The Epitranscriptome and Innate Immunity

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Publikace nespadá pod Ústav výpočetní techniky, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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O´CONNELL Mary MANNION Niamh M. KEEGAN Liam

Rok publikování 2015
Druh Článek v odborném periodiku
Časopis / Zdroj PLOS GENETICS
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
Doi http://dx.doi.org/10.1371/journal.pgen.1005687
Obor Genetika a molekulární biologie
Klíčová slova DOUBLE-STRANDED-RNA; EDITING ENZYME ADAR1; LACTIS GAMMA-TOXIN; PRE-MESSENGER-RNA; I-LIKE RECEPTORS; ADENOSINE-DEAMINASE; RIG-I; SUBSTRATE-SPECIFICITY; STRUCTURAL INSIGHTS; MAMMALIAN ADARS
Popis Our knowledge of the variety and abundances of RNA base modifications is rapidly increasing. Modified bases have critical roles in tRNAs, rRNAs, translation, splicing, RNA interference, and other RNA processes, and are now increasingly detected in all types of transcripts. Can new biological principles associated with this diversity of RNA modifications, particularly in mRNAs and long non-coding RNAs, be identified? This review will explore this question by focusing primarily on adenosine to inosine (A-to-I) RNA editing by the adenine deaminase acting on RNA (ADAR) enzymes that have been intensively studied for the past 20 years and have a wide range of effects. Over 100 million adenosine to inosine editing sites have been identified in the human transcriptome, mostly in embedded Alu sequences that form potentially innate immune-stimulating dsRNA hairpins in transcripts. Recent research has demonstrated that inosine in the epitranscriptome and ADAR1 protein establish innate immune tolerance for host dsRNA formed by endogenous sequences. Innate immune sensors that detect viral nucleic acids are among the readers of epitranscriptome RNA modifications, though this does preclude a wide range of other modification effects.
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