Novel Staufen1 ribonucleoproteins prevent formation of stress granules but favour encapsidation of HIV-1 genomic RNA

• Autores: Abrahamyan, L.G.; Chatel-Chaix, L.; Ajamian, L.; Milev, M.P.; Monette, A.; Clément, J.-F.; Song, R.; Lehmann, M.; DesGroseillers, L.; Laughrea, M.; Boccaccio, G.; Mouland, A.J.
• Año de publicación: 2010
• Idioma: inglés
• Tipo de recurso: artículo
• Fuente: J. Cell Sci. 2010;123(3):369-383
• Materia: AIDS; HIV-1; Intracellular traffic; Ribonucleoprotein; RNA encapsidation; SHRNP; sIRNA; Staufen1; Staufen1 HIV-1-dependent RNP; Virus-host interaction; Gag protein; genomic RNA; ribonucleoprotein; Staufen 1 ribonucleoprotein; unclassified drug; virus RNA; article; cell granule; cell level; cell stress; cellular distribution; controlled study; human; human cell; Human immunodeficiency virus 1; nonhuman; oxidative stress; polysome; priority journal; protein assembly; protein depletion; protein function; protein localization; virion; virus capsid; virus cell interaction; virus expression; Blotting, Western; Cell Line; Cytoplasmic Granules; Cytoskeletal Proteins; gag Gene Products, Human Immunodeficiency Virus; Hela Cells; Humans; Immunoprecipitation; In Situ Hybridization, Fluorescence; Models, Biological; Protein Binding; Reverse Transcriptase Polymerase Chain Reaction; Ribonucleoproteins; RNA, Viral; RNA-Binding Proteins; Virus Assembly; Human immunodeficiency virus 1
• Institución: Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales

Human immunodeficiency virus type 1 (HIV-1) Gag selects for and mediates genomic RNA (vRNA) encapsidation into progeny virus particles. The host protein, Staufen1 interacts directly with Gag and is found in ribonucleoprotein (RNP) complexes containing vRNA, which provides evidence that Staufen1 plays a role in vRNA selection and encapsidation. In this work, we show that Staufen1, vRNA and Gag are found in the same RNP complex. These cellular and viral factors also colocalize in cells and constitute novel Staufen1 RNPs (SHRNPs) whose assembly is strictly dependent on HIV-1 expression. SHRNPs are distinct from stress granules and processing bodies, are preferentially formed during oxidative stress and are found to be in equilibrium with translating polysomes. Moreover, SHRNPs are stable, and the association between Staufen1 and vRNA was found to be evident in these and other types of RNPs. We demonstrate that following Staufen1 depletion, apparent supraphysiologic-sized SHRNP foci are formed in the cytoplasm and in which Gag, vRNA and the residual Staufen1 accumulate. The depletion of Staufen1 resulted in reduced Gag levels and deregulated the assembly of newly synthesized virions, which were found to contain several-fold increases in vRNA, Staufen1 and other cellular proteins. This work provides new evidence that Staufen1-containing HIV-1 RNPs preferentially form over other cellular silencing foci and are involved in assembly, localization and encapsidation of vRNA.
Fil:Boccaccio, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.