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Open AccessJournal ArticleDOI

Association of the Influenza A Virus RNA-Dependent RNA Polymerase with Cellular RNA Polymerase II

Othmar G. Engelhardt, +2 more
- 01 May 2005 - 
- Vol. 79, Iss: 9, pp 5812-5818
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TLDR
It is demonstrated for the first time that the influenza virus RNA polymerase complex interacts with the large subunit of Pol II via its C-terminal domain, indicating that it targets actively transcribing Pol II.
Abstract
Transcription by the influenza virus RNA-dependent RNA polymerase is dependent on cellular RNA processing activities that are known to be associated with cellular RNA polymerase II (Pol II) transcription, namely, capping and splicing. Therefore, it had been hypothesized that transcription by the viral RNA polymerase and Pol II might be functionally linked. Here, we demonstrate for the first time that the influenza virus RNA polymerase complex interacts with the large subunit of Pol II via its C-terminal domain. The viral polymerase binds hyperphosphorylated forms of Pol II, indicating that it targets actively transcribing Pol II. In addition, immunofluorescence analysis is consistent with a new model showing that influenza virus polymerase accumulates at Pol II transcription sites. The present findings provide a framework for further studies to elucidate the mechanistic principles of transcription by a viral RNA polymerase and have implications for the regulation of Pol II activities in infected cells.

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Citations
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Interferon-induced Mx proteins in antiviral host defense.

TL;DR: In general, Mx GTPases appear to detect viral infection by sensing nucleocapsid-like structures and are trapped and sorted to locations where they become unavailable for the generation of new virus particles.
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At the centre: influenza A virus ribonucleoproteins

TL;DR: This Review discusses current knowledge about vRNP trafficking within host cells and the function of these complexes in the context of the virus life cycle, highlighting how structure contributes to function and the crucial interactions with host cell pathways, as well as on the information gaps that remain.
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Influenza virus RNA polymerase: insights into the mechanisms of viral RNA synthesis.

TL;DR: Current knowledge of the structure of the influenza virus RNA polymerase is discussed, and insights that have been gained into the molecular mechanisms of viral transcription and replication, and their regulation by viral and host factors are discussed.
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Host and viral determinants of influenza A virus species specificity.

TL;DR: The host barriers that influenza A viruses of animals, especially birds, must overcome to initiate a pandemic in humans are examined and how, on crossing the species barrier, the virus mutates to establish new interactions with the human host is described.
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Influenza A Virus Cell Entry, Replication, Virion Assembly and Movement.

TL;DR: The aim of this review is to present the current mechanistic understanding for how IAVs facilitate cell entry, replication, virion assembly, and intercellular movement, in an effort to highlight some of the unanswered questions regarding the coordination of the IAV infection process.
References
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Journal ArticleDOI

The tandem affinity purification (TAP) method: a general procedure of protein complex purification.

TL;DR: The TAP method is developed as a tool that allows rapid purification under native conditions of complexes, even when expressed at their natural level, and is a very useful procedure for protein purification and proteome exploration.
Journal ArticleDOI

Integrating mRNA Processing with Transcription

TL;DR: The phosphorylated CTD of RNA polymerase II provides key molecular contacts with these mRNA processing reactions throughout transcriptional elongation and termination.
Journal ArticleDOI

Influenza Virus NS1 Protein Interacts with the Cellular 30 kDa Subunit of CPSF and Inhibits 3′ End Formation of Cellular Pre-mRNAs

TL;DR: It is demonstrated that the NS1 effector domain functionally interacts with the cellular 30 kDa subunit of CPSF, an essential component of the 3' end processing machinery of cellular pre-mRNAs.
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