Clinical and mutational characterization of three patients with multiple sulfatase deficiency: Report of a new splicing mutation

• Published in: Molecular genetics and metabolism Vol. 86; no. 1; pp. 206 - 211
• Main Authors: Díaz-Font, Anna, Santamaría, Raül, Cozar, Mònica, Blanco, Mariana, Chamoles, Néstor, Coll, Maria Josep, Chabás, Amparo, Vilageliu, Lluïsa, Grinberg, Daniel
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.2005
• Subjects: Base Sequence; Child, Preschool; DNA Primers; Female; Humans; Infant; Male; Minigene analysis; Multiple sulfatase deficiency; Mutation; Polymerase Chain Reaction; RNA Splicing; Sphingolipidoses - genetics; Sphingolipidoses - pathology; Splicing mutation; Sulfatases - genetics; SUMF1 gene; SUMF1 gene; Multiple sulfatase deficiency; Splicing mutation; Minigene analysis
• ISSN: 1096-7192; 1096-7206
• DOI: 10.1016/j.ymgme.2005.07.004

Multiple sulfatase deficiency (MSD) is a rare autosomal recessive lysosomal storage disease characterized by impaired activity of all known sulfatases. The gene SUMF1, recently identified, encodes the enzyme responsible for post-translational modification of a cysteine residue, which is essential for the activity of sulfatases. Fewer than 30 MSD patients have been reported to date and 23 different mutations in the SUMF1 gene have been identified. Here, we present the characterization of the mutant alleles of two Spanish and one Argentinean MSD patients. While the two Spanish patients were homozygous for the previously described mutations, c.463T>C (p.S155P) and c.1033C>T (p.R345C), the Argentinean patient was homozygous for the new mutation IVS7 + 5 G>T. A minigene approach was used to analyze the effect of the splice site mutation identified, due to the lack of sample from the patient. This experiment showed that this change altered the normal splicing of the RNA, which strongly suggests that this is the molecular cause of the disease in this patient.