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- W2158155220 abstract "The inherited metabolic disease propionic acidemia (PA) can result from mutations in either of the genes PCCA or PCCB, which encode the alpha and beta subunits, respectively, of the mitochondrial enzyme propionyl CoA-carboxylase. In this work we have analyzed the molecular basis of PCCA gene defects, studying mRNA levels and identifying putative disease causing mutations. A total of 10 different mutations, none predominant, are present in a sample of 24 mutant alleles studied. Five novel mutations are reported here for the first time. A neutral polymorphism and a variant allele present in the general population were also detected. To examine the effect of a point mutation (M348K) involving a highly conserved residue, we have carried out in vitro expression of normal and mutant PCCA cDNA and analyzed the mitochondrial import and stability of the resulting proteins. Both wild-type and mutant proteins were imported into mitochondria and processed into the mature form with similar efficiency, but the mature mutant M348K protein decayed more rapidly than did the wild-type, indicating a reduced stability, which is probably the disease-causing mechanism." @default.
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- W2158155220 date "1999-03-01" @default.
- W2158155220 modified "2023-10-18" @default.
- W2158155220 title "Genetic heterogeneity in propionic acidemia patients with α-subunit defects. Identification of five novel mutations, one of them causing instability of the protein" @default.
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- W2158155220 doi "https://doi.org/10.1016/s0925-4439(99)00008-3" @default.
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