Institute of Cytology and Genetics SB RAS, Novosibirsk, 630090, Russia.
Novosibirsk State University, Novosibirsk, 630090, Russia.
Mol Neurobiol. 2018 Aug;55(8):6533-6546. doi: 10.1007/s12035-017-0851-5. Epub 2018 Jan 11.
Copy number variations (CNVs) of the human CNTN6 gene caused by megabase-scale microdeletions or microduplications in the 3p26.3 region are often the cause of neurodevelopmental disorders, including intellectual disability and developmental delay. Surprisingly, patients with different copy numbers of this gene display notable overlapping of neuropsychiatric symptoms. The complexity of the study of human neuropathologies is associated with the inaccessibility of brain material. This problem can be overcome through the use of reprogramming technologies that permit the generation of induced pluripotent stem (iPS) cells from fibroblasts and their subsequent in vitro differentiation into neurons. We obtained a set of iPS cell lines derived from a patient carrier of the CNTN6 gene duplication and from two healthy donors. All iPS cell lines displayed the characteristics of pluripotent cells. Some iPS cell lines derived from the patient and from healthy donors were differentiated in vitro by exogenous expression of the Ngn2 transcription factor or by spontaneous neural differentiation of iPS cells through the neural rosette stage. The obtained neurons showed the characteristics of mature neurons as judged by the presence of neuronal markers and by their electrophysiological characteristics. Analysis of allele-specific expression of the CNTN6 gene in these neuronal cells by droplet digital PCR demonstrated that the level of expression of the duplicated allele was significantly reduced compared to that of the wild-type allele. Importantly, according to the sequencing data, both copies of the CNTN6 gene, which were approximately 1 Mb in size, showed no any additional structural rearrangements.
人类 CNTN6 基因的拷贝数变异(CNVs),由 3p26.3 区域的大片段微缺失或微重复引起,通常是神经发育障碍的原因,包括智力残疾和发育迟缓。令人惊讶的是,具有该基因不同拷贝数的患者表现出显著重叠的神经精神症状。研究人类神经病理学的复杂性与大脑物质的不可及性有关。这个问题可以通过使用重编程技术来克服,这些技术允许从成纤维细胞生成诱导多能干细胞(iPS),并随后在体外分化为神经元。我们获得了一组源自携带 CNTN6 基因重复的患者和两个健康供体的 iPS 细胞系。所有 iPS 细胞系均显示出多能细胞的特征。通过外源性表达 Ngn2 转录因子或通过 iPS 细胞通过神经玫瑰阶段的自发神经分化,从患者和健康供体中获得的一些 iPS 细胞系在体外分化。通过神经元标记物的存在及其电生理特性来判断,获得的神经元表现出成熟神经元的特征。通过液滴数字 PCR 对这些神经元细胞中 CNTN6 基因的等位基因特异性表达进行分析表明,与野生型等位基因相比,重复等位基因的表达水平显著降低。重要的是,根据测序数据,大小约为 1Mb 的 CNTN6 基因的两个拷贝没有任何其他结构重排。