Chromosome 15 (C15) imprinting disorders including Prader–Willi (PWS), Angelman (AS) and chromosome 15 duplication (Dup15q) syndromes are severe neurodevelopmental disorders caused by abnormal expression of genes from the 15q11–q13 region, associated with abnormal DNA methylation and/or copy number changes. This study compared changes in mRNA levels of UBE3A and SNORD116 located within the 15q11–q13 region between these disorders and their subtypes and related these to the clinical phenotypes. The study cohort included 58 participants affected with a C15 imprinting disorder (PWS = 27, AS = 21, Dup15q = 10) and 20 typically developing controls. Semi-quantitative analysis of mRNA from peripheral blood mononuclear cells (PBMCs) was performed using reverse transcription droplet digital polymerase chain reaction (PCR) for UBE3A and SNORD116 normalised to a panel of internal control genes determined using the geNorm approach. Participants completed an intellectual/developmental functioning assessment and the Autism Diagnostic Observation Schedule-2nd Edition. The Dup15q group was the only condition with significantly increased UBE3A mRNA levels when compared to the control group (p < 0.001). Both the AS and Dup15q groups also had significantly elevated SNORD116 mRNA levels compared to controls (AS: p < 0.0001; Dup15q: p = 0.002). Both UBE3A and SNORD116 mRNA levels were positively correlated with all developmental functioning scores in the deletion AS group (p < 0.001), and autism features (p < 0.001) in the non-deletion PWS group. The findings suggest presence of novel interactions between expression of UBE3A and SNORD116 in PBMCs and brain specific processes underlying motor and language impairments and autism features in these disorders.
Angelman syndrome (AS), Prader–Willi syndrome (PWS) and chromosome 15 duplication syndrome (Dup15q) are neurodevelopmental disorders that are associated with varying degrees of intellectual disability (ID) and social communication deficits1,2, and arise from different deletions or duplications at the 15q11–q13 imprinted region3.
PWS was the first example of genomic imprinting identified in humans4. Cardinal features include a poor suck with failure to thrive, infantile hypotonia and hypogonadism. Food seeking and hyperphagia emerges at approximately 6 years of age, leading to morbidity if not externally controlled. Mild ID (mean full scale IQ [FSIQ] between 55 and 69) is typical, frequently accompanied by compulsions, tantrums and skin picking5. AS is characterised by microcephaly, gait ataxia, seizures, ID, and absence of speech6. Dup15q is associated with variable cognitive impairment and motor delays. An overlapping feature between AS and Dup15q is the presence of seizures3.
DNA methylation and/or copy number changes on chromosome 15 are thought to cause PWS and AS specific phenotypes3,7. Loss of paternal gene expression from the chromosome 15q11–q13 region is the primary cause of PWS7, while the absence of the maternal gene expression in the same region is the primary cause of AS3. For PWS the lack of expression of key genes result from: (i) two deletion subtypes (typical—type I and type II deletions; and atypical smaller or larger 15q deletions) in ~60% of cases; (ii) three maternal disomy subtypes in ~35% of cases; and (ii) two imprinting centre defects (ICD; epimutation and microdeletion) in ~5% of cases5,8. Similarly, deletions from the maternally contributed chromosome 15 are the most common cause of AS (~70% of cases). Paternal uniparental disomy (patUPD) occurs in approximately 8% of AS cases and ICD in approximately 7% of cases3. Approximately, 10% of AS cases result from a mutation in the ubiquitin-protein ligase E3A gene (UBE3A). Both PWS and AS have a frequency of approximately 1 in 15,000 births9.
Dup15q syndrome results from duplications or triplications of the PWS/AS imprinted 15q11–q13 region. Triplication typically arises through the presence of a supernumerary chromosome (isodicentric 15 [idic15]), while the duplication is caused by interstitial tandem duplication (int dup). Hereafter, we use Dup15q to encompass these subtypes, unless otherwise stated. In maternal Dup15q, autism features are more common and severe, as compared to AS and PWS, with severity directly proportional to the number of maternal copies present9. In contrast, paternal Dup15q has a less severe phenotype than maternal Dup15q10. Despite Dup15q being a cause of autism spectrum disorder (ASD), reported in 1–3% of ASD cases9, prevalence in the general population has not been well established, with one study reporting 1 in 14,000 in the general population11.
While some genotype–phenotype correlations have emerged in each of the syndromes, primarily around the different molecular classes, there is a need for peripheral tissue biomarkers in humans as the phenotypes are highly variable in each disorder, and their specific subtypes do not fully explain this variability12. For PWS, those with the typical 15q11–q13 deletions have been reported to have lower Verbal IQ (VIQ) scores than those with matUPD13. In addition, PWS individuals with the larger typical 15q11–q13 type I deletion involving chromosome 15 breakpoints BP1 and BP3 have been reported to have more behavioural problems, specifically self-injury and compulsions compared to those having the smaller typical 15q11–q13 type II deletion involving breakpoints BP2 and BP314. The larger type I deletion encompasses four extra genes (i.e., NIPA2, NIPA1, GCP5, and CYFIP1), which may account for the additional clinical findings.
For AS, mouse models have been used to implicate loss of UBE3A expression in the brain as the primary cause of specific deficits in AS15. However, few studies have been performed in human peripheral tissues16,17. UBE3A is a key gene in neurodevelopment and is thought to be imprinted only in neurons, where it is expressed from the maternal allele in humans and mice15. Interestingly in other cell types UBE3A has bi-allelic expression18 and is thought to be consistently expressed from both alleles in different peripheral tissues15. The silencing of UBE3A on the paternal allele in neurons is thought to be regulated by a paternally expressed antisense transcript of UBE3A. This antisense transcript is part of the 3′end of SNRPN–SNURF transcript that comprises multiple small nuclear RNAs (snoRNAs)19. SnoRNA C/D box cluster 116 (SNORD116) is one of the snoRNAs that serves as a precursor to the antisense UBE3A, and through this process may regulate UBE3A silencing on the paternal allele16. Importantly, in PWS SNORD116 has been reported to be completely silenced, in neurons as well as other cell types in peripheral tissues, and this may contribute to phenotype severity17.
This study, for the first time, examines UBE3A and SNORD116 mRNA levels (controlled for the allele copy number and subtype) in peripheral blood mononuclear cells (PBMCs) using a highly sensitive and quantitative droplet digital PCR (ddPCR) method developed for analysis of gene expression. Expression changes for these genes in PBMCs are investigated between the chromosome 15 imprinting disorders, the different subtypes and typically developing controls. For AS and PWS subtypes genotype–phenotype studies are also described, with the focus on relationships between the UBE3A and SNORD116 mRNA levels in PBMCs and brain specific phenotypes including formal assessments targeting behavioural features and intellectual functioning. It was hypothesised that expression of these genes in PBMCs reflects immune processes in the brain related to gene expression in microglial cells (of the same cellular lineage) that support neuronal processes in the brain related to intellectual/developmental functioning and autism features in these disorders20.
Subjects and methods
This study comprised 58 individuals with a chromosome 15 imprinting disorder aged between 1 and 45 years. Twenty-seven individuals with PWS, 21 individuals with AS and 10 individuals with Dup15q were included in the study. The molecular classes for each syndrome are presented in the supplementary material (Table S1). Samples from 20 de-identified controls, aged 8–52 years, from our earlier studies21,22 were included as reference data for gene expression comparisons.
Participants were recruited through Victorian Clinical Genetics Services; Hunter Genetics; the PWS Clinic at the Royal Children’s Hospital, Melbourne; Genetic Services of Western Australia; and various support organisations including the Foundation for Angelman Syndrome Therapeutics, the PWS Clinic at the Royal Children’s Hospital, Melbourne; the Prader–Willi Association of Australia. Inclusion criteria were that verbal participants be able to speak English and non-verbal participants to be exposed to English within the home. Exclusion criteria were having another genetic condition of known clinical significance, or having any significant medical condition (e.g., stroke and head trauma).
For all participants their diagnosis was confirmed using DNA methylation analysis, methylation-specific multiple ligation-dependent probe amplification and/or microarray testing for copy number changes within the 15q11–q13 region, as per standard diagnostic testing protocol23.
At the time of assessment, 5 ml of venous blood were collected in ethylenediaminetetraacetic acid tubes, followed by PBMC isolation using Ficoll gradient separation, as previously described24. RNA was extracted from 1 to 4 million viable PBMCs using RNeasy kit as per manufacturer’s instructions (Qiagen, Germany). RNA samples were diluted between approximately 10 and 20 µl/ng depending on the concentration, resulting in an average input of 100 ng per reverse-transcription reaction. Reverse transcription was performed using the High-Capacity cDNA Reverse Transcription Kit as per manufacturer’s instructions (Thermos-Fisher, Global).
Gene expression analysis utilising ddPCR
To establish the optimal reference genes for our samples, eight assays (EIF4A2, RPL13A, SDHA, TOP1, YWHAZ, APT5B and GAPDH) were used from the geNorm reference 12 gene kit, as per manufacturer’s instructions (PrimerDesign, Ltd., Camberley, United Kingdom). For each assay, 1.1 µl of the primer/probe mix was added to 1× ddPCR SuperMix for probes (no dUTPs) (Biorad, Global) and RNAse/DNAse free water, and then aliquoted into 96-well PCR plates. One to two microlitre of cDNA was then added to the reaction mix.
For target genes, SNORD116 used the forward (5′-CAGGAAAGATCAAAACGATGCA-3′) and reverse (5′-TCCAAAGGAGGCAGTTGGAT-3′) primers with a HEX labelled probe (5′- TGCAAGTGTGATTGGTCCAGATAGCTGC-3′). This target region was referred to as SNURF–SNRPN exons 57–58, in a previous study16. The UBE3A assay was a premade TaqMan Assay (ID: Hs00166580_m1) with specific primer sequences not made available by the manufacturer (Thermo Fisher Scientific, MN, USA). The assay targets an amplicon with Chr.15: 25337234–25439086 coordinates [on Build GRCh38] present in most UBE3A transcripts, utilising a FAM-labelled probe. Both UBE3A and SNORD116 assays utilised a Deep Hole Quencher and were duplexed. Briefly, each 20 μL reaction mixture contained 2.0 μl cDNA, 1× ddPCR SuperMix for probes, no dUTPs (Bio-Rad Laboratories; Hercules, California), 125 nM SNRPN forward primer, 125 nM SNRPN reverse primer, 500 nM SNRPN HEX tagged probe, 1× UBE3A FAM-tagged TaqMan assay, and RNAse/DNAse free water. Prepared reactions were run on a Bio-Rad QX200 system (Bio-Rad, Hercules, California). Data were analysed using the QuantaSoft Analysis Pro software, as per manufacturer’s instructions (Bio-Rad, Hercules, California), with data collected from two different channels specific for HEX and FAM signals (with no confirmed signal overlap).
All individuals with AS were assessed with the Mullen Scales of Early Learning (MSEL)25, a developmental assessment that assessed the domains of visual reception, fine motor, receptive language, and expressive language. Developmental assessments are commonly used for individuals with AS and Dup15q, given the significant developmental delay that is commonly observed in these individuals and the subsequent propensity to have scores that fall at the “floor” on standardised age-appropriate assessments. The MSEL provides age equivalent scores in months for the domains of visual reception, fine motor, receptive language and expressive language. All PWS participants completed an age appropriate standardised assessment. Standardised intellectual functioning assessments included the MSEL (children aged under 3 years), the Wechsler Preschool and Primary Scale of Intelligence-3rd Edition (WPPSI-III; children aged 3–6 years, 11 months)26, the Wechsler Intelligence Scale for Children-4th Edition Australian (WISC-IV; Australian children aged 7–16 years, 11 months)27 or the Wechsler Adult Intelligence Scale-4th Edition Australian edition (WAIS-IV; individuals aged 17+ years)28. The following intellectual functioning variables were included in the analyses: VIQ, performance IQ (PIQ) and FSIQ.
The Autism Diagnostic Observation Schedule-2nd Edition (ADOS-2)29 was used to assess social communication skills and the presence of repetitive and restricted behaviours. The ADOS-2 was used in all children who were cruising/walking and had a mental age of 12 months or greater. The ADOS-2 provides an overall calibrated severity score (CSS), in addition to CSS for the social affect (SA CSS) and repetitive and restricted behaviours (RRB CSS) domain. All assessments were completed by the first author, a certified ADOS-2 trainer in Australia, who regularly engages in reliability coding meetings to maintain research reliability of >80%.
Participants attended an appointment at a clinic or within their own home for the developmental/intellectual functioning assessment and the ADOS-2. Venous blood was collected at the cessation of the clinical appointment. All procedures were approved by The Royal Children’s Hospital Human Research Ethics Committee (HREC #33066). All parents/caregivers provided written informed consent, and those aged 18 years and above, who were deemed cognitively able, also provided written consent.
UBE3A and SNORD116 mRNA copy numbers were normalised to copy numbers from a stably expressed set of internal control genes determined using the geNorm approach30 on the same set of cDNA samples from PWS (n = 21) and control (n = 23) cohorts (Fig. 1). Given the sample size for each group was small, the summary statistics were presented by median and interquartile range, and the nonparametric Kruskal–Wallis test or Mann-Whitney test were used for comparisons of the groups. For binary data, such as sex, the percentage was given and Fisher’s exact test was used for comparison. The robust regression, using M-estimator and robust standard errors, was used to assess the relationship between each phenotypic measure (intellectual functioning and ADOS scores) and UBE3A and SNORD116 mRNA levels. Adjustments for confounders was undertaken where appropriate, especially for age, where the youngest participant was 0.8 years and the oldest was 45.6 years (e.g., age adjusted for MSEL equivalent scores in AS or for ADOS in Dup 15q group, and age and FSIQ for ADOS in PWS). The Bonferroni correction method was used to correct for multiple testing. All analyses were conducted using the software STATA (http://www.stata.com).
Technical validation of ddPCR assays
Nine ddPCR assays were validated including seven from an internal control gene panel (Supplemental Fig. 1) and two target genes, UBE3A and SNORD116 (Supplemental Fig. 2). The validation experiments involved establishing positive call threshold and dynamic linear range (DLR) for each assay on serially diluted RNA reference sample, with RNA input ranging between 170.4 and 1.33 ng. For all assays the positive call thresholds were set on the ddPCR 2-D plots using no template controls (no RNA input—1st column of each 2-D plot included in every run) at the amplitude of the droplet/s with the highest amplitude unit value, representing non-specific signal.
For the GAPDH assay that showed multiple distinct droplet population above the non-specific signal amplitude in the no-template control sample, we trialled two different thresholds. The second threshold was set just below the most prominent positive droplet population. Supplemental Fig. 1D and 1E demonstrate that the correlation between expected and observed RNA input for the GAPDH essay are not significantly different between the no-template control-based threshold and the higher amplitude threshold set below the main positive droplet population. All of the internal control assays showed the DLR between 170.4 and 5.325 ng RNA input, with every serial dilution there was a proportional decrease in copy numbers detected. However, the target gene assays showed wider DLR, between 170.4 and 2.7 ng RNA input for SNORD116, and 170.4 and 1.33 ng RNA input for UBE3A. Subsequently, all RNA samples from chromosome 15 imprinting disorder cohorts and controls were diluted to equate to 10 ng input per cDNA synthesis reaction. This input overlapped with the approximate middle dilution for DLR of all internal control and target gene assays tested.
Selection of most stably expressed internal control genes
The geNorm strategy was used to determine the minimum number of genes required to calculate a reliable normalisation factor for gene expression studies in PBMCs of 21 individuals with PWS and 23 typically developing controls (Fig. 1). Of the seven reference genes evaluated for different abundance and functional classes, the geometric mean of mRNA levels for SDHA, ATP5B and EIF4A2 provided an accurate normalisation factor in the system tested. This is evident from the geNorm V score of 0.123, which is below the recommendation of the V score of 0.15 used to assess if expression of the selected genes are sufficiently stable. Moreover, inclusion of additional genes in the geometric average of the top three most stably expressed genes, did not significantly impact the V score for gene expression normalisation in the tested settings (Fig. 1B).
Intergroup comparisons on clinical measures, UBE3A and SNORD116 mRNA levels
The AS, PWS and Dup15q groups did not significantly differ on age at time of assessment (PWS: median (Md) = 7.15, interquartile range (IQR) = 12.31; AS: Md = 6.93, IQR = 16.03; Dup15q: Md = 6.38, IQR = 9.83; p = 0.672). Similarly, the proportion of males in each group did not significantly differ (PWS: 40.7%; AS: 52.4%; Dup15q: 60.0%; p = 0.520). Both the Dup15q and PWS groups had a significantly higher ADOS-2 CSS and SA CSS compared to the AS group (Table 1), but the three groups did not differ on RRB CSS. The PWS and Dup15q groups did not significantly differ on ADOS-2 scores. Descriptive intellectual functioning data are provided in Supplemental Table S2.
The Dup15q group had significantly elevated UBE3A mRNA levels compared to the PWS, AS and control groups (Table 1; Fig. 2A), while the AS, PWS and control groups did not significantly differ on UBE3A mRNA levels (Table 1; Fig. 2A). The AS and Dup15q groups did not significantly differ on SNORD116 mRNA levels (Table 1). The normalised levels of SNORD116 mRNA were significantly elevated in the AS and Dup15q groups as compared to the control group (Fig. 2A, B). In the Dup15q group the UBE3A median was more than threefold higher than the levels found in the AS group (Table 1) and more than twofold higher than controls (Fig. 2A). SNORD116 mRNA levels showed the greatest variability in the AS group (range: 0.015–0.121 a.u). For the Dup15q group UBE3A mRNA levels (range: 0.268–0.574) were significantly more variable than those for SNORD116 mRNA (range: 0.026–0.052). In contrast SNORD116 mRNA was completely absent in the PWS group, but the levels of UBE3A mRNA were not significantly different between the PWS and control groups (Fig. 2A).
Comparison of deletion and non-deletion subtypes in the AS and PWS groups demonstrated that the deletion groups had significantly lower UBE3A mRNA levels compared to their non-deletion counterparts (AS: p = 0.002; PWS: p < 0.001; Supplement Table S3). However, SNORD116 mRNA levels did not differ between the deletion and non-deletion subtypes in AS individuals (p = 0.197; Supplement Table S3). UBE3A mRNA levels in the methylation mosaic, ICD and UPD individuals were considerably higher (almost double) than those found in the deletion subtype (Fig. 2B) with the exception of one deletion individual who had the highest UBE3A mRNA level in the AS group.
Relationships between mRNA and phenotypic measures
In the AS deletion subtype, both UBE3A and SNORD116 mRNA levels were significantly associated with all age equivalent (months) scores derived from the MSEL (Table 2; Fig. 2C and 2D) and RRB CSS. Although higher UBE3A mRNA levels were significantly associated with higher expressive language age equivalent scores in the non-deletion AS subtype, this relationship did not survive adjustment for multiple comparisons. SNORD116 expression was not significantly associated with any MSEL age equivalent or ADOS scores in the non-deletion subtype (Table 2). Analyses for the combined AS group showed significant associations between UBE3A expression and receptive and expressive language age equivalent scores (Table S4), primarily driven by the deletion subtype.
In the PWS non-deletion subtype, UBE3A mRNA levels were significantly negatively correlated with PIQ scores and FSIQ scores, though the latter did not survive adjustment for multiple comparisons (Table 3). UBE3A mRNA levels were also positively correlated with ADOS CSS (Fig. 2E) and SA CSS (Table 3), after adjustment for age at time of assessment and multiple comparisons (Table 3; Fig. 2E). In contrast, in the PWS deletion subtype, UBE3A mRNA levels were significantly negatively associated with SA CSS and ADOS CSSS, though the association with ADOS CSS did not survive Bonferroni adjustment. When the PWS group was analysed with all subtypes combined (Table S5), no significant associations were observed between ADOS scores and UBE3A mRNA levels.
In the Dup15q group UBE3A and SNORD116 mRNA levels were not significantly associated with any of the ADOS scores (Table S6). Due to high variability in the intellectual functioning assessments used and small sample size, analyses were not conducted for intellectual/developmental functioning variables for the Dup15q group.
This study highlights the potential utility of gene expression in peripheral tissues as biomarkers for phenotypic severity in chromosome 15 imprinting disorders. While these syndromes are predominantly thought to be caused by abnormal functioning of neurons in the brain, the significant associations observed between UBE3A mRNA in peripheral blood and phenotypic variables suggest that changes in gene expression in PBMCs reflect brain specific processes indirectly measured through formal assessments of intellectual functioning and autism features. Specifically, this study demonstrated that increased UBE3A mRNA levels were associated with age equivalent scores derived from the MSEL in AS individuals with the deletion subtype and ADOS scores in PWS individuals, though the direction of association differed between the deletion and non-deletion PWS groups. No significant associations were observed between gene expression of UBE3A and SNORD116 and autism features in the Dup15q group.
This study was also the first to utilise ddPCR, as a more precise and reproducible technique to quantify UBE3A and SNORD116 mRNA levels from human peripheral tissues in chromosome 15 imprinting disorders. This may explain the associations between gene expression in blood and phenotype severity observed in this study, not previously examined. One of the strengths of the approach used is characterisation of the most stably expressed internal control genes using the geNorm approach in PBMCs of PWS and control groups in this study30. This approach is in line with the broad best practice recommendations for locus specific gene expression analyses31. However, we are not aware of previous studies examining gene expression in peripheral tissues of patients with chromosome 15 imprinting disorders that have tested a panel of genes (as in this study) to determine the optimal combination of most stably expressed genes, to be chosen as appropriate reference controls. This is a significant limitation of the earlier studies16,32 that needs to be taken into consideration, when interpreting and comparing results from this study with those conducted earlier.
Together, our approach addresses two potential technical limitations associated with previous gene expression studies in chromosome 15 imprinting disorders including: (i) use of techniques15,16,32 that are not as precise or quantitative as ddPCR for locus specific analysis33; (ii) target gene(s) normalised to a single internal control gene such as β-actin16, β-2 microglobulin15 or GAPDH32 that were not validated as part of gene expression stability studies, and may be themselves affected in the tested conditions. In this study, SDHA, ATP5B and EIF4A2 were identified as the combination of reference genes most stably expressed in these settings, and were used to normalise expression of target genes, UBE3A and SNORD116. Future studies aiming to examine expression of other genes in these settings, now have evidence supporting use of the same normalisation strategy as described here for UBE3A and SNORD116.
Dissociation between UBE3A and SNORD 116 expression in PBMCs
The SNORD116 mRNA levels showed the greatest variability in the AS group as compared to UBE3A. However, for UBE3A there was almost a clear split, with the deletion AS individuals showing lower mRNA levels than the non-deletion group, with the exception of one individual with AS and the deletion subtype, who had one of the highest levels of expression reported for all individuals examined. For SNORD116 the UBE3A mutation group appeared to cluster with the deletion subtype. This suggests that there is a dissociation between UBE3A and SNORD116 expression in AS, at least in peripheral blood; a similar phenomenon to what was observed in blood of PWS and AS patients previously16.
For the Dup15q group, the expression of UBE3A was the highest from all groups examined with significant variability observed. As expected, those with the int dup15 subtype had the lowest UBE3A mRNA levels within the Dup15q group. Moreover, the results for the combined Dup15q group were approximately four times those of controls. This is consistent with UBE3A not being imprinted in PBMCs, and further demonstrates the reliability of the ddPCR method developed and used to quantify mRNA levels in PBMCs in this study. However, this does not necessarily rule out that factors other than copy number changes impact mRNA levels in Dup15q individuals with the idic15 subtype, consistent with results previously observed in idic1534. In contrast, SNORD116 mRNA levels were less variable within the Dup15q group, with expression being not significantly different from the AS group, but still significantly above the control levels. Since SNORD116 in PWS is completely silenced in PBMCs on maternal alleles, one would expect to see mat idic15 to have SNORD116 expressed at normal levels (as one of the four alleles would be paternal and expressing SNORD116 as in controls). The observed elevated levels, however, suggest that SNORD116 on the paternal allele is being upregulated in PBMCs, though the mechanism is yet to be characterised. These findings should be confirmed in a larger independent cohort, as elevated levels of SNORD116 mRNA from the paternal allele may contribute to mat idic15 pathology.
Moreover, in a study describing methylation-sensitive high-resolution melting-curve analysis on genomic DNA of post-mortem human brain tissues obtained from 8 Dup15q syndrome, 10 idiopathic autism and 21 typical control individuals34, PWS-IC methylation, and UBE3A transcript and protein levels were higher in Dup15q than in control or autism samples. Methylation of the PWS-IC region showed a positive correlation with UBE3A and GABRB3 levels, but a negative correlation with SNRPN levels. This led the authors to suggest that gene expression within 15q11–q13 is not completely based on copy number changes, but it can also be influenced by epigenetic mechanisms in the brain.
In PWS (regardless of the molecular class) UBE3A mRNA levels were not significantly different compared to controls, while SNORD16 expression was completely silenced. This was consistent with the real-time PCR results from an earlier study of SNORD116 (referred to as SNRPN exons 57–58)16 that used exactly the same primers and probe as in this study. The previous study tested blood of two PWS participants, and also did not detect any SNORD116 mRNA levels by real-time PCR. For quantitative analysis in AS and controls, however, it is not possible to accurately compare the results between the studies16 because: (i) the previous study reported quantitative real-time PCR results as a ratio of SNORD116 over UBE3A mRNA, rather than normalising expression of each of the target genes to a set of stably expressed internal control genes; (ii) the number of participants was too low to perform statistical analysis as part of intergroup comparisons.
To examine potential clinical and biological significance of the detected variation in UBE3A and SNORD116 mRNA levels in PBMCs, genotype–phenotype relationships were examined. Both UBE3A and SNORD116 mRNA levels in PBMCs were significantly correlated with all age equivalent scores on the MSEL and the RRB CSS in the deletion AS group; higher gene expression levels were associated with better developmental functioning and less repetitive and restricted behaviours in this subtype. In the PWS deletion group, higher UBE3A mRNA levels were associated with lower SA CSS scores. In contrast, for the PWS non-deletion subtype, increased UBE3A mRNA levels were significantly associated with lower PIQ scores and increased SA CSS, reflecting poorer visuo-spatial and social communication skills, respectively. No significant associations were observed between UBE3A and ADOS scores in the Dup15q group. This may be attributed to the highly heterogenous molecular and clinical profiles of individuals with Dup15q and a significantly smaller sample size than the AS and PWS groups with available ADOS-2 data. Nonetheless, all Dup15q participants who completed the ADOS-2 (n = 8) met the cut-off for ‘Autism’ indicating a high level of autism symptoms
Overexpression of UBE3A has been linked to severity in Dup15q, where the increased number of maternal alleles is thought to be the primary driver of Dup15q pathology34. Similarly, PWS individuals with the UPD subtype are also thought to be ‘at a greater risk’ for ASD due to overexpression of UBE3A35. The findings provide support to this theory, however, it is possible that overexpression of UBE3A is more specifically related to the social communication deficits associated with ASD rather than RRBs. Several of the findings in this study support this notion: (i) higher UBE3A levels were associated with lower SA deficits in the PWS deletion subtype, which clustered at the bottom of the PWS group on UBE3A levels; (ii) in those with the non-deletion subtype higher UBE3A levels were associated with more SA difficulties; (iii) RRBs did not significantly differ across the three clinical groups, despite differences in UBE3A expression. Moreover, in ASD and other psycho-pathologies, such as schizotypy, gain of function UBE3A mutations have been suggested to be linked to phenotype severity36,37,38. It should be noted that ADOS scores in individuals with PWS may also be capturing other psychiatric difficulties including mood disorders and schizotypy traits, which are also linked to social communication deficits39. There is now a large amount of evidence supporting UBE3A dosage effects on schizotypy in the general population38 as well as those with PWS and Dup15q.
The associations between UBE3A and SNORD116 mRNA levels and brain related processes, including developmental functioning and autism features, are consistent with the patho-mechanism proposed in a recent study examining transcriptomic signatures in the hypothalamus from post-mortem brain tissues in PWS40. This previous study demonstrated that genes associated with inflammatory response (including TNF-alpha and Il1-beta) were upregulated in PWS hypothalamus40. Together with the genotype-phenotype relationships reported in this study using PBMCs, this suggests that the immune response regulated by microglial cells (comprising almost half of all cells in the brain) may play a broader role in chromosome 15 imprinting disorder pathology. Abnormal expression of UBE3A in AS leucocytes, where UBE3A is not imprinted, may also have implications for clinical trials targeting UBE3A re-activation in the brain41. Specifically, UBE3A expression and regulation in other tissues may need to be monitored for non-specific impacts of the intervention on pathways regulated by UBE3A in non-neuronal cell types. Moreover, future studies should explore UBE3A expression in microglial cells in post-mortem human tissues of individuals affected with different chromosome 15 imprinting disorders, to confirm or refute these proposed patho-mechanisms.
Strengths and limitations
One of the strengths of this study is the utility of ddPCR to accurately measure differences in gene expression of 30% or less—a feat not possible with most other methods including real-time quantitative PCR and RNA-seq33. Another strength is the characterisation of the most stably expressed internal control genes (SDHA, ATP5B and EIF4A2) using the geNorm approach in PBMCs of PWS and control groups30. This approach to select stably expressed reference genes for quantitative real-time PCR30 and ddPCR42 based studies has been widely recommended in other settings to ensure that the variation identified is not due to changes in genes used for target gene normalisation. Yet, previous studies for locus specific gene expression analysis in the chromosome 15 imprinting disorders in peripheral tissues and/or neurons, mostly utilised expression of β-actin16, β-2 microglobulin15 or GAPDH32 as a single internal control gene. Of note is that β-actin and β-2 microglobulin are involved in cell migration, which may be affected in chromosome 15 imprinting disorders43.
A limitation of the current study is the relatively small sample sizes for each of the subtypes in each condition as compared to similar studies performed in other rare disorders such as fragile X syndrome (FXS)44. Given these are rare genetic syndromes, obtaining large sample sizes can be difficult for each subtype. Nonetheless, this is one of the largest studies to date that has examined the utility of gene expression in peripheral tissues as biomarkers for brain related phenotypes in chromosome 15 imprinting disorders. Another limitation is that cellular and secreted protein product of UBE3A was not examined in this study. This is an important direction for future studies to confirm functional significance of changes in UBE3A mRNA levels and relationships with clinical phenotypes reported here.
While the use of peripheral tissues may not be entirely reflective of what is happening in the brain, the primary advantage of examining peripheral tissues is that the collection is less invasive than other tissues, such as cerebral spinal fluid (CSF), and will therefore likely increase sample sizes which is important for recruitment of individuals with rare genetic disorders. Evidence from other neurodevelopmental disorders, including FXS, has demonstrated significant relationships between promoter methylation, mRNA and protein and gene expression in peripheral tissues (e.g., blood and buccal epithelial cells) and the severity of the clinical phenotype, including intellectual functioning and autism features22,44. Nonetheless, future research exploring relationships between peripheral tissue biomarkers and other tissues such as CSF and brain tissue, where available, will further confirm the utility of peripheral biomarkers in understanding the molecular underpinnings of these rare genetic syndromes.
In conclusion this study has demonstrated the utility of ddPCR for accurate quantification of gene expression in PBMCs in chromosome 15 imprinting disorders and characterisation of a stably expressed set of internal control genes. This ensured that variation reflected in the target genes analysed is not attributed to the variability in expression of the internal control gene/s used. UBE3A mRNA levels in PBMCs were shown to be significantly correlated with brain related phenotypes in both the PWS and AS cohorts. Specifically, increased UBE3A mRNA levels correlated with increased autism features in PWS and receptive language skills in AS, suggesting the utility of gene expression analysis in peripheral tissues as non-invasive biomarkers for future studies. Future research exploring clinical and biological significance of the relationships between UBE3A and SNORD116 transcription in human peripheral and post-mortem brain tissues in PWS, AS and Dup15q patients are warranted to further explain the findings and the underlying mechanisms proposed in this study.
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This study was supported by the Victorian Government’s Operational Infrastructure Support Programme, with the salaries supported by NHMRC project grants (Nos. 1049299 and 1103389 to D.E.G.); Murdoch Children’s Research Institute, Royal Children’s Hospital Foundation (D.E.G.); Next Generation Clinical Researchers Programme—Career Development Fellowship, funded by the Medical Research Future Fund (MRF1141334 to D.E.G.); the Financial Markets Foundation for Children (Australia; No. 2017—361 to D.E.G. and D.J.A.); the Genetics of Learning Disability (GOLD) Service (M.F.); the Foundation for Prader–Willi Syndrome Research, USA (grant Nos. 43445 and 501393 to D.E.G. and D.J.A., respectively); the National Institute of Child Health and Human Development (NICHD; grant No. HD02528 to M.G.B.); and joint funding from the Prader–Willi Syndrome Association (Australia), Foundation for Angelman Syndrome Therapeutics (Australia) and Dup15q Australia Ltd. The authors would like to thank all the study participants and their families for being involved in the study. We would also like to thank James O’Brien from the Prader–Willi Syndrome Association (Australia), Meagan Cross and Chloe Simons from the Foundation for Angelman Syndrome Therapeutics (Australia), and Chris Cahir from Dup15q Australia Ltd. for their assistance with the recruitment of participants.
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The authors declare that they have no conflict of interest.
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Baker, E.K., Butler, M.G., Hartin, S.N. et al. Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders. Transl Psychiatry 10, 362 (2020). https://doi.org/10.1038/s41398-020-01034-7