Evidence for recent positive selection at the human AIM1 locus in a European population

被引:67
作者
Soejima, M
Tachida, H
Ishida, T
Sano, A
Koda, Y [1 ]
机构
[1] Kurume Univ, Sch Med, Dept Forens Med & Human Genet, Kurume, Fukuoka 830, Japan
[2] Kyushu Univ, Fac Sci, Dept Biol, Fukuoka 812, Japan
[3] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, Tokyo 113, Japan
关键词
AIM1; directional selection; pigmentation;
D O I
10.1093/molbev/msj018
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
Two missense polymorphisms (E272K and L374F) of the AIM1 locus, encoding a melanocyte differentiation antigen, were shown to have a clear association with human ethnicities. These two nonpathogenic single nucleotide polymorphisms (SNPs) may be associated with human pigmentation variation. In this study, we investigated sequence variation in the coding region and exon-flanking sequence and found low genetic variation only in subjects of European descent. All four statistical tests applied to the 7.55-kb region surrounding the L374F polymorphism detected statistically significant deviations from selective neutrality in Europeans. In addition, haplotype analysis revealed that one haplotype carrying 374F was overrepresented in this population, and the low rate of variation, with some features of selective sweeps, was shown to be statistically significant. These results suggest that positive selection recently has been acting or has acted on at least this region of the melanogenic gene and that an advantageous haplotype spread rapidly in Europe.
引用
收藏
页码:179 / 188
页数:10
相关论文
共 38 条
[1]   Median-joining networks for inferring intraspecific phylogenies [J].
Bandelt, HJ ;
Forster, P ;
Röhl, A .
MOLECULAR BIOLOGY AND EVOLUTION, 1999, 16 (01) :37-48
[2]   The 8818G allele of the agouti signaling protein (ASIP) gene is ancestral and is associated with darker skin color in African Americans [J].
Bonilla, C ;
Boxill, LA ;
McDonald, SA ;
Williams, T ;
Sylvester, N ;
Parra, E ;
Dios, S ;
Norton, H ;
Shriver, MD ;
Kittles, RA .
HUMAN GENETICS, 2005, 116 (05) :402-406
[3]   Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation.: A model for oculocutaneous albinism (OCA) type 4 [J].
Costin, GE ;
Valencia, JC ;
Vieira, WD ;
Lamoreux, ML ;
Hearing, VJ .
JOURNAL OF CELL SCIENCE, 2003, 116 (15) :3203-3212
[4]  
Fay JC, 2000, GENETICS, V155, P1405
[5]  
FU YX, 1993, GENETICS, V133, P693
[6]   Mutations in the gene encoding B, a novel transporter protein, reduce melanin content in medaka [J].
Fukamachi, S ;
Shimada, A ;
Shima, A .
NATURE GENETICS, 2001, 28 (04) :381-385
[7]   Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation [J].
Graf, J ;
Hodgson, R ;
van Daal, A .
HUMAN MUTATION, 2005, 25 (03) :278-284
[8]  
Harada M, 2001, CANCER RES, V61, P1089
[9]   Evidence for variable selective pressures at MC1R [J].
Harding, RM ;
Healy, E ;
Ray, AJ ;
Ellis, NS ;
Flanagan, N ;
Todd, C ;
Dixon, C ;
Sajantila, A ;
Jackson, IJ ;
Birch-Machin, MA ;
Rees, JL .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (04) :1351-1361
[10]  
HUDSON RR, 1994, GENETICS, V136, P1329