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Approaching the cellular mechanism that supports the intercellular spread of Tobacco mosaic virus
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 98712
Author(s) Sambade, Adrian; Heinlein, Manfred
Author(s) at UniBasel Heinlein, Manfred
Year 2009
Title Approaching the cellular mechanism that supports the intercellular spread of Tobacco mosaic virus
Journal Plant Signaling & Behavior
Volume 4
Number 1
Pages / Article-Number 35-8
Keywords Tobacco mosaic virus, movement protein, RNA transport, plasmodesmata, microtubules, endoplasmic reticulum
Abstract Plant viruses spread cell-to-cell in infected plants by exploiting plasmodesmata (PD), gatable channels in the cell wall that provide cytoplasmic passageways for the trafficking of informational macromolecules. Since it became known that the intercellular spread of Tobacco mosaic virus (TMV) depends on virus-encoded movement protein (MP), the mechanism by which this protein mediates in the targeting of this virus to PD is subject to intense studies. TMV movement occurs in a non-encapsidated form and thus promises to reveal important host functions involved in the intra-and intercellular trafficking of RNA molecules. We have recently presented new evidence that the cell-to-cell trafficking of TMV RNA (vRNA) involves the formation and intracellular trafficking of distinct MP particles. Upon assembly, these particles detach from cortical microtubule (MT) sites and then move with the flow of ER through the cell. During passage the particles continue to undergo transient interactions with MT which may guide the particles to their destination. The comprehensive analysis of particle composition may lead to important insights into the regulation of RNA transport in plants and may also reveal potential similarities to RNA transport mechanisms in animals and humans.
Publisher Taylor & Francis
ISSN/ISBN 1559-2316 ; 1559-2324
edoc-URL http://edoc.unibas.ch/45443/
Full Text on edoc No
Digital Object Identifier DOI 10.4161/psb.4.1.7253
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/19704702
ISI-Number BCI:BCI201700612263
Document type (ISI) Comment, Journal Article
 
   

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25/04/2024