| Literature DB >> 33736931 |
Jaclyn Quin1, Jiří Sedmík1, Dragana Vukić1, Anzer Khan1, Liam P Keegan2, Mary A O'Connell3.
Abstract
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.Entities:
Keywords: RNA editing; antiviral responses; autoinflammatory disease; double-stranded RNA (dsRNA); interferon; pattern recognition receptors (PRRs)
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Year: 2021 PMID: 33736931 DOI: 10.1016/j.tibs.2021.02.002
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807