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https://hdl.handle.net/2440/51915
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dc.contributor.author | Garrido, E. | - |
dc.contributor.author | Cormand, B. | - |
dc.contributor.author | Hopwood, J. | - |
dc.contributor.author | Chabas, A. | - |
dc.contributor.author | Grinberg, D. | - |
dc.contributor.author | Vilageliu, L. | - |
dc.date.issued | 2008 | - |
dc.identifier.citation | Molecular Genetics and Metabolism, 2008; 94(3):305-312 | - |
dc.identifier.issn | 1096-7192 | - |
dc.identifier.issn | 1096-7206 | - |
dc.identifier.uri | http://hdl.handle.net/2440/51915 | - |
dc.description.abstract | Mucopolysaccharidosis VI (MPS VI; Maroteaux-Lamy syndrome) is an autosomal recessive lysosomal disorder caused by deficiency of N-acetylgalactosamine-4-sulfatase (ARSB), which is required for the degradation of dermatan sulfate. We recently reported mutational screening of 12 Spanish and 4 Argentinian MPS VI patients. In the present study, seven missense mutations (c.245T>G [p.L82R], c.413A>G [p.Y138C], c.719C>T [p.S240F], c.922G>A [p.G308R], c.937C>G [p.P313A], c.1340G>T [p.C447F] and c.1415T>C [p.L472P]) were transiently expressed in COS-7 cells and 4-sulfatase activity was measured in cell extracts. All mutations resulted in less than 6% of wild-type enzyme activity, in most cases undetectable. Mutations were expressed in their original haplotype context with respect to two non-synonymous polymorphisms present in the ARSB protein, p.V358M and p.S384N. The three less frequent haplotype combinations yielded an ARSB activity of 16%, 57% and 70%, when compared to the most frequent haplotype (p.358V and p.384S). Western blot analyses showed that the expressed mutations significantly reduced the amount of mature protein. Sub-cellular localization studies of mutant ARSB proteins in fibroblasts of MPS VI patients were performed. RNA analysis confirmed that nonsense-mediated RNA decay had taken place for all mutant alleles (c.1143-1G>C, c.1143-8T>G, p.W322X, c.427delG and c.1142+2T>A) which were candidates for causing RNA degradation by this mechanism. In summary, all the ARSB mutations studied had a significant effect on enzyme activity, protein processing and/or mRNA stability. | - |
dc.description.statementofresponsibility | Elena Garrido, Bru Cormand, John J. Hopwood, Amparo Chabás, Daniel Grinberg and Lluïsa Vilageliu | - |
dc.description.uri | http://www.elsevier.com/wps/find/journaldescription.cws_home/622920/description#description | - |
dc.language.iso | en | - |
dc.publisher | Academic Press Inc Elsevier Science | - |
dc.source.uri | http://dx.doi.org/10.1016/j.ymgme.2008.02.012 | - |
dc.subject | Cells, Cultured | - |
dc.subject | COS Cells | - |
dc.subject | Animals | - |
dc.subject | Humans | - |
dc.subject | Mucopolysaccharidosis VI | - |
dc.subject | N-Acetylgalactosamine-4-Sulfatase | - |
dc.subject | Codon, Nonsense | - |
dc.subject | Transfection | - |
dc.subject | DNA Mutational Analysis | - |
dc.subject | Protein Processing, Post-Translational | - |
dc.subject | Enzyme Activation | - |
dc.subject | RNA Stability | - |
dc.subject | Mutation | - |
dc.subject | Polymorphism, Single Nucleotide | - |
dc.subject | Models, Molecular | - |
dc.subject | Chlorocebus aethiops | - |
dc.title | Maroteaux-Lamy syndrome: Functional characterization of pathogenic mutations and polymorphisms in the arylsulfatase B gene | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1016/j.ymgme.2008.02.012 | - |
pubs.publication-status | Published | - |
Appears in Collections: | Aurora harvest Paediatrics publications |
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