Conserved determinants of lentiviral genome dimerization
Date
Type of Work
Department
Program
Citation of Original Publication
Tran, 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.
Rights
Attribution 4.0 International
Subjects
Non-coding RNAs
Gel electrophoresis
Nucleocapsid protein (NC)
RNA structure
UMBC Howard Hughes Medical Institute
Non-homologous-end joining
SIVcpzUS
Labile dimer
SIVcpzTAN1
Retrovirus
RNA folding
HIV-1NL4-3
Long non-coding RNAs
Non-labile dimer
HIV-2ROD
Retroviral genome dimerization
UMBC Howard Hughes Medical Institute
2016 UMBC Phage Hunters
Ribozymes
Gel electrophoresis
Nucleocapsid protein (NC)
RNA structure
UMBC Howard Hughes Medical Institute
Non-homologous-end joining
SIVcpzUS
Labile dimer
SIVcpzTAN1
Retrovirus
RNA folding
HIV-1NL4-3
Long non-coding RNAs
Non-labile dimer
HIV-2ROD
Retroviral genome dimerization
UMBC Howard Hughes Medical Institute
2016 UMBC Phage Hunters
Ribozymes
Abstract
Retroviruses 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.
