NGS-based identification of a MYO7A mutation in a Korean family with DFNB2, a subtype of autosomal recessive non-syndromic hearing loss.

IF 1.6 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ye-Ri Kim, Byeonghyeon Lee, Hong-Joon Park, Tae-Jun Kwon, Un-Kyung Kim
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引用次数: 0

Abstract

Background: Hereditary hearing loss (HHL) exhibits considerable genetic heterogeneity. Among the known causative genes, MYO7A is frequently linked to autosomal recessive non-syndromic hearing loss (ARNSHL), contributing to auditory dysfunction through impaired inner ear cellular mechanics.

Objective: This study aimed to identify the genetic cause of ARNSHL in a Korean family (SR-323) and to assess the pathogenicity of candidate MYO7A variants.

Methods: Whole-exome sequencing (WES) was performed on five family members (two affected individuals and three unaffected relatives). Variant filtering, co-segregation analysis, and Sanger sequencing validation were conducted to identify candidate mutations. Conservation analysis across vertebrate species and in silico pathogenicity predictions were used to evaluate the biological impact of the variants. Additionally, 100 unrelated normal-hearing Korean individuals were screened to determine the frequency of the variant in the general population.

Results: Two MYO7A variants, c.4501G > A (p.Val1501Met) and c.6070 C > T (p.Arg2024Stop), were identified in affected individuals in a compound heterozygous state. Unaffected family members carried only one heterozygous variant. Both amino acid residues were highly conserved across seven vertebrate species. In silico analyses predicted p.Val1501Met to be pathogenic, while c.6070 C > T was previously classified as likely pathogenic. These variants were absent in the normal-hearing cohort, and only individuals with both variants exhibited hearing loss, supporting a compound heterozygous inheritance.

Conclusion: Compound heterozygosity of the MYO7A variants c.4501G > A and c.6070 C > T likely underlies the ARNSHL phenotype in the SR-323 family. These findings expand the known mutational spectrum of MYO7A and highlight the importance of genetic screening in hereditary hearing loss within the Korean population.

基于ngs的韩国DFNB2家族MYO7A突变鉴定,DFNB2是常染色体隐性非综合征性听力损失的一种亚型。
背景:遗传性听力损失(HHL)表现出相当大的遗传异质性。在已知的致病基因中,MYO7A常与常染色体隐性非综合征性听力损失(ARNSHL)相关,通过内耳细胞力学受损导致听力功能障碍。目的:本研究旨在确定韩国家族(SR-323) ARNSHL的遗传原因,并评估MYO7A候选变异的致病性。方法:对5名家庭成员(2名患病个体和3名未患病亲属)进行全外显子组测序(WES)。通过变异过滤、共分离分析和Sanger测序验证来确定候选突变。利用脊椎动物物种的保护分析和计算机致病性预测来评估变异的生物学影响。此外,筛选了100名无血缘关系的听力正常的韩国人,以确定该变体在一般人群中的频率。结果:两种MYO7A变异,c.4501G . >a (p. val151met)和c.6070C b> T (p.a g2024stop),在受影响个体中鉴定出复合杂合状态。未受影响的家庭成员只携带一个杂合变体。这两个氨基酸残基在7种脊椎动物中高度保守。计算机分析预测p. val151met具有致病性,而c.6070C - bbb10t以前被归类为可能致病。这些变异在听力正常的人群中不存在,只有具有这两种变异的个体表现出听力损失,支持复合杂合遗传。结论:MYO7A突变体c.4501G . >a和c.6070具有复合杂合性C b> T可能是SR-323家族中ARNSHL表型的基础。这些发现扩大了已知的MYO7A突变谱,并强调了韩国人群遗传性听力损失基因筛查的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genes & genomics
Genes & genomics 生物-生化与分子生物学
CiteScore
3.70
自引率
4.80%
发文量
131
审稿时长
6-12 weeks
期刊介绍: Genes & Genomics is an official journal of the Korean Genetics Society (http://kgenetics.or.kr/). Although it is an official publication of the Genetics Society of Korea, membership of the Society is not required for contributors. It is a peer-reviewed international journal publishing print (ISSN 1976-9571) and online version (E-ISSN 2092-9293). It covers all disciplines of genetics and genomics from prokaryotes to eukaryotes from fundamental heredity to molecular aspects. The articles can be reviews, research articles, and short communications.
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