Two beta-globin cluster-linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin

Eur J Haematol. 2005 Jul;75(1):47-53. doi: 10.1111/j.1600-0609.2005.00416.x.

Abstract

Objective: To correlate different polymorphisms of the beta-globin cluster with fetal hemoglobin (HbF) level in beta-thalassemia and E-beta thalassemia patients.

Methods: Fifteen thalassemia patients, seven with high HbF and not requiring transfusion, eight with lower HbF and requiring transfusion were studied for beta-globin mutation, concurrent inheritance of alpha-thalassemia, RFLP haplotype, a C-->T polymorphism at -158 of Ggamma and configuration of an (AT)(x)T(y) motif at -540 of beta-globin gene.

Results: Senegal 5'beta-haplotype and the polymorphism at -158 of G(gamma) was (P = 0.063) was linked to the high-HbF phenotype but the (AT)(9)T(5) configuration of the (AT)(x)T(y) motif was not (P = 0.6). Study of 30 chromosomes revealed 7 different configurations of the (AT)(x)T(y) motif. Association of these motifs with specific beta-globin mutations of this region has also been determined.

Conclusion: The senegal haplotype and the polymorphism at -158 of G(gamma) was linked to the high-HbF phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Fetal Hemoglobin* / analysis
  • Genetic Linkage
  • Hemoglobins, Abnormal / genetics*
  • Humans
  • Male
  • Multigene Family / genetics
  • Phenotype*
  • Point Mutation*
  • Polymorphism, Restriction Fragment Length*
  • Quantitative Trait Loci / genetics
  • alpha-Thalassemia / blood
  • alpha-Thalassemia / genetics*

Substances

  • Hemoglobins, Abnormal
  • hemoglobin Senegal
  • Fetal Hemoglobin