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Clinical, biochemical and genetic findings in two siblings with a dihydropyrimidinase deficiency
Karolinska Institutet. (Molecular Structural Biology)
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2007 (English)In: Molecular Genetics and Metabolism, ISSN 1096-7192, E-ISSN 1096-7206, Vol. 91, no 2, 157-164 p.Article in journal (Refereed) Published
Abstract [en]

Dihydropyrimidinase (DHP) is the second enzyme of the pyrimidine degradation pathway and it catalyses the ring opening of 5,6-dihydrouracil and 5,6-dihydrothymine to N-carbamyl-beta-alanine and N-carbamyl-beta-aminoisobutyric acid, respectively. To date, only nine individuals have been reported suffering from a complete DHP deficiency. We report two siblings presenting with strongly elevated levels of 5,6-dihydrouracil and 5,6-dihydrothymine in plasma, cerebrospinal fluid and urine. One of the siblings had a severe delay in speech development and white matter abnormalities, whereas the other one was free of symptoms. Analysis of the DHP gene (DPYS) showed that both patients were compound heterozygous for the missense mutation 1078T>C (W360R) in exon 6 and a novel missense mutation 1235G>T (R412M) in exon 7. Heterologous expression of the mutant enzymes in Escherichia coli showed that both missense mutations resulted in a mutant DHP enzyme without residual activity. Analysis of the crystal structure of eukaryotic DHP from the yeast Saccharomyces kluyveri and the slime mold Dictyostelium discoideum suggests that the W360R and R412M mutations lead to structural instability of the enzyme which could potentially impair the assembly of the tetramer.

Place, publisher, year, edition, pages
2007. Vol. 91, no 2, 157-164 p.
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Medical Genetics
URN: urn:nbn:se:uu:diva-214432DOI: 10.1016/j.ymgme.2007.02.008ISI: 000247408300006PubMedID: 17383919OAI: oai:DiVA.org:uu-214432DiVA: diva2:684921
Available from: 2014-01-08 Created: 2014-01-08 Last updated: 2014-01-15Bibliographically approved

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Dobritzsch, Doreen
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