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蛋白酶体亚基 PSMC3 变体导致神经感觉综合征,表现为耳聋和白内障,原因是蛋白毒性应激。

Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress.

机构信息

Laboratoire de Génétique Médicale, INSERM, UMRS_1112, Institut de Génétique Médicale d'Alsace (IGMA), Université de Strasbourg, Faculté de médecine de Strasbourg, Strasbourg, France.

Karlsruhe Institute of Technology (KIT), Institut für Biologische und Chemische Systeme (IBCS, BIP), Eggenstein-Leopoldshafen, Germany.

出版信息

EMBO Mol Med. 2020 Jul 7;12(7):e11861. doi: 10.15252/emmm.201911861. Epub 2020 Jun 5.

DOI:10.15252/emmm.201911861
PMID:32500975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7338805/
Abstract

The ubiquitin-proteasome system degrades ubiquitin-modified proteins to maintain protein homeostasis and to control signalling. Whole-genome sequencing of patients with severe deafness and early-onset cataracts as part of a neurological, sensorial and cutaneous novel syndrome identified a unique deep intronic homozygous variant in the PSMC3 gene, encoding the proteasome ATPase subunit Rpt5, which lead to the transcription of a cryptic exon. The proteasome content and activity in patient's fibroblasts was however unaffected. Nevertheless, patient's cells exhibited impaired protein homeostasis characterized by accumulation of ubiquitinated proteins suggesting severe proteotoxic stress. Indeed, the TCF11/Nrf1 transcriptional pathway allowing proteasome recovery after proteasome inhibition is permanently activated in the patient's fibroblasts. Upon chemical proteasome inhibition, this pathway was however impaired in patient's cells, which were unable to compensate for proteotoxic stress although a higher proteasome content and activity. Zebrafish modelling for knockout in PSMC3 remarkably reproduced the human phenotype with inner ear development anomalies as well as cataracts, suggesting that Rpt5 plays a major role in inner ear, lens and central nervous system development.

摘要

泛素-蛋白酶体系统通过降解泛素化修饰的蛋白来维持蛋白质的内稳态并调控信号通路。对患有严重耳聋和早发性白内障的患者进行全基因组测序,发现了一种新的神经、感觉和皮肤综合征的独特纯合性深内含子突变,该突变位于编码蛋白酶体 ATP 酶亚基 Rpt5 的 PSMC3 基因中,导致一个隐蔽外显子的转录。然而,患者成纤维细胞中的蛋白酶体含量和活性并未受到影响。尽管如此,患者细胞的蛋白质内稳态受损,表现为泛素化蛋白的积累,这表明存在严重的蛋白毒性应激。事实上,允许蛋白酶体抑制后恢复的 TCF11/Nrf1 转录途径在患者的成纤维细胞中被永久激活。然而,在蛋白酶体受到化学抑制时,患者细胞中的这条途径受损,尽管蛋白酶体含量和活性较高,但它们无法代偿蛋白毒性应激。敲除 PSMC3 的斑马鱼模型惊人地重现了人类表型,包括内耳发育异常和白内障,这表明 Rpt5 在内耳、晶状体和中枢神经系统发育中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/9239e0a7b778/EMMM-12-e11861-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/2744e544ed9a/EMMM-12-e11861-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/312c2800f8f1/EMMM-12-e11861-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/1c71f40f3a88/EMMM-12-e11861-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/c35fdf878679/EMMM-12-e11861-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/9239e0a7b778/EMMM-12-e11861-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/2744e544ed9a/EMMM-12-e11861-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/312c2800f8f1/EMMM-12-e11861-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/4f47476f7048/EMMM-12-e11861-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/d865a5f34d17/EMMM-12-e11861-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/1c71f40f3a88/EMMM-12-e11861-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/c35fdf878679/EMMM-12-e11861-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71ba/7338805/9239e0a7b778/EMMM-12-e11861-g008.jpg

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