Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder‐Haplotype Analysis

• Published in: Annals of human genetics Vol. 70; no. 6; pp. 802 - 811
• Main Authors: Yuasa, I., Umetsu, K., Harihara, S., Kido, A., Miyoshi, A., Saitou, N., Dashnyam, B., Jin, F., Lucotte, G., Chattopadhyay, P. K., Henke, L., Henke, J.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.11.2006
• Subjects: African Continental Ancestry Group - genetics; Antigens, Neoplasm - genetics; Asian Continental Ancestry Group - genetics; European Continental Ancestry Group - genetics; Founder Effect; Gene Frequency; Genetics, Population; Genotype; haplotype; Haplotypes; Humans; Linkage Disequilibrium; Membrane Transport Proteins - genetics; membrane‐associated transporter protein; polymorphism; Polymorphism, Single Nucleotide; population study; Racemases and Epimerases - genetics; Receptors, G-Protein-Coupled - genetics; SLC45A2
• ISSN: 0003-4800; 1469-1809
• DOI: 10.1111/j.1469-1809.2006.00261.x

Summary The membrane‐associated transporter protein (MATP) plays an important role in melanin synthesis. The L374F mutation in the SLC45A2 gene encoding MATP has been suggested to be associated with skin colour in major human populations. In this study more detailed distribution of the F374 allele was investigated in 1649 unrelated subjects from 13 Eurasian populations and one African population. The highest allele frequency was observed in Germans (0.965); French and Italians showed somewhat lower frequencies; and Turks had an intermediate value (0.615). Indians and Bangladeshis from South Asia were characterized by low frequencies (0.147 and 0.059, respectively). We also found the F374 allele in some East and Southeast Asian populations, and explained this by admixture. Haplotype analysis revealed that the haplotype diversity was much lower in Germans than in Japanese, and suggest that the L374F mutation occurred only once in the ancestry of Caucasians. The large differences in distribution of the F374 allele and its haplotypes suggest that this allele may be an important factor in hypopigmentation in Caucasian populations.