Department of Ophthalmology and Central Lab, The Second People's Hospital of Yunnan Province, Kunming, Yunnan Province, China.
Hainan Western Central Hospital, Danzhou, Hainan Province, China.
Sci Rep. 2020 Oct 1;10(1):16225. doi: 10.1038/s41598-020-73190-1.
Duane retraction syndrome (DRS) is a neuromuscular dysfunction of the eyes. Although many causative genes of DRS have been identified in Europe and the United States, few reports have been published in regard to Chinese DRS. The aim of the present study was to explore the genetic defect of DRS in a Chinese family. Exome sequencing was used to identify the disease-causing gene for the two affected family members. Ophthalmic and physical examinations, as well as genetic screenings for variants in chimerin 1 (CHN1), were performed for all family members. Functional analyses of a CHN1 variant in 293T cells included a Rac-GTP activation assay, α2-chimaerin translocation assay, and co-immunoprecipitation assay. Genetic analysis revealed a NM_001822.7: c.637T > G variant in the CHN1 gene, which resulted in the substitution of a highly conserved C1 domain with valine at codon 213 (NP_001813.1: p.(Phe213Val)) (ClinVar Accession Number: SCV001335305). In-silico analysis revealed that the p.(Phe213Val) substitution affected the protein stability and connections among the amino acids of CHN1 in terms of its tertiary protein structure. Functional studies indicated that the p.(Phe213Val) substitution reduced Rac-GTP activity and enhanced membrane translocation in response to phorbol-myristoyl acetate (PMA). Together with previous studies, our present findings demonstrate that CHN1 may be an important causative gene for different ethnicities with DRS.
杜安退缩综合征(DRS)是一种眼部神经肌肉功能障碍。尽管许多导致 DRS 的基因已在欧美被鉴定,但在中国 DRS 的相关报道较少。本研究旨在探讨一个中国家系中 DRS 的遗传缺陷。对两名受影响的家族成员进行外显子组测序以鉴定致病基因。对所有家族成员进行眼科和体格检查,以及对奇美拉 1(CHN1)基因变异的基因筛查。在 293T 细胞中对 CHN1 变异体进行功能分析,包括 Rac-GTP 激活测定、α2-奇美拉转移测定和共免疫沉淀测定。遗传分析显示 CHN1 基因中的 NM_001822.7:c.637T>G 变异导致高度保守的 C1 结构域中第 213 位的脯氨酸被缬氨酸取代(NP_001813.1:p.(Phe213Val))(ClinVar 访问号:SCV001335305)。计算机分析表明,p.(Phe213Val)取代会影响 CHN1 的蛋白质稳定性及其三级蛋白质结构中氨基酸之间的连接。功能研究表明,p.(Phe213Val)取代会降低 Rac-GTP 活性并增强对佛波醇-12,13-二乙酸酯(PMA)的膜易位。结合以前的研究,我们的研究结果表明 CHN1 可能是 DRS 不同种族的重要致病基因。