Novel GALTvariations and mutation spectrum in the Korean population with decreased galactose-1-phosphate uridyltransferase activityReportar como inadecuado




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BMC Medical Genetics

, 15:94

Clinical-Molecular Genetics and Cytogenetics

Abstract

BackgroundClassic galactosemia OMIM #230400 is an autosomal recessive metabolic disorder caused by a deficiency of the galactose-1-phosphate uridyltransferase GALT, EC2.7.7.12 protein due to mutations in the GALT gene. The aim of this study was to provide a comprehensive and updated mutation spectrum of GALT in a Korean population.

MethodsThirteen unrelated patients screened positive for galactosemia in a newborn screening program were included in this study. They showed a reduced GALT enzyme activity in red blood cells. Direct sequencing of the GALT gene and in silico analyses were done to evaluate the impact of novel variations upon GALT enzyme activity. We also reviewed previous reports for GALT mutations in Koreans.

ResultsWe identified six novel likely pathogenic variations including three missense p.Ala101Asp, p.Tyr165His, and p.Pro257Thr, one small deletion-insertion c.826 827delinsAA p.Ala276Asn, one frameshift p.Asn96Serfs*5, and one splicing c.378-1G > C likely pathogenic variations. The most frequent variation was the Duarte variant c.940A > G, 35.3%, followed by c.507G > C p.Gln169His, 9.6%, among 34 Korean patients. Other mutations were widely scattered. None of the eight common mutations used for targeted mutation analysis in Western countries including p.Gln188Arg, p.Ser135Leu, p.Lys285Asn, p.Leu195Pro, p.Tyr209Cys, p.Phe171Ser, c.253-2A > G, and a 5 kb deletion, had been found in Koreans until this study.

ConclusionsConsidering the mutation spectrum in Koreans, direct sequence analysis of entire GALT exons is recommended for accurate diagnosis. The mutations responsible for GALT deficiency in the Korean population were clearly different from those of other populations.

KeywordsGalactosemia Galactose-1-phosphate uridyltransferase GALT Metabolic disease Mutation Electronic supplementary materialThe online version of this article doi:10.1186-s12881-014-0094-5 contains supplementary material, which is available to authorized users.

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Autor: Rihwa Choi - Kyoung Il Jo - Dae-Hyun Ko - Dong Hwan Lee - Junghan Song - Dong-Kyu Jin - Chang-Seok Ki - Soo-Youn Lee - J

Fuente: https://link.springer.com/







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