| Literature DB >> 22922033 |
Brad R Evans1, Rebecca A Mosig, Mollie Lobl, Chiara R Martignetti, Catalina Camacho, Valerie Grum-Tokars, Marc J Glucksman, John A Martignetti.
Abstract
The "vanishing bone" syndromes represent a group of rare skeletal disorders characterized by osteolysis and joint destruction, which can mimic severe rheumatoid arthritis. Winchester syndrome was one of the first recognized autosomal-recessive, multicentric forms of the disorder. It was originally described nearly 50 years ago in two sisters with a severe crippling osteolysis. Using cultured fibroblasts from the proband, we have now identified homozygous mutations in membrane type-1 metalloproteinase (MT1-MMP or MMP14). We demonstrate that the resulting hydrophobic-region signal-peptide substitution (p.Thr17Arg) decreases MT1-MMP membrane localization with consequent impairment of pro-MMP2 activation, and we propose a structure-based mechanism for this effect.Entities:
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Year: 2012 PMID: 22922033 PMCID: PMC3512002 DOI: 10.1016/j.ajhg.2012.07.022
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025