Cyclic mismatch binding ligands interact with disease-associated CGG trinucleotide repeats in RNA and suppress their translation

dc.contributor.authorKonieczny, Patryk
dc.contributor.authorMukherjee, Sanjukta
dc.contributor.authorStepniak-Konieczna, Ewa
dc.contributor.authorTaylor, Katarzyna
dc.contributor.authorNiewiadomska, Daria
dc.contributor.authorPiasecka, Agnieszka
dc.contributor.authorWalczak, Agnieszka
dc.contributor.authorBaud, Anna
dc.contributor.authorDohno, Chikara
dc.contributor.authorNakatani, Kazuhiko
dc.contributor.authorSobczak, Krzysztof
dc.date.accessioned2023-08-10T05:59:51Z
dc.date.available2023-08-10T05:59:51Z
dc.date.issued2021
dc.description.abstractFragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder caused by a limited expansion of CGG repeats in the FMR1 gene. Degeneration of neurons in FXTAS cell models can be triggered by accumulation of polyglycine protein (FMRpolyG), a by-product of translation initiated upstream to the repeats. Specific aims of our work included testing if naphthyridine-based molecules could (1) block FMRpolyG synthesis by binding to CGG repeats in RNA, (2) reverse pathological alterations in affected cells and (3) preserve the content of FMRP, translated from the same FMR1 mRNA. We demonstrate that cyclic mismatch binding ligand CMBL4c binds to RNA structure formed by CGG repeats and attenuates translation of FMRpolyG and formation of nuclear inclusions in cells transfected with vectors expressing RNA with expanded CGG repeats. Moreover, our results indicate that CMBL4c delivery can reduce FMRpolyG-mediated cytotoxicity and apoptosis. Importantly, its therapeutic potential is also observed once the inclusions are already formed. We also show that CMBL4c-driven FMRpolyG loss is accompanied by partial FMRP reduction. As complete loss of FMRP induces FXS in children, future experiments should aim at evaluation of CMBL4c therapeutic intervention in differentiated tissues, in which FMRpolyG translation inhibition might outweigh adverse effects related to FMRP depletion.
dc.description.sponsorshipThis work was supported by the National Centre for Research and Development grant ERA- NET-E-Rare-2/III/DRUG_FXSPREMUT/01/2016 (to KS), Foundation for Polish Science-TEAM program cofinanced by the European Union within the European Regional Development Fund (TEAM POIR.04.04.00-00-5C0C/17-00 to KS), by the National Science Centre grants: 2020/38/A/NZ3/00498 (to KS), 2018/30/E/NZ5/00065 (to PK), 2014/15/B/NZ5/00142 (to ESK), 2020/37/B/NZ5/01263 (to ESK) and 2017/24/C/NZ1/00112(to KT), and JSPS KAKENHI Grant-in-Aid for Specially Promoted Research (26000007 to KN).
dc.identifier.citationNucleic Acids Research 2021, Vol. 49, nr 16, s. 9479–9495.
dc.identifier.doihttps://doi.org/10.1093/nar/gkab669
dc.identifier.urihttps://hdl.handle.net/10593/27341
dc.language.isoen
dc.publisherOxford University Press
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectfragile X-associated tremor/ataxia syndrome
dc.subjectFXTAS
dc.subjectrepeat-associated non-AUG (RAN) translation
dc.subjectRAN translation
dc.subjectCGG repeats
dc.subjectcyclic mismatch binding ligands
dc.subjectCMBL
dc.subjectCMBLs
dc.titleCyclic mismatch binding ligands interact with disease-associated CGG trinucleotide repeats in RNA and suppress their translation
dc.typeinfo:eu-repo/semantics/article

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Uniwersytet im. Adama Mickiewicza w Poznaniu
Biblioteka Uniwersytetu im. Adama Mickiewicza w Poznaniu
Ministerstwo Nauki i Szkolnictwa Wyższego