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hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles
The influenza A virus polymerase associates with a number of cellular transcription-related factors, including the RNA polymerase II (RNAP II). We previously described that the cellular protein hCLE/C14orf166 interacts with and stimulates influenza virus polymerase as well as RNAP II activities. Her...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749964/ https://www.ncbi.nlm.nih.gov/pubmed/26864902 http://dx.doi.org/10.1038/srep20744 |
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author | Rodriguez-Frandsen, Ariel de Lucas, Susana Pérez-González, Alicia Pérez-Cidoncha, Maite Roldan-Gomendio, Alejandro Pazo, Alejandra Marcos-Villar, Laura Landeras-Bueno, Sara Ortín, Juan Nieto, Amelia |
author_facet | Rodriguez-Frandsen, Ariel de Lucas, Susana Pérez-González, Alicia Pérez-Cidoncha, Maite Roldan-Gomendio, Alejandro Pazo, Alejandra Marcos-Villar, Laura Landeras-Bueno, Sara Ortín, Juan Nieto, Amelia |
author_sort | Rodriguez-Frandsen, Ariel |
collection | PubMed |
description | The influenza A virus polymerase associates with a number of cellular transcription-related factors, including the RNA polymerase II (RNAP II). We previously described that the cellular protein hCLE/C14orf166 interacts with and stimulates influenza virus polymerase as well as RNAP II activities. Here we show that, despite the considerable cellular shut-off observed in infected cells, which includes RNAP II degradation, hCLE protein levels increase throughout infection in a virus replication-dependent manner. Human and avian influenza viruses of various subtypes increase hCLE levels, but other RNA or DNA viruses do not. hCLE colocalises and interacts with viral ribonucleoproteins (vRNP) in the nucleus, as well as in the cytoplasm late in infection. Furthermore, biochemical analysis of purified virus particles and immunoelectron microscopy of infected cells show hCLE in virions, in close association with viral vRNP. These findings indicate that hCLE, a cellular protein important for viral replication, is one of the very few examples of transcription factors that are incorporated into particles of an RNA-containing virus. |
format | Online Article Text |
id | pubmed-4749964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47499642016-02-17 hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles Rodriguez-Frandsen, Ariel de Lucas, Susana Pérez-González, Alicia Pérez-Cidoncha, Maite Roldan-Gomendio, Alejandro Pazo, Alejandra Marcos-Villar, Laura Landeras-Bueno, Sara Ortín, Juan Nieto, Amelia Sci Rep Article The influenza A virus polymerase associates with a number of cellular transcription-related factors, including the RNA polymerase II (RNAP II). We previously described that the cellular protein hCLE/C14orf166 interacts with and stimulates influenza virus polymerase as well as RNAP II activities. Here we show that, despite the considerable cellular shut-off observed in infected cells, which includes RNAP II degradation, hCLE protein levels increase throughout infection in a virus replication-dependent manner. Human and avian influenza viruses of various subtypes increase hCLE levels, but other RNA or DNA viruses do not. hCLE colocalises and interacts with viral ribonucleoproteins (vRNP) in the nucleus, as well as in the cytoplasm late in infection. Furthermore, biochemical analysis of purified virus particles and immunoelectron microscopy of infected cells show hCLE in virions, in close association with viral vRNP. These findings indicate that hCLE, a cellular protein important for viral replication, is one of the very few examples of transcription factors that are incorporated into particles of an RNA-containing virus. Nature Publishing Group 2016-02-11 /pmc/articles/PMC4749964/ /pubmed/26864902 http://dx.doi.org/10.1038/srep20744 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Rodriguez-Frandsen, Ariel de Lucas, Susana Pérez-González, Alicia Pérez-Cidoncha, Maite Roldan-Gomendio, Alejandro Pazo, Alejandra Marcos-Villar, Laura Landeras-Bueno, Sara Ortín, Juan Nieto, Amelia hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
title | hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
title_full | hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
title_fullStr | hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
title_full_unstemmed | hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
title_short | hCLE/C14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
title_sort | hcle/c14orf166, a cellular protein required for viral replication, is incorporated into influenza virus particles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749964/ https://www.ncbi.nlm.nih.gov/pubmed/26864902 http://dx.doi.org/10.1038/srep20744 |
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