Background

Sleep is an optimized state for memory consolidation compared to wake (Rasch and Born, 2013). Indeed, sleep is thought to reorganize and strengthen the neural connections required for novel memory formation and long-term memory consolidation, and sleep disruption leads to impaired memory consolidation (Roselli et al., 2021). Beneficial effects of sleep on memory have also been attributed to post-learning neuronal reactivation (Wagner et al., 2007; Dag et al., 2019).

We recently demonstrated that Drosophila switch between sleep-dependent and sleep-independent memory consolidation based on food availability (Chouhan et al., 2021). Flies that are fed after appetitive conditioning show sleep-dependent memory consolidation, which is mediated by the anterior posterior (ap) α’/β’ neurons of the mushroom body. On the other hand, flies starved after training display sleep- independent memory mediated by medial (m) neurons of the α’/β’ lobes. Neurotransmission from ap α’/β’ neurons in the first 4 hours after training in the fed flies is not only required for long term memory but also increased sleep post-training. Activation of ap α’/β’ neurons also promotes baseline sleep, supporting the idea that post training sleep is triggered by the same neurons that are required for sleep- dependent memory consolidation. However, how sleep and memory consolidation are coordinated in ap α’/β’ neurons in this time window is not understood.

Since both post-training sleep and memory consolidation occur rapidly within a few hours after training, we investigated transient gene expression changes in the ap α’/β’ neurons after training to elucidate the interplay of sleep and memory consolidation. Here, we profiled the transcriptome of ap α’/β’ neurons 1 hour after flies were fed and trained, as well as under control conditions in which flies were starved and trained or fed and untrained. We knocked down the differentially expressed genes in trained and fed flies and identified two RNA processing genes that affect sleep. Knockdown of one of these, Polr1F, a regulator of ribosomal RNA synthesis, promotes sleep and translation, both of which are required for consolidation of memory in trained and fed flies.

Knockdown of Polr1F does not affect memory, which is consistent with downregulation of this gene during memory consolidation. Knockdown of Regnase-1, an mRNA decay protein, reduces sleep and disrupts short and long term memory, suggesting an early role, perhaps in learning. These results suggest that RNA processing is an important mechanism linking sleep to memory.

Results

Transient transcriptome profiling of ap α’/β’ neurons after training

We previously demonstrated that flies fed after appetitive memory training exhibit increased sleep and form sleep-dependent memory, which is mediated by ap α’/β’ neurons of the mushroom body (MB) α’/β’ lobes (Chouhan et al., 2021). To address the mechanisms that mediate increases in sleep and consolidation of memory in ap α’/β’ neurons, we assayed gene expression changes in ap α’/β’ neurons of flies fed after training in an appetitive conditioning paradigm. We crossed ap α’/β’ neuron driver R35B12-Gal4 (BDSC #49822) with UAS-nGFP (BDSC #4775) to label all ap α’/β’ neurons with nuclear GFP and collected 5-7 day old F1 progeny subjected to three different conditions: Trained-Fed, Trained-Starved, Untrained-Fed as illustrated (Figure 1A). The trained-starved flies served as controls for sleep-dependent changes, while flies that were fed but untrained served as controls for training-dependent changes. After one-hour, 50 mixed sex (25 for each sex) fly brains from each condition were dissected, and 500 GFP+ cells were sorted for bulk-RNA sequencing using the protocol described by Hongjie Li et al (Li et al., 2017).

Figure 1.

Our analysis of the bulk RNA-seq data revealed that most genes are not altered in ap α’/β’ neurons after one hour, so there are no significant global changes observed among the three conditions. The correlation matrix calculated using the top 75% genes showed high similarity between samples, with most values exceeding 0.9 (Figure 1 – source data 1). Nonetheless, we did observe a small subset of genes that were rapidly responsive and differentially expressed between the groups. Principal component analysis (PCA) of these differentially expressed genes (DEGs) indicated that samples from different conditions are separable, and pathway analysis of PCA indicated that transcription and RNA biosynthetic processes were influenced by the training and feeding paradigm (Figure 1B). In total, we identified 59 DEGs, of which 56 were downregulated and only three were upregulated in the Trained-Fed condition compared to the control conditions (Figure 1C, Figure 1 – source data 1). Gene ontology (GO) analysis of these 59 genes using FlyEnrichr (https://maayanlab.cloud/FlyEnrichr/) indicated that they encode cellular components of the 90S preribosome, Cajal body, DNA-directed RNA polymerase complex, nuclear euchromatin, and condensed chromosome, consistent with the PCA enrichment (Figure 1 – source data 1). Our transcriptome results suggest that ribosome biosynthesis and transcription are the initial changes in ap α’/β’ neurons of trained and fed flies.

Two genes expressed differentially in ap α’/β’ neurons of trained and fed flies predominately affect sleep

To investigate if any of the 59 DEGs identified in the ap α’/β’ neurons of trained and fed flies affect baseline sleep, we knocked down each of the genes using UAS- RNAi lines and screened for their potential effects on sleep. We used the ap α’/β’ neuron constitutive driver R35B12-Gal4 line to drive the RNAi constructs and compared the sleep patterns of knockdown flies with those of R35B12-Gal4 and UAS-RNAi control flies (Figure 2A, B). Using a cutoff of a 200 min change in sleep relative to each control group, we identified two genes, Polr1F and Regnase-1, that showed significant effects on baseline sleep. Knockdown of Polr1F, a component of RNA polymerase I complex, led to an increase in sleep. Although Polr1F has not been extensively studied in Drosophila (Marygold et al., n.d.), its human ortholog hRPA43 is part of the multi- subunit protein complex Pol I that regulates the transcription of ribosomal RNA (Beckouët et al., 2011). Knockdown of Regnase-1, an RNA-binding protein that binds to mRNA undergoing active translation and promotes mRNA decay via its ribonuclease activity, in ap α’/β’ neurons resulted in a reduction of both nighttime and daytime sleep (Figure 2A, B). Further analysis of sleep architecture revealed that knockdown of Polr1F and Regnase-1 did not significantly impact the total activity of flies, while knockdown of either Polr1F and Regnase-1 resulted in increased and decreased average length of sleep episodes, respectively (Figure 2 – supplemental figure1).

Figure 2.

Given that these two genes reduce expression rapidly in response to training under fed conditions, we next used the inducible pan-neuronal GeneSwitch driver nSyb- GeneSwitch (GS) to determine if restricting knockdown of these two genes to the adult stage recapitulates changes in sleep and/or memory. RU486 (mifepristone) was added to normal fly food and transgene expression is induced when flies are loaded into Drosophila Activity Monitor (DAM) glass tubes (Robles-Murguia et al., 2019). We crossed the nSyb-GS flies with Polr1F or Regnase-1 RNAi flies and transferred the adult F1 progeny to RU486 tubes to induce expression of the RNAi 3-5 hours before dusk, and continuously monitored sleep for 5 days. Knockdown of Polr1F resulted in immediate inactivity and sleep (Figure 3A-C). However, with knockdown of Regnase-1, immediate changes in sleep were not noted (Figure 3 – supplemental figure 1A-C).

Figure 3.

This could be due to potential leakiness of the nSyb-GS, such that it reduced sleep even without RU486 treatment, coupled with the fact that sleep before dusk is already quite low. We also analyzed sleep for the next 3 consecutive days from day 3 to day 5 and found that constitutive pan-neuronal Polr1F knockdown increased sleep while Regnase-1 knockdown seemed to have no effect, again perhaps due to the leakiness of nSyb-GS. However, it is also possible that Regnase-1 affects sleep differently in different brain areas (Figure 3D, E; Figure 3 – supplemental figure 1 D, E). In general, these results indicate that adult specific knockdown of Polr1F promotes sleep while brain-wide adult-specific knockdown of Regnase-1 has limited effect on sleep.

Knockdown of Regnase-1 affects memory consolidation

We next evaluated the impact of Polr1F and Regnase-1 knockdown on memory consolidation using our olfactory conditioning paradigm (Figure 4A). Starved flies were subjected to training to associate an odor with a reward, and then post-training, they were either kept on food vials for sleep-dependent memory consolidation or kept starved to promote sleep-independent memory consolidation. Memory tests were conducted 24 hours after training for starved flies, while fed flies were restarved for 42 hours before testing, as starvation is necessary for memory retrieval (Krashes and Waddell, 2008). We observed that constitutive knockdown of Polr1F in ap α’/β’ neurons did not affect sleep-dependent or sleep-independent memory as memory performance was comparable to that of genetic controls (Figure 4B-C). These results were consistent with the fact that Polr1F levels typically decrease during memory consolidation. Monitoring of sleep from ZT8 to ZT12 after training at zeitgeber time (ZT) 6 showed that the post-training increase in sleep was also not affected by Polr1F knockdown in ap α’/β’ neurons (Figure 4E), suggesting that acute downregulation of Polr1F may not be essential to the post-training increased sleep.

Figure 4.

On the other hand, Regnase-1 knockdown in ap α’/β’ neurons resulted in a significant decrease in long-term memory performance in both fed and starved flies and eliminated the increase in post-training sleep (Figure 4 B-E). These findings suggested that Regnase-1 expression in ap α’/β’ neurons is necessary for both sleep-dependent and sleep-independent memory consolidation or that it is required for learning or short- term memory formation. Short-term memory tests confirmed that Regnase-1 knockdown flies performed significantly worse than control flies (Figure 4F), indicating that Regnase-1 expression is essential for the increase in post-training sleep and for short- term memory, which precedes both sleep-dependent and sleep-independent long-term memory.

Knockdown of Polr1F promotes translation

Since Polr1F knockdown promotes sleep and a 22 amino acid peptide within Polr1F inhibits ribosomal DNA transcription (Rothblum et al., 2014), we predicted that Polr1F acted as a suppressor for ribosomal DNA transcription, and thus knockdown of Polr1F would enhance the transcription and translation of ribosomal RNA and thereby overall protein synthesis. As Regnase-1 is thought to promote decay of mRNAs undergoing translation, its knockdown, or its downregulation following training, might also be expected to promote translation, or at least the translation of its target mRNAs. The role of protein synthesis in long-term memory consolidation is well-established across organisms (Alberini and Kandel, 2015), and nascent rRNA synthesis was also shown to be induced by training and required for memory consolidation in mouse (Allen et al., 2018). We thus used real-time qPCR of total RNA extracted from vehicle control and RU-treated fly brains to measure how precursor ribosomal RNA (Pre-rRNA) is affected by knockdown of Polr1F. We found that the pre-rRNA level increased significantly in the RU486 induction (RU+) group compared with vehicle control (RU-) group for nSyb-GS>polr1F RNAi flies (Figure 5A), indicating Polr1F knockdown results in higher levels of pre-rRNA, which is consistent with studies of Polr1F homologs in yeast cells (Thuriaux et al., 1995; Rothblum et al., 2014).

Figure 5.

The increasing ribosomal RNA should help translation and so we also used incorporation of puromycin into newly synthesized peptides as a measure of translation after inducing pan-neuronal knockdown of Polr1F. We observed high levels of translation when Porl1F was knockdown pan-neuronally (RU+) compared to the control (RU-) group (Figure 5B), indicating that Polr1F suppresses translation, probably by suppressing ribosomal RNA transcription (Rothblum et al., 2014). Thus, it may need to be downregulated after training to support translation and memory. Given that knockdown of Porl1F enhances rRNA synthesis and sleep, there is a question as to whether global alterations in rRNA synthesis impact sleep. However, feeding of rRNA inhibitor (CX5461) failed to produce rapid sleep phenotypes in both fed and starved flies (Figure 5 – supplemental figure 1), suggesting that rRNA synthesis may not directly influence sleep. Using puromycin to address effects of Regnase-1 on translation revealed an insignificant slight increase in translation (data not shown); given that Regnase-1 may specifically affect pre-existing translationally active mRNA or may act only on specific target mRNAs, its effects on de novo translation may not be obvious.

Discussion

The anterior-posterior (ap) α’/β’ neurons of the mushroom body make critical and privileged contributions to sleep-dependent memory consolidation and post-training sleep (Krashes et al., 2007; Chouhan et al., 2021), but the mechanisms that link memory and sleep in these neurons are not known. To address this gap, we conducted transcriptomic analysis of ap α’/β’ neurons from trained and fed flies to identify genes that change rapidly under conditions that drive sleep-dependent memory. By uncovering two RNA processing genes involved in memory and sleep, our transcriptome profiling of ap α’/β’ neurons suggests that genes regulating rRNA transcription and translation are altered in the context of sleep-dependent memory consolidation.

RNA processing genes mediate sleep-dependent memory consolidation and sleep

Many of the 59 DEGs we identified are implicated in RNA processing. Among them, Polr1F and CG11920 affect ribosomal RNA processing, CG5654 is predicted to be part of the 90S pre-ribosome and involved in endonucleoytic cleavages (Herold et al., 2009), WDR79 encodes a small Cajal body specific RNA binding protein, Nup133 encodes a component of nuclear pore complex, Regnase-1 degrades mRNA, and CG18011, CG17568, Koko, CG11398 and Meics are all involved in RNA polymerase II- specific transcription (Di Giorgio et al., 2017; Rogg et al., 2022). The enrichment of RNA processing and translation genes is consistent with the notion that memory consolidation requires transcription and translation (Seibt and Frank, 2012; Alberini and Kandel, 2015). More importantly, our findings here indicate that alterations of some of RNA processing genes may impact sleep as well.

Polr1F regulates ribosome RNA synthesis and memory

Learning-induced changes in gene expression in memory-related neurons are often critical for long-term memory formation (Cavallaro et al., 2002; Hoedjes et al., 2015; Tadi et al., 2015). Our findings with Polr1F implicate changes in Pol I transcription during sleep-dependent memory. Polr1F(Rpa43) is predicted to be part of the RNA polymerase I complex and is involved in DNA-dependent RNA polymerase activity/rDNA transcription in yeast, especially for the initiation of ribosomal RNA (Beckouët et al., 2011; Marygold et al., 2020). As suggested by our data, Polr1F has an inhibitory role in the RNA polymerase I complex, which is also consistent with aforementioned study that found a 22 amino acid peptide within Polr1F can inhibit rDNA transcription (Rothblum et al., 2014). Based upon our finding that inducible knockdown of Polr1F rapidly promotes translation, it is likely that the rapid and dramatic decline of Polr1F after training in fed flies serves to increase de novo ribosome RNA synthesis.

This is consistent with the report that ribosomal RNA is induced by learning and required for memory consolidation in mice (Allen et al., 2018). While we do not know how knockdown of Polr1F promotes sleep, an attractive possibility is that higher translation is a result of elevated sleep. Sleep is thought to promote translation and it is required for sleep-dependent memory consolidation (Seibt and Frank, 2012; Chouhan et al., 2021). Alternatively, increased translation or rRNA synthesis could promote sleep. However, translation is typically thought of as a consequence of sleep rather than a cause (Zimmerman et al., 2006). Also, rRNA transcription rates remain constant throughout the day in the liver (Sinturel et al., 2017), although it is still possible that these rates vary in particular regions of the brain and affect sleep. The role of rRNA synthesis in Drosophila learning and memory has barely been explored, but our work, together with that of Allen et al. (2018), indicates that the well-known requirement for de novo protein synthesis during long-term memory consolidation (Jarome and Helmstetter, 2014) includes increased synthesis of ribosomal RNA and protein.

Rapid Regnase-1 inactivation may affect memory through effects on translation

The role of RNA binding protein Regnase-1 in the innate immune response has been extensively studied (Mino et al., 2015; Mao et al., 2017; Wei et al., 2019). However, our study sheds light on a novel function of neuronal Regase-1 in ap α’/β’ neurons on sleep and memory. Regnase-1 is an anti-inflammatory enzyme that inhibits mRNA translation during acute inflammatory responses. It localizes to the ribosomes on the surface of the endoplasmic reticulum (ER) and binds to translationally active mRNAs with specialized stem-loop structures at the 3’UTR (Uehata et al., 2013; Mino et al., 2015). When phosphorylated, Regnase-1 is released from the ER (Tanaka et al., 2019). Because functional Regnase-1 binds and degrades its bound mRNA, Regnase-1 inactivation leads to an increase of its target mRNA (Uehata et al., 2013). The target mRNAs of Regnase-1 in immune cells encode proinflammatory cytokines, which can then be expressed when Regnase-1 is inactivated. However, Regnase-1 has also been reported to modulate cytokines and neuronal injury in the microglia in rats (Liu et al., 2016). Regulation of Regnase-1 is usually rapid and transient, and its rapid response to microenvironmental changes, different pathological states and stress are critical for cellular adaption (Mao et al., 2017).

Our study reveals that the expression of Regnase-1 changes after training, and constitutive downregulation of Regnase-1 in ap α’/β’ neurons reduces sleep and causes deficits in learning and memory consolidation. We suggest that downregulation of Regnase-1 following training in fed flies may be crucial for the promotion of long-term memory, perhaps by promoting translation of specific transcripts. For instance, downregulation of Regnase-1 after training may release a pool of mRNAs that are normally targeted by it for decay and that are important for consolidation of memory. On the other hand, we find that constitutive loss of Regnase-1 impairs sleep-independent memory and also short-term memory, suggesting that it is required early in the learning and memory process, likely for learning. Interestingly, constitutive knockdown of Regnase-1 also reduces sleep and prevents sleep increase after training. The requirement for sleep is linked most to long-term memory rather than to learning, but increases in neural activity after training and cognitive tasks are thought to increase the need to sleep (Wagner et al., 2007; Diekelmann and Born, 2010), so it is possible that the reduced sleep phenotype of the constitutive Regnase-1 knockdown is related to its role in learning.

Our study of local molecular changes in ap α’/β’ neurons after training highlights how ribosomal RNA transcription and mRNA translation work in concert during the consolidation of sleep-dependent memory. Neurons are regulated to generate short bursts of boosted transcription and boosted translation, which are required for new protein synthesis. How sleep is involved in this boosted protein synthesis process is unclear, but we suggest that sleep affects several steps of the central dogma, and that deleterious consequences of sleep deprivation are also mediated through effects on rRNA transcription and translation. Overall, our findings indicate the importance of maintaining RNA homeostasis for sleep and memory.

Conflict of interest statement

The authors declare no competing interests.

Acknowledgements

This work was supported by Howard Hughes Medical Institute (HHMI). We thank all members of the Sehgal lab for reagents, comments and support, especially rotation undergraduate Arielle Ketchum for help with molecular cloning. We thank Hongjie Li of Liqun Luo lab with technical assistance and protocol sharing from Stanford University.

Author contributions

Conceptualization, Y.J.L., N.S.C. and A.S.; Methodology, Y.J.L., N.S.C., S.Z. and R.M. Software, Y.J.L; Validation, Y.J.L., N.S.C., S.Z., R.M., J.S., A.K. and Z.F.Y.; Formal analysis, Y.J.L., N.S.C. and R.M.; Investigation, Y.J.L. and N.S.C.; Resources, Y.J.L., N.S.C., S.Z., R.M., J.S., A.K. and Z.F.Y.; Data Curation, Y.J.L., N.S.C. and R.M.; Writing – Original Draft, Y.J.L. and N.S.C. Writing – Review & Editing, Y.J.L., N.S.C. and A.S. Visualization, Y.J.L., N.S.C. and R.M.; Supervision, Y.J.L., N.S.C. and A.S.; Project administration, A.S.; Funding acquisition, A.S.

Materials and Methods

Contact for reagent and resource sharing

Amita Sehgal (amita@pennmedicine.upenn.edu)

Key resource table

Fly stock and maintenance

All the stock information of the flies used in this project are listed in the key resource table and flies were reared on the standard cornmeal vials or bottles at 25 °C with 12:12 hours light dark cycle in the preset incubator. The genetic background control used in the paper is White-CantonS (wCS) unless specified.

Behavior measurement in Drosophila

We have used both single beam and updated multibeam Drosophila activity monitoring (DAM) system from Trikinetics (https://trikinetics.com/) in our experiments. Briefly, 5-7 days old female flies were loaded into 60/90 mm glass locomotor tubes for behavior tests, using DAM2/5H Drosophila activity monitors from Trikinetics. 1/15 infrared beams bisect each tube, providing movement (position in multibeam) information of the fly across the tube. Locomotor tubes are loaded with 2% agar with 5% sucrose as fly food on one side, and yarn is put on the other side to restrain the behavior of flies inside the glass tubes. For experiments with the inducible Gene Switch system, 0.5mM RU-486 (mifepristone) was added to the fly food to activate the expression of the transgenes under the control of UAS. Three constitutive days of data were used for sleep analysis by Pysolo (https://www.pysolo.net/).

Appetitive conditioning

∼100 4-7 old flies were starved for 12 hours in Drosophila bottles with water -soaked filtered paper and then trained at 25°C and 70% relative humidity to associate sucrose with odor A for 2 minutes, and then a blank with odor B for 2 minutes with 30-second clean air in between. After conditioning, flies were moved back to normal fly food or starved for 1 hour and dissected for subsequent ap cell sorting and RNA-sequencing. For the short-term memory test, flies were tested immediately after conditioning in the same wheel for 2 mins.

To assess post-training sleep, flies were introduced in glass tubes containing 2% agar and 5% sucrose through an aspirator without anesthesia and loaded into the DAM system after training. For long-term memory assessment, trained flies were either kept on food vials for 24 h or were further starved. Starved flies were tested for memory 24 h after training, while fed flies were re-starved for 42 h before memory tests. Memory was tested by giving flies a choice between odor A and odor B for 2 min in a T-maze.

Performance index (PI) was calculated as the number of flies selecting CS⁺ odor minus the number of flies selecting CS^- odor divided by the total number of flies. Each PI is the average of PIs from reciprocal experiments with two odors swapped to minimize non- associative effects.

Cell isolation and sorting

Dissected brains are dissociated by following the protocol from (Li et al., 2017). Briefly, brains are dissected in Schneider’s medium, and then are placed in a shaker and dissociated in Papain solution, filtered through a 100 μm cell strainer, and re-suspended in Schneider’s medium. 500 GFP+ cells from the same conditions were sorted into 96 well microplate with lysis buffer from Smart-seq2 HT kit and frozen. We dissected 50 brains for each group to ensure enough GFP+ cells. Cell sorting were conducted by either BD FACSMelody or BD FACSAria (BD Biosciences), and dead cells were excluded with 4’, 6-diamidino-2-phenylindole (DAPI). Doublets were excluded using and forward scatter (FSC-H by FSC-W) and side scatter (SSC-H by SSC-W). Size of cells was selected by FSC-A by FSC-A and validated for fly neurons using cells from flies expressing nsyb-nGFP. Length of time from tissue harvest to cell collection approximated 4 hours.

RNA-seq and data analysis

GFP+ cells were sorted and immediately frozen, then sent to Admera Health (https://www.admerahealth.com/) for RNA extraction, RNA library construction, and sequencing using the Smart-seq2 HT kit. To analyze the RNA-sequence data, we used Hisat2 (http://daehwankimlab.github.io/hisat2/) to map the sequencing data FASTQ files to the fly genome (BDSG6). The alignment results were then counted by LiBiNorm (https://warwick.ac.uk/fac/sci/lifesci/research/libinorm/) using the GENCODE reference genome. Raw count and TPM were used separately in further analysis. Raw count data were analyzed by IDEP v0.95 to identify genes expressed differentially between three conditions. We filtered out low-expressed genes using a cutoff of CPM>0.5, at least detected in 3 independent samples, and treated missing values as gene median.

Regularized log transformation was used to transform raw count data for clustering and PCA. Differentially expressed genes were identified using DESeq2 with an FDR cutoff of 0.1 and minimum fold change of 2.

Puromycin assay and imaging

We developed a puromycin assay to measure the rate and localization of nascent peptide synthesis in the fly brain, and similar method has been described in the fly larvae (Deliu et al., 2017). Fly brains were dissected in Schneiders’ medium and incubated with puromycin for 40 min in vitro to allow puromycin to incorporate into the newly synthesized peptide. Subsequently, using an anti-puromycin antibody, standard immunostaining protocols were applied to detect the number and position of newly synthesized puromycin-tagged peptides (Aviner, 2020), which provided a measure of translation rate. The brains were then imaged with a 40X oil immersion confocal microscope with a resolution of 1024*1024. The intensity of the images was then measured by FUJI (ImageJ) and the average intensity of the samples was analyzed for comparison.

RNA polymerase I inhibitor II, CX-5461 protocol

CX-5461 was mixed with 2% agar and 5% sucrose to make fly motor tubes at a final concentration of 0.2 mM or 0.6 mM. Flies are loaded into these CX-5461 tubes or vehicle control tubes 4 hours before light turns off and transient sleep changes are measured.

Quantitative Real-time PCR (qPCR)

10 flies’ brains from each group were dissected for RNA extraction using Qiagen’s RNeasy Plus Mini Kit. Total RNA was then reverse transcribed to cDNA by using random hexamers and Superscript II from Invitrogen. qPCR was performed using SYBR-green master mix and oligonucleotide information is provided in the Key Resources table. Relative gene expression was analyzed using the ΔΔCt method.

Statistical Analysis

Fly sleep behavioral data extracted from Pysolo was analyzed by GraphPad Prism (https://www.graphpad.com/). Data from different replicates were pooled directly and first tested for normality using D’Agostino-Pearson and Shapiro-Wilk tests. For normally distributed data, unpaired parametric Student’s t-test is used for two-sample experiments and one-way ANOVA with Turkey post hoc test for three-sample or more experiments. Non-normally distributed data were analyzed using nonparametric tests, the Mann-Whitney test for two-sample experiments and the Kruskal-Wallis test with

Dunn’s multiple comparisons test for three or more samples experiments. For all graphs, unless otherwise stated, data are presented as mean and standard error of the mean (SEM) and statistical significance was accepted for p value < 0.05.

Data availability

Sequencing data will be available at GEO. All other data for this study are included in the manuscript and supporting files.

Supplemental information

Supplemental information includes 2 figures and 1 table.