Multicentric osteolysis, nodulosis and arthropathy (MONA) is a rare autosomal recessive disorder. To date, 13 mutations of the matrix metalloproteinase 2 (MMP2) gene have been detected in 26 patients with MONA and other osteolytic syndromes. Here, we describe the molecular and functional analysis of a novel MMP2 mutation in two adult Italian siblings with MONA. Both siblings displayed palmar-plantar subcutaneous nodules, tendon retractions, limb arthropathies, osteolysis in the toes and pigmented fibrous skin lesions. Molecular analysis identified a homozygous MMP2 missense mutation in exon 8 c.1228G>C (p.G410R), not detected in 260 controls and predicted by several bioinformatic tools to be pathogenic. By protein modelling, the mutant residue was predicted to affect the main chain conformation of the catalytic domain. Gelatin zymography, the gold standard test for MMP2 function, of serum-free conditioned medium from G410R-MMP2-expressing human embryonic kidney (HEK) cells, showed a complete loss of gelatinolytic activity. The novel mutation is located in the catalytic domain, as are 3 (p.E404K, p.V400del and p.G406D) of the other 13 MMP2 mutations described to date; however, p.G410R underlies a phenotype that is only partially overlapping that of other MMP2 exon 8 mutation carriers. Our results further delineate the complexity of genotype-phenotype correlations in MONA, broaden the repertoire of reported MMP2 mutation and enhance the comprehension of the protein motifs crucial for MMP2 catalytic activity.
Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy / J. Azzollini, D. Rovina, C. Gervasini, I. Parenti, A. Fratoni, M. Cubellis, A. Cerri, L. Pietrogrande, L. Larizza. - In: JOURNAL OF HUMAN GENETICS. - ISSN 1434-5161. - 59:11(2014 Nov), pp. 631-637.
|Titolo:||Functional characterisation of a novel mutation affecting the catalytic domain of MMP2 in siblings with multicentric osteolysis, nodulosis and arthropathy|
AZZOLLINI, JACOPO VITO (Primo)
ROVINA, DAVIDE (Secondo)
PIETROGRANDE, LUCA (Penultimo)
LARIZZA, LIDIA (Corresponding)
|Parole Chiave:||Winchester-syndrome; matrix metalloproteinase-2; Torgs-syndrome; arthritis; family; matrix-metalloproteinase-2; disease; patient; genes; NAO|
|Settore Scientifico Disciplinare:||Settore MED/03 - Genetica Medica|
Settore MED/33 - Malattie Apparato Locomotore
Settore MED/35 - Malattie Cutanee e Veneree
|Data di pubblicazione:||nov-2014|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1038/jhg.2014.84|
|Appare nelle tipologie:||01 - Articolo su periodico|