone20, impairs presynaptic plasticity, with reduced evoked and spontaneous vesicle release frequency15,21,22 and generates a compensatory increase in post-synaptic density size20,23.

Drosophila has served as a model organism to study the contribution of genes to several complex behaviours in humans, and also to diseases, including neurodegenerative and neuropsychiatric disorders, such as schizophrenia24,25,26,27,28. So far Drosophila studies assessing the function of RIM1 have mostly been conducted at the peripheral and developing larval neuromuscular junction (NMJ). These studies revealed that the Drosophila RIM1 ortholog called Rim, showed conserved functions in evoked neurotransmission, VGCC clustering and synaptic plasticity29,30. The need for tractable animal models to advance our understanding of schizophrenia pathophysiology makes the Drosophila Rim mutant a potentially important tool to gain new insights on the underlying causes of this disorder; however, there is a paucity of knowledge on its behavioural role in adults.

The olfactory and the clock circuits are particularly well characterized and tractable in Drosophila and show high molecular, anatomical and functional conservation with their counterparts in mammals31,32,33,34, thereby facilitating the study of olfactory and circadian phenotypes related to schizophrenia in flies. In the Drosophila olfactory circuit, odorants are received by olfactory receptor neurons, which connect with the antennal lobe projection neurons (AL PNs) in the antennal lobe (AL)35,36. AL PNs send olfactory information to higher processing centres, namely the MB which generates olfactory memories and the lateral horn (LH) which is important for innate olfactory behaviours37,38. Multi-modal sensory information conveyed to both brain regions is also used for the generation of different behavioural outputs39,40,41,42.

Likewise, the neural circuit that regulates circadian rhythms has been intensively studied in Drosophila and is highly tractable, consisting of 75 pairs of clock neurons targetable with defined clock gene promoters43,44. This network is composed of dorsal and ventral groups of clock neurons43,45,46. The lateral ventral group of neurons, the PDF-containing LNvs, can be divided into the small and large LNvs (s-LNvs and l-LNvs, respectively) with the s-LNvs being the most important in maintaining the behavioural and molecular circadian rhythms under constant darkness (DD)43,47. The s-LNvs neurons send projections to the dorsal part of the brain, where they connect with dorsal clock neurons and output circuits of the clock such as the central complex, a fly brain region that controls movement34,48. Two important features that seem to contribute to the output of these neurons are the circadian structural plasticity of s-LNvs axons and PDF release from these terminals34,48. Firstly, the dorsal axonal arborization of s-LNvs goes from a higher morphological complexity, the open state during the day, with high accumulation of PDF, to a more compact, lower complexity state during the night, with low PDF abundance43,49.

In the present study, we manipulated the expression of Rim in different neural circuits to assess its contribution to behaviour. Knocking down Rim in defined sets of neurons reduced olfactory performance, decreased social behaviour and impaired locomotor circadian rhythmicity. In contrast, lack of Rim in memory-associated MB neurons had no effect on memory, suggesting a differential contribution of Rim in different CNS synapses. Structural and functional changes were found to underlie some of the behavioural changes reported and were consistent with Rim functioning in Ca2+ signalling and neuropeptide release.

## Materials and methods

### Fly stock

Flies were raised at 25 °C on 12 h light:12 h dark (LD) cycles on a standard corn-yeast meal diet. CSw flies (kindly donated by Dr. Scott Waddell, University of Oxford, UK) were crossed with flies bearing UAS (UAS/+) transgenes and used as control genotypes. Due to the high contribution of the genetic background to circadian phenotypes33, we have also included the GAL4 controls (GAL4/+) for circadian locomotor analysis in Fig. 3. Tim-GAL4 and PDF-GAL4, flies were a gift from Dr. Ralf Stanewsky (University of Münster, Germany). PDF-GAL4; UAS-Tub:GFP (PDF; Tub:GFP) flies were kindly donated by Dr. Herman Wijnen (University of Southampton, UK). The following strains were obtained from Bloomington Drosophila Stock Center (BDSC; stock number provided in brackets): c309-GAL4 (6906)50,51, OK107-Gal4 (854)26, GH146-GAL4 (30026)52,53, RimMI03470 (37056), RimEx98 (78047), Df(3R)ED5785 (9207, hereon referred to as Df) which is a mutant bearing a deficiency in the third chromosome and therefore lacks the Rim gene, UAS-Rim-RNAi (44541; chromosome II insert, hereon referred to as Rim-RNAi II), UAS-Rim-RNAi (27300; chromosome III insert, hereon referred to as Rim-RNAi III), UAS-Rim:GFP (78051), UAS-GCaMP6f (42747) and UAS-eGFP (5431). The RimEx98/Df flies were generating by crossing the RimEx98 and the Df flies, as previously described30.

### Behavioural test

#### Olfactory performance using single fly tracking

Experiments were carried out as previously reported25,54. Single male flies were placed in a 3.9 cm-diameter circular arena and their behavioural response to an aversive odorant (1% benzaldehyde, Bz, Sigma) was recorded for 3 min. Buritrack software and the Centroid Trajectory Analysis application55 were used to generate heat plots of flies behaviour and Fiji software was used to compute an olfactory index (OI) calculated as

$${\rm {OI}} = \frac{{({\rm {AUC}}\,{\rm {H}}_2{\rm {O}} - {\rm {AUC}}\,{\rm {Bz}})}}{{({\rm {AUC}}\,{\rm {H}}_2{\rm {O}} + {\rm {AUC}}\,{\rm {Bz}})}}$$

where AUC means area under the curve in the pixel profile; AUC H2O = time spent in the water side; and AUC Bz = time spent in the Bz side. Flies were also recorded for three-min in absence of Bz to quantify centrophobism and locomotion as previously reported54, and to discard preference bias within the arena.

Social space experiments were carried out using the same setup described by Simon et al. (2012)56. Groups of 30–40 flies were collected 2 days post eclosion and then kept on fresh food at 24 °C overnight. To avoid sexual dimorphism in social space phenotypes and confounding effects of courtship, only male flies were used. After 2 h of acclimatization in the room where the experiment would take place, flies were loaded into the social space arena, consisting in an isosceles triangle with base of 14.5 cm and height of 14.8 cm, giving a free space area of about 86.5 cm2. The arena was homemade out of glass and acrylic as previously reported56,57. A period of 30 min was given to allow the flies to assume static positions within the arena56. Afterwards, a single photo was taken and the distance of each fly to its nearest neighbour was calculated using Fiji software56,57.

### Aversive olfactory conditioning

Olfactory memory experiments were performed as previously described26. Briefly, groups of 20–50 flies were collected and kept for at least 24 h at 25 °C and 70% relative humidity in the behavioural room to allow acclimatization. On the day of the experiment, flies were transferred into a training tube lined with an electrifiable grid. After 90 s rest, flies were exposed to an odorant (conditioned stimulus, CS+) paired with twelve 70 V DC electric shocks (unconditioned stimulus, US) over 60 s. This was followed by a 45 s rest with fresh air. Flies were then exposed to the reciprocal odorant (CS) with no electric shock. Odorants used were either 3-octanol (OCT, Sigma) or 4-methylcyclohexanol (MCH, Sigma). Memory was evaluated 2 min or 1 h post-conditioning to test short-term memory (STM) or intermediate-term memory (ITM), respectively; a performance index (PI) was calculated using the following equation:

$${\rm {PI}} = \frac{{(N_{{\rm {CS}} - } - N_{{\rm {CS}} + })}}{{(N_{{\rm {CS}} - } + N_{{\rm {CS}} + })}}$$

where NCS− and NCS+ is the number of flies choosing CS and CS+, respectively. The CS+ odour was reversed in alternate groups of flies to account for innate bias toward one odorant; a n = 1 was calculated as the average of the performance of the two groups where CS+ odour was reversed. Sensorimotor controls were performed to assess whether electric shock and odorant avoidance were comparable between different strains. Briefly, for olfactory acuity the odorant and air were pumped through opposite arms of the T-maze and flies were allowed to decide between both stimuli for 2 min. For electric shock avoidance, flies are allowed to choose between two training tubes, one of them connected to the stimulator providing electric shocks. The flies that correctly avoided the shock tube over the total number of flies were quantified and reported as percentage avoidance (Table S1).

### Drosophila activity monitoring (DAM)

Locomotor activity monitoring experiments were conducted as previously described58,59. The activity of 2–5 days old male flies was measured using the DAM system (DAM2, TriKinetics Inc., USA). Flies were transferred into DAM tubes and maintained for 2–5 days under 12:12 LD conditions to assure proper entrainment had taken place, followed by DD, where the first 2 or 5 days were used for circadian rhythm analysis. To assess the rhythm strength, autocorrelation analysis was used following previously published protocols58,59. From this analysis, it was possible to obtain a rhythmicity statistic (RS) value, defined as the ratio between the rhythmicity index and the absolute value of the 95% confidence interval in the derived autocorrelogram. By convention, values > 1.5 indicate strong rhythmicity characteristic of a normal wild type fly59,60,61. Additionally, an estimated period length under free-running conditions (i.e. DD without external circadian cues) was calculated from the distance between the autocorrelation peaks (i.e. lag between the peaks)60. Flies with RS < 1.5 were excluded from the period calculation58,59. All data were analysed in MATLAB using the Sleep and Circadian Analysis MATLAB Program60. Only flies that survived until the last day of DD were used for analysis.

### Imaging

#### Calcium imaging

Calcium imaging using the genetically encoded GCaMP6f optogenetic reporter was performed as previously described26,62 and adapting protocols for live imaging of [Ca2+] fluorescence in presynaptic buttons of AL neurons63. Flies were anesthetised under CO2, decapitated and their brains dissected in extracellular saline containing (in mM): 101 NaCl, 1 CaCl2, 4 MgCl2, 3 KCl, 5 d-glucose, 1.25 NaH2PO4, and 20.7 NaHCO3, pH 7.2. Brains were held with the dorsal part facing up, using a custom-made anchor and visualized with a ×40 water-immersion lens on an upright microscope (Zeiss Examiner Z1). Extracellular saline (3 mL/min) was used to perfuse the brains and transient (12 s) bath application of 100 mM potassium chloride (KCl) in extracellular solution was used to transiently depolarize and stimulate the neurons.

Images were acquired at 4 frames/s with 100 ms exposure using a charge-coupled device camera (Zeiss Axiocam) and a 470 nm light-emitting diode light source (Thor Labs). Baseline fluorescence (F0) was calculated as the mean fluorescence during the first 20 s of recordings (80 images), prior to the start of the high [KCl] perfusion. The change in fluorescence was expressed relative to baseline fluorescence. Data is expressed as [(FF0)/F0], where F is fluorescence at any given time following high KCl exposure; thus, data is expressed as a metric of transient Ca2+ increase. Data were processed and analysed using RStudio version 1.1.463 (RStudio, Inc., Boston, MA).

### Immunohistochemistry and imaging analysis

Immunohistochemistry procedure was conducted as previously described58. Brains were dissected at two day-points: 2 h after lights were switched on (zeitgeber (ZT)2, i.e. at 11 a.m.) and 2 h after lights were switched off (ZT14 i.e. 11 p.m.). Samples were fixed in 4% paraformaldehyde (in PBS plus 0.5% Triton X-100) avoiding tissue exposure to white light. Brains were washed and blocked in 5% normal goat serum (NGS, Thermo Fisher Scientific # 50197Z) and then incubated with primary antibodies in 5% NGS at 4 °C for 48 h. To detect PDF a monoclonal antibody specific to the neuropeptide was used (1:200; Developmental Studies Hybridoma Bank, #PDF-C7) and green fluorescent protein (GFP) detection was enhanced by using an anti-GFP antibody (1:1000; Life Technologies #A11122). Vectashield hard set medium (Vector Laboratories) was used as a mounting media for confocal visualization. Confocal stacks images were acquired at 2 μm steps using a Leica TCS SP8 AOBS confocal laser scanning microscope attached to a Leica DMi8 inverted epifluorescence microscope. Axonal arborization of the dorsal projections was quantified using Sholl analysis, with some modifications49,58,64,65. Ten evenly spaced (5 μm) concentric rings centred at the first branching of the dorsal projections were drawn and the number of intersections of each projection with the rings was quantified. To assess PDF intensity within the clusters a homemade Fiji macro was used defining the fluorescence intensity in each PDF cluster. Scoring of both, axonal arborization and PDF intensity was automatized and blind to avoid observer bias. Data recorded in the two hemispheres in a brain was averaged and that number was reported as the result for that animal (n = 1).

### Drug exposure for behavioural assay

Drug exposure was conducted as previously described66. Haloperidol (H1512, Merck) was dissolved in 100% ethanol to generate a stock solution and a 1 mM concentration in food was achieved by mixing the required volume in molten fly food. Flies were given the haloperidol as adults four days prior and throughout the behavioural experiment. Circadian and locomotor activity data for these experiments was obtained by using the ShinyR-DAM app67. When carrying out these experiments we noticed a difference in fly survival after the 3rd day in DD conditions in mutant and control flies fed haloperidol compared to control conditions (mutant and control flies fed vehicle; not shown). Therefore, in this particular experiment, we only report data collected during 2 consecutive days in DD conditions. Morning anticipation was calculated as the difference between the averaged activity in ZT21.5–24 and ZT17–19.5 and evening anticipation was calculated as the difference between the averaged activity in ZT9.5–12 and ZT5–7.558.

### Statistical analysis

No sample size calculation was carried out. No randomization was performed to carry out experiments. Analysis for data was not performed blindly. No data exclusion criteria were pre-determined. All statistical analyses were performed using GraphPad Prism (version 8.00, GraphPad Software, La Jolla, CA, USA). Datasets were scrutinized for normal distribution using the Shapiro–Wilk test in order to choose the appropriate parametric or non-parametric analysis to be used. Data are presented as mean ± standard error of the mean (SEM), of the n (number of animals, trials, brains) indicated in each figure legend. Data presented was acquired from animals/brains obtained from different crosses/vials, and therefore are biological replicates. Statistical tests used for each comparison are detailed in figure legends. Also, statistical descriptions for each comparison are provided throughout the manuscript. Statistical levels are denoted as following *p < 0.05, **p < 0.01 and ***p < 0.001.

## Results

### Effect of Rim knockdown in olfactory processing and social behaviour

Olfactory impairments are widely reported in patients with schizophrenia and are known to be a prodromal symptom of frontal and temporal-limbic disorders related to schizophrenia8,68,69. We used Drosophila to assess olfactory acuity by tracking behaviour of single flies exposed to the aversive odorant benzaldehyde, Bz. Initially, we used a previously described Rim mutant, RimEx98, which lacks part of the Rim gene including the PDZ and C2 domains, over a deficiency chromosome (Df) lacking the entire Rim gene30.

RimEx98/Df mutants showed less reactivity to the odorant compared to control flies (Fig. 1A, bottom and top panels, respectively). Quantification of the effect showed a reduction in the olfactory index (OI) in this mutant (F(2, 66) = 5.412, p = 0.0067, Fig. 1B). We also characterized flies that carried a transposon insertion in the 23rd exon of the Rim gene (Mi{MIC} insertion; RimMI03470). This second loss of function allele of Rim also displayed a reduction in the OI (Fig. 1B, open blue bar). In addition, flies with targeted reduction of Rim in the AL PNs (GH146>Rim-RNAi (II)) also displayed a reduction in the OI to about 70% that is seen in controls (F(2, 57) = 3.399, p < 0.05, Fig. 1C). Results were further confirmed using an independent RNAi line against a non-overlapping region of Rim (GH146>Rim-RNAi (III), F(2, 58) = 11.75, p < 0.0001, Fig. 1D). In contrast, knocking down Rim in the MBs did not influence the olfactory performance of flies with either of the two RNAi lines tested (c309>Rim-RNAi (II), p = 0.50; c309>Rim-RNAi (III), p > 0.05, Fig. 1C, D).

As the olfactory system has been shown to be a key mediator of social behaviour in different animals70,71,72, we tested whether flies that displayed impaired olfaction are also deficient in social space behaviour. To do this, we used a social space paradigm56 in which flies are kept in a closed arena for 30 min before assessing the distance of each fly to its closest neighbour.

While control animals formed groups within the arena, RimMI03470 flies failed to do so (Fig. 1E), as reflected by an increase in distance between each fly and its nearest neighbour (Mann–Whitney U test, hereafter U = 21418, p < 0.0001, Fig. 1F). Knocking down Rim in the AL PNs (Fig. 1G) resulted in a similar defect in clustering behaviour as RimMI03470. A 1.4-fold increase in social distance was observed in Rim deficient flies compared to control (Kruskal–Wallis statistic H, hereafter H = 14.06, p < 0.0001, Fig. 1H). A similar effect was observed using a different RNAi strain (H = 7.254, p < 0.05, Fig. 1I). Knocking down Rim in the MBs with either RNAi did not result in a change in distance to the closest neighbour compared to control flies. No differences were found in single-fly locomotion or centrophobism, after knocking-down Rim in the AL or MB. This suggests that the differences observed in these experiments arise from social impairments as opposed to locomotor or centrophobism deficits (Supplemental Fig. S1).

Although Rim knockdown in the MBs does not affect either Bz aversion or social space, we went onto investigate the role of Rim in olfactory learning and memory, which is known to be mediated by this structure39,73,74. Using the aversive olfactory conditioning paradigm, memory performance was tested at 2 min and 1 h after training to test for STM and ITM, respectively26,62. No effect was observed on STM (F(4, 27) = 1.382, p = 0.27, Supplemental Fig. S2) or ITM (F(4, 23) = 1.492, p = 0.24, Supplemental Fig. S2) when knocking down Rim in the MB (c309>Rim-RNAi). Similar results were found when using another GAL4 driver that expresses throughout the MB (OK107-Gal426) (STM: F(4, 18) = 2.725, p = 0.06, ITM: H = 2.035, p = 0.36, Supplemental Fig. S2). Therefore, Rim expression in the MBs is not required for any of these behaviours.

### Rim loss-of-function affects the structure and function of presynaptic terminals of AL PNs innervating the LH

Given the effects of Rim knockdown in AL PNs on olfaction and social behaviour, we looked for any underlying structural and/or functional defects of these neurons. However, no gross-morphological alterations were found when the inner antenno-cerebral tract or the median antenno-cerebral tract pathways were studied in knockdown and control animals (Fig. 2A–C, Supplemental Fig. S3). Furthermore, similar AL diameter (F(2, 33) = 0.9314, p = 0.40, Fig. 2D) and an equal number of labelled cells were observed (U = 21, p = 0.72, Supplemental Fig. S3) between strains. Nonetheless, close inspection of the presynaptic terminals reaching the LH (Fig. 2E) showed an approximate 50% reduction of the area covered by the AL PNs terminals in Rim knockdowns compared to control (F(2, 21) = 50.03, p < 0.0001, Fig. 2F).

In order to determine if these changes in synaptic morphology were accompanied by changes in neural activity, the genetically encoded calcium sensor, GCaMP6f, was expressed in the AL PNs and high [KCl] evoked Ca2+ transients were assessed in terminals of Rim knockdown versus control (Fig. 2G). Bath application of depolarizing high KCl evoked a robust signal in normalized fluorescence, that decayed once it was washed out in both control and knockdown neurons (Fig. 2H, traces in left panel). Quantification of independent experiments revealed a reduction in peak amplitude in Rim knockdown compared to control flies (U = 6.5, p < 0.05, Fig. 2H, right panel).

### Rim contribution to circadian locomotor activity under constant darkness

In order to determine the role of Rim in circadian rhythms, locomotor activity was measured in constant darkness (referred as to DD). As opposed to control flies whose behaviour appeared rhythmic under constant-dark conditions (Supplemental Fig. S4), RimEx98/Df flies appeared less rhythmic in DD (Supplemental Fig. S4).

Autocorrelation analysis revealed a reduction in the RS, a measure of the strength of the behaviour rhythms of about 3-times in RimEx98/Df mutants compared to control flies (Fig. 3A). 100% of control flies showed the expected wildtype rhythmic behaviour, this was in contrast with RimEx98/Df mutants where only 58% of flies were rhythmic (Table S2). A reduction in the period length was observed in a portion of RimEx98/Df rhythmic flies compared to controls (Fig. 3B). Similar reductions in rhythmic behaviour resulted from Rim knockdown throughout the clock circuit using timeless (tim)-Gal444,75 (Tim>Rim-RNAi, Supplemental Fig. S4), resulting in a reduction in rhythm strength to ~50% of that of controls (Fig. 3C, Table S2). There appeared to be a reduction in the period length in Tim>Rim-RNAi compared to Tim/+ control, but not when compared to the UAS/+ controls (Fig. 3D). Moreover, we observed an unexpected difference between the Gal4/+ and UAS/+ control lines. In order to clarify the potential inconsistency between genotypes as well as to map the Rim circadian phenotypes to subpopulations of neurons in the clock circuit, Rim-RNAi expression was restricted to just the LNvs using the clock-neuron-specific PDF-Gal444,76 (PDF>Rim-RNAi, Supplemental Fig. S4). Consistent with the RimEx98/Df and Tim>Rim-RNAi arrhythmic behaviour, knocking down Rim only in the LNvs reduced rhythm strength (Fig. 3E), with only 66% and 51% of the PDF>Rim-RNAi flies being rhythmic compared to a 100% and 90% of controls (Table S2). Moreover, a comparison of the period of the rhythmic flies in each group again revealed a reduction in period length in PDF>Rim-RNAi flies (Fig. 3F).

### Rim knockdown affects circadian-dependent remodelling of pacemaker s-LNvs terminals and PDF cycling

Given the changes in rhythmic behaviour in Rim mutants, we studied whether Rim knockdown had an effect on the structural plasticity of s-LNvs. A GFP-tagged version of tubulin expressed in the LNvs allow the visualization of l-LNvs projections to the medulla and the s-LNvs dorsal and ventral projections, which co-localized with the PDF peptide assessed by immunohistochemistry (Fig. 4A). Dorsal terminals from s-LNvs in control flies displayed day/night remodelling, as previously described58,64, with a complex axonal arborization during the day which was significantly more branched compared to at night (Fig. 4B, top left and right panels, respectively). However, Rim knockdown in the LNvs removed this day/night difference in terminal complexity (Fig. 4B, bottom left and right panels), resulting in an intermediate level of complexity between control day and night levels (Fig. 4C).

In order to assess whether Rim was involved in the rhythmic accumulation of PDF in s-LNvs terminals, PDF levels were quantified at these two-time points. PDF signal intensity was measured in each PDF marked area within the dorsal terminals of the s-LNvs, making the quantification of structural remodelling and changes in PDF accumulation independent of one another (Supplemental Fig. S5). PDF shows circadian cycling in control flies, as previously described75, with high levels of PDF at ZT2 and lower levels at ZT14. In contrast, PDF accumulated to similar levels at ZT2 and ZT14 in PDF>Rim-RNAi (Fig. 4D).

In order to determine if Rim co-localized with PDF in the s-LNvs terminals, a GFP-tagged version of Rim was expressed using a PDF driver and PDF localization was determined by immunohistochemistry. This revealed that Rim:GFP was preferentially localized in the s-LNvs terminals as well as in the soma, whereas it appeared to be absent in the l-LNvs terminals terminating in the medulla (Fig. 5A). Interestingly, co-localization images showed PDF was in close proximity to Rim:GFP but they were not directly co-localized (Fig. 5B). Higher magnification images of the PDF containing terminals revealed that Rim:GFP formed aggregates around the sites where PDF might be released, lending further support to Rim regulating PDF release (Fig. 5C).

### Pharmacological effect of the antipsychotic haloperidol on Rim mutant phenotypes

In order to provide pharmacological validation of our Drosophila Rim model, we analysed the effect of a typical antipsychotic, haloperidol66,77, on circadian locomotor activity. Flies were collected after hatching and then exposed for 4 days to 1 mM haloperidol in regular food. Afterward, animals were entrained for 2 full days in 12L:12D cycles. Then, locomotor activity was monitored for 3 days in LD conditions, followed by 5 days in DD. Flies were maintained on food supplemented with drug for the entire procedure, while in the control condition animals were maintained in regular food (Fig. 6A).

As it has been reported a disruption in day and night locomotor activity in schizophrenia78, we sought to determine if similar deficits occur in our model and whether these alterations could be affected by haloperidol treatment. Therefore, we measured the average daily locomotor activity of flies in LD (Fig. 6B). Under these conditions, daytime activity in RimEx98 homozygotes was not different from that recorded in control flies. While haloperidol treatment did not have an effect on daytime activity in control flies, it induced an increase in this parameter in RimEx98 animals (F (1, 252) = 11.12, p = 0.001, Fig. 6C). On the other hand, night-time activity was reduced in the RimEx98 flies when compared to control animals. Treatment with haloperidol restored the night activity to control levels in the mutants. However, it did not show any effect on w1118 control flies.

From the activity profiles showed in Fig. 6B, a reduction in the morning anticipation can be observed in RimEx98 flies when compared to control animals (Fig. 6B, red and black traces). This effect can be quantified by comparing the average morning anticipation of control and mutant flies (F(1, 254) = 68.67, p < 0.0001, Fig. 6E). Haloperidol treatment did not affect the average morning anticipation in either genotype (F(1, 254) = 0.1560, p = 0.69). On the other hand, the evening anticipation was not different between w1118 and RimEx98 flies. Interestingly, there was an increase in evening anticipation in mutants treated with haloperidol, an effect not observed in control flies (F(1, 254) = 68.67, p < 0.0001, Fig. 6F).

We also analysed the effect of haloperidol treatment on the circadian defects we described in Rim mutants in DD conditions (Fig. 7A, red box). As shown for the mutant and knockdown animals (Fig. 3), RimEx98 homozygotes displayed reduced rhythmicity strength under DD compared to control flies (F(1, 207) = 38.94, p < 0.0001, Fig. 7B, C). Haloperidol treatment did not affect circadian strength (F(1, 207) = 0.1713, p = 0.679) in control (p = 0.976) or mutant flies (p = 0.976) and did not rescue the circadian defect observed in RimEx98 flies (Fig. 7C).

Finally, we observed a reduction in locomotor activity in RimEx98 flies as compared to control flies under DD conditions (F(1, 211) = 8.387, p = 0.004, Fig. 7E). Noteworthy, haloperidol treatment (F(1, 211) = 22.03, p < 0.0001) restored RimEx98 locomotion to levels indistinguishable from control flies (w1118ctrl 997.91 ± 51.29 vs. RimEx98haloperidol 1146.23 ± 155.83 counts/day, p > 0.05). The chemical did not affect locomotor activity in control flies (w1118ctrl 997.91 ± 51.29 vs. w1118haloperidol 1121.14 ± 53.90 counts/day, p = 0.736).

## Discussion

Schizophrenia is commonly diagnosed by the presence of different symptoms, including psychosis and asociality. Little is known about the underlying molecular mechanisms5,79. Drugs currently used only treat some of the symptoms observed in a percentage of patients. Thus, animal models based on the genetic changes observed in schizophrenia continue to be a powerful tool to uncover the pathophysiology of the disorder and to study new potential targets for therapeutic intervention80,81,82. Here we demonstrated that the Drosophila orthologue of the schizophrenia-associated gene RIM1, Rim, has an important role in distinct neuronal populations mediating different behaviours relevant to the disease.

Rim loss of function mutants and animals where Rim expression was knocked down in the AL PNs, showed impaired olfactory acuity to the normally highly aversive odorant benzaldehyde. Reduced olfaction is commonly observed in schizophrenia patients83. Several studies have established that the threshold for odour detection is decreased in patients by a mechanism that is independent of environmental factors such as the use of neuroleptics or smoking84,85,86. Although well documented, it is not fully understood how olfactory impairments arise in schizophrenia. However, since they occur at the early stages of the disorder, they have been proposed to be a prodromal marker of the disease83. Hence, the Drosophila olfactory system offers a simple platform to evaluate olfactory dysfunction resulting from mutations in schizophrenia-associated genes.

Previous work has shown that expression in mice of the schizophrenia-associated human splice isoforms of the G72/G30 overlapping genes resulted in impaired smell87. Moreover, a null mutation in the schizophrenia-associated gene ortholog dtnbp-1 (dysb1), showed impaired olfactory habituation in flies, an effect that was mimicked by knocking down dysb expression in the AL PNs88. It is not known whether mutations in RIM1 can cause similar olfactory impairments in humans; however, its high expression in the olfactory bulb is consistent with the idea that it could play a role in olfaction89.

Impaired social behaviour is a hallmark of schizophrenia, with animal models of this disorder showing phenotypes resembling such deficits in social interaction4,82. There are many levels at which social impairments can manifest in people with schizophrenia, including reduced social skills, shyness and disrupted social communication, which can often lead to social withdrawal4,82. Studies have reported that one specific aspect of social interaction, namely social space, is a good descriptor of social withdrawal in schizophrenia90. Social space is understood as a space where a person interacts with others, and strikingly, schizophrenia patients consistently exhibited increased social space regardless of the different setups used to study this symptom90,91,92,93. Here we found that social behaviour was affected in Rim mutants resulting in them also showing an increase in social space. Similar social impairments were described in RIM1α−/− mutant mouse17,22. In particular, RIM1α−/− mutant mice display decreased time engaged in social recognition of novel mice17 and also exhibit deficits in maternal behaviour22.

Interestingly, a relationship between olfactory performance and social behaviour has been proposed for schizophrenia and other neuropsychiatric disorders like autism in humans94,95,96. Our results show that the fly social space deficits are also mediated by the olfactory system as they occurred when Rim was just knocked down in the olfactory AL PNs. Recent evidence in ants suggested that nesting, a social grouping behaviour, also relies on olfactory processing97, in agreement with the idea that similar mechanisms regulate social behaviour in flies. It is known that olfactory information is sent by the AL PNs to two major areas: the MB and the LH98. While LH mediates innate olfactory behaviours, the MB participates in odour learning99,100. Interestingly, Rim knockdown in the AL PNs resulted in prominent structural and functional changes in the terminals reaching the LH. These terminals were smaller and displayed reduced Ca2+ responses to depolarizing high [KCl] stimulation.

The LH is known to have a highly defined neuronal structure101; therefore it would be interesting to determine if there are any Rim-mediated reductions in the AL projections to particular regions of the LH as opposed to a general loss of neuronal connectivity. Based on our images, we were not able to test if this was the case. Our data did suggest that social space information is being processed through the olfactory system and is mediated by the LH with no effect seen with Rim knockdown in MBs. We also did not see a decrease in olfactory learning and memory in these flies, even though memory and cognitive impairments have been described in schizophrenia6,102. Studies in mammals have also been equivocal in describing the potential role of RIM in memory. While RIM1α−/− mice showed impaired memory in fear-conditioning test18, deletion of RIM1 in the dentate gyrus or pyramidal neurons of the CA3 regions resulted in normal memory. This is a puzzling observation since the hippocampus is known to be critical for this type of memory19. Therefore, the lack of effect described here is consistent with mammalian studies showing that RIMs can have distinct roles in different types of synapses103. Rim expression has not currently been characterized in the fly brain, and to our knowledge, there remains no functioning antibody for such studies; therefore the reason why there are no phenotypes due to knockdown of Rim in the MB could be that the gene is not expressed there.

Sleep and circadian disruption are also common manifestations of schizophrenia, affecting up to 80% of individuals with this disorder104,105. However, the symptoms are highly heterogeneous, with changes in total sleep, sleep activity patterns and circadian misalignment being the most frequently observed7,104,105. Consistently, reduced rhythmicity and shorter free-running period length were observed in Rim mutants, phenotypes replicated when Rim knockdown was restricted to the LNvs. These neurons have been described as the major pacemakers under DD, sustaining locomotor rhythmicity43,106 with flies lacking these PDF-containing neurons exhibiting shorter periods and a lack of rhythmicity107. Likewise, pdf-null flies also display arrhythmicity under the same conditions108. Hence, our results agree with the notion that Rim and the LNvs are important in maintaining rhythmicity under DD34,43,59,106.

Another consistent feature of schizophrenia pathology is changes in synaptic and neuronal structure5,109,110,111, with patients showing reduced cortical thickness109,112 and decreased brain volume110,111. Intriguingly, we also found changes in synaptic and neuronal structure related to the behavioural deficits of the Rim mutants. As shown for the AL PNs, Rim expression in the LNvs was necessary to support the synaptic structure of the s-LNvs dorsal terminals. Normally the dorsal projections of the s-LNvs undergo circadian structural plasticity in their axonal branching which goes from a higher terminal complexity during the day, to reduced complexity during the night49,58,64. This structural reorganization is accompanied by changes in the number of active zones64 and PDF release34,49,75, allowing the s-LNvs to potentially change how they interact with postsynaptic clock neurons during different times of the day64. Because of this, it is suggested that these clock outputs could be fundamental for the accurate expression of circadian activity. This is supported by our results, as the behavioural phenotypes in the PDF>Rim-RNAi flies, were accompanied by loss of this remodelling and accumulation of PDF at perpetually high levels throughout the day and night. Although there is a lack of information on the molecular machinery required for the release of PDF113, these data are consistent with Rim regulating PDF release from the s-LNvs dorsal terminals. A recently published study showed that RIM1/2 and RAB3 are essential for neuropeptide release from dense core vesicles114, further supporting the idea that Rim might regulate PDF release from the s-LNvs. Moreover, we show that PDF and Rim were localized to dorsal s-LNvs synaptic terminals, with Rim surrounding clusters of PDF neuropeptide. Remarkably, a similar organization of peptidergic vesicles is observed in different neuronal populations, where dense-core vesicles are in close proximity to the presynaptic releasing site113, further supporting this idea. Additionally, it is possible that the loss of circadian structural plasticity observed upon Rim knockdown might arise from the same impairment of PDF release. Herrero et al. recently showed that PDF is required for this process, through local action of the peptide115. Interestingly, RimEx98 displayed reduced morning anticipation (Fig. 7) possibly arising from a reduced PDF expression or terminal accumulation that has been shown to be essential for this component of the locomotor circadian activity45,116.

Antipsychotic drugs have been used in the treatment of schizophrenia and mood disorders for several years117. The antagonist of the dopamine receptor D2 was the first type to be described and is considered now typical antipsychotics81. Although they are effective in treating the positive symptoms of schizophrenia, they have several adverse effects that are associated with extrapyramidal action of the drugs117,118,119. Hence, there is a need to developing new therapeutic tools to address this problem and easy ways to test them. Here we show that feeding adult flies with haloperidol was sufficient to rescue Rim mutant locomotion deficits to normal levels under constant darkness. This result validates our model for high throughput in vivo testing of novel compounds that reverse this behavioural deficit, which similarly occurs in people with schizophrenia78. Although the treatment was sufficient to increase the locomotion in mutant flies, it did not have an effect on circadian strength. It is possible that the drug did not have any impact on this behaviour because, to the best of our knowledge, D2 receptors are not involved in fly circadian rhythms. Also, it has been shown that other dopamine receptors underlie phenotypes observed in Drosophila schizophrenia models120. It is known, however, that dopamine does have a role in clock output48. Therefore, future studies would be useful to clarify if different durations and doses of haloperidol might rescue all the phenotypes including circadian, olfactory or social activity in Rim and other Drosophila models of the disorder.

In summary, we have shown that loss of function of the fly ortholog of the schizophrenia-associated gene RIM1 in different neuronal populations of the central brain leads to a range of behavioural deficits. Similar to mice models and consistent with human studies, this Drosophila model displayed impaired social behaviour and olfactory performance, likely due to the requirement of Rim for normal structure and Ca2+ responses of AL PN presynaptic terminals onto the LH. Likewise, circadian deficits have been associated with schizophrenia. We also found Rim mutants exhibited circadian defects including a loss of circadian rhythmicity and decreased period length phenotypes that mapped to the s-LNvs pacemaker neurons. Moreover, loss of Rim expression resulted in a loss of day/night differences in s-LNvs dorsal terminal complexity and PDF synaptic abundance. Finally, we showed daily locomotor activity of RimEx98 flies was reduced in constant darkness a phenotype that could be reversed by the common schizophrenia treatment, haloperidol, providing pharmacological validation of our model.

Further studies should be conducted to explore whether similar phenotypes are observed with other schizophrenia-associated genes in Drosophila. We have recently described that the Drosophila dysb1 mutant displays similar olfactory and social deficits as the ones here described for Rim57, further supporting the use of Drosophila mutants to test schizophrenia pathophysiology. In addition, new drug treatments could be tested in this model, for instance, to compare their efficiency with currently available treatments.

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## Acknowledgements

The authors would like to thank Dr. Anne Simon (The University of Western Ontario, Canada) for help setting up the social space paradigm. We thank Drs. Scott Waddell, Ralf Stanewsky, Herman Wijnen and the Bloomington Drosophila Stock Center for sharing flies. We thank Drs. Valentina Zavala and Edgar Buhl for providing comments on the manuscript and acknowledge the Wolfson Bioimaging facilities at University of Bristol. This work was supported by PUC-VRI Puente Grants No. P-1805 to J.M.C. S.H. was supported by CONICYT-PCHA/Doctorado Nacional/2016-21161611 (Chile) and J.J.L.H. by a Leverhulme Trust grant (RPG-2016-318).

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Hidalgo, S., Campusano, J.M. & Hodge, J.J.L. Assessing olfactory, memory, social and circadian phenotypes associated with schizophrenia in a genetic model based on Rim. Transl Psychiatry 11, 292 (2021). https://doi.org/10.1038/s41398-021-01418-3