Genomic basis of mucopolysaccharidosis type IIID (MIM 252940) revealed by sequencing of GNS encoding N-acetylglucosamine-6-sulfatase.

Abstract

Mucopolysaccharidosis type IIID (MPS IIID; Sanfilippo syndrome type D; MIM 252940) is caused by deficiency of the activity of N-acetylglucosamine-6-sulfatase (GNS), which is normally required for degradation of heparan sulfate. The clinical features of MPS IIID include progressive neurodegeneration, with relatively mild somatic symptoms. Biochemical features include accumulation of heparan sulfate and N-acetylglucosamine-6-sulfate in the brain and viscera. To date, diagnosis required a specific lysosomal enzyme assay for GNS activity. From genomic DNA of a subject with MPS IIID, we amplified and sequenced the promoter and 14 exons of GNS. We found a homozygous nonsense mutation in exon 9 (1063C --> T), which predicted premature termination of translation (R355X). We also identified two common synonymous coding single-nucleotide polymorphisms and genotyped these in samples from four ethnic groups. This first report of a mutation in GNS resulting in MPS IIID indicates the potential utility of molecular diagnosis for this rare condition.

• Authors: Andrea Mok, Henian Cao, Robert A Hegele
• Journal: Genomics (Genomics) Vol. 81 Issue 1 Pg. 1-5 (Jan 2003) ISSN: 0888-7543 [Print] United States
• PMID: 12573255 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Heparitin Sulfate
• Sulfatases
• N-acetylglucosamine-6-sulfatase

Topics

• Genome, Human
• Heparitin Sulfate (metabolism)
• Humans
• Mucopolysaccharidosis III (etiology, genetics)
• Polymorphism, Single Nucleotide
• Sequence Analysis, DNA
• Sulfatases (deficiency, genetics)