β-Thalassemia in American Blacks: Novel mutations in the 'TATA' box and an acceptor splice site

S. E. Antonarakis, S. H. Irkin, T. C. Cheng, A. F. Scott, J. P. Sexton, S. P. Trusko, S. Charache, H. H. Kazazian

Research output: Contribution to journalArticle

Abstract

β-Thalassemia genes, although often mild in their effects, are common among American Blacks. We have begun a systematic molecular analysis of β-Thalassemia mutations in this group. DNA polymorphisms in the β-globin gene cluster were examined among 22 β-Thalassemia chromosomes. Six different haplotypes were observed. β-globin genes of two of these were cloned, and their phenotypes were examined both in heterologous cells upon transient expression and in vivo. The gene found in the most common haplotype (9 of 22 chromosomes) contained a single base substitution (A → G) at position -29 within the highly conserved proximal promoter element (the 'TATA' box). This mutant gene directed β-globin RNA at 25% of normal levels both in heterologous cells and in vivo. It was associated with a mild β+-thalassemia phenotype. A different gene, isolated from an apparently rare haplotype (1 of 22 chromosomes), had a single base substitution (A → G) within the acceptor splice site of the second intervening sequence. This mutation abolished normal RNA splicing so that the only RNA made from the gene in vitro was an alternatively spliced RNA, which could not encode β-globin. The mild deficit in β-globin production attributable to the -29 A → G mutant allele most likely accounts for the frequently mild nature of β-thalassemia among American Blacks.

Original languageEnglish (US)
Pages (from-to)1154-1158
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume81
Issue number4 I
DOIs
StatePublished - May 24 1984
Externally publishedYes

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