Analysis of the LEMD3 gene in individuals affected with ... · osteopoikilosis, melorheostosis,...
Transcript of Analysis of the LEMD3 gene in individuals affected with ... · osteopoikilosis, melorheostosis,...
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Analysis of the LEMD3 gene in individuals affected with melorheostosis
Geert MortierCenter for Medical GeneticsGhent University Hospital
Ghent - Belgium
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Genome search in three families
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Family with melorheostosis
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Osteopoikilosis
Benign conditionAutosomal dominantHyperostotic spotsIsolated or in association withother skin/bone lesions
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Buschke-Ollendorff syndrome
BOS = osteopoikilosis + connective tissue nevi (elastic type)
elastic-type nevus
Light micrograph – Van Gieson – x100Widely disseminated, multiple,skin-colored to yellow, smallpapules (few mm in diameter)
Localized, asymmetricallydistributed, larger lesions(yellow plaques)
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Melorheostosis
joint contracturescurving or shortening of limb(s)chronic pain, swelling of jointsskin, subcutaneous tissue ormuscle involvementirregular linear areas of increased radiodensity along the major axis of the tubular bonesareas of osteophytic periostealexcrescences (dripping candlewax)ectopic bone formation
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LEMD3
Nature Genetics Nov 2004; 36:1213
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LEMD3: integral protein of the inner nuclear membrane
LEMD3
Adapted from Gruenbaum Y et al. Nature Rev Mol Cell Biol 6,21,2005
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The cell
nucleus
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LEMD3 function
A. Zwijsen et al. FEBS Letters 546 (2003) 133-139
LEMD3
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LEMD3 mutations
Smad interacting part
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Analysis of LEMD3 in a larger series of patients
• group A: patients with osteopoikilosis, short stature and learning problems
n=3
• group B: patients with osteopoikilosis with(out) BOS skin lesions
n=15
• group C: patients with melorheostosis belonging to a family with OP/BOS
n=5
• group D: patients with melorheostosis (sporadic occurrence)
n=23
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LEMD3 analysisgroup phenotype nucleotide and residue changes reference
osteopoikilosis, melorheostosis, short stature, MR Not tested Jurenka and Van Allen 1995osteopoikilosis, short stature, MR, ectopic kidney microdeletion Hellemans et al. 2004osteopoikilosis, short stature, MR microdeletion Hellemans et al. 2006
BOS c.2134dupT; p.Met712fsX Hellemans et al. 2004BOS c.1185dupT; p.Gly395fsX Hellemans et al. 2004osteopoikilosis c.1033_1035delGGGinsC; p.Gly345fsX Hellemans et al. 2004osteopoikilosis c.1921+5delG; exon skip - frameshift Hellemans et al. 2004osteopoikilosis c.457C>T; p.Gln153X Hellemans et al. 2004osteopoikilosis c.1801G>T; p.Glu601X Hellemans et al. 2006BOS c.1323C>A; p.Tyr441X Hellemans et al. 2006BOS c.1873C>T; p.Arg625X Hellemans et al. 2006BOS c.1914dupA; p.Leu638fsX Hellemans et al. 2006osteopoikilosis c.2494-9A>G; splice site Hellemans et al. 2006BOS c.1873C>T; p.Arg625X Hellemans et al. 2006BOS c.2245C>T;p.Gln749X Hellemans et al. 2006BOS c.1707_1708delTG; p.Pro569fsX unpublishedosteopoikilosis c.1813delA; p.Ile605fsX unpublishedosteopoikilosis normal Hellemans et al. 2006
melorheostosis (BOS in other relatives) c.1609C>T; p.Arg537X Hellemans et al. 2004, Debeer et al. 2003melorheostosis (BOS in other relatives) c.830dupA; p.Lys277X Hellemans et al. 2006melorheostosis (BOS in other relatives) [c.1963C>T,c.2488C>T]; p.Arg655X Hellemans et al. 2006, Butkus et al. 1997melorheostosis (BOS in other relatives) c.2275_2278delGTTA; p.Val759fsX unpublishedmelorheostosis (BOS in other relatives) normal unpublished
melorheostosis c.1913T>A; p.Leu638X Hellemans et al. 2006melorheostosis (22 patients) normal Hellemans et al. 2006 + unpublished
D
C
B
A
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Group C – familial melorheostosis
p.Val759fsX
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Group D – sporadic melorheostosis
p.Leu638fsX
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normal LEMD3 gene
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Germline LEMD3 mutations
MUTATION
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Germline LEMD3 mutations
normal LEMD3 gene abnormal LEMD3 gene
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Germline LEMD3 mutations
? ?
Other genes mutated?
melorheostosis
osteopoikilosis
?
normal LEMD3 gene abnormal LEMD3 gene
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Somatic mutations
Somatic LEMD3 mutations responsible for the spotty, localized character of the lesions?
skin biopsy from:elastic type nevus (BOS patient)hard sclerodermic-like lesion (melorheostosis patient in BOS family)
No LOH or allelic imbalanceNo second hit in LEMD3Only cDNA of wild type LEMD3
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Sporadic melorheostosis
normal LEMD3 gene
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Sporadic melorheostosis
melorheostosis?
? ?
Other genes mutated?
normal LEMD3 gene abnormal LEMD3 gene
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Somatic mutations
Somatic LEMD3 mutations in melorheostosis patientswithout an identifiable germline mutation?
biopsies from skin and bone of 2 patientsNo somatic LOH or mutation in LEMD3
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Conclusions (1)
Heterozygous loss-of-function mutations in LEMD3 resultin osteopoikilosis and Buschke-Ollendorff syndrome
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Conclusions (1)
Heterozygous loss-of-function mutations in LEMD3 resultin osteopoikilosis and Buschke-Ollendorff syndrome
Individuals with melorheostosis and osteopoikilosis(usually belonging to a family) have heterozygous LEMD3 mutations in the germline
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Conclusions (1)
Heterozygous loss-of-function mutations in LEMD3 resultin osteopoikilosis and Buschke-Ollendorff syndrome
Individuals with melorheostosis and osteopoikilosis(usually belonging to a family) have heterozygous LEMD3 mutations in the germline
Individuals with melorheostosis (sporadic and isolated) do not have germline mutations in LEMD3
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Conclusions (1)
Heterozygous loss-of-function mutations in LEMD3 resultin osteopoikilosis and Buschke-Ollendorff syndrome
Individuals with melorheostosis and osteopoikilosis(usually belonging to a family) have heterozygous LEMD3 mutations in the germline
Individuals with melorheostosis (sporadic and isolated) do not have germline mutations in LEMD3
Somatic defects in LEMD3 have not yet been identified in melorheostosis lesions
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Conclusions (1)
Heterozygous loss-of-function mutations in LEMD3 resultin osteopoikilosis and Buschke-Ollendorff syndrome
Individuals with melorheostosis and osteopoikilosis(usually belonging to a family) have heterozygous LEMD3 mutations in the germline
Individuals with melorheostosis (sporadic and isolated) do not have germline mutations in LEMD3
Somatic defects in LEMD3 have not yet been identified in melorheostosis lesions
The cause of sporadic, isolated melorheostosis remains tobe unravelled
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Conclusions (2)
Microdeletions encompassing the LEMD3 gene result in a syndromic condition with osteopoikilosis, mental retardation and short stature
LEMD3
short stature gene
mental retardation gene
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Heterozygous knock-out mouse: development of melorheostosis?
?
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Acknowledgments
Center for Medical GeneticsGent
Andy WillaertBjorn MentenNadine Van RoyJo Vandesompele Frank SpelemanPaul CouckeAnne De PaepeGeert Mortier
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Acknowledgments
Referring physicians
Lina BaselTeresa CostaAlbert DavidPhilippe DebeerKlaus KjaerCelia MossAndreas JaneckeJohannes RothRavi SavarirayanPeter VerdonkMichael Wright
Dept Medical Genetics - Antwerp
Katrien JanssensWim Van Hul
Olena PreobrazhenskaKristin VerschuerenDanny Huylebroeck
Dept Developmental Biology - Leuven
Fund for Scientific Research (Flanders)European Commission grant (QLG1-CT-2001-02188)European Skeletal dysplasia Network (www.esdn.org)