Gao Xue, Ma Ying, Wang Wei-Qian, Wang Guo-Jian, Yang Kun, Xu Jin-Cao, Huang Sha-Sha, Wang Xiang, Hu Li-Min, Wang Xi, Wang Qiu-Quan, Wang Zhen-Dong, Han Ming-Yu, Dai Pu, Yuan Yong-Yi
Department of Otolaryngology, PLA Rocket Force Characteristic Medical Center, 16# XinWai Da Jie, Beijing, 100088, People's Republic of China.
College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, 28 Fuxing Road, Beijing, 100853, China.
Hum Genet. 2025 Sep 8. doi: 10.1007/s00439-025-02774-6.
Recessive variants in TWNK cause syndromes arising from mitochondrial DNA (mtDNA) depletion. Hearing loss is the most prevalent manifestation in individuals with these disorders. However, the clinical and pathophysiological features have not been fully elucidated. In this study, we collected five cases of hearing loss carrying bi-allelic TWNK variants from three unrelated Chinese families and identified two cases with isolated auditory neuropathy (AN) and three cases segregating with Perrault syndrome, characterized by AN, global developmental delay, and ovarian dysgenesis in females. All patients with cochlear implantation (CI) show poor speech discrimination outcomes, suggesting that the defect involves post-synaptic sites. In the mouse inner ear, Twinkle was immunolocalized to inner phalangeal cells and spiral ganglion neurons. Additionally, the broad expression pattern of Twinkle was observed in the auditory cortex, which to some extent explains the poor rehabilitation outcomes following CI. At the cellular level, Twinkle is localized at the mtDNA membrane, and the p.(Arg609AlaTer6) variant prevents the protein from reaching the mtDNA while the p.(Arg65Trp) variant exhibits a similar localization to the wild type, indicating a second mechanism of action. RT-PCR results indicated that the canonical transcript was abundant in the inner ear, while the shorter transcript was more abundant in the brain. Our findings revealed that bi-allelic TWNK variants lead to AN, which can be either syndromic or non-syndromic, with the molecular pathogenesis involving defects in mtDNA replication at post-synaptic sites. Patients with TWNK-associated conditions are not ideal candidates for CI and gene therapy may offer a solution for hearingrehabilitation.
TWNK基因的隐性变异会导致线粒体DNA(mtDNA)耗竭引起的综合征。听力损失是患有这些疾病个体中最常见的表现。然而,其临床和病理生理特征尚未完全阐明。在本研究中,我们从三个不相关的中国家庭收集了五例携带双等位基因TWNK变异的听力损失病例,鉴定出两例孤立性听觉神经病(AN)和三例与佩罗特综合征相关的病例,其特征为AN、全面发育迟缓以及女性卵巢发育不全。所有接受人工耳蜗植入(CI)的患者语音辨别结果均较差,提示缺陷涉及突触后位点。在小鼠内耳中,Twinkle免疫定位在内指细胞和螺旋神经节神经元。此外,在听觉皮层观察到Twinkle广泛的表达模式,这在一定程度上解释了CI后康复效果不佳的原因。在细胞水平上,Twinkle定位于mtDNA膜,p.(Arg609AlaTer6)变异阻止蛋白质到达mtDNA,而p.(Arg65Trp)变异与野生型表现出相似的定位,表明存在第二种作用机制。RT-PCR结果表明,典型转录本在内耳中丰富,而较短的转录本在大脑中更丰富。我们的研究结果表明,双等位基因TWNK变异导致AN,可为综合征性或非综合征性,分子发病机制涉及突触后位点mtDNA复制缺陷。患有TWNK相关疾病的患者并非CI的理想候选者,基因治疗可能为听力康复提供解决方案。