Species-Specific Features of DARC, the Primate Receptor for Plasmodium vivax and Plasmodium knowlesi

被引:29
|
作者
Demogines, Ann [1 ]
Truong, Kimberly A. [1 ]
Sawyer, Sara L. [1 ]
机构
[1] Univ Texas Austin, Inst Cellular & Mol Biol, Sect Mol Genet & Microbiol, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
malaria; positive selection; arms race; species tropism; zoonosis; HUMAN MALARIA PARASITE; DUFFY ANTIGEN/RECEPTOR; EVOLUTION; ANTIGEN; PROTEIN; IDENTIFICATION; ERYTHROCYTES; FALCIPARUM; LIKELIHOOD; CHEMOKINES;
D O I
10.1093/molbev/msr204
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The DARC (Duffy antigen/receptor for chemokines) gene, also called Duffy or FY, encodes a membrane-bound chemokine receptor. Two malaria parasites, Plasmodium vivax and Plasmodium knowlesi, use DARC to trigger internalization into red blood cells. Although much has been reported on the evolution of DARC null alleles, little is known about the evolution of the coding portion of this gene or the role that protein sequence divergence in this receptor may play in disease susceptibility or zoonosis. Here, we show that the Plasmodium interaction domain of DARC is nearly invariant in the human population, suggesting that coding polymorphism there is unlikely to play a role in differential susceptibility to infection. However, an analysis of DARC orthologs from 35 simian primate species reveals high levels of sequence divergence in the Plasmodium interaction domain. Signatures of positive selection in this domain indicate that species-specific mutations in the protein sequence of DARC could serve as barriers to the transmission of Plasmodium between primate species.
引用
收藏
页码:445 / 449
页数:5
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