Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, EH9 3FL Edinburgh, United Kingdom.
Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, EH9 3FL Edinburgh, United Kingdom
RNA. 2024 Mar 18;30(4):327-336. doi: 10.1261/rna.079942.124.
RNA caps are deposited at the 5' end of RNA polymerase II transcripts. This modification regulates several steps of gene expression, in addition to marking transcripts as self to enable the innate immune system to distinguish them from uncapped foreign RNAs, including those derived from viruses. Specialized immune sensors, such as RIG-I and IFITs, trigger antiviral responses upon recognition of uncapped cytoplasmic transcripts. Interestingly, uncapped transcripts can also be produced by mammalian hosts. For instance, 5'-triphosphate RNAs are generated by RNA polymerase III transcription, including tRNAs, Alu RNAs, or vault RNAs. These RNAs have emerged as key players of innate immunity, as they can be recognized by the antiviral sensors. Mechanisms that regulate the presence of 5'-triphosphates, such as 5'-end dephosphorylation or RNA editing, prevent immune recognition of endogenous RNAs and excessive inflammation. Here, we provide a comprehensive overview of the complexity of RNA cap structures and 5'-triphosphate RNAs, highlighting their roles in transcript identity, immune surveillance, and disease.
RNA 帽在 RNA 聚合酶 II 转录本的 5' 端被沉积。这种修饰除了将转录本标记为自身以使其能够被先天免疫系统从无帽的外来 RNA 中区分出来,包括那些来自病毒的 RNA 之外,还调节了几个基因表达的步骤。专门的免疫传感器,如 RIG-I 和 IFITs,在识别无帽的细胞质转录本时会引发抗病毒反应。有趣的是,无帽的转录本也可以由哺乳动物宿主产生。例如,5'-三磷酸 RNA 是由 RNA 聚合酶 III 转录产生的,包括 tRNA、Alu RNA 或 vault RNA。这些 RNA 已经成为先天免疫的关键参与者,因为它们可以被抗病毒传感器识别。调节 5'-三磷酸存在的机制,如 5'-末端去磷酸化或 RNA 编辑,可防止内源性 RNA 的免疫识别和过度炎症。在这里,我们全面概述了 RNA 帽结构和 5'-三磷酸 RNA 的复杂性,强调了它们在转录本身份、免疫监测和疾病中的作用。