Mild beta+(-87)-thalassemia CACCC box mutation is associated with elevated fetal hemoglobin expression in cis

Am J Hematol. 1994 Mar;45(3):265-7. doi: 10.1002/ajh.2830450316.

Abstract

The beta zero-thalassemia codon 39 nonsense mutation predominant in Sardinia is severe, and homozygotes are transfusion dependent. Two-thirds of beta zero 39 alleles are linked to A gamma T (haplotype II). One-fourth are linked to A gamma I (haplotypes I and IX), as is the mild beta +-thalassemia -87 C-->G mutation (haplotype VIII). beta +/beta zero-Thalassemia VIII/II compound heterozygotes have significantly higher A gamma I:A gamma T (23:7) than beta zero-thalassemia I/II (24:20) or IX/II (16:17) cases. This suggests that the beta + -87 mutation is associated with elevated gamma expression in cis, which may contribute to the lack of transfusion-dependence in beta +/beta zero cases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Base Sequence
  • Fetal Hemoglobin / biosynthesis*
  • Gene Expression
  • Globins / genetics*
  • Haplotypes
  • Heterozygote
  • Humans
  • Italy
  • Molecular Sequence Data
  • Point Mutation*
  • Promoter Regions, Genetic / genetics*
  • Severity of Illness Index
  • beta-Thalassemia / blood
  • beta-Thalassemia / genetics*

Substances

  • Globins
  • Fetal Hemoglobin