神经退行性变
核糖核酸
翻译(生物学)
髓鞘
信使核糖核酸
多发性硬化
生物
细胞生物学
神经科学
化学
生物化学
中枢神经系统
医学
病理
基因
免疫学
疾病
作者
Prakash Kharel,Naveen Kumar Singhal,Thulasi Mahendran,Nicole West,Brintha Croos,Joram Rana,Lindsey Smith,Ernest Freeman,Ansuman Chattopadhyay,Jennifer McDonough,Soumitra Basu
标识
DOI:10.1016/j.chembiol.2023.02.007
摘要
RNA oxidation has been implicated in neurodegeneration, but the underlying mechanism for such effects is unclear. Extensive RNA oxidation occurs within the neurons in multiple sclerosis (MS) brains. Here, we identified selectively oxidized mRNAs in neuronal cells that pertained to neuropathological pathways. N-acetyl aspartate transferase 8 like (NAT8L) is one such transcript, whose translation product enzymatically synthesizes N-acetyl aspartic acid (NAA), a neuronal metabolite important for myelin synthesis. We reasoned that impediment of translation of an oxidized NAT8L mRNA will result in a reduction in its cognate protein, thus lowering the NAA level. This hypothesis is supported by our studies on cells, an animal model, and postmortem human MS brain. Reduced brain NAA level hampers myelin integrity making neuronal axons more susceptible to damage, which contributes to MS neurodegeneration. Overall, this work provides a framework for a mechanistic understanding of the link between RNA oxidation and neurodegeneration.
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