A new polymorphism in the human beta-globin gene useful in antenatal diagnosis.
Open Access
- 1 October 1981
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 68 (4) , 915-919
- https://doi.org/10.1172/jci110346
Abstract
A new polymorphism in the beta-globin is described, using the restriction enzyme Asu I. A radioactive probe specifically representing the large intervening sequence (IVS 2) of the beta-globin gene has been used to detect this polymorphism. Normally, a 0.8-kilobase fragment containing beta-IVS 2 is generated by Asu I; however, a 1.0-kilobase fragment is seen in association with 18% of beta A-genes, and 38% of beta-thalassemia genes in an Israeli population studied. By contrast, the Asu I polymorphism has rarely been seen in blacks examined to date. An additional Asu I change is seen the the delta-globin gene with a delta-IVS probe. The beta-Asu I polymorphism is shown to be useful in the antenatal diagnosis of beta-thalassemia.Keywords
This publication has 21 references indexed in Scilit:
- Polymorphism of DNA Sequence in the β-Globin Gene RegionNew England Journal of Medicine, 1980
- DNA sequence variants in the Gγ-, Aγ-, δ- and β-globin genes of manCell, 1979
- Heterogeneity of DNA fragments associated with the sickle-globin gene.Journal of Clinical Investigation, 1979
- The structure of the human β-globin gene in β-thalassaemiaNucleic Acids Research, 1979
- beta 0 thalassemia, a nonsense mutation in man.Proceedings of the National Academy of Sciences, 1979
- Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia.Proceedings of the National Academy of Sciences, 1979
- Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.Proceedings of the National Academy of Sciences, 1978
- Changes in restricted human cellular DNA fragments containing globin gene sequences in thalassemias and related disordersProceedings of the National Academy of Sciences, 1978
- ABSENCE OF BETA-MESSENGER MESSENGER-RNA IN BETA-0-THALASSEMIA IN KURDISH JEWS1978
- Homozygous βd` - and β+- Thalassemia in Kurdish Jews and ArabsHemoglobin, 1977