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Updated: Apr 6, 2026

Co-immunoprecipitation of the Mouse Mx1 Protein with the Influenza A Virus Nucleoprotein
Published on: April 21, 2015
The Cellular Factor NXP2/MORC3 Is a Positive Regulator of Influenza Virus Multiplication
Lorena S Ver1, Laura Marcos-Villar1, Sara Landeras-Bueno1
1Centro Nacional de Biotecnología (CSIC), Darwin 3, Madrid, Spain CIBER de Enfermedades Respiratorias, ISCIII, Madrid, Spain.
Unlabelled:
Transcription and replication of influenza A virus are carried out in the nuclei of infected cells in the context of viral ribonucleoproteins (RNPs). The viral polymerase responsible for these processes is a protein complex composed of the PB1, PB2, and PA proteins. We previously identified a set of polymerase-associated cellular proteins by proteomic analysis of polymerase-containing intracellular complexes expressed and purified from human cells. Here we characterize the role of NXP2/MORC3 in the infection cycle. NXP2/MORC3 is a member of the Microrchidia (MORC) family that is associated with the nuclear matrix and has RNA-binding activity. Influenza virus infection led to a slight increase in NXP2/MORC3 expression and its partial relocalization to the cytoplasm. Coimmunoprecipitation and immunofluorescence experiments indicated an association of NXP2/MORC3 with the viral polymerase and RNPs during infection. Downregulation of NXP2/MORC3 by use of two independent short hairpin RNAs (shRNAs) reduced virus titers in low-multiplicity infections. Consistent with these findings, analysis of virus-specific RNA in high-multiplicity infections indicated a reduction of viral RNA (vRNA) and mRNA after NXP2/MORC3 downregulation. Silencing of NXP2/MORC3 in a recombinant minireplicon system in which virus transcription and replication are uncoupled showed reductions in cat mRNA and chloramphenicol acetyltransferase (CAT) protein accumulation but no alterations in cat vRNA levels, suggesting that NXP2/MORC3 is important for influenza virus transcription.
Importance:
Influenza virus infections appear as yearly epidemics and occasional pandemics of respiratory disease, with high morbidity and occasional mortality. Influenza viruses are intracellular parasites that replicate and transcribe their genomic ribonucleoproteins in the nuclei of infected cells, in a complex interplay with host cell factors. Here we characterized the role of the human NXP2/MORC3 protein, a member of the Microrchidia family that is associated with the nuclear matrix, during virus infection. NXP2/MORC3 associates with the viral ribonucleoproteins in infected cells. Downregulation of NXP2/MORC3 reduced virus titers and accumulations of viral genomic RNA and mRNAs. Silencing of NXP2/MORC3 in an influenza virus CAT minireplicon system diminished CAT protein and cat mRNA levels but not genomic RNA levels. We propose that NXP2/MORC3 plays a role in influenza virus transcription.
Insights
The cellular protein NXP2/MORC3 associates with influenza A virus components, aiding viral transcription. Downregulating NXP2/MORC3 reduces viral RNA and protein production, highlighting its role in the virus life cycle.
Area of Science:
- Virology
- Molecular Biology
- Cell Biology
Background:
- Influenza A virus (IAV) replication and transcription occur in the host cell nucleus, involving viral ribonucleoproteins (RNPs) and a complex viral polymerase.
- Host cell factors play a critical role in the IAV life cycle, interacting with viral components.
- NXP2/MORC3, a nuclear matrix-associated protein with RNA-binding activity, belongs to the Microrchidia (MORC) family.
Purpose of the Study:
- To investigate the role of the host cell protein NXP2/MORC3 in the influenza A virus infection cycle.
- To determine the association of NXP2/MORC3 with viral components during infection.
- To assess the impact of NXP2/MORC3 on viral replication and transcription.
Main Methods:
- Proteomic analysis to identify polymerase-associated cellular proteins.
- Coimmunoprecipitation and immunofluorescence to confirm protein-protein interactions and localization.
- Short hairpin RNA (shRNA)-mediated knockdown to downregulate NXP2/MORC3 expression.
- Analysis of viral titers, viral RNA (vRNA), and mRNA levels.
- Use of a recombinant influenza virus CAT minireplicon system.
Main Results:
- Influenza virus infection caused a slight increase in NXP2/MORC3 expression and partial cytoplasmic relocalization.
- NXP2/MORC3 was found to associate with the viral polymerase and RNPs in infected cells.
- Downregulation of NXP2/MORC3 led to reduced virus titers and decreased accumulation of viral RNA and mRNA.
- In a minireplicon system, NXP2/MORC3 silencing reduced viral mRNA and protein but not vRNA levels.
Conclusions:
- NXP2/MORC3 is a host factor that associates with influenza A virus polymerase and RNPs.
- NXP2/MORC3 plays a significant role in influenza virus transcription.
- NXP2/MORC3 is important for efficient viral replication and production.
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