Abstract
DNA from healthy Malaysian newborns was studied on gene maps after digestion with different restriction endonucleases. Of 65 newborns, two were found to be carriers of two different variants of triplicated alpha-globin loci. In variant no. 1, found in an Malay, the three alpha-globin genes are in an elongated DNA fragment on digestion with Eco RI and Bam HI. The third alpha-globin gene was found in a additional 3.7-kb fragment on digestion with Hpa I, Bgl II and Hind III. In variant no. 2, a new type of triplicated alpha-globin loci, found in a Chinese, the three alpha-globin genes reside in an elongated DNA fragment longer than that of variant no. 1 on digestion with Eco RI and Bam HI. The third alpha-globin gene was found in an additional 4.2-kb fragment on digestion with Hpa I and Hind III. Digestion of this variant DNA with Bg1 II produced an abnormal 16.7-kb fragment in addition to the normal 7.0-kb Bgl-II fragment. The locations of the restriction sites in the two types of triplicated alpha-globin loci are compatible with a mechanism of unequal crossing over following two different modes of misalignment.
MeSH Terms
Base Sequence
DNA Restriction Enzymes
Erythrocytes/metabolism
Fetal Blood
Genes
Genetic Variation
Globins/genetics
Hemoglobins, Abnormal/genetics
Humans
Infant, Newborn
Leukocytes/metabolism
Nucleic Acid Hybridization
Chemicals
Hemoglobins, Abnormal
Globins
DNA Restriction Enzymes
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Lie-Injo L E
Herrera A R
Kan Y W
References (19)
19 references, click to expand
-
Genetic lesion in homozygous alpha thalassaemia (hydrops fetalis).
Nature. 1974 Oct 4;251(5474):392-3
PMID: 4424635
-
Nucleotide sequence of the rightward operator of phage lambda.
Proc Natl Acad Sci U S A. 1975 Mar;72(3):1184-8
PMID: 1055375
-
Deletion of alpha-globin genes in haemoglobin-H disease demonstrates multiple alpha-globin structural loci.
Nature. 1975 May 15;255(5505):255-6
PMID: 1170497
-
Detection of specific sequences among DNA fragments separated by gel electrophoresis.
J Mol Biol. 1975 Nov 5;98(3):503-17
PMID: 1195397
-
Identification of a nondeletion defect in alpha-thalassemia.
N Engl J Med. 1977 Nov 17;297(20):1081-4
PMID: 909565
-
Insertion of synthetic copies of human globin genes into bacterial plasmids.
Nucleic Acids Res. 1978 Feb;5(2):563-81
PMID: 345245
-
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.
J Clin Invest. 1979 Jun;63(6):1307-10
PMID: 447845
-
The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.
Cell. 1979 May;17(1):33-42
PMID: 455460
-
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia.
Blood. 1979 Dec;54(6):1407-16
PMID: 508945
-
Triplicated alpha-globin loci in humans.
Proc Natl Acad Sci U S A. 1980 Jan;77(1):518-21
PMID: 6928643
-
A novel alpha-globin gene arrangement in man.
Nature. 1980 Apr 17;284(5757):632-5
PMID: 6245373
-
The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions.
Cell. 1980 May;20(1):119-30
PMID: 6446404
-
The structure of a human alpha-globin pseudogene and its relationship to alpha-globin gene duplication.
Cell. 1980 Sep;21(2):537-44
PMID: 7407925
-
Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
J Clin Invest. 1980 Dec;66(6):1319-25
PMID: 7440717
-
Homology and concerted evolution at the alpha 1 and alpha 2 loci of human alpha-globin.
Nature. 1981 Mar 5;290(5801):26-9
PMID: 7010180
-
Cloning and complete nucleotide sequence of human 5'-alpha-globin gene.
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7054-8
PMID: 6452630
-
Alpha-chain thalassemia and hydrops fetalis in Malaya: report of five cases.
Blood. 1962 Nov;20:581-90
PMID: 13930509
-
HAEMOGLOBIN H DISEASE IN THAILAND: A GENETICAL STUDY.
Nature. 1964 Nov 28;204:907-8
PMID: 14235731
-
The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion.
Nature. 1974 Oct 4;251(5474):389-92
PMID: 4138824