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轴丝外动力蛋白臂 docking 复合物基因 CCDC114 的剪接位点突变导致原发性纤毛运动障碍。

Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia.

机构信息

Molecular Medicine Unit and Birth Defects Research Centre, Institute of Child Health, University College London, London WC1N 1EH, UK.

出版信息

Am J Hum Genet. 2013 Jan 10;92(1):88-98. doi: 10.1016/j.ajhg.2012.11.002. Epub 2012 Dec 20.

Abstract

Defects in motile cilia and sperm flagella cause primary ciliary dyskinesia (PCD), characterized by chronic airway disease, infertility, and left-right laterality disturbances, usually as a result of loss of the outer dynein arms (ODAs) that power cilia/flagella beating. Here, we identify loss-of-function mutations in CCDC114 causing PCD with laterality malformations involving complex heart defects. CCDC114 is homologous to DCC2, an ODA microtubule-docking complex component of the biflagellate alga Chlamydomonas. We show that CCDC114 localizes along the entire length of human cilia and that its deficiency causes a complete absence of ciliary ODAs, resulting in immotile cilia. Thus, CCDC114 is an essential ciliary protein required for microtubular attachment of ODAs in the axoneme. Fertility is apparently not greatly affected by CCDC114 deficiency, and qPCR shows that this may explained by low transcript expression in testis compared to ciliated respiratory epithelium. One CCDC114 mutation, c.742G>A, dating back to at least the 1400s, presents an important diagnostic and therapeutic target in the isolated Dutch Volendam population.

摘要

动力臂缺陷和精子鞭毛导致原发性纤毛运动障碍(PCD),其特征是慢性气道疾病、不孕和左右侧位障碍,通常是由于外动力臂(ODAs)丧失导致纤毛/鞭毛跳动。在这里,我们发现 CCDC114 失活突变导致 PCD 伴有侧位畸形,涉及复杂的心脏缺陷。CCDC114 与 DCC2 同源,DCC2 是双鞭毛藻类衣藻的 ODAs 微管 docking 复合物的组成部分。我们表明 CCDC114 沿人类纤毛的全长定位,其缺乏导致纤毛 ODAs 的完全缺失,导致纤毛不动。因此,CCDC114 是纤毛轴突微管附着 ODAs 所必需的纤毛蛋白。CCDC114 缺乏显然不会极大地影响生育能力,qPCR 显示,与呼吸上皮纤毛相比,睾丸中这种蛋白的转录表达水平较低,可能解释了这一点。CCDC114 的一个突变,c.742G>A,至少可以追溯到 15 世纪,为孤立的荷兰 Volendam 人群提供了一个重要的诊断和治疗靶点。

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