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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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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 |
format | Online Article Text |
id | pubmed-4337731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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