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Development and RNA-synthesizing activity of coronavirus replication structures in the absence of protein synthesis.

Identifieur interne : 002130 ( Main/Exploration ); précédent : 002129; suivant : 002131

Development and RNA-synthesizing activity of coronavirus replication structures in the absence of protein synthesis.

Auteurs : Sjoerd H E. Van Den Worm [Pays-Bas] ; Kèvin Knoops ; Jessika C. Zevenhoven-Dobbe ; Corrine Beugeling ; Yvonne Van Der Meer ; A Mieke Mommaas ; Eric J. Snijder

Source :

RBID : pubmed:21430047

Descripteurs français

English descriptors

Abstract

The RNA replication and transcription complex of coronaviruses is associated with an elaborate reticulovesicular network (RVN) of modified endoplasmic reticulum. Using cycloheximide and puromycin, we have studied the effect of translation inhibition on the RNA synthesis of severe acute respiratory syndrome coronavirus and mouse hepatitis virus. Both inhibitors prevented the usual exponential increase in viral RNA synthesis, with immunofluorescence and electron microscopy indicating that RVN development came to a standstill. Nevertheless, limited RNA synthesis was supported, implying that continued translation is not an absolute requirement and suggesting a direct link between RVN formation and accumulation of coronavirus proteins.

DOI: 10.1128/JVI.00403-11
PubMed: 21430047


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Zevenhoven Dobbe, Jessika C" sort="Zevenhoven Dobbe, Jessika C" uniqKey="Zevenhoven Dobbe J" first="Jessika C" last="Zevenhoven-Dobbe">Jessika C. Zevenhoven-Dobbe</name>
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<name sortKey="Van Der Meer, Yvonne" sort="Van Der Meer, Yvonne" uniqKey="Van Der Meer Y" first="Yvonne" last="Van Der Meer">Yvonne Van Der Meer</name>
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<term>Microscopy, Fluorescence</term>
<term>Murine hepatitis virus (physiology)</term>
<term>Protein Biosynthesis (drug effects)</term>
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<term>RNA, Viral (biosynthesis)</term>
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<front>
<div type="abstract" xml:lang="en">The RNA replication and transcription complex of coronaviruses is associated with an elaborate reticulovesicular network (RVN) of modified endoplasmic reticulum. Using cycloheximide and puromycin, we have studied the effect of translation inhibition on the RNA synthesis of severe acute respiratory syndrome coronavirus and mouse hepatitis virus. Both inhibitors prevented the usual exponential increase in viral RNA synthesis, with immunofluorescence and electron microscopy indicating that RVN development came to a standstill. Nevertheless, limited RNA synthesis was supported, implying that continued translation is not an absolute requirement and suggesting a direct link between RVN formation and accumulation of coronavirus proteins.</div>
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