Serveur d'exploration sur la rapamycine et les champignons

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Tombusvirus RNA replication depends on the TOR pathway in yeast and plants.

Identifieur interne : 000438 ( Main/Exploration ); précédent : 000437; suivant : 000439

Tombusvirus RNA replication depends on the TOR pathway in yeast and plants.

Auteurs : Jun-Ichi Inaba [États-Unis] ; Peter D. Nagy [États-Unis]

Source :

RBID : pubmed:29734044

Descripteurs français

English descriptors

Abstract

Similar to other (+)RNA viruses, tomato bushy stunt virus (TBSV) utilizes metabolites, lipids, membranes, and co-opted host factors during replication. The coordination of cell metabolism and growth with environmental cues is performed by the target of rapamycin (TOR) kinase in eukaryotic cells. In this paper, we find that TBSV replication partially inhibits TOR activity, likely due to recruitment of glycolytic enzymes to the viral replication compartment, which results in reduced ATP levels in the cytosol. Complete inhibition of TOR activity with rapamycin in yeast or AZD8055 inhibitor in plants reduces tombusvirus replication. We find that high glucose concentration, which stimulates TOR activity, enhanced tombusvirus replication in yeast. Depletion of yeast Sch9 or plant S6K1 kinase, a downstream effector of TOR, also inhibited tombusvirus replication in yeast and plant or the assembly of the viral replicase in vitro. Altogether, the TOR pathway is crucial for TBSV to replicate efficiently in hosts.

DOI: 10.1016/j.virol.2018.04.010
PubMed: 29734044


Affiliations:


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Le document en format XML

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<term>Glycolysis (MeSH)</term>
<term>Host-Pathogen Interactions (MeSH)</term>
<term>Mechanistic Target of Rapamycin Complex 1 (antagonists & inhibitors)</term>
<term>Mechanistic Target of Rapamycin Complex 1 (metabolism)</term>
<term>Morpholines (pharmacology)</term>
<term>RNA Replicase (metabolism)</term>
<term>RNA, Viral (biosynthesis)</term>
<term>Ribonucleotides (biosynthesis)</term>
<term>Saccharomyces cerevisiae (drug effects)</term>
<term>Saccharomyces cerevisiae (genetics)</term>
<term>Saccharomyces cerevisiae (metabolism)</term>
<term>Saccharomyces cerevisiae (virology)</term>
<term>Saccharomyces cerevisiae Proteins (antagonists & inhibitors)</term>
<term>Saccharomyces cerevisiae Proteins (metabolism)</term>
<term>Sirolimus (pharmacology)</term>
<term>Tobacco (drug effects)</term>
<term>Tobacco (metabolism)</term>
<term>Tobacco (virology)</term>
<term>Tombusvirus (genetics)</term>
<term>Tombusvirus (physiology)</term>
<term>Transcription Factors (antagonists & inhibitors)</term>
<term>Transcription Factors (metabolism)</term>
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<term>ARN viral (biosynthèse)</term>
<term>Adénosine triphosphate (métabolisme)</term>
<term>Complexe-1 cible mécanistique de la rapamycine (antagonistes et inhibiteurs)</term>
<term>Complexe-1 cible mécanistique de la rapamycine (métabolisme)</term>
<term>Facteurs de transcription (antagonistes et inhibiteurs)</term>
<term>Facteurs de transcription (métabolisme)</term>
<term>Glycolyse (MeSH)</term>
<term>Interactions hôte-pathogène (MeSH)</term>
<term>Morpholines (pharmacologie)</term>
<term>Protéines de Saccharomyces cerevisiae (antagonistes et inhibiteurs)</term>
<term>Protéines de Saccharomyces cerevisiae (métabolisme)</term>
<term>RNA replicase (métabolisme)</term>
<term>Ribonucléotides (biosynthèse)</term>
<term>Réplication virale (MeSH)</term>
<term>Saccharomyces cerevisiae (effets des médicaments et des substances chimiques)</term>
<term>Saccharomyces cerevisiae (génétique)</term>
<term>Saccharomyces cerevisiae (métabolisme)</term>
<term>Saccharomyces cerevisiae (virologie)</term>
<term>Sirolimus (pharmacologie)</term>
<term>Tabac (effets des médicaments et des substances chimiques)</term>
<term>Tabac (métabolisme)</term>
<term>Tabac (virologie)</term>
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<term>Tombusvirus (physiologie)</term>
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<term>Mechanistic Target of Rapamycin Complex 1</term>
<term>Saccharomyces cerevisiae Proteins</term>
<term>Transcription Factors</term>
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<term>Ribonucleotides</term>
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<term>Mechanistic Target of Rapamycin Complex 1</term>
<term>RNA Replicase</term>
<term>Saccharomyces cerevisiae Proteins</term>
<term>Transcription Factors</term>
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<term>Complexe-1 cible mécanistique de la rapamycine</term>
<term>Facteurs de transcription</term>
<term>Protéines de Saccharomyces cerevisiae</term>
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<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>ARN viral</term>
<term>Ribonucléotides</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
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<term>Tobacco</term>
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<term>Saccharomyces cerevisiae</term>
<term>Tabac</term>
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<term>Saccharomyces cerevisiae</term>
<term>Tombusvirus</term>
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<term>Saccharomyces cerevisiae</term>
<term>Tombusvirus</term>
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<term>Complexe-1 cible mécanistique de la rapamycine</term>
<term>Facteurs de transcription</term>
<term>Protéines de Saccharomyces cerevisiae</term>
<term>RNA replicase</term>
<term>Saccharomyces cerevisiae</term>
<term>Tabac</term>
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<term>Morpholines</term>
<term>Sirolimus</term>
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<term>Tombusvirus</term>
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<term>Virus Replication</term>
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<term>Interactions hôte-pathogène</term>
<term>Réplication virale</term>
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<div type="abstract" xml:lang="en">Similar to other (+)RNA viruses, tomato bushy stunt virus (TBSV) utilizes metabolites, lipids, membranes, and co-opted host factors during replication. The coordination of cell metabolism and growth with environmental cues is performed by the target of rapamycin (TOR) kinase in eukaryotic cells. In this paper, we find that TBSV replication partially inhibits TOR activity, likely due to recruitment of glycolytic enzymes to the viral replication compartment, which results in reduced ATP levels in the cytosol. Complete inhibition of TOR activity with rapamycin in yeast or AZD8055 inhibitor in plants reduces tombusvirus replication. We find that high glucose concentration, which stimulates TOR activity, enhanced tombusvirus replication in yeast. Depletion of yeast Sch9 or plant S6K1 kinase, a downstream effector of TOR, also inhibited tombusvirus replication in yeast and plant or the assembly of the viral replicase in vitro. Altogether, the TOR pathway is crucial for TBSV to replicate efficiently in hosts.</div>
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Data generation: Thu Nov 19 21:55:41 2020. Site generation: Thu Nov 19 22:00:39 2020