Literature DB >> 17148142

'Genome gating'; polarized intranuclear trafficking of influenza virus RNPs.

Debra Elton1, Maria Joao Amorim, Liz Medcalf, Paul Digard.   

Abstract

Many viruses exploit cellular polarity to constrain the assembly and release of progeny virions to a desired surface. Influenza virus particles are released only from the apical surface of epithelial cells and this polarization is partly owing to specific targeting of the viral membrane proteins to the apical plasma membrane. The RNA genome of the virus is transcribed and replicated in the nucleus, necessitating nuclear export of the individual ribonucleoprotein (RNP) segments before they can be incorporated into budding virus particles. We show that the process of polarized virus assembly begins in the nucleus with the RNPs adopting a novel asymmetric distribution at the inner nuclear membrane prior to their export to the cytoplasm. The viral nucleoprotein, the major protein component of RNPs, displays the same polarized intranuclear distribution in the absence of other influenza virus components, suggesting the existence of a hitherto unrecognized polarity within the mammalian cell nucleus.

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Year:  2005        PMID: 17148142      PMCID: PMC1626216          DOI: 10.1098/rsbl.2004.0253

Source DB:  PubMed          Journal:  Biol Lett        ISSN: 1744-9561            Impact factor:   3.703


  16 in total

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Journal:  Dev Cell       Date:  2003-06       Impact factor: 12.270

Review 6.  Transport of viral proteins to the apical membranes and interaction of matrix protein with glycoproteins in the assembly of influenza viruses.

Authors:  S Barman; A Ali; E K Hui; L Adhikary; D P Nayak
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  18 in total

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Review 4.  Deciphering the Structure and Function of Nuclear Pores Using Single-Molecule Fluorescence Approaches.

Authors:  Siegfried M Musser; David Grünwald
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5.  Studies of an influenza A virus temperature-sensitive mutant identify a late role for NP in the formation of infectious virions.

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6.  Host- and strain-specific regulation of influenza virus polymerase activity by interacting cellular proteins.

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7.  Influenza virus ribonucleoprotein complexes gain preferential access to cellular export machinery through chromatin targeting.

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Review 8.  Influenza virus morphogenesis and budding.

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9.  Identification of the domains of the influenza A virus M1 matrix protein required for NP binding, oligomerization and incorporation into virions.

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10.  Colocalization of different influenza viral RNA segments in the cytoplasm before viral budding as shown by single-molecule sensitivity FISH analysis.

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Journal:  PLoS Pathog       Date:  2013-05-09       Impact factor: 6.823

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