先天免疫系统
肌苷
核糖核酸
生物
RNA沉默
阿达尔
RNA编辑
解旋酶
免疫
细胞生物学
基因
病毒学
腺苷
RNA干扰
免疫系统
遗传学
生物化学
作者
Jaclyn Quin,Jiří Sedmík,Dragana Vukić,Aalia Khan,Liam P. Keegan,Mary A. O’Connell
标识
DOI:10.1016/j.tibs.2021.02.002
摘要
Modified bases act as marks on cellular RNAs so that they can be distinguished from foreign RNAs, reducing innate immune responses to endogenous RNA. In humans, mutations giving reduced levels of one base modification, adenosine-to-inosine deamination, cause a viral infection mimic syndrome, a congenital encephalitis with aberrant interferon induction. These Aicardi-Goutières syndrome 6 mutations affect adenosine deaminase acting on RNA 1 (ADAR1), which generates inosines in endogenous double-stranded (ds)RNA. The inosine base alters dsRNA structure to prevent aberrant activation of antiviral cytosolic helicase RIG-I-like receptors. We review how effects of inosines, ADARs, and other modified bases have been shown to be important in innate immunity and cancer.
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