Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/42782

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Campo DCValorIdioma
dc.contributor.authorCarvalho, Andreia Alexandra Nevespor
dc.contributor.authorLogarinho, Elsapor
dc.contributor.authorFreitas, Anapor
dc.contributor.authorSilva, Sara Duartepor
dc.contributor.authorCosta, Maria do Carmopor
dc.contributor.authorFernandes, Anabela Silvapor
dc.contributor.authorMartins, Margarida Isabel Barros Coelhopor
dc.contributor.authorSerra, Sofia Cravinopor
dc.contributor.authorLopes, André Teixeirapor
dc.contributor.authorPaulson, Henry L.por
dc.contributor.authorHeutink, Peterpor
dc.contributor.authorRelvas, João B.por
dc.contributor.authorMaciel, P.por
dc.date.accessioned2016-10-13T13:45:19Z-
dc.date.available2016-10-13T13:45:19Z-
dc.date.issued2015-
dc.identifier.issn0964-6906por
dc.identifier.urihttps://hdl.handle.net/1822/42782-
dc.description.abstractThe physiological function of Ataxin-3 (ATXN3), a deubiquitylase (DUB) involved in Machado–Joseph Disease (MJD), remains elusive. In this study, we demonstrate that ATXN3 is required for neuronal differentiation and for normal cell morphology, cytoskeletal organization, proliferation and survival of SH-SY5Y and PC12 cells. This cellular phenotype is associated with increased proteasomal degradation of a5 integrin subunit (ITGA5) and reduced activation of integrin signalling and is rescued by ITGA5 overexpression. Interestingly, silencing of ATXN3, overexpression of mutant versions of ATXN3 lacking catalytic activity or bearing an expanded polyglutamine (polyQ) tract led to partially overlapping phenotypes. In vivo analysis showed that both Atxn3 knockout and MJD transgenic mice had decreased levels of ITGA5 in the brain. Furthermore, abnormal morphology and reduced branching were observed both in cultured neurons expressing shRNA for ATXN3 and in those obtained from MJD mice. Our results show that ATXN3 rescues ITGA5 from proteasomal degradation in neurons and that polyQ expansion causes a partial loss of this cellular function, resulting in reduced integrin signalling and neuronal cytoskeleton modifications, which may be contributing to neurodegeneration.por
dc.description.sponsorshipFundação para a Ciência e a Tecnologia (FCT) and COMPETE through the project ‘(PTDC/SAU-GMG/ 101572/2008)por
dc.description.sponsorshipNational Institutes of Health (NIH) ‘(R01NS038712)por
dc.description.sponsorshipFundação para a Ciência e a Tecnologia (FCT) - fellowships SFRH/BD/51059/2010, SFRH/BD/ 78388/2011 and SFRH/BPD/91562/2012por
dc.language.isoengpor
dc.publisherOxford University Presspor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/101572/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F51059%2F2010/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F91562%2F2012/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F78388%2F2011/PTpor
dc.rightsopenAccesspor
dc.titleDominant negative effect of polyglutamine expansion perturbs normal function of ataxin-3 in neuronal cellspor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://oxfordjournals.org/por
sdum.publicationstatusinfo:eu-repo/semantics/publishedVersionpor
oaire.citationStartPage100por
oaire.citationEndPage117por
oaire.citationIssue1por
oaire.citationTitleHuman Molecular Geneticspor
oaire.citationVolume24por
dc.date.updated2016-10-13T10:59:44Z-
dc.identifier.doi10.1093/hmg/ddu422por
dc.identifier.pmid25143392por
dc.subject.wosScience & Technologypor
sdum.journalHuman Molecular Geneticspor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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