Diversity of the MBL2 gene in various Brazilian populations and the case of selection at the Mannose-binding lectin locus

被引:57
作者
Boldt, A. B. W.
Culpi, L.
Tsuneto, L. T.
de Souza, I. R.
Kun, J. F. J.
Petzl-Erler, M. L.
机构
[1] Univ Fed Parana, Lab Genet Mol Humana, Dept Genet, Setor Ciencias Biol, BR-81531990 Curitiba, Parana, Brazil
[2] Univ Fed Parana, Lab Polimorfismos & Ligacao, Dept Genet, Setor Ciencias Biol, Curitiba, Parana, Brazil
[3] Univ Tubingen, Inst Trop Med, Tubingen, Germany
关键词
D O I
10.1016/j.humimm.2006.05.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The mannose binding lectin (MBL2) polymorphism is responsible for a common immunodeficiency in the human species. There were suggestions that the MBL2 polymorphism has been under balancing selection, based on the high global frequency of alleles generating MBL deficiency and on the worldwide distribution of diseases negatively associated with them. To describe the distribution of MBL2 allelic haplotypes in Brazilian populations and to discuss the evolution of this polymorphism, we analyzed six South Brazilian populations (152 Guarani Amerindian, 239 Kaingang Amerindian, 107 admixed, Brazilian 32 Afro-Brazilian, 202 Euro-Brazilian and 16 Oriental-Brazilian). Eight haplotypes were observed: MBL2*HYPA, LYQA, LYPA, LXPA, LYPB, LYQC, HYPD, and LYPD. In addition, through sequencing of the promoter and exon I from Amerindian and Oriental individuals, three new single-nucleotide polymorphisms (SNPs) were found in the MBL2 promoter region in the Kaingang. Analysis of the sequencing data by neutrality tests (Tajima's D and Fu and Li's D* and F*) revealed no deviation from selective neutrality equilibrium in the Guarani and Kaingang. Significant Fay and Wu's H results are explained by the recent gene flow in these populations. Contrarily to previous thoughts, stochastic evolutionary factors seem therefore to have bad a predominant role in shaping the MBL2 polymorphism, at least in the Amerindians. Human Immunology 67, 722-734 (2006). (c) American Society for Histocompatibility and Immunogenetics, 2006. Published by Elsevier Inc.
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页码:722 / 734
页数:13
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