MBE Advance Access originally published online on September 14, 2005
Molecular Biology and Evolution 2006 23(1):179-188; doi:10.1093/molbev/msj018
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Article |
Evidence for Recent Positive Selection at the Human AIM1 Locus in a European Population


* Department of Forensic Medicine and Human Genetics, Kurume University School of Medicine, Kurume, Japan;
Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka, Japan; and
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Tokyo, Japan
E-mail: ykoda{at}med.kurume-u.ac.jp.
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.
Key Words: AIM1 directional selection pigmentation
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
R. A. Sturm Molecular genetics of human pigmentation diversity Hum. Mol. Genet., April 15, 2009; 18(R1): R9 - R17. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Suzuki, A. Pasch, O. Bonny, M. G. Mohaupt, M. A. Hediger, and F. J. Frey Gain-of-function haplotype in the epithelial calcium channel TRPV6 is a risk factor for renal calcium stone formation Hum. Mol. Genet., June 1, 2008; 17(11): 1613 - 1618. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Fujimoto, R. Kimura, J. Ohashi, K. Omi, R. Yuliwulandari, L. Batubara, M. S. Mustofa, U. Samakkarn, W. Settheetham-Ishida, T. Ishida, et al. A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness Hum. Mol. Genet., March 15, 2008; 17(6): 835 - 843. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Fukamachi, M. Kinoshita, T. Tsujimura, A. Shimada, S. Oda, A. Shima, A. Meyer, S. Kawamura, and H. Mitani Rescue From Oculocutaneous Albinism Type 4 Using Medaka slc45a2 cDNA Driven by Its Own Promoter Genetics, February 1, 2008; 178(2): 761 - 769. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. McEvoy, S. Beleza, and M. D. Shriver The genetic architecture of normal variation in human pigmentation: an evolutionary perspective and model Hum. Mol. Genet., October 15, 2006; 15(suppl_2): R176 - R181. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Lamason, M.-A. P.K. Mohideen, J. R. Mest, A. C. Wong, H. L. Norton, M. C. Aros, M. J. Jurynec, X. Mao, V. R. Humphreville, J. E. Humbert, et al. SLC24A5, a Putative Cation Exchanger, Affects Pigmentation in Zebrafish and Humans Science, December 16, 2005; 310(5755): 1782 - 1786. [Abstract] [Full Text] [PDF] |
||||


