| Literature DB >> 26027498 |
Roberto Mendoza-Londono1, Somayyeh Fahiminiya2, Jacek Majewski2, Martine Tétreault2, Javad Nadaf2, Peter Kannu1, Etienne Sochett3, Andrew Howard4, Jennifer Stimec5, Lucie Dupuis1, Paul Roschger6, Klaus Klaushofer6, Telma Palomo7, Jean Ouellet7, Hadil Al-Jallad7, John S Mort7, Pierre Moffatt7, Sergei Boudko8, Hans-Peter Bächinger8, Frank Rauch9.
Abstract
Secreted protein, acidic, cysteine-rich (SPARC) is a glycoprotein that binds to collagen type I and other proteins in the extracellular matrix. Using whole-exome sequencing to identify the molecular defect in two unrelated girls with severe bone fragility and a clinical diagnosis of osteogenesis imperfecta type IV, we identified two homozygous variants in SPARC (GenBank: NM_003118.3; c.497G>A [p.Arg166His] in individual 1; c.787G>A [p.Glu263Lys] in individual 2). Published modeling and site-directed mutagenesis studies had previously shown that the residues substituted by these mutations form an intramolecular salt bridge in SPARC and are essential for the binding of SPARC to collagen type I. The amount of SPARC secreted by skin fibroblasts was reduced in individual 1 but appeared normal in individual 2. The migration of collagen type I alpha chains produced by these fibroblasts was mildly delayed on SDS-PAGE gel, suggesting some overmodification of collagen during triple helical formation. Pulse-chase experiments showed that collagen type I secretion was mildly delayed in skin fibroblasts from both individuals. Analysis of an iliac bone sample from individual 2 showed that trabecular bone was hypermineralized on the material level. In conclusion, these observations show that homozygous mutations in SPARC can give rise to severe bone fragility in humans.Entities:
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Year: 2015 PMID: 26027498 PMCID: PMC4457955 DOI: 10.1016/j.ajhg.2015.04.021
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025