Complex signatures of natural selection at the Duffy blood group locus

被引:215
作者
Hamblin, MT [1 ]
Thompson, EE [1 ]
Di Rienzo, A [1 ]
机构
[1] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
关键词
D O I
10.1086/338628
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Duffy blood group locus (FY) has long been considered a likely target of natural selection, because of the extreme pattern of geographic differentiation of its three major alleles (FY* B, FY* A, and FY* O). In the present study, we resequenced the FY region in samples of Hausa from Cameroon (fixed for FY* O), Han Chinese (fixed for FY* A), Italians, and Pakistanis. Our goals were to characterize the signature of directional selection on FY* O in sub-Saharan Africa and to understand the extent to which natural selection has also played a role in the extreme geographic differentiation of the other derived allele at this locus, FY* A. The data from the FY region are compared with the patterns of variation observed at 10 unlinked, putatively neutral loci from the same populations, as well as with theoretical expectations from the neutral-equilibrium model. The FY region in the Hausa shows evidence of directional selection in two independent properties of the data (i.e., level of sequence variation and frequency spectrum), observations that are consistent with the FY* O mutation being the target. The Italian and Chinese FY data show patterns of variation that are very unusual, particularly with regard to frequency spectrum and linkage disequilibrium, but do not fit the predictions of any simple model of selection. These patterns may represent a more complex and previously unrecognized signature of positive selection.
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页码:369 / 383
页数:15
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共 45 条
[11]  
FLINT J, 1993, HUM GENET, V91, P91
[12]   Effects of natural selection on patterns of DNA sequence variation at the transferrin, somatolactin, and p53 genes within and among chinook salmon (Oncorhynchus tshawytscha) populations [J].
Ford, MJ .
MOLECULAR ECOLOGY, 2000, 9 (07) :843-855
[13]   Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels [J].
Frisse, L ;
Hudson, RR ;
Bartoszewicz, A ;
Wall, JD ;
Donfack, J ;
Di Rienzo, A .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) :831-843
[14]   From malaria to chemokine receptor: The emerging physiologic role of the duffy blood group antigen [J].
Hadley, TJ ;
Peiper, SC .
BLOOD, 1997, 89 (09) :3077-3091
[15]   Detection of the signature of natural selection in humans: Evidence from the Duffy blood group locus [J].
Hamblin, MT ;
Di Rienzo, A .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (05) :1669-1679
[16]   ESTIMATION OF LINKAGE DISEQUILIBRIUM IN RANDOMLY MATING POPULATIONS [J].
HILL, WG .
HEREDITY, 1974, 33 (OCT) :229-239
[17]  
HUDSON RR, 1987, GENETICS, V116, P153
[18]  
HUDSON RR, IN PRESS GENETICS
[19]   Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting [J].
Ishihara, K ;
Hatano, N ;
Furuumi, H ;
Kato, R ;
Iwaki, T ;
Miura, K ;
Jinno, Y ;
Sasaki, H .
GENOME RESEARCH, 2000, 10 (05) :664-671
[20]   BALANCING SELECTION AT ALLOZYME LOCI IN OYSTERS - IMPLICATIONS FROM NUCLEAR RFLPS [J].
KARL, SA ;
AVISE, JC .
SCIENCE, 1992, 256 (5053) :100-102