Abstract |
Thanatophoric dysplasia is a lethal chondrodysplasia caused by heterozygous fibroblast growth factor receptor 3 (FGFR3) missense mutations. Mutations have been identified in several domains of the receptor. The most frequent mutations (p.R248C, p.S249C, p.Y373C) create a cysteine residue within the extracellular domain, whereas the others eliminate the termination codon (p.X807R, p.X807C, p.X807G, p.X807S, p.X807W). Here, we report a unique patient with thanatophoric dysplasia and a double de novo FGFR3 mutation, located on the same allele, (c.[1620C>A;1454A>G]), which corresponds to p.[N540K;Q485R]. The p.N540K mutation is associated with 60% of patients with hypochondroplasia and the p.Q485R mutation is a novel mutation located in a highly conserved domain of FGFRs. Evidence for the structural impact of the two concurrent missense mutations was achieved using protein alignments and three-dimensional structural prediction, in agreement with our modeling of the FGFR3 structure. In this patient with thanatophoric dysplasia, we conclude that the presence of the double FGFR3 missense mutation on the same allele alters the receptor structure, holding the receptor in its fully activated state, thus leading to lethal chondrodysplasia.
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Authors | Stéphanie Pannier, Jelena Martinovic, Solange Heuertz, Anne-Lise Delezoide, Arnold Munnich, Laurent Schibler, Valérie Serre, Laurence Legeai-Mallet |
Journal | American journal of medical genetics. Part A
(Am J Med Genet A)
Vol. 149A
Issue 6
Pg. 1296-301
(Jun 2009)
ISSN: 1552-4833 [Electronic] United States |
PMID | 19449430
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | (c) 2009 Wiley-Liss, Inc. |
Chemical References |
- Receptor, Fibroblast Growth Factor, Type 3
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Topics |
- Aborted Fetus
- Abortion, Induced
- Alleles
- Amino Acid Sequence
- Bone Diseases, Developmental
(genetics)
- DNA Mutational Analysis
- Humans
- Models, Molecular
- Molecular Sequence Data
- Mutation, Missense
- Osteochondrodysplasias
(diagnostic imaging, genetics, pathology)
- Protein Conformation
- Protein Structure, Tertiary
- Radiography
- Receptor, Fibroblast Growth Factor, Type 3
(chemistry, genetics)
- Sequence Homology, Amino Acid
- Thanatophoric Dysplasia
(diagnostic imaging, genetics, pathology)
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