Abstract
Primary transcripts of certain microRNA (miRNA) genes are subject to RNA editing that converts adenosine to inosine. However, the importance of miRNA editing remains largely undetermined. Here we report that tissue-specific adenosine-to-inosine editing of miR-376 cluster transcripts leads to predominant expression of edited miR-376 isoform RNAs. One highly edited site is positioned in the middle of the 5'-proximal half "seed" region critical for the hybridization of miRNAs to targets. We provide evidence that the edited miR-376 RNA silences specifically a different set of genes. Repression of phosphoribosyl pyrophosphate synthetase 1, a target of the edited miR-376 RNA and an enzyme involved in the uric-acid synthesis pathway, contributes to tight and tissue-specific regulation of uric-acid levels, revealing a previously unknown role for RNA editing in miRNA-mediated gene silencing.
MeSH Terms
3' Untranslated Regions
Adenosine/metabolism
Adenosine Deaminase/genetics,metabolism
Animals
Base Sequence
Brain/metabolism
HeLa Cells
Humans
Inosine/metabolism
Liver/metabolism
Mice
MicroRNAs/chemistry,genetics,metabolism
Molecular Sequence Data
Nucleic Acid Conformation
Organ Specificity
Protein Serine-Threonine Kinases/genetics,metabolism
RNA Editing
RNA Interference
RNA-Binding Proteins
Ribose-Phosphate Pyrophosphokinase/genetics,metabolism
Uric Acid/metabolism
Chemicals
3' Untranslated Regions
MicroRNAs
RNA-Binding Proteins
Uric Acid
Inosine
Ttk protein, mouse
Protein Serine-Threonine Kinases
Ribose-Phosphate Pyrophosphokinase
ADARB1 protein, human
Adenosine Deaminase
Adenosine
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Zinshteyn Boris
Sethupathy Praveen
Iizasa Hisashi
Hatzigeorgiou Artemis G
Nishikura Kazuko
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