Department of Genetics, Stanford University, Stanford, CA 94305, USA.
Curr Opin Genet Dev. 2024 Jun;86:102195. doi: 10.1016/j.gde.2024.102195. Epub 2024 Apr 20.
Adenosine-to-inosine RNA editing, catalyzed by the enzymes ADAR1 and ADAR2, stands as a pervasive RNA modification. A primary function of ADAR1-mediated RNA editing lies in labeling endogenous double-stranded RNAs (dsRNAs) as 'self', thereby averting their potential to activate innate immune responses. Recent findings have highlighted additional roles of ADAR1, independent of RNA editing, that are crucial for immune control. Here, we focus on recent progress in understanding ADAR1's RNA editing-dependent and -independent roles in immune control. We describe how ADAR1 regulates various dsRNA innate immune receptors through distinct mechanisms. Furthermore, we discuss the implications of ADAR1 and RNA editing in diseases, including autoimmune diseases and cancers.
腺嘌呤核苷到肌苷核苷 RNA 编辑,由 ADAR1 和 ADAR2 等酶催化,是一种普遍存在的 RNA 修饰。ADAR1 介导的 RNA 编辑的一个主要功能是将内源性双链 RNA(dsRNA)标记为“自身”,从而避免它们激活先天免疫反应的潜在风险。最近的研究结果强调了 ADAR1 的其他非 RNA 编辑依赖性功能,这些功能对于免疫控制至关重要。在这里,我们重点介绍了最近在理解 ADAR1 在免疫控制中的 RNA 编辑依赖性和非依赖性作用方面的进展。我们描述了 ADAR1 通过不同的机制调节各种 dsRNA 先天免疫受体。此外,我们还讨论了 ADAR1 和 RNA 编辑在包括自身免疫性疾病和癌症在内的疾病中的意义。