短重复核糖核酸通过防止 TDP-43 及其 25 KDa 羧基末端片段的聚集来降低细胞毒性

IF 8.5 Q1 CHEMISTRY, MULTIDISCIPLINARY JACS Au Pub Date : 2024-09-24 eCollection Date: 2024-10-28 DOI:10.1021/jacsau.4c00566
Ai Fujimoto, Masataka Kinjo, Akira Kitamura
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引用次数: 0

摘要

TAR DNA/RNA 结合蛋白 43 kDa(TDP-43)蛋白病是肌萎缩侧索硬化症等神经退行性疾病的特征之一,在这种疾病中,退行性神经元细胞中会出现含有 TDP-43 及其 C 端片段(如 TDP-25)的细胞质聚集。然而,很少有报道关注能减少其聚集和细胞毒性的小分子。在这里,我们发现 GGGGCC 和 AAAAUU 的短 RNA 重复序列是 TDP-43 和 TDP-25 的聚集抑制因子。利用荧光交叉相关光谱,尽管缺乏主要的 RNA 识别基序,TDP-25 仍能与这些 RNA 以及 TDP-43 相互作用。表达这些 RNA 能显著减少携带 TDP-43 和 TDP-25 细胞质聚集体的细胞数量,并能改善 TDP-25 和 TDP-43 误定位造成的细胞死亡,而不会改变分子伴侣的细胞转录组。因此,GGGGCC 和 AAAAUU 的短 RNA 重复序列可以通过防止 TDP-43 和 TDP-25 的聚集来维持蛋白稳态。
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Short Repeat Ribonucleic Acid Reduces Cytotoxicity by Preventing the Aggregation of TDP-43 and Its 25 KDa Carboxy-Terminal Fragment.

TAR DNA/RNA-binding protein 43 kDa (TDP-43) proteinopathy is a hallmark of neurodegenerative disorders, such as amyotrophic lateral sclerosis, in which cytoplasmic aggregates containing TDP-43 and its C-terminal fragments, such as TDP-25, are observed in degenerative neuronal cells. However, few reports have focused on small molecules that can reduce their aggregation and cytotoxicity. Here, we show that short RNA repeats of GGGGCC and AAAAUU are aggregation suppressors of TDP-43 and TDP-25. TDP-25 interacts with these RNAs, as well as TDP-43, despite the lack of major RNA-recognition motifs using fluorescence cross-correlation spectroscopy. Expression of these RNAs significantly decreases the number of cells harboring cytoplasmic aggregates of TDP-43 and TDP-25 and ameliorates cell death by TDP-25 and mislocalized TDP-43 without altering the cellular transcriptome of molecular chaperones. Consequently, short RNA repeats of GGGGCC and AAAAUU can maintain proteostasis by preventing the aggregation of TDP-43 and TDP-25.

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