Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106851
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dc.contributor.authorCosta, Rui O.-
dc.contributor.authorMartins, Helena-
dc.contributor.authorMartins, Luís F.-
dc.contributor.authorCwetsch, Andrzej W-
dc.contributor.authorMele, Miranda-
dc.contributor.authorPedro, Joana R.-
dc.contributor.authorTomé, Diogo-
dc.contributor.authorJeon, Noo Li-
dc.contributor.authorCancedda, Laura-
dc.contributor.authorJaffrey, Samie R.-
dc.contributor.authorAlmeida, Ramiro D.-
dc.date.accessioned2023-04-27T08:55:20Z-
dc.date.available2023-04-27T08:55:20Z-
dc.date.issued2019-07-23-
dc.identifier.issn22111247pt
dc.identifier.urihttps://hdl.handle.net/10316/106851-
dc.description.abstractRibosomes and a subset of cellular mRNAs are trafficked into axons of developing neurons. The axonal localization of translational machinery allows new proteins to be rapidly and locally synthesized during axonal growth and pathfinding. However, in mature neurons, axonal ribosomes are significantly reduced or even absent. The mechanism that elicits this removal is currently unknown. Here, we demonstrate that synapse formation is the trigger for ribosome reduction in mature axons. In vivo analysis shows that axonal ribosome levels decrease in rat brain at a developmental stage coincident with synapse formation. Next, we observe in vitro that different synaptogenic inducers trigger an overall decrease of ribosomal proteins and rRNA in the axons of spinal motor neurons. We further observe that this process is dependent on the ubiquitin-proteasome system but not on autophagy. Together, these data identify synaptogenesis as the long missing biological trigger that leads to ribosome disappearance during axonal maturation.pt
dc.language.isoengpt
dc.publisherElsevierpt
dc.relationThis work was funded by FEDER - Fundo Europeu de Desenvolvimento Regional, through COMPETE 2020 - Operational Programme for Competitiveness and Internationalisation and Portuguese national funds via FCT - Fundac¸ ~ao para a Ci^encia e a Tecnologia, under the projects PTDC/SAUNEU/ 104100/2008, EXPL/NEU-NMC/0541/2012, UID/BIM/04501/2013, UID/ NEU/04539/2019, POCI-01-0145-FEDER-007628, and CENTRO-01-0145- FEDER-000008:BrainHealth 2020, individual grants SFRH/BPD/84593/2012 (R.O.C.), PD/BD/114170/2016 (L.F.M.), SFRH/BPD/115546/2016 (M.M.), SFRH/BD/77789/2011 (J.R.P.), and SFRH/BD/139368/2018 (D.T.), and by Marie Curie Actions - IRG - 7th Research Framework Programme, and NIH grants R35NS111631 and NS056306 (S.R.J.).pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt
dc.subjectUPSpt
dc.subjectaxonal maturationpt
dc.subjectco-culturespt
dc.subjectneuromuscular junctionpt
dc.subjectpresynaptic differentiationpt
dc.subjectproteasomept
dc.subjectribosomal proteinspt
dc.subjectribosomept
dc.subjectsynapse formationpt
dc.subjectsynaptogenesispt
dc.subject.meshAnimalspt
dc.subject.meshAxonspt
dc.subject.meshCell Differentiationpt
dc.subject.meshFemalept
dc.subject.meshHEK293 Cellspt
dc.subject.meshHumanspt
dc.subject.meshMicept
dc.subject.meshNeuromuscular Junctionpt
dc.subject.meshPresynaptic Terminalspt
dc.subject.meshProteasome Endopeptidase Complexpt
dc.subject.meshRNA, Ribosomalpt
dc.subject.meshRats, Sprague-Dawleypt
dc.subject.meshRibosomespt
dc.subject.meshSynapsespt
dc.subject.meshUbiquitinpt
dc.subject.meshNeurogenesispt
dc.titleSynaptogenesis Stimulates a Proteasome-Mediated Ribosome Reduction in Axonspt
dc.typearticle-
degois.publication.firstPage864pt
degois.publication.lastPage876.e6pt
degois.publication.issue4pt
degois.publication.titleCell Reportspt
dc.peerreviewedyespt
dc.identifier.doi10.1016/j.celrep.2019.06.080pt
degois.publication.volume28pt
dc.date.embargo2019-07-23*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypearticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextCom Texto completo-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-2652-7500-
crisitem.author.orcid0000-0002-1084-7913-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
IIIUC - Artigos em Revistas Internacionais
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