The molecular language of RNA 5′ ends: guardians of RNA identity and immunity

被引:7
作者
Avila-Bonilla, Rodolfo Gamaliel [1 ,2 ]
Macias, Sara [1 ]
机构
[1] Univ Edinburgh, Inst Immunol & Infect Res, Sch Biol Sci, Edinburgh EH9 3FL, Scotland
[2] Ctr Invest & Estudios Avanzados IPN CINVESTAV, Dept Genet & Biol Mol, Gustavo A Madero 07360, Cdmx, Mexico
基金
英国惠康基金;
关键词
5'cap; m7G; IFIT; RIG-I; capping; CMTR1; CMTR2; type I interferon; antiviral; MESSENGER-RNA; RIG-I; SACCHAROMYCES-CEREVISIAE; 5'-TRIPHOSPHATE RNA; PATTERN-RECOGNITION; ANTIVIRAL IMMUNITY; STRUCTURAL BASIS; CAPPED RNAS; HUMAN IFIT1; PROTEIN;
D O I
10.1261/rna.079942.124
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
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.
引用
收藏
页码:327 / 336
页数:10
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