ADAR2 enzymes: efficient site-specific RNA editors with gene therapy aspirations

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Publikace nespadá pod Filozofickou fakultu, ale pod Středoevropský technologický institut. Oficiální stránka publikace je na webu muni.cz.
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HAJJI Khadija SEDMÍK Jiří CHERIAN Anna AMORUSO Damiano KEEGAN Liam O'CONNELL Mary Anne

Rok publikování 2022
Druh Článek v odborném periodiku
Časopis / Zdroj RNA
Fakulta / Pracoviště MU

Středoevropský technologický institut

Citace
www https://rnajournal.cshlp.org/content/28/10/1281
Doi http://dx.doi.org/10.1261/rna.079266.122
Klíčová slova ADAR; ADARB1; dsRNA; recoding RNA editing; neurons
Popis The adenosine deaminase acting on RNA (ADAR) enzymes are essential for neuronal function and innate immune control. ADAR1 RNA editing prevents aberrant activation of antiviral dsRNA sensors through editing of long, double-stranded RNAs (dsRNAs). In this review, we focus on the ADAR2 proteins involved in the efficient, highly site-specific RNA editing to recode open reading frames first discovered in the GRIA2 transcript encoding the key GLUA2 subunit of AMPA receptors; ADAR1 proteins also edit many of these sites. We summarize the history of ADAR2 protein research and give an up-to-date review of ADAR2 structural studies, human ADARBI (ADAR2) mutants causing severe infant seizures, and mouse disease models. Structural studies on ADARs and their RNA substrates facilitate current efforts to develop ADAR RNA editing gene therapy to edit disease-causing single nucleotide polymorphisms (SNPs). Artificial ADAR guide RNAs are being developed to retarget ADAR RNA editing to new target transcripts in order to correct SNP mutations in them at the RNA level. Site-specific RNA editing has been expanded to recode hundreds of sites in CNS transcripts in Drosophila and cephalopods. In Drosophila and C. elegans, ADAR RNA editing also suppresses responses to self dsRNA.
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