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Osteopoikilosis and multiple exostoses caused by novel mutations in LEMD3 and EXT1 genes respectively - coincidence within one family
- Sevjidmaa Baasanjav†1, 6,
- Aleksander Jamsheer†2, 3,
- Mateusz Kolanczyk†1, 4Email author,
- Denise Horn1,
- Tomasz Latos5,
- Katrin Hoffmann1, 4,
- Anna Latos-Bielenska2, 3 and
- Stefan Mundlos1, 4
© Baasanjav et al; licensee BioMed Central Ltd. 2010
Received: 20 January 2010
Accepted: 9 July 2010
Published: 9 July 2010
Osteopoikilosis is a rare autosomal dominant genetic disorder, characterised by the occurrence of the hyperostotic spots preferentially localized in the epiphyses and metaphyses of the long bones, and in the carpal and tarsal bones . Heterozygous LEMD3 gene mutations were shown to be the primary cause of the disease . Association of the primarily asymptomatic osteopokilosis with connective tissue nevi of the skin is categorized as Buschke-Ollendorff syndrome (BOS) . Additionally, osteopoikilosis can coincide with melorheostosis (MRO), a more severe bone disease characterised by the ectopic bone formation on the periosteal and endosteal surface of the long bones [4–6]. However, not all MRO affected individuals carry germ-line LEMD3 mutations . Thus, the genetic cause of MRO remains unknown. Here we describe a familial case of osteopoikilosis in which a novel heterozygous LEMD3 mutation coincides with a novel mutation in EXT1, a gene involved in aetiology of multiple exostosis syndrome. The patients affected with both LEMD3 and EXT1 gene mutations displayed typical features of the osteopoikilosis. There were no additional skeletal manifestations detected however, various non-skeletal pathologies coincided in this group.
We investigated LEMD3 and EXT1 in the three-generation family from Poland, with 5 patients affected with osteopoikilosis and one child affected with multiple exostoses.
We found a novel c.2203C > T (p.R735X) mutation in exon 9 of LEMD3, resulting in a premature stop codon at amino acid position 735. The mutation co-segregates with the osteopoikilosis phenotype and was not found in 200 ethnically matched controls. Another new substitution G > A was found in EXT1 gene at position 1732 (cDNA) in Exon 9 (p.A578T) in three out of five osteopoikilosis affected family members. Evolutionary conservation of the affected amino acid suggested possible functional relevance, however no additional skeletal manifestations were observed other then those specific for osteopoikilosis. Finally in one member of the family we found a splice site mutation in the EXT1 gene intron 5 (IVS5-2 A > G) resulting in the deletion of 9 bp of cDNA encoding three evolutionarily conserved amino acid residues. This child patient suffered from a severe form of exostoses, thus a causal relationship can be postulated.
We identified a new mutation in LEMD3 gene, accounting for the familial case of osteopoikilosis. In the same family we identified two novel EXT1 gene mutations. One of them A598T co-incided with the LEMD3 mutation. Co-incidence of LEMD3 and EXT1 gene mutations was not associated with a more severe skeletal phenotype in those patients.
Osteopoikilosis is a rare and primarily benign autosomal dominant genetic entity caused by heterozygous mutations in the LEMD3 gene. It is characterised by the occurrence of the hyperostotic spots throughout the skeleton, with most frequent localization in the epiphyses and metaphyses of the long bones, as well as in the carpal and tarsal bones . The clinical features of osteopoikilosis are relatively mild, therefore the condition is usually diagnosed by chance or because of the association with other medical problems (fractures, joint dislocations, etc.). In addition to spotty bone changes, some patients affected by osteopoikilosis develop the superficial skin lesions (elastic-type nevi) and/or subcutaneous foci of dermatofibrosis. Such combination of clinical features is categorized as a separate condition named the Buschke-Ollendorff syndrome . Osteopoikilosis has also been found in association with a more severe and detrimental bone disease called melorheostosis. Melorheostosis manifests with predominantly asymmetric depositions of dense compact bone on the periosteal and endosteal surface of the long bones, resembling a dripping wax of a candle. Bone deformations are often associated with the ossification of the soft tissue in the joint proximity, which can cause compression of the adjacent nerves, and result in pain. Heterozygous LEMD3 gene mutations were detected in all such cases. In contrast, no germline LEMD3 mutations were found in the isolated cases of melorheostosis [7, 8]. Thus, genetic cause of isolated melorheostosis remains unknown. Melorheostosis belongs to a group of osteogenic lesions together with another disease called hereditary multiple exostoses (HME) . Multiple exostoses (enchondromas) are caused by heterozygous mutations in EXT1, EXT2 and/or EXT3 genes. The EXT proteins function in the proteoglycan synthesis and play tumour suppressor roles. EXT1 and EXT2 have both been shown to encode a heparan sulphate polymerase with both D-glucuronyl (GlcA) and N-acetyl-D-glycosaminoglycan (GlcNAC) transferase activities and their functions are indispensable for heparin-sulphate biosynthesis . The nature of the tumour suppressor effects of the heparan sulphate biosynthesis is not entirely clear, however the regulation of Ihh signalling was proposed to play an important role . Here we describe a family with 5 patients affected by osteopoikilosis caused by novel mutation in the LEMD3 gene. Interestingly, three of the patients affected with this new LEMD3 mutation additionally carry a new mutation in the EXT1 gene. We discuss possible implications.
We studied a two-branch family of Polish descent. The main branch comprised three generations with five individuals affected by osteopoikilosis. We also examined a more distant kindred affected by the severe deformational condition of the long bones. The local ethics committee approved the study and written, informed consent was obtained from all participants or their legal guardians for publication of this case report, including clinical data, pedigree and X-ray images. Copies of all written consents are available for review on request.
Sequences of the primers used for LEMD3 and EXT1 gene amplification and sequencing.
F Primer sequence 5'- 3'
R Primer sequence 5' - 3'
Sequences of the primers used for EXT1 cDNA amplification and sequencing.
F Primer sequence 5'- 3'
R Primer sequence 5' - 3'
Isolation of the primary osteoblast cells
Surgically removed exostosis was placed in alphaMEM medium supplemented with 10% FCS, Penicilin-Streptomycin and Glutamine and transported to laboratory within 24 h. Bone was cleaned of any remaining connective tissue and 3 rounds of collagenase IV (2 mg/ml) digest 1× 5 min. and 2× 20 min. each at 37°C were performed. Cells from the first digestion were discarded whereas second and third digests were pooled and seeded in the alpha-MEM medium. Cells were cultured till confluent.
RNA isolation and cDNA synthesis
Total RNA was isolated with peqGOLD TriFast™ reagent (PeqLab) according to supplied protocol. cDNAs were synthesised from 1 μg total RNAs with SuperscriptII (Invitrogen) according to manufacturer's guidelines.
Clinical symptoms identified in the patients presenting with osteopoikilosis.
(female; 26 years)
(female; 24 years)
(male; 60 years)
(female; 54 years)
(male; 19 years)
EXT1 mutation status
Painful hands and feet
Additional skin changes
TOF, Ovarian cyst
Laboratory tests (Ca, P, AP, ACP)
We also consulted a more distant relative of this family (V:1), who was independently referred to a clinical geneticist at the age of 7 years. X-ray examination showed large multiple exostoses predominantly localized in the ends of the long bones (Figure 2). The boy was operated at the age of 7 years for a large exostosis affecting proximal part of the right humerus. Histopathological examination of the removed bone was suggestive of enchondromatosis.
A different mutation in EXT1 gene was identified in the patient (V:1), diagnosed with multiple exostoses syndrome. The patient carried a heterozygotic splice site mutation in intron 5 (IVS5-2 A > G), as detected in blood lymphocytes and primary osteoblast progenitor cells obtained from the surgically removed exostoses. Sequencing of the exostoses derived cDNA (obtained from the cells isolated from the affected bone) showed that splice site mutation resulted in the in-frame deletion of 9 bp of the exon 5 leading to a deletion of three amino acids (pos. 429-431 - two conserved isoleucin residues and a conserved glutamic acid residue) (Figure 3B). Functional relevance of the deleted amino acids was predicted based on their evolutionary conservation.
We identified a family with five members affected by osteopoikilosis caused by a novel nonsense heterozygous mutation (p.R735X) localised in exon 9 of the LEMD3 gene. In other branch of this family we identified a boy affected by more severe bone deformations. The boy was initially suspected of the melorheostosis, but upon X-ray examination, the diagnosis was corrected to the multiple exostoses syndrome. Clinical diagnosis was subsequently confirmed by sequence analysis of the EXT1 gene and identification of a previously undescribed splice site mutation (IVS5-2 A>G). This finding led us to sequence EXT1 gene in the rest of the family. Surprisingly, three of the osteopoikilosis affected patients additionally to LEMD3 mutation carried a yet unreported amino acid variant (p.A578T) in the EXT1 gene. Of note was a wide spectrum of the clinical symptoms observed in these family members, which ranged from heart defect, diabetes mellitus, vitiligo to ovarian and sinus cyst formation. None of these pathologies was observed in the examined family members who carried LEMD3 mutation only (patients III:10 and IV:8), nor in the family members who were free of mutations in both genes (patients III:5, III:8, III:14, IV:3). However, since we were unable to examine other unaffected family members, the relevance of this observation remains uncertain. The EXT1 splice site mutation and other identified mutations must have occurred independently in the two branches of the family.
The exact mechanism by which LEMD3 gene mutations lead to the formation of the bone lesions is not clear. LEMD3 inactivation in mice was recently shown to result in the mid-gestation lethality . However, heterozygous mice were healthy and no bone lesions reminiscent of osteopoikilosis could be detected, leaving question mark over patho-mechanism of the disease. Co-occurrence of the LEMD3 gene mutation with the mutation in another gene has not yet been reported. Presented case constitutes first such report. Following considerations appear relevant based on the review of the available literature. It has been shown that LEM domain containing proteins interact with the barrier-to-autointegration factor (BAF) . BAF is a component of the chromatin remodelling complex, which uses energy from ATP to dismantle DNA-histone complexes . This is on one hand necessary for initiation of transcription, and it has been postulated that LEMD3, through BAF and SMAD interactions might regulate the expression of osteogenic genes . On the other hand it is known that chromatin remodelling is necessary for the efficient DNA repair . LEMD3 closely associates with the intranuclear lamina and mutations in other lamin interacting proteins are known to result in the DNA damage accumulation . Indeed, it has been suggested that lamin complexes acts as assembly scaffolds for DNA repair machinery . Thus, it seems legitimate to ask if inactivation of LEMD3 could also result in an increased mutational susceptibility and increased frequency of the post-zygotic second hit mutation occurrence. In this context it is interesting to note that osteopoikilosis was previously reported to coincide with other pathological entities, including various types of cancers: synovial chondromatosis , synoviosarcoma , chondrosarcoma , osteosarcoma , giant cell tumor , metastatic breast carcinoma , as well as developmental dysplasias: dental, facial abnormalities, coarctation of the aorta, double urether, mental retardation and other reviewed by Gunal et.al. .
Clearly, further research is needed to address possible association of the LEMD3 loss of function with DNA mutation susceptibility. Presented study constitutes first example of the LEMD3 gene mutation co-occurrence with additional genetic alteration, which could potentially modify and/or constitute the nature of the osteopoikilosis.
The presented case points to importance of the thorough clinical evaluation of the osteopoikilosis patients as phenotypic features of osteopoikilosis with melorheostosis might be confused with the co-occurrence of osteopoikilosis and multiple exostoses. The data encourage re-evaluation of the known osteopoikilosis families for the possible co-occurrence of other than Buschke-Ollendorff and melorheostosis disease entities and investigation of the possible LEMD3 function in the DNA repair.
M.K. and N.K. were supported by the by the Young Investigator Award from Children Tumour Fundation - New York (Grant #2007-01-038) and Bundesministerium für Bildung und Forschung; Grant (NF1-01GM0844).
This work was also supported by the Sixth Framework of the European Commission (EuroGrow project LSHM-CT-2007-037471) and by a grant from the Polish Ministry of Science and Higher Education (495/N-NIEMCY/2009/0)
We thank Monika Osswald and Carola Dietrich for excellent technical assistance.
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