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dc.contributor.authorByk, Laura A.-
dc.contributor.authorIglesias, Nestor G.-
dc.contributor.authorDe Maio, Federico Andrés-
dc.contributor.authorGebhard, Leopoldo G.-
dc.contributor.authorRossi, Mario.-
dc.contributor.authorGamarnik, Andrea V.-
dc.date.accessioned2019-07-30T12:28:30Z-
dc.date.available2019-07-30T12:28:30Z-
dc.date.issued2016-06-
dc.identifier.citationByk, Laura A., Iglesias, Nestor G., de Maio, Federico A., Gebhard, Leopoldo G., Rossi, Mario., et al. (2016). Dengue Virus Genome Uncoating Requires Ubiquitination. American Society for Microbiology; mBio; 7; 3; pp. 1-10es_ES
dc.identifier.issn2150-7511es_ES
dc.identifier.urihttp://mbio.asm.org/content/7/3/e00804-16.long-
dc.identifier.urihttp://hdl.handle.net/11336/25157-
dc.identifier.urihttps://rid.unrn.edu.ar/jspui/handle/20.500.12049/2631-
dc.format.extentp. 1-10es_ES
dc.format.mediumimpresoes_ES
dc.format.mediumdigitales_ES
dc.language.isoenes_ES
dc.titleDengue Virus Genome Uncoating Requires Ubiquitinationes_ES
dc.typeArticuloes_ES
dc.rights.licensehttps://creativecommons.org/licenses/by-nc-sa/4.0/es_ES
dc.description.filiationFil: Byk, Laura A. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario; Argentinaes_ES
dc.description.filiationFil: Byk, Laura A. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir; Argentinaes_ES
dc.description.filiationFil: Iglesias, Nestor G. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario; Argentinaes_ES
dc.description.filiationFil: Iglesias, Nestor G. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentinaes_ES
dc.description.filiationFil: de Maio, Federico A. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario; Argentinaes_ES
dc.description.filiationFil: de Maio, Federico A. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentinaes_ES
dc.description.filiationFil: Gebhard, Leopoldo G. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario; Argentinaes_ES
dc.description.filiationFil: Gebhard, Leopoldo G. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentinaes_ES
dc.description.filiationFil: Rossi, Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario; Argentinaes_ES
dc.description.filiationFil: Rossi, Mario. Instituto de Investigación en Biomedicina de Buenos Aires - Instituto Partner de la Sociedad Max Planck; Argentinaes_ES
dc.description.filiationFil: Gamarnik, Andrea V. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario; Argentinaes_ES
dc.description.filiationFil: Gamarnik, Andrea V. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentinaes_ES
dc.subject.keywordDengue Viruses_ES
dc.subject.keywordNucleocapside Uncoatimges_ES
dc.subject.keywordUbiquitinationes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.materiaCiencias Biológicases_ES
dc.origin.lugarDesarrolloAmerican Society for Microbiologyes_ES
dc.relation.journalissue7es_ES
dc.description.reviewsies_ES
dc.description.resumenThe process of genome release or uncoating after viral entry is one of the least-studied steps in the flavivirus life cycle. Flaviviruses are mainly arthropod-borne viruses, including emerging and reemerging pathogens such as dengue, Zika, and West Nile viruses. Currently, dengue virus is one of the most significant human viral pathogens transmitted by mosquitoes and is responsible for about 390 million infections every year around the world. Here, we examined for the first time molecular aspects of dengue virus genome uncoating. We followed the fate of the capsid protein and RNA genome early during infection and found that capsid is degraded after viral internalization by the host ubiquitin-proteasome system. However, proteasome activity and capsid degradation were not necessary to free the genome for initial viral translation. Unexpectedly, genome uncoating was blocked by inhibiting ubiquitination. Using different assays to bypass entry and evaluate the first rounds of viral translation, a narrow window of time during infection that requires ubiquitination but not proteasome activity was identified. In this regard, ubiquitin E1-activating enzyme inhibition was sufficient to stabilize the incoming viral genome in the cytoplasm of infected cells, causing its retention in either endosomes or nucleocapsids. Our data support a model in which dengue virus genome uncoating requires a nondegradative ubiquitination step, providing new insights into this crucial but understudied viral process. IMPORTANCE: Dengue is the most significant arthropod-borne viral infection in humans. Although the number of cases increases every year, there are no approved therapeutics available for the treatment of dengue infection, and many basic aspects of the viral biology remain elusive. After entry, the viral membrane must fuse with the endosomal membrane to deliver the viral genome into the cytoplasm for translation and replication. A great deal of information has been obtained in the last decade regarding molecular aspects of the fusion step, but little is known about the events that follow this process, which leads to viral RNA release from the nucleocapsid. Here, we investigated the fate of nucleocapsid components (capsid protein and viral genome) during the infection process and found that capsid is degraded by the ubiquitin-proteasome system. However, in contrast to that observed for other RNA and DNA viruses, dengue virus capsid degradation was not responsible for genome uncoating. Interestingly, we found that dengue virus genome release requires a nondegradative ubiquitination step. These results provide the first insights into dengue virus uncoating and present new opportunities for antiviral intervention.es_ES
dc.identifier.doihttps://doi.org/10.1128/mBio.00804-16-
dc.relation.journalTitlemBioes_ES
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