Suppr超能文献

使用全外显子组测序在原发性纤毛运动障碍患者中鉴定新型的轴丝动力蛋白装配因子 1 突变。

Novel dynein axonemal assembly factor 1 mutations identified using whole‑exome sequencing in patients with primary ciliary dyskinesia.

机构信息

Department of Pulmonary Medicine, Qingpu Branch of Zhongshan Hospital, Shanghai 201700, P.R. China.

2Department of Pulmonary and Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai 200032, P.R. China.

出版信息

Mol Med Rep. 2020 Dec;22(6):4707-4715. doi: 10.3892/mmr.2020.11562. Epub 2020 Oct 6.

Abstract

Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder caused by dysfunction of the cilia and flagella; however, causative genetic defects have not been detected in all patients with PCD. Seven Chinese Han patients with Kartagener syndrome were enrolled onto the present study. Transmission electron microscopy (TEM) was performed to evaluate the cilial defects and whole‑exome sequencing was used to analyze relevant genetic variations in all patients. In two of the seven patients with PCD, four novel dynein axonemal assembly factor 1 (DNAAF1) mutations were identified (NM_178452.6:c.3G>A, c.124+1G>C, c.509delG and c.943A>T) in three alleles. Both of these patients had long‑standing infertility. Their chest computed tomography results showed bronchiectasis, lung infections and situs inversus, and paranasal computed tomography revealed sinusitis. Semen analysis of the male patient showed poor sperm motility. TEM showed defects in the inner and outer dynein arms in both patients. The DNAAF1 sequences of family members were then analyzed. Bioinformatics analysis indicated that these mutations may be the cause of the cilial defects in these two probands. Thus, the present study identified novel PCD‑causing mutations in DNAAF1 in two patients with PCD. These genetic variations were predicted to alter DNAAF1 amino acid residues and lead to loss of function, thereby inhibiting cilia‑mediated motility. Accordingly, the two probands had PCD symptoms, and one of them died due to PCD‑associated complications.

摘要

原发性纤毛运动障碍(PCD)是一种罕见的、遗传异质性疾病,由纤毛和鞭毛功能障碍引起;然而,并非所有 PCD 患者都能检测到致病的遗传缺陷。本研究纳入了 7 名患有卡塔格内综合征的汉族中国患者。通过透射电子显微镜(TEM)评估纤毛缺陷,并对所有患者进行全外显子组测序以分析相关的遗传变异。在 7 名 PCD 患者中的 2 名患者中,在 3 个等位基因中发现了 4 种新型动力蛋白轴突组装因子 1(DNAAF1)突变(NM_178452.6:c.3G>A、c.124+1G>C、c.509delG 和 c.943A>T)。这两名患者均有长期不孕史。他们的胸部计算机断层扫描结果显示支气管扩张、肺部感染和内脏转位,以及副鼻窦计算机断层扫描显示鼻窦炎。男性患者的精液分析显示精子活动力差。TEM 显示这两名患者的内外动力蛋白臂均存在缺陷。然后分析了家庭成员的 DNAAF1 序列。生物信息学分析表明,这些突变可能是这两个先证者纤毛缺陷的原因。因此,本研究在 2 名 PCD 患者中鉴定了 DNAAF1 引起的新型 PCD 致病突变。这些遗传变异预计会改变 DNAAF1 的氨基酸残基并导致功能丧失,从而抑制纤毛介导的运动。因此,这两个先证者都有 PCD 症状,其中一个因 PCD 相关并发症而死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce64/7646867/131a8b8e2156/MMR-22-06-4707-g00.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验