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Research Article

Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients with Suspected Smith-Magenis Syndrome without the 17p11.2 Deletion

  • Thierry Vilboux,

    Affiliation: Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Carla Ciccone,

    Affiliation: Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Jan K. Blancato,

    Affiliation: Department of Oncology, Georgetown University Medical Center, Washington, D.C., United States of America

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  • Gerald F. Cox,

    Affiliations: Division of Genetics, Department of Pediatrics, Harvard Medical School, Children's Hospital Boston, Boston, Massachusetts, United States of America, Genzyme Corporation, Cambridge, Massachusetts, United States of America

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  • Charu Deshpande,

    Affiliation: Department of Genetics, Guy's Hospital, London, United Kingdom

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  • Wendy J. Introne,

    Affiliation: Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • William A. Gahl,

    Affiliations: Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America, Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Ann C. M. Smith,

    Affiliation: Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Marjan Huizing mail

    mhuizing@mail.nih.gov

    Affiliation: Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America

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  • Published: August 08, 2011
  • DOI: 10.1371/journal.pone.0022861

Abstract

Smith-Magenis syndrome (SMS) is a complex neurobehavioral disorder characterized by multiple congenital anomalies. The syndrome is primarily ascribed to a ~3.7 Mb de novo deletion on chromosome 17p11.2. Haploinsufficiency of multiple genes likely underlies the complex clinical phenotype. RAI1 (Retinoic Acid Induced 1) is recognized as a major gene involved in the SMS phenotype. Extensive genetic and clinical analyses of 36 patients with SMS-like features, but without the 17p11.2 microdeletion, yielded 10 patients with RAI1 variants, including 4 with de novo deleterious mutations, and 6 with novel missense variants, 5 of which were familial. Haplotype analysis showed two major RAI1 haplotypes in our primarily Caucasian cohort; the novel RAI1 variants did not occur in a preferred haplotype. RNA analysis revealed that RAI1 mRNA expression was significantly decreased in cells of patients with the common 17p11.2 deletion, as well as in those with de novo RAI1 variants. Expression levels varied in patients with familial RAI1 variants and in non-17p11.2 deleted patients without identified RAI1 defects. No correlation between SNP haplotype and RAI1 expression was found. Two clinical features, ocular abnormalities and polyembolokoilomania (object insertion), were significantly correlated with decreased RAI1 expression. While not significantly correlated, the presence of hearing loss, seizures, hoarse voice, childhood onset of obesity and specific behavioral aspects and the absence of immunologic abnormalities and cardiovascular or renal structural anomalies, appeared to be specific for the de novo RAI1 subgroup. Recognition of the combination of these features will assist in referral for RAI1 analysis of patients with SMS-like features without detectable microdeletion of 17p11.2. Moreover, RAI1 expression emerged as a genetic target for development of therapeutic interventions for SMS.

Introduction

Smith-Magenis syndrome (SMS; OMIM 182290) is a complex neurobehavioral syndrome characterized by multiple congenital anomalies and behavior problems, including craniofacial and skeletal abnormalities, variable intellectual disability, self-injurious and attention-seeking behaviors, speech and motor delay, and sleep disturbance [1], [2], [3], [4], [5]. The estimated prevalence of SMS in the general population is ~1:15000–25000, but it is likely underdiagnosed [6]. The syndrome is caused primarily by de novo interstitial deletions of chromosome 17p11.2, which can range from 1.5 to 9 megabases (Mb) in size, detectable by cytogenetic G-banding and/or by fluorescence in situ hybridization (FISH) analysis. The most common ~3.7 Mb deletion occurs in approximately 75% of the patients [3], [4], [5], [7], [8].

Several genes have been mapped to the 17p11.2 SMS critical region, and the exact functions of many of these genes remain unknown [5], [9], [10]. Haploinsufficiency for several genes is likely to account for the SMS phenotype, but haploinsufficiency for the retinoic acid induced 1 gene (RAI1), located within the minimal critical SMS deletion region, is considered to play a major role in SMS. This is supported by the identification of heterozygous point mutations in RAI1 in SMS patients without detectable 17p11.2 deletions. Such individuals share most, but not all, characteristics of the SMS phenotype [11], [12], [13], [14], but their levels of RAI1 mRNA transcription and RAI1 protein translation have not been assessed.

The RAI1 gene (OMIM 607642; GenBank NM_030665) consists of 6 exons, of which exons 3 through 6 encode a 1,906 amino acid RAI1 protein [15]. An RAI1 mRNA transcript of approximately 8 kb is expressed in all adult and fetal tissues examined [16], with heart and neuronal tissues showing the highest expression levels [15]. RAI1 is thought to function as a transcription factor, based on the presence of a bipartite nuclear localization signal and a zinc finger-like plant homeodomain (PHD) that is conserved in the trithorax group of chromatin-based transcription regulators [12], [17]. It also has homology to the transcription factor TCF20 [16], and contains polyglutamine (polyQ) stretches capable of modulating transcriptional activation [18]. Recently, RAI1 was shown to localize to the nucleus and have transcription factor activity in a neuronal cell line [19]. The RAI1 promotor region contains several regulatory protein binding sites, including a retinoic acid-responsive element [15]. A variety of mouse studies have identified additional Rai1 features, including upregulation of Rai1 in mouse carcinoma cells following retinoic acid treatment [20], localization of the Rai1 mRNA transcript and protein to neurons suggesting a role in neuronal differentiation [20], and a dosage-dependent role for Rai1 in the serotonin pathway [21].

To date, only 14 de novo RAI1 mutations (in 16 patients) have been associated with SMS [9], [10], [11], [12], [13], [14], [22], so more patients need to be evaluated to understand the complete role of RAI1 in the SMS phenotype. We analyzed 36 patients with SMS features but without a detectable 17p11.2 microdeletion, for variations in RAI1 and RAI1 SNP haplotypes. We report 4 de novo RAI1 mutations, 1 unclassified variant, and 5 novel familial variants. In addition, we demonstrate for the first time that RAI1 mRNA expression is decreased in lymphoblastoid cells of SMS patients with the common 17p11.2 deletion, as well as in cells with RAI1 mutations. We also extensively compare the clinical features of patients bearing the common 17p11.2 deletion with the manifestations of patients having RAI1 variants, to further delineate which aspects of the SMS phenotype are influenced by RAI1 expression.

Results

Copy Number Analysis

Of ~120 investigated patients with SMS features, 36 were cytogenetically ascertained to have no detectable deletion of 17p11.2. For patients without prior cytogenetic studies, FISH analysis was performed (Figure 1A). Genomic DNA from whole blood was then used to confirm the presence of two RAI1 alleles in all 36 patients by copy number qPCR (Figure 1B). In selected cases, MLPA analysis confirmed the presence of two RAI1 alleles (Figure 1C).

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Figure 1. RAI1 copy number analysis.

(A) Representative images of two-color FISH analysis on metaphase chromosomes of lymphoblastoid cells of an SMS patient without (M2717) and with (M2606) the 17p11.2 deletion. The probes were specific for the RAI1 locus (RP1–253P7; red) and for the chromosome 17 centromere (green). The chromosomes were counterstained with DAPI (blue). (B) Copy number analysis by qPCR using TaqMan primer-probe assays targeting exon 6 of RAI1 (Hs025670777_s1) and the endogenous control gene RNaseP. The comparative Ct method (RQ, relative quantification) was used to determine the RAI1 gene copy number as shown for a non-deleted patient (M2485), a 17p11.2 deleted patient (M2173) and a non-deleted patient with a familial RAI1 variant (M2900). (C) Results of MLPA copy number analysis, shown for 6 genes including RAI1 from the P245-A2 kit. Results are shown for an SMS patient without the 17p11.2 deletion (M2543) and a patient with 17p11.2 deletion (M0119).

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RAI1 Molecular Analysis

The RAI1 coding exons 3, 4, 5 and 6, including their intron-exon boundaries, were sequenced for all 36 undeleted patients and available parents and/or siblings. The identified coding variants (excluding known SNPs) are listed in Table 1. In 4 patients, a severe RAI1 mutation was identified; we classified these as ‘de novo’ variants. Patient M2377 was heterozygous for c.1449delC [p.E484KfsX35], a frameshift mutation leading to a premature stop codon (Figure 2A). This case was previously reported as SMS159 [14]; this variation was absent from parental DNA. Patient M2719 was heterozygous for a novel nonsense mutation, c.1973G>A [p.W658X] (Figure 2B); parental DNA was not available for testing. Patient M2754 was heterozygous for a frameshift mutation, c.3103insC [p.Q1034PfsX31], leading to a premature stop codon (Figure 2C). This case was recently reported as SMS335 [22], and the C-nucleotide at position 3103 was recognized as a frameshift mutation hotspot due to the presence of a heptameric C-tract [22]. This variant was not present in parental DNA. Patient M2911 had an unreported heterozygous frameshift mutation c.548delT [p.L183RfsX69] (Figure 2D). Parental DNA did not contain this variant.

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Figure 2. SMS patients and their identified RAI1 variants.

(A) Patient M2377 (pictured at age 20 years) carried the de novo frameshift variant c.1449delC. (B) Patient M2719 (pictured at age 17 years) carried the de novo nonsense variant c.1973G>A. (C) Patient M2754 (pictured at age 18 years) carried the de novo frameshift variant c.3103insC. (D) Patient M2911 (pictured at age 5 years) carried the de novo frameshift variant c.548delT. (E) Patient M2543 (pictured at age 14 years) was heterozygous for the c.725C>T and c.2907C>T variants. The pedigree of his family contains the genotypes of his mother (M2812) and his unaffected brother (M2811) for the identified variants as well as the informative SNP rs11078398 and the polyQ repeat sequence. His father's genotype could be partially reconstructed; no paternal DNA was available for sequencing. (F) Patient M2900 (pictured at age 6 years) was heterozygous for the c.1500G>A and c.3791A>G (rs61746214) variants, which were also present in his brother with developmental delay (M2901) and in his unaffected sister (M2902). His family pedigree shows these variants as well as the informative SNP rs11078398 and the polyQ repeat sequence. His father's genotype could be partially reconstructed (no DNA was available).

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Table 1. RAI1 variants in SMS patients without 17p11.2 deletion identified in the current study.

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Patient M2543 had a novel heterozygous missense variant, c.725C>T [p.P242L], as well as a novel heterozygous silent variant c.2907C>T [p.D969D] (Figure 2E) and 13 polyQ residues on each allele. The missense variant c.725C>T was not present in his mother (13 and 14 allelic polyQ residues) or brother (13 and 14 allelic polyQ residues). The silent variant c.2907C>T was present in his mother, but not in his brother, indicating that these variants occurred on separate alleles and that the c.2907C>T variant occurred on an allele with 13 polyQ residues that was inherited from his mother. The allele carrying the missense variant c.725C>T was inherited from his father and carried 13 polyQ residues (see pedigree Figure 2E). Since father's DNA was not available, we could not determine whether this variant was de novo or paternally inherited, and therefore subgrouped this patient as unclassified (Table 1).

In the previously reported patient SMS175 [13], with RAI1 p.Q1562R, we confirmed absence of the 17p11.2 deletion (M2390, Table S1). However, we did not identify p.Q1562R in whole blood or fibroblast DNA, raising the possibility of mosaicism.

Furthermore, we identified 3 novel heterozygous nonsynonymous (missense) variants, one 3bp deletion and one synonymous (silent) variant (Table 1), all of which were also found in one of the parents. None of these ‘familial’ variants were reported SNPs, nor were any identified in our other screened patients or reported in previous RAI1 sequencing studies [9], [10], [11], [12], [13], [14]. Patient M2365 carried the missense variant c.5653G>A [p.D1885N] as well as the silent variant c.3183G>A [p.T1061T], both of which were identified in his unaffected father but absent from his mother's DNA; they are, therefore, expected to exist on the same allele/in the same haplotype (see also Table S1). Of interest is that p.D1885N is located in RAI1 exon 4, which is the first reported RAI1 variant located in this exon.

Patient M2732 and her unaffected mother were heterozygous for the unreported variant c.707A>T [p.Y236F]. Patient M2826 was heterozygous for the novel missense variant c.3208G>A [p.G1070R] as well as a novel silent variant c.4512G>T [p.L1504L], which were both also identified in her mother indicating that they may exist on the same allele/in the same haplotype (see also Table S1). Her mother has a history of learning problems (see Clinical Information S1). Patient M2867 had a novel heterozygous in-frame deletion of 3 bp, c.3781_3783delGAG [p.del1262E] that was also present in her unaffected father and absent in maternal DNA. Patient M2900 carried a heterozygous unreported silent variant c.1500G>A [p.P500P], which was present in the homozygous state in his mildly dysmorphic mother (M2903) and heterozygous in his brother with developmental delay (M2901) and unaffected sister (M2902) (Figure 2F and Clinical Information S1). The paternal DNA was not available for analysis. Further familial molecular studies, including SNP analysis, identified a rare reported SNP, c.3791A>G [p.E1264G] (rs61746214), heterozygous in the proband (M2900), his mother, and his siblings. The more common synonymous SNP c.837G>A [p.Q279Q] (rs11078398) occurred homozygous in the proband and his siblings, and heterozygous in their mother (Figure 2F). These findings indicate that neither the novel silent variant c.1500G>A, nor the identified SNPs are likely to be related to the SMS phenotype in proband M2900.

For the other 26 undeleted SMS patients, no novel RAI1 variants were detected in the coding region or intron/exon boundaries, other than a variety of reported SNPs (Table S1A).

Missense Variant Analysis

Table 2 lists all RAI1 missense variants (detected in this study and those previously reported), as well as nonsynonymous SNPs (indicated with their rs identification numbers from dbSNP http://www.ncbi.nlm.nih.gov/snp). Since the pathogenicity of missense mutations is difficult to predict, we analyzed the potential pathogenicity of each variant using different prediction software programs (Polyphen, Panther and PMut). Please note that these are predicted values only, not based on cellular data.

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Table 2. Severity predictions of missense variants.

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The identified p.P242L missense variant (patient M2543) has a high probability to be deleterious predicted by at least 2 programs. The previously published RAI1 missense mutations p.Q1562R (SMS175) [13] and p.S1808N (SMS195) [13] were predicted to be benign or ambiguous deleterious by all 3 prediction programs. Interestingly, a recent report demonstrated that neither of these two variants impair RAI1 nuclear localization or transcription factor activity [19], suggesting that these variants may not cause the SMS phenotype, or that other factors (post-translational modifications, interactions) related to these mutations may induce their SMS phenotype.

The familial missense variants p.Y236F, p.S1212G, p.D1885N, and p.del1261E were predicted to be benign overall, based on at least 2 prediction programs (except for p.del1261E, which could only be analyzed by the Polyphen program, Table 2).

Of the 3 nonsynonymous SNPs, p.G90A (rs3803763) was predicted to be benign, p.P165T (rs11649804) has variable predictions, but p.E1264G (rs61746214) was predicted by Pmut and Polyphen to be deleterious and warrants further research.

RAI1 is highly polymorphic; more than 30 SNPs are reported in the coding region in dbSNP. All identified variants of our molecular analyses are listed in Table 3. For each variant, the minor allele frequency (MAF; the frequency of the SNP's less frequent allele in a given population) reported in dbSNP, as well as the MAF calculated from our study are indicated in Table 3 (see also Table S1 for allele distributions). Our SMS patient contingent was of Caucasian origin (except patient M2900 who was Hispanic, and M2543 who had a mother of Indian descent). For most variants, the MAF identified in our study is similar to that reported in dbSNP, except for three variants, rs8067439 and rs3803763, which occurred more frequently in our SMS cohort and rs35686634, which occurred less frequently in our SMS cohort (gray highlighted in Table 3).

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Table 3. Minor allele frequencies (MAF) of RAI1 variants.

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SNP Haplotype Analysis

We attempted to reconstruct the haplotype for each patient by assigning the variant nucleotides to each allele, using all sequencing data including sequences from available family members. For most patients, the listed haplotypes are the only possible combination of variants; for other patients the haplotype is the most likely prediction (Table S1). We prioritized the presence of a ‘common haplotype’ allele (Haplotype H1 in Table S1), and then assigned the nucleotides of the second allele. These analyses revealed various allelic haplotypes among 72 studied alleles, with one predominant haplotype existing on 44% of the alleles (H1: 32 of 72 alleles, yellow highlighted in Table S1), one moderately common haplotype existing on 15% of alleles (H2, green highlighted) and several rare haplotypes, with existence ranging from 3%–7% of alleles, and 11 unique haplotypes (u, white background, 17%) (Table S1).

RAI1 mRNA Expression

RAI1 mRNA expression levels were determined by qPCR on RNA isolated from lymphoblastoid cells (Figure 3). SMS patients with the common 17p11.2 deletion (M2370, M0119, M2844; haploinsufficient for RAI1) had significantly (p<0.05) lower expression of RAI1 mRNA, with an average of ~30% of control. In addition, all patients with de novo RAI1 variants displayed significantly decreased RAI1 expression (p<0.05 by at least one statistical test) to about 52% of normal; cells from patient M2911 were not available. Decreased RAI1 expression was not only determined in cells with RAI1 frame-shift and nonsense mutations (36% in M2377, 59% in M2719, and 55% in M2754), but also in the patient with a missense mutation (60% in M2543).

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Figure 3. RAI1 mRNA expression in lymphoblastoid cells.

RNA extracted from lymphoblastoid cells from SMS patients in 4 subgroups: cases with common 17p11.2 deletion, de novo RAI1 variants (including the ‘unclassified’ variant M2543), familial RAI1 variants, and non-17p11.2 deleted without identified RAI1 variants, as well as from 3 control cell lines were used for RAI1 mRNA expression analysis by qPCR. Two Taqman primer-probe assays were used per sample (assay 1 and assay 2). Displayed values represent the relative quantification (RQ) compared to the average of all control assays (set to 1). *: Average RQ of the sample is statistically different (p<0.05) from the average of all control cases (t: using the ANOVA post hoc Tukey-Kramer test; g: using the ANOVA post hoc Games-Howell test).

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Expression levels varied among the familial RAI1 variants (M2365, M2732, M2826, M2867, M2900) and three selected non-deleted cases without novel RAI1 variants (M2390, M2647, M2712). In this group, RAI1 expression varied from normal and non-significant (98% in M2365, 104% in M2732, 80% M2647, 76% in M2712), to moderately but significantly (p<0.05) decreased (61% in M2900 and 59% in M2390), to significantly severely decreased (47% in M2826 and 21% in M2867). An alternative normalizing gene (instead of β-actin), G6PC3 was used for qPCR on selected mRNA samples from each group, demonstrating that normalizing to a control assay with a similar threshold cycle (Ct) as the RAI1 assays provided comparable results to using β-actin as normalizing gene (Figure S1).

Since genomic copy number variations are a concern when using EBV transformed cells [23], [24], we also performed MLPA analysis on genomic DNA from all lymphoblastoid cell lines (Figure S2). We verified that all cell lines had two alleles for RAI1, except for the 17p11.2 deleted cases (M2370, M0119, M2844), who were confirmed to have one copy of the 17p11.2 genes RAI1, LRRC48, and LLGL1. Cell lines M2365, M2370 and M2867 showed a variety of abnormal copy number variations outside the 17p11.2 region (Figure S2).

We were unable to analyze the translated amounts of RAI1 protein, since the commercially available RAI1 antibodies that we tested (RAI-1 C-14 from Santa Cruz Biotechnology and LS-C46854 from LifeSpan) did not yield a RAI1 signal by western blotting of lymphoblastoid cell extracts.

Clinical Analysis

Detailed clinical descriptions of the cases with de novo and familial RAI1 variants are provided in the Clinical Information S1. Comparison of clinical features of our de novo subgroup with previously reported RAI1 mutation and 17p11.2 deletion cases is summarized in Table S2, and evaluated below. We provide clinical comparison data with and without the ‘unclassified’ variant M2543 included in the ‘de novo’ cohort, and mention where he is an outlier. We did not analyze the RAI1 familial variants as a discrete phenotypic group, partly due to the heterogeneity of their RAI1 levels (Figure 3).

Growth parameters.

Birth parameters for de novo RAI1 variant cases included term (mean 39.6±2.2 weeks) delivery and appropriate-for-gestational age (AGA) birth weights and lengths, consistent with published data for both 17p11.2 deletion (~80% term) [25] and RAI1 mutation cases [11], [12], [13], [14]. Among the de novo RAI1 subgroup, four patients had current weights >98th centile (obese) and lacked short stature (<5th centile), including the youngest (M2911, 5y). Only M2543 appeared to be an outlier in this group with weight in the normal range and short stature (height <2nd centile). Head circumferences were normal for three (M2719, M2754, M2911) and >95th centile for one (M2377); microcephaly (OFC<2nd centile) was observed only in M2543, the potential outlier.

The mean BMI for the de novo group (n = 5; 31.3±10.1 kg/m2) was significantly higher than for the SMS 17p11.2 common deletion group (n = 49; 20.3±5.8 kg/m2) by the two-tailed unpaired t-test (t = 3.7, df = 51; p<0.0005 (Figure 4A and 4B). BMI values above 25.0–29.9 kg/m2 are considered overweight and ≥30 kg/m2 are consistent with obesity as defined by the Centers for Disease Control and Prevention (http://www.cdc.gov/growthcharts/). Based on this classification, except for patient M2543 (the missense variant outlier), all de novo RAI1 cases are obese, including the youngest (M2911, 5y) in contrast to 57% (28 out of 49) of common 17p11.2 deletion cases (Figure 4B and 4C). The observed frequency distribution of body types (Figure 4B) by subgroup was not statistically significant (Chi square 6.0; p = 0.42). Age was significantly correlated to BMI for the entire study group (Spearman's rho 0.60; p<0.0001) (Figure 4C). However, analysis by subgroup showed a significant correlation between BMI and age for only the two largest subgroups: the common deletion cases (n = 49; Spearman's rho 0.576; p<0.0001) and the non 17p11.2 deletion cases without RAI1 variants (n = 24; Spearman's rho 0.585; p = 0.005). Both the de novo (n = 5) and familial (n = 5) RAI1 variant subgroups were non-significant (Figure 4C).

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Figure 4. Body mass index (BMI) analysis of SMS patients.

Comparison of BMI (kg/m2) for common 17p11.2 deletion cases (n = 49), and cases with de novo (n = 5, including unclassified variant M2543) or familial (n = 5) RAI1 variants. (A) The mean BMI for each subgroup. The value for the de novo RAI1 group was calculated with and without the outlier unclassified case (M2543) who carried an RAI1 missense variant. (B) Frequency of body description type (normal, overweight, or obese) based on BMI values considering age (as plotted in (C)) and gender. Interpretation of BMI levels for age 2–20 years: underweight, <5th percentile; normal range, 5th–85th percentile; overweight, 85th–95th percentile; and obese, >95th percentile. For adults: underweight, BMI below 18.5; normal range, BMI 18.5–24.9; overweight, BMI 25–29.9; and obese, BMI 30 and over. (C) Comparison of BMI by age for subjects 2–20 years of age. BMI percentile curves (5th, 85th and 95th) for ages 2–20 years were extracted from growth data from the Centers for Disease Control and Prevention. BMI values are not plotted for 6 subjects over age 20 years; 3 with common deletions and 3 without deletions or RAI1 mutations (their values are displayed in upper left of the figure).

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Neurobehavioral features.

cases included: problems with food intake and/or food foraging (5/5 de novo cases); nail yanking (4/5 de novo; not M2543 outlier); and to a lesser extent anxiety/mood shifts (5/5 de novo; including M2543 outlier). Speech delay was seen less frequently in the de novo group (3/5) compared to published deletion cases (>90%) and remains close to prior studies (70%) [9], [10]. All subjects without the 17p11.2 deletion and SMS diagnosis in our study cohort had neurobehavioral features that overlap with deletion cases (Table S2), likely reflective of referrals for study by experienced clinicians. Behavioral features that might distinguish the de novo subgroup from common deletion.

Concordant features with 17p11.2 deletion cases.

Hypotonia, frequent otitis media, ocular anomalies, dental anomalies, hoarse voice, and brachydactyly occurred in our de novo RAI1 cases with frequencies consistent with published 17p11.2 deletion cases (Table S2). Scoliosis was seen in 3/5 de novo (M2377, M2719, M2754) cases, consistent with published frequencies for common deletion (40–70%) and RAI1 mutation (36%) cases [9], [10]. Psychomotor delay, sleep disturbance and typical behavioral features occurred in over 80% of the RAI1 cases (Table S2). Hearing loss occurred in 4/4 de novo cases tested compared with 60–79% for 17p11.2 deletions and 10–25% for published RAI1 mutation cases [3], [9], [10]. Our two oldest cases (M2377 and M2754) had sensorineural hearing loss (SNHL).

Discordant features with 17p11.2 deletion cases.

Seizures occurred in all but one of the de novo cases, compared with only 11–30% for deletion cases and 17% for published RAI1 mutation cases [4], [9], [10]. Obstructive sleep apnea (OSA)/tonsillectomy/adenoidectomy were more prevalent in the de novo cases (5/5) compared to our deletion cases (50%). Cardiovascular and renal abnormalities were not documented in any de novo cases, consistent with prior reports [3], [9], [10]. While structural genitourinary anomalies were absent, issues of incontinence and/or nighttime enuresis were common, and frequent urinary tract infections occurred in all three females in the de novo subgroup. Other genital findings included hypogonadism (M2377) and labial adhesions (M2911). With the exception of a bifid uvula documented in M2719, facial clefts were absent. Immunological abnormalities were not identified. In addition, failure to thrive (FTT)/feeding issues were less frequent (3/5) in de novo RAI1 mutation cases compared to deletion cases (19/19) [26]. Both gastroesophageal reflux disease (GERD) and constipation issues occurred in de novo cases (2/5), but less frequently than reported for deletion cases [27].

Discussion

In most microdeletion syndromes, haploinsufficiency of more than one gene underlies the phenotype [28], [29]. In others, such as Alagille syndrome (deletion of 20p12; OMIM 118450) or Rubinstein-Taybi syndrome (deletion of 16p13.3; OMIM 180849), haploinsufficiencies of a single gene (Jagged1 (JAG1) or CREBBP, respectively) accounts for all the characteristic features [30], [31], [32]. In still other syndromes, haploinsufficiency of one gene in the deleted region explains only some specific feature(s); haploinsufficiency of the elastin gene accounts for the cardiac defects in Williams-Beuren syndrome (deletion of 7q11.23; OMIM 194050) [33] and haploinsufficiency of the LIS1 gene explains the lissencephaly of Miller-Dieker syndrome (deletion of 17p13.3; OMIM 247200) [34], [35].

SMS is considered a microdeletion syndrome in which haploinsufficiency of multiple genes underlies the phenotypic features [3], [5], [9]. However, heterozygous mutations in RAI1 have been identified in clinically typical SMS patients without detectable 17p11.2 deletions. This raises the issue of how RAI1 haploinsufficiency influences RAI1 RNA transcription, and which clinical features of SMS result from RAI1 haploinsufficiency.

According to BioGPS (Human Gene Atlas U133A; http://biogps.gnf.org) [36], [37], RAI1 is expressed in 84 different human tissues, including B-lymphoblasts. We employed lymphoblastoid lines to assess RAI1 expression in our patients, after ruling out copy number variations due to the immortalization process by MLPA (Figure S2).

Our results indicated that haploinsufficiency of RAI1 (through deletion of 17p11.2) results in a greater than 50% decrease in RAI1 expression (Figure 3). Other factors, likely deleted ancillary genes in 17p11.2, may influence RAI1 expression to decrease below the expected 50% level. For example, it was recently demonstrated that HDAC4 haploinsufficiency (on chromosome 2q37) decreased RAI1 mRNA expression to lower than 50% levels [38]. All our 4 patients with de novo RAI1 variants had approximately 50% decreased RAI1 levels (Figure 3), likely due to RNA decay of the nonsense (M2719) and frame-shift mutated (M2377, M2754, M2911) alleles. These findings are consistent with RAI1 expression levels reported for a haploinsufficient RAI1 mouse model [39]. Our ‘unclassified’ patient M2543 carried a missense (and a silent) RAI1 variant and displayed decreased RAI1 expression; whether his RNA expression level is directly related to these variants is unknown. We found no obvious correlation between RAI1 haplotype (Table S1) and RNA expression (Figure 3).

Surprisingly, selected SMS patients without truncating RAI1 mutations displayed significantly decreased RAI1 expression in both the familial variant group (47% in M2826; 21% in M2867, and 61% in M2900) and in a non-deleted case (59% in M2390; SMS175 in ref. [13]) (Figure 3). These reduced levels may help explain their clinical SMS-like phenotype, supported by recent data of patients mutated in HDAC4, showing impaired RAI1 mRNA expression (without RAI1 mutations) and exhibiting a SMS-like phenotype [38]. In addition, sequence variations in non-coding RAI1 exons 1 and 2, the 3′untranslated region (UTR), or in (conserved) intronic regions may underlie the decreased RAI1 levels. In addition, RAI1 expression may be affected by (epigenetic) modifiers within or outside the common 17p11.2 deletion region; environmental or physiological factors may also play a role [40]. These findings emphasize that RAI1 expression is a promising genetic target for development of therapeutic interventions for SMS.

In evaluating the clinical features of SMS in relation to molecular results, we found that a high BMI and obesity are characteristic of the de novo RAI1 variant cases (4/5), as previously reported (6/9 or 67%) [3]. In our common deletion cases, the frequency of obesity (28/49 or 57%; Figure 4B) was higher than previously reported (4/31 or 13%) [3], perhaps reflecting age at assessment and pubertal status. In the study by Edelman et al. [3], median assessment ages were 15 years (de novo RAI1 mutation cases) and 8 years (17p11.2 deletion cases), compared to 15 years (de novo RAI1 cases) and 14 years (17p11.2 deletion cases) in our analysis. A trend toward obesity in common deletion cases was reported [25], beginning around age 9 years, coinciding with pubertal onset, and reaching >95th centile for weight in teenage years to adulthood.

Past reports suggest that several features occur less often or are less severe among RAI1 mutation cases compared to common 17p11.2 deletion cases. These include infantile hypotonia, short stature, speech and motor delay, hearing loss, frequent otitis media, and structural cardiac and renal defects [3], [9], [10]. Consistent with previously published reports, our de novo RAI1 variant cases (Table S2) were less cognitively impaired (mild intellectual disability), lacked short stature (except for outlier M2543), and had normal cardiac and renal structure. While delays in growth (height/weight) in early childhood were previously recognized for de novo RAI1 mutation cases [13], the frequency of failure to thrive (FTT) and feeding issues in infancy has not been documented. In our study group, FTT and early feeding issues occurred less frequently among de novo RAI1 variant cases (3/5) compared to reported for SMS deletion cases (19/19; 100%) [26].

We identified several features that occurred more frequently in our de novo RAI1 variant cases than in previously reported cases. Infantile hypotonia was documented more often in our de novo subgroup (5/5) than previously reported (44%–61%) [3], [9], [10]. Seizures (with/without EEG abnormalities) also occurred more frequently in our de novo (4/5) group than previously reported (17%) [9], [10]. As expected, behavioral features occurred across all subgroups, reflecting syndrome-specific features that include sleep disturbance and various maladaptive and self-injurious behaviors. Interestingly, only 3/5 of our de novo RAI1 variant cases demonstrated the characteristic “self-hug”, which is more consistent with the reported rate for deletion cases (50–80%) compared to the 100% (9/9) previously reported for RAI1 mutation cases [3], [9], [10]. As expected, sleep disturbance was universal, but we also documented increased symptoms of OSA and/or T&A for our de novo (5/5) group. In addition, anxiety issues, rapid mood shifts and emotional lability were present in 5/5 of our de novo RAI1 variant group, raising future research questions concerning the role of RAI1 in neurodevelopment.

Only two clinical features (Table 4) demonstrated a significant relationship to RAI1 mRNA levels, i.e., ocular abnormalities (Mann-Whitney Z = −2.35; p = 0.0188) and object insertion (Mann-Whitney Z = −2.21; p = 0.03). Some ocular abnormalities, either strabismus (2/4), esotropia (3/4), or hyperopia (1/4), were present in all our de novo RAI1 cases; this frequency is higher than previously appreciated [9], [10]; and more consistent with common 17p11.2 deletion cases (Table 4 and Table S2). Although object insertion was significantly associated with lower RAI1 expression levels (Table 4), this behavioral feature may reflect a bias of ascertainment since it would lead to referral for RAI1 mutation analysis of suspected SMS non-deleted cases.

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Table 4. Comparison of mean RAI1 levels based on presence/absence of phenotypic features.

doi:10.1371/journal.pone.0022861.t004

While not significantly associated with RAI1 level, several clinical features (Table 4) may differentiate cases with de novo RAI1 variants from the other sub-groups. All four de novo cases tested demonstrated hearing loss in contrast to 25% (2/8) previously reported, the role of RAI1 in hearing abnormalities is unknown [3]. Since the Myosin 15A (MYO15A) gene, located in the 17p11.2 SMS critical region, was implicated as a candidate gene for the hearing abnormalities of SMS [41], it is of interest to explore MYO15A expression in SMS patients as well as the role of RAI1 in MYO15A expression. The absence of immunologic abnormalities (Table 4) in our de novo cases, versus the increased frequency reported for deletion cases (23–50%) [42], [43], suggests that a gene other than RAI1 may regulate immune involvement in SMS. The TNFRSF13B gene, located in 17p11.2, encoding the transmembrane activator and CAML interactor (TACI) protein, was proposed as a candidate for the immune abnormalities, including reduced IgA levels in SMS patients [43], [44]. The presence of a hoarse voice occurred in all our de novo cases, but was not significantly related to RAI1 expression levels. Furthermore, no apparent correlation between specific clinical features and RAI1 haplotype or polyQ repeat length (Table S1) could be identified. It is of interest to note that a spina bifida occulta (SBO) variant occurred in one de novo (M2377) and one familial (M2826) case, both with RAI1 levels <50%.

Failing to document a direct correlation between RAI1 level and most features may reflect the small sample size and/or bias introduced by features leading to referral for suspected SMS in non 17p11.2 deletion cases. It is also possible that our group categorization of subjects reflects an arbitrary designation. The familial variants were not analyzed as a discrete clinical subgroup due to the heterogeneity of their RAI1 levels. No feature(s) emerged to distinguish the two females with low mRAI1 levels (M2826, 47%; M2867, 20.7%) from others in the familial subgroup. Familial cases may be similar to non-deletion cases without RAI1 variants or, in cases where family members present with subtle overlapping symptoms, further familial analysis of RAI1 expression could shed more light on the role of the RAI1 variants. For example, our case M2900, the mother and developmentally delayed brother both showed features not observed in his cognitively normal sister (see Clinical Information S1), yet all have the same familial RAI variant. Such cases reiterate the importance of family studies to verify the inheritance of the variant. We classified M2543, who has a severe missense RAI1 variant, as ‘unclassified’ since his father was unavailable for genetic testing. Reasons to analyze the clinical and molecular findings of M2543 with the ‘de novo’ subgroup were the severity of his missense variant (Table 2) and his decreased RAI1 expression level of 60% (Figure 3, Table 4), although this level was the highest in the de novo group. On the other hand, M2543 appears to be an outlier from the de novo group for several clinical features, including short stature (<5th centile), normal BMI (non-obese), less characteristic facial appearance (See Figure 2E) with OFC at 2%, and increased level of cognitive impairment with significant speech delay.

Our clinical analysis as well as our large group of undeleted patients without detected RAI1 variants (26 patients, Table S1) indicates that other genes may be involved in the complex SMS phenotype. A future approach would be to determine RAI1 expression levels in this group of non-deleted cases as well as expression levels for other genes in the 17p11.2 critical region that have been implicated to play a role in some SMS features, including MYO15A (hearing) [41], TNFRSF13B (immune) [43], PEMT (fatty liver) [45], and ALDH3A2 (dry skin) [46]. We realize that defects in other chromosomal regions could be present in these patients, which will be pursued by whole genome array studies, as recently described for other SMS patients [47].

An ancillary dividend of this study is our analysis of the pathogenicity of RAI1 variants. It is reasonable to assume that the nonsense and frame-shift RAI1 variants would lead to nonsense-mediated decay [48]; the resulting haploinsufficiency of RAI1 could lead to the SMS phenotype, as suggested for patients with the common 17p11.2 deletion [7], [49]. However, it remains unknown how RAI1 missense mutations can underlie the SMS phenotype. Our haplotype analysis showed that de novo and familial RAI1 variants did not appear to occur on a preferred haplotype (Table S1). Our pathogenicity assessments of RAI1 missense variants (Table 2) showed that p.P242L (M2543) was predicted to be deleterious by at least 2 programs. However, before calling this variant a mutation, paternal DNA (not available to us) should be analyzed, and we therefore sub-grouped this patient as ‘unclassified’. Two previously published missense variants, p.Q156R and p.S1808N (SMS175 and SMS195 respectively [13]), were predicted to be benign or ambiguously deleterious by all 3 prediction programs (Table 2), and did not influence RAI1 nuclear localization or transcription activity [19]. This warrants further research regarding the pathogenicity of these two variants.

Most familial missense variants were predicted to be benign by at least 2 prediction programs. These predictions, in cases where the carrier parents are apparently unaffected, render these variants unlikely to be disease causing. The familial variant p.G1070R (patient M2826) was predicted to be ambiguous and deleterious. This variant was also present in the patient's mother, who had learning problems (see Clinical Information S1), and may play a role in the severe clinical phenotype of the patient and mild symptoms in her mother.

One of the three nonsynonymous RAI1 SNPs, p.E1264G (rs61746214), was predicted to be deleterious, but familial analysis showed that this variant may not be disease causing in patient M2900 (Figure 2F). The allele frequency of rs61746214 is not reported in dbSNP; we only identified this allele (of 72 analyzed) in patient M2900. Since this individual was the only Hispanic in our study, the frequency of rs61746214 should be determined in the Hispanic population.

In sum, identification of additional de novo RAI1 cases is required to further delineate phenotypic heterogeneity in this SMS subgroup. Our study adds two newly ascertained de novo RAI1 mutation cases, one unclassified case, and provides further assessment of two previously reported cases (M2377/SMS159 [14] and M2754/SMS335 [22]). As noted, early published RAI1 mutation cases may reflect a bias of ascertainment due to the striking phenotypic similarity to deletion cases, especially with respect to the physical and neurobehavioral features of the syndrome that become more evident with age. Cases suspected to have SMS, but without a 17p11.2 deletion, should prompt consideration of RAI1 mutation analysis, if their features include AGA term birth, childhood onset obesity (increased BMI for age), ocular abnormalities, hoarse voice, middle ear dysfunction and hearing loss, and behavioral aspects, especially self-injurious behavior, nail damage, and problems regulating food intake (i.e., insatiable appetite), in the absence of immunological abnormalities and cardiovascular or renal structural anomalies.

Materials and Methods

Ethics Statement

All patients were enrolled in NIH clinical protocol 01-HG-0109 approved by the National Human Genome Research Institute (NHGRI) institutional review board to evaluate the clinical and molecular manifestations of Smith-Magenis syndrome (www.clinicaltrials.gov, NCT00013559). Written informed consent was obtained from each patient or their parents. All clinical investigations were conducted according to the principles expressed in the Declaration of Helsinki.

Study Group

Since universally agreed minimum diagnostic criteria for SMS are lacking, patients were included based on the clinical impression of experienced clinicians of clustering of features (i.e., facial appearance, unusual sleep pattern, behavioral and developmental concerns) suggestive of SMS.

Clinical data for participating subjects were derived from chart review of medical records and genetic evaluations at the NIH or offsite. Descriptive statistics including weight and height percentiles and body mass index (BMI) were calculated using an on-line body surface area calculator for medication doses (http://www.halls.md/body-surface-area/bs​a.htm). For statistical analysis, growth parameters of ‘de novo’ and ‘familialRAI1 variants were compared to a common 17p11.2 SMS deletion group of 49 patients (30 female/19 male; mean age 9.6±8.4 years; range 1.4 to 49 years), also evaluated under our NIH clinical protocol.

Peripheral blood was collected from the patients and employed for extraction of genomic DNA and for Epstein Barr Virus (EBV) immortalization of B-lymphocytes, using standard protocols. Primary cultures of epidermal fibroblasts were obtained from selected patients from a forearm skin biopsy or from tissue procured from a surgical sample and cultured as previously described [50].

Cytogenetic Analysis

A subset of patients enrolled in our protocol had prior fluorescent in situ hybridization (FISH) results from studies performed by outside laboratories. For most patients without prior cytogenetic studies, we performed FISH with DNA probes specific for the RAI1 locus (RP1–253P7), as well as a distal SMS-REP (RP11–416I2) and a proximal SMS-REP (RP5–836L9) 17p11.2 probe, as described [51].

Copy Number Analysis

Genomic DNA (gDNA) of all enrolled patients was subjected to RAI1 copy number analysis by quantitative PCR (qPCR). For qPCR, TaqMan primer-probe assays targeting exon 6 of RAI1 (Hs025670777_s1) and the endogenous control gene RNaseP were purchased from Applied Biosystems (Foster City, CA). gDNA samples of SMS patients, along with control samples, were PCR-amplified in triplicate as described [52] for both assays on an ABI PRISM 7900 HT Sequence Detection System (Applied Biosystems). The comparative Ct method was used to determine the RAI1 gene copy number [52], [53], [54]. For copy number analysis by multiplex ligation-dependent probe amplification (MLPA), the P245-A2 Microdeletion Syndromes-1 kit was employed, which includes a probe for RAI1, following the manufacturer's recommendations (MLPA® MRC-Holland, Amsterdam, The Netherlands). Genescan-ROX 500 (Applied Biosystems) was added to the reaction mixtures to facilitate estimation of fragment sizes. MLPA fluorescent PCR products were separated on an ABI 3130×l genetic analyzer (Applied Biosystems). Peak height values obtained in probands were compared to those obtained in healthy controls, using GeneMarker 1.8 software (SoftGenetics, LLC, State College, PA).

RAI1 Sequence Analysis

Some patients were referred by their clinicians for commercial RAI1 sequencing of exon 3 (GeneDx, Gaithersburg, MD) and enrolled in the NIH protocol with a confirmed RAI1 mutation. DNA samples of these referred RAI1 mutated patients, as well as DNA of our NIH contingent of other enrolled non-17p11.2 deleted SMS-like patients, were subsequently analyzed for all 4 RAI1 coding exons, to accurately assess all gene variants (including SNPs). Primers were designed to amplify the 4 coding exons of RAI1, including their intronic boundaries in 22 amplicons (primer sequences available on request). Standard PCR amplification procedures were employed. All amplified products were directly sequenced using the BigDye 3 Terminator chemistry (Applied Biosystems) and separated on an ABI 3130×l genetic analyzer (Applied Biosystems). Data were evaluated using Sequencher 4.8 software (Gene Codes Corporation, Ann Arbor, MI).

Missense Variant Prediction Tools

The effect of missense variations on protein function was evaluated using the mutation prediction programs POLYPHEN, PANTHER and PMUT.

POLYPHEN.

(http://genetics.bwh.harvard.edu/pph/; POLYmorphism PHENotyping) predicts the effect of an amino acid substitution on the structure and function of a protein. POLYPHEN predictions are based on empirical rules that are applied to the sequence, as well as phylogenetic and known structural information that characterize the substitution. The Position-Specific Independent Counts (PSIC) is calculated for the two different alleles and the score for wild type and variant mapping to the known 3D structure [55].

PANTHER.

(http://www.pantherdb.org/; Protein ANalysis THrough Evolutionary Relationships) estimates the likelihood of a non-synonymous variant to cause loss of function of the protein. The output, the subPSEC (substitution position-specific evolutionary conservation), is the negative logarithm of the probability ratio of the wild-type and mutant amino acids at a particular position based on a library. This library contains over 5,000 protein families and 30,000 subfamilies, each represented by a multiple sequence alignment and Hidden Markov Model. PANTHER subPSEC scores are continuous from 0 to −10. A value of 0 is interpreted as a functionally neutral variant; the more negative the subPSEC value, the more deleterious the substitution. The cutoff value suggested is −3 [56], [57], [58].

PMUT.

(http://mmb2.pcb.ub.es:8080/PMut/) uses neural networks that have been trained with a large database of disease-associated and neutral variants to predict the impact of a given amino acid substitution. The output gives a neural network (NN) value between 0 and 1 (the higher this value, the more deleterious the variant) and a confidence value between 0 and 9 (the higher this value, the more reliable the NN) [59].

RAI1 mRNA Expression

Total RNA was isolated from patients' or control lymphoblastoid cells using the RNeasy Mini-Kit (Qiagen, Valencia, CA). RNA was subsequently treated with DNase (Applied Biosystems). RNA concentration and purity were assessed on a NanoDrop ND-1000 spectrophotometer (Thermo Fisher Scientific, Wilmington, DE). First strand cDNA was synthesized using a high capacity RNA-to-cDNA kit (Applied Biosystems). qPCR was performed utilizing two RAI1 Assays-On-Demand Taqman primer-probe assays (Applied Biosystems), Hs00430773_m1 (Assay 1; located at the RAI1 exon 2–3 boundary) and Hs01554690_m1 (Assay 2; located at the RAI1 exon 3–4 boundary), and a control assay for the β-actin housekeeping gene (Hs99999903_m1). PCR amplifications were performed on 100 ng of cDNA using TaqMan Gene Expression Master Mix reagent (Applied Biosystems) and were carried out on an ABI PRISM 7900 HT Sequence Detection System (Applied Biosystems). Results were analyzed with the comparative Ct method as described [53], [60]. All assays were performed at least three times, and each sample was measured in triplicate. Displayed values in Figure 3 represent the relative quantification (RQ) normalized to the average of all control assays in all three control cell lines (arbitrary set to 1). For verification of results with an alternative control gene (to β-actin) with a similar threshold cycle (Ct) as RAI1, a G6PC3 TaqMan assay (Hs00292720_m1) was used on selected mRNA samples (Figure S1). The average Ct for both RAI1 assay 1 and G6PC3 assays was ~34–35 cycles in lymphoblastoid mRNA.

Statistics

Data were compiled for statistical analysis using Statview. Differences between data groups were evaluated for significance using different standard statistical tests depending on the variables. For RNA expression data (Figure 3), where the number of patients/datapoints was not equal between the groups, the ANOVA post hoc Tukey-Kramer as well as the ANOVA Games-Howell tests were used. For phenotype-genotype correlations, specific tests (indicated in the text where used) included two-tailed unpaired t-test, non-parametric tests, Spearman's rank correlation coefficient (Spearman's rho). Chi-Square tests of independence were employed depending on whether the dependent variable was continuous or categorical. Given the concern for a potential outlier (M2543), the nonparametric Mann-Whitney test was used for means analysis of phenotypic features (Table 4). All data are presented as the mean ± SD (standard deviation). A p-value less than 0.05 was considered statistically significant.

Supporting Information

Clinical Information S1.

Clinical description of RAI1 de novo variants, RAI1 unclassified variant, RAI1 familial variants.

doi:10.1371/journal.pone.0022861.s001

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Figure S1.

RAI1 mRNA expression in lymphoblastoid cells with different control assays.

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Figure S2.

Results of MLPA copy number analysis on genomic DNA from all lymphoblastoid cell lines used for RAI1 expression analysis.

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Table S1.

(A) RAI1 haplotype assignments to our non 17p11.2 deleted SMS patient cohort. (B) Haplotype analysis of alleles in A.

doi:10.1371/journal.pone.0022861.s004

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Table S2.

Clinical data.

doi:10.1371/journal.pone.0022861.s005

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Acknowledgments

The NHGRI SMS Research Team gratefully acknowledges the referrals from PRISMS and genetics colleagues, including Sarah Elsea, PhD, Virginia Commonwealth University, Richmond, VA; Sherri Bale, PhD, GeneDX, Gaithersburg, MD; Emily Chen, MD and Helen Levy, MS, Kaiser Permanente, Oakland, CA; Pat Himes, MS, Kaiser Permanente, Portland OR; Meredith Wilson, MD, and David Dossetor, MD, Westmead Children's Hospital, Sydney, NSW, Australia; Livija Medne, MS, Children's Hospital of Philadelphia; and Margarita Raygada, PhD, NICHD/NIH. We also thank Ms. Roxanne Fischer, Ms. Angelica Garcia, Ms. Hailey Edwards and Ms. Jennifer Parkes for their excellent laboratory assistance.

Author Contributions

Conceived and designed the experiments: TV ACMS MH. Performed the experiments: TV JKB CC. Analyzed the data: TV CC ACMS MH. Wrote the paper: TV WAG ACMS MH. Recruited patients and performed clinical investigations of the patients: GFC CD WJI WAG ACMS.

References

  1. 1. Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, et al. (1986) Interstitial deletion of (17)(p11.2p11.2) in nine patients. Am J Med Genet 24: 393–414.
  2. 2. Stratton RF, Dobyns WB, Greenberg F, DeSana JB, Moore C, et al. (1986) Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome. Am J Med Genet 24: 421–432.
  3. 3. Edelman EA, Girirajan S, Finucane B, Patel PI, Lupski JR, et al. (2007) Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. Clin Genet 71: 540–550.
  4. 4. Potocki L, Shaw CJ, Stankiewicz P, Lupski JR (2003) Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)]. Genet Med 5: 430–434.
  5. 5. Gropman AL, Elsea S, Duncan WC Jr, Smith AC (2007) New developments in Smith-Magenis syndrome (del 17p11.2). Curr Opin Neurol 20: 125–134.
  6. 6. Greenberg F, Guzzetta V, Montes de Oca-Luna R, Magenis RE, Smith AC, et al. (1991) Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2). Am J Hum Genet 49: 1207–1218.
  7. 7. Vlangos CN, Yim DK, Elsea SH (2003) Refinement of the Smith-Magenis syndrome critical region to approximately 950 kb and assessment of 17p11.2 deletions. Are all deletions created equally? Mol Genet Metab 79: 134–141.
  8. 8. Juyal RC, Figuera LE, Hauge X, Elsea SH, Lupski JR, et al. (1996) Molecular analyses of 17p11.2 deletions in 62 Smith-Magenis syndrome patients. Am J Hum Genet 58: 998–1007.
  9. 9. Girirajan S, Vlangos CN, Szomju BB, Edelman E, Trevors CD, et al. (2006) Genotype-phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical spectrum. Genet Med 8: 417–427.
  10. 10. Elsea SH, Girirajan S (2008) Smith-Magenis syndrome. Eur J Hum Genet 16: 412–421.
  11. 11. Bi W, Saifi GM, Girirajan S, Shi X, Szomju B, et al. (2006) RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome. Am J Med Genet A 140: 2454–2463.
  12. 12. Bi W, Saifi GM, Shaw CJ, Walz K, Fonseca P, et al. (2004) Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome. Hum Genet 115: 515–524.
  13. 13. Girirajan S, Elsas LJ 2nd, Devriendt K, Elsea SH (2005) RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions. J Med Genet 42: 820–828.
  14. 14. Slager RE, Newton TL, Vlangos CN, Finucane B, Elsea SH (2003) Mutations in RAI1 associated with Smith-Magenis syndrome. Nat Genet 33: 466–468.
  15. 15. Toulouse A, Rochefort D, Roussel J, Joober R, Rouleau GA (2003) Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia. Genomics 82: 162–171.
  16. 16. Seranski P, Hoff C, Radelof U, Hennig S, Reinhardt R, et al. (2001) RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients. Gene 270: 69–76.
  17. 17. Aasland R, Gibson TJ, Stewart AF (1995) The PHD finger: implications for chromatin-mediated transcriptional regulation. Trends Biochem Sci 20: 56–59.
  18. 18. Gerber HP, Seipel K, Georgiev O, Hofferer M, Hug M, et al. (1994) Transcriptional activation modulated by homopolymeric glutamine and proline stretches. Science 263: 808–811.
  19. 19. Carmona-Mora P, Encina CA, Canales CP, Cao L, Molina J, et al. (2010) Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome. BMC Mol Biol 11: 63.
  20. 20. Imai Y, Suzuki Y, Matsui T, Tohyama M, Wanaka A, et al. (1995) Cloning of a retinoic acid-induced gene, GT1, in the embryonal carcinoma cell line P19: neuron-specific expression in the mouse brain. Brain Res Mol Brain Res 31: 1–9.
  21. 21. Girirajan S, Elsea SH (2009) Abnormal maternal behavior, altered sociability, and impaired serotonin metabolism in Rai1-transgenic mice. Mamm Genome 20: 247–255.
  22. 22. Truong HT, Dudding T, Blanchard CL, Elsea SH (2010) Frameshift mutation hotspot identified in Smith-Magenis syndrome: case report and review of literature. BMC Med Genet 11: 142.
  23. 23. Gualandi G, Giselico L, Carloni M, Palitti F, Mosesso P, et al. (2001) Enhancement of genetic instability in human B cells by Epstein-Barr virus latent infection. Mutagenesis 16: 203–208.
  24. 24. Jeon JP, Shim SM, Nam HY, Baik SY, Kim JW, et al. (2007) Copy number increase of 1p36.33 and mitochondrial genome amplification in Epstein-Barr virus-transformed lymphoblastoid cell lines. Cancer Genet Cytogenet 173: 122–130.
  25. 25. Smith ACM, Leonard AK, Gropman A, Krasnewich D (2004) Growth Assessment of Smith-Magenis Syndrome (SMS). Am Soc Hum Genetics, Toronto, Canada, Oct 2004, Poster 700.
  26. 26. Gropman AL, Duncan WC, Smith AC (2006) Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2). Pediatr Neurol 34: 337–350.
  27. 27. Smith ACM, Gropman A (2005) Smith-Magenis Syndrome. In: Cassidy S, Allanson J, editors. Clinical Management of Genetic Syndromes, 2nd Edition. Wiley-Liss, New York, NY, 2005.
  28. 28. Devriendt K, Vermeesch JR (2004) Chromosomal phenotypes and submicroscopic abnormalities. Hum Genomics 1: 126–133.
  29. 29. Stankiewicz P, Lupski JR (2010) Structural variation in the human genome and its role in disease. Annu Rev Med 61: 437–455.
  30. 30. Li L, Krantz ID, Deng Y, Genin A, Banta AB, et al. (1997) Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nat Genet 16: 243–251.
  31. 31. Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, et al. (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet 16: 235–242.
  32. 32. Petrij F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RC, et al. (1995) Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Nature 376: 348–351.
  33. 33. Ewart AK, Morris CA, Atkinson D, Jin W, Sternes K, et al. (1993) Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat Genet 5: 11–16.
  34. 34. Hirotsune S, Fleck MW, Gambello MJ, Bix GJ, Chen A, et al. (1998) Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat Genet 19: 333–339.
  35. 35. Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, et al. (1998) LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet 7: 2029–2037.
  36. 36. Su AI, Wiltshire T, Batalov S, Lapp H, Ching KA, et al. (2004) A gene atlas of the mouse and human protein-encoding transcriptomes. Proc Natl Acad Sci U S A 101: 6062–6067.
  37. 37. Wu C, Orozco C, Boyer J, Leglise M, Goodale J, et al. (2009) BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources. Genome Biol 10: R130.
  38. 38. Williams SR, Aldred MA, Der Kaloustian VM, Halal F, Gowans G, et al. (2010) Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems. Am J Hum Genet 87: 219–228.
  39. 39. Burns B, Schmidt K, Williams SR, Kim S, Girirajan S, et al. (2010) Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome. Hum Mol Genet 19: 4026–4042.
  40. 40. Yan H, Yuan W, Velculescu VE, Vogelstein B, Kinzler KW (2002) Allelic variation in human gene expression. Science 297: 1143.
  41. 41. Liburd N, Ghosh M, Riazuddin S, Naz S, Khan S, et al. (2001) Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Hum Genet 109: 535–541.
  42. 42. Greenberg F, Lewis RA, Potocki L, Glaze D, Parke J, et al. (1996) Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2). Am J Med Genet 62: 247–254.
  43. 43. Introne W, Jurinka A, Krasnwich D, Candotti F, Smith A (2005) Immunologic Abnormalities in Smith-Magenis syndrome (del 17p11.2). Am Soc Hum Genetics, Salt Lake City, Oct, 2005 Poster 605.
  44. 44. Rachid R, Castigli E, Geha RS, Bonilla FA (2006) TACI mutation in common variable immunodeficiency and IgA deficiency. Curr Allergy Asthma Rep 6: 357–362.
  45. 45. Song J, da Costa KA, Fischer LM, Kohlmeier M, Kwock L, et al. (2005) Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD). FASEB J 19: 1266–1271.
  46. 46. Rizzo WB, Carney G (2005) Sjogren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2). Hum Mutat 26: 1–10.
  47. 47. Williams SR, Girirajan S, Tegay D, Nowak N, Hatchwell E, et al. (2010) Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay. J Med Genet 47: 223–229.
  48. 48. Frischmeyer PA, Dietz HC (1999) Nonsense-mediated mRNA decay in health and disease. Hum Mol Genet 8: 1893–1900.
  49. 49. Chen KS, Manian P, Koeuth T, Potocki L, Zhao Q, et al. (1997) Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome. Nat Genet 17: 154–163.
  50. 50. Huizing M, Anikster Y, Fitzpatrick DL, Jeong AB, D'Souza M, et al. (2001) Hermansky-Pudlak syndrome type 3 in Ashkenazi Jews and other non-Puerto Rican patients with hypopigmentation and platelet storage-pool deficiency. Am J Hum Genet 69: 1022–1032.
  51. 51. Vlangos CN, Wilson M, Blancato J, Smith AC, Elsea SH (2005) Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith-Magenis syndrome should contain the RAI1 gene. Am J Med Genet A 132A: 278–282.
  52. 52. Griffin AE, Cobb BR, Anderson PD, Claassen DA, Helip-Wooley A, et al. (2005) Detection of hemizygosity in Hermansky-Pudlak syndrome by quantitative real-time PCR. Clin Genet 68: 23–30.
  53. 53. Livak K (1997) Comparative Ct method. ABI Prism 7700 Sequence Detection System.
  54. 54. Truong HT, Solaymani-Kohal S, Baker KR, Girirajan S, Williams SR, et al. (2008) Diagnosing Smith-Magenis syndrome and duplication 17p11.2 syndrome by RAI1 gene copy number variation using quantitative real-time PCR. Genet Test 12: 67–73.
  55. 55. Ramensky V, Bork P, Sunyaev S (2002) Human non-synonymous SNPs: server and survey. Nucleic Acids Res 30: 3894–3900.
  56. 56. Thomas PD, Campbell MJ, Kejariwal A, Mi H, Karlak B, et al. (2003) PANTHER: a library of protein families and subfamilies indexed by function. Genome Res 13: 2129–2141.
  57. 57. Thomas PD, Kejariwal A (2004) Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects. Proc Natl Acad Sci U S A 101: 15398–15403.
  58. 58. Thomas PD, Kejariwal A, Guo N, Mi H, Campbell MJ, et al. (2006) Applications for protein sequence-function evolution data: mRNA/protein expression analysis and coding SNP scoring tools. Nucleic Acids Res 34: W645–650.
  59. 59. Ferrer-Costa C, Gelpi JL, Zamakola L, Parraga I, de la Cruz X, et al. (2005) PMUT: a web-based tool for the annotation of pathological mutations on proteins. Bioinformatics 21: 3176–3178.
  60. 60. Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods 25: 402–408.