| Autor: |
Linares, Gabriel R., Li, Yichen, Chang, Wen-Hsuan, Rubin-Sigler, Jasper, Mendonca, Stacee, Hong, Sarah, Eoh, Yunsun, Guo, Wenxuan, Huang, Yi-Hsuan, Chang, Jonathan, Tu, Sharon, Dorjsuren, Nomongo, Santana, Manuel, Hung, Shu-Ting, Yu, Johnny, Perez, Joscany, Chickering, Michael, Cheng, Tze-Yuan, Huang, Chi-Chou, Lee, Shih-Jong James, Deng, Hao-Jen, Bach, Kieu-Tram, Gray, Kamden, Subramanyam, Vishvak, Rosenfeld, Jeffrey, Alworth, Samuel V., Goodarzi, Hani, Ichida, Justin K. |
| Zdroj: |
Cell Stem Cell; February 2023, Vol. 30 Issue: 2 p171-187.e14 |
| Abstrakt: |
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease caused by many diverse genetic etiologies. Although therapeutics that specifically target causal mutations may rescue individual types of ALS, such approaches cannot treat most patients since they have unknown genetic etiology. Thus, there is a critical need for therapeutic strategies that rescue multiple forms of ALS. Here, we combine phenotypic chemical screening on a diverse cohort of ALS patient-derived neurons with bioinformatic analysis of large chemical and genetic perturbational datasets to identify broadly effective genetic targets for ALS. We show that suppressing the gene-encoding, spliceosome-associated factor SYF2 alleviates TDP-43 aggregation and mislocalization, improves TDP-43 activity, and rescues C9ORF72and causes sporadic ALS neuron survival. Moreover, Syf2suppression ameliorates neurodegeneration, neuromuscular junction loss, and motor dysfunction in TDP-43 mice. Thus, suppression of spliceosome-associated factors such as SYF2may be a broadly effective therapeutic approach for ALS. |
| Databáze: |
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