Literature DB >> 20696450

Analysis of the function of cytoplasmic fibers formed by the rubella virus nonstructural replicase proteins.

Jason D Matthews1, Wen-Pin Tzeng, Teryl K Frey.   

Abstract

The P150 and P90 replicase proteins of rubella virus (RUBV), a plus-strand RNA Togavirus, produce a unique cytoplasmic fiber network resembling microtubules. Pharmacological and mutagenic approaches were used to determine if these fibers functioned in virus replication. The pharmacological approach revealed that microtubules were required for fiber formation, but neither was necessary for virus replication. Through the mutagenic approach it was found that α-helices near both termini of P150 were necessary for fiber assembly and infectivity, but fiber formation and viability could not be correlated because most of these mutations were lethal. The N-terminal α-helix of P150 affected both proteolytic processing of P150 and P90 from the P200 precursor and targeting of P200, possibly through directing conformational folding of P200. Finally, we made the unexpected discovery that RUBV genomes can spread from cell-to-cell without virus particles, a process that we hypothesize utilizes RUBV-induced cytoplasmic projections containing fibers and replication complexes.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20696450      PMCID: PMC2939240          DOI: 10.1016/j.virol.2010.07.025

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  40 in total

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Journal:  J Virol       Date:  2009-01-28       Impact factor: 5.103

3.  Determinants of subcellular localization of the rubella virus nonstructural replicase proteins.

Authors:  Jason D Matthews; Wen-Pin Tzeng; Teryl K Frey
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5.  Analysis of subcellular G3BP redistribution during rubella virus infection.

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6.  Involvement of p32 and microtubules in alteration of mitochondrial functions by rubella virus.

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7.  Determinants in the maturation of rubella virus p200 replicase polyprotein precursor.

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8.  Specific, sensitive, high-resolution detection of protein molecules in eukaryotic cells using metal-tagging transmission electron microscopy.

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