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The ribotoxin -sarcin can cleave the sarcin/ricin loop on late 60S pre-ribosomes

dc.contributor.authorOlombrada, Miriam
dc.contributor.authorPeña, Cohue
dc.contributor.authorRodríguez Galán, Olga
dc.contributor.authorKlingauf Nerurkar, Purnima
dc.contributor.authorPortugal Calisto, Daniela
dc.contributor.authorOborská Oplová, Michaela
dc.contributor.authorAltvater, Martin
dc.contributor.authorGavilanes, José G.
dc.contributor.authorMartínez Del Pozo, Álvaro
dc.contributor.authorCruz, Jesús de la
dc.contributor.authorGarcía Ortega, Lucía
dc.contributor.authorGovind Panse, Vikram
dc.date.accessioned2023-06-16T15:23:54Z
dc.date.available2023-06-16T15:23:54Z
dc.date.issued2020
dc.description.abstractThe ribotoxin -sarcin belongs to a family of ribonucleases that cleave the sarcin/ricin loop (SRL), a critical functional rRNA element within the large ribosomal subunit (60S), thereby abolishing translation. Whether -sarcin targets the SRL only in mature 60S subunits remains unresolved. Here, we show that, in yeast, -sarcin can cleave SRLs within late 60S pre-ribosomes containing mature 25S rRNA but not nucleolar/nuclear 60S pre-ribosomes containing 27S pre-rRNA in vivo. Conditional expression of -sarcin is lethal, but does not impede early pre-rRNA processing, nuclear export and the cytoplasmic maturation of 60S pre-ribosomes. Thus, SRL-cleaved containing late 60S pre-ribosomes seem to escape cytoplasmic proofreading steps. Polysome analyses revealed that SRL-cleaved 60S ribosomal subunits form 80S initiation complexes, but fail to progress to the step of translation elongation. We suggest that the functional integrity of a -sarcin cleaved SRL might be assessed only during translation.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipUnión Europea. FP7
dc.description.sponsorshipMinisterio de Economía y Competitividad (MINECO)
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/62256
dc.identifier.doidoi.org/10.1093/nar/gkaa315
dc.identifier.issn1362-4962
dc.identifier.officialurlhttps://doi.org/10.1093/nar/gkaa315
dc.identifier.relatedurlhttps://academic.oup.com/nar/article/48/11/6210/5828919
dc.identifier.urihttps://hdl.handle.net/20.500.14352/6574
dc.issue.number11
dc.journal.titleNucleic Acids Research
dc.language.isoeng
dc.page.final6222
dc.page.initial6210
dc.publisherOxford university press
dc.relation.projectIDEURIBIO (260676)
dc.relation.projectID(BFU2012-32404; BFU2016-75352-P)
dc.rightsAtribución-NoComercial 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/es/
dc.subject.cdu577.1
dc.subject.keywordRibosomes
dc.subject.keywordPeptide Elongation Factor G
dc.subject.keywordAnticodons
dc.subject.ucmBiología molecular (Química)
dc.subject.ucmBioquímica (Química)
dc.titleThe ribotoxin -sarcin can cleave the sarcin/ricin loop on late 60S pre-ribosomes
dc.typejournal article
dc.volume.number48
dspace.entity.typePublication
relation.isAuthorOfPublication4d35a8a6-8bd3-4ff4-b179-57581d8d36d8
relation.isAuthorOfPublicationb8f84062-84af-45de-876d-9ee1b31aa47a
relation.isAuthorOfPublication.latestForDiscoveryb8f84062-84af-45de-876d-9ee1b31aa47a

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