Genotypic and phenotypic characteristics of ADGRV1 mutations in four children and functional validation in a zebrafish model.

IF 2.6 3区 生物学 Q2 GENETICS & HEREDITY
Gene Pub Date : 2025-03-20 Epub Date: 2025-01-16 DOI:10.1016/j.gene.2025.149246
Xiao Xiao, Hao Zheng, Miao Xiong, Xiaoqi Chen, Li Jiang, Yue Hu
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引用次数: 0

Abstract

Mutations in ADGRV1 can cause seizures, but the mechanism remains unclear. The zebrafish model can be used to assess the functions of human ADGRV1 and its variant alleles during embryonic development. In this study, we summarized the phenotypic and genotypic characteristics of four children with ADGRV1 variation and based on this, we validated the ADGRV1 loss phenotype in an adgrv1-knockout zebrafish model. We retrospectively analyzed the clinical and genotypic characteristics of four pediatric patients diagnosed as having ADGRV1 mutations at Children's Hospital Affiliated to Chongqing Medical University from April 2019 to February 2022. Moreover, we used the adgrv1-knockout zebrafish larvae model and performed morphological, behavioral, and neuroelectrophysiological testing. We found that of the four included children, two had epilepsy, one had paroxysmal kinesigenic dyskinesia, and one had febrile seizure plus. Three children had a history of febrile seizures, whereas two had a family history of febrile seizures. Three children had well-controlled clinical epilepsy seizures or motor disorders. Finally, one child with spontaneous mutation had epigenetic abnormalities and comprehensive developmental delay, one had language developmental delay, and two (paternal or maternal) had a good prognosis. Regarding the zebrafish model, the cas9-control and adgrv1-edited groups demonstrated significant differences in the interocular areas of the zebrafish observed in the open field and the maximum swimming velocity under light stimulus. In neuroelectrophysiological testing, epilepsy-related signals were observed in 2 of 26 adgrv1-edited group fish. We believe that, mutations in the ADGRV1 may lead to epileptic seizures and movement disorders. The patients usually have a history of febrile seizures or a family history. Through research using the zebrafish model, it has been found that ADGRV1 mutations can affect the expression of eye and the neuromotor development of zebrafish larvae. This might be one of the reasons for epileptic seizures caused by ADGRV1 gene mutations.

四名儿童ADGRV1突变的基因型和表型特征及其在斑马鱼模型中的功能验证
ADGRV1突变可引起癫痫发作,但其机制尚不清楚。斑马鱼模型可用于评估人类ADGRV1及其变异等位基因在胚胎发育过程中的功能。在本研究中,我们总结了4例ADGRV1变异儿童的表型和基因型特征,并以此为基础,在ADGRV1基因敲除斑马鱼模型中验证了ADGRV1缺失表型。回顾性分析2019年4月至2022年2月重庆医科大学附属儿童医院诊断为ADGRV1突变的4例儿科患者的临床和基因型特征。此外,我们使用adgrv1敲除斑马鱼幼虫模型,并进行形态学、行为学和神经电生理测试。我们发现在这四名儿童中,两名患有癫痫,一名患有阵发性运动发生障碍,一名患有发热性癫痫发作。3例患儿有热性惊厥史,2例患儿有热性惊厥家族史。三名儿童有控制良好的临床癫痫发作或运动障碍。最后,1例自发性突变患儿存在表观遗传异常和综合发育迟缓,1例存在语言发育迟缓,2例(父系或母系)预后良好。在斑马鱼模型中,cas9对照组和adgrv1编辑组在开阔视野下观察到的斑马鱼眼间面积和光刺激下的最大游动速度存在显著差异。在神经电生理测试中,26条adgrv1编辑组鱼中有2条观察到癫痫相关信号。我们认为,ADGRV1的突变可能导致癫痫发作和运动障碍。患者通常有发热性惊厥史或家族史。通过斑马鱼模型研究发现,ADGRV1突变可以影响斑马鱼幼体眼睛的表达和神经运动发育。这可能是ADGRV1基因突变引起癫痫发作的原因之一。
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来源期刊
Gene
Gene 生物-遗传学
CiteScore
6.10
自引率
2.90%
发文量
718
审稿时长
42 days
期刊介绍: Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.
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