Degradation of circular RNA by the ribonuclease DIS3
- PMID: 39965568
- DOI: 10.1016/j.molcel.2025.01.012
Degradation of circular RNA by the ribonuclease DIS3
Abstract
Features of circular RNAs (circRNAs) produced by back-splicing of eukaryotic exon(s) make them resistant to degradation by linear RNA decay machineries. Thus, a general circRNA degradation pathway under normal conditions has remained largely elusive. Here, we report that the endonucleolytic enzyme DIS3 is responsible for the degradation of circRNAs. Depletion of DIS3 leads to the upregulation of more than 60% of circRNAs with little effect on their linear cognates. Such DIS3-mediated circRNA degradation is conserved, occurs in the cytoplasm, and relies on DIS3's endonucleolytic activity but is independent of the RNA exosome complex. Sequence enrichment analyses suggest that DIS3 prefers to degrade circRNAs containing U-rich motifs. Correspondingly, synthesized RNA circles with or without U-rich motifs exhibit decreased or increased stabilities, respectively. Together, these findings suggest a general regulation of circRNA turnover by DIS3.
Keywords: DIS3; RNA decay; U-rich motifs; circRNAs; circular RNAs; degradation; endonuclease; turnover.
Copyright © 2025 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests L.-L.C. and C.-X.L. are named as inventors on patents related to circular RNA held by CAS Center for Excellence in Molecular Cell Science (CEMCS). Ling-Ling Chen is a member of the Molecular Cell advisory board.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources