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CCDC39 和 CCDC40 基因突变是轴丝结构紊乱和内动力蛋白臂缺失的原发性纤毛运动障碍的主要原因。

Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms.

机构信息

Molecular Medicine Unit and Birth Defects Research Centre, University College London (UCL) Institute of Child Health, London, UK.

出版信息

Hum Mutat. 2013 Mar;34(3):462-72. doi: 10.1002/humu.22261. Epub 2013 Feb 11.

Abstract

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder caused by cilia and sperm dysmotility. About 12% of cases show perturbed 9+2 microtubule cilia structure and inner dynein arm (IDA) loss, historically termed "radial spoke defect." We sequenced CCDC39 and CCDC40 in 54 "radial spoke defect" families, as these are the two genes identified so far to cause this defect. We discovered biallelic mutations in a remarkable 69% (37/54) of families, including identification of 25 (19 novel) mutant alleles (12 in CCDC39 and 13 in CCDC40). All the mutations were nonsense, splice, and frameshift predicting early protein truncation, which suggests this defect is caused by "null" alleles conferring complete protein loss. Most families (73%; 27/37) had homozygous mutations, including families from outbred populations. A major putative hotspot mutation was identified, CCDC40 c.248delC, as well as several other possible hotspot mutations. Together, these findings highlight the key role of CCDC39 and CCDC40 in PCD with axonemal disorganization and IDA loss, and these genes represent major candidates for genetic testing in families affected by this ciliary phenotype. We show that radial spoke structures are largely intact in these patients and propose this ciliary ultrastructural abnormality be referred to as "IDA and microtubular disorganisation defect," rather than "radial spoke defect."

摘要

原发性纤毛运动障碍(PCD)是一种由纤毛和精子运动障碍引起的遗传异质性疾病。约有 12%的病例显示出 9+2 微管纤毛结构和内动力蛋白臂(IDA)缺失的紊乱,这在历史上被称为“辐射状鞘缺陷”。我们对 54 个“辐射状鞘缺陷”家族进行了 CCDC39 和 CCDC40 的测序,因为这两个基因是迄今为止被发现导致这种缺陷的两个基因。我们在 69%(37/54)的家族中发现了显著的双等位基因突变,包括鉴定出 25 个(19 个新的)突变等位基因(12 个在 CCDC39 中,13 个在 CCDC40 中)。所有的突变都是无义的、剪接的和移码的,预测早期蛋白截断,这表明这种缺陷是由“无效”等位基因导致完全蛋白丢失引起的。大多数家族(73%;27/37)存在纯合突变,包括来自混血人群的家族。鉴定出一个主要的假定热点突变,CCDC40 c.248delC,以及其他几个可能的热点突变。这些发现共同强调了 CCDC39 和 CCDC40 在 PCD 中轴丝紊乱和 IDA 缺失中的关键作用,这两个基因是受这种纤毛表型影响的家族进行基因测试的主要候选基因。我们表明,这些患者的辐射状鞘结构基本完整,并提出将这种纤毛超微结构异常称为“IDA 和微管组织缺陷”,而不是“辐射状鞘缺陷”。

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