PHYSICAL MAPPING OF THE GLOBIN GENE DELETION IN (DELTA-BETA)-DEGREES-THALASSAEMIA

被引:78
作者
BERNARDS, R
KOOTER, JM
FLAVELL, RA
机构
[1] Section for Medical Enzymology and Molecular Biology, Laboratory of Biochemistry, University of Amsterdam, 10005 GA Amsterdam
关键词
filter hybridization; Foetal-adult gene switch; genomic blotting; plasmid pCRI vector; recombinant DNA;
D O I
10.1016/0378-1119(79)90062-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have constructed a physical map of restriction endonuclease cleavage sites in the (δ+β)-globin gene region in the DNA of patients with (δβ)°-thalassaemia. This map shows that a 10 kb deletion has occurred in (δβ)°-thalassaemia to remove the entire β-globin gene and the 3′ portion of the δ-globin gene. The 5′ terminus of the deletion is in the large intron of the δ-globin gene and the 3′ terminus 1.8 kb to the 3′-side of the β-globin gene. A similar deletion of about 7 kb has been described previously in the DNA of patients with Hb Lepore; the 5′ terminus of the deletion is also in the δ-globin gene but the 3′ terminus is in the β-globin gene. Comparison of the foetal (γ) globin gene expression in adults with (δβ)°-thalassaemia and Hb Lepore suggests that the 3′ extragenic regions of the β-globin gene contain DNA sequences involved in the regulation of γ-globin gene expression. © 1979.
引用
收藏
页码:265 / 280
页数:16
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