The heritage of pathogen pressures and ancient demography in the human innate-immunity CD209/CD209L region

被引:74
作者
Barreiro, LB
Patin, E
Neyrolles, O
Cann, HM
Gicquel, B
Quintana-Murci, L
机构
[1] Inst Pasteur, FRE 2849, Unit Mol Prevent & Therapy Human Dis, CNRS, F-75724 Paris, France
[2] Inst Pasteur, Unite Genet Mycobacterienne, F-75724 Paris, France
[3] Fdn Jean Dausset, Ctr Etud Polymorphisme Humain, Paris, France
关键词
D O I
10.1086/497613
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The innate immunity system constitutes the first line of host defense against pathogens. Two closely related innate immunity genes, CD209 and CD209L, are particularly interesting because they directly recognize a plethora of pathogens, including bacteria, viruses, and parasites. Both genes, which result from an ancient duplication, possess a neck region, made up of seven repeats of 23 amino acids each, known to play a major role in the pathogen-binding properties of these proteins. To explore the extent to which pathogens have exerted selective pressures on these innate immunity genes, we resequenced them in a group of samples from sub-Saharan Africa, Europe, and East Asia. Moreover, variation in the number of repeats of the neck region was defined in the entire Human Genome Diversity Panel for both genes. Our results, which are based on diversity levels, neutrality tests, population genetic distances, and neck-region length variation, provide genetic evidence that CD209 has been under a strong selective constraint that prevents accumulation of any amino acid changes, whereas CD209L variability has most likely been shaped by the action of balancing selection in non-African populations. In addition, our data point to the neck region as the functional target of such selective pressures: CD209 presents a constant size in the neck region populationwide, whereas CD209L presents an excess of length variation, particularly in non- African populations. An additional interesting observation came from the coalescent-based CD209 gene tree, whose binary topology and time depth (similar to 2.8 million years ago) are compatible with an ancestral population structure in Africa. Altogether, our study has revealed that even a short segment of the human genome can uncover an extraordinarily complex evolutionary history, including different pathogen pressures on host genes as well as traces of admixture among archaic hominid populations.
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页码:869 / 886
页数:18
相关论文
共 110 条
[91]   DC-SIGN (CD209) mediates dengue virus infection of human dendritic cells [J].
Tassaneetrithep, B ;
Burgess, TH ;
Granelli-Piperno, A ;
Trumpfherer, C ;
Finke, J ;
Sun, W ;
Eller, MA ;
Pattanapanyasat, K ;
Sarasombath, S ;
Birx, DL ;
Steinman, RM ;
Schlesinger, S ;
Marovich, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (07) :823-829
[92]   Patterns of human genetic diversity: Implications for human evolutionary history and disease [J].
Tishkoff, SA ;
Verrelli, BC .
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, 2003, 4 :293-340
[93]   Haplotype diversity and linkage disequilibrium at human G6PD:: Recent origin of alleles that confer malarial resistance [J].
Tishkoff, SA ;
Varkonyi, R ;
Cahinhinan, N ;
Abbes, S ;
Argyropoulos, G ;
Destro-Bisol, G ;
Drousiotou, A ;
Dangerfield, B ;
Lefranc, G ;
Loiselet, J ;
Piro, A ;
Stoneking, M ;
Tagarelli, A ;
Tagarelli, G ;
Touma, EH ;
Williams, SM ;
Clark, AG .
SCIENCE, 2001, 293 (5529) :455-462
[94]   Defense strategies and immunity-related genes [J].
Trowsdale, J ;
Parham, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (01) :7-17
[95]   Y chromosome sequence variation and the history of human populations [J].
Underhill, PA ;
Shen, PD ;
Lin, AA ;
Jin, L ;
Passarino, G ;
Yang, WH ;
Kauffman, E ;
Bonné-Tamir, B ;
Bertranpetit, J ;
Francalacci, P ;
Ibrahim, M ;
Jenkins, T ;
Kidd, JR ;
Mehdi, SQ ;
Seielstad, MT ;
Wells, RS ;
Piazza, A ;
Davis, RW ;
Feldman, MW ;
Cavalli-Sforza, LL ;
Oefner, PJ .
NATURE GENETICS, 2000, 26 (03) :358-361
[96]   Positive selection on the human genome [J].
Vallender, EJ ;
Lahn, BT .
HUMAN MOLECULAR GENETICS, 2004, 13 :R245-R254
[97]   Molecular basis of the differences in binding properties of the highly related C-type lectins DC-SIGN and L-SIGN to Lewis x trisaccharide and Schistosoma mansoni egg antigens [J].
Van Liempt, E ;
Imberty, A ;
Bank, CMC ;
Van Vliet, SJ ;
Van Kooyk, Y ;
Geijtenbeek, TBH ;
Van Die, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) :33161-33167
[98]  
Van Valen L., 1973, Evol. Theory, V1, P1, DOI DOI 10.1038/344864A0
[99]   Evidence for balancing selection from nucleotide sequence analyses of human G6PD [J].
Verrelli, BC ;
McDonald, JH ;
Argyropoulos, G ;
Destrol-Bisol, G ;
Froment, A ;
Drousiotou, A ;
Lefranc, G ;
Helal, AN ;
Loiselet, J ;
Tishkoff, SA .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (05) :1112-1128
[100]   Metapopulation models for historical inference [J].
Wakeley, J .
MOLECULAR ECOLOGY, 2004, 13 (04) :865-875