1. An initiation codon mutation as a cause of a beta-thalassemia.
- Author
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Jankovic L, Efremov GD, Josifovska O, Juricic D, Stoming TA, Kutlar A, and Huisman TH
- Subjects
- Adult, Base Sequence, Female, Heterozygote, Humans, Male, Middle Aged, Molecular Sequence Data, Polymorphism, Genetic genetics, Codon genetics, Mutation, Peptide Chain Initiation, Translational genetics, Thalassemia genetics
- Abstract
During the course of a screening program for beta-thalassemia mutations among beta-thalassemia heterozygotes in Yugoslavia we observed a mutation (ATG----ACG) in the initiation codon of the beta-globin gene which has not been described before. The abnormality was initially detected through mapping of the beta-globin gene by Southern blot analysis using the restriction enzyme Nco I. The loss of the Nco I site resulted in the presence of an 8.3 kb band in addition to the normal 5.2 kb band. The mutation was identified by sequence analysis of amplified DNA and by dot-blot analysis of this DNA with a 32P-labeled oligonucleotide probe. An additional polymorphism (CAC----CAT) was present at codon 2 on the same chromosome; this mutation was detected by Orkin et al in 1982 (1). Hematological and in vitro chain synthesis data suggest that the beta-thalassemia is of the beta zero type.
- Published
- 1990
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