NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models
Authors:
Mayanglambam Dhruba Singh aff001; Matthew Jensen aff001; Micaela Lasser aff002; Emily Huber aff001; Tanzeen Yusuff aff001; Lucilla Pizzo aff001; Brian Lifschutz aff001; Inshya Desai aff001; Alexis Kubina aff001; Sneha Yennawar aff001; Sydney Kim aff002; Janani Iyer aff001; Diego E. Rincon-Limas aff003; Laura Anne Lowery aff002; Santhosh Girirajan aff001
Authors place of work:
Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, Pennsylvania, United States of America
aff001; Department of Biology, Boston College, Chestnut Hill, Massachusetts, United States of America
aff002; Department of Neurology, McKnight Brain Institute, University of Florida, Gainesville, Florida, United States of America
aff003; Department of Medicine, Boston University Medical Center, Boston, Massachusetts, United States of America
aff004; Department of Anthropology, Pennsylvania State University, University Park, Pennsylvania, United States of America
aff004; Department of Anthropology, Pennsylvania State University, University Park, Pennsylvania, United States of America
aff005
Published in the journal:
NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models. PLoS Genet 16(2): e32767. doi:10.1371/journal.pgen.1008590
Category:
Research Article
doi:
https://doi.org/10.1371/journal.pgen.1008590
Summary
The 1.6 Mbp deletion on chromosome 3q29 is associated with a range of neurodevelopmental disorders, including schizophrenia, autism, microcephaly, and intellectual disability. Despite its importance towards neurodevelopment, the role of individual genes, genetic interactions, and disrupted biological mechanisms underlying the deletion have not been thoroughly characterized. Here, we used quantitative methods to assay Drosophila melanogaster and Xenopus laevis models with tissue-specific individual and pairwise knockdown of 14 homologs of genes within the 3q29 region. We identified developmental, cellular, and neuronal phenotypes for multiple homologs of 3q29 genes, potentially due to altered apoptosis and cell cycle mechanisms during development. Using the fly eye, we screened for 314 pairwise knockdowns of homologs of 3q29 genes and identified 44 interactions between pairs of homologs and 34 interactions with other neurodevelopmental genes. Interestingly, NCBP2 homologs in Drosophila (Cbp20) and X. laevis (ncbp2) enhanced the phenotypes of homologs of the other 3q29 genes, leading to significant increases in apoptosis that disrupted cellular organization and brain morphology. These cellular and neuronal defects were rescued with overexpression of the apoptosis inhibitors Diap1 and xiap in both models, suggesting that apoptosis is one of several potential biological mechanisms disrupted by the deletion. NCBP2 was also highly connected to other 3q29 genes in a human brain-specific interaction network, providing support for the relevance of our results towards the human deletion. Overall, our study suggests that NCBP2-mediated genetic interactions within the 3q29 region disrupt apoptosis and cell cycle mechanisms during development.
Keywords:
Drosophila melanogaster – Phenotypes – RNA interference – Hyperexpression techniques – Xenopus – Eyes – Cell staining
Introduction
Rare copy number variants (CNVs), including deletions and duplications in the human genome, significantly contribute to complex neurodevelopmental disorders such as schizophrenia, intellectual disability/developmental delay, autism, and epilepsy [1,2]. Despite extensive phenotypic heterogeneity associated with recently described CNVs [3], certain rare CNVs have been linked to specific neuropsychiatric diagnoses. For example, the 22q11.2 deletion (DiGeorge/velocardiofacial syndrome), the most frequently occurring pathogenic CNV, is found in about 1–2% of individuals with schizophrenia [4,5], and animal models of several genes within the region show neuronal and behavioral phenotypes on their own [6,7]. Similarly, the 1.6 Mbp recurrent deletion on chromosome 3q29, encompassing 21 genes, was initially identified in individuals with a range of neurodevelopmental features, including intellectual disability, microcephaly, craniofacial features, and speech delay [8,9]. Further studies have implicated this deletion as a major risk factor for multiple disorders [10]. In fact, the deletion confers a >40-fold increase in risk for schizophrenia [11,12] as well as a >20-fold increase in risk for autism [13]. More recently, two studies have reported decreases in body and brain sizes as well as a range of behavioral and social defects in mouse models of the entire deletion, mimicking the human developmental phenotypes associated with the deletion [14,15].
Identifying the biological underpinnings of the 3q29 deletion is contingent upon uncovering the conserved molecular mechanisms linking individual genes or combinations of genes within the 3q29 region to the neurodevelopmental phenotypes observed in individuals with the entire deletion. Recent studies have suggested a subset of genes in the 3q29 region as potential candidates for these phenotypes based on their established roles in neuronal development [16,17]. For example, DLG1 is a scaffolding protein that organizes the synaptic structure at neuromuscular junctions [18], affecting both synaptic density and plasticity during development [19]. However, mouse models of Dlg1+/- did not recapitulate the behavioral and developmental phenotypes observed in mice with the entire deletion [14], suggesting that haploinsufficiency of DLG1 by itself does not account for the wide range of phenotypes associated with the deletion. Given that genes within rare pathogenic CNV regions tend to share similar biological functions [20] and interact with each other to contribute towards developmental phenotypes [21,22], it is likely that multiple genes within 3q29 jointly contribute to these phenotypes through shared cellular pathways. Therefore, an approach that integrates functional analysis of individual genes within the 3q29 deletion and their combinatorial effects on neuronal and cellular phenotypes is necessary to understand the pathways and mechanisms underlying the deletion.
Systematic testing of genes within 3q29 towards developmental and cellular phenotypes requires model systems that are amenable for rapid phenotypic evaluation and allow for testing interactions between multiple dosage-imbalanced genes without affecting the viability of the organism. Drosophila melanogaster and Xenopus laevis provide such powerful genetic models for studying conserved mechanisms that are altered in neurodevelopmental disorders, with the ability to manipulate gene expression in a tissue-specific manner in Drosophila [23] and examine developmental defects in X. laevis [24]. Both model systems contain homologs for a majority of disease-causing genes in humans, and show a high degree of conservation in key developmental pathways [23,25–27]. For example, Drosophila knockdown models of the candidate schizophrenia gene DTNBP1 showed dysregulation of synaptic homeostasis and altered glutamatergic and dopaminergic neuron function [28,29], and fly models for UBE3A, the gene associated with Angelman syndrome, showed sleep, memory and locomotor defects [30]. Furthermore, X. laevis models have been widely used to identify morphological and neuronal defects associated with developmental disorders [24], such as dendritic connectivity defects with overexpression of MECP2, the causative gene for Rett syndrome [31]. Thus, Drosophila and X. laevis models of individual CNV homologs and their interactions would allow for a deeper dissection of the molecular mechanisms disrupted by the deletion, complementing the phenotypes documented in mouse models of the entire deletion [14,15].
Here, we used a mechanistic approach to understand the role of individual homologs of 3q29 genes and their interactions towards the cellular processes underlying the deletion. We systematically characterized developmental, cellular, and nervous system phenotypes for 14 conserved homologs of human 3q29 genes and 314 pairwise interactions using Drosophila, and validated these phenotypes using X. laevis. We found that multiple homologs of genes within the 3q29 region, including NCBP2, DLG1, FBXO45, PIGZ, and BDH1, contribute to disruptions in apoptosis and cell cycle pathways, leading to neuronal and developmental defects in both model systems. These defects were further enhanced when each of the homologs were concomitantly knocked down with homologs of NCBP2 in Drosophila (Cbp20) and X. laevis (ncbp2), resulting in increased apoptosis and dysregulation of cell cycle genes. Our results support an oligogenic model for the 3q29 deletion, and implicate specific cellular mechanisms disrupted by genes in the deletion region.
Results
Reduced expression of individual homologs of 3q29 genes causes global developmental defects
We used reciprocal BLAST and orthology prediction tools (see Methods) to identify fly homologs for 15 of the 21 genes within the 3q29 deletion region (Fig 1, S1 Table). We note that the genes and crosses tested in this study are represented as fly gene names along with the human counterparts at first mention in the text, i.e. Cbp20 (NCBP2), and fly genes with allele names in the figures, i.e. Cbp20KK109448. We found that the biological functions of these 15 genes were also conserved between Drosophila and humans, as 61 of the 69 Gene Ontology (88.4%) annotations for the human genes were also annotated for their respective fly homologs (S1 File). For example, dlg1 (DLG1) and Cbp20 (NCBP2) share the same roles in both flies and vertebrates, as a scaffolding protein at the synaptic junction [32] and a member of the RNA cap binding complex [33], respectively. We used RNA interference (RNAi) and the UAS-GAL4 system to knockdown expression levels of fly homologs of genes within the 3q29 region ubiquitously and in neuronal, wing and eye tissues [34] (Fig 1). A stock list of the fly lines used in this study and full genotypes for all experiments are provided in S2 File. Quantitative PCR (qPCR) confirmed partial knockdown of gene expression for each of the tested homologs (S2 Table); fly lines for CG5359 (TCTEX1D2) were excluded from further analysis after additional quality control assessment (see Methods). To identify genes essential for organism survival and neurodevelopment, we first assessed the effect of ubiquitous knockdown of homologs of 3q29 genes using the da-GAL4 driver (Fig 2A). Seven of the 14 homologs, including dlg1, Cbp20, and Tsf2 (MFI2), showed lethality or severe developmental defects with ubiquitous knockdown, suggesting that multiple homologs of 3q29 genes are essential for viability during early development. Similarly, wing-specific bxMS1096-GAL4 knockdown of Tsf2, Cbp20, CG8888 (BDH1), and Pak (PAK2) showed severe wing defects, and wing-specific knockdown of dlg1 showed larval lethality (S1 Fig).
Several fly homologs for genes within the 3q29 region have previously been associated with a range of neuronal defects during fly development (S3 Table). For example, loss of dlg1 contributed to morphological and physiological defects at the neuromuscular junction (NMJ), as well as increased brain size, abnormal courtship behavior, and loss of gravitaxis response [35–37]. Similarly, Pak mutant flies exhibited extensive defects in the axonal targeting of sensory and motor neurons [38,39], in addition to abnormal NMJ and mushroom body development [40,41]. We sought to determine whether fly homologs for other genes in the 3q29 region also contribute to defects in neuronal function, and therefore performed climbing assays for motor defects and staining of larval brains for axonal targeting with pan-neuronal knockdown of the fly homologs. Interestingly, Elav-GAL4 mediated pan-neuronal knockdown caused larval or pupal lethality in dlg1, Tsf2, and CG5543 (WDR53) flies (Fig 2A), and about 30% of adult flies with knockdown of dlg1 did not survive beyond day 5 (S1 Fig), indicating an essential role for these genes in neuronal development. Furthermore, we found that flies with pan-neuronal knockdown of several homologs of 3q29 genes, including dlg1 and Cbp20, exhibited a strong reduction in climbing ability over ten days (Fig 2B, S1 Video), suggesting that these genes could contribute to abnormalities in synaptic and motor functions [42]. We next examined the axonal projections of photoreceptor cells into the optic lobe by staining third instar larval brains with anti-chaoptin. We found that GMR-GAL4 mediated eye-specific knockdown of Cbp20, dlg1, Pak and Fsn (FBXO45) showed several axonal targeting defects (S1 Fig, S4 Table). Our results recapitulated the previous findings in Pak mutant flies [38], and were similar to targeting defects observed in models of other candidate neurodevelopmental genes, including Drosophila homologs for human DISC1 and FMR1 [43,44]. Overall, our data show that multiple conserved homologs of genes in the 3q29 region beyond just dlg1 or Pak are important for Drosophila neurodevelopment.
Drosophila eye models for genes within the 3q29 region show cellular defects
The Drosophila compound eye has been classically used to perform high-throughput genetic screens and quantitative assays of cellular and neurodevelopmental defects [45]. In fact, about two-thirds of all vital genes in the fly genome are predicted to be involved in fly eye development [46]. For instance, the Drosophila eye model was recently used to screen a large set of intellectual disability genes [47], and genetic interaction studies using the fly eye have identified modifier genes for Rett syndrome, spinocerebellar ataxia type 3, and other conserved developmental processes [48–50]. We used the developing fly eye as an in vivo system to quantify the effect of gene knockdown on adult eye morphology, cellular organization in the pupal eye, and cell proliferation and death in the larval imaginal eye disc (Fig 1, S2 Fig). The wild-type adult Drosophila eye consists of about 750 ommatidia containing different cell types arranged in a regular hexagonal structure, which can be easily perturbed by genetic modifications [51,52]. Because of this, we first performed eye-specific RNAi knockdown of fly homologs of genes in the 3q29 region using GMR-GAL4, and measured the rough eye phenotype of each knockdown line using Flynotyper, a quantitative tool that calculates a phenotypic score based on defects in ommatidial arrangement [53]. We found that eye-specific knockdown of 8/13 homologs of 3q29 genes showed significant external eye phenotypes compared with control GMR-GAL4 flies, while knockdown of Tsf2 caused lethality (Fig 2C, S3 Fig). For example, knockdown of Cbp20 resulted in a severe rough eye phenotype that was comparable to knockdown of other neurodevelopmental genes [53], such as Prosap (SHANK3) and kis (CHD8) (S5 Table).
To examine the cellular mechanisms underlying the rough eye phenotypes observed with knockdown of fly homologs of 3q29 genes, we first measured changes in area and ommatidial size of the adult eyes. We found a significant reduction in eye size with knockdown of CG8888 and Cbp20, while the eyes of flies with knockdown of dlg1 were significantly larger than GMR-GAL4 controls (Fig 2D). Similarly, we observed decreases in ommatidial diameter with knockdown of Cbp20 and CG8888, suggesting that these genes may also contribute to abnormal cell growth phenotypes (S3 Fig). We also assessed the cellular structure of 44 hour-old pupal eyes by staining the ommatidial and photoreceptor cells with anti-DLG, a septate junction marker, and Phalloidin, a marker for F-actin at cell boundaries (S2 Fig). We found that knockdown of 11/12 tested homologs of 3q29 genes caused disorganization or loss of the photoreceptor neurons and ommatidial cells (Fig 2E, S4 Fig, S6 Table). For example, pupal eyes with knockdown of CG8888, dlg1, Cbp20 and CG5543 all showed defects in cone cell orientation and ommatidial rotation compared with control GMR-GAL4 flies. Furthermore, Cbp20 and dlg1 knockdown flies showed hexagonal defects and severe disorganization of photoreceptor neurons, while Cbp20 knockdown flies also showed fused secondary cells and dlg1 knockdown flies showed a complete loss of bristle cells.
We next hypothesized that abnormal proliferation and apoptosis could contribute to the cellular defects observed with knockdown of fly homologs of 3q29 genes. To test this, we stained the third instar larval eye discs for select knockdowns of individual homologs of 3q29 genes with anti-pH3 (phospho-Histone H3 (Ser10)) and Drosophila caspase-1 (dcp1), markers for proliferating and apoptotic cells, and quantified the number of cells posterior to the morphogenetic furrow (S2 Fig). We observed a significant decrease in pH3-positive cells for CG8888 knockdown flies and trends towards increased pH3-positive cells for PIG-Z (PIGZ) knockdown flies compared with GMR-GAL4 controls (p = 0.165) (Fig 2F, S4 Fig), while knockdown of dlg1 led to significant increases in cells stained with bromodeoxyuridine (BrdU), a marker for replicating cells (S4 Fig). Flies with knockdown of Cbp20 or dlg1 also showed a significant increase in apoptotic dcp1-positive cells compared with controls (Fig 2G), which we validated using TUNEL assays for these lines (S4 Fig). We further tested for proliferation and apoptosis in the third instar larval wing discs of flies with knockdown of homologs of 3q29 genes using the bxMS1096-GAL4 driver, and observed changes in both processes with knockdown of dlg1, CG8888 and Cbp20 (S5 Fig). Knockdown of Cbp20 in particular showed dcp1-positive staining across the entire wing pouch in the larval wing disc. These data suggest that knockdown of multiple fly homologs of genes in the 3q29 region contribute to defects in apoptosis and proliferation during early development, leading to the observed defects in cell count and organization (Table 1).
Interactions between fly homologs of 3q29 genes enhance neuronal phenotypes
As knockdown fly models for homologs of multiple 3q29 genes showed a variety of neuronal, developmental, and cellular defects, we hypothesized that these genes could interact with each other to further disrupt cellular processes during development. We therefore generated GMR-GAL4 recombined lines for nine fly homologs of 3q29 genes, and crossed these lines with multiple RNAi or mutant lines for other homologs to generate 161 two-hit crosses for testing 94 pairwise gene interactions (Fig 1, S7 Table). We found a significant enhancement in eye phenotypic severity, measured using Flynotyper and validated with a second line when available, for 39 pairwise knockdowns compared with recombined lines crossed with control flies (represented in the figures as Cbp20KK109448/Control) (Fig 3A, S6 Fig, S7 Fig). In fact, we found that 19 out of 21 pairwise interactions involving Cbp20 as either a first or second-hit gene resulted in more severe eye phenotypes, suggesting that reduced expression of Cbp20 drastically modifies the morphological phenotypes of other homologs of 3q29 genes (Fig 3B–3D). For further validation, we compared pairs of reciprocal crosses (i.e. Fsn/CG8888 versus CG8888/Fsn) and confirmed concordant results for 19/26 reciprocal interactions, including 14/16 reciprocal interactions involving Cbp20 (S7 Table). We also found a non-significant increase in severity for dlg1/Pak knockdown flies using both RNAi and mutant lines, concordant with enhanced neuromuscular junction and circadian rhythm defects observed in mutant dlg1/Pak flies described by Grice and colleagues [54].
As Cbp20 knockdown enhanced the rough eye phenotypes of multiple other homologs, we next tested for enhancement of neuronal defects among flies with knockdown of Cbp20 and homologs of other 3q29 genes. We found that simultaneous knockdown of Cbp20 with dlg1 or Fsn led to an increase in severity of axon targeting defects (Fig 3E). For instance, while knockdown of Cbp20 mostly led to mild-to-moderate axon targeting defects, such as loss of R7-R8 axon projection into the medulla, we observed more severe loss of projection for all axons with simultaneous knockdown of Cbp20 and dlg1 or Fsn (S4 Table). We also tested pan-neuronal Elav-GAL4 knockdown of select pairs of homologs, and found that both Cbp20/dlg1 and Cbp20/Fsn significantly enhanced the climbing defects observed with knockdown of Cbp20 alone (Fig 3F, S2 Video). Overall, these data show that Cbp20 interacts with other homologs of genes in the 3q29 region to enhance the observed cellular and neuronal defects (Table 1).
To further characterize the functional effects of interactions between homologs of 3q29 genes, we analyzed changes in gene expression by performing RNA-sequencing of heads from flies with select pan-neuronal knockdown of individual (Cbp20, dlg1, Fsn, and Pak) and pairs (Cbp20/dlg1 and Cbp20/Fsn) of homologs of 3q29 genes. We identified differentially-expressed genes in each of the tested fly models compared with Elav-GAL4 controls, and performed enrichment analysis on both differentially-expressed fly genes and their corresponding human homologs (S3 File). We found that knockdown of each individual homolog showed enrichment for dysregulation of cellular and developmental processes (S8 Fig). For example, flies with knockdown of dlg1 and Cbp20 showed enrichment for dysregulation of homologs for human synaptic transmission genes, such as Glt (NLGN1) and nAChRβ3 (HTR3A). Furthermore, flies with knockdown of Cbp20 were enriched for dysregulated fly genes related to metabolic processes, while knockdown of Fsn led to dysregulation of fly genes involved in response to external stimuli and immune response. We also found that homologs of key signaling genes dysregulated in mouse models of the 3q29 deletion, reported by Baba and colleagues [15], were differentially expressed in our fly models for homologs of 3q29 genes. In fact, knockdown of Fsn led to altered expression for each of the “early immediate” signaling genes dysregulated in the deletion mouse model [15]. While dysregulated genes in Cbp20/dlg1 knockdown flies showed enrichments for protein folding and sensory perception, Cbp20/Fsn knockdown flies were uniquely enriched for dysregulated homologs of cell cycle genes, including Aura (AURKA), Cdk1 (CDK1), lok (CHEK2), and CycE (CCNE1) (S8 Fig). We similarly found 17 differentially-expressed homologs corresponding to human apoptosis genes in Cbp20/Fsn knockdown flies, including the DNA fragmentation gene Sid (ENDOG) and the apoptosis signaling genes tor (RET) and Hsp70Bb (HSPA1A). Furthermore, we found a strong enrichment for fly genes whose human homologs are preferentially expressed in early and mid-fetal brain tissues among the dysregulated genes in Cbp20/Fsn knockdown flies (S8 Fig). These data suggest that Cbp20 interacts with other homologs of genes in the 3q29 region to disrupt a variety of key biological functions, including apoptosis and cell cycle pathways as well as synaptic transmission and metabolic pathways (Table 1).
Finally, to complement the interactions among homologs of 3q29 genes that we identified in Drosophila, we examined the connectivity patterns of 3q29 genes within the context of human gene interaction databases. Gene interaction networks derived from co-expression and protein-protein interaction data [55,56] showed large modules of connected genes within the 3q29 region, including a strongly-connected component involving 11/21 3q29 genes (Fig 4A and 4B). However, the average connectivity among 3q29 genes within a brain-specific interaction network [57] was not significantly different from the connectivity of randomly-selected sets of genes throughout the genome (Fig 4C), suggesting that a subset of genes drive the complexity of genetic interactions within the region. This paradigm was previously observed among genes in the 22q11.2 deletion region, where interactions between PRODH and COMT modulate neurotransmitter function independently of other genes in the region [58]. In fact, five genes in the 3q29 region, including NCBP2, PAK2, and DLG1, showed significantly higher connectivity to other 3q29 genes compared with the average connectivity of random sets of genes (Fig 4D). Interestingly, NCBP2 showed the highest connectivity of all genes in the region, further highlighting its role as a key modulator of genes within the region.
Interactions between Cbp20 and other homologs of 3q29 genes enhance apoptosis defects
Cell death and proliferation are two antagonistic forces that maintain an appropriate number of neurons during development [59]. In fact, both processes have been previously identified as candidate mechanisms for several neurodevelopmental disorders [60–62]. While knockdown of Cbp20 with other homologs of 3q29 genes likely disrupts multiple cellular processes that contribute towards the enhanced cellular defects, we next specifically investigated the role of apoptosis towards these defects, as larval eye and wing discs with knockdown of Cbp20 showed strong increases in apoptosis. We observed black necrotic patches on the ommatidia in adult eyes with knockdown of Cbp20/dlg1 and Cbp20/Fsn, indicating that an increase in cell death occurs with these interactions (Fig 5A, S9 Fig). In fact, significantly larger regions of necrotic patches were observed in flies homozygous for Cbp20 RNAi and heterozygous for dlg1 RNAi (see S2 File for full genotype annotation), suggesting that the knockdown of both homologs contributes to ommatidial cell death (Fig 5A). Furthermore, we found an enhanced disruption of ommatidial cell organization and loss of photoreceptors in pupal flies with concomitant knockdown of Cbp20 with dlg1, Fsn or CG8888, emphasizing the role of these genes in maintaining cell count and organization (Fig 5B and 5C, S9 Fig, S8 Table). Based on these observations, we next assayed for apoptotic cells in the larval eye discs of flies with knockdown of Cbp20 and other homologs of 3q29 genes. We observed significant increases in the number of apoptotic cells, as measured by dcp1 (Fig 5D and 5E) and TUNEL staining (S9 Fig), when Cbp20 was knocked down along with CG8888, dlg1, or Fsn. Cbp20/CG8888 knockdown flies also showed a decreased number of pH3-positive cells, suggesting that both apoptosis and proliferation are affected by the interaction between these two genes (Fig 5F).
To validate apoptosis as a candidate mechanism for the cellular defects of flies with knockdown of homologs of 3q29 genes, we crossed recombined fly lines for Cbp20 and dlg1 with flies overexpressing Diap1 (death-associated inhibitor of apoptosis). Diap1 is an E3 ubiquitin ligase that targets Dronc, the fly homolog of caspase-9, and prevents the subsequent activation of downstream caspases that lead to apoptosis [63]. We found that overexpression of Diap1 rescued the adult rough eye phenotypes (Fig 6A and 6B, S10 Fig) and increased the eye sizes of Cbp20 and dlg1 flies (S10 Fig). These observations were corroborated by the reversal of cellular changes in the eye upon Diap1 overexpression, including the rescue of ommatidial structure and cell count deficits observed with knockdown of Cbp20 and dlg1 (Fig 6D, S10 Fig). Furthermore, overexpression of Diap1 led to significant reductions in the number of TUNEL and dcp1-positive cells in the larval eye discs of flies with knockdown of Cbp20 and dlg1, confirming the rescue of apoptosis defects in these flies (Fig 6E and 6F, S10 Fig). Interestingly, Diap1 overexpression also suppressed the photoreceptor axon targeting defects observed with knockdown of Cbp20 (Fig 6G, S4 Table), suggesting that the neuronal defects observed in these flies could be attributed to increased apoptosis. We further confirmed these mechanistic findings by observing increased severity in cellular phenotypes upon overexpression of Dronc in Cbp20 and dlg1 knockdown flies. For example, we observed black necrotic patches (Fig 6A and 6C) and exaggerated apoptotic responses (Fig 6E and 6F, S10 Fig) in Cbp20 knockdown flies with overexpression of Dronc. These results suggest that apoptosis mediates the cellular defects observed in flies with knockdown of Cbp20 and dlg1.
Homologs of 3q29 genes interact with canonical neurodevelopmental genes
We further explored the role of 3q29 genes in neurodevelopmental pathways by screening four fly homologs with strong neurodevelopmental phenotypes (Cbp20, dlg1, CG8888, and Pak) for interactions with homologs of 15 known human neurodevelopmental genes, for a total of 60 pairwise interactions and 153 two-hit crosses (Fig 7A). We selected these neurodevelopmental genes for screening based on their association with developmental disorders in humans [53,64], and included eight genes associated with apoptosis or cell cycle functions as well as four genes associated with microcephaly [65], a key phenotype observed in approximately 50% of 3q29 deletion carriers [8]. We found that 34 pairwise interactions, validated with a second line when available, led to significant increases in eye phenotypes compared with recombined lines for individual homologs of 3q29 genes (S9 Table, S11 Fig). These interactions included 19 validated interactions of homologs of 3q29 genes with apoptosis or cell cycle genes as well as ten interactions with microcephaly genes. We found that 13/15 homologs of neurodevelopmental genes, including all four microcephaly genes, enhanced the phenotypes observed with knockdown of Cbp20 alone. Furthermore, knockdown of dlg1 significantly enhanced the ommatidial necrotic patches observed with knockdown of arm (CTNNB1), while flies with concomitant knockdown of Cbp20 and arm also showed increased necrotic patches (Fig 7B, S9 Fig). Interestingly, we also found that knockdown of CG8888 and dlg1 suppressed the rough eye phenotypes observed with knockdown of Prosap (SHANK3), while knockdown of Pak suppressed the phenotypes of both Prosap and Pten (PTEN) knockdown flies (Fig 7B). Several of these interactions have been previously observed to modulate neuronal function in model systems. For example, SHANK3 interacts with DLG1 through the mediator protein DLGAP1 to influence post-synaptic density in mice [66] and binds to proteins in the Rac1 complex, including PAK2, to regulate synaptic structure [67,68]. These results suggest that homologs of 3q29 genes interact with key developmental genes in conserved pathways to modify cellular phenotypes.
Reduction of 3q29 gene expression causes developmental defects in Xenopus laevis
After identifying a wide range of neurodevelopmental defects due to knockdown of fly homologs of 3q29 genes, we sought to gain further insight into the conserved functions of these genes in vertebrate embryonic brain development using the Xenopus laevis model system. We examined the effect of targeted knockdown of ncbp2, fbxo45, and pak2, as homologs of these genes displayed multiple severe phenotypes with reduced gene expression in flies. Knockdown of X. laevis homologs for each 3q29 gene was accomplished using antisense morpholino oligonucleotides (MOs) targeted to early splice sites of each homolog (Fig 1). X. laevis embryos were injected at either the two- or four-cell stage with various concentrations of MO for each homolog or a standard control, and knockdown of each homolog was validated using qPCR (S12 Fig). As knockdown of Cbp20, Fsn, and Pak each resulted in neuronal defects in Drosophila, we first examined the effects of knockdown of these homologs on X. laevis brain development at stage 47. To test this, we knocked down each gene in half of the embryo at the two-cell stage, and left the other half uninjected to create a side-by-side comparison of brain morphology (Fig 8A). We performed whole-mount immunostaining with anti-alpha tubulin and found that reduced expression of ncbp2, fbxo45, and pak2 each resulted in smaller forebrain and midbrain size compared with controls (Fig 8A–8C). We also found that simultaneous knockdown of ncbp2 with fbxo45 caused a significant decrease in forebrain size and a trend towards decreased midbrain size (p = 0.093) compared with ncbp2 knockdown (Fig 8A–8C). Knockdown of pak2 with ncbp2 showed a similar trend towards decreased forebrain size (p = 0.051). Interestingly, the reduced brain volumes we observed with knockdown of homologs of 3q29 genes in X. laevis recapitulate the reduced brain volume observed in 3q29 deletion mice [14,15], suggesting that multiple genes in the 3q29 region contribute to this phenotype. We further examined the effect of knocking down homologs of 3q29 genes on X. laevis eye development at stage 42, and found that knockdown of these homologs caused irregular shapes and decreased size compared with controls (S13 Fig). The reductions in eye size were rescued to control levels when mRNA was co-injected along with MO for each homolog (S13 Fig). Together, these data show that individual and pairwise knockdown of homologs of 3q29 genes in X. laevis leads to abnormal brain and eye morphology, confirming the conserved role of these genes during vertebrate development.
To determine if the knockdown of homologs of 3q29 genes also disrupted apoptotic processes in X. laevis, we tested whether overexpression of the X-linked inhibitor of apoptosis gene (xiap) could rescue the observed developmental defects. We found that overexpression of xiap rescued the midbrain and forebrain size deficits observed with ncbp2 knockdown to control levels (Fig 8A–8C). Similarly, we found that the decreased eye sizes and morphological defects observed with knockdown of ncbp2 were rescued with xiap overexpression (S13 Fig). To further validate these findings, we performed a western blot following knockdown of fbxo45 and ncbp2 using anti-cleaved caspase-3 (Asp175) as a marker for apoptosis (Fig 8D, S12 Fig). We found that reduction of fbxo45 and ncbp2 expression each led to an increase in cleaved caspase-3 levels compared with controls, which were restored to control levels with concomitant overexpression of xiap (Fig 8E). Caspase-3 levels were also enhanced when fbxo45 and ncbp2 were knocked down together (Fig 8E), suggesting that these two homologs interact with each other and contribute towards developmental phenotypes through increased apoptosis. Overall, these results suggest involvement of apoptotic processes towards the developmental phenotypes observed with knockdown of homologs of 3q29 genes in a vertebrate model (Table 1).
Discussion
Using complementary Drosophila and X. laevis models, we interrogated developmental effects, cellular mechanisms, and genetic interactions of individual homologs of genes within the 3q29 region. Our major findings were recapitulated across both model systems (Table 1) and could also potentially account for the developmental phenotypes reported in mouse models of the entire deletion. Several themes have emerged from our study that exemplify the genetic and mechanistic complexity of the 3q29 deletion region.
First, our analysis of developmental phenotypes with knockdown of homologs for individual 3q29 genes showed that a single gene within the region may not be solely responsible for the effects of the deletion. In fact, we found that knockdown of 12 out of 14 fly homologs showed developmental defects in Drosophila, while every fly homolog showed an enhanced rough eye phenotype when knocked down along with at least one other homolog (Fig 2). Although our study is limited to examining conserved cellular phenotypes of homologs of 3q29 genes in Drosophila and X. laevis, evidence from other model organisms also supports an oligogenic model for the deletion. In fact, knockout mouse models for several 3q29 genes have been reported to exhibit severe developmental phenotypes, including axonal and synaptic defects in Fbxo45-/- and embryonic lethality in Pak2-/- and Pcyt1a-/- knockout mice [69–71] (S3 Table). Notably, although Dlg1+/- or Pak2+/- mice showed a range of neuronal phenotypes compared with control mice, they did not recapitulate the major developmental and behavioral features observed in mouse models of the entire deletion [14,15,72], suggesting that the deletion phenotypes are contingent upon haploinsufficiency of multiple genes in the region (S10 Table). Furthermore, several 3q29 genes including PAK2, DLG1, PCYT1A, and UBXN7 are under evolutionary constraint in humans, based on gene pathogenicity metrics (S1 File). Two genes in the 3q29 region without fly homologs, CEP19 and TFRC, are also under evolutionary constraint in humans, with TFRC having been implicated in neural tube defects and embryonic lethality in mouse models [73]. While no common variants associated with neurodevelopmental traits have been observed in the 3q29 region [74], rare variants of varying effects in 9/21 genes have been identified among patients with different developmental disorders [75–77] (S1 File). These data, combined with our findings in Drosophila and X. laevis, implicate multiple genes within the 3q29 region as potential candidates for neurodevelopmental defects.
Second, our screening of 161 crosses between pairs of fly homologs of 3q29 genes identified 44 interactions that showed enhanced rough eye phenotypes, suggesting that complex interactions among genes in the 3q29 region could contribute towards developmental defects (Fig 9A). While we only tested a subset of all possible interactions among the non-syntenic homologs of 3q29 genes in Drosophila, our results highlight conserved mechanistic relationships between “parts”, or the individual genes, towards understanding the effects of the “whole” deletion. For example, knockdown of Cbp20 enhanced the phenotypes of 11 out of 12 other fly homologs, suggesting that NCBP2 could be a key modulator of other genes within the region. NCBP2 encodes a subunit of the nuclear cap-binding complex (CBC), which binds to the 5’ end of mRNA and microRNA in the nucleus [78]. Given the role of the CBC in post-transcriptional regulatory mechanisms such as nonsense-mediated decay, alternative splicing and mRNA transport [79,80], it is possible that disruption of this complex could result in changes to a broad set of genes and biological processes. In fact, our analysis of differentially-expressed genes in Cbp20 knockdown flies showed disruption of synaptic transmission, cellular respiration, and several metabolic pathways. In contrast to other proposed candidate genes in the 3q29 region, NBCP2 is not predicted to be pathogenic on its own in humans (S1 File) and does not have identified deleterious mutations in sequencing studies of neurodevelopmental disease cohorts so far, indicating its potential role as a modifier of the other candidate genes in the region (Fig 9B). Our results also complement previous reports of synergistic interactions among fly homologs of 3q29 genes in the nervous system [54], representing another hallmark of an oligogenic model for the deletion. As these genetic interactions may vary across different species, developmental timepoints, and tissues, the role of these interactions should be more deeply explored using mouse and human cell culture models.
Third, we identified disruptions to several cellular processes due to both single and pairwise knockdown of homologs in Drosophila and X. laevis models (Table 1). For example, simultaneous knockdown of homologs of NCBP2 and FBXO45 in Drosophila led to enhanced cellular disorganization (Fig 5) and altered expression of cell cycle and apoptosis genes (S8 Fig), as well as enhanced morphological defects and increased caspase-3 levels in X. laevis (Fig 8). We further found that overexpression of the apoptosis inhibitors Diap1 and xiap rescued the cellular and neuronal phenotypes observed with knockdown of homologs of 3q29 genes (Fig 6), providing important validations for the potential involvement of apoptosis in the deletion (Table 1). We propose that NCBP2 could modify several cellular and molecular processes that may not be directly related to apoptosis, but could instead lead to a cascade of biological events that ultimately result in apoptosis (Fig 9B). Apoptosis mechanisms are well-conserved between Drosophila, X. laevis, and humans, with key genes such as XIAP (Diap1), CASP2 (Dronc), CASP3 (DrICE), and CASP7 (Dcp-1) sharing the same roles in programmed cell death across the three organisms [81–83]. In fact, we found that fly homologs of human genes annotated for apoptosis function in the Gene Ontology database were also enriched for apoptosis function (n = 1,063 fly homologs from 1,789 human apoptosis genes; p = 5.30×10−13, Fisher’s Exact test with Benjamini-Hochberg correction). Although we focused on testing apoptosis phenotypes with knockdown of homologs of 3q29 genes, we note that apoptosis is potentially one of many cellular pathways disrupted by the 3q29 deletion (Fig 9B). In fact, our data implicated knockdown of several homologs of 3q29 genes, including dlg1 and CG8888 (BDH1), towards abnormal cell proliferation during development. Furthermore, several 3q29 genes have been previously associated with apoptosis or cell cycle regulation functions (S1 File). For example, DLG1 is a tumor suppressor gene whose knockdown in Drosophila leads to neoplasms in the developing brain and eye disc [84,85], while PAK2 is a key downstream mediator of the ERK signaling pathway for neuronal extension and is activated by caspases during apoptosis [70,86,87]. Our results recapitulate the role of DLG1 towards cell cycle regulation, and also implicate NCBP2 and its interactions towards multiple cellular and developmental phenotypes.
More broadly, genes involved with apoptosis and cell proliferation have been implicated in several neurodevelopmental disorders. For example, we previously observed disrupted cell proliferation upon knockdown of Drosophila homologs of genes in the 16p11.2 deletion region, as well as an enrichment of cell cycle function among connector genes between pairs of 16p11.2 genes in a human brain-specific network [21]. Furthermore, abnormal apoptosis in the early developing brain has been suggested as a possible mechanism for the decreased number of neurons observed in individuals with autism and schizophrenia [62,88,89]. For example, increased apoptosis was observed in both postmortem brain tissue from autism patients [90] and primary fibroblasts from schizophrenia patients [91,92]. We found further support for the role of apoptosis in these disorders by identifying significant enrichments for genes associated with apoptotic processes among candidate genes for autism (empirical p<1.00×10−5) [77], intellectual disability (p<1.00×10−5) [93], and schizophrenia (p = 0.014) [76] (S11 Table). In fact, out of the 525 neurodevelopmental genes involved in apoptosis, 20 genes were present within pathogenic CNV regions [94], including CORO1A, MAPK3 and TAOK2 in the 16p11.2 region as well as TBX1, the causative gene for heart defects in DiGeorge/velocardiofacial syndrome [95] (S4 File). In addition to neuropsychiatric disorders, apoptosis has also been implicated in syndromic forms of microcephaly in humans [96] as well as decreased brain size in animal models of microcephaly genes [97,98]. For example, a mouse model of the Nijmegen breakage syndrome gene NBN exhibited increased neuronal apoptosis, leading to microcephaly and decreased body mass [99]. Overall, these findings highlight the importance of cell cycle-related processes, particularly apoptosis and proliferation, towards modulating neuronal phenotypes that could be responsible for developmental disorders.
In this study, the use of Drosophila and X. laevis models, both of which are amenable to high-throughput screening of developmental phenotypes, allowed us to systematically examine the conserved cellular and mechanistic roles of homologs of 3q29 genes and their interactions. Follow-up studies in more evolutionarily advanced systems, such as mouse or human cell lines, will be useful to overcome limitations of Drosophila and X. laevis models, including testing the neurodevelopmental phenotypes and interactions of 3q29 genes without fly homologs. Collectively, these results emphasize the utility of quantitative functional assays for identifying conserved pathways associated with neurodevelopmental disorders, which will hopefully allow for future discoveries of treatments for these disorders.
Materials and methods
Ethics statement
All X. laevis experiments were approved by the Boston College Institutional Animal Care and Use Committee (Protocol #2016–012) and were performed according to national regulatory standards.
Fly stocks and genetics
Using reciprocal BLAST searches and orthology predictions from the DRSC Integrative Ortholog Prediction Tool (DIOPT) v.7.1 [100], we identified 15 fly homologs for the 21 human genes within the chromosome 3q29 region (S1 Table). No fly homologs were present for six genes, including LRRC33, CEP19, RNF168, SMCO1, TFRC, and TM4SF19. We used a similar strategy to identify homologs for other neurodevelopmental genes tested for interactions in this study. Gene Ontology-Slim (GO-Slim) terms for each human gene and fly homolog were obtained from PantherDB [101] and are provided in S1 File. RNAi lines for fly homologs were obtained from the Vienna Drosophila Resource Centre [102] (VDRC), including both KK and GD lines, and the Bloomington Drosophila Stock Center (BDSC) (NIH P40OD018537). A list of fly RNAi lines used in this study is provided in S2 File. Fly RNAi lines for homologs of 3q29 genes were tested for gene knockdown using quantitative PCR (S1 Table). As the available KK line for CG5359 (TCTEX1D2) showed a wing phenotype consistent with tiptop overexpression due to RNAi insertion at the 5’UTR of the gene [103], which we confirmed using qPCR analysis (S5 File), we excluded this gene from our experiments. Microarray data and modENCODE Anatomy RNA-Seq from FlyBase [104,105] showed that all of the 14 tested homologs were expressed in the fly central nervous system and eye tissues (S1 Table).
All fly stocks and crosses were cultured on conventional cornmeal-sucrose-dextrose-yeast medium at 25°C, unless otherwise indicated. RNAi lines were crossed with a series of GAL4 driver lines to achieve tissue-specific knockdown of genes, including w1118;da-GAL4 (Scott Selleck, Penn State) for ubiquitous, w1118;dCad-GFP,GMR-GAL4/CyO (Zhi-Chun Lai, Penn State) and w1118;GMR-GAL4;UAS-Dicer2 (Claire Thomas, Penn State) for eye-specific, w1118,bxMS1096-GAL4;;UAS-Dicer2 (Zhi-Chun Lai, Penn State) for wing-specific, and w1118,Elav-GAL4 (Mike Groteweil, VCU) and w1118,Elav-GAL4;;UAS-Dicer2 (Scott Selleck, Penn State) for pan-neuronal knockdown of gene expression. A list of full genotypes for all crosses tested in this study is provided in S2 File. To perform interaction studies, we generated recombined stock lines of GMR-GAL4 with reduced expression of nine select homologs of 3q29 genes (S2 File). Females from these stocks with constitutively reduced gene expression for each of these genes were crossed with RNAi lines of other homologs to achieve simultaneous knockdown of two genes (Fig 1). We previously demonstrated that these two-hit crosses had adequate GAL4 to bind to two independent UAS-RNAi constructs [21]. All unique biological materials described in the manuscript, such as recombined fly stocks, are readily available from the authors upon request.
Quantitative polymerase chain reaction for Drosophila RNAi knockdowns
Levels of gene expression knockdown were confirmed using quantitative reverse-transcriptase PCR (qPCR) on RNA isolated from pooled groups of 35 fly heads per line tested (S2 Table). Briefly, RNAi lines were crossed with Elav-GAL4 (to test RNAi line efficacy) or Elav-GAL4;;UAS-Dicer2 (to test for tiptop overexpression) at 25°C to achieve pan-neuronal knockdown of the fly homolog. Adult fly heads at day 3 were separated by vortexing, and total RNA was isolated using TRIzol (Invitrogen, Carlsbad, CA, USA). cDNA was prepared using the qScript cDNA synthesis kit (Quantabio, Beverly, MA, USA). Quantitative PCR was performed using an Applied Biosystems Fast 7500 system with SYBR Green PCR master mix (Quantabio) to estimate the level of gene expression. All experiments were performed using three biological replicates of 35 fly heads each. Primers were designed using NCBI Primer-BLAST [106], with primer pairs separated by an intron in the corresponding genomic DNA. A list of primers used in the experiments is provided in S2 Table. The delta-delta Ct value method was used to obtain the relative expression of fly homologs in the RNAi lines compared with Elav-GAL4 controls [107].
Climbing assay
We set up fly crosses at 25°C with Elav-GAL4 to obtain pan-neuronal knockdown for select homologs of 3q29 genes. For each RNAi line tested, groups of ten female flies were first allowed to adjust at room temperature for 30 minutes and then transferred to a climbing apparatus, made by joining two vials, and allowed to adjust for 5 minutes. The flies were tapped down to the bottom, and the number of flies climbing past the 8 cm mark measured from the bottom of the apparatus in 10 seconds was then counted (S1 Video, S2 Video). This assay was repeated nine additional times for each group, with a one-minute rest between trials. The sets of 10 trials for each group were repeated daily for ten days, capturing data for 100 replicates from day 1 until day 10, starting the experiments with 1-2-day old flies. All experiments were performed during the same time of the day for consistency of results.
Imaging of adult fly eyes and wings
We crossed RNAi lines with GMR-GAL4 and reared at 29°C for eye-specific knockdown and bxMS1096-GAL4 at 25°C for wing-specific knockdown. For eye imaging, adult 2-3-day old female progenies from the crosses were collected, immobilized by freezing at -80°C, mounted on Blu-tac (Bostik Inc, Wauwatosa, WI, USA), and imaged with an Olympus BX53 compound microscope with LMPLan N 20X air objective using a DP73 c-mount camera at 0.5X magnification and a z-step size of 12.1μm. (Olympus Corporation, Tokyo, Japan). We used CellSens Dimension software (Olympus Corporation, Tokyo, Japan) to capture the images, and stacked the image slices using Zerene Stacker (Zerene Systems LLC, Richland, WA, USA). All eye images presented in this study are maximum projections of 20 consecutive optical z-sections. Adult wings were plucked from 2–5 day old female flies, mounted on a glass slide, covered with a coverslip and sealed with clear nail polish. The wings were imaged using a Zeiss Discovery V20 stereoscope (Zeiss, Thornwood, NY, USA) with ProgRes Speed XT Core 3 camera (Jenoptik AG, Jena, Germany) using a 40X objective, and wing images were captured with ProgRes CapturePro v.2.8.8 software.
Quantitative phenotyping of fly eyes using Flynotyper
We used a computational method called Flynotyper (http://flynotyper.sourceforge.net) to measure the degree of roughness of the adult eyes with knockdown of individual or pairs of homologs [53]. The software uses an algorithm to detect the center of each ommatidium, and calculates a phenotypic score based on the number of ommatidia detected, the lengths of six local vectors with direction pointing from each ommatidium to the neighboring ommatidia, and the angle between these six local vectors (S2 Fig). Eye areas, ommatidial diameter, and areas of necrotic patches, which may not be reflected in the Flynotyper scores, were measured using ImageJ [108]. Significant pairwise interactions were reported as “validated” when multiple RNAi or mutant lines, if available, showed the same phenotype (S7 Table, S9 Table).
Immunohistochemistry of eye and wing discs
Third instar larval and 44-hour-old pupal eye discs, reared at 29°C, and third instar larval wing discs, reared at 25°C, were dissected in 1X phosphate-buffered saline (PBS) and fixed in 4% paraformaldehyde for 20 minutes. The eye and wing discs were then washed thrice in PBT (PBS with 0.1% Triton-X) for 10 minutes each, treated with blocking solution (PBS with 1% normal goat serum (NGS) for eye discs, or 1% bovine serum albumin (BSA) for wing discs) for 30 minutes, and then incubated overnight with primary antibodies at 4°C. Rabbit anti-cleaved Drosophila dcp1 (Asp216) (1:100; 9578S, Cell Signaling Technology, Danvers, MA, USA), a marker for cells undergoing apoptosis, and Mouse anti-phospho-Histone H3 (S10) antibody (1:100; 9706L, Cell Signaling Technology), a mitotic marker for measuring proliferating cells, were used to assay cell proliferation and apoptosis defects in larval eye and wing discs. Mouse anti-DLG (1:200; 4F3, DSHB, Iowa City, Iowa, USA), a septate junction marker, and Rhodamine Phalloidin (1:200; R415, Invitrogen Molecular Probes, Carlsbad, CA, USA), an F-actin marker, were used to visualize and count ommatidial cells and photoreceptor cells in pupal eyes. Mouse anti-chaoptin (1:200; 24B10, DSHB) was used to visualize retinal axon projections. Preparations were then washed thrice with PBT for 10 minutes, and incubated for two hours with fluorophore-conjugated secondary antibodies (Alexa fluor 568 goat anti-mouse (1:200) (A11031), Alexa fluor 488 goat anti-mouse (1:200) (A11029), Alexa fluor 647 goat anti-rabbit (1:200) (A21245), and Alexa fluor 647 goat anti-mouse (1:200) (A21236), Invitrogen Molecular Probes, Carlsbad, CA, USA)) with gentle shaking. Preparations were washed thrice in PBT for 10 minutes, and the tissues were then mounted in Prolong Gold antifade mounting media with DAPI (P36930, Thermo Fisher Scientific, Waltham, MA, USA) or Vectashield hard set mounting media with DAPI (H-1500, Vector Laboratories, Burlingame, CA, USA) for imaging.
Bromouridine staining
Third instar larval eye discs were dissected in 1X PBS and immediately transferred to Schneider’s Insect Media (Sigma-Aldrich, St. Louis, MO). The tissues were then incubated in 10 μM BrdU (Sigma-Aldrich) at 25°C for one hour with constant agitation to allow for incorporation of BrdU into DNA of replicating cells during the S-phase of cell cycle. The samples were washed thrice with PBS for five minutes each and fixed in 4% paraformaldehyde for 20 minutes. To denature DNA, the tissues were acid-treated in 2N HCl for 20 minutes, neutralized in 100 mM Borax solution for 2 minutes, washed thrice in 10X PBT (PBS with 0.1% Tween-20) for 10 minutes, and treated with blocking solution (PBS, 0.2% Triton X-100, 5% NGS) for one hour. The tissues were then incubated in mouse anti-BrdU (1:200; G3G4, DSHB, Iowa City, Iowa, USA) and diluted in blocking solution overnight at 4°C. The next day, the tissues were washed thrice in PBT for 20 minutes each and incubated in Alexa fluor 568 goat anti-mouse (1:200, Invitrogen Molecular Probes, Carlsbad, CA, USA) for two hours with constant agitation. Finally, the samples were mounted in Prolong Gold antifade reagent with DAPI (Thermo Fisher Scientific, Waltham, MA, USA) for imaging.
Terminal deoxynucleotidyl transferase (TUNEL) Assay
The levels of cell death in the developing eye were evaluated by staining using the In Situ Cell Death Detection Kit, TMR Red (Roche, Basel, Switzerland). The third instar larval eye discs were dissected in 1X PBS and fixed in 4% paraformaldehyde for 20 minutes at room temperature, followed by three 10-minute washes with PBS. The dissected tissues were permeabilized by treating with 20 μg/ml proteinase K (Sigma-Aldrich, St. Louis, MO, USA) for two minutes, washed thrice in PBT (PBS with 0.1% Triton-X) for 5 minutes each, fixed in 4% paraformaldehyde for 15 minutes, and washed thrice again in PBT for 10 minutes each. The tissues were then incubated overnight with TUNEL (terminal deoxynucleotidyl transferase dUTP nick end labeling) reaction mixture at 4°C per the manufacturer’s instructions, and washed five times in PBT for 15 minutes each. Finally, tissues were mounted in Prolong Gold antifade containing DAPI (Thermo Fisher Scientific, Waltham, MA, USA) for imaging.
Confocal imaging and analysis
Confocal images of larval and pupal eye and wing discs were captured using an Olympus Fluoview FV1000 laser scanning confocal microscope (Olympus America, Lake Success, NY). Maximum projections of all optical sections were generated for display. As DLG staining was only used to visualize cell boundaries in the pupal eye and not for any expression or quantitative analysis, we increased the laser intensity from 400-490V in control flies to 530-570V in flies with knockdown of dlg1 to account for decreased DLG expression. Acquisition and processing of images was performed using the Fluoview FV10-ASW 2.1 software (Olympus Corporation, Tokyo, Japan), and the z-stacks of images were merged using ImageJ [108]. The number of pH3, BrdU, TUNEL, and dcp1-positive cells from larval eye discs were counted using two ImageJ plugins, AnalyzeParticles and Image-based Tool for Counting Nuclei (ITCN). As we found a strong correlation (Pearson correlation, r = 0.736, p<2.2x10-16) between the two methods (S2 Fig), all cell counts displayed for eye data were derived from ITCN analysis. Proliferating cells in larval wing discs stained with pH3 were counted using AnalyzeParticles, and apoptotic cells in wing discs stained with dcp1 were analyzed using manual counting. Images stained with anti-chaoptin were manually scored as having either “mild” (minor axon disorganization compared with control), “moderate” (partial loss of axon projection. i.e. loss of R7-R8 projection into the medulla), or “severe” (loss of projections for most axons at the lamina) axon targeting defects.
Differential expression analysis of transcriptome data
We performed RNA sequencing (RNA-Seq) of samples isolated from three biological replicates of 35 fly heads each for individual (Cbp20, dlg1, Fsn, Pak) and pairwise (Cbp20/dlg1, Cbp20/Fsn) Elav-GAL4 mediated knockdowns of homologs of 3q29 genes. We compared gene expression levels of each cross to VDRC control flies carrying the same genetic background (GD or KK control lines crossed with Elav-GAL4). We prepared cDNA libraries for the three biological replicates per genotype using TruSeq Stranded mRNA LT Sample Prep Kit (Illumina, San Diego, CA), and performed single-end sequencing using Illumina HiSeq 2000 at the Penn State Genomics Core Facility to obtain 100 bp reads at an average coverage of 36.0 million aligned reads/sample. We used Trimmomatic v.0.36 [109] for quality control assessment, TopHat2 v.2.1.1 [110] to align the raw sequencing data to the reference fly genome and transcriptome (build 6.08), and HTSeq-Count v.0.6.1 [111] to calculate raw read counts for each gene. edgeR v.3.20.1 [112] (generalized linear model option) was used to perform differential expression analysis, and genes with log2-fold changes >1 or <-1 and false-discovery rates <0.05 (Benjamini-Hochberg correction) were considered to be differentially expressed (S3 File). Human homologs of differentially-expressed fly genes (top matches for each fly gene, excluding matches with “low” rank) were identified using DIOPT [100]. Enrichment analysis of Panther GO-Slim Biological Process terms among the differentially-expressed fly genes and their human homologs was performed using the PantherDB Gene List Analysis tool [101]. Enrichments for genes preferentially expressed in the developing brain were calculated using the Cell-type Specific Expression Analysis tool [113] based on expression data from the BrainSpan Atlas [114].
X. laevis embryos
Eggs collected from female X. laevis frogs were fertilized in vitro, dejellied, and cultured following standard methods [115,116]. Embryos were staged according to Nieuwkoop and Faber [117].
Morpholino and RNA constructs
Morpholinos (MOs) were targeted to early splice sites of X. laevis ncbp2, fbxo45, pak2, or standard control MO, purchased from Gene Tools LLC (Philomath, OR, USA). MO sequences are listed in S12 Table. For knockdown experiments, all MOs were injected at either the 2-cell or 4-cell stage, with embryos receiving injections two or four times total in 0.1X MMR media containing 5% Ficoll. Control and fbxo45 MOs were injected at 10ng/embryo, ncbp2 and control MOs were injected at 20ng/embryo, and pak2 and control MOs were injected at 50ng/embryo. For rescue experiments (S13 Fig), the same amounts of MOs used in the KD experiments were injected along with gene-specific mRNA tagged with GFP (800pg/embryo for xiap-GFP; 1000pg/embryo for ncbp2-GFP and fbxo45-GFP, and 300pg/embryo for pak2-GFP) in the same injection solution. Capped mRNAs were transcribed in vitro using SP6 or T7 mMessage mMachine Kit (Thermo Fisher Scientific, Waltham, MA, USA). RNA was purified with LiCl precipitation. X. laevis ncbp2, fbxo45, pak2, and xiap ORFs obtained from the European Xenopus Resource Center (EXRC, Portsmouth, UK) were gateway-cloned into pCSf107mT-GATEWAY-3’GFP destination vectors. Constructs used included ncbp2-GFP, fbxo45-GFP, pak2-GFP, xiap-GFP, and GFP in pCS2+. Embryos either at the 2-cell or 4-cell stage received four injections in 0.1X MMR containing 5% Ficoll with the following total mRNA amount per embryo: 300pg of GFP, 800pg of xiap-GFP, 1000pg of ncbp2-GFP, 1000pg of fbxo45-GFP, and 300pg of pak2-GFP.
qPCR for X. laevis morpholino knockdown
Morpholino validation and knockdown was assessed using qPCR. Total RNA was extracted using TRIzol reagent (Life Technologies, Grand Island, NY, USA), followed by chloroform extraction and ethanol precipitation from 2-day old embryos injected with increasing concentrations of MO targeted to each homolog of the tested 3q29 gene. cDNA synthesis was performed with SuperScript II Reverse Transcriptase (Life Technologies, Grand Island, NY, USA) and random hexamers. PCR primers are listed in S13 Table. qPCR was performed in triplicate (S12 Fig), with band intensities quantified by densitometry in ImageJ and normalized to the uninjected control mean relative to ODC1, which was used as a housekeeping control.
Brain and eye morphology assays
In brain morphology experiments, all embryos received two injections at the 2-cell stage in 0.1X MMR containing 5% Ficoll. One cell was left uninjected and the other cell was injected with either control MO or MO targeted to the tested 3q29 gene, along with 300pg of GFP mRNA in the same injection solution. Stage 47 tadpoles were fixed in 4% PFA diluted in PBS for one hour, rinsed in PBS and gutted to reduce autofluorescence. Embryos were incubated in 3% bovine serum albumin and 1% Triton-X 100 in PBS for two hours, and then incubated in anti-acetylated tubulin primary antibody (1:500, monoclonal, clone 6-11B-1, AB24610, Abcam, Cambridge, UK) and goat anti-mouse Alexa fluor 488 conjugate secondary antibody (1:1000, polyclonal, A11029, Invitrogen Life Technologies, Carlsbad, CA). Embryos were then rinsed in 1% PBS-Tween and imaged in PBS. Skin dorsal to the brain was removed if the brain was not clearly visible due to pigment. For eye phenotype experiments, all embryos received four injections at the 2-cell or 4-cell stage in 0.1X MMR containing 5% Ficoll with either the control MO or MOs targeted to each 3q29 gene. Stage 42 tadpoles were fixed in 4% PFA diluted in PBS. Tadpoles were washed three times in 1% PBS-Tween for one hour at room temperature before imaging.
X. laevis image acquisition and analysis
Lateral view images of stage 42 tadpoles for eye experiments and dorsal view images of state 47 tadpoles for brain experiments were each collected on a SteREO Discovery.V8 microscope using a Zeiss 5X objective and Axiocam 512 color camera (Zeiss, Thornwood, NY, USA). Areas of the left and right eye, forebrain, and midbrain were determined from raw images using the polygon area function in ImageJ. Eye size was quantified by taking the average area of both the left and right eye, while forebrain and midbrain area were quantified by taking the ratio between the injected and uninjected sides for each sample.
Western blot for apoptosis
Two replicate western blot experiments were performed to test for apoptosis markers in X. laevis with 3q29 gene knockdown (S12 Fig). Embryos at stages 20–22 were lysed in buffer (50mM Tris pH 7.5, 1% NP40, 150mM NaCl, 1mM PMSF, 0.5 mM EDTA) supplemented with cOmplete Mini EDTA-free Protease Inhibitor Cocktail (Sigma-Aldrich, Basel, Switzerland). Blotting was carried out using rabbit polyclonal antibody to cleaved caspase-3 (1:500, 9661S, Cell Signaling Technology, Danvers, MA, USA), with mouse anti-beta actin (1:2500, AB8224, Abcam, Cambridge, UK) as a loading control on a Mini-PROTEAN TGX precast 4–15% gradient gel (Bio-Rad, Hercules, CA, USA). Chemiluminescence detection was performed using Amersham ECL western blot reagent (GE Healthcare Bio-Sciences, Pittsburgh, PA, USA). Band intensities were quantified by densitometry in ImageJ and normalized to the control mean relative to beta-actin. Due to the low number of replicates, we did not perform any statistical tests on data derived from these experiments.
Human brain-specific network analysis of 3q29 gene interactions
We used a human brain-specific gene interaction network that was previously built using a Bayesian classifier trained on gene co-expression datasets [56,57]. We extracted interactions between pairs of genes with predicted weights >2.0 (containing the top 0.5% most likely interactions) and measured the length of the shortest paths connecting pairs of 3q29 genes within the network, excluding genes not present in the network from final calculations. As a control, we also measured the connectivity of 500 randomly selected genes with 100 replicates each of 20 other random genes. All network analysis was performed using the NetworkX Python package [118].
Overlap between neurodevelopmental and apoptosis gene sets
We obtained a set of 1,794 genes annotated with the Gene Ontology term for apoptotic processes (GO:0006915) or children terms from the Gene Ontology Consortium (AmiGO v.2.4.26) [119], and overlapped this gene set with sets of 756 candidate autism genes (SFARI Gene Tiers 1–4) [77], 1,854 candidate intellectual disability genes [93], and 2,546 curated candidate schizophrenia genes [76]. Genes in these three sets that were annotated for apoptosis function are listed in S4 File. To determine the statistical significance of these overlaps, we performed 100,000 simulations to identify the number of apoptosis genes among groups of genes randomly selected from the genome, and determined the percentiles for each observed overlap among the simulated overlaps as empirical p-values.
Statistical analysis
Details of each dataset and the associated statistical tests are provided in S5 File. All statistical analyses of functional data were performed using R v.3.4.2 (R Foundation for Statistical Computing, Vienna, Austria). Non-parametric one-tailed and two-tailed Mann-Whitney tests were used to analyze Drosophila functional data and human network data, as several datasets were not normally distributed (p<0.05, Shapiro-Wilk tests for normality). Climbing ability and survival data for each fly RNAi line across each experiment day were analyzed using two-way and one-way repeated values ANOVA tests with post-hoc pairwise t-tests. We also used parametric t-tests to analyze Drosophila qPCR data and all X. laevis data, as these data were either normally distributed (p>0.05, Shapiro-Wilk tests for normality) or had a robust sample size (n>30) for non-normality. All p-values from statistical tests derived from similar sets of experiments (i.e. Flynotyper scores for pairwise interactions, dcp1 rescue experiments with Diap1) were corrected using Benjamini-Hochberg correction.
Reproducibility
Drosophila eye area and pH3 and TUNEL staining experiments for select individual knockdown lines, as well as climbing ability experiments for a subset of individual and pairwise knockdown lines, were performed on two independent occasions with similar sample sizes. Data displayed in the main figures were derived from single batches, while data from the repeated experiments are shown in S14 Fig. X. laevis brain and eye area experiments were performed on three independent occasions, with the data shown in the figures representing pooled results of each of the three experimental batches (normalized to the respective controls from each batch). X. laevis qPCR experiments were performed three times and western blot experiments were performed twice, with the blots/gels for each replicate experiment shown in S12 Fig. Sample sizes for each experiment were determined by testing all available organisms; no prior power calculations for sample size estimation were performed. No data points or outliers were excluded from the experiments presented in the manuscript.
Code availability
All source code and datasets for generating genomic data (RNA-Seq, network analysis, and neurodevelopment/apoptosis gene overlap) are available on the Girirajan lab GitHub page at https://github.com/girirajanlab/3q29_project.
Supporting information
S1 Fig [a]
Developmental defects in flies with tissue-specific knockdown of individual homologs of 3q29 genes.
S2 Fig [a]
Examination of cellular phenotypes in the eye.
S3 Fig [a]
Phenotypic screening for flies with eye-specific knockdown of individual fly homologs of 3q29 genes.
S4 Fig [a]
Cellular phenotypes of flies with eye-specific knockdown of individual fly homologs of 3q29 genes.
S5 Fig [a]
Cellular phenotypes of flies with wing-specific knockdown of individual fly homologs of 3q29 genes.
S6 Fig [a]
Phenotypic screening for pairwise interactions of homologs of 3q29 genes in the adult fly eye.
S7 Fig [pdf]
Validation lines for pairwise interactions of homologs of 3q29 genes in the adult fly eye.
S8 Fig [a]
Transcriptome analysis of flies with knockdown of select homologs of 3q29 genes.
S9 Fig [a]
Cellular phenotypes for pairwise knockdowns of homologs of 3q29 genes.
S10 Fig [a]
Rescue of cellular phenotypes due to knockdown of fly homologs of 3q29 genes with overexpression of .
S11 Fig [pdf]
Phenotypic scores for interactions between homologs of 3q29 genes and known neurodevelopmental genes in the adult fly eye.
S12 Fig [a]
Quantification of 3q29 morpholino knockdown and apoptosis marker levels in models.
S13 Fig [a]
Eye phenotypes observed with knockdown of homologs of 3q29 genes in models.
S14 Fig [a]
Replication of experimental results for individual and pairwise knockdown of homologs of 3q29 genes.
S1 Table [pdf]
homologs of human 3q29 genes and expression of homologs during development.
S2 Table [pdf]
qPCR primers and expression values for RNAi knockdown of fly homologs of 3q29 genes.
S3 Table [pdf]
Comparison of animal model phenotypes with knockdown or knockout of homologs of 3q29 genes.
S4 Table [pdf]
Summary of scoring for phenotypic severity of axon targeting defects upon individual and pairwise knockdown of homologs of 3q29 genes.
S5 Table [pdf]
Comparison of eye phenotypic scores for homologs of 3q29 genes and neurodevelopmental genes.
S6 Table [pdf]
Analysis of defects in ommatidial cells with RNAi knockdown of fly homologs of 3q29 genes.
S7 Table [pdf]
Screening for pairwise interactions among fly homologs of 3q29 genes.
S8 Table [pdf]
Analysis of defects in ommatidial cells with pairwise RNAi knockdown of fly homologs of 3q29 genes.
S9 Table [pdf]
Screening for interactions between fly homologs of 3q29 genes and other known neurodevelopmental genes.
S10 Table [pdf]
Developmental phenotypes observed in mouse models of the 3q29 deletion and individual homologs of 3q29 genes.
S11 Table [pdf]
Summary of apoptosis function enrichment among candidate neurodevelopmental genes.
S12 Table [pdf]
Morpholinos used for experiments.
S13 Table [pdf]
qPCR primers used for experiments.
S1 File [rvis]
Pathogenicity metrics, mutations in disease cohorts, and biological functions of 3q29 genes.
S2 File [xlsx]
List of fly stocks and full genotypes for all crosses tested.
S3 File [fdr]
Transcriptome analysis of flies with knockdown of homologs of 3q29 genes.
S4 File [xlsx]
List of candidate neurodevelopmental genes with apoptosis function.
S5 File [xlsx]
Statistical analysis of experimental data.
S1 Video [mp4]
Climbing ability of flies with knockdown of individual homologs of 3q29 genes.
S2 Video [mp4]
Climbing ability of flies with pairwise knockdowns of homologs of 3q29 genes.
Zdroje
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