GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.
Hoenen, T, Volchkov, V, Kolesnikova, L, Mittler, E, Timmins, J, Ottmann, M, Reynard, O, Becker, S and Weissenhorn, W (2005) VP40 octamers are essential for Ebola virus replication. J. Virol. 79:1898-905
Matrix protein VP40 of Ebola virus is essential for virus assembly and budding. Monomeric VP40 can oligomerize in vitro into RNA binding octamers, and the crystal structure of octameric VP40 has revealed that residues Phe125 and Arg134 are the most important residues for the coordination of a short single-stranded RNA. Here we show that full-length wild-type VP40 octamers bind RNA upon HEK 293 cell expression. While the Phe125-to-Ala mutation resulted in reduced RNA binding, the Arg134-to-Ala mutation completely abolished RNA binding and thus octamer formation. The absence of octamer formation, however, does not affect virus-like particle (VLP) formation, as the VLPs generated from the expression of wild-type VP40 and mutated VP40 in HEK 293 cells showed similar morphology and abundance and no significant difference in size. These results strongly indicate that octameric VP40 is dispensable for VLP formation. The cellular localization of mutant VP40 was different from that of wild-type VP40. While wild-type VP40 was present in small patches predominantly at the plasma membrane, the octamer-negative mutants were found in larger aggregates at the periphery of the cell and in the perinuclear region. We next introduced the Arg134-to-Ala and/or the Phe125-to-Ala mutation into the Ebola virus genome. Recombinant wild-type virus and virus expressing the VP40 Phe125-to-Ala mutation were both rescued. In contrast, no recombinant virus expressing the VP40 Arg134-to-Ala mutation could be recovered. These results suggest that RNA binding of VP40 and therefore octamer formation are essential for the Ebola virus life cycle.
Animals; Cell Line; Cercopithecus aethiops; Dimerization; Ebolavirus/genetics; Ebolavirus/metabolism; Ebolavirus/physiology; Gene Expression Regulation, Viral; Humans; Models, Molecular; Mutation; Protein Conformation; RNA, Viral/chemistry; RNA, Viral/metabolism; Vero Cells; Viral Matrix Proteins/chemistry; Viral Matrix Proteins/genetics; Viral Matrix Proteins/metabolism; Virion/metabolism; Virus Assembly; Virus Replication/physiology
|Gene product||Qualifier||GO Term||Evidence Code||with/from||Aspect||Extension||Notes||Status|
|GO:0020002: host cell plasma membrane||
Figure 4. Indirect immunofluroescence with anti-VP40 monoclonal antibody was used to localize VP40 in small patches in the plasma membrane.
See Help:References for how to manage references in GONUTS.