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Understanding plant cell-wall remodelling during the symbiotic interaction between Tuber melanosporum and Corylus avellana using a carbohydrate microarray.

Identifieur interne : 001118 ( Main/Corpus ); précédent : 001117; suivant : 001119

Understanding plant cell-wall remodelling during the symbiotic interaction between Tuber melanosporum and Corylus avellana using a carbohydrate microarray.

Auteurs : Fabiano Sillo ; Jonatan U. Fangel ; Bernard Henrissat ; Antonella Faccio ; Paola Bonfante ; Francis Martin ; William G T. Willats ; Raffaella Balestrini

Source :

RBID : pubmed:27072675

English descriptors

Abstract

MAIN CONCLUSION

A combined approach, using a carbohydrate microarray as a support for genomic data, has revealed subtle plant cell-wall remodelling during Tuber melanosporum and Corylus avellana interaction. Cell walls are involved, to a great extent, in mediating plant-microbe interactions. An important feature of these interactions concerns changes in the cell-wall composition during interaction with other organisms. In ectomycorrhizae, plant and fungal cell walls come into direct contact, and represent the interface between the two partners. However, very little information is available on the re-arrangement that could occur within the plant and fungal cell walls during ectomycorrhizal symbiosis. Taking advantage of the Comprehensive Microarray Polymer Profiling (CoMPP) technology, the current study has had the aim of monitoring the changes that take place in the plant cell wall in Corylus avellana roots during colonization by the ascomycetous ectomycorrhizal fungus T. melanosporum. Additionally, genes encoding putative plant cell-wall degrading enzymes (PCWDEs) have been identified in the T. melanosporum genome, and RT-qPCRs have been performed to verify the expression of selected genes in fully developed C. avellana/T. melanosporum ectomycorrhizae. A localized degradation of pectin seems to occur during fungal colonization, in agreement with the growth of the ectomycorrhizal fungus through the middle lamella and with the fungal gene expression of genes acting on these polysaccharides.


DOI: 10.1007/s00425-016-2507-5
PubMed: 27072675

Links to Exploration step

pubmed:27072675

Le document en format XML

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<term>Ascomycota (enzymology)</term>
<term>Ascomycota (genetics)</term>
<term>Ascomycota (physiology)</term>
<term>Carbohydrate Metabolism (MeSH)</term>
<term>Cell Wall (metabolism)</term>
<term>Cell Wall (ultrastructure)</term>
<term>Corylus (metabolism)</term>
<term>Corylus (microbiology)</term>
<term>Corylus (ultrastructure)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Mycorrhizae (MeSH)</term>
<term>Pectins (analysis)</term>
<term>Pectins (genetics)</term>
<term>Pectins (metabolism)</term>
<term>Plant Roots (metabolism)</term>
<term>Plant Roots (microbiology)</term>
<term>Plant Roots (ultrastructure)</term>
<term>Transcriptome (MeSH)</term>
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<term>Pectins</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en">
<term>Ascomycota</term>
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<b>MAIN CONCLUSION</b>
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<p>A combined approach, using a carbohydrate microarray as a support for genomic data, has revealed subtle plant cell-wall remodelling during Tuber melanosporum and Corylus avellana interaction. Cell walls are involved, to a great extent, in mediating plant-microbe interactions. An important feature of these interactions concerns changes in the cell-wall composition during interaction with other organisms. In ectomycorrhizae, plant and fungal cell walls come into direct contact, and represent the interface between the two partners. However, very little information is available on the re-arrangement that could occur within the plant and fungal cell walls during ectomycorrhizal symbiosis. Taking advantage of the Comprehensive Microarray Polymer Profiling (CoMPP) technology, the current study has had the aim of monitoring the changes that take place in the plant cell wall in Corylus avellana roots during colonization by the ascomycetous ectomycorrhizal fungus T. melanosporum. Additionally, genes encoding putative plant cell-wall degrading enzymes (PCWDEs) have been identified in the T. melanosporum genome, and RT-qPCRs have been performed to verify the expression of selected genes in fully developed C. avellana/T. melanosporum ectomycorrhizae. A localized degradation of pectin seems to occur during fungal colonization, in agreement with the growth of the ectomycorrhizal fungus through the middle lamella and with the fungal gene expression of genes acting on these polysaccharides.</p>
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<AbstractText Label="MAIN CONCLUSION" NlmCategory="CONCLUSIONS">A combined approach, using a carbohydrate microarray as a support for genomic data, has revealed subtle plant cell-wall remodelling during Tuber melanosporum and Corylus avellana interaction. Cell walls are involved, to a great extent, in mediating plant-microbe interactions. An important feature of these interactions concerns changes in the cell-wall composition during interaction with other organisms. In ectomycorrhizae, plant and fungal cell walls come into direct contact, and represent the interface between the two partners. However, very little information is available on the re-arrangement that could occur within the plant and fungal cell walls during ectomycorrhizal symbiosis. Taking advantage of the Comprehensive Microarray Polymer Profiling (CoMPP) technology, the current study has had the aim of monitoring the changes that take place in the plant cell wall in Corylus avellana roots during colonization by the ascomycetous ectomycorrhizal fungus T. melanosporum. Additionally, genes encoding putative plant cell-wall degrading enzymes (PCWDEs) have been identified in the T. melanosporum genome, and RT-qPCRs have been performed to verify the expression of selected genes in fully developed C. avellana/T. melanosporum ectomycorrhizae. A localized degradation of pectin seems to occur during fungal colonization, in agreement with the growth of the ectomycorrhizal fungus through the middle lamella and with the fungal gene expression of genes acting on these polysaccharides.</AbstractText>
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<Affiliation>Dipartimento di Scienze Della Vita e Biologia dei Sistemi, Università di Torino, Torino, Italy.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Dipartimento di Scienze Agrarie, Forestali e Alimentari, Università di Torino, Largo Paolo Braccini 2, Grugliasco, 10095, Turin, Italy.</Affiliation>
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<Affiliation>Section for Plant Glycobiology, Department of Plant and Environmental Sciences, Copenhagen University, Copenhagen, Denmark.</Affiliation>
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<AffiliationInfo>
<Affiliation>Architecture et Fonction des Macromolécules Biologiques, Aix-Marseille University, 13288, Marseille, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>INRA, USC 1408 AFMB, 13288, Marseille, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.</Affiliation>
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