Publication:
HIV-1 Cis Enhancing Sequence (CES) enhances CTE-dependent Gag expression

dc.contributor.authorOrnpreya Suptawiwaten_US
dc.contributor.authorTun Hou Leeen_US
dc.contributor.authorPrasert Auewarakulen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherHarvard School of Public Healthen_US
dc.date.accessioned2018-06-21T08:14:49Z
dc.date.available2018-06-21T08:14:49Z
dc.date.issued2005-11-10en_US
dc.description.abstractIn order to export intron-containing RNA from nucleus, retroviruses use either viral trans-acting factors or constitutive cellular factors interacting with cis-elements in their intron-containing RNA. We have previously identified a Cis Enhancing Sequence (CES) in HIV-1 env region that could co-operate with Rev and RRE to enhance Gag expression by promoting RNA stabilization and exportation. In this study, we found that CES could function in a Rev-independent manner by co-operating with a Constitutive Transport Element (CTE) of Mason-Pfizer monkey viruses (MPMV). RRE and CTE promote intron-containing RNA exportation through different pathways. The fact that CES could function in both pathways of RNA export suggested that CES might function at a common step either up- or downstream to Rev/RRE or CTE functions. Known hnRNP-A1-binding sites as well as other 3 highly conserved sequences in the CES were found to be required for its activity. © 2005 Elsevier Inc. All rights reserved.en_US
dc.identifier.citationVirology. Vol.342, No.1 (2005), 111-118en_US
dc.identifier.doi10.1016/j.virol.2005.07.027en_US
dc.identifier.issn10960341en_US
dc.identifier.issn00426822en_US
dc.identifier.other2-s2.0-27444436229en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16539
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27444436229&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleHIV-1 Cis Enhancing Sequence (CES) enhances CTE-dependent Gag expressionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27444436229&origin=inwarden_US

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