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PMID: 6268660 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Sickle gene. Its origin and diffusion from West Africa.

The Journal of clinical investigation ·Vol. 68 ·No. 3 ·1981-09-00 ·Pages 606-10

Mears JG, Lachman HM, Cabannes R, Amegnizin KP, Labie D, Nagel RL

Abstract

Linked DNA polymorphisms can be used to study the evolution of structural gene mutations. Both the beta S-(beta 6Glu leads to Val) and beta C-(beta 6Glu leads to Lys) genes are common in West Africa. We have analyzed their linkage to a polymorphic Hpa 1 site appearing 3' to the beta-globin gene locus in selected populations from Wes Africa. A large reservoir of beta A-genes linked to 13-kilobase Hpa 1 fragments with a frequency of 17-18% has been identified. In addition, the beta S- and beta C-genes in Togo are found to be tightly linked to the 13-kilobase Hpa 1 fragment, whereas 72% of the beta S-genes in the Ivory Coast reside on the 7.6-kilobase Hpa 1 fragment. These studies are consistent with the selection and expansion of two different chromosomes bearing beta S-genes in at least two physically close, but ethnically separate regions of West Africa, with subsequent diffusion to North, Equatorial, and East Africa.

MeSH Terms
Africa/ethnology Anemia, Sickle Cell/genetics Biological Evolution DNA Restriction Enzymes Genes Genetics, Population Hemoglobin, Sickle/genetics Humans Polymorphism, Genetic
Chemicals
Hemoglobin, Sickle DNA Restriction Enzymes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mears J G
Lachman H M
Cabannes R
Amegnizin K P
Labie D
Nagel R L
References (13)
13 references, click to expand
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1981-09-00
Pages
606-10
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC370840
Subset
IM
Grants
NIGMS NIH HHS · GM 28841 · United States
NHLBI NIH HHS · HL 21016 · United States
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