Some Mexican glucose-6-phosphate dehydrogenase variants revisited
✍ Scribed by Ernest Beutler; Wanda Kuhl; Eva Ramirez; Ruben Lisker
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 369 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
✦ Synopsis
Glucose-6-phosphate dehydrogenase (G6PD) deficiency appears to be fairly common in Mexico. We have now examined the DNA of three previously reported electrophoretically fast Mexican G6PD variants, -G6PD Distrito Federal, G6PD Tepic, and G6PD Castilla. All three of these variants, believed on the basis of biochemical characterization and population origin to be unique, have the G--~A transition at nucleotide 202 and the A---~G transition at nucleotide 376, mutations that we now recognize to be characteristic of G6PD A-. Two other Mexican males with G6PD deficiency were found to have the same mutation. All five have the (NlaIII! FokI/PvulI/PstI) haplotype characteristic of G6PD Ain Africa. Since the PvuII+ genotype seems to be rare in Europe, we conclude that all of these G6PD A-genes had their ancient origin in Africa, although in many of the Mexican patients with G6PD A -202A/376G the gene may have been imported more recently from Spain, where this variant, formerly known as G6PD Betica, is also prevalent.
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