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Giusti, S.A.* ; Pino, N.S. ; Pannunzio, C.* ; Ogando, M.B.* ; Armando, N.G.* ; Garrett, L. ; Zimprich, A. ; Becker, L. ; Gimeno, M.L.* ; Lukin, J.* ; Merino, F.L.* ; Pardi, M.B.* ; Pedroncini, O.* ; Di Mauro, G.C.* ; Gailus-Durner, V. ; Fuchs, H. ; Hrabě de Angelis, M. ; Patop, I.L.* ; Turck, C.W.* ; Deussing, J.M.* ; Vogt Weisenhorn, D.M. ; Jahn, O.* ; Kadener, S.* ; Hölter, S.M. ; Brose, N.* ; Giesert, F. ; Wurst, W. ; Marin-Burgin, A.* ; Refojo, D.*

A brain-enriched circular RNA controls excitatory neurotransmission and restricts sensitivity to aversive stimuli.

Sci. Adv. 10:eadj8769 (2024)
Publ. Version/Full Text DOI PMC
Open Access Gold
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Circular RNAs (circRNAs) are a large class of noncoding RNAs. Despite the identification of thousands of circular transcripts, the biological significance of most of them remains unexplored, partly because of the lack of effective methods for generating loss-of-function animal models. In this study, we focused on circTulp4, an abundant circRNA derived from the Tulp4 gene that is enriched in the brain and synaptic compartments. By creating a circTulp4-deficient mouse model, in which we mutated the splice acceptor site responsible for generating circTulp4 without affecting the linear mRNA or protein levels, we were able to conduct a comprehensive phenotypic analysis. Our results demonstrate that circTulp4 is critical in regulating neuronal and brain physiology, modulating the strength of excitatory neurotransmission and sensitivity to aversive stimuli. This study provides evidence that circRNAs can regulate biologically relevant functions in neurons, with modulatory effects at multiple levels of the phenotype, establishing a proof of principle for the regulatory role of circRNAs in neural processes.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Gene-expression; Mice; Quantification; Biogenesis; Database; Abundant; Cells; State; Seq
Language english
Publication Year 2024
HGF-reported in Year 2024
ISSN (print) / ISBN 2375-2548
e-ISSN 2375-2548
Quellenangaben Volume: 10, Issue: 21, Pages: , Article Number: eadj8769 Supplement: ,
Publisher American Association for the Advancement of Science (AAAS)
Publishing Place Washington, DC [u.a.]
Reviewing status Peer reviewed
POF-Topic(s) 30204 - Cell Programming and Repair
30201 - Metabolic Health
Research field(s) Genetics and Epidemiology
PSP Element(s) G-500500-001
G-500692-001
G-500600-001
Grants Volkswagen Foundation
Swiss National Science Foundation-SNSF
Max Planck Society
German Federal Ministry of Education and Research
Fondo para la Convergencia Estructural del Mercosur-FOCEM
Consejo Nacional de Investigaciones Cientificas y Tecnicas
Agencia Nacional de Promoción Científica y Tecnológica
Scopus ID 85194218757
PubMed ID 38787942
Erfassungsdatum 2024-06-03