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Article ; Online: RNA Editing Alterations Define Disease Manifestations in the Progression of Experimental Autoimmune Encephalomyelitis (EAE).

Dafou, Dimitra / Kanata, Eirini / Pettas, Spyros / Bekas, Nikolaos / Dimitriadis, Athanasios / Kempapidou, Garyfalia / Lagoudaki, Roza / Theotokis, Paschalis / Touloumi, Olga / Delivanoglou, Nikoleta / Kesidou, Evangelia / Xanthopoulos, Konstantinos / Grigoriadis, Nikolaos / Papavasiliou, Fotini Nina / Sklaviadis, Theodoros

Cells

2022  Volume 11, Issue 22

Abstract: RNA editing is an epitranscriptomic modification, leading to targeted changes in RNA transcripts. It is mediated by the action of ADAR (adenosine deaminases acting on double-stranded (ds) RNA and APOBEC (apolipoprotein B mRNA editing enzyme catalytic ... ...

Abstract RNA editing is an epitranscriptomic modification, leading to targeted changes in RNA transcripts. It is mediated by the action of ADAR (adenosine deaminases acting on double-stranded (ds) RNA and APOBEC (apolipoprotein B mRNA editing enzyme catalytic polypeptide-like) deaminases and appears to play a major role in the pathogenesis of many diseases. Here, we assessed its role in experimental autoimmune encephalomyelitis (EAE), a widely used non-clinical model of autoimmune inflammatory diseases of the central nervous system (CNS), which resembles many aspects of human multiple sclerosis (MS). We have analyzed in silico data from microglia isolated at different timepoints through disease progression to identify the global editing events and validated the selected targets in murine tissue samples. To further evaluate the functional role of RNA editing, we induced EAE in transgenic animals lacking expression of APOBEC-1. We found that RNA-editing events, mediated by the APOBEC and ADAR deaminases, are significantly reduced throughout the course of disease, possibly affecting the protein expression necessary for normal neurological function. Moreover, the severity of the EAE model was significantly higher in APOBEC-1 knock-out mice, compared to wild-type controls. Our results implicate regulatory epitranscriptomic mechanisms in EAE pathogenesis that could be extrapolated to MS and other neurodegenerative disorders (NDs) with common clinical and molecular features.
MeSH term(s) Humans ; Mice ; Animals ; RNA Editing/genetics ; APOBEC-1 Deaminase/genetics ; Encephalomyelitis, Autoimmune, Experimental/genetics ; RNA, Double-Stranded ; Mutagenesis, Site-Directed ; Mice, Knockout
Chemical Substances APOBEC-1 Deaminase (EC 3.5.4.36) ; RNA, Double-Stranded
Language English
Publishing date 2022-11-12
Publishing country Switzerland
Document type Journal Article
ZDB-ID 2661518-6
ISSN 2073-4409 ; 2073-4409
ISSN (online) 2073-4409
ISSN 2073-4409
DOI 10.3390/cells11223582
Database MEDical Literature Analysis and Retrieval System OnLINE

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