Abstract
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 noncoding 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.
Lingua originale | Inglese |
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pagine (da-a) | 1-13 |
Numero di pagine | 13 |
Rivista | Cancers |
Volume | 12 |
Numero di pubblicazione | 10 |
DOI | |
Stato di pubblicazione | Pubblicato - 2020 |
All Science Journal Classification (ASJC) codes
- Oncologia
- Ricerca sul Cancro
Keywords
- Brain
- Glioblastoma
- LncRNA
- RNA editing