PhytophthoraV1, Main, Exploration, bibRecord, 000D80

Rerouting of plant late endocytic trafficking toward a pathogen interface.

Identifieur interne : 000D80 ( Main/Exploration ); précédent : 000D79; suivant : 000D81

Rerouting of plant late endocytic trafficking toward a pathogen interface.

Auteurs : Tolga O. Bozkurt [Royaume-Uni] ; Khaoula Belhaj ; Yasin F. Dagdas ; Angela Chaparro-Garcia ; Chih-Hang Wu ; Liliana M. Cano ; Sophien Kamoun

Source :

Traffic (Copenhagen, Denmark) [ 1600-0854 ] ; 2015.

RBID : pubmed:25430691

Descripteurs français

English descriptors

KwdEn :
- Arabidopsis (genetics), Arabidopsis Proteins (genetics), Arabidopsis Proteins (metabolism), Endocytosis (MeSH), Endosomes (metabolism), Host-Pathogen Interactions (MeSH), Membrane Transport Proteins (genetics), Membrane Transport Proteins (metabolism), Phytophthora infestans (pathogenicity), Plant Proteins (genetics), Plant Proteins (metabolism), Protein Kinases (genetics), Protein Kinases (metabolism), Protein Transport (MeSH), Protein-Serine-Threonine Kinases (genetics), Protein-Serine-Threonine Kinases (metabolism), Tobacco (genetics), Tobacco (metabolism), Tobacco (microbiology), rab GTP-Binding Proteins (genetics), rab GTP-Binding Proteins (metabolism).
MESH :
- chemical , genetics : Arabidopsis Proteins, Membrane Transport Proteins, Plant Proteins, Protein Kinases, Protein-Serine-Threonine Kinases, rab GTP-Binding Proteins.
- genetics : Arabidopsis, Tobacco.
- chemical , metabolism : Arabidopsis Proteins, Endosomes, Membrane Transport Proteins, Plant Proteins, Protein Kinases, Protein-Serine-Threonine Kinases, Tobacco, rab GTP-Binding Proteins.
- microbiology : Tobacco.
- pathogenicity : Phytophthora infestans.
- Endocytosis, Host-Pathogen Interactions, Protein Transport.

Abstract

A number of plant pathogenic and symbiotic microbes produce specialized cellular structures that invade host cells where they remain enveloped by host-derived membranes. The mechanisms underlying the biogenesis and functions of host-microbe interfaces are poorly understood. Here, we show that plant late endocytic trafficking is diverted toward the extrahaustorial membrane (EHM); a host-pathogen interface that develops in plant cells invaded by Irish potato famine pathogen Phytophthora infestans. A late endosome and tonoplast marker protein Rab7 GTPase RabG3c, but not a tonoplast-localized sucrose transporter, is recruited to the EHM, suggesting specific rerouting of vacuole-targeted late endosomes to a host-pathogen interface. We revealed the dynamic nature of this process by showing that, upon activation, a cell surface immune receptor traffics toward the haustorial interface. Our work provides insight into the biogenesis of the EHM and reveals dynamic processes that recruit membrane compartments and immune receptors to this host-pathogen interface.

DOI: 10.1111/tra.12245
PubMed: 25430691

Affiliations:

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

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Le document en format XML

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<author><name sortKey="Kamoun, Sophien" sort="Kamoun, Sophien" uniqKey="Kamoun S" first="Sophien" last="Kamoun">Sophien Kamoun</name>
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<term>Arabidopsis Proteins (genetics)</term>
<term>Arabidopsis Proteins (metabolism)</term>
<term>Endocytosis (MeSH)</term>
<term>Endosomes (metabolism)</term>
<term>Host-Pathogen Interactions (MeSH)</term>
<term>Membrane Transport Proteins (genetics)</term>
<term>Membrane Transport Proteins (metabolism)</term>
<term>Phytophthora infestans (pathogenicity)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Protein Kinases (genetics)</term>
<term>Protein Kinases (metabolism)</term>
<term>Protein Transport (MeSH)</term>
<term>Protein-Serine-Threonine Kinases (genetics)</term>
<term>Protein-Serine-Threonine Kinases (metabolism)</term>
<term>Tobacco (genetics)</term>
<term>Tobacco (metabolism)</term>
<term>Tobacco (microbiology)</term>
<term>rab GTP-Binding Proteins (genetics)</term>
<term>rab GTP-Binding Proteins (metabolism)</term>
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<term>Endocytose (MeSH)</term>
<term>Endosomes (métabolisme)</term>
<term>Interactions hôte-pathogène (MeSH)</term>
<term>Phytophthora infestans (pathogénicité)</term>
<term>Protein kinases (génétique)</term>
<term>Protein kinases (métabolisme)</term>
<term>Protein-Serine-Threonine Kinases (génétique)</term>
<term>Protein-Serine-Threonine Kinases (métabolisme)</term>
<term>Protéines G rab (génétique)</term>
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<term>Protéines d'Arabidopsis (génétique)</term>
<term>Protéines d'Arabidopsis (métabolisme)</term>
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<term>Tabac (génétique)</term>
<term>Tabac (microbiologie)</term>
<term>Tabac (métabolisme)</term>
<term>Transport des protéines (MeSH)</term>
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<term>Membrane Transport Proteins</term>
<term>Plant Proteins</term>
<term>Protein Kinases</term>
<term>Protein-Serine-Threonine Kinases</term>
<term>rab GTP-Binding Proteins</term>
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<term>Tobacco</term>
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<term>Protein kinases</term>
<term>Protein-Serine-Threonine Kinases</term>
<term>Protéines G rab</term>
<term>Protéines d'Arabidopsis</term>
<term>Protéines de transport membranaire</term>
<term>Protéines végétales</term>
<term>Tabac</term>
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<term>Protein Transport</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Endocytose</term>
<term>Interactions hôte-pathogène</term>
<term>Transport des protéines</term>
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<front><div type="abstract" xml:lang="en">A number of plant pathogenic and symbiotic microbes produce specialized cellular structures that invade host cells where they remain enveloped by host-derived membranes. The mechanisms underlying the biogenesis and functions of host-microbe interfaces are poorly understood. Here, we show that plant late endocytic trafficking is diverted toward the extrahaustorial membrane (EHM); a host-pathogen interface that develops in plant cells invaded by Irish potato famine pathogen Phytophthora infestans. A late endosome and tonoplast marker protein Rab7 GTPase RabG3c, but not a tonoplast-localized sucrose transporter, is recruited to the EHM, suggesting specific rerouting of vacuole-targeted late endosomes to a host-pathogen interface. We revealed the dynamic nature of this process by showing that, upon activation, a cell surface immune receptor traffics toward the haustorial interface. Our work provides insight into the biogenesis of the EHM and reveals dynamic processes that recruit membrane compartments and immune receptors to this host-pathogen interface. </div>
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<Abstract><AbstractText>A number of plant pathogenic and symbiotic microbes produce specialized cellular structures that invade host cells where they remain enveloped by host-derived membranes. The mechanisms underlying the biogenesis and functions of host-microbe interfaces are poorly understood. Here, we show that plant late endocytic trafficking is diverted toward the extrahaustorial membrane (EHM); a host-pathogen interface that develops in plant cells invaded by Irish potato famine pathogen Phytophthora infestans. A late endosome and tonoplast marker protein Rab7 GTPase RabG3c, but not a tonoplast-localized sucrose transporter, is recruited to the EHM, suggesting specific rerouting of vacuole-targeted late endosomes to a host-pathogen interface. We revealed the dynamic nature of this process by showing that, upon activation, a cell surface immune receptor traffics toward the haustorial interface. Our work provides insight into the biogenesis of the EHM and reveals dynamic processes that recruit membrane compartments and immune receptors to this host-pathogen interface. </AbstractText>
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       | NlmPubMed2Wicri -a PhytophthoraV1

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	Serveur d'exploration Phytophthora
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Serveur d'exploration Phytophthora

Rerouting of plant late endocytic trafficking toward a pathogen interface.

Rerouting of plant late endocytic trafficking toward a pathogen interface.

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