High diversity and no significant selection signal of human ADH1B gene in Tibet

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Abstract

Background: 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. 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.Methods: In 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.Results: The 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.Conclusions: We 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. © 2012 Lu et al.; licensee BioMed Central Ltd.

Figures

  • Figure 1 Distribution of the population samples and ADH1B haplogroup frequencies.
  • Table 1 Frequencies ofADH1Bhaplogroups in Tibet
  • Table 2 Diversities (23 SNPs) ofADH1Bhaplogroup H7 among linguistic families
  • Figure 2 Geographic distributions ofADH1B*48His(rs1229984*T) and rs3811801*A andADH1BH7 haplotype diversity in eastern Asia.
  • Figure 3 Long-range haplotype networks of ADH1B. We examined 23 SNPs covering 173.5 kb of the ADH region, extending from rs1154473 upstream (telomeric) of ADH7 through ADH1C, ADH1B (including ADH1B*48His), and ADH1A to rs1230025 downstream (centromeric) of the ADH1 cluster. For haplogroups H5, H6, and H7 the relationships among the haplotypes of 23 SNPs were displayed by networks using Network 4.5.1.6. The ‘Tibetan larger’ included 909 individuals from central Tibet (Qamdo 157, Lhasa 334, Nagqu 24, Nyingchi 55, Shannan 147, Shigatse 192), while the ‘Tibetan smaller’ included 216 individuals distributed in other parts of Tibet (Gongbo 50, Tingri 50, Lhoba 50, Monba 16, Deng 50, and Sherpa 50). The reference samples are all the population data from reference [12].
  • Figure 4 Positive selection test (EHH and REHH) on ADH1B among populations in Tibet.
  • Figure 5 Principal component analysis of the estimated haplotype frequencies of the Sino-Tibetan populations.
  • Figure 6 A Delaunay triangulation (green lines) and the genetic barrier

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Lu, Y., Kang, L., Hu, K., Wang, C., Sun, X., Chen, F., … Li, H. (2012). High diversity and no significant selection signal of human ADH1B gene in Tibet. Investigative Genetics, 3(1). https://doi.org/10.1186/2041-2223-3-23

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