Cargando…

Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1

The human immunodeficiency virus type 1 (HIV-1) unspliced, 9 kb genomic RNA (vRNA) is exported from the nucleus for the synthesis of viral structural proteins and enzymes (Gag and Gag/Pol) and is then transported to sites of virus assembly where it is packaged into progeny virions. vRNA co-exists in...

Descripción completa

Detalles Bibliográficos
Autores principales: Milev, Miroslav P., Ravichandran, Mukunthan, Khan, Morgan F., Schriemer, David C., Mouland, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486646/
https://www.ncbi.nlm.nih.gov/pubmed/23125841
http://dx.doi.org/10.3389/fmicb.2012.00367
_version_ 1782248383512051712
author Milev, Miroslav P.
Ravichandran, Mukunthan
Khan, Morgan F.
Schriemer, David C.
Mouland, Andrew J.
author_facet Milev, Miroslav P.
Ravichandran, Mukunthan
Khan, Morgan F.
Schriemer, David C.
Mouland, Andrew J.
author_sort Milev, Miroslav P.
collection PubMed
description The human immunodeficiency virus type 1 (HIV-1) unspliced, 9 kb genomic RNA (vRNA) is exported from the nucleus for the synthesis of viral structural proteins and enzymes (Gag and Gag/Pol) and is then transported to sites of virus assembly where it is packaged into progeny virions. vRNA co-exists in the cytoplasm in the context of the HIV-1 ribonucleoprotein (RNP) that is currently defined by the presence of Gag and several host proteins including the double-stranded RNA-binding protein, Staufen1. In this study we isolated Staufen1 RNP complexes derived from HIV-1-expressing cells using tandem affinity purification and have identified multiple host protein components by mass spectrometry. Four viral proteins, including Gag, Gag/Pol, Env and Nef as well as >200 host proteins were identified in these RNPs. Moreover, HIV-1 induces both qualitative and quantitative differences in host protein content in these RNPs. 22% of Staufen1-associated factors are virion-associated suggesting that the RNP could be a vehicle to achieve this. In addition, we provide evidence on how HIV-1 modulates the composition of cytoplasmic Staufen1 RNPs. Biochemical fractionation by density gradient analyses revealed new facets on the assembly of Staufen1 RNPs. The assembly of dense Staufen1 RNPs that contain Gag and several host proteins were found to be entirely RNA-dependent but their assembly appeared to be independent of Gag expression. Gag-containing complexes fractionated into a lighter and another, more dense pool. Lastly, Staufen1 depletion studies demonstrated that the previously characterized Staufen1 HIV-1-dependent RNPs are most likely aggregates of smaller RNPs that accumulate at juxtanuclear domains. The molecular characterization of Staufen1 HIV-1 RNPs will offer important information on virus-host cell interactions and on the elucidation of the function of these RNPs for the transport of Gag and the fate of the unspliced vRNA in HIV-1-producing cells.
format Online
Article
Text
id pubmed-3486646
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-34866462012-11-02 Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1 Milev, Miroslav P. Ravichandran, Mukunthan Khan, Morgan F. Schriemer, David C. Mouland, Andrew J. Front Microbiol Microbiology The human immunodeficiency virus type 1 (HIV-1) unspliced, 9 kb genomic RNA (vRNA) is exported from the nucleus for the synthesis of viral structural proteins and enzymes (Gag and Gag/Pol) and is then transported to sites of virus assembly where it is packaged into progeny virions. vRNA co-exists in the cytoplasm in the context of the HIV-1 ribonucleoprotein (RNP) that is currently defined by the presence of Gag and several host proteins including the double-stranded RNA-binding protein, Staufen1. In this study we isolated Staufen1 RNP complexes derived from HIV-1-expressing cells using tandem affinity purification and have identified multiple host protein components by mass spectrometry. Four viral proteins, including Gag, Gag/Pol, Env and Nef as well as >200 host proteins were identified in these RNPs. Moreover, HIV-1 induces both qualitative and quantitative differences in host protein content in these RNPs. 22% of Staufen1-associated factors are virion-associated suggesting that the RNP could be a vehicle to achieve this. In addition, we provide evidence on how HIV-1 modulates the composition of cytoplasmic Staufen1 RNPs. Biochemical fractionation by density gradient analyses revealed new facets on the assembly of Staufen1 RNPs. The assembly of dense Staufen1 RNPs that contain Gag and several host proteins were found to be entirely RNA-dependent but their assembly appeared to be independent of Gag expression. Gag-containing complexes fractionated into a lighter and another, more dense pool. Lastly, Staufen1 depletion studies demonstrated that the previously characterized Staufen1 HIV-1-dependent RNPs are most likely aggregates of smaller RNPs that accumulate at juxtanuclear domains. The molecular characterization of Staufen1 HIV-1 RNPs will offer important information on virus-host cell interactions and on the elucidation of the function of these RNPs for the transport of Gag and the fate of the unspliced vRNA in HIV-1-producing cells. Frontiers Media S.A. 2012-10-25 /pmc/articles/PMC3486646/ /pubmed/23125841 http://dx.doi.org/10.3389/fmicb.2012.00367 Text en Copyright © 2012 Milev, Ravichandran, Khan, Schriemer and Mouland. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Microbiology
Milev, Miroslav P.
Ravichandran, Mukunthan
Khan, Morgan F.
Schriemer, David C.
Mouland, Andrew J.
Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1
title Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1
title_full Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1
title_fullStr Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1
title_full_unstemmed Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1
title_short Characterization of Staufen1 Ribonucleoproteins by Mass Spectrometry and Biochemical Analyses Reveal the Presence of Diverse Host Proteins Associated with Human Immunodeficiency Virus Type 1
title_sort characterization of staufen1 ribonucleoproteins by mass spectrometry and biochemical analyses reveal the presence of diverse host proteins associated with human immunodeficiency virus type 1
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486646/
https://www.ncbi.nlm.nih.gov/pubmed/23125841
http://dx.doi.org/10.3389/fmicb.2012.00367
work_keys_str_mv AT milevmiroslavp characterizationofstaufen1ribonucleoproteinsbymassspectrometryandbiochemicalanalysesrevealthepresenceofdiversehostproteinsassociatedwithhumanimmunodeficiencyvirustype1
AT ravichandranmukunthan characterizationofstaufen1ribonucleoproteinsbymassspectrometryandbiochemicalanalysesrevealthepresenceofdiversehostproteinsassociatedwithhumanimmunodeficiencyvirustype1
AT khanmorganf characterizationofstaufen1ribonucleoproteinsbymassspectrometryandbiochemicalanalysesrevealthepresenceofdiversehostproteinsassociatedwithhumanimmunodeficiencyvirustype1
AT schriemerdavidc characterizationofstaufen1ribonucleoproteinsbymassspectrometryandbiochemicalanalysesrevealthepresenceofdiversehostproteinsassociatedwithhumanimmunodeficiencyvirustype1
AT moulandandrewj characterizationofstaufen1ribonucleoproteinsbymassspectrometryandbiochemicalanalysesrevealthepresenceofdiversehostproteinsassociatedwithhumanimmunodeficiencyvirustype1