Unknown

Dataset Information

0

Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome.


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.

SUBMITTER: Evans BR 

PROVIDER: S-EPMC3512002 | BioStudies | 2012-01-01

REPOSITORIES: biostudies

Similar Datasets

2020-01-01 | S-EPMC7609061 | BioStudies
2017-08-01 | GSE100661 | GEO
2020-01-01 | S-EPMC7253023 | BioStudies
1000-01-01 | S-EPMC4547893 | BioStudies
1000-01-01 | S-EPMC4847008 | BioStudies
1000-01-01 | S-EPMC3117651 | BioStudies
2016-01-01 | S-EPMC4773521 | BioStudies
1000-01-01 | S-EPMC3322893 | BioStudies
2015-01-01 | S-EPMC4362532 | BioStudies
2009-01-01 | S-EPMC2721823 | BioStudies