Türk Matthias, Schröder Rolf, Khuller Katharina, Hofmann Andreas, Berwanger Carolin, Ludolph Albert C, Dekomien Gabriele, Müller Kathrin, Weishaupt Jochen H, Thiel Christian T, Clemen Christoph S
Department of Neurology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.
Institute of Neuropathology, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.
Neurobiol Aging. 2017 Aug;56:213.e1-213.e5. doi: 10.1016/j.neurobiolaging.2017.04.023. Epub 2017 May 3.
Mutations of the human valosin-containing protein, p97 (VCP) and Wiskott-Aldrich syndrome protein and SCAR homolog (WASH) complex genes cause motor neuron and cognitive impairment disorders. Here, we analyzed a cohort of German patients with sporadic amyotrophic lateral sclerosis and frontotemporal lobar degeneration comorbidity (ALS/FTD) for VCP and WASH complex gene mutations. Next-generation panel sequencing of VCP, WASH1, FAM21C, CCDC53, SWIP, strumpellin, F-actin capping protein of muscle Z-line alfa 1 (CAPZA1), and CAPZB genes was performed in 43 sporadic ALS/FTD patients. Subsequent analyses included Sanger sequencing, in silico analyses, real-time PCR, and CCDC53 immunoblotting. We identified 1 patient with the heterozygous variant c.26C>T in CAPZA1, predicted to result in p.Ser9Leu, and a second with the heterozygous start codon variant c.2T>C in CCDC53. In silico analysis predicted structural changes in the N-terminus of CAPZα1, which may interfere with CAPZα:CAPZβ dimerization. Though the translation initiation codon of CCDC53 is mutated, real-time PCR and immunoblotting did neither reveal any evidence for a CCDC53 haploinsufficiency nor for aberrant CCDC53 protein species. Moreover, a disease-causing C9orf72 repeat expansion mutation was later on identified in this patient. Thus, with the exception of a putatively pathogenic heterozygous c.26C>T CAPZA1 variant, our genetic analysis did not reveal mutations in VCP and the remaining WASH complex subunits.
人类含缬酪肽蛋白p97(VCP)以及威斯科特-奥尔德里奇综合征蛋白和SCAR同源物(WASH)复合体基因的突变会导致运动神经元和认知障碍疾病。在此,我们分析了一组患有散发性肌萎缩侧索硬化症和额颞叶痴呆合并症(ALS/FTD)的德国患者,以检测VCP和WASH复合体基因突变情况。对43例散发性ALS/FTD患者进行了VCP、WASH1、FAM21C、CCDC53、SWIP、斯特伦佩林、肌肉Z线α1肌动蛋白封端蛋白(CAPZA1)和CAPZB基因的二代测序。后续分析包括桑格测序、计算机分析、实时PCR和CCDC53免疫印迹。我们鉴定出1例患者的CAPZA1基因存在杂合变异c.26C>T,预测会导致p.Ser9Leu,另1例患者的CCDC53基因存在杂合起始密码子变异c.2T>C。计算机分析预测CAPZα1的N端会发生结构变化,这可能会干扰CAPZα:CAPZβ二聚化。虽然CCDC53的翻译起始密码子发生了突变,但实时PCR和免疫印迹均未发现任何CCDC53单倍体不足或异常CCDC53蛋白种类的证据。此外,后来在该患者中鉴定出了致病的C9orf72重复扩增突变。因此,除了一个可能致病的杂合c.26C>T CAPZA1变异外,我们的基因分析未发现VCP和其余WASH复合体亚基存在突变。