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. 1981 Apr;78(4):2455–2459. doi: 10.1073/pnas.78.4.2455

Base substitution in an intervening sequence of a beta+-thalassemic human globin gene.

R A Spritz, P Jagadeeswaran, P V Choudary, P A Biro, J T Elder, J K deRiel, J L Manley, M L Gefter, B G Forget, S M Weissman
PMCID: PMC319365  PMID: 6264477

Abstract

beta globin gene fragments from a patient with homozygous beta+-thalassemia have been cloned and subjected to restriction endonuclease, nucleotide sequence, and in vitro trancription analyses. Restriction endonuclease mapping of the cloned gene fragments revealed no deletions or other rearrangements, and transcription of the thalassemic gene appeared to be normal in vitro. However, nucleotide sequence analysis of the beta+-thalassemic gene fragments permitted identification of a single base change in the body of the small intervening sequence. This nucleotide change creates a sequence much like that of the 3' splice site of the small intervening sequence. The presence of a potential anomalous splicing site as a result of this base change suggests a mechanism for defective posttranscriptional processing of beta globin mRNA precursor molecules in beta+-thalassemia.

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Selected References

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