Abstract

BackgroundADH1B is one of the most studied human genes with many polymorphic sites. One of the single nucleotide polymorphism (SNP), rs1229984, coding for the Arg48His substitution, have been associated with many serious diseases including alcoholism and cancers of the digestive system. The derived allele, ADH1B*48His, reaches high frequency only in East Asia and Southwest Asia, and is highly associated with agriculture. Micro-evolutionary study has defined seven haplogroups for ADH1B based on seven SNPs encompassing the gene. Three of those haplogroups, H5, H6, and H7, contain the ADH1B*48His allele. H5 occurs in Southwest Asia and the other two are found in East Asia. H7 is derived from H6 by the derived allele of rs3811801. The H7 haplotype has been shown to have undergone significant positive selection in Han Chinese, Hmong, Koreans, Japanese, Khazak, Mongols, and so on.MethodsIn the present study, we tested whether Tibetans also showed evidence for selection by typing 23 SNPs in the region covering the ADH1B gene in 1,175 individuals from 12 Tibetan populations representing all districts of the Tibet Autonomous Region. Multiple statistics were estimated to examine the gene diversities and positive selection signals among the Tibetans and other populations in East Asia.ResultsThe larger Tibetan populations (Qamdo, Lhasa, Nagqu, Nyingchi, Shannan, and Shigatse) comprised mostly farmers, have around 12% of H7, and 2% of H6. The smaller populations, living on hunting or recently switched to farming, have lower H7 frequencies (Tingri 9%, Gongbo 8%, Monba and Sherpa 6%). Luoba (2%) and Deng (0%) have even lower frequencies. Long-range haplotype analyses revealed very weak signals of positive selection for H7 among Tibetans. Interestingly, the haplotype diversity of H7 is higher in Tibetans than in any other populations studied, indicating a longer diversification history for that haplogroup in Tibetans. Network analysis on the long-range haplotypes revealed that H7 in the Han Chinese did not come from the Tibetans but from a common ancestor of the two populations.ConclusionsWe argue that H7 of ADH1B originated in the ancestors of Sino-Tibetan populations and flowed to Tibetans very early. However, as Tibetans depend less on crops, and therefore were not significantly affected by selection. Thus, H7 has not risen to a high frequency, whereas the diversity of the haplogroup has accumulated to a very high level.

Highlights

  • ADH1B is one of the most studied human genes with many polymorphic sites

  • Further study revealed that several single nucleotide polymorphism (SNP) in ADH1B form different haplotypes, and haplotypes with the ADH1B*48His allele are different in East Asia and Southwest Asia [4], with evidence in East Asia of strong positive natural selection [11,12] during the history of agriculture [13]

  • Important questions are whether the ADH1B*48His alleles of Tibetans and Han Chinese have a common origin and, if so, why the frequency of this allele did not rise in Tibetans as it did in Han Chinese

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Summary

Introduction

ADH1B is one of the most studied human genes with many polymorphic sites. One of the single nucleotide polymorphism (SNP), rs1229984, coding for the Arg48His substitution, have been associated with many serious diseases including alcoholism and cancers of the digestive system. The derived allele, ADH1B*48His, reaches high frequency only in East Asia and Southwest Asia, and is highly associated with agriculture. Micro-evolutionary study has defined seven haplogroups for ADH1B based on seven SNPs encompassing the gene. Three of those haplogroups, H5, H6, and H7, contain the ADH1B*48His allele. The derived allele reaches high frequency only in eastern East Asia and Southwest Asia and is almost absent in the rest of the world [3]. Further study revealed that several SNPs in ADH1B form different haplotypes, and haplotypes with the ADH1B*48His allele are different in East Asia and Southwest Asia [4], with evidence in East Asia of strong positive natural selection [11,12] during the history of agriculture [13]. Important questions are whether the ADH1B*48His alleles of Tibetans and Han Chinese have a common origin and, if so, why the frequency of this allele did not rise in Tibetans as it did in Han Chinese

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