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HNRNPK 通过拮抗 C9orf72 ALS 中的 DNA 损伤来减轻 RNA 毒性。

HNRNPK alleviates RNA toxicity by counteracting DNA damage in C9orf72 ALS.

机构信息

Department of Neurosciences, Experimental Neurology and Leuven Brain Institute (LBI), KU Leuven-University of Leuven, Leuven, Belgium.

Center for Brain & Disease Research, Laboratory of Neurobiology, VIB, Campus Gasthuisberg, O&N5, Herestraat 49, PB 602, 3000, Leuven, Belgium.

出版信息

Acta Neuropathol. 2022 Sep;144(3):465-488. doi: 10.1007/s00401-022-02471-y. Epub 2022 Jul 27.

Abstract

A 'GGGGCC' repeat expansion in the first intron of the C9orf72 gene is the most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). The exact mechanism resulting in these neurodegenerative diseases remains elusive, but C9 repeat RNA toxicity has been implicated as a gain-of-function mechanism. Our aim was to use a zebrafish model for C9orf72 RNA toxicity to identify modifiers of the ALS-linked phenotype. We discovered that the RNA-binding protein heterogeneous nuclear ribonucleoprotein K (HNRNPK) reverses the toxicity of both sense and antisense repeat RNA, which is dependent on its subcellular localization and RNA recognition, and not on C9orf72 repeat RNA binding. We observed HNRNPK cytoplasmic mislocalization in C9orf72 ALS patient fibroblasts, induced pluripotent stem cell (iPSC)-derived motor neurons and post-mortem motor cortex and spinal cord, in line with a disrupted HNRNPK function in C9orf72 ALS. In C9orf72 ALS/FTD patient tissue, we discovered an increased nuclear translocation, but reduced expression of ribonucleotide reductase regulatory subunit M2 (RRM2), a downstream target of HNRNPK involved in the DNA damage response. Last but not least, we showed that increasing the expression of HNRNPK or RRM2 was sufficient to mitigate DNA damage in our C9orf72 RNA toxicity zebrafish model. Overall, our study strengthens the relevance of RNA toxicity as a pathogenic mechanism in C9orf72 ALS and demonstrates its link with an aberrant DNA damage response, opening novel therapeutic avenues for C9orf72 ALS/FTD.

摘要

在 C9orf72 基因的第一个内含子中,“GGGGCC”重复扩展是肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD)最常见的遗传原因。导致这些神经退行性疾病的确切机制仍难以捉摸,但 C9 重复 RNA 毒性已被认为是一种功能获得机制。我们的目的是使用斑马鱼模型来研究 C9orf72 RNA 毒性,以确定与 ALS 相关表型的修饰因子。我们发现,异质核核糖核蛋白 K(HNRNPK)这种 RNA 结合蛋白可以逆转正义和反义重复 RNA 的毒性,这依赖于其亚细胞定位和 RNA 识别,而不依赖于 C9orf72 重复 RNA 结合。我们观察到 C9orf72 ALS 患者成纤维细胞、诱导多能干细胞(iPSC)衍生的运动神经元以及死后运动皮层和脊髓中的 HNRNPK 细胞质定位异常,这与 C9orf72 ALS 中 HNRNPK 功能的中断一致。在 C9orf72 ALS/FTD 患者组织中,我们发现核转位增加,但 HNRNPK 的下游靶标核糖核苷酸还原酶调节亚基 M2(RRM2)的表达减少,后者参与 DNA 损伤反应。最后但并非最不重要的是,我们表明增加 HNRNPK 或 RRM2 的表达足以减轻我们的 C9orf72 RNA 毒性斑马鱼模型中的 DNA 损伤。总的来说,我们的研究加强了 RNA 毒性作为 C9orf72 ALS 致病机制的相关性,并证明了它与异常的 DNA 损伤反应有关,为 C9orf72 ALS/FTD 开辟了新的治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b145/9381635/f98001f672c4/401_2022_2471_Fig1_HTML.jpg

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