Univ Fed Sao Paulo, Ctr Res & Mol Diagnost Genet Dis, Dept Biophys, Sao Paulo - Brazil
 Dept Nephrol URONEFRO Hemodialise & Especialidade, Belem, Para - Brazil
Número total de Afiliações: 2
Tipo de documento:
FRONTIERS IN GENETICS;
SEP 27 2019.
Citações Web of Science:
Fabry disease (FD) is a rare and underdiagnosed X-linked disorder resulting from the deficient activity of the lysosomal hydrolase alpha-galactosidase A, which leads to storage of complex glycosphingolipids inside of lysosomes in critical organs and tissues, impairing their functions and consequently resulting in a progressive multisystem disease. FD is caused by mutations in the GLA gene, and only 4.6% of described mutations are located in the splice site regions. RNA splicing is an essential step to the formation of functional proteins, and mutations in splice site regions can cause formation of aberrant transcripts leading to disease. Here we report a novel GLA insertion at position c.801+3 in intron 5 (c.801+2\_801+3insT) in a Brazilian family with suspicion of FD. The index case, a 46-year-old male, presented undetectable alpha-galactosidase A activity. Analysis of blood cDNA found two aberrant GLA transcripts. In the first transcript, a novel donor splice site was created promoting formation of an intron inclusion with 37 bp. The splice site was not recognized in the second transcript and the intron 5 was not excised. The wild-type transcript was not formed and both aberrant transcripts lead to a premature stop codon. Despite not being in the canonical site, this new mutation disrupts existing 5' splice site and produces two aberrant transcripts leading to FD. (AU)