Conserved determinants of lentiviral genome dimerization

dc.contributor.authorTran, Thao
dc.contributor.authorLiu, Yuanyuan
dc.contributor.authorMarchant, Jan
dc.contributor.authorMonti, Sarah Ann
dc.contributor.authorSeu, Michelle
dc.contributor.authorZaki, Jessica
dc.contributor.authorYang, Ae Lim
dc.contributor.authorBohn, Jennifer
dc.contributor.authorRamakrishnan, Venkateswaran
dc.contributor.authorSingh, Rashmi
dc.contributor.authorHernandez, Mateo
dc.contributor.authorVega, Alexander
dc.contributor.authorSummers, Michael
dc.date.accessioned2025-07-30T19:22:10Z
dc.date.issued2015-09-29
dc.description.abstractRetroviruses selectively package two copies of their unspliced genomes by what appears to be a dimerization-dependent RNA packaging mechanism. Dimerization of human immunodeficiency virus Type-1 (HIV-1) genomes is initiated by “kissing” interactions between GC-rich palindromic loop residues of a conserved hairpin (DIS), and is indirectly promoted by long-range base pairing between residues overlapping the gag start codon (AUG) and an upstream Unique 5' element (U5). The DIS and U5:AUG structures are phylogenetically conserved among divergent retroviruses, suggesting conserved functions. However, some studies suggest that the DIS of HIV-2 does not participate in dimerization, and that U5:AUG pairing inhibits, rather than promotes, genome dimerization. We prepared RNAs corresponding to native and mutant forms of the 5' leaders of HIV-1 (NL4-3 strain), HIV-2 (ROD strain), and two divergent strains of simian immunodeficiency virus (SIV; cpz-TAN1 and -US strains), and probed for potential roles of the DIS and U5:AUG base pairing on intrinsic and NC-dependent dimerization by mutagenesis, gel electrophoresis, and NMR spectroscopy.
dc.description.sponsorshipSupport from the National Institutes of Health (R01 GM42561) is gratefully acknowledged. R.S. was supported by a NIH NIGMS Grant for enhancing minority access to research careers (MARC U*STAR 2T34 GM008663). We thank the Howard Hughes Medical Institute staff at University of Maryland, Baltimore County for the technical assistance and Dr. Sarah Keane for reviewing the manuscript.
dc.description.urihttps://retrovirology.biomedcentral.com/articles/10.1186/s12977-015-0209-x
dc.format.extent16 pages
dc.genrejournal articles
dc.identifierdoi:10.13016/m26fqo-nnov
dc.identifier.citationTran, Thao, Yuanyuan Liu, Jan Marchant, et al. “Conserved Determinants of Lentiviral Genome Dimerization.” Retrovirology 12, no. 1 (2015): 83. https://doi.org/10.1186/s12977-015-0209-x.
dc.identifier.urihttps://doi.org/10.1186/s12977-015-0209-x
dc.identifier.urihttp://hdl.handle.net/11603/39502
dc.language.isoen_US
dc.publisherSpringer Nature
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Biological Sciences Department
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Chemistry & Biochemistry Department
dc.relation.ispartofUMBC Student Collection
dc.relation.ispartofThe Shriver Center at UMBC
dc.relation.ispartofUMBC Meyerhoff Scholars Program
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectNon-coding RNAs
dc.subjectGel electrophoresis
dc.subjectNucleocapsid protein (NC)
dc.subjectRNA structure
dc.subjectUMBC Howard Hughes Medical Institute
dc.subjectNon-homologous-end joining
dc.subjectSIVcpzUS
dc.subjectLabile dimer
dc.subjectSIVcpzTAN1
dc.subjectRetrovirus
dc.subjectRNA folding
dc.subjectHIV-1NL4-3
dc.subjectLong non-coding RNAs
dc.subjectNon-labile dimer
dc.subjectHIV-2ROD
dc.subjectRetroviral genome dimerization
dc.subjectUMBC Howard Hughes Medical Institute
dc.subject2016 UMBC Phage Hunters
dc.subjectRibozymes
dc.titleConserved determinants of lentiviral genome dimerization
dc.typeText
dcterms.creatorhttps://orcid.org/0000-0002-2418-6247
dcterms.creatorhttps://orcid.org/0000-0003-1045-6274
dcterms.creatorhttps://orcid.org/0000-0003-4267-4380

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