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Molecular Impairment Mechanisms of Novel OPA1 Mutations Predicted by Molecular Modeling in Patients With Autosomal Dominant Optic Atrophy and Auditory Neuropathy Spectrum Disorder.分子建模预测的常染色体显性遗传性视神经萎缩和听觉神经病谱系障碍患者中新型OPA1突变的分子损伤机制
Otol Neurotol. 2016 Apr;37(4):394-402. doi: 10.1097/MAO.0000000000000978.
2
Auditory neuropathy--neural and synaptic mechanisms.听觉神经病——神经和突触机制。
Nat Rev Neurol. 2016 Mar;12(3):135-49. doi: 10.1038/nrneurol.2016.10. Epub 2016 Feb 19.
3
Cellular iron uptake, trafficking and metabolism: Key molecules and mechanisms and their roles in disease.细胞铁摄取、转运与代谢:关键分子、机制及其在疾病中的作用
Biochim Biophys Acta. 2015 May;1853(5):1130-44. doi: 10.1016/j.bbamcr.2015.01.021. Epub 2015 Feb 4.
4
Functional reconstitution of mitochondrial Fe/S cluster synthesis on Isu1 reveals the involvement of ferredoxin.Isu1 上线粒体 Fe/S 簇合成的功能重建揭示了铁氧还蛋白的参与。
Nat Commun. 2014 Oct 31;5:5013. doi: 10.1038/ncomms6013.
5
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6
Mammalian Fe-S cluster biogenesis and its implication in disease.哺乳动物铁硫簇生物合成及其在疾病中的意义。
Biochimie. 2014 May;100:48-60. doi: 10.1016/j.biochi.2014.01.009. Epub 2014 Jan 17.
7
Auditory dyssynchrony or auditory neuropathy: understanding the pathophysiology and exploring methods of treatment.听觉失同步或听觉神经病:理解其病理生理学并探索治疗方法。
Int J Pediatr Otorhinolaryngol. 2014 Feb;78(2):171-3. doi: 10.1016/j.ijporl.2013.12.021. Epub 2013 Dec 24.
8
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.FDX1L基因中的有害突变与一种新型线粒体肌肉肌病相关。
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10
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss.PNPTA1 基因突变导致线粒体 RNA 输入蛋白 PNPase 缺失,引起遗传性耳聋。
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FDXR突变导致感觉神经病变并扩大线粒体铁硫合成疾病的范围。

FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis Diseases.

作者信息

Paul Antoine, Drecourt Anthony, Petit Floriane, Deguine Delphine Dupin, Vasnier Christelle, Oufadem Myriam, Masson Cécile, Bonnet Crystel, Masmoudi Saber, Mosnier Isabelle, Mahieu Laurence, Bouccara Didier, Kaplan Josseline, Challe Georges, Domange Christelle, Mochel Fanny, Sterkers Olivier, Gerber Sylvie, Nitschke Patrick, Bole-Feysot Christine, Jonard Laurence, Gherbi Souad, Mercati Oriane, Ben Aissa Ines, Lyonnet Stanislas, Rötig Agnès, Delahodde Agnès, Marlin Sandrine

机构信息

UMR 1163, Université Paris Descartes, Sorbonne Paris Cité, Institut IMAGINE, 24 Boulevard du Montparnasse, 75015 Paris, France.

Service de Génétique Médicale, Hôpital Purpan, 40031 Toulouse, France.

出版信息

Am J Hum Genet. 2017 Oct 5;101(4):630-637. doi: 10.1016/j.ajhg.2017.09.007. Epub 2017 Sep 28.

DOI:10.1016/j.ajhg.2017.09.007
PMID:28965846
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5630197/
Abstract

Hearing loss and visual impairment in childhood have mostly genetic origins, some of them being related to sensorial neuronal defects. Here, we report on eight subjects from four independent families affected by auditory neuropathy and optic atrophy. Whole-exome sequencing revealed biallelic mutations in FDXR in affected subjects of each family. FDXR encodes the mitochondrial ferredoxin reductase, the sole human ferredoxin reductase implicated in the biosynthesis of iron-sulfur clusters (ISCs) and in heme formation. ISC proteins are involved in enzymatic catalysis, gene expression, and DNA replication and repair. We observed deregulated iron homeostasis in FDXR mutant fibroblasts and indirect evidence of mitochondrial iron overload. Functional complementation in a yeast strain in which ARH1, the human FDXR ortholog, was deleted established the pathogenicity of these mutations. These data highlight the wide clinical heterogeneity of mitochondrial disorders related to ISC synthesis.

摘要

儿童期听力损失和视力损害大多源于遗传,其中一些与感觉神经元缺陷有关。在此,我们报告了来自四个独立家庭的八名受听觉神经病和视神经萎缩影响的受试者。全外显子组测序揭示了每个家庭受影响受试者中FDXR的双等位基因突变。FDXR编码线粒体铁氧化还原蛋白还原酶,这是唯一参与铁硫簇(ISC)生物合成和血红素形成的人类铁氧化还原蛋白还原酶。ISC蛋白参与酶催化、基因表达以及DNA复制和修复。我们观察到FDXR突变成纤维细胞中铁稳态失调以及线粒体铁过载的间接证据。在缺失人类FDXR直系同源基因ARH1的酵母菌株中的功能互补确定了这些突变的致病性。这些数据突出了与ISC合成相关的线粒体疾病广泛的临床异质性。