Department of Pathology and Matrix Biology, Mie University Graduate School of Medicine, Tsu, Japan.
Department of Genomic Medicine, Mie University Hospital, Tsu, Japan.
J Hum Genet. 2024 Dec;69(12):655-661. doi: 10.1038/s10038-024-01289-8. Epub 2024 Aug 16.
Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by ciliary structural abnormalities and dysfunction, leading to chronic rhinosinusitis, otitis media with effusion, bronchiectasis, and infertility. Approximately half of Japanese PCD cases are attributed to variants in the dynein regulatory complex subunit 1 (DRC1) gene, predominantly featuring homogeneous deletions of exons 1-4 spanning 27,748 base pairs on chromosome 2. Here, we report 10 new PCD cases (9 families) in addition to 29 previously reported cases (24 families) caused by DRC1 variants. Among these 39 cases, biallelic DRC1 exon 1-4 deletions were detected in 38 (97.4%). These DRC1 deletions exhibited an identical breakpoint in all PCD cases in the Japanese and Korean populations, strongly suggesting a founder effect. In this study, we performed haplotype analysis, using a whole-exome sequencing dataset of 18 Japanese PCD patients harboring large biallelic DRC1 deletions. We estimated that the founder allele likely emerged 115.1 generations ago (95% confidence interval: 33.7-205.1), suggesting an origin of approximately 3050 years ago, coinciding with the transition from the Jomon period to the early Yayoi period in Japan. Considering the formation of the modern Japanese population, the founder with the DRC1 exon 1-4 deletion likely lived on the Korean peninsula, with the allele later transmitted to Japan through migration. This study provides insights into the origin of the DRC1 copy number variant, the most frequent PCD variant in the Japanese and Korean populations, highlighting the importance of understanding population-specific genetic variations in the context of human migration and disease prevalence.
原发性纤毛运动障碍(PCD)是一种遗传性疾病,其特征为纤毛结构异常和功能障碍,导致慢性鼻窦炎、中耳炎伴渗出、支气管扩张和不孕。大约一半的日本 PCD 病例归因于动力蛋白调节复合物亚单位 1(DRC1)基因的变异,主要表现为跨越染色体 2 的 27748 个碱基对的外显子 1-4 的同质缺失。在这里,我们报告了除 29 例先前报道的病例(24 个家族)之外的另外 10 例 PCD 病例(9 个家族),这些病例均由 DRC1 变异引起。在这 39 例病例中,38 例(97.4%)检测到双等位基因 DRC1 外显子 1-4 缺失。所有日本和韩国 PCD 病例的 DRC1 缺失均具有相同的断裂点,强烈提示存在一个共同的起源。在这项研究中,我们对携带大片段双等位基因 DRC1 缺失的 18 例日本 PCD 患者的全外显子组测序数据集进行了单倍型分析。我们估计,该起源等位基因可能在 115.1 代前(95%置信区间:33.7-205.1)出现,这表明起源大约在 3050 年前,与日本从绳纹时代向弥生时代早期的过渡时间相吻合。考虑到现代日本人口的形成,该 DRC1 外显子 1-4 缺失的起源等位基因可能生活在朝鲜半岛,该等位基因随后通过移民传播到日本。本研究提供了对 DRC1 拷贝数变异起源的见解,这是日本和韩国人群中最常见的 PCD 变异,强调了在人类迁移和疾病流行的背景下了解特定人群遗传变异的重要性。