ADAR RNA Modifications, the Epitranscriptome and Innate Immunity

被引:86
作者
Quin, Jaclyn [1 ]
Sedmik, Jiri [1 ]
Vukic, Dragana [1 ]
Khan, Anzer [1 ]
Keegan, Liam P. [1 ]
O'Connell, Mary A. [1 ]
机构
[1] Masaryk Univ Brno, Cent European Inst Technol, Kamenice 753-5,Pavil A35, CZ-62500 Brno, Czech Republic
基金
欧盟地平线“2020”;
关键词
DYSCHROMATOSIS SYMMETRICA HEREDITARIA; GENETIC POLYMORPHISMS; ANTIVIRAL ACTIVITY; CELLULAR-IMMUNITY; MUTATIONS; RECOGNITION; RNASEH2B; VARIANTS; THERAPY; ASSOCIATIONS;
D O I
10.1016/j.tibs.2021.02.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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-Goutieres 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 modi-fied bases have been shown to be important in innate immunity and cancer.
引用
收藏
页码:758 / 771
页数:14
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