斑马鱼 gabra1 种系功能缺失等位基因的特征证实了 Gabra1 在运动和神经系统发育中的功能。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-06-15 DOI:10.1016/j.diff.2024.100790
Nayeli G. Reyes-Nava , David Paz , Briana E. Pinales, Isaiah Perez, Claudia B. Gil, Annalise V. Gonzales, Brian I. Grajeda , Igor L. Estevao , Cameron C. Ellis , Victoria L. Castro, Anita M. Quintana
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引用次数: 0

摘要

GABRA1 基因突变与神经发育缺陷和癫痫有关。GABRA1 编码γ-氨基丁酸 A 型受体(GABAAR)的α1 亚基,该受体调节神经系统的快速抑制冲动。为了了解 GABRA1 的功能,人们开发了多种模型系统,但这些模型产生了复杂的数据,有时甚至是不一致的数据。因此,需要更多的模型系统来验证和证实以前的结果。我们试图对一种新型种系突变等位基因进行初步表型分析。我们的分析为将来利用该等位基因通过斑马鱼鉴定 gabra1 的功能和药理特性奠定了坚实的基础。我们研究了与斑马鱼gabra1基因无义突变(sa43718等位基因)相关的行为游泳模式。sa43718 等位基因导致 gabra1 mRNA 表达减少,这与光诱导的过度运动有关,而这种表型以前曾与斑马鱼的癫痫样行为有关。伴随着 gabra1 的突变,gabra2、gabra3 和 gabra5 的 mRNA 表达也有所下降,这表明 GABAAR 的其他 α 亚单位的表达也有所下降。虽然多个亚单位的表达量减少,但幼虫对戊烯四唑(PTZ)仍有反应,表明在 sa43718 等位基因中存在残余的 GABAAR。蛋白质组学分析表明,gabra1 的突变与调节突触小泡融合、小泡转运、突触发育和线粒体蛋白复合物的蛋白质表达异常有关。这些数据支持了之前通过 CRISPR/Cas9 在斑马鱼无义等位基因中进行的研究,并验证了 gabra1 基因的功能缺失突变会导致 GABA 突触发育异常的癫痫样表型。我们的研究结果丰富了关于 GABRA1 在发育过程中的功能的现有知识,并验证了斑马鱼可用于提供该基因的完整功能特征。
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Characterization of the zebrafish gabra1sa43718/sa43718 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development

Mutation of the GABRA1 gene is associated with neurodevelopmental defects and epilepsy. GABRA1 encodes for the α1 subunit of the γ-aminobutyric acid type A receptor (GABAAR), which regulates the fast inhibitory impulses of the nervous system. Multiple model systems have been developed to understand the function of GABRA1, but these models have produced complex and, at times, incongruent data. Thus, additional model systems are required to validate and substantiate previous results. We sought to provide initial phenotypic analysis of a novel germline mutant allele. Our analysis provides a solid foundation for the future use of this allele to characterize gabra1 functionally and pharmacologically using zebrafish. We investigated the behavioral swim patterns associated with a nonsense mutation of the zebrafish gabra1 (sa43718 allele) gene. The sa43718 allele causes a decrease in gabra1 mRNA expression, which is associated with light induced hypermotility, one phenotype previously associated with seizure like behavior in zebrafish. Mutation of gabra1 was accompanied by decreased mRNA expression of gabra2, gabra3, and gabra5, indicating a reduction in the expression of additional α sub-units of the GABAAR. Although multiple sub-units were decreased, larvae continued to respond to pentylenetetrazole (PTZ), indicating that a residual GABAAR exists in the sa43718 allele. Proteomics analysis demonstrated that mutation of gabra1 is associated with abnormal expression of proteins that regulate synaptic vesicle fusion, vesicle transport, synapse development, and mitochondrial protein complexes. These data support previous studies performed in a zebrafish nonsense allele created by CRISPR/Cas9 and validate that loss of function mutations in the gabra1 gene result in seizure-like phenotypes with abnormal development of the GABA synapse. Our results add to the existing body of knowledge as to the function of GABRA1 during development and validate that zebrafish can be used to provide complete functional characterization of the gene.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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