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dc.contributor.authorUroda, Tina
dc.contributor.authorAnastasakou, Eleni
dc.contributor.authorRossi, Annalisa
dc.contributor.authorTeulon, Jean Marie
dc.contributor.authorPellequer, Jean-Luc
dc.contributor.authorAnnibale, Paolo
dc.contributor.authorPessey, Ombeline
dc.contributor.authorInga, Alberto
dc.contributor.authorChillón, Isabel
dc.contributor.authorMarcia, Marco
dc.date.accessioned2022-01-17T16:30:22Z
dc.date.available2022-01-17T16:30:22Z
dc.date.issued2019-09-05
dc.identifier.citationUroda , T , Anastasakou , E , Rossi , A , Teulon , J M , Pellequer , J-L , Annibale , P , Pessey , O , Inga , A , Chillón , I & Marcia , M 2019 , ' Conserved pseudoknots in lncRNA MEG3 are essential for stimulation of the p53 pathway ' , Molecular Cell , vol. 75 , no. 5 , pp. 982-995 . https://doi.org/10.1016/j.molcel.2019.07.025en
dc.identifier.issn1097-2765
dc.identifier.otherPURE: 277343461
dc.identifier.otherPURE UUID: fc0ec7ae-a25d-451e-b068-0bd201f5eb20
dc.identifier.otherScopus: 85071560684
dc.identifier.otherPubMed: 31444106
dc.identifier.otherORCID: /0000-0003-3208-5347/work/105957255
dc.identifier.urihttp://hdl.handle.net/10023/24687
dc.descriptionFunding Information: Work in the Marcia lab is partly funded by the Agence Nationale de la Recherche (ANR-15-CE11-0003-01), the Agence Nationale de Recherche sur le Sida et les H?patites Virales (ANRS, ECTZ18552), and ITMO Cancer (18CN047-00). The Marcia lab uses the platforms of the Grenoble Instruct Center (ISBG UMS 3518 CNRS-CEA-UJF-EMBL) with support from FRISBI (ANR-10-INSB-05-02) and GRAL (ANR-10-LABX-49-01) within the Grenoble Partnership for Structural Biology (PSB). IBS acknowledges integration into the Interdisciplinary Research Institute of Grenoble (IRIG, CEA). This work acknowledges the AFM platform at the IBS.en
dc.description.abstractLong non-coding RNAs (lncRNAs) are key regulatory molecules, but unlike with other RNAs, the direct link between their tertiary structure motifs and their function has proven elusive. Here we report structural and functional studies of human maternally expressed gene 3 (MEG3), a tumor suppressor lncRNA that modulates the p53 response. We found that, in an evolutionary conserved region of MEG3, two distal motifs interact by base complementarity to form alternative, mutually exclusive pseudoknot structures (“kissing loops”). Mutations that disrupt these interactions impair MEG3-dependent p53 stimulation in vivo and disrupt MEG3 folding in vitro. These findings provide mechanistic insights into regulation of the p53 pathway by MEG3 and reveal how conserved motifs of tertiary structure can regulate lncRNA biological function.
dc.format.extent24
dc.language.isoeng
dc.relation.ispartofMolecular Cellen
dc.rightsCopyright © 2019 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license.en
dc.subjectAlternative splicingen
dc.subjectAtomic force microscopyen
dc.subjectCell cycle regulationen
dc.subjectEpigeneticsen
dc.subjectImprintingen
dc.subjectp53 stress responseen
dc.subjectPituitary adenomaen
dc.subjectRNA evolutionen
dc.subjectRNA pseudoknotsen
dc.subjectRNA structureen
dc.subjectQH301 Biologyen
dc.subjectCell Biologyen
dc.subjectMolecular Biologyen
dc.subjectDASen
dc.subject.lccQH301en
dc.titleConserved pseudoknots in lncRNA MEG3 are essential for stimulation of the p53 pathwayen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Physics and Astronomyen
dc.identifier.doihttps://doi.org/10.1016/j.molcel.2019.07.025
dc.description.statusPeer revieweden


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