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Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane

The HIV-1 entry-route is a matter of ongoing controversy, and there is evidence for fusion either at the cell surface or from within endosomes. A recent report demonstrated that isoform 4 of nuclear receptor coactivator 7 (NCOA7(iso4)) interacts with endolysosomal vacuolar-type H(+)-ATPase (V-ATPase...

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Autor principal: Herold, Nikolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410169/
https://www.ncbi.nlm.nih.gov/pubmed/30700004
http://dx.doi.org/10.3390/v11020121
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author Herold, Nikolas
author_facet Herold, Nikolas
author_sort Herold, Nikolas
collection PubMed
description The HIV-1 entry-route is a matter of ongoing controversy, and there is evidence for fusion either at the cell surface or from within endosomes. A recent report demonstrated that isoform 4 of nuclear receptor coactivator 7 (NCOA7(iso4)) interacts with endolysosomal vacuolar-type H(+)-ATPase (V-ATPase), increasing lytic activity and thereby severely affecting the entry of vesicular stomatitis virus glycoprotein (VSV-G)-mediated, but not HIV-Env-mediated, entry and infection. As basal expression of NCOA7(iso4) is low in the absence of type-1 interferons, its overexpression is a novel tool to study viral entry.
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spelling pubmed-64101692019-04-01 Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane Herold, Nikolas Viruses Commentary The HIV-1 entry-route is a matter of ongoing controversy, and there is evidence for fusion either at the cell surface or from within endosomes. A recent report demonstrated that isoform 4 of nuclear receptor coactivator 7 (NCOA7(iso4)) interacts with endolysosomal vacuolar-type H(+)-ATPase (V-ATPase), increasing lytic activity and thereby severely affecting the entry of vesicular stomatitis virus glycoprotein (VSV-G)-mediated, but not HIV-Env-mediated, entry and infection. As basal expression of NCOA7(iso4) is low in the absence of type-1 interferons, its overexpression is a novel tool to study viral entry. MDPI 2019-01-29 /pmc/articles/PMC6410169/ /pubmed/30700004 http://dx.doi.org/10.3390/v11020121 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Commentary
Herold, Nikolas
Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane
title Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane
title_full Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane
title_fullStr Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane
title_full_unstemmed Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane
title_short Overexpression of the Interferon-Inducible Isoform 4 of NCOA7 Dissects the Entry Route of Enveloped Viruses and Demonstrates that HIV Enters Cells via Fusion at the Plasma Membrane
title_sort overexpression of the interferon-inducible isoform 4 of ncoa7 dissects the entry route of enveloped viruses and demonstrates that hiv enters cells via fusion at the plasma membrane
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410169/
https://www.ncbi.nlm.nih.gov/pubmed/30700004
http://dx.doi.org/10.3390/v11020121
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