The SNORD116 locus lies in the 15q11-13 region of paternally expressed genes implicated in Prader–Willi Syndrome (PWS), a complex disease accompanied by obesity and severe neurobehavioural disturbances. Cases of PWS patients with a deletion encompassing the SNORD116 gene cluster, but preserving the expression of flanking genes, have been described. We report a 23-year-old woman who presented clinical criteria of PWS, including the behavioural and nutritional features, obesity, developmental delay and endocrine dysfunctions with hyperghrelinemia. We found a paternally transmitted highly restricted deletion of the SNORD116 gene cluster, the shortest described to date (118 kb). This deletion was also present in the father. This finding in a human case strongly supports the current hypothesis that lack of the paternal SNORD116 gene cluster has a determinant role in the pathogenesis of PWS. Moreover, targeted analysis of the SNORD116 gene cluster, complementary to SNRPN methylation analysis, should be carried out in subjects with a phenotype suggestive of PWS.
Prader–Willi Syndrome (PWS) is a neurodevelopmental disorder caused by the lack of expression of paternal alleles in 15q11-13.1, 2 The PWS phenotype includes neonatal hypotonia, early hyperphagia, morbid obesity, short stature, hypogonadism, cognitive impairment, and behavioural and psychiatric problems. Molecular mechanisms including large deletions, maternal uniparental disomy or imprinting defects explain 98% of cases which are easily diagnosed with a SNRPN methylation analysis. The study of rare cases resulting from reciprocal translocations and atypical 15q11q12 microdeletions without methylation abnormalities has defined a critical region containing the functional PWS gene locus.3 This minimal region contains several snoRNAs gene clusters including SNORD116 and SNORD115. Mice lacking the SNORD116 orthologue display a partial PWS phenotype.4, 5 However, so far, all reported clinical cases of limited deletion of the SNORD116 cluster associated with PWS have also involved adjacent genes: SNURF-SNRPN or SNORD115.6, 7, 8, 9 We report the first case of a patient with the highly typical features of PWS who presented a restricted deletion of the SNORD116 region which did not affect the expression of SNURF-SNRPN and did not delete any portion of the SNORD115 locus.
A girl was born after 35 weeks gestation with appropriate weight (2780 g), length (48 cm) and cranial perimeter (35 cm). Because of severe neonatal hypotonia and poor suck, she required exclusive tube feeding during the first 2 weeks of life and hospital care for 1 month. She had mild developmental delay and walked at 18 months. She had an orthoptic treatment for a strabism. Excessive aggressiveness and stubbornness were observed at 30 months. She displayed poor abstraction skills and difficulties in coping with stress and frustrations, with frequent temper tantrums. She gained excessive weight after 18 months and became obese by the age of 3 (Supplementary Figure 1Sa). Strict control of food access allowed BMI stabilisation until the age of 12. She presented frequent skin picking. Growth hormone deficiency (GHD) was diagnosed at age 9 years with low IGF-1 level (Table 1), but GH treatment was not indicated as her height was above −2 SDS. GHD was again documented at age 12 years; GH treatment was started and discontinued after 6 months by the parents. L-thyroxin was given from age 10 to 13 years due to central hypothyroidism. At age 12, the GnRH test suggested central hypogonadism. At age 16, incomplete pubertal development with no menarche required substitution with oestrogen and progesterone. The patient did not accept to perform an IQ test; however, she had a mild impairment of cognitive functions. Nevertheless she remained in mainstream education until secondary school. Adult height was −1.5 SDS (Supplementary Figure 1Sb).
The patient was 23 when admitted to our PWS reference centre. Her phenotype suggested PWS with morphologic features (narrow forehead, thin and down-turned upper lip, hypopigmented skin, acromicria) (Figure 1). She had thick saliva and presented skin picking (visible in Figure 1). Abnormal sleep-wakefulness scoring and excessive daytime sleepiness were noted with an apnea-hypopnea index score of 3 per hour, a mild level. She had hyperphagia, temper tantrums and difficulties in organisation of daily life. Strict control of food access had allowed stabilisation of BMI at 31 kg/m2 (Supplementary Figure 1Sa). GHD with low IGF-1, hypogonadism and hyperghrelinemia10 were documented (Table 1). The mother (height 168 cm, weight 55 kg, BMI 19.5 kg/m2) had a history of four miscarriages associated with positive anti-nuclear antibodies. The father (height 168 cm, weight 80 kg, BMI 28.3 kg/m2) was healthy; his brother and his parents, deceased, were otherwise asymptomatic. The couple previously had a preterm baby girl who died at the fourth day of life with severe hypotonia.
All subjects agreed to participate and gave their signed informed consent for genetic testing. Methods are described in Supplementary Methods.
Methyl-specific PCR at the SNURF-SNRPN locus was normal in the proband. As the phenotype was highly suggestive of PWS (Figure 1), we performed quantitative multiplex PCR of short fluorescent fragments (QMPSF) analysis of 15q11q12 in order to detect atypical deletions in the 15q11.2 region (Figure 2a). Analysis of fragments revealed 50% reduction of a unique marker consistent with a heterozygous deletion in the SNORD116 region (Supplementary Figure 2S). We determined the boundaries of the deletion using specifically designed 15q oligonucleotide-based array comparative genomic hybridisation (array-CGH). We found negative hybridisation of 333 SNP probes encompassing a segment of 116.5 kb (Figure 2b). PCR analysis and sequencing identified breakpoints at positions g.25257217 and g.25375376 based on the UCSC hg19 genome assembly (size of the deletion: 118 159 bp). Two perfectly homologous six-bp short sequences flanked the deleted region, suggesting a breakage mechanism by microhomology-mediated end joining (Figure 2c). The paternal origin of the deletion was demonstrated by a PCR assay directed to the breakpoint regions (Figure 2d). The deletion encompassed the SNORD109A gene, the complete SNORD116 cluster 1–29 and the four non-coding exons of the IPW transcript (Figure 2a). Expression of SNRPN and SNORD116 transcripts was studied by RT-PCR in lymphocytes and fibroblasts from the proband and her parents (Figures 2e and f). SNRPN was normally expressed (Figure 2e). Conversely, SNORD116 expression was detected in both parents but was absent in the proband (Figure 2f). From RT-quantitative PCR analysis in fibroblasts, the expression of SNRPN and NECDIN genes was abolished in patients with a type 1 PWS deletion,2 but did not differ between control subjects and the proband (Supplementary Figure 4S). The genotype and phenotype data of the proband were deposited with the online DECIPHER database (http://decipher.sanger.ac.uk, patient ID: 285216).
The proband presented the complete phenotype that is characteristic of PWS, including neonatal hypotonia, endocrine phenotype with GHD, central hypothyroidism, hypogonadism and hyperghrelinemia, and cognitive and behavioural impairment.1, 10, 11, 12 Obesity was not extreme due to the strict control of food access, but she clearly displayed hyperphagia and deficit of satiety. Overall, hyperphagia and behavioural problems are milder than generally observed in patients with PWS but typical.
We report the shortest, paternally transmitted, deletion of the SNORD116 region that has been described to date, associated with a clear PWS phenotype. SNORD109A and IPW were also deleted in the proband. Their role has never been highlighted in PWS pathophysiology.2 Moreover, we found that SNORD116 expression was fully abolished in lymphocytes and fibroblasts of this patient (Figures 2e and f). The father carried the deletion and because he was asymptomatic, it was strongly assumed that the deletion is located on his maternal allele. Supporting this assumption, RT-PCR analysis of his lymphocytes showed normal expression of SNORD116 (Figure 2e). The study of the maternal parent of the father would provide the definitive answer. Unfortunately, both the parents of the father were deceased and no material was available to test this hypothesis (Supplementary Figure 3S). Comparison of demonstrative cases of PWS-like cases with short deletions of the minimal functional PWS gene locus including the SNORD116 region6, 7, 8 shows that the phenotypes are very similar (Supplementary Table 1S). Nevertheless, in the proband, SNORD107, SNORD64, SNORD108, SNORD109B and, more importantly, SNURF-SNRPN and the SNORD115 cluster were not deleted (Figure 2a). In all previously described cases, at least one of these genes was preserved. Of note, deletions encompassing SNURF-SNRPN may result in atypical PWS phenotype.13 While the SNORD115 region is genetically intact, its expression could be affected by the absence of the SNORD116 gene cluster or hypothetical regulatory elements in the surrounding region. SNORD115 expression in normal subjects has been shown to be present in neuronal cells and absent in peripheral tissues.14 However, de Smith et al8 using RT-PCR found an expression of SNORD115 in the lymphocyte-derived RNA of a SNORD116 microdeletion PWS patient while it is undetectable in his normal father. The expression of SNORD115 (analysed by RT-PCR and microarrays) was found undetectable in the skin fibroblasts and lymphocytes of both the proband and the normal control (data not shown). These results do not rule out the possibility that the neuronal expression of SNORD115 might be altered in our proband, but this hypothesis is impossible to verify in our living patient. Nevertheless, we can argue that the deletion of SNORD116 gene cluster is highly contributive to generate PWS phenotype as observed in the proband. In agreement, the SNORD116 cluster expressed in the hypothalamus seems to be regulated developmentally, playing a role in the maturation of feeding circuits.15 Knockout mice with deletion of SNORD116 display hyperphagia.5 This finding is also in accordance with the recent data demonstrating the regulatory role of GC skew repeat elements or long non-coding RNA (116HG) derived from the SNORD116 region.14, 16
This case therefore strengthens an evidence for the role of the SNORD116 region that has recently been highlighted in the molecular pathophysiology of PWS,6, 7, 8 either as fully processed box C/D snoRNA species or as long non-coding host transcripts (116HG).16, 17, 18, 19
Next step will be to investigate the functions of these RNAs and their role in the pathogenesis of PWS. More distant genes potentially implicated in PWS syndrome as NDN and MAGEL2,2 which were not deleted, were normally expressed in the fibroblasts of the proband (Supplementary Figure 4Sb). Recently, truncating mutations of MAGEL2 were also associated with PWS.20 The discussion regarding expression of SNORD115 by non-neuronal cells can be applied to MAGEL2. Therefore, like for SNORD115, MAGEL2 expression could not be tested here. As for SNORD115, it cannot be excluded that lack of SNORD116 cluster acts as a host gene to modify MAGEL2 expression.
Altogether, the present case suggests that the SNORD116 is an aetiological factor in PWS. Targeted analysis of the SNORD116 cluster by array-CGH or qPCR should be performed in patients with PW-like features in whom the diagnosis was not confirmed by more conventional cytogenetic methods and DNA methylation analysis.
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We thank the patient and her family. SE was the recipient of a grant from Pfizer (grant 08766A10). This work was part of the National Programme for Clinical Research from the French government (PHRC) (grant 0811601) and the Clinical Research Programme of Midi Pyrénées (grant 09004797). We thank Sandoz France and Ipsen France for financial support.
The authors declare no conflict of interest.
Supplementary Information accompanies this paper on European Journal of Human Genetics website
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Bieth, E., Eddiry, S., Gaston, V. et al. Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome. Eur J Hum Genet 23, 252–255 (2015). https://doi.org/10.1038/ejhg.2014.103
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