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AbstractThe 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.
Cytoplasm, Article, Madin Darby Canine Kidney Cells, Viral Proteins, Dogs, Influenza A Virus, H1N1 Subtype, Influenza A Virus, H9N2 Subtype, Animals, Humans, Microscopy, Immunoelectron, Cell Nucleus, Influenza A Virus, H3N2 Subtype, Virion, HEK293 Cells, Gene Expression Regulation, Ribonucleoproteins, A549 Cells, Host-Pathogen Interactions, Proteolysis, Trans-Activators, RNA polymerase II, RNA Polymerase II
Cytoplasm, Article, Madin Darby Canine Kidney Cells, Viral Proteins, Dogs, Influenza A Virus, H1N1 Subtype, Influenza A Virus, H9N2 Subtype, Animals, Humans, Microscopy, Immunoelectron, Cell Nucleus, Influenza A Virus, H3N2 Subtype, Virion, HEK293 Cells, Gene Expression Regulation, Ribonucleoproteins, A549 Cells, Host-Pathogen Interactions, Proteolysis, Trans-Activators, RNA polymerase II, RNA Polymerase II
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