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PMID: 1376298 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A novel sickle cell mutation of yet another origin in Africa: the Cameroon type.

Human genetics ·Vol. 89 ·No. 3 ·1992-05-00 ·Pages 333-7

Lapouméroulie C, Dunda O, Ducrocq R, Trabuchet G, Mony-Lobé M, Bodo JM, Carnevale P, Labie D, Elion J, Krishnamoorthy R

Abstract

The sickle cell mutation (beta s) arose as at least three independent events in Africa and once in Asia, being termed the Senegal, Benin, Bantu and Indian types respectively. An investigation in Cameroon was carried out to determine whether the atypical sickle genes observed in the neighboring countries are the result of recombination or the presence of a sickle cell mutation of a different genetic origin. It was conducted on 40 homozygous SS patients followed at the Blood Transfusion Center in the capital city of Yaoundé. On 80 beta s chromosomes, 13 exhibited a novel polymorphic pattern that was observed three times in the homozygous state. This chromosome contains an A gamma T gene. The restriction fragment length polymorphism haplotype is different from all the other beta s chromosomes in both the 5' and 3' regions, but has previously been reported in sporadic cases. The (AT)8(T)5 sequence in the -500 region of the beta gene is specific and different from that of the Senegal, Benin, Bantu or Indian beta s genes. All the carriers of this specific chromosome belong to the Eton ethnic group and originate from the Sanaga river valley. This observation strongly argues for yet another independent origin of the sickle cell mutation in Africa, here referred to as the "Cameroon type". The Benin haplotype and a Benin/Bantu recombinant haplotype have been observed in the other studied populations: Ewondo, Bamiléké, Bassa, Yambassa and Boulou.

MeSH Terms
Anemia, Sickle Cell/genetics Base Sequence Blotting, Southern Cameroon Fetal Hemoglobin Hemoglobin, Sickle/genetics Humans Linkage Disequilibrium Molecular Sequence Data Mutation/genetics Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Recombination, Genetic/genetics
Chemicals
Hemoglobin, Sickle Fetal Hemoglobin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Lapouméroulie C
INSERM U 120, Hôpital Robert Debré, Paris, France.
Dunda O
Ducrocq R
Trabuchet G
Mony-Lobé M
Bodo J M
Carnevale P
Labie D
Elion J
Krishnamoorthy R
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Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1992-05-00
Pages
333-7
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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