ADAR Enzyme and miRNA Story: A Nucleotide that Can Make the Difference |
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Authors: | Sara Tomaselli Barbara Bonamassa Anna Alisi Valerio Nobili Franco Locatelli Angela Gallo |
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Affiliation: | 1.Laboratory of RNA Editing, Onco-haematology Department, Bambino Gesù Children’s Hospital, IRCCS, Piazza S. Onofrio 4, Rome 00165, Italy; E-Mails: (S.T.); (B.B.); (F.L.);2.Hepato-Metabolic Disease Unit and Liver Research Unit, Bambino Gesù Children’s Hospital, IRCCS, Piazza S. Onofrio 4, Rome 00165, Italy; E-Mail: ;3.Department of Pediatric Science, Università di Pavia, Strada Nuova 65, Pavia 27100, Italy |
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Abstract: | Adenosine deaminase acting on RNA (ADAR) enzymes convert adenosine (A) to inosine (I) in double-stranded (ds) RNAs. Since Inosine is read as Guanosine, the biological consequence of ADAR enzyme activity is an A/G conversion within RNA molecules. A-to-I editing events can occur on both coding and non-coding RNAs, including microRNAs (miRNAs), which are small regulatory RNAs of ~20–23 nucleotides that regulate several cell processes by annealing to target mRNAs and inhibiting their translation. Both miRNA precursors and mature miRNAs undergo A-to-I RNA editing, affecting the miRNA maturation process and activity. ADARs can also edit 3′ UTR of mRNAs, further increasing the interplay between mRNA targets and miRNAs. In this review, we provide a general overview of the ADAR enzymes and their mechanisms of action as well as miRNA processing and function. We then review the more recent findings about the impact of ADAR-mediated activity on the miRNA pathway in terms of biogenesis, target recognition, and gene expression regulation. |
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Keywords: | microRNA Adenosine deaminase acting on RNA (ADAR) A-to-I RNA editing double-stranded RNA (dsRNA) non-coding sequence |
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