Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia

• Published in: The Journal of clinical investigation 1970-05, Vol.49 (5), p.1035-1040
• Main Authors: Huisman, T H, Schroeder, W A, Stamatoyannopoulos, G, Bouver, N, Shelton, J R, Shelton, J B, Apell, G
• Format: Article
• Language: English
• Subjects: Alanine; Amino Acid Metabolism, Inborn Errors - blood; Chromatography, Paper; Fetal Hemoglobin - analysis; Glycine; Hemoglobinopathies - genetics; Heterozygote; Molecular Biology; Pedigree; Thalassemia - blood; Thalassemia - complications
• ISSN: 0021-9738
• DOI: 10.1172/JCI106303

The fetal hemoglobin in the affected members of three Greek families with the hereditary persistence of fetal hemoglobin has only gamma-chains of the type with alanine in position 136. Although certain Negro families had been considered to have only this type of gamma-chains in their fetal hemoglobin, further studies required that they be reclassified. Consequently, the Greek cases are the sole examples of this class among the heterozygotes for the hereditary persistence of fetal hemoglobin. In Greek double heterozygotes for beta-thalassemia and the hereditary persistence of fetal hemoglobin, fetal hemoglobin is increased above the level of hemoglobin F in simple heterozygotes and gamma-chains with glycine in position 136 become apparent. In these individuals, gamma-chains with alanine in position 136 apparently derive from the chromosome for the hereditary persistence of fetal hemoglobin and are present in the hemoglobin F with gamma-chains of both types from the chromosome for beta-thalassemia. When these data are correlated with earlier knowledge of the genetic state of the Greek individuals, modifications of our previous ideas about deletions as the genetic basis of the hereditary persistence of fetal hemoglobin must be considered.