Beckwith–wiedemann syndrome caused by maternally inherited mutation of an oct-binding motif in the igf2/h19-imprinting control region, icr1

ABSTRACT The imprinted expression of the _IGF2_ and _H19_ genes is controlled by the imprinting control region 1 (ICR1) located at chromosome 11p15.5. DNA methylation defects involving ICR1

result in two growth disorders with opposite phenotypes: an overgrowth disorder, the Beckwith–Wiedemann syndrome (maternal ICR1 hypermethylation in 10% of BWS cases) and a growth retardation

disorder, the Silver–Russell syndrome (paternal ICR1 loss of methylation in 60% of SRS cases). In familial BWS, hypermethylation of ICR1 has been found in association with microdeletion of

repetitive DNA motifs within ICR1 that bind the zinc finger protein CTCF; but more recently, ICR1 point mutations were described in BWS pedigrees. We present a case report of two brothers

with BWS and prolonged post-pubertal growth resulting in very large stature. A maternally inherited point mutation was identified in ICR1 in both brothers, which altered binding of OCT

transcription factors. The same mutation was present on the paternally inherited allele of their unaffected mother. This is a second report of a point mutation causing ICR1 hypermethylation

by altering an OCT-binding motif. The atypical growth phenotype of the brothers may be connected to the unusual underlying cause of their BWS. SIMILAR CONTENT BEING VIEWED BY OTHERS

IDENTIFICATION OF RESPONSIBLE SEQUENCES WHICH MUTATIONS CAUSE MATERNAL _H19_-ICR HYPERMETHYLATION WITH BECKWITH–WIEDEMANN SYNDROME-LIKE OVERGROWTH Article Open access 02 December 2024 A

PATERNALLY INHERITED 1.4 KB DELETION OF THE 11P15.5 IMPRINTING CENTER 2 IS ASSOCIATED WITH A MILD FAMILIAL SILVER–RUSSELL SYNDROME PHENOTYPE Article 11 November 2020 IMPRINTING DISORDERS

Article 29 June 2023 INTRODUCTION Human chromosome 11p15 contains two clusters of imprinted genes that are critical regulators of early human growth, each expressed under the control of an

imprinting control region (ICR). Genetic and epigenetic mutations of these genes cause Beckwith–Wiedemann syndrome (BWS: OMIM 130650), an overgrowth disorder, or Silver–Russell syndrome

(SRS: OMIM 180860), which is characterised by growth restriction. Clinical features of BWS include prenatal overgrowth, macroglossia, abdominal wall abnormalities, ear pits and creases,

organomegaly, neonatal hypoglycaemia and elevated tumour risk.1 Molecular abnormalities associated with BWS include: paternal uniparental disomy (20–25%), numerical and chromosomal

abnormalities of chr11p15 (<1%), hypomethylation of ICR2 (60% of cases), maternally inherited mutation of CDKN1C (5%) and hypermethylation of ICR1 (10% of cases).1 ICR1 directs parent of

origin-specific expression of insulin-like growth factor 2 (IGF2). IGF2 is normally expressed only from the paternal allele, while the untranslated _H19_ gene is expressed from the maternal

allele. Differential methylation of ICR1 (normally on the paternal allele) mediates differential binding of CTCF and formation of chromatin structures supporting expression of either H19 or

IGF2, but not both, under control of distant enhancer sequences (reviewed in Ideraabdullah _et al_2). CTCF binds to tandem repeat elements in ICR1, and maternally inherited deletion of

CTCF-binding elements is associated with hypermethylation of ICR1 and BWS, though in paternal inheritance there is no phenotypic effect.3, 4, 5, 6 We recently described BWS pedigrees with

novel deletions/mutations involving binding sites other than CTCF-binding sites, and in particular binding sites for the OCT4 and SOX2 pluripotency factors, including a point mutation in an

OCT4-binding site.6 In this study, we report another BWS family with a point mutation affecting an OCT-binding DNA sequence. CASE REPORT Case 1 (Figure 1a) was born to non-consanguineous

parents following natural conception. _In utero_ he was noted to have bilateral large kidneys and his term birth weight was 5600 g (>99th centile). He had macroglossia, undescended

testes, a minor right-sided ear anomaly with bifid tragus and diastasis recti, and documented episodes of neonatal hypoglycaemia. He had feeding difficulties initially and repeated mild

infections. Ultrasound kidney scans revealed unilateral cysts but with no evidence of change into adulthood. His tongue was surgically reduced at 5 years. His development was relatively

normal with normal early milestones (sat at 9 months and walked before a year). He was diagnosed with ADHD at school, and although he attended a normal school he finished schooling at the

age of 15 years without formal qualifications. Age of puberty was normal. Aged 24 years, endocrine tests revealed random GH 5 U/l, IGF1 19.4 nM, IGF2 63.6 nM, IGF1/IGF2 ratio 3.3 (<10)

and normal glucose tolerance. At 24 years, his height of 204 cm, weight of 119.6 kg and head circumference of 58.2 cm were all ≫99th centile for age. His height was proportionate and his

span length 211.5 cm. He had prominent supraorbital ridges and a large mouth, but no ear abnormalities other than the bifid right tragus. He had large hands and feet with deepset ingrowing

toenails of the halices. Joint movement was not restricted. The rest of the examination was normal with no evidence of asymmetry and a normal neurological examination. Case 2 (Figure 1a) is

the younger brother of case 1. He was born at term following normal conception and an uneventful pregnancy with a birth weight of 6270 g (≫99th centile). Like his brother he had macroglossia

requiring surgical correction, undescended testes, diastasis recti and documented neonatal hypoglycaemia. At 14 months he was found to have mild spasticity of both lower limbs and later

required surgical release of a tight left Achilles tendon. By 6 years, mild left sided hemiparesis was apparent, and brain MRI showed a right-sided infarct of perinatal origin. He also has a

mild right-sided hemihypertrophy with a leg length discrepancy of 0.5 cm. Routine renal scanning at 14 months identified a right-sided Stage I Wilms' tumour, which was treated with

nephrectomy and chemotherapy. He needed a special educational statement, which was described as having poor concentration and lethargy, and after education at normal school with additional

help left without formal qualifications. He has generalised joint hypermobility and significantly restricted mobility owing to a severe planovalgus deformity of the left ankle. Puberty was

delayed and now at 22 years he has minimal body hair. Current height is 208 cm and weight 139.7 kg. The mother and father of both the boys were born with normal birth weights and final

heights of 163 and 183 cm, respectively. Neither had any features of Beckwith–Wiedemann syndrome. MOLECULAR STUDIES Methylation analysis of H19 and IGF2P0 was performed by

methylation-specific PCR (MSP) and pyrosequencing as described.7 H19 and IGF2P0 interrogated methylation of cytosines by MSP of the amplicons chr11:1975598-1981477 and chr11:2,126,061-2,126

and 227, while pyrosequencing amplicons spanned chr11:1977650-1977877 and chr11:2,125,904-2,126 and 158, respectively (sequence build NCBI36/hg18); further details are available on request.

Methylation-specific MLPA was performed using kit ME-030 v1 (MRC-Holland, Amsterdam, The Netherlands) according to the manufacturer's instructions. Microsatellite analysis of chr11p15

was performed by standard methods. Array analysis utilised a highly tiled aCGH array as described.8 Long-range PCR of H19 was performed as described.5 The H19 ICR and proximal promoter

(HG18:chr11:1976978-1981258) were sequenced by standard methods from a single amplicon of 4281 bp; further details are available on request. For some experiments, 200 ng genomic DNA was

cleaved using restriction enzyme _BstUI_ (New England Biolabs, Ipswich, MA, USA) following the manufacturer's instructions; then DNA was desalted and concentrated using Amicon 30 K

microconcentrator columns (Millipore, Billerica, MA, USA) before amplification and sequencing. Electrophoretic mobility shift assay was carried out as described.6 Briefly, radiolabelled

double-stranded probes were incubated with nuclear extracts from mouse ES cells or from 293FT cells overexpressing human OCT4 and SOX2 proteins, in the presence of wild-type

(5′-CTCAAACCTGCACTGAATGGGAATGTTAATGTCTGGCCACTTAAGATTG-3′) or mutated (5′-CTCAAACCTGCACTGAATGGGAATGTTCA TGTCTGGCCACTTAAGATTG-3′) probes as indicated. Reaction mixtures were resolved on

non-denaturing 4% polyacrylamide gel and exposed on film. MOLECULAR RESULTS Molecular testing of blood DNA in probands 1 and 2 indicated ICR1 hypermethylation: methylation-specific PCR of

ICR1 gave methylation indices of 0.23 and 0.27, respectively, while MS-MLPA gave methylation indices 0.33 and 0.32, and methylation at the KCNQ1OT1 promoter was normal (data not shown).

These results were confirmed by pyrosequencing of ICR1 and IGF2P0 (Figure 1b). Methylation of maternal DNA was normal, and paternal DNA was not available. The presence of ICR1

hypermethylation in both probands suggested an underlying genetic anomaly. Microsatellite analysis showed that both brothers inherited identical alleles from both parents around ICR1 (Figure

1c), but showed no evidence of allelic imbalance. MS-MLPA revealed no copy number change at 11p15. Long-range PCR of ICR1 showed no evidence of microdeletions (data not shown). Tiling

array-CGH using a highly tiled array spanning the entire imprinted region on 11p15 revealed no copy number change of any kind (data not shown). Sanger sequencing of the H19 ICR and proximal

promoter revealed a single sequence change: NCBI36:11:g.[1979624A>C]+[=], in both probands and their unaffected mother (Figure 1e). The variant was not found in published databases of

sequence variation, nor in 100 normal control samples. To determine the parental origin of the polymorphism, genomic DNA was digested with the methylation-sensitive restriction enzyme

_Bst_UI, which would be expected to cleave the unmethylated maternal allele of ICR1. As predicted, in both probands both alleles were detectable after restiction digest, as both alleles were

methylated. However, in maternal DNA the wild-type allele was undetectable after restriction digest (Figure 1e), indicating that the variant was present on the paternal allele and would be

without effect on ICR1. The sequence change is 29 nucleotides from a mutation recently reported in a BWS pedigree (Family 1, Demars _et al_6). Both variants lie within the A2 repeat of ICR1

and are predicted to alter binding sites for OCT transcription factors. The functional significance of this variant was tested by the electrophoretic mobility shift assay (EMSA; Figure 1e).

With mouse ES cell nuclear extracts the 32P-labelled wild-type probe formed two complexes, whereas only one complex was observed with the 32P-labelled mutated probe. When using cell lysate

overexpressing human OCT4 and SOX2 proteins, one complex was identified with both the 32P-labelled wild-type and mutated probes, but the complex obtained with the mutated probe was retarded

on the gel. Moreover, the complex obtained with the 32P-labelled wild-type probe was more efficiently competed by an excess of cold wild type than an excess of cold-mutated probe. These data

demonstrate that the variant nucleotide alters the binding of nuclear factors, most likely OCT4. Taken together, with its parental origin, this strongly suggests that the variant is the

mutation causing BWS in the two probands. We sequenced DNA from nine other individuals with BWS and H19 hypermethylation, all apparently sporadic, and found no evidence of this mutation or

any other novel variant in the H19 ICR or promoter (data not shown). DISCUSSION Although recombinative deletions of B-type repeats in ICR1 have been identified in several BWS pedigrees,3, 4,

5, 6 and in apparently sporadic Wilms' tumours,9 the group of Gicquel were the first to describe a mutation in a pluripotency factor-binding site.6 Interestingly, the point mutation in

our pedigree, like that described by Demars _et al_,6 disrupted a conserved OCT-binding motif within repeat A2 of ICR1. In a mouse model, A-type motifs binding OCT family proteins were

involved in maintaining the unmethylated status of the neighbouring B-type repeats.10 Because this function is required only on the maternally inherited allele, neither brother is at the

risk of transmitting BWS to his offspring, and inheritance by subsequent generations can be monitored molecularly. Therefore, the provision of a concrete molecular diagnosis provides

reassurance to the family. ICR1 hypermethylation accounts for ∼10% of BWS cases.1 Approximately 20% of these have genetic defects, including ICR1 deletions and OCT or SOX binding site

mutations or deletions. In all, ∼50% of patients with maternally transmitted ICR1 mutations have an apparently sporadic presentation with no family history of BWS. In this study we found no

mutations in ICR1 or the H19 promoter among nine patients with apparently sporadic H19 hypermethylation. More extensive sequencing may identify cis-acting mutations outside the regions

already examined. Alternatively, as suggested by the studies of Riccio and co-workers,5 ICR1 hypermethylation may arise from a stochastic error in the binding of regulatory proteins during

the earliest cell divisions of the embryo. This suggestion receives some support from the observation that even inherited mutations in H19 do not cause universal somatic hypermethylation,

but partial hypermethylation. Either these mutations do not inevitably cause methylation errors in all affected cells, or universal somatic hypermethylation of H19 is incompatible with life,

such that the only individuals seen with this disorder are necessarily those with partial rescue from the mutant epigenotype. The two siblings in this pedigree showed many of the cardinal

features of BWS: prenatal overgrowth, macroglossia, neonatal hypoglycaemia, ear dysmorphism, Wilms' tumour and asymmetry. Interestingly, the siblings continued to grow into their

twenties, whereas most individuals with BWS show rapid growth in early childhood but decelerating growth in the teens. The height of both probands is >99th centile while adult height in

BWS is typically at the upper range of normal.11 Identification of similar cases will help determine whether this atypical growth is particularly related to the genotype. Genetic counselling

is increasingly complex for BWS, and this case report illustrates the importance of considering a genetic cause for an epigenetic aberration when giving recurrence risks. In summary, this

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Washington, 1993 (http://www.ncbi.nlm.nih.gov/sites/GeneTests/review?db=GeneTests). Google Scholar  Download references ACKNOWLEDGEMENTS This study was funded by the Newlife Foundation for

Disabled Children. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Faculty of Medicine, University of Southampton, Southampton, UK Rebecca L Poole, Donald J Leith, Louise E Docherty, I Karen

Temple & Deborah J G Mackay * Wessex Genetics Service, Southampton University Hospitals Trust, Southampton, UK and Salisbury Hospital NHS Foundation Trust, Salisbury, UK Rebecca L Poole,

 Donald J Leith, Louise E Docherty, I Karen Temple & Deborah J G Mackay * Epigenetics in Human Health and Disease Laboratory, Baker IDI Heart and Diabetes Institute, Melbourne, Victoria,

Australia Mansur E Shmela & Christine Gicquel * Northern Genetics Service, Institute of Human Genetics, International Centre for Life, Newcastle upon Tyne, UK Miranda Splitt Authors *

Rebecca L Poole View author publications You can also search for this author inPubMed Google Scholar * Donald J Leith View author publications You can also search for this author inPubMed 

Google Scholar * Louise E Docherty View author publications You can also search for this author inPubMed Google Scholar * Mansur E Shmela View author publications You can also search for

this author inPubMed Google Scholar * Christine Gicquel View author publications You can also search for this author inPubMed Google Scholar * Miranda Splitt View author publications You can

also search for this author inPubMed Google Scholar * I Karen Temple View author publications You can also search for this author inPubMed Google Scholar * Deborah J G Mackay View author

publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Deborah J G Mackay. ETHICS DECLARATIONS COMPETING INTERESTS The authors

declare no conflict of interest. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Poole, R., Leith, D., Docherty, L. _et al._ Beckwith–Wiedemann syndrome

caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1. _Eur J Hum Genet_ 20, 240–243 (2012). https://doi.org/10.1038/ejhg.2011.166

Download citation * Received: 01 March 2011 * Revised: 03 June 2011 * Accepted: 28 June 2011 * Published: 24 August 2011 * Issue Date: February 2012 * DOI:

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currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative KEYWORDS * Beckwith–Wiedemann syndrome * IGF2/H19 ICR1 *

OCT-binding site * DNA methylation * imprinting disorder