S. Rahbar et al., A NOVEL INTRACHROMOSOMAL REARRANGEMENT IN THE BETA-GLOBIN GENE FOUND IN AN AFRICAN-AMERICAN FAMILY, Hemoglobin, 19(6), 1995, pp. 375-388
We describe here a deletion of 34 nucleotides from the 3' end of the f
irst intervening sequence of the beta-globin gene covering the AGGC sp
lice junction, and the insertion of 32 nucleotides of the delta-globin
gene at the same location. This gene rearrangement was detected in th
ree members of an African-American family. The proband, a 28-year-old
female, and her mother had a history of chronic anemia. One of her two
brothers, who inherited the same gene defect, was apparently healthy
with no symptoms of hemolytic anemia. The proband, her rather, and her
two brothers, including the one who carried the beta-globin gene rear
rangement, were found to be heterozygous for alpha-thalassemia-2 (-alp
ha(3.7)). Although the AGGC splice junction is disrupted (AGGC-->AGAT)
, the invariant AG has remained intact after this gene rearrangement.
Our investigations could not detect any defect in RNA processing in th
e affected beta-globin genes. The discrepancies between the phenotypes
and the globin chain synthesis ratios of the mother, her daughter, an
d her son who inherited the same gene defect at their beta-globin gene
s, remain unexplained.