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Updated: Dec 5, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
Published on: April 21, 2022
De Novo A-to-I RNA Editing Discovery in lncRNA
Domenico Alessandro Silvestris1, Chiara Scopa1, Sara Hanchi1
1RNA Editing Lab, Department of Hematology and Oncology and Cell and Gene Therapy, Bambino Gesù Children's Hospital (OPBG), IRCCS, 00146 Rome, Italy.
Background:
Adenosine to inosine (A-to-I) RNA editing is the most frequent editing event in humans. It converts adenosine to inosine in double-stranded RNA regions (in coding and non-coding RNAs) through the action of the adenosine deaminase acting on RNA (ADAR) enzymes. Long non-coding RNAs, particularly abundant in the brain, account for a large fraction of the human transcriptome, and their important regulatory role is becoming progressively evident in both normal and transformed cells.
Results:
Herein, we present a bioinformatic analysis to generate a comprehensive inosinome picture in long non-coding RNAs (lncRNAs), using an ad hoc index and searching for de novo editing events in the normal brain cortex as well as in glioblastoma, a highly aggressive human brain cancer. We discovered >10,000 new sites and 335 novel lncRNAs that undergo editing, never reported before. We found a generalized downregulation of editing at multiple lncRNA sites in glioblastoma samples when compared to the normal brain cortex.
Conclusion:
Overall, our study discloses a novel layer of complexity that controls lncRNAs in the brain and brain cancer.
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