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Angiomotin functions in HIV-1 assembly and budding

Many retroviral Gag proteins contain PPXY late assembly domain motifs that recruit proteins of the NEDD4 E3 ubiquitin ligase family to facilitate virus release. Overexpression of NEDD4L can also stimulate HIV-1 release but in this case the Gag protein lacks a PPXY motif, suggesting that NEDD4L may f...

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Autores principales: Mercenne, Gaelle, Alam, Steven L, Arii, Jun, Lalonde, Matthew S, Sundquist, Wesley I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337731/
https://www.ncbi.nlm.nih.gov/pubmed/25633977
http://dx.doi.org/10.7554/eLife.03778
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author Mercenne, Gaelle
Alam, Steven L
Arii, Jun
Lalonde, Matthew S
Sundquist, Wesley I
author_facet Mercenne, Gaelle
Alam, Steven L
Arii, Jun
Lalonde, Matthew S
Sundquist, Wesley I
author_sort Mercenne, Gaelle
collection PubMed
description Many retroviral Gag proteins contain PPXY late assembly domain motifs that recruit proteins of the NEDD4 E3 ubiquitin ligase family to facilitate virus release. Overexpression of NEDD4L can also stimulate HIV-1 release but in this case the Gag protein lacks a PPXY motif, suggesting that NEDD4L may function through an adaptor protein. Here, we demonstrate that the cellular protein Angiomotin (AMOT) can bind both NEDD4L and HIV-1 Gag. HIV-1 release and infectivity are stimulated by AMOT overexpression and inhibited by AMOT depletion, whereas AMOT mutants that cannot bind NEDD4L cannot function in virus release. Electron microscopic analyses revealed that in the absence of AMOT assembling Gag molecules fail to form a fully spherical enveloped particle. Our experiments indicate that AMOT and other motin family members function together with NEDD4L to help complete immature virion assembly prior to ESCRT-mediated virus budding. DOI: http://dx.doi.org/10.7554/eLife.03778.001
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spelling pubmed-43377312015-03-04 Angiomotin functions in HIV-1 assembly and budding Mercenne, Gaelle Alam, Steven L Arii, Jun Lalonde, Matthew S Sundquist, Wesley I eLife Biochemistry Many retroviral Gag proteins contain PPXY late assembly domain motifs that recruit proteins of the NEDD4 E3 ubiquitin ligase family to facilitate virus release. Overexpression of NEDD4L can also stimulate HIV-1 release but in this case the Gag protein lacks a PPXY motif, suggesting that NEDD4L may function through an adaptor protein. Here, we demonstrate that the cellular protein Angiomotin (AMOT) can bind both NEDD4L and HIV-1 Gag. HIV-1 release and infectivity are stimulated by AMOT overexpression and inhibited by AMOT depletion, whereas AMOT mutants that cannot bind NEDD4L cannot function in virus release. Electron microscopic analyses revealed that in the absence of AMOT assembling Gag molecules fail to form a fully spherical enveloped particle. Our experiments indicate that AMOT and other motin family members function together with NEDD4L to help complete immature virion assembly prior to ESCRT-mediated virus budding. DOI: http://dx.doi.org/10.7554/eLife.03778.001 eLife Sciences Publications, Ltd 2015-01-29 /pmc/articles/PMC4337731/ /pubmed/25633977 http://dx.doi.org/10.7554/eLife.03778 Text en © 2015, Mercenne et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biochemistry
Mercenne, Gaelle
Alam, Steven L
Arii, Jun
Lalonde, Matthew S
Sundquist, Wesley I
Angiomotin functions in HIV-1 assembly and budding
title Angiomotin functions in HIV-1 assembly and budding
title_full Angiomotin functions in HIV-1 assembly and budding
title_fullStr Angiomotin functions in HIV-1 assembly and budding
title_full_unstemmed Angiomotin functions in HIV-1 assembly and budding
title_short Angiomotin functions in HIV-1 assembly and budding
title_sort angiomotin functions in hiv-1 assembly and budding
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337731/
https://www.ncbi.nlm.nih.gov/pubmed/25633977
http://dx.doi.org/10.7554/eLife.03778
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