Beta-globin gene cluster haplotypes as evidence of African gene flow to the northeastern coast of Venezuela

被引:15
作者
De Lugo, MV [1 ]
Rodríguez-Larralde, A [1 ]
De Guerra, DC [1 ]
机构
[1] Inst Venezolano Invest Cient, Ctr Med Expt, Lab Genet Humana, Caracas 1020A, Venezuela
关键词
D O I
10.1002/ajhb.10120
中图分类号
Q98 [人类学];
学科分类号
030303 ;
摘要
In order to study the origin of mutation HBB*S in Sucre and Anzoategui states and the genetic affinities of these Venezuelan populations with other human groups, the beta-globin gene cluster haplotypes were determined for 28 sickle cell and/or S-beta thalassemia patients and for 37 individuals with normal hematological parameters. Bantu, Benin, Senegal, and atypical haplotypes were identified in 50%, 36%, 2%, and 12% of the HBB*S chromosomes, respectively. Similar results have been published for Venezuelan patients from the central states, but a different trend is shown in a publication based on a group of patients from different regions of the country. For HBB*A, haplotype 2 (+ - - - - ), characteristic of non-African groups, was the most common (39%), followed by haplotype 3 (- - - - +) of African origin, and haplotype 6 (- + + - +), also typical of non-Africans. The results reveal a high level of admixture of the Sucre-Anzoategui population. The importance of specific conditions which have acted differently in the Venezuelan populations, such as founder. effect, genetic drift, isolation, and endogamy are discussed. Genetic distances between the Sucre-Anzoategui sample and several other human populations calculated on the basis of the HBB*S and HBB*A haplotypes revealed similar results, the closest genetic relationships being observed in relation to Bantu-speaking groups. These results confirm the utility of the beta-globin haplotypes for population studies and contribute to knowledge of the Venezuelan gene pool. (C) 2002 Wiley-Liss, Inc.
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页码:29 / 37
页数:9
相关论文
共 60 条
[31]  
LI QL, 1985, J BIOL CHEM, V260, P4901
[32]   PHYLOGENY OF HUMAN BETA-GLOBIN HAPLOTYPES AND ITS IMPLICATIONS FOR RECENT HUMAN-EVOLUTION [J].
LONG, JC ;
CHAKRAVARTI, A ;
BOEHM, CD ;
ANTONARAKIS, S ;
KAZAZIAN, HH .
AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, 1990, 81 (01) :113-130
[33]   SICKLE-CELL-ANEMIA AND BETA-GENE CLUSTER HAPLOTYPES IN CUBA [J].
MUNIZ, A ;
CORRAL, L ;
ALAEZ, C ;
SVARCH, E ;
ESPINOSA, E ;
CARBONELL, N ;
DILEO, R ;
FELICETTI, L ;
NAGEL, RL ;
MARTINEZ, G .
AMERICAN JOURNAL OF HEMATOLOGY, 1995, 49 (02) :163-164
[34]  
NAGEL RL, 1991, BLOOD, V77, P1371
[35]  
NAGEL RL, 1990, SEMIN HEMATOL, V27, P342
[36]  
NAGEL RL, 1987, BLOOD, V69, P1026
[37]   HEMATOLOGICALLY AND GENETICALLY DISTINCT FORMS OF SICKLE-CELL ANEMIA IN AFRICA - THE SENEGAL TYPE AND THE BENIN TYPE [J].
NAGEL, RL ;
FABRY, ME ;
PAGNIER, J ;
ZOHOUN, I ;
WAJCMAN, H ;
BAUDIN, V ;
LABIE, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (14) :880-884
[38]   ACCURACY OF ESTIMATED PHYLOGENETIC TREES FROM MOLECULAR-DATA .2. GENE-FREQUENCY DATA [J].
NEI, M ;
TAJIMA, F ;
TATENO, Y .
JOURNAL OF MOLECULAR EVOLUTION, 1983, 19 (02) :153-170
[39]  
NEI M, 1993, MOL BIOL EVOL, V10, P927
[40]  
OLIVERO R, 1996, ACTA CIENT VENEZ, V47, P61