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利用微基因检测验证 SLC26A4 基因中稀有变异的剪接效果。

Validating the splicing effect of rare variants in the SLC26A4 gene using minigene assay.

机构信息

Department of Otorhinolaryngology-Head and Neck Surgery, Peking University People's Hospital, No.11 Xizhimen South Street, Beijing, 100044, China.

Department of Clinical Laboratory, Peking University People's Hospital, No.11 Xizhimen South Street, Xicheng District, Beijing, 100044, China.

出版信息

BMC Med Genomics. 2024 Sep 27;17(1):233. doi: 10.1186/s12920-024-02007-1.

Abstract

BACKGROUND

The SLC26A4 gene is the second most common cause of hereditary hearing loss in human. The aim of this study was to utilize the minigene assay in order to identify pathogenic variants of SLC26A4 associated with enlarged vestibular aqueduct (EVA) and hearing loss (HL) in two patients.

METHODS

The patients were subjected to multiplex PCR amplification and next-generation sequencing of common deafness genes (including GJB2, SLC26A4, and MT-RNR1), then bioinformatics analysis was performed on the sequencing data to identify candidate pathogenic variants. Minigene experiments were conducted to determine the potential impact of the variants on splicing.

RESULTS

Genetic testing revealed that the first patient carried compound heterozygous variants c.[1149 + 1G > A]; [919-2 A > G] in the SLC26A4 gene, while the second patient carried compound heterozygous variants c.[2089 + 3 A > T]; [919-2 A > G] in the same gene. Minigene experiments demonstrated that both c.1149 + 1G > A and c.2089 + 3 A > T affected mRNA splicing. According to the ACMG guidelines and the recommendations of the ClinGen Hearing Loss Expert Panel for ACMG variant interpretation, these variants were classified as "likely pathogenic".

CONCLUSIONS

This study identified the molecular etiology of hearing loss in two patients with EVA and elucidated the impact of rare variants on splicing, thus contributing to the mutational spectrum of pathogenic variants in the SLC26A4 gene.

摘要

背景

SLC26A4 基因是人类遗传性听力损失的第二大常见原因。本研究旨在利用微基因检测来鉴定与前庭水管扩大(EVA)和听力损失(HL)相关的 SLC26A4 致病变体在两名患者中。

方法

对患者进行常见耳聋基因(包括 GJB2、SLC26A4 和 MT-RNR1)的多重 PCR 扩增和下一代测序,然后对测序数据进行生物信息学分析,以鉴定候选致病变体。微基因实验用于确定变体对剪接的潜在影响。

结果

基因检测显示,第一位患者携带 SLC26A4 基因中的复合杂合变体 c.[1149 + 1G > A]; [919-2A > G],而第二位患者携带相同基因中的复合杂合变体 c.[2089 + 3A > T]; [919-2A > G]。微基因实验表明,c.1149 + 1G > A 和 c.2089 + 3A > T 均影响 mRNA 剪接。根据 ACMG 指南和 ClinGen 听力损失专家小组对 ACMG 变异解释的建议,这些变体被归类为“可能致病”。

结论

本研究鉴定了两名 EVA 患者听力损失的分子病因,并阐明了稀有变体对剪接的影响,从而丰富了 SLC26A4 基因中致病变体的突变谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2fd/11430457/96d9484bc0ad/12920_2024_2007_Fig1_HTML.jpg

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