Influenza A virus polymerase co-opts distinct sets of host proteins for RNA transcription or replication

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Authors: Amalie B. Rasmussen, Olivia C. Swann, Jonathan C. Brown, Ksenia Sukhova, Nancy Liu, M. Brown, Charles J.L. Levitt, Laura Martin-Sancho, Carol Sheppard, Wendy S. Barclay
Cited by: 2
References: 68

Abstract

The influenza A virus polymerase, consisting of a heterotrimer of three viral proteins, carries out both transcription and replication of the viral RNA genome. These distinct activities are regulated by viral proteins and various co-opted host cell proteins, which serve as targets for the development of novel antiviral interventions. However, little is known about which host proteins direct transcription versus replication. In this report, we performed a differential interactome screen to identify host proteins co-opted downstream or upstream of primary transcription, some of which may be transcription- or replication-specific factors. We found that distinct sets of host proteins interact with the influenza polymerase as it carries out the different activities. We functionally characterized HMGB2 and RUVBL2 as replication cofactors and RPAP2 as a transcription cofactor. Our data demonstrate that comparative proteomics can be used as a targeted approach to uncover virus-host interactions that regulate specific stages of the viral life cycle.

Fields of Study & Subjects

Influenza Virus Research Studies interferon and immune responses Infectious Encephalopathies and Encephalitis

Publication details

Journal / source
Cell chemical biology
Publisher
Elsevier BV
Volume
33
Issue
3
Pages
338–352.e7
Publication date
1 March 2026
Language
EN