Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430022, P.R. China.
Mol Med Rep. 2020 Jul;22(1):77-86. doi: 10.3892/mmr.2020.11100. Epub 2020 Apr 30.
Mutations in mitochondrial DNA (mtDNA), especially in mitochondrial 12S rRNA and transfer RNA(tRNA)Ser(UCN) genes, are important causes of non‑syndromic hearing loss. However, the molecular mechanism underlying mt‑tRNA mutations in clinical hearing impairment are not fully understood. The present study assessed the molecular characterization of two Chinese families with non‑syndromic hearing loss, who both exhibited very low penetrance of deafness (9.1 and 12.5% for Family 1 and 2, respectively). Mutational analysis of the complete mtDNA genes identified the presence of cytochrome c oxidase 1/tRNASer(UCN) G7444A and tRNASer(UCN) C7492T mutations, together with polymorphisms belonging to human mitochondrial haplogroup D4 and G2b, respectively. Moreover, the G7444A and C7492T mutations occurred at highly conserved tRNASer(UCN) nucleotides and may cause tRNA metabolism failure, which is involved in mitochondrial translation defects. Therefore, the G7444A and C7492T mutations may lead to the mitochondrial dysfunction that responsible for deafness. However, the absence of any functional variants in Gap junction β‑2, Solute Carrier Family 26 Member 4 and TRNA 5‑methylaminomethyl‑2‑thiouridylate methyltransferase suggested that nuclear genes may not play active roles in the occurrence of deafness. In the present study, the observed incomplete penetrance of hearing loss and mild mitochondrial dysfunction indicated that mtDNA G7444A and C7492T mutations are insufficient to produce the deafness phenotype. Therefore, other risk factors such as environmental factors and epigenetic regulation may be involved in the pathogenesis of hearing loss in the families recruited in the present study.
线粒体 DNA(mtDNA)突变,尤其是线粒体 12S rRNA 和转移 RNA(tRNA)Ser(UCN)基因的突变,是导致非综合征性耳聋的重要原因。然而,mt-tRNA 突变导致临床听力损伤的分子机制尚不完全清楚。本研究评估了两个中国非综合征性耳聋家系的分子特征,这两个家系的耳聋外显率均非常低(家系 1 和 2 分别为 9.1%和 12.5%)。对完整 mtDNA 基因的突变分析发现存在细胞色素 c 氧化酶 1/tRNA Ser(UCN)G7444A 和 tRNA Ser(UCN)C7492T 突变,分别与属于人类线粒体单倍群 D4 和 G2b 的多态性有关。此外,G7444A 和 C7492T 突变发生在高度保守的 tRNA Ser(UCN)核苷酸上,可能导致 tRNA 代谢失败,从而导致线粒体翻译缺陷。因此,G7444A 和 C7492T 突变可能导致导致耳聋的线粒体功能障碍。然而,缝隙连接β-2、溶质载体家族 26 成员 4 和 tRNA 5-甲基氨基甲酰基-2-硫代尿嘧啶甲基转移酶的核基因中没有任何功能变体,提示核基因可能不会在耳聋的发生中发挥积极作用。在本研究中,观察到听力损失的不完全外显率和轻度线粒体功能障碍表明,mtDNA G7444A 和 C7492T 突变不足以产生耳聋表型。因此,其他风险因素,如环境因素和表观遗传调控,可能参与了本研究中招募的家族的听力损失发病机制。