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关于TWNK基因参与佩罗综合征的新神经听力学发现及进一步证据。

Novel neuro-audiological findings and further evidence for TWNK involvement in Perrault syndrome.

作者信息

Ołdak Monika, Oziębło Dominika, Pollak Agnieszka, Stępniak Iwona, Lazniewski Michal, Lechowicz Urszula, Kochanek Krzysztof, Furmanek Mariusz, Tacikowska Grażyna, Plewczynski Dariusz, Wolak Tomasz, Płoski Rafał, Skarżyński Henryk

机构信息

Department of Genetics, World Hearing Center, Institute of Physiology and Pathology of Hearing, Mokra 17, Kajetany/Warsaw, 05-830, Nadarzyn, Poland.

Laboratory of Functional and Structural Genomics, Centre of New Technologies, University of Warsaw, Warsaw, Poland.

出版信息

J Transl Med. 2017 Feb 8;15(1):25. doi: 10.1186/s12967-017-1129-4.

Abstract

BACKGROUND

Hearing loss and ovarian dysfunction are key features of Perrault syndrome (PRLTS) but the clinical and pathophysiological features of hearing impairment in PRLTS individuals have not been addressed. Mutations in one of five different genes HSD17B4, HARS2, LARS2, CLPP or TWNK (previous symbol C10orf2) cause the autosomal recessive disorder but they are found only in about half of the patients.

METHODS

We report on two siblings with a clinical picture resembling a severe, neurological type of PRLTS. For an exhaustive characterisation of the phenotype neuroimaging with volumetric measurements and objective measures of cochlear hair cell and auditory nerve function (otoacustic emissions and auditory brainstem responses) were used. Whole exome sequencing was applied to identify the genetic cause of the disorder. Co-segregation of the detected mutations with the phenotype was confirmed by Sanger sequencing. In silico analysis including 3D protein structure modelling was used to predict the deleterious effects of the detected variants on protein function.

RESULTS

We found two rare biallelic mutations in TWNK, encoding Twinkle, an essential mitochondrial helicase. Mutation c.1196A>G (p.Asn399Ser) recurred for the first time in a patient with PRLTS and the second mutation c.1802G>A (p.Arg601Gln) was novel for the disorder. In both patients neuroimaging studies showed diminished cervical enlargement of the spinal cord and for the first time in PRLTS partial atrophy of the vestibulocochlear nerves and decreased grey and increased white matter volumes of the cerebellum. Morphological changes in the auditory nerves, their desynchronized activity and partial cochlear dysfunction underlay the complex mechanism of hearing impairment in the patients.

CONCLUSIONS

Our study unveils novel features on the phenotypic landscape of PRLTS and provides further evidence that the newly identified for PRLTS TWNK gene is involved in its pathogenesis.

摘要

背景

听力损失和卵巢功能障碍是佩罗特综合征(PRLTS)的关键特征,但PRLTS患者听力障碍的临床和病理生理特征尚未得到探讨。五个不同基因HSD17B4、HARS2、LARS2、CLPP或TWNK(先前符号为C10orf2)中的一个发生突变会导致常染色体隐性疾病,但仅在约一半的患者中发现这些突变。

方法

我们报告了两名临床表现类似于严重神经型PRLTS的同胞。为了全面描述该表型,使用了体积测量的神经影像学以及耳蜗毛细胞和听神经功能的客观测量方法(耳声发射和听性脑干反应)。应用全外显子组测序来确定该疾病的遗传原因。通过桑格测序确认检测到的突变与表型的共分离。使用包括三维蛋白质结构建模在内的计算机分析来预测检测到的变体对蛋白质功能的有害影响。

结果

我们在编码Twinkle(一种必需的线粒体解旋酶)的TWNK中发现了两个罕见的双等位基因突变。突变c.1196A>G(p.Asn399Ser)在一名PRLTS患者中首次复发,第二个突变c.1802G>A(p.Arg601Gln)是该疾病的新突变。在两名患者中,神经影像学研究均显示脊髓颈膨大减小,并且在PRLTS患者中首次出现前庭蜗神经部分萎缩以及小脑灰质体积减少和白质体积增加。听神经的形态变化、其不同步活动和部分耳蜗功能障碍是患者听力障碍复杂机制的基础。

结论

我们的研究揭示了PRLTS表型特征的新特点,并提供了进一步的证据表明新确定的PRLTS相关基因TWNK参与了其发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa1e/5299684/d2c890b61ec3/12967_2017_1129_Fig1_HTML.jpg

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