Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome
Molecular Autism volume 4, Article number: 28 (2013)
Rare genetic variation is an important class of autism spectrum disorder (ASD) risk factors and can implicate biological networks for investigation. Altered serotonin (5-HT) signaling has been implicated in ASD, and we and others have discovered multiple, rare, ASD-associated variants in the 5-HT transporter (SERT) gene leading to elevated 5-HT re-uptake and perturbed regulation. We hypothesized that loci encoding SERT regulators harbor variants that impact SERT function and/or regulation and therefore could contribute to ASD risk. The adenosine A3 receptor (A3AR) regulates SERT via protein kinase G (PKG) and other signaling pathways leading to enhanced SERT surface expression and catalytic activity.
To test our hypothesis, we asked whether rare variants in the A3AR gene (ADORA3) were increased in ASD cases vs. controls. Discovery sequencing in a case-control sample and subsequent analysis of comparison exome sequence data were conducted. We evaluated the functional impact of two variants from the discovery sample on A3AR signaling and SERT activity.
Sequencing discovery showed an increase of rare coding variants in cases vs. controls (P=0.013). While comparison exome sequence data did not show a significant enrichment (P=0.071), combined analysis strengthened evidence for association (P=0.0025). Two variants discovered in ASD cases (Leu90Val and Val171Ile) lie in or near the ligand-binding pocket, and Leu90Val was enriched individually in cases (P=0.040). In vitro analysis of cells expressing Val90-A3AR revealed elevated basal cGMP levels compared with the wildtype receptor. Additionally, a specific A3AR agonist increased cGMP levels across the full time course studied in Val90-A3AR cells, compared to wildtype receptor. In Val90-A3AR/SERT co-transfections, agonist stimulation elevated SERT activity over the wildtype receptor with delayed 5-HT uptake activity recovery. In contrast, Ile171-A3AR was unable to support agonist stimulation of SERT. Although both Val90 and Ile171 were present in greater numbers in these ASD cases, segregation analysis in families showed incomplete penetrance, consistent with other rare ASD risk alleles.
Our results validate the hypothesis that the SERT regulatory network harbors rare, functional variants that impact SERT activity and regulation in ASD, and encourages further investigation of this network for other variation that may impact ASD risk.
Serotonin (5-hydroxytryptamine (5-HT)) is a prominent monoamine neurotransmitter in the central and peripheral nervous systems, influencing mood, aggression, anxiety, impulsivity, and other behaviors. Serotonergic signaling has been implicated in multiple neuropsychiatric phenotypes, including major depression, obsessive-compulsive disorder (OCD), anxiety disorders, and autism spectrum disorder (ASD), among others (reviewed in ref. ). The presynaptic, antidepressant-sensitive 5-HT transporter (SERT; gene symbol: SLC6A4) is a critical regulator of 5-HT signaling by modulating synaptic 5-HT levels via presynaptic, Na+/Cl- dependent re-uptake. Given the significance of SERT in regulating 5-HT function and its targeting by widely used medications, SLC6A4 has been an attractive target for genetic studies in neuropsychiatric disorders. A significant focus of SLC6A4 genetic studies is a common insertion/deletion polymorphism (5-HTTLPR) in the promoter region reported to impact SLC6A4 gene expression . Although some evidence supports association of 5-HTTLPR with psychiatric phenotypes including ASD, results overall are mixed [3–5], potentially influenced by the inherent difficulty of diagnosing behaviorally defined disorders and heterogeneity within and across cohorts examined. Additionally, single nucleotide variants (SNPs) within 5-HTTLPR and the promoter region are inherent confounds to many earlier studies [6–8].
The phenomenon of hyperserotonemia, or elevated whole blood or platelet 5-HT seen in approximately 35% of ASD cases, is the oldest ASD biomarker and is a highly heritable trait . The presence of SERT on the platelet surface and its role in acquiring 5-HT from the blood provides a plausible biological mechanism for SERT involvement in hyperserotonemia [10–12]. Genetic association related to SLC6A4 gene expression , as well as an interaction of SLC6A4 with the gene encoding integrin β3 (ITGB3), which physically interacts with SERT, supports this idea [14–16].
Following observations of significant genetic linkage at 17q11.2 (harboring SLC6A4) in multiplex ASD families [17–19], we screened exons of SLC6A4 specifically in families contributing to the observed linkage and found multiple, novel coding variants (Ile425Leu, Phe465Leu, and Leu550Val) and an elevated frequency of a previously documented coding variant (Gly56Ala) to a degree that profoundly deviated from expectations under Hardy-Weinberg equilibrium . Further support for a role of these variants in ASD comes from studies reporting an Ile425Val variant that segregated in pedigrees harboring multiple psychiatric phenotypes, with Asperger syndrome (an ASD), OCD, and other anxiety disorders being the most prominent [20–22]. Functional characterization of these SERT variants revealed that each elevated 5-HT transport function, as well as altered protein kinase G (PKG) and p38 mitogen activated protein kinase (MAPK) regulation [23, 24]. Our characterization of one of these variants (Gly56Ala) in knock-in transgenic mice revealed elevated 5-HT clearance and p38 MAPK-dependent transporter hyperphosphorylation in vivo accompanied by deficits in the three classical behavioral domains associated with ASD . Collectively, these results suggest that altered 5-HT signaling, and SERT activity and/or regulation represents an important biological endpoint for the functional impact of genetic variation at other genes contributing to SERT regulation and ASD risk.
Modulation of synaptic 5-HT is a dynamic and tightly controlled process, subject to influence through multiple signaling pathways and interacting proteins that act on SERT (reviewed in ). Enhanced SERT activity can be achieved via PKG and p38 MAPK signaling pathways acting through trafficking-dependent and trafficking-independent (that is, functional modulation) mechanisms. A trigger for both of these uptake-enhancing pathways, and the focus of this paper, is activation of the A3 adenosine receptor (A3AR; gene symbol: ADORA3), a G-protein-coupled receptor (GPCR) that is expressed by 5-HT synthesizing neurons at synaptic terminals [27, 28]. A3ARs physically interact and influence SERT  through a Gq-linked stimulation of guanyl cyclase (GC)-mediated cGMP synthesis. cGMP activation of PKG elevates SERT surface expression and, in parallel, a p38 MAPK-dependent elevation of surface resident SERT proteins [26, 28, 30]. Importantly, A3AR agonist stimulation of SERT is lost in A3AR knockout mice , providing evidence for the specificity of the current tools used to study receptor/transporter coupling.
Given a role of A3ARs in SERT regulation, we targeted ADORA3 as a candidate locus to determine whether rare or common variants at this locus are correlated with ASD risk and/or with altered A3AR-mediated SERT function or regulation. To test for common allele effects on ASD risk, single nucleotide polymorphisms (SNPs) that index common haplotypes at ADORA3 were assessed using family-based association methods. The alternative rare variant hypothesis was tested by Sanger sequencing of ADORA3 exons in a sample of ASD probands and ethnically matched controls and followed by a replication analysis using data from whole exome sequencing of independent ASD cases and controls. Nonsynonymous variants identified as being increased in cases from these studies were evaluated functionally through heterologous expression of wildtype and variant A3ARs to test for changes in basal and agonist-activated modulation of SERT activity.
Sample for allelic association analysis
The sample for analysis of common alleles in this study consisted of 958 combined simplex and multiplex ASD families (1,649 probands; 4,150 samples) recruited at Vanderbilt University, Tufts-New England Medical Center (including the Collaborative Linkage Study of Autism (CLSA)) , or obtained from the NIMH Genetics Repository (http://nimhgenetics.org). Samples from the NIMH Repository were submitted by one of three groups: the Autism Genetics Resource Exchange Consortium (AGRE), University of Iowa (CLSA) , or Stanford University . All ASD probands were assessed with the Autism Diagnostic Interview (ADI) or its revision (ADI-R)  and most with the Autism Diagnostic Observation Schedule (ADOS) . Affection status was assigned using a classification scheme employed by the Autism Genome Project  in which subjects were classified with either a ‘strict’ diagnosis if criteria for ‘autism’ were met on both the ADI-R and ADOS, or a more inclusive ‘spectrum’ (that is, ASD) diagnosis for subjects that met algorithm criteria for (1) ‘autism’ on the ADI-R alone; (2) ‘ASD’  on both the ADI-R and ADOS; or (3) ‘autism’ on the ADOS alone. Other ‘unaffected’ family members were designated as ‘unknown’ for purposes of genetic analyses described below. Demographic information for this sample is shown in Additional file 1: Table S1. All studies were approved by the Vanderbilt Institutional Review Board and with the informed consent of participating families.
Genotyping and analysis of common alleles at ADORA3
To test for association of common alleles at ADORA3 in ASD, we selected SNPs to represent all common haplotypes (that is, ≥5%) across the transcriptional unit and flanking sequence taking into account linkage disequilibrium patterns. We used Haploview (http://www.broadinstitute.org/haploview)  to analyze CEPH (CEU; Caucasian) SNP data from the HapMap database (http://www.hapmap.org), given that the vast majority of the sample was of European ancestry. The Haploview implementation of Tagger identified tag-SNPs to capture common alleles across ADORA3 at an r2 ≥0.8 and minor allele frequency (MAF) ≥5%. TaqMan™ allelic discrimination assays for four SNPs that span 14.4 kb were obtained from Applied Biosystems (ABI, Foster City, CA, USA) as Assays-on-Demand (AoD) or designed as Assays-by-Design.
PCR amplification was conducted in a 5-μL volume in accordance with manufacturer’s recommendations. In brief, cycling conditions included an initial denaturation at 95°C for 7 min, followed by 50 cycles of 92°C for 15 s and 60°C for 1 min. Post-PCR allelic discrimination was conducted using an ABI 7900HT genotypes ABI Sequence Detection System software. Genotypes were checked for completeness (≥98%) and conformity to expectations under Hardy Weinberg Equilibrium (HWE). Other quality control procedures included inter- and intra-plate replicates and checks for Mendelian inconsistencies using PEDCHECK . Families containing Mendelian inconsistencies were identified and excluded from additional analysis. Family-based allelic association testing was used to evaluate transmission of alleles in the autism families being studied. Single marker analysis was conducted using the family based association test (FBAT) . FBAT analysis was conducted under the additive model, and significance was determined using the empirical variance (−e) option, as this provides a more conservative estimate of association, given the presence of multiplex families in the dataset. Statistical power required to detect a meaningful association was determined by power calculations using the Genetic Power Calculator (http://pngu.mgh.harvard.edu/~purcell/gpc/) . We assumed ASD as a discrete trait with a prevalence of 1/100 and a sample size of 1,000 trios, further assuming MAFs of 5%, 10%, and 30%, respectively, and a D´=0.8. Based on these calculations, we would have ≥80% power to detect odds ratios (ORs) of ≥1.59, ≥1.44, and ≥1.36 for (risk) allele frequencies of ≥5%, 10%, and 30%, respectively.
Determination of ancestry from genotype data
To permit association analysis within the major European subset of the family-based sample and for subsequent matching of cases and controls (see below), ancestry was determined using STRUCTURE  and multidimensional scaling (MDS) in PLINK  (http://pngu.mgh.harvard.edu/~purcell/plink) to analyze genome-wide parental (founder) genotype data [35, 43] from autism families. Genome-wide (GW) genotypes were derived from different platforms and in substantially different numbers. Many multiplex families were genotyped by the Autism Genome Project (AGP) in its Phase I linkage study using the Affymetrix 10 k SNP platform , and 10 k data were analyzed at that time using STRUCTURE. Other families had genotypes from Illumina 550 k  and/or 1 M SNP  arrays, and these were analyzed recently using MDS. Fortuitously, numerous families had both sets of genotypes and analyzed using both applications, and identical ancestry classifications provided confirmation that both STRUCTURE and MDS yielded consistent and robust assignments that also agreed with self-report information. A small number of families from the overall association sample (1) did not have GW genotypes, in which case self-report information determined classification or (2) had neither GW genotype data nor self-report information, in which case they were classified as being of ‘unknown’ ancestry.
Discovery and analysis of rare variants at ADORA3
Initial screening for sequence variants at ADORA3 utilized whole blood derived DNA samples from 185 unrelated (predominantly Caucasian) cases (94% Caucasian; 5% African-American; 1% Hispanic). Non-clinical comparison samples were drawn from reference collections and consisted of lymphoblastoid cell lines DNA from 305 subjects: (1) 96 samples from the ‘Caucasian’ subset of the Coriell Human Genome Diversity Panel (http://ccr.coriell.org/sections/Search/Panel_Detail.aspx?Ref=HD100CAU&PgId=202); (2) 192 samples from the Human Random Control (HRC) collection corresponding to subjects of European ancestry recruited in the UK and obtained from Sigma-Aldrich (St. Louis, MO, USA; http://www.sigmaaldrich.com/life-science/molecular-biology/pcr/human-genomic-dna.html); and (3) 24 subjects from the neurologically-normal NINDS/Coriell African-American panel (http://ccr.coriell.org/Sections/Search/Panel_Detail.aspx?Ref=NDPT111&PgId=202). Thus, the comparison samples were 92% Caucasian and 8% African-American. This discovery sample of cases and controls provides 80% power to detect rare risk variants of 0.1%, 0.5%, 1% allele frequencies with ORs of 16.2, 5.25, and 3.71, respectively. Our a priori expectation is that functional ADORA3-containing, SERT-altering functional variants would confer large genetic effects, and thus we are reasonably powered under this assumption. However, we would be significantly underpowered if hypothetical rare variants conferred ORs <2.
PCR amplifying primers (Additional file 2: Table S2) were designed using Primer3 (http://frodo.wi.mit.edu/primer3/), and all potential amplicons were subjected to a BLAST-Like Alignment Tool search to ensure no significant matches existed elsewhere in the genome. Amplicons were optimized using a gradient of annealing temperatures, followed by agarose gel electrophoresis to determine ideal annealing temperature. PCR was then performed on the case (185) and control (305) screening samples. PCR reactions contained 7.1 nM of amplifying primers, 10 μL of 2× Mastermix, and 12 ng of DNA in a final volume of 20 μL. ADORA3 primers were designed for exons 1 to 2 and >500 bp of promoter sequence. PCR amplification conditions were 7 min at 95°C, 40 cycles of 15 s at 95°C, 12 s at the annealing temperature, and 60 s at 72°C, with a final extension at 72°C for 7 min. Following PCR, each product was examined by gel-electrophoresis, and once verified for expected size and specificity, excess primers and nucleotides were removed using Millipore 96 well filter plates. Samples were quantitated, subjected to Sanger sequencing, and data analyzed for variants using Sequencher v4.9 (Gene Codes Corporation, Ann Arbor, MI, USA). Specific variants were confirmed by independent PCR and sequencing, and for ASD cases with simultaneous determination of segregation by inclusion of other available family members, affected or unaffected.
Variants were assessed using multiple approaches. We noted whether or not they were previously documented in dbSNP or the 1000 Genomes project. In silico algorithms PolyPhen2 , SIFT , and SNAP  were used to provide a bioinformatic estimate of whether amino acid substitutions were likely to be ‘damaging’ or ‘not tolerated’ or benign. Cross-species conservation of the amino acid residue and surrounding sequence was also evaluated, along with available literature regarding structural features of the A3AR protein. Finally, to ask whether there might be evidence to support a global burden of rare (<1%) coding variants, the cohort allelic sums test (CAST) was used. CAST is a grouping method in which the number of individuals with one or more variants in a gene is compared between affected and unaffected individuals [48, 49]. Thus, we compared differences in rare allele counts in matched cases and controls in a 2 × 2 contingency table, and a Fisher’s Exact test was performed.
An independent replication sample for comparison to variation identified in the discovery phase corresponded to ASD cases and controls from the NIMH Repository. Cases and controls were pair-matched for ancestry, and samples used for whole exome sequence analysis as recently described . SLC6A4 coding variants (described above) that affect SERT function and regulation are associated with not only ASD but also OCD, anxiety and mood disorders [17, 20, 21]. Therefore, case-control pairs were excluded if control subjects had any history of OCD or anxiety disorders. Sequence data at ADORA3 for a total of 339 case-control pairs were examined for ‘functional’ (that is, missense, nonsense, consensus splice site, and read-through) variants. Details regarding quality control procedures and read depth for case and control samples are detailed in the Supplemental Material of Neale et al. .
A full-length cDNA encoding human SERT in the mammalian expression vector pcDNA3.1 (Invitrogen, Carlsbad, CA, USA) and a full-length cDNA encoding the human A3AR (myc-A3AR/pCMV) have been described previously . In vitro mutagenesis of the A3AR cDNA clone to introduce Val90 and Ile171 variants were performed using the QuikChange mutagenesis kit (Stratagene, La Jolla, CA, USA). Variant constructs were later confirmed by direct sequencing of the entire open reading frame.
Cell culture and transfection
Chinese Hamster Ovary (CHO) cells were maintained at 37°C in Dulbecco’s modified Eagle’s medium containing 10% fetal bovine serum, 1% L-glutamine, 100 IU/mL penicillin, and 100 μg/mL streptomycin. Transfections were performed using the TransIT-CHO Transfection reagent (Mirus, Madison, WI, USA). Quantities of 50 ng/well SERT and 20 ng/well of A3AR cDNAs were preincubated with Mirus reagent for 30 min at room temperature prior to adding to plated cells, seeded at 20,000 cells/well. Transfected cells were cultured for an additional 24-48 h after transfection and prior to assay of [3H]5-HT transport activities.
cGMP activity assays
The concentration of the second messenger cyclic guanosine monophosphate (cGMP) was measured using the CatchPoint cGMP fluorescent assay kit (Molecular Devices, Sunnyvale, CA, USA). In brief, CHO cells co-transfected with wildtype A3AR or A3AR coding variants and SERT cDNAs were plated at 50,000 cells/well. Cells were initially washed in a Krebs-Ringer bicarbonate (KRGB) prestimulation buffer containing 0.8 mM 3-isobutyl-1-methylxanthine (IBMX), an inhibitor of cGMP-phosphodiesterases. Following a 10 min incubation period, cGMP accumulation was measured in response to a 1 μM IB-MECA or vehicle treatment at various time points (0 min, 10 min, 20 min, 30 min, 40 min, 60 min) according to the manufacture’s protocol. The 1 μM IB-MECA concentration was selected on the basis of previous studies [28, 30] that found optimal stimulation of A3ARs under those conditions. All values were normalized to 100% representing basal (that is, time = 0 min) wildtype (WT) cGMP levels. Statistical analyses comparing the effects of IB-MECA treatment on variant and wildtype A3ARs were performed with Prism (GraphPad, La Jolla, CA, USA) using two-way analysis of variance (ANOVA). We used a t-test to compare overall differences of IB-MECA treatment on variant and wildtype A3ARs for cGMP synthesis (and 5-HT below) over the full time course, area under the curve (AUC) was calculated with Prism using total cGMP production (or 5-HT uptake) for each 60 min time course experiment. Means and standard errors of the mean were calculated using each experiment. P values <0.05 were considered significant.
5-HT transport assays
Assays measuring transport of [3H]5-HT were conducted as described previously [28, 30]. Briefly, medium from CHO cells were removed and cells washed with Krebs-Ringer-Hepes (KRH) buffer containing 130 nM NaCl, 1.3 nM KCL, 2.2 mM CaCl2, 1.2 mM MgSO4, 1.2 mM KH2P04, 1.8 g/L glucose, 10 mM HEPES, pH 7.4, 100 mM pargyline, and 100 mM ascorbic acid. Cells were incubated in triplicate at 37°C in KRH buffer containing 100 μM pargyline and 100 μM ascorbic acid, with and without the adenosine A3 selective agonist and adenosine analog IB-MECA. Following incubation with IB-MECA, a 10 min incubation with [3H]5-HT (20 nM) at 37°C was performed, followed by aspiration of buffer and three washes with ice-cold KRH buffer. Cells were then solubilzed with 0.5 mL Microscint-20, and [3H]5-HT accumulation was quantified using a TopCount plate scintillation counter (PerkinElmer Life and Analytical Sciences, Waltham, MA, USA). Specific 5-HT uptake was determined by subtracting the amount of [3H]5-HT accumulated in the presence of 10 μM paroxetine, a selective SERT inhibitor. A minimum of three independent replicates were performed for each experiment. Analyses comparing basal (time = 0 min) and IB-MECA-modified uptake for wildtype vs. variant A3AR/SERT co-transfections at individual time points and for the full time course was calculated and plotted using Prism as described above.
Molecular modeling to predict location of A3AR coding variants
The A3AR residue positions of Leu90 and Val171 were determined for the human adenosine A2a receptor (A2aAR) by amino acid sequence alignment and were found to correspond to Val84 and Val171, respectively. The relative positions and structural conformation of the corresponding A2aAR residues were determined using structural data obtained using an adenosine-bound, thermostabilized A2aAR (PDB ID:Y2DO) as a model. Images were prepared using PyMOL (DeLano Scientific Ltd).
Family-based association analysis
To test whether common alleles at ADORA3 contribute to ASD risk, we genotyped a sample consisting of 958 autism families using four SNPs representing common haplotypes that span the ADORA3 locus. Primary FBAT analyses of genotype data were designed to test allelic transmissions along two axes of stratification: strict vs. spectrum diagnostic classifications and European vs. all ancestries, yielding four primary analyses. Analysis for each of the resulting four strata (strict-European and strict-all ancestries; spectrum-European and spectrum-all ancestries) showed no evidence to support common variant association at ADORA3 using data for the four SNPs tested (Additional file 3: Table S3). Analysis of haplotypes (>5%) across the locus that were captured by these SNPs also showed no significant association, consistent with single marker analysis (data not shown).
Sequence-based discovery of functional variation at ADORA3
To identify potentially functional, risk variants in ADORA3, we screened all exons and the promoter region in 185 unrelated ASD cases and 305 non-clinical comparison samples by direct Sanger sequencing. Comparison samples were selected to ethnically match case samples for Caucasian and African-American subjects, which represented the vast majority of the case screening panel (see Methods). Multiple synonymous and non-synonymous variants were identified and are documented in Table 1. Three novel variants, two non-synonymous (ns) and one synonymous, were detected in cases (Leu90Val, Val171Ile, Cys194) but were not previously documented in dbSNP or 1000 Genomes (1 kG) . A novel Ala195Thr substitution was identified in a single control sample. Experimental validation of variants by sequencing independent PCR products included parents and other siblings (when applicable). No de novo variants were detected, and thus all were inherited in ASD families. Bioinformatic algorithms PolyPhen2 , SIFT , and SNAP  that predict the likelihood of functional effect of coding variants on protein function were applied to rare (<1%) ns-variants identified. Val171Ile (detected only in cases) was predicted to be ‘damaging’ or ‘not tolerated’, however, Leu90Val along with Ala195Thr were predicted to be benign substitutions. We note that subsequent to our discovery of novel Leu90Val and Ile171Val variants, but during subsequent functional and follow-up genetic experiments, both variants emerged from 1 kG sequence data and were thus deposited into dbSNP, as reflected in Table 1.
We sought to determine whether there was evidence for an increase of rare ADORA3 coding variants in cases compared with controls. Both Leu90Val and Val171Ile were detected only in ASD cases and not controls (3/370 case chromosomes for each variant vs. 0/562 control chromosomes). A case-control comparison of these individual rare alleles does not reach significance given the small number of observations (Fisher’s Exact P=0.064 for Leu90Val and Val171Ile each). Given the inherent limitation in power to compare rates of single rare alleles, a gene-wide discovery model suggests that a better approach is to model all ‘functional’ (that is, non-synonymous, consensus splice site, and read-through) rare variants simultaneously for case-control comparisons. Therefore, we employed the Cohort Allelic Sums Test (CAST) to test for an overall increased burden of rare (<1%) nsSNPs in ADORA3 in ASD. We reasoned that any risk effect of higher frequency, common coding variants would be indexed by SNP and haplotype-based association studies described above. Allele counts obtained from sequence discovery in 185 cases and 305 controls were tabulated for Leu90Val, Val171Ile, and Ala195Thr, and a Fisher’s Exact test was conducted (Table 2). This analysis showed a significant burden effect (6/185 ASD individuals vs. 1/310 controls; P=0.013; OR=10.19, CI = 1.20-81.56). We note that, as described in Methods, we have low power to detect rare variants of only modest risk effect. Nevertheless, we observed a nominal increase in rare ‘functional’ variants in the discovery case sample vs. controls, and this prompted us to: (1) conduct functional studies of the novel variants found in ASD cases for effects on SERT; and (2) subsequently compare the putative increase of rare, ‘functional’ variants in ASD cases to data from exome sequence that became available from the NIH ARRA Autism Sequencing Consortium [50, 52]. Consistent with published data on accepted risk CNVs (for example, 16p11.2, 1q21.1, 22q11.2, 22q13.3, and so on) [53–55], novel variants Leu90Val and Val171Ile did not always segregate to only (or all) affected individuals in a family, consistent with incomplete penetrance of these variants (Figure 1).
The availability of crystal structure for a human ligand-bound adenosine A2a receptor (A2aAR)  provides an important source of structure-function information that can inform predictions of a potential functional impact of the Leu90Val and Ile171Leu variants. Figure 2 depicts the structure of the A2aAR, modeling the positions of residues equivalent to Leu90 and Val171 in A3AR, in relation to bound adenosine. Our model predicts that the A3AR residues Leu90 and Val171 flank the adenosine-binding site, supporting a hypothesis that one or both of these variants may affect A3AR function. Leu90 and Val171 show consistent cross-species conservation in mammals, while Ala195 is less conserved (Figure 3). Functional studies therefore focused solely on the two variants identified in cases.
Functional analysis of Leu90Val- and Val171Ile-A3AR effects on cGMP production and SERT activity
To test for potential functional effects caused by the Leu90Val and Val171Ile substitutions, we engineered human A3AR cDNA expression constructs to harbor either Leu90Val or Val171Ile variants for experimentation in a heterologous transfection system using CHO cells. In prior studies, we have found that CHO cells support both the investigation of A3AR regulation of SERT as well as studies of A3AR/SERT physical association [29, 30]. Western blot analysis of cell lysates using an anti-myc probe confirmed equivalent expression of myc-tagged wildtype and both variant A3AR constructs, Leu90Val  and Val171Ile (data not shown). We first asked whether either variant (G-protein coupled) receptors produced increased (or otherwise altered) levels of cGMP that might result in a downstream increase of SERT activity. The human A3AR and SERT constructs were co-transfected into CHO cells, and we assessed basal cGMP levels for both variants, and then following activation of receptors with the A3AR selective agonist IB-MECA. Figure 4A (at 0 min) demonstrates that CHO cells co-transfected with the Leu90Val variant display significantly elevated basal cGMP compared to wildtype A3AR co-transfected cells (L90V: 207.85% ± 45.71 vs. WT: 100.0% ± 0.02; P=0.015, n=3). Stimulation of the Leu90Val A3AR by IB-MECA (1 μM) revealed that the elevated cGMP production seen in the basal state persisted over the full time course and paralleled wildtype A3AR with both returning to their respective basal states after 40 min (Figure 4A and Additional file 4: Figure S1A; L90V: 163.3% ± 29.15 vs. WT: 100.0% ± 6.32; 1-tailed t-test P=0.049, n=3).
In contrast with Leu90Val, cells co-transfected with Val171Ile-A3AR/SERT displayed basal cGMP levels similar to those observed in wildtype A3AR co-transfected cells (V171I: 116.1% ± 16.3 vs. WT: 100.0% ± 9.2, n=3). Additionally, IB-MECA treatment in Val171Ile co-transfections failed to show any stimulation of cGMP production that was seen with wildtype A3AR. This inability of the Val171Ile receptor to be stimulated by IB-MECA appeared as a slightly diminished cGMP synthesis over the time course compared with wildtype, although this difference was not statistically significant (Additional file 4: Figure S1A; V171I: 90.14% ± 12.22 vs. WT: 100.0% ± 16.18; 1-tailed t-test P=0.303, n=3).
The IB-MECA induced stimulation of cGMP production in wildtype A3AR/SERT co-transfections displayed in Figure 4A paralleled the expected stimulation of SERT-mediated 5-HT uptake activity by wildtype A3AR (Figure 4B and ). Although the elevation in peak 5-HT uptake (that is, at 10 min) in Leu90Val A3AR/SERT co-transfections was not significantly greater than that for wildtype A3AR (Figure 4B; L90V: 148.5% ± 7.1 vs. WT: 140.3% ± 4.5; n=4), the IB-MECA-stimulated increase in 5-HT uptake activity mediated by the variant receptor persisted above that seen in cells transfected with the wildtype receptor throughout the time of our observations. Indeed, the significantly increased 5-HT uptake, seen at 40 min for Leu90Val A3AR transfected cells, the time by which wildtype A3AR-stimulated SERT activity had already returned to baseline levels (L90V: 131.3% ± 7.1 vs. WT: 108.3% ± 3.7; two-way ANOVA P=0.001, n=4) did not return to wildtype levels until the next time point measure, 20 min later (Figure 4B). These observations reflect an overall greater 5-HT uptake in Leu90Val-A3AR cells compared to wildtype A3AR (Additional file 4: Figure S1B; L90V: 112.2% ± 8.80 vs. WT: 100.0% ± 3.22; 1-tailed t-test P=0.020, n=4).
In striking contrast to the enhanced SERT activity observed with Val90 co-transfected cells, IB-MECA treatment of Ile171, compared with wildtype co-transfected cells failed to stimulate SERT activity (Figure 4C) across all agonist doses tested (for example, 1 μM IB-MECA Val171Ile: 101.8% ± 12.5 vs. WT: 136.3% ± 7.2; two-way ANOVA P=0.005; n=3-4).
Replication test of an increased rate of rare functional variants in cases vs. controls
With support from both initial Sanger discovery experiments and subsequent functional studies that potentially ASD-related, functional variation had been identified in ADORA3, we sought replication of the putative increase of such variants in ASD cases vs. controls. We examined whole exome sequence data from 339 cases and pair-matched controls of European ancestry generated by the NIH ARRA Autism Sequencing Consortium  for the presence of functional variants at ADORA3 (see methods for exclusion criteria). Nine non-synonymous and numerous synonymous variants were discovered in these pair-matched samples that were completely independent from the discovery sample. In total, nine of 12 subjects harboring non-synonymous variants were detected in cases, and the remaining three in controls (9/339 ASD individuals vs. 3/339 controls); although that relative increase was not statistically significant (Fisher’s Exact 1-tailed P=0.071; OR = 3.06, CI: 0.82-10.99; Table 3). Specifically, Leu90Val was found in one additional case and no controls, while Val171Ile was found in two additional cases but also one control. Of the remainder, four additional missense variants (Ile22Thr, Phe48Ser, Ala69Ser, and Leu294Thr) were found in one case each and no controls, and a single read-through mutation (*319Gln) predicted to add an additional 38 residues (>10% of the native protein) was found in two cases and zero controls. Two additional missense variants were detected in controls (Phe180Leu and Ala273Thr). Each of these variants passed stringent quality control thresholds and have read-depths that, based on empirical data, have an extremely high positive predictive value for being valid calls , although they have not been experimentally validated. Prediction of functional consequences using PolyPhen2  indicated that two missense variants were forecast to be benign (Ala69Ser and Leu294Thr) and four missense to be damaging (Ile22Thr, Phe48Ser, Phe180Leu, and Ala273Thr). Combining both discovery and replication findings strengthens evidence for an increase of ‘functional’ variants in ASD, with counts of 15 of 524 cases compared with four of 644 controls harboring such variants (Fisher’s Exact 1-tailed, Bonferroni-corrected P=0.0025; OR = 4.72, CI: 1.56-14.30). Moreover, taking into account replication data, the enrichment of Leu90Val in ASD cases vs. controls becomes statistically significant (Fisher’s Exact 1-tailed P=0.040; 4/1,048 ASD vs. 0/1,288 control chromosomes). Although present in greater numbers in ASD cases, enrichment for Leu171Ile by itself did not reach significance (Fisher’s Exact 1-tailed P=0.068; 5/1,048 ASD vs. 1/1,288 controls).
Exploring phenotypic and genomic characteristics of ADORA3variant carriers
We explored the possibility that dimensions of the ASD phenotype might stand out in affected carriers of Val90 and Ile171 or other ADORA3 variants. We examined domain and item-level data from the ADI-R to explore the possibility that certain ASD features might be more pronounced in ADORA3 rare variant-carriers. Such comparisons are inherently limited by a small number of carriers relative to hypothetical phenotypic effect sizes and different mechanistic effects on A3AR for a given variant. Our examination of available data showed no consistent pattern of elevated or diminished ADI-R domain scores in carriers vs. non-carriers (Additional file 5: Table S4). We found a similar lack of correlation upon examination of ADI-derived principal components analysis-derived scores ), as a complementary set of dimensional ASD traits (data not shown).
To determine whether rare ADORA3 variant carriers also harbored other known or likely risk factors, we examined data from published work describing CNVs in respective samples [58, 59]. Some inherited CNVs were identified in the six cases for which CNV data were available; for the remaining nine samples, CNV data were not available and several of these have not been subjected to array based genotyping or analysis. Most CNVs corresponded to regions also detected in controls, however, a single de novo duplication of approximately 211 kb (hg18: ChrX:153263157–153474401) was found in the male proband (NIMH ID: 217-14216-3470) harboring a Ala69Ser substitution in ADORA3.
Based upon our knowledge that SERT and 5-HT have a longstanding connection to ASD, that A3AR plays a key role in SERT regulation via PKG and p38 MAPK signaling pathways, and that SERT is an essential regulator of 5-HT signaling, we screened ADORA3 for SERT-altering and ASD-associated alleles. Our experiments were premised on a specific hypothesis: functional risk variants at ADORA3 would lead to a signaling-mediated elevation of SERT-dependent 5-HT uptake activity, phenocopying in vitro the elevated function seen with rare, ASD-associated SERT coding variants [17, 20, 23]. Regarding association of ASD with SERT variants, we note that sequencing of SLC6A4 by another group testing unrelated ASD probands from singleton or multiplex families (and controls) but without obligate allele sharing (linkage) at 17q11.2 did not show a similar pattern of enriched coding variants, and thus association with ASD risk . We believe therefore that screening of multiplex probands with allele sharing in this region was an important factor in our initial discovery of novel, functional variants, given the extreme genetic heterogeneity underlying ASD. Moreover, results from genotyping of ASD and related cohorts by Delorme and colleagues [20, 21] further support ASD association initially suggested by Ozaki et al. [20, 21] and reinforced by our own studies.
Consistent with results from large-scale GWA scans for common allele susceptibility effects [35, 43], we found no evidence to support a main effect on ASD association attributable to common variants at ADORA3. The current study is limited in power to detect alleles of small effect size (for example, OR <1.3), so we cannot exclude the possibility that common ADORA3 variants confer very small effect sizes or interact with alleles at other genes to confer risk.
Mechanistically, we anticipated that a more likely scenario was for ADORA3 to harbor coding variants, likely rare, that might impact A3 function directly and SERT function indirectly. Numerous, recent studies focused on CNV or sequencing [44, 50, 58, 61–64] have documented that rare variation affecting a large number of genes is collectively a major source of genetic liability in autism. Our results are consistent with ADORA3 being one such gene that contributes to ASD liability in rare cases. Here, we present the identification of novel coding variants in ADORA3 in a Sanger sequencing-based screen of cases and non-clinical comparison samples ethnically matched to the case sample. This screen showed a statistically significant increase in coding variants in cases vs. controls (P=0.013). Subsequent availability and analysis of exome sequence data from cases and clinically-screened controls  showed a greater number of ‘functional’ variants at ADORA3 in cases compared with controls (15/524 vs. 4/644), but a difference that was not significant (P=0.07). Nevertheless, combining Sanger discovery and newly available exome sequence data strengthens evidence for association, even after Bonferroni correction for multiple comparisons (Fisher’s exact 1-tailed P=0.0025; OR = 4.72, CI: 1.56-14.30).
Encouraged by the initial discovery of Leu90Val and Val171Ile, functional studies focused on these two rare non-synonymous variants identified from the ASD discovery sample. To test our central SERT regulatory network hypothesis, analysis of Leu90Val and Val171Ile examined the effect of receptor stimulation to induce cGMP synthesis via G-protein coupling and on downstream SERT-dependent 5-HT uptake. IB-MECA stimulation of the Val90-encoded A3AR showed enhanced cGMP synthesis compared with wildtype A3AR under basal conditions, and enhanced cGMP levels extended over the full time course ending with a return to the elevated baseline. These results mirrored our findings that the IB-MECA induced increase in SERT-dependent 5-HT uptake activity across the experimental time course including a delayed return to baseline in co-transfections with the Leu90Val mutant A3 receptor compared with wildtype A3AR. Thus, overall 5-HT uptake is significantly increased in cells expressing the mutant A3 receptor. Increases in both cGMP and 5-HT uptake activity parallels our recent report of enhanced Leu90Val-A3AR/SERT complex formation , which implies (1) enhanced basal receptor-G protein coupling, (2) reduced receptor desensitization, and/or possible differences in the binding kinetics of IB-MECA to Val90-A3AR as a consequence of its location proximal to the A3AR ligand binding site upon agonist stimulation. Taken together, our results are consistent with our prior expectation, based on increased 5-HT uptake caused by rare autism-associated coding mutations in SERT [17, 20, 23]. In particular, the Gly56Ala SERT variant, exhibited increased catalytic activity as would be achieved through stimulation by PKG and p38 MAPK signaling, which represent the primary pathways for A3AR-mediated upregulation of SERT.
In contrast to Leu90Val, the Val171Ile variant rendered A3AR insensitive to the selective IB-MECA agonist to induce increased cGMP synthesis and a downstream increase in SERT-dependent 5-HT uptake activity. The molecular mechanism underlying this effect is not yet clear, however, we postulate that the proximity of the Val171 residue to the ligand binding pocket may prevent or hinder the ability of the adenosine analog IB-MECA to bind A3AR, resulting in a more rapid dissociation and/or less efficient (or absence of) receptor-G protein coupling. Additional experiments will be required to fully elucidate the molecular mechanisms of these two coding variants on receptor function. Although the functional impact on SERT of the Leu90Val and Val171Ile variants are in opposite directions, it is possible that both elevated and diminished capacity for regulation of SERT through A3AR pathways can impact 5-HT clearance in a manner that disrupts 5-HT’s ability to coordinate brain development [65, 66] and/or adult 5-HT signaling [67, 68].
We initially conceptualized dysregulation of a SERT regulatory network based not only on the molecular impact ASD-associated SERT mutations, rather within a broader context that implicates disruptions in 5-HT signaling in autism. Hyperserotonemia in 35% of ASD cases and efficacy of selective 5-HT re-uptake inhibitors (for example, fluoxetine, citalopram) and atypical antipsychotics (for example, risperidone) in ameliorating irritability and other anxiety-related problems in ASD are just two of many themes that implicate 5-HT dysregulation in ASD. We previously demonstrated a proof-of-principal for genetic variation in SERT-binding and regulatory proteins being associated with ASD. Here we refer to the common Leu33Pro variant in ITGB3, which has been statistically associated with both elevated 5-HT levels in blood  and ASD risk , and which causes allele-dependent effects on SERT activity and regulation . We recently observed hyperserotonemia in a knock-in mouse model of the Gly56Ala SERT variant, along with p38 MAPK-dependent hyperphosphorylation of SERT, increased SERT-dependent 5-HT clearance and 5-HT receptor hypersensitivity in vivo, as well as social behavior impairments, repetitive behaviors, and deficits in communication . Nonetheless, we recognize that statistical association of rare ADORA3 variants (especially Leu90Val) requires further validation in larger samples. This is the case for rare variants in any specific locus implicated in ASD, and has led many investigators to emphasize the network as a better substrate to elucidate the underlying mechanisms. We recognize that the magnitude of ASD risk conferred by these variants is unknown. Indeed, the single male case harboring an Ala69Ser variant (of unknown functional effect) at ADORA3 also possessed a de novo duplication of an X-linked interval including RPL10, a gene for which inherited and de novo point mutations and gene-disrupting and/or CNV deletion has been associated with ASD and ID . Duplication effects here are unknown, but this variant is likely to confer risk. Nevertheless, we believe these studies will add to the growing body of data implicating specific gene/protein networks in contributing to ASD liability. Taken together our studies support the case for 5-HT and more specifically SERT regulatory pathways as one gene/protein network in which perturbations contribute to the underlying pathophysiology of ASD. Further studies within this network may provide new leads to ASD therapeutics.
There are a few limitations or caveats of the studies we present. First, while the discovery sequence sample was ethnically matched, subjects were not matched based on genome-wide genotype data. It is possible therefore, that subtle population stratification effects could lead to inflation of the observed increase in numbers of rare, ‘functional’ variants in cases vs. controls. Given that the case and control samples from the AASC were pair-matched based on genotype data, and the greater number of functional variants in those cases (15/524 vs. 4/644) was not statistically significant in a Fisher’s Exact test, we recognize that both discovery (P=0.0143) and combined (P=0.0025) evidence for gene-based association of rare, ‘functional’ variants should be interpreted with caution. Second, while multiple comparisons were conducted in functional experiments, we are reassured that the increases in cGMP production and 5-HT uptake parallel one another, supporting our conclusions regarding the ability of Leu90Val A3AR to augment SERT-dependent 5-HT uptake over time. Finally, we note that the functional experiments were conducted in CHO cells, and may not reflect the function during or after development in vivo. While this is certainly possible, our study of multiple variants in SERT and other proteins that influence SERT regulation (for example, ITGB3) present a consistent picture of results from in vitro transfection-based experiments ultimately relating very well to effects on SERT function in mouse models harboring these variants [70, 72, 73].
Our results validate the hypothesis that the SERT regulatory network harbors rare, functional variants that impact SERT activity and regulation in ASD, and encourages further investigation of this network as a site for additional functional variation that may impact ASD risk.
A3 subtype adenosine receptor
Analysis of variance
Autism spectrum disorder
Cohort allelic sums test
Cyclic guanosine monophosphate
Chinese hamster ovary
Copy number variation/variant
Family-based association test
G-protein coupled receptor
Mitogen-activated protein kinase
- A3AR, MDS:
Nitric oxide synthase
Polymerase chain reaction
Protein kinase C
Protein kinase G
SLC6A4: serotonin transporter.
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This work was supported by grants NS049261, MH061009 and MH084962 to JSS and MH094527, MH078028 and MH096972 to RDB, the NIH NCRR grant UL1 RR024975 for the Vanderbilt CTSA, and P30 HD15052 to the Vanderbilt Kennedy Center for Research on Human Development. This work would not have been possible without the DNA Resources Core, invaluable assistance by Melissa Potter for Data Coordination and statistical genetics support from Lan Jiang, both in the Computational Genomics Core at Vanderbilt. In particular, we recognize important technical contributions to this work by Emily L. Crawford and Anna G. McGrew.
The authors gratefully acknowledge investigators in the NIH ARRA Autism Sequencing Consortium: Eric Boerwinkle (University of Texas Health Science Center), Joseph D. Buxbaum (Mount Sinai School of Medicine), Edwin H. Cook, Jr. (University of Illinois at Chicago), Mark J. Daly (Communicating PI; Massachusetts General Hospital, Harvard Medical School and Broad Institute of Harvard and MIT), Bernie Devlin (University of Pittsburgh Medical School), Richard Gibbs (Baylor College of Medicine), Elaine T. Lim (Broad Institute of Harvard and MIT), Benjamin M. Neale (Massachusetts General Hospital, Harvard Medical School and Broad Institute of Harvard and MIT), Kathryn Roeder (Carnegie Mellon University), Aniko Sabo (Baylor College of Medicine), Gerard D. Schellenberg (University of Pennsylvania), Christine Stevens (Massachusetts General Hospital, Harvard Medical School, Broad Institute of Harvard and MIT) and James S. Sutcliffe (Vanderbilt University).
The authors declare that they have no competing interests.
NGC, RDB, and JSS designed the study. NGC performed genetic studies including sequencing, genotyping, and exome replication analysis. NGC, CBZ, KML, and WAH performed in vitro functional assays. BLY and EKG preformed ancestry determination. CGT compared the A3AR with A2aAR and generated Figure 2. ARRA Sequencing Consortium performed exome sequencing and variant calls. NGC, RDB, and JSS prepared the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Table S1: Characteristics of genotyped families with autism stratified by ancestry. A total of 958 families were genotype for common variants (MAF >5%). Ancestral background was determined using classical multidimensional scaling (MDS) using PLINK. (DOC 222 KB)
Additional file 3: Table S3: Association analysis of common variants in the ADORA3 gene loci. Analysis was conducted using the family-based association test (FBAT) suite and genotype data generated from TaqMan allelic discrimination assays in a sample of 940 autism families. SNP ID, alleles, minor allele frequency (MAF), informative families, observed and expected transmission counts, and corresponding P values (empirical variance ‘-e’ option) are provided. Significant P values indicated evidence for distortion of allele transmission. (DOC 32 KB)
Additional file 4: Figure S1: Activation of Leu90Val-A3AR expressing cells leads to prolonged cGMP production and 5-HT uptake. (A) CHO cells co-transfected with either WT-A3AR or Leu90Val-A3AR or Val171Ile-A3AR and SERT and were stimulated using IB-MECA (1 μM). Leu90Val-A3AR/SERT cells display elevated area under the curves (AUC) for cGMP production compared to wildtype-A3AR/SERT. (B) IB-MECA induced Leu90Val-A3AR activation enhances total SERT dependent 5-HT uptake compared to wildtype. Significant (P <0.05) findings are indicated by an asterisk (*). (EPS 99 KB)
Additional file 5: Table S4: Autism phenotypic profile of rare variants in the ADORA3 gene. Ancestry (AA: African American, EUR: European); IQ (Composite score on the Wechsler Preschool and Primary Scale of Intelligence (WPPSI) test); The Western Psychological Services (WPS) domain scores of the Autism Diagnostic Interview-Revised are provided. *: AGP ID, no NIMH ID available. (DOC 245 KB)
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Campbell, N.G., Zhu, CB., Lindler, K.M. et al. Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome. Molecular Autism 4, 28 (2013). https://doi.org/10.1186/2040-2392-4-28
- Autism spectrum disorder
- Serotonin transporter
- Adenosine receptor
- DNA sequencing
- Rare variant
- Single nucleotide polymorphisms (SNPs)
- Allelic association