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Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), which causes COVID-19, utilizes angiotensin-converting enzyme 2 (ACE2) for entry into target cells. ACE2 has been proposed as an interferon-stimulated gene (ISG). Thus, interferon-induced variability in ACE2 expression levels could be imp...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386494/ https://www.ncbi.nlm.nih.gov/pubmed/32743577 http://dx.doi.org/10.1101/2020.07.19.210955 |
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author | Onabajo, Olusegun O. Banday, A. Rouf Yan, Wusheng Obajemu, Adeola Stanifer, Megan L. Santer, Deanna M. Florez-Vargas, Oscar Piontkivska, Helen Vargas, Joselin Kee, Carmon Tyrrell, D. Lorne J. Mendoza, Juan L. Boulant, Steeve Prokunina-Olsson, Ludmila |
author_facet | Onabajo, Olusegun O. Banday, A. Rouf Yan, Wusheng Obajemu, Adeola Stanifer, Megan L. Santer, Deanna M. Florez-Vargas, Oscar Piontkivska, Helen Vargas, Joselin Kee, Carmon Tyrrell, D. Lorne J. Mendoza, Juan L. Boulant, Steeve Prokunina-Olsson, Ludmila |
author_sort | Onabajo, Olusegun O. |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), which causes COVID-19, utilizes angiotensin-converting enzyme 2 (ACE2) for entry into target cells. ACE2 has been proposed as an interferon-stimulated gene (ISG). Thus, interferon-induced variability in ACE2 expression levels could be important for susceptibility to COVID-19 or its outcomes. Here, we report the discovery of a novel, primate-specific isoform of ACE2, which we designate as deltaACE2 (dACE2). We demonstrate that dACE2, but not ACE2, is an ISG. In vitro, dACE2, which lacks 356 N-terminal amino acids, was non-functional in binding the SARS-CoV-2 spike protein and as a carboxypeptidase. Our results reconcile current knowledge on ACE2 expression and suggest that the ISG-type induction of dACE2 in IFN-high conditions created by treatments, inflammatory tumor microenvironment, or viral co-infections is unlikely to affect the cellular entry of SARS-CoV-2 and promote infection. |
format | Online Article Text |
id | pubmed-7386494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-73864942020-07-31 Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 Onabajo, Olusegun O. Banday, A. Rouf Yan, Wusheng Obajemu, Adeola Stanifer, Megan L. Santer, Deanna M. Florez-Vargas, Oscar Piontkivska, Helen Vargas, Joselin Kee, Carmon Tyrrell, D. Lorne J. Mendoza, Juan L. Boulant, Steeve Prokunina-Olsson, Ludmila bioRxiv Article Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), which causes COVID-19, utilizes angiotensin-converting enzyme 2 (ACE2) for entry into target cells. ACE2 has been proposed as an interferon-stimulated gene (ISG). Thus, interferon-induced variability in ACE2 expression levels could be important for susceptibility to COVID-19 or its outcomes. Here, we report the discovery of a novel, primate-specific isoform of ACE2, which we designate as deltaACE2 (dACE2). We demonstrate that dACE2, but not ACE2, is an ISG. In vitro, dACE2, which lacks 356 N-terminal amino acids, was non-functional in binding the SARS-CoV-2 spike protein and as a carboxypeptidase. Our results reconcile current knowledge on ACE2 expression and suggest that the ISG-type induction of dACE2 in IFN-high conditions created by treatments, inflammatory tumor microenvironment, or viral co-infections is unlikely to affect the cellular entry of SARS-CoV-2 and promote infection. Cold Spring Harbor Laboratory 2020-07-20 /pmc/articles/PMC7386494/ /pubmed/32743577 http://dx.doi.org/10.1101/2020.07.19.210955 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Onabajo, Olusegun O. Banday, A. Rouf Yan, Wusheng Obajemu, Adeola Stanifer, Megan L. Santer, Deanna M. Florez-Vargas, Oscar Piontkivska, Helen Vargas, Joselin Kee, Carmon Tyrrell, D. Lorne J. Mendoza, Juan L. Boulant, Steeve Prokunina-Olsson, Ludmila Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 |
title | Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 |
title_full | Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 |
title_fullStr | Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 |
title_full_unstemmed | Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 |
title_short | Interferons and viruses induce a novel primate-specific isoform dACE2 and not the SARS-CoV-2 receptor ACE2 |
title_sort | interferons and viruses induce a novel primate-specific isoform dace2 and not the sars-cov-2 receptor ace2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7386494/ https://www.ncbi.nlm.nih.gov/pubmed/32743577 http://dx.doi.org/10.1101/2020.07.19.210955 |
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