eIF5A has a function in the elongation step of translation in yeast

dc.contributor.authorGregio, Ana P. B. [UNESP]
dc.contributor.authorCano, Veridiana P. S. [UNESP]
dc.contributor.authorAvaca, Juliana S. [UNESP]
dc.contributor.authorValentini, Sandro Roberto [UNESP]
dc.contributor.authorZanelli, Cleslei Fernando [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:24:15Z
dc.date.available2014-05-20T13:24:15Z
dc.date.issued2009-03-20
dc.description.abstractThe putative translation factor eIF5A is essential for cell viability and is highly conserved throughout evolution. Here, we describe genetic interactions between an eIF5A Mutant and a translation initiation mutant (eIF4E) or a translation elongation mutant (eEF2). Polysome profile analysis of single and double mutants revealed that mutation in eIF5A reduces polysome run-off, contrarily to translation initiation mutants. Moreover, the polysome profile of an eIF5A mutant alone is very similar to that of a translation elongation mutant. Furthermore, depletion of eIF5A causes a significant decrease in total protein synthesis and an increase of the average ribosome transit time. Finally, we, demonstrate that the formation of P bodies is inhibited in an eIF5A mutant, similarly to the effect of the translation elongation inhibitor cycloheximide. taken together, these results not only reinforce a role for eIF5A in translation but also strongly support a function for eIF5A in the elongation step of protein synthesis. (C) 2009 Elsevier B.V. All rights reserved.en
dc.description.affiliationSão Paulo State Univ, Dept Biol Sci, Sch Pharmaceut Sci, UNESP,Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Dept Biol Sci, Sch Pharmaceut Sci, UNESP,Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent785-790
dc.identifierhttp://dx.doi.org/10.1016/j.bbrc.2009.01.148
dc.identifier.citationBiochemical and Biophysical Research Communications. San Diego: Academic Press Inc. Elsevier B.V., v. 380, n. 4, p. 785-790, 2009.
dc.identifier.doi10.1016/j.bbrc.2009.01.148
dc.identifier.issn0006-291X
dc.identifier.lattes5333250355049814
dc.identifier.lattes1525665408900195
dc.identifier.orcid0000-0001-7831-1149
dc.identifier.urihttp://hdl.handle.net/11449/7475
dc.identifier.wosWOS:000264271100013
dc.language.isoeng
dc.publisherAcademic Press Inc. Elsevier B.V.
dc.relation.ispartofBiochemical and Biophysical Research Communications
dc.relation.ispartofjcr2.559
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjecteIF5Aen
dc.subjectTranslation elongationen
dc.subjecteEF2en
dc.subjectRibosome transit timeen
dc.subjectEF-Pen
dc.subjectHypusineen
dc.titleeIF5A has a function in the elongation step of translation in yeasten
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderAcademic Press Inc. Elsevier B.V.
unesp.author.lattes5333250355049814
unesp.author.lattes1525665408900195[5]
unesp.author.orcid0000-0001-7831-1149[5]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt

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