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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Functional Characterization and Pharmacological Evaluation of a Novel GLA Missense Mutation Found in a Severely Affected Fabry Disease Family

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Autor(es):
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Varela, Patricia [1] ; Mastroianni Kirsztajn, Gianna [2] ; Ferrer, Henrique [1] ; Aranda, Carolina [3] ; Wallbach, Krissia [3] ; Ferreira da Mata, Gustavo [2] ; Moura, Luiz A. [2] ; Moreira, Silvia R. [2] ; Mendes, Carmen [3] ; Curiati, Marco A. [3] ; Martins, Ana Maria [3] ; Bosco Pesquero, Joao [1]
Número total de Autores: 12
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Dept Biophys, Ctr Res & Mol Diagnost Genet Dis, Rua Pedro Toledo 669, 9 Andar, BR-04039032 Sao Paulo, SP - Brazil
[2] Univ Fed Sao Paulo, Dept Med, Div Nephrol, Rua Pedro Toledo 669, 9 Andar, BR-04039032 Sao Paulo, SP - Brazil
[3] Univ Fed Sao Paulo, Dept Pediat, Reference Ctr Inborn Errors Metab, Sao Paulo - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: NEPHRON; v. 144, n. 3, p. 147-155, MAR 2020.
Citações Web of Science: 1
Resumo

Background: Fabry disease (FD) is a rare X-linked storage disorder resulting from the deficient activity of the lysosomal hydrolase alpha-galactosidase A (alpha-Gal A). Here we describe a 23-year-old man with FD possessing a novel mutation in the GLA gene, the evaluation of his family, and the functional characterization of the novel variant. Methods: Two generations of a family were screened for FD by clinical symptoms and low enzymatic activity. This step was followed by DNA sequencing that showed a novel GLA missense mutation. To confirm the pathogenicity potential of the mutation, we employed site-directed polymerase chain reaction mutagenesis. GLA wild-type and mutant plasmids were transfected into mammalian cells; RNA and proteins were extracted for expression and analysis of enzymatic activity. Results: The patient presents the variant p.Asn34Asp in the GLA and had several manifestations of FD since adolescence. The investigation of the deficiency of alpha-Gal A was initiated due to stage 4 of chronic kidney disease. All family members carrying the novel mutation presented early symptoms, including index case's mother, who received a renal transplant when she was 35 years old. In silico and in vitro analysis confirmed the pathogenic potential of the mutation p.Asn34Asp showing that the enzyme had only 4% of residual activity due to protein misfolding. The ability of the pharmacological chaperone 1-deoxygalactonojirimycin to recover the mutant was confirmed, producing 37.5% of residual activity. Conclusion: In this work, we present a novel missense mutation in GLA that leads to the production of a catalytically competent alpha-Gal A, which is degraded before its delivery to the lysosome, promoting severe manifestations of FD, with a very similar disease course in affected men and women. (AU)

Processo FAPESP: 14/27198-8 - Estabelecimento de um centro de pesquisa genética e molecular para desafios clínicos
Beneficiário:João Bosco Pesquero
Linha de fomento: Auxílio à Pesquisa - Temático