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Structure and function of the influenza virus transcription and replication machinery

Accepted version
Peer-reviewed

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Authors

Fodor, Ervin 

Abstract

Transcription and replication of the influenza virus RNA genome is catalysed by the viral heterotrimeric RNA-dependent RNA polymerase in the context of viral ribonucleoprotein (vRNP) complexes. Atomic resolution structures of the viral RNA synthesis machinery have offered insights into the initiation mechanisms of viral transcription and genome replication, and the interaction of the viral RNA polymerase with host RNA polymerase II, which is required for the initiation of viral transcription. Replication of the viral RNA genome by the viral RNA polymerase depends on host ANP32A, and host-specific sequence differences in ANP32A underlie the poor activity of avian influenza virus polymerases in mammalian cells. A failure to faithfully copy the viral genome segments can lead to the production aberrant viral RNA products, such as defective interfering (DI) RNAs and mini viral RNAs (mvRNAs). Both aberrant RNA types have been implicated in innate immune responses against influenza virus infection. This chapter discusses recent insights into the structure-function relationship of the viral RNA polymerase and its role in determining host range and virulence.

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Keywords

Host-Pathogen Interactions, Humans, Influenza A virus, Influenza, Human, Nuclear Proteins, RNA, Viral, RNA-Binding Proteins, RNA-Dependent RNA Polymerase, Viral Transcription, Virus Replication

Journal Title

Cold Spring Harbor Perspectives in Medicine

Conference Name

Journal ISSN

2157-1422
2157-1422

Volume Title

10

Publisher

Cold Spring Harbor Laboratory Press

Rights

All rights reserved
Sponsorship
Wellcome Trust (206579/Z/17/Z)
Isaac Newton Trust (17.37 (r))
National Institutes of Health (NIH) (1R21AI147172-01)
E. Fodor is supported by UK Medical Research Council programme grant MR/R009945/1. A. te Velthuis is supported by joint Wellcome Trust and Royal Society grant 206579/Z/17/Z, Isaac Newton Trust grant 17.37(r), and the National Institutes of Health grant R21AI147172.