The HTLV-1 oncoprotein Tax is modified by the ubiquitin related modifier 1 (Urm1)

dc.contributor.authorHleihel, Rita S.
dc.contributor.authorKhoshnood, Behzad
dc.contributor.authorDacklin, Ingrid
dc.contributor.authorOmran, Hayssam
dc.contributor.authorMouawad, Carine
dc.contributor.authorDassouki, Zeina
dc.contributor.authorEl-Sabban, Marwan E.
dc.contributor.authorShirinian, Margret
dc.contributor.authorGrabbe, Caroline
dc.contributor.departmentInternal Medicine
dc.contributor.departmentExperimental Pathology, Microbiology, and Immunology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:52:35Z
dc.date.available2025-01-24T11:52:35Z
dc.date.issued2018
dc.description.abstractBackground: Adult T-cell leukemia/lymphoma (ATL) is an aggressive malignancy secondary to chronic human T-cell lymphotropic virus 1 infection, triggered by the virally encoded oncoprotein Tax. The transforming activity and subcellular localization of Tax is strongly influenced by posttranslational modifications, among which ubiquitylation and SUMOylation have been identified as key regulators of the nuclear/cytoplasmic shuttling of Tax, as well as its ability to activate NF-ΚB signaling. Results: Adding to the complex posttranslational modification landscape of Tax, we here demonstrate that Tax also interacts with the ubiquitin-related modifier 1 (Urm1). Conjugation of Urm1 to Tax results in a redistribution of Tax to the cytoplasm and major increase in the transcription of the NF-κB targets Rantes and interleukin-6. Utilizing a tax-transgenic Drosophila model, we show that the Urm1-dependent subcellular targeting of Tax is evolutionary conserved, and that the presence of Urm1 is strongly correlated with the transcriptional output of Diptericin, an antimicrobial peptide and established downstream target of NF-ΚB in flies. Conclusions: These data put forward Urm1 as a novel Tax modifier that modulates its oncogenic activity and hence represents a potential novel target for developing new strategies for treating ATL. © 2018 The Author(s).
dc.identifier.doihttps://doi.org/10.1186/s12977-018-0415-4
dc.identifier.eid2-s2.0-85045527544
dc.identifier.pmid29665857
dc.identifier.urihttp://hdl.handle.net/10938/31066
dc.language.isoen
dc.publisherBioMed Central Ltd.
dc.relation.ispartofRetrovirology
dc.sourceScopus
dc.subjectAtl
dc.subjectHtlv-1
dc.subjectNf-κb
dc.subjectOncogenesis
dc.subjectTax
dc.subjectUrm1
dc.subjectAnimals
dc.subjectCell nucleus
dc.subjectCytoplasm
dc.subjectGene products, tax
dc.subjectHost-pathogen interactions
dc.subjectHtlv-i infections
dc.subjectHuman t-lymphotropic virus 1
dc.subjectHumans
dc.subjectI-kappa b kinase
dc.subjectLeukemia-lymphoma, adult t-cell
dc.subjectProtein processing, post-translational
dc.subjectProtein transport
dc.subjectSumoylation
dc.subjectTranscriptional activation
dc.subjectUbiquitins
dc.subjectImmunoglobulin enhancer binding protein
dc.subjectInterleukin 6
dc.subjectOncoprotein
dc.subjectPolypeptide antibiotic agent
dc.subjectRantes
dc.subjectTax protein
dc.subjectUbiquitin
dc.subjectUbiquitin related modifier 1
dc.subjectUnclassified drug
dc.subjectI kappa b kinase
dc.subjectUrm1 protein, human
dc.subjectArticle
dc.subjectCancer prognosis
dc.subjectControlled study
dc.subjectDownstream processing
dc.subjectDrosophila
dc.subjectHuman immunodeficiency virus 1
dc.subjectImmunoprecipitation
dc.subjectIn vitro study
dc.subjectIn vivo study
dc.subjectNonhuman
dc.subjectPathogenicity
dc.subjectProtein degradation
dc.subjectProtein localization
dc.subjectProtein modification
dc.subjectProtein phosphorylation
dc.subjectProtein processing
dc.subjectProtein protein interaction
dc.subjectT cell leukemia
dc.subjectUbiquitination
dc.subjectWestern blotting
dc.subjectAnimal
dc.subjectHost pathogen interaction
dc.subjectHtlv-1 infection
dc.subjectHuman
dc.subjectMetabolism
dc.subjectPhysiology
dc.subjectTranscription initiation
dc.subjectVirology
dc.titleThe HTLV-1 oncoprotein Tax is modified by the ubiquitin related modifier 1 (Urm1)
dc.typeArticle

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