Clinical and Genetic Heterogeneity in Black Patients With Homozygous β-Thalassemia From the Southeastern United States

Abstract

AbstractThe presence of various substitutions and deletions resulting in β-thalassemia was studied in 19 black patients with homozygous β-thalassemia and in numerous relatives; all patients were from Georgia, South Carolina, and Alabama. Methodology included gene mapping, amplification of genomic DNA with Taq polymerase, identification of known nucleotide substitutions or a single nucleotide deletion through hybridization with synthetic oligonucleotides, cloning and sequencing of a β-globin gene, and sequencing of amplified genomic DNA. Of the 38 chromosomes tested, 21 (55%) had the A →G substitution at nt -29, eight (21%) had the C → T substitution at nt —88, three (8%) had the substitution at codon 24, while one each of the following abnormalities were also detected: frameshift at codon 6, a C → A mutation at nt 848 of the βIVS-II (new), an A→ T mutation at codon 61 (new), a deletion of 1.35 kilobases including the 5’ end of β a Gγ(Aγδβ)°-thalassemia, and one thalassemia determinant that remained unidentified. The C → A mutation at nt 848 of IVS-II occurred at a position 3 nucleotides 5’ to the third exon, adjacent to the invariant AG dinucleotide of the acceptor sequence. The A →T mutation in codon 61 (AAG → TAG) resulted in the creation of a stop codon and thus in β°-thalassemia. The various mutations occurred on chromosomes with different haplotypes; however, chromosomes with a specific mutation but with different haplotypes belonged to one specific framework, which suggested that crossovers were responsible for these different types. Hemoglobin (Hb) F levels were generally high (55% to 75% with 98.5% in one patient with β°/β°); a few patients with specific haplotypes and an a-thalassemia-2 heterozygosity had a lower Hb F level. The Gγ in the Hb F was consistently high when the C →T mutation occurred at nt — 158 to the Cap site of the Gγ-globin gene; seven patients with + / + at this site had an average Gγof 73.8%, eight patients with + /- had 64.8%, and one patient with — / — had 34.2%. Variations in hematologic values and in Hb F, Gγ, and Hb A2 levels of relatives with a β-thalassemia heterozygosity depended to some extent on the types of mutations or deletions and on the haplotypes of the chromosomes with the β-thalasse-mia determinant.© 1988 by Grune & Stratton, Inc. 0006-4971/88/7203-0014$3.00/0