Department of General Pediatrics, University Children's Hospital Muenster, 48149 Muenster, Germany.
Am J Hum Genet. 2012 Oct 5;91(4):672-84. doi: 10.1016/j.ajhg.2012.08.016. Epub 2012 Sep 27.
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder characterized by defective cilia and flagella motility. Chronic destructive-airway disease is caused by abnormal respiratory-tract mucociliary clearance. Abnormal propulsion of sperm flagella contributes to male infertility. Genetic defects in most individuals affected by PCD cause randomization of left-right body asymmetry; approximately half show situs inversus or situs ambiguous. Almost 70 years after the hy3 mouse possessing Hydin mutations was described as a recessive hydrocephalus model, we report HYDIN mutations in PCD-affected persons without hydrocephalus. By homozygosity mapping, we identified a PCD-associated locus, chromosomal region 16q21-q23, which contains HYDIN. However, a nearly identical 360 kb paralogous segment (HYDIN2) in chromosomal region 1q21.1 complicated mutational analysis. In three affected German siblings linked to HYDIN, we identified homozygous c.3985G>T mutations that affect an evolutionary conserved splice acceptor site and that subsequently cause aberrantly spliced transcripts predicting premature protein termination in respiratory cells. Parallel whole-exome sequencing identified a homozygous nonsense HYDIN mutation, c.922A>T (p.Lys307(∗)), in six individuals from three Faroe Island PCD-affected families that all carried an 8.8 Mb shared haplotype across HYDIN, indicating an ancestral founder mutation in this isolated population. We demonstrate by electron microscopy tomography that, consistent with the effects of loss-of-function mutations, HYDIN mutant respiratory cilia lack the C2b projection of the central pair (CP) apparatus; similar findings were reported in Hydin-deficient Chlamydomonas and mice. High-speed videomicroscopy demonstrated markedly reduced beating amplitudes of respiratory cilia and stiff sperm flagella. Like the hy3 mouse model, all nine PCD-affected persons had normal body composition because nodal cilia function is apparently not dependent on the function of the CP apparatus.
原发性纤毛运动障碍(PCD)是一种遗传性异质性隐性疾病,其特征是纤毛和鞭毛运动功能缺陷。慢性破坏性气道疾病是由异常呼吸道黏液纤毛清除引起的。精子鞭毛的异常推进导致男性不育。大多数受 PCD 影响的个体的遗传缺陷导致左右身体不对称的随机化;约有一半表现为 situs inversus 或 situs ambiguus。在描述具有 Hydin 突变的 hy3 小鼠作为隐性脑积水模型近 70 年后,我们报告了 PCD 患者中无脑积水的 HYDIN 突变。通过纯合子作图,我们鉴定了一个与 PCD 相关的位点,染色体 16q21-q23 区域,其中包含 HYDIN。然而,在染色体 1q21.1 区域的一个几乎相同的 360kb 旁系同源片段(HYDIN2)使突变分析复杂化。在与 HYDIN 连锁的三个受影响的德国兄弟姐妹中,我们鉴定了纯合的 c.3985G>T 突变,该突变影响了一个进化上保守的剪接受体位点,随后导致呼吸细胞中异常剪接的转录物预测提前终止蛋白质。平行全外显子组测序在来自三个法罗群岛 PCD 受影响家庭的六个个体中鉴定出纯合的无义 HYDIN 突变,c.922A>T(p.Lys307(∗)),这些个体都携带 HYDIN 跨越 8.8Mb 的共享单倍型,表明在这个孤立的人群中存在一个祖先的起始突变。我们通过电子显微镜断层扫描证明,与功能丧失突变的影响一致,HYDIN 突变的呼吸纤毛缺乏中央对(CP)装置的 C2b 投影;在缺乏 Hydin 的衣藻和小鼠中也有类似的发现。高速视频显微镜显示呼吸纤毛的拍打幅度明显减小,精子鞭毛僵硬。与 hy3 小鼠模型一样,所有 9 名 PCD 患者的身体成分都正常,因为节点纤毛功能显然不依赖于 CP 装置的功能。