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Reversing the effect of the IDUA GENE W402X mutation?

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Abstract(s)

Introduction: Mucopolysaccharidosis type I (MPS I; OMIM #252800) is an autosomal recessive disorder, which results from the defective activity of the lysosomal enzyme α-L-iduronidase (IDUA, EC 3.2.1.76). The gene encoding α-L-iduronidase (IDUA; OMIM #252800) maps to chromosome 4p16.3 and contains 14 exons. The W402X mutation is the most common in patients of European Caucasian origin, appearing in over 45% of alleles in unrelated patients of various western European origins. In addition, this mutation has been considered to play an important role in terms of the pathophysiology of MPS I. The main objective of this work was to functionally evaluate the susceptibility of the nonsense mutation W402X of the IDUA gene to mechanisms of nonsense suppression with two individual compounds.

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Presenting author: Diogo Ribeiro; Corresponding author: Olga Amaral

Keywords

Doenças Genéticas Genética Humana

Pedagogical Context

Citation

Livro de resumos da 16ª Reunião anual da Sociedade Portuguesa de Genética Humana, 2012: 124 (P 64)

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Sociedade Portuguesa de Genética Humana (SPGH)

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