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Molecular pathologyof galactosialidosisin a patient affectedwith two newframeshift mutationsin the cathepsinA/protective proteingene Catherine RichardJulie TranchemontagneMarc‐André Elsliger1998 год

Molecular pathology of galactosialidosis in a patient affected with two new frameshift mutations in the cathepsin A/protective protein gene
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Аннотация: Galactosialidosis is a recessively inherited lysosomal storage disease characterized by the combined deficiency of neuraminidase and β-galactosidase secondary to the genetic deficiency of cathepsin A/protective protein. In lysosomes, cathepsin A forms a high-molecular-weight complex with β-galactosidase and neuraminidase that protects these enzymes against intralysosomal proteolysis. In a patient affected with late infantile form of galactosialidosis, we found two new cathepsin A mutations, a two-nucleotide deletion, c517delTT and an intronic mutation, IVS8+9C→G resulting in abnormal splicing and a five-nucleotide insertion in the cathepsin A cDNA. Both mutations cause frameshifts and result in the synthesis of truncated cathepsin A proteins, which, as suggested by structural modeling, are incapable of dimerization, complex formation, and catalysis. However, enzymatic assays, gel-filtration, and Western blot analysis of the patient's cultured skin fibroblast extracts showed the presence of a small amount of normal-size, catalytically active cathepsin A and cathepsin A-β-galactosidase 680 kDa complex, suggesting that a low amount of cathepsin A mRNA is spliced normally and produces the wild-type protein. This may contribute to the relatively mild phenotype of the patient and illustrates the importance of critically comparing molecular results with clinical and biochemical phenotypes. Hum Mutat 11:461–469, 1998. © 1998 Wiley-Liss, Inc.
Год издания: 1998
Авторы: Catherine Richard, Julie Tranchemontagne, Marc‐André Elsliger, Grant A. Mitchell, Michel Potier, Alexey V. Pshezhetsky
Издательство: Wiley
Источник: Human Mutation
Ключевые слова: Lysosomal Storage Disorders Research, Research on Leishmaniasis Studies, Trypanosoma species research and implications
Другие ссылки: Human Mutation (HTML)
PubMed (HTML)