The g.1170C > T polymorphism of the 5 ' untranslated region of the human alpha-galactosidase gene is associated with decreased enzyme expression-Evidence from a family study

• Type: Article in International Scientific Journal
• Date: 2008

Authors

João Paulo Oliveira (Author) FMUP; Ferreira, S (Author) Other; reguenga, c (Author) FMUP; carvalho, f (Author) FMUP; Mansson, JE (Author) Other

Journal

Title: Journal of Inherited Metabolic Disease

Vol. 31

Pages: S405-S413

ISSN: 0141-8955

Publisher: Springer Nature

Indexing

ISI Web of Knowledge - 16 Citations

Scopus - 1 Citation

Other information

Authenticus ID: P-003-TJM

DOI: 10.1007/s10545-008-0972-0

Abstract (EN): Subnormal leukocyte alpha-galactosidase (alpha-Gal) activity was found during evaluation of an adolescent male with cryptogenic cerebrovascular small-vessel disease. The only molecular abnormality found was the g.1170C>T single-nucleotide polymorphism (SNP) in the 5' untranslated region of exon 1 in the alpha-Gal gene (GLA). Historically, this polymorphism has been considered to be biologically neutral. To test the hypothesis that the g.1170T allele might be associated with lower alpha-Gal expression, we genotyped GLA exon 1 and measured leukocyte and plasma alpha-Gal in the parents, brother and sister of the index case. The g.1170T allele co-segregated with a subnormal leukocyte alpha-Gal activity in the three siblings. Although plasma enzyme activities were within the normal range in all five relatives, the ranking of their values suggested a dosage effect of the g.1170T allele. Western blotting assays of leukocyte protein extracts showed that the relative expression of alpha-Gal in both the patient and his sister was significantly lower than in sex-matched hemizygous or homozygous controls for the g.1170C allele, either normalized to the beta-actin immunoblot expression or standardized to a known amount of recombinant human alpha-Gal. These family data, in combination with results from a recent GLA SNP screening study among healthy Portuguese individuals, suggest that the g.1170C>T SNP may be co-dominantly associated with a relatively decreased GLA expression at the transcription and/or translation level. Larger population studies are needed to confirm these findings and to test the hypothesis that the GLA g.1170C>T may contribute to the multifactorial risk of ischaemic small-vessel cerebrovascular disease.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9