Laboratory for Statistical and Translational Genetics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Clinical Research Center, Shizuoka General Hospital, Shizuoka, Japan.
Mol Biol Evol. 2023 Oct 4;40(10). doi: 10.1093/molbev/msad231.
Natural selection signatures across Japanese subpopulations are under-explored. Here we conducted genome-wide selection scans with 622,926 single nucleotide polymorphisms for 20,366 Japanese individuals, who were recruited from the main-islands of Japanese Archipelago (Hondo) and the Ryukyu Archipelago (Ryukyu), representing two major Japanese subpopulations. The integrated haplotype score (iHS) analysis identified several signals in one or both subpopulations. We found a novel candidate locus at IKZF2, especially in Ryukyu. Significant signals were observed in the major histocompatibility complex region in both subpopulations. The lead variants differed and demonstrated substantial allele frequency differences between Hondo and Ryukyu. The lead variant in Hondo tags HLA-A33:03-C14:03-B44:03-DRB113:02-DQB106:04-DPB104:01, a haplotype specific to Japanese and Korean. While in Ryukyu, the lead variant tags DRB115:01-DQB106:02, which had been recognized as a genetic risk factor for narcolepsy. In contrast, it is reported to confer protective effects against type 1 diabetes and human T lymphotropic virus type 1-associated myelopathy/tropical spastic paraparesis. The FastSMC analysis identified 8 loci potentially affected by selection within the past 20-150 generations, including 2 novel candidate loci. The analysis also showed differences in selection patterns of ALDH2 between Hondo and Ryukyu, a gene recognized to be specifically targeted by selection in East Asian. In summary, our study provided insights into the selection signatures within the Japanese and nominated potential sources of selection pressure.
自然选择在日本亚群中的特征研究还不够充分。在这里,我们对来自日本列岛主岛(本州)和琉球群岛(琉球)的 20366 名日本人进行了全基因组选择扫描,共使用了 622926 个单核苷酸多态性。综合单倍型得分(iHS)分析在一个或两个亚群中确定了几个信号。我们在 IKZF2 中发现了一个新的候选基因座,特别是在琉球。在两个亚群的主要组织相容性复合体区域都观察到了显著的信号。主要变体不同,并且在本州和琉球之间显示出相当大的等位基因频率差异。本州的主要变体标记 HLA-A33:03-C14:03-B44:03-DRB113:02-DQB106:04-DPB104:01,这是一种特定于日本和韩国的单倍型。而在琉球,主要变体标记 DRB115:01-DQB106:02,它已被认为是嗜睡症的遗传风险因素。相反,据报道,它对 1 型糖尿病和人类 T 淋巴细胞病毒 1 型相关的骨髓病/热带痉挛性截瘫具有保护作用。FastSMC 分析确定了 8 个在过去 20-150 代中可能受到选择影响的位点,包括 2 个新的候选基因座。该分析还显示了本州和琉球之间 ALDH2 选择模式的差异,该基因被认为是东亚特有的选择目标。总之,我们的研究提供了对日本人群中的选择特征的深入了解,并提名了潜在的选择压力来源。