Study of the WFS1 gene and mitochondrial DNA in Spanish Wolfram syndrome families.

Abstract

Wolfram syndrome (WS) is an autosomal recessive neurodegenerative disorder characterized by early onset diabetes mellitus and progressive optic atrophy. Patients with WS frequently develop deafness, diabetes insipidus, renal tract abnormalities, and diverse psychiatric illnesses, among others. A gene responsible for WS was identified on 4p16.1 (WFS1). It encodes a putative 890 amino acid transmembrane protein present in a wide spectrum of tissues. A new locus for WS has been located on 4q22-24, providing evidence for the genetic heterogeneity of this syndrome. Six Spanish families with a total of seven WS patients were screened for mutations in the WFS1-coding region by direct sequencing. We found three previously undescribed mutations c.873C > A, c.1949_50delAT, and c.2206G > C, as well as the duplication c.409_424dup16, formerly published as 425ins16. Several groups had detected deletions in the mitochondrial DNA (mtDNA) of WS patients. For this reason, we also studied the presence of mtDNA rearrangements as well as Leber's hereditary optic neuropathy, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes, and A1555G point mutations in the WS families. No mtDNA abnormalities were detected.

• Authors: E Domènech, M Gómez-Zaera, V Nunes
• Journal: Clinical genetics (Clin Genet) Vol. 65 Issue 6 Pg. 463-9 (Jun 2004) ISSN: 0009-9163 [Print] Denmark
• PMID: 15151504 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA, Mitochondrial
• Membrane Proteins
• wolframin protein

Topics

• Alleles
• DNA, Mitochondrial (genetics)
• Gene Frequency
• Humans
• Membrane Proteins (genetics)
• Mutation (genetics)
• Pedigree
• Spain
• Wolfram Syndrome (genetics)