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  3. Influence of RNA circularity on Target RNA-Directed MicroRNA Degradation.
 

Influence of RNA circularity on Target RNA-Directed MicroRNA Degradation.

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BORIS DOI
10.48350/193152
Date of Publication
April 12, 2024
Publication Type
Article
Division/Institute

Institut für Zellbiol...

Author
Fuchs Wightman, Federico
Lukin, Jerónimo
Giusti, Sebastián A
Soutschek, Michael
Bragado, Laureano
Pozzi, Maria Berta
Institut für Zellbiologie (IZB)
Pierelli, María L
González, Paula
Fededa, Juan P
Schratt, Gerhard
Fujiwara, Rina
Wilusz, Jeremy E
Refojo, Damián
de la Mata, Manuel
Subject(s)

500 - Science::570 - ...

Series
Nucleic acids research
ISSN or ISBN (if monograph)
0305-1048
Publisher
Oxford University Press
Language
English
Publisher DOI
10.1093/nar/gkae094
PubMed ID
38381063
Description
A subset of circular RNAs (circRNAs) and linear RNAs have been proposed to 'sponge' or block microRNA activity. Additionally, certain RNAs induce microRNA destruction through the process of Target RNA-Directed MicroRNA Degradation (TDMD), but whether both linear and circular transcripts are equivalent in driving TDMD is unknown. Here, we studied whether circular/linear topology of endogenous and artificial RNA targets affects TDMD. Consistent with previous knowledge that Cdr1as (ciRS-7) circular RNA protects miR-7 from Cyrano-mediated TDMD, we demonstrate that depletion of Cdr1as reduces miR-7 abundance. In contrast, overexpression of an artificial linear version of Cdr1as drives miR-7 degradation. Using plasmids that express a circRNA with minimal co-expressed cognate linear RNA, we show differential effects on TDMD that cannot be attributed to the nucleotide sequence, as the TDMD properties of a sequence often differ when in a circular versus linear form. By analysing RNA sequencing data of a neuron differentiation system, we further detect potential effects of circRNAs on microRNA stability. Our results support the view that RNA circularity influences TDMD, either enhancing or inhibiting it on specific microRNAs.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/174634
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s00259-024-06649-2.pdftextAdobe PDF2.04 MBAttribution (CC BY 4.0)publishedOpen
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