Bantu βs cluster haplotype predominates among Brazilian Blacks
- 1 July 1992
- journal article
- research article
- Published by Wiley in American Journal of Physical Anthropology
- Vol. 88 (3) , 295-298
- https://doi.org/10.1002/ajpa.1330880304
Abstract
We describe the combination of polymorphic restriction-enzyme sites in the β globin gene cluster (haplotypes) for 74 chromosomes from Brazilian Blacks bearing the sickle hemoglobin gene (βs). The three most common African βs haplotypes account for 67 chromosomes: 49/74 (66.2%) were identified as Central African Republic (CAR or Bantu) type, 17 (23.0%) as Benin, and one as Senegal; seven chromosomes (9.5%) had minor atypical haplotypes. This distribution is different from that observed in the United States or Jamaica, where the Benin haplotype predominates, and results from different patterns of slave trades to North and South Americas. Since the βs gene cluster polymorphisms modulate the severity of sickle cell anemia, this heterogeneity may explain differences of the clinical behavior of the disease in the United States and South America, and should also be considered in relation to other features and diseases.Keywords
This publication has 20 references indexed in Scilit:
- βS-Gene-Cluster Haplotypes in Sickle Cell AnemiaJournal of Pediatric Hematology/Oncology, 1990
- Nonblack patients with sickle cell disease have African beta S gene cluster haplotypesJAMA, 1989
- Haplotypes of βSChromosomes Among Patients with Sickle Cell Anemia from GeorgiaHemoglobin, 1986
- A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?British Journal of Haematology, 1985
- An HbF enrichment procedure for the HPLC analysis of γ chainsClinica Chimica Acta; International Journal of Clinical Chemistry, 1985
- Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in AfricaNew England Journal of Medicine, 1985
- The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell DiseaseNew England Journal of Medicine, 1982
- Concurrent Sickle-Cell Anemia and α-ThalassemiaNew England Journal of Medicine, 1982
- α-Globin gene organisation in blacks precludes the severe form of α-thalassaemiaNature, 1979
- Protection Afforded by Sickle-cell Trait Against Subtertian Malarial InfectionBMJ, 1954