Serveur d'exploration sur la mycorhize

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Blumenols as shoot markers of root symbiosis with arbuscular mycorrhizal fungi.

Identifieur interne : 000A49 ( Main/Exploration ); précédent : 000A48; suivant : 000A50

Blumenols as shoot markers of root symbiosis with arbuscular mycorrhizal fungi.

Auteurs : Ming Wang [Allemagne] ; Martin Sch Fer [Allemagne] ; Dapeng Li [Allemagne] ; Rayko Halitschke [Allemagne] ; Chuanfu Dong [Allemagne] ; Erica Mcgale [Allemagne] ; Christian Paetz [Allemagne] ; Yuanyuan Song [Allemagne] ; Suhua Li [Allemagne] ; Junfu Dong [Allemagne, République populaire de Chine] ; Sven Heiling [Allemagne] ; Karin Groten [Allemagne] ; Philipp Franken [Allemagne] ; Michael Bitterlich [Allemagne] ; Maria J. Harrison [États-Unis] ; Uta Paszkowski [Royaume-Uni] ; Ian T. Baldwin [Allemagne]

Source :

RBID : pubmed:30152755

Descripteurs français

English descriptors

Abstract

High-through-put (HTP) screening for functional arbuscular mycorrhizal fungi (AMF)-associations is challenging because roots must be excavated and colonization evaluated by transcript analysis or microscopy. Here we show that specific leaf-metabolites provide broadly applicable accurate proxies of these associations, suitable for HTP-screens. With a combination of untargeted and targeted metabolomics, we show that shoot accumulations of hydroxy- and carboxyblumenol C-glucosides mirror root AMF-colonization in Nicotiana attenuata plants. Genetic/pharmacologic manipulations indicate that these AMF-indicative foliar blumenols are synthesized and transported from roots to shoots. These blumenol-derived foliar markers, found in many di- and monocotyledonous crop and model plants (Solanum lycopersicum, Solanum tuberosum, Hordeum vulgare, Triticum aestivum, Medicago truncatula and Brachypodium distachyon), are not restricted to particular plant-AMF interactions, and are shown to be applicable for field-based QTL mapping of AMF-related genes.

DOI: 10.7554/eLife.37093
PubMed: 30152755
PubMed Central: PMC6156081


Affiliations:


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Le document en format XML

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<term>Biomarkers (metabolism)</term>
<term>Cyclohexanones (chemistry)</term>
<term>Cyclohexanones (metabolism)</term>
<term>Genes, Plant (MeSH)</term>
<term>High-Throughput Screening Assays (MeSH)</term>
<term>Metabolomics (MeSH)</term>
<term>Mycorrhizae (growth & development)</term>
<term>Mycorrhizae (metabolism)</term>
<term>Plant Leaves (metabolism)</term>
<term>Plant Shoots (metabolism)</term>
<term>RNA, Messenger (genetics)</term>
<term>RNA, Messenger (metabolism)</term>
<term>Stress, Physiological (MeSH)</term>
<term>Symbiosis (MeSH)</term>
<term>Time Factors (MeSH)</term>
<term>Tobacco (genetics)</term>
<term>Tobacco (metabolism)</term>
<term>Tobacco (microbiology)</term>
</keywords>
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<term>ARN messager (génétique)</term>
<term>ARN messager (métabolisme)</term>
<term>Cyclohexanones (composition chimique)</term>
<term>Cyclohexanones (métabolisme)</term>
<term>Facteurs temps (MeSH)</term>
<term>Feuilles de plante (métabolisme)</term>
<term>Gènes de plante (MeSH)</term>
<term>Marqueurs biologiques (métabolisme)</term>
<term>Mycorhizes (croissance et développement)</term>
<term>Mycorhizes (métabolisme)</term>
<term>Métabolomique (MeSH)</term>
<term>Pousses de plante (métabolisme)</term>
<term>Stress physiologique (MeSH)</term>
<term>Symbiose (MeSH)</term>
<term>Tabac (génétique)</term>
<term>Tabac (microbiologie)</term>
<term>Tabac (métabolisme)</term>
<term>Tests de criblage à haut débit (MeSH)</term>
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<term>Cyclohexanones</term>
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<term>RNA, Messenger</term>
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<term>Biomarkers</term>
<term>Cyclohexanones</term>
<term>RNA, Messenger</term>
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<term>Cyclohexanones</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Mycorhizes</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Tobacco</term>
</keywords>
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<term>Mycorrhizae</term>
</keywords>
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<term>ARN messager</term>
<term>Tabac</term>
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<term>Mycorrhizae</term>
<term>Plant Leaves</term>
<term>Plant Shoots</term>
<term>Tobacco</term>
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<term>Tabac</term>
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<term>Tobacco</term>
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<term>Cyclohexanones</term>
<term>Feuilles de plante</term>
<term>Marqueurs biologiques</term>
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<term>Gènes de plante</term>
<term>Métabolomique</term>
<term>Stress physiologique</term>
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<front>
<div type="abstract" xml:lang="en">High-through-put (HTP) screening for functional arbuscular mycorrhizal fungi (AMF)-associations is challenging because roots must be excavated and colonization evaluated by transcript analysis or microscopy. Here we show that specific leaf-metabolites provide broadly applicable accurate proxies of these associations, suitable for HTP-screens. With a combination of untargeted and targeted metabolomics, we show that shoot accumulations of hydroxy- and carboxyblumenol C-glucosides mirror root AMF-colonization in
<i>Nicotiana attenuata</i>
plants. Genetic/pharmacologic manipulations indicate that these AMF-indicative foliar blumenols are synthesized and transported from roots to shoots. These blumenol-derived foliar markers, found in many di- and monocotyledonous crop and model plants (
<i>Solanum lycopersicum, Solanum tuberosum, Hordeum vulgare, Triticum aestivum, Medicago truncatula</i>
and
<i>Brachypodium distachyon</i>
), are not restricted to particular plant-AMF interactions, and are shown to be applicable for field-based QTL mapping of AMF-related genes.</div>
</front>
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<DateCompleted>
<Year>2019</Year>
<Month>01</Month>
<Day>21</Day>
</DateCompleted>
<DateRevised>
<Year>2020</Year>
<Month>03</Month>
<Day>18</Day>
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<Volume>7</Volume>
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<Year>2018</Year>
<Month>08</Month>
<Day>28</Day>
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<Title>eLife</Title>
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<ArticleTitle>Blumenols as shoot markers of root symbiosis with arbuscular mycorrhizal fungi.</ArticleTitle>
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<Abstract>
<AbstractText>High-through-put (HTP) screening for functional arbuscular mycorrhizal fungi (AMF)-associations is challenging because roots must be excavated and colonization evaluated by transcript analysis or microscopy. Here we show that specific leaf-metabolites provide broadly applicable accurate proxies of these associations, suitable for HTP-screens. With a combination of untargeted and targeted metabolomics, we show that shoot accumulations of hydroxy- and carboxyblumenol C-glucosides mirror root AMF-colonization in
<i>Nicotiana attenuata</i>
plants. Genetic/pharmacologic manipulations indicate that these AMF-indicative foliar blumenols are synthesized and transported from roots to shoots. These blumenol-derived foliar markers, found in many di- and monocotyledonous crop and model plants (
<i>Solanum lycopersicum, Solanum tuberosum, Hordeum vulgare, Triticum aestivum, Medicago truncatula</i>
and
<i>Brachypodium distachyon</i>
), are not restricted to particular plant-AMF interactions, and are shown to be applicable for field-based QTL mapping of AMF-related genes.</AbstractText>
<CopyrightInformation>© 2018, Wang et al.</CopyrightInformation>
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<ForeName>Ming</ForeName>
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<Keyword MajorTopicYN="Y">Nicotiana attenuata</Keyword>
<Keyword MajorTopicYN="Y">Rhizophagus irregularis</Keyword>
<Keyword MajorTopicYN="Y">arbuscular mycorrhizal fungi</Keyword>
<Keyword MajorTopicYN="Y">blumenol</Keyword>
<Keyword MajorTopicYN="Y">colonization rate</Keyword>
<Keyword MajorTopicYN="Y">ecology</Keyword>
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<CoiStatement>MW European patent application EP 18 15 8922.7, MS Martin Schäfer: European patent application EP 18 15 8922.7, DL Dapeng Li: European patent application EP 18 15 8922.7, RH Rayko Halitschke: European patent application EP 18 15 8922.7, CD, CP, YS, SL, JD, KG, PF, MB, UP No competing interests declared, EM Erica McGale: European patent application EP 18 15 8922.7, SH Sven Heiling: European patent application EP 18 15 8922.7, MH Reviewing editor, eLife, IB Senior editor, eLife; European patent application EP 18 15 8922.7</CoiStatement>
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