Molecular genetics and metabolism · 2012
Fabry disease: biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Togawa Tadayasu, Tsukimura Takahiro, Kodama Takashi, Tanaka Toshie, Kawashima Ikuo, Saito Seiji, Ohno Kazuki, Fukushige Tomoko, Kanekura Takuro, Satomura Atsushi, Kang Duk-Hee, Lee Beom Hee, Yoo Han-Wook, Doi Kent, Noiri Eisei, Sakuraba Hitoshi
Аннотация
Recently, male subjects harboring the c.196G>C nucleotide change which leads to the E66Q enzyme having low α-galactosidase A (GLA) activity have been identified at an unexpectedly high frequency on Japanese and Korean screening for Fabry disease involving dry blood spots and plasma/serum samples. Individuals with the E66Q enzyme have been suspected to have the later-onset Fabry disease phenotype leading to renal and cardiac disease. However, there has been no convincing evidence for this. To determine whether c.196G>C (E66Q) is disease-causing or not, we performed biochemical, pathological and structural studies. It was predicted that the E66Q amino acid substitution causes a small conformational change on the molecular surface of GLA, which leads to instability of the enzyme protein. However, biochemical studies revealed that subjects harboring the E66Q enzyme exhibited relatively high residual enzyme activity in white blood cells, and that there was no accumulation of globotriaosylceramide in cultured fibroblasts or an increased level of plasma globotriaosylsphingosine in these subjects. An electron microscopic examination did not reveal any pathological changes specific to Fabry disease in biopsied skin tissues from a male subject with the E66Q enzyme. These results strongly suggest that the c.196G>C is not a pathogenic mutation but is a functional polymorphism.
Предметные рубрики MeSH
AgedAged, 80 and overAmino Acid SubstitutionAsian PeopleCells, CulturedChild, PreschoolDNA Mutational AnalysisFabry DiseaseFibroblastsHeterozygoteHumansImmunoblottingMaleMicroscopy, ElectronMiddle AgedModels, MolecularMutationPhenotypeReal-Time Polymerase Chain ReactionSkinTrihexosylceramidesalpha-Galactosidase