The genetic basis of "Scarsdale Gourmet Diet" variegate porphyria: a missense mutation in the protoporphyrinogen oxidase gene.

Abstract

The porphyrias are disorders of porphyrin or porphyrin-precursor metabolism that result from inherited or acquired aberrations in the control of the porphyrin-heme biosynthetic pathway. Variegate porphyria (VP), one of the acute hepatic porphyrias, is characterized by a partial reduction in the activity of protoporphyrinogen oxidase (PPO), and recently, mutations in the PPO gene on chromosome 1q22-23 have been described. Our purpose was to identify the underlying genetic lesion in a severely affected patient with VP and to detect the silent mutation carriers in her family. The disease in this patient was precipitated by carbohydrate restriction as outlined in the "Scarsdale Gourmet Diet". Our mutation detection and confirmation strategy included PCR, automated sequencing, and restriction enzyme digestion. We identified a missense mutation in the patient and five family members. The mutation consisted of a previously unreported C-to-T transition in exon 5 of the PPO gene, resulting in the substitution of arginine by cysteine, designated R152C. This arginine residue is evolutionarily highly conserved in humans, mice, bacteria, yeast, and plants, indicating the importance of this residue in PPO. Our study established that a missense mutation in the PPO gene was the underlying mutation in this patient with VP and explained the occurrence of the phenotype in this family.

• Authors: J Frank, M B Poh-Fitzpatrick, L E King Jr, A M Christiano
• Journal: Archives of dermatological research (Arch Dermatol Res) Vol. 290 Issue 8 Pg. 441-5 (Aug 1998) ISSN: 0340-3696 [Print] Germany
• PMID: 9763307 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Flavoproteins
• Mitochondrial Proteins
• Oxidoreductases
• Oxidoreductases Acting on CH-CH Group Donors
• PPOX protein, human
• Protoporphyrinogen Oxidase

Topics

• Amino Acid Sequence
• Amino Acid Substitution
• Diet, Reducing
• Family
• Female
• Flavoproteins
• Genes (genetics)
• Humans
• Middle Aged
• Mitochondrial Proteins
• Molecular Sequence Data
• Mutation, Missense
• Oxidoreductases (genetics)
• Oxidoreductases Acting on CH-CH Group Donors
• Pedigree
• Porphyrias (diet therapy, enzymology, genetics)
• Protoporphyrinogen Oxidase
• Sequence Homology, Amino Acid