Abstract |
The first feline model of human congenital erythropoietic porphyria (CEP) due to deficient uroporphyrinogen III synthase (URO-synthase) activity was identified by its characteristic clinical phenotype, and confirmed by biochemical and molecular genetic studies. The proband, an adult domestic shorthair cat, had dark-red urine and brownish discolored teeth with red fluorescence under ultraviolet light. Biochemical studies demonstrated markedly increased uroporphyrinogen I in urine and plasma (2,650- and 10,700-fold greater than wild type, respectively), whereas urinary 5-aminolevulinic acid and porphobilinogen were lower than normal. Erythrocytic URO-synthase activity was <1% of mean wild-type activity, confirming the diagnosis and distinguishing it from feline phenocopies having acute intermittent porphyria. Sequencing of the affected cat's UROS gene revealed two missense mutations, c.140C>T (p.S47F) in exon 3 and c.331G>A (p.G111S) in exon 6, both of which were homozygous, presumably owing to parental consanguinity. Neither was present in 100 normal cat alleles. Prokaryotic expression and thermostability studies of the purified monomeric wild-type, p.S47F, p.G111S, and p.S47F/G111S enzymes showed that the p.S47F enzyme had 100% of wild-type specific activity but ~50% decreased thermostability, whereas the p.G111S and p.S47F/G111S enzymes had about 60% and 20% of wild-type specific activity, respectively, and both were markedly thermolabile. Molecular modeling results indicated that the less active/less stable p.G111S enzyme was further functionally impaired by a structural interaction induced by the presence of the S47F substitution. Thus, the synergistic interaction of two rare amino acid substitutions in the URO-synthase polypeptide caused the feline model of human CEP.
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Authors | Sonia Clavero, David F Bishop, Urs Giger, Mark E Haskins, Robert J Desnick |
Journal | Molecular medicine (Cambridge, Mass.)
(Mol Med)
2010 Sep-Oct
Vol. 16
Issue 9-10
Pg. 381-8
ISSN: 1528-3658 [Electronic] England |
PMID | 20485863
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Mutant Proteins
- Porphyrins
- Uroporphyrinogen III Synthetase
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Topics |
- Animals
- Cat Diseases
(blood, enzymology, genetics, urine)
- Cats
- Erythrocytes
(metabolism)
- Homozygote
- Male
- Models, Molecular
- Molecular Sequence Data
- Mutant Proteins
(chemistry, genetics, metabolism)
- Mutation, Missense
(genetics)
- Porphyria, Erythropoietic
(blood, enzymology, urine, veterinary)
- Porphyrins
(blood, metabolism, urine)
- Uroporphyrinogen III Synthetase
(chemistry, genetics, metabolism)
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