Serveur d'exploration sur les interactions arbre microorganisme

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Identification of Populus Small RNAs Responsive to Mutualistic Interactions With Mycorrhizal Fungi, Laccaria bicolor and Rhizophagus irregularis.

Identifieur interne : 000074 ( Main/Exploration ); précédent : 000073; suivant : 000075

Identification of Populus Small RNAs Responsive to Mutualistic Interactions With Mycorrhizal Fungi, Laccaria bicolor and Rhizophagus irregularis.

Auteurs : Ritesh Mewalal [États-Unis] ; Hengfu Yin [République populaire de Chine] ; Rongbin Hu [États-Unis] ; Sara Jawdy [États-Unis] ; Patrice Vion [France] ; Gerald A. Tuskan [États-Unis] ; François Le Tacon [France] ; Jessy L. Labbé [États-Unis] ; Xiaohan Yang [États-Unis]

Source :

RBID : pubmed:30936859

Abstract

Ecto- and endo-mycorrhizal colonization of Populus roots have a positive impact on the overall tree health and growth. A complete molecular understanding of these interactions will have important implications for increasing agricultural or forestry sustainability using plant:microbe-based strategies. These beneficial associations entail extensive morphological changes orchestrated by the genetic reprogramming in both organisms. In this study, we performed a comparative analysis of two Populus species (Populus deltoides and P. trichocarpa) that were colonized by either an arbuscular mycorrhizal fungus (AmF), Rhizophagus irregularis or an ectomycorrhizal fungus (EmF), Laccaria bicolor, to describe the small RNA (sRNA) landscape including small open reading frames (sORFs) and micro RNAs (miRNAs) involved in these mutualistic interactions. We identified differential expression of sRNAs that were, to a large extent, (1) within the genomic regions lacking annotated genes in the Populus genome and (2) distinct for each fungal interaction. These sRNAs may be a source of novel sORFs within a genome, and in this regard, we identified potential sORFs encoded by the sRNAs. We predicted a higher number of differentially-expressed miRNAs in P. trichocarpa (4 times more) than in P. deltoides (conserved and novel). In addition, 44 miRNAs were common in P. trichocarpa between the EmF and AmF treatments, and only 4 miRNAs were common in P. deltoides between the treatments. Root colonization by either fungus was more effective in P. trichocarpa than in P. deltoides, thus the relatively few differentially-expressed miRNAs predicted in P. deltoides might reflect the extent of the symbiosis. Finally, we predicted several genes targets for the plant miRNAs identified here, including potential fungal gene targets. Our findings shed light on additional molecular tiers with a role in Populus-fungal mutualistic associations and provides a set of potential molecular targets for future enhancement.

DOI: 10.3389/fmicb.2019.00515
PubMed: 30936859
PubMed Central: PMC6431645


Affiliations:


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Le document en format XML

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Small RNAs Responsive to Mutualistic Interactions With Mycorrhizal Fungi,
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and
<i>Rhizophagus irregularis</i>
.</title>
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<div type="abstract" xml:lang="en">Ecto- and endo-mycorrhizal colonization of
<i>Populus</i>
roots have a positive impact on the overall tree health and growth. A complete molecular understanding of these interactions will have important implications for increasing agricultural or forestry sustainability using plant:microbe-based strategies. These beneficial associations entail extensive morphological changes orchestrated by the genetic reprogramming in both organisms. In this study, we performed a comparative analysis of two
<i>Populus</i>
species (
<i>Populus deltoides</i>
and
<i>P. trichocarpa</i>
) that were colonized by either an arbuscular mycorrhizal fungus (AmF),
<i>Rhizophagus irregularis</i>
or an ectomycorrhizal fungus (EmF),
<i>Laccaria bicolor</i>
, to describe the small RNA (sRNA) landscape including small open reading frames (sORFs) and micro RNAs (miRNAs) involved in these mutualistic interactions. We identified differential expression of sRNAs that were, to a large extent, (1) within the genomic regions lacking annotated genes in the
<i>Populus</i>
genome and (2) distinct for each fungal interaction. These sRNAs may be a source of novel sORFs within a genome, and in this regard, we identified potential sORFs encoded by the sRNAs. We predicted a higher number of differentially-expressed miRNAs in
<i>P. trichocarpa</i>
(4 times more) than in
<i>P. deltoides</i>
(conserved and novel). In addition, 44 miRNAs were common in
<i>P. trichocarpa</i>
between the EmF and AmF treatments, and only 4 miRNAs were common in
<i>P. deltoides</i>
between the treatments. Root colonization by either fungus was more effective in
<i>P. trichocarpa</i>
than in
<i>P. deltoides</i>
, thus the relatively few differentially-expressed miRNAs predicted in
<i>P. deltoides</i>
might reflect the extent of the symbiosis. Finally, we predicted several genes targets for the plant miRNAs identified here, including potential fungal gene targets. Our findings shed light on additional molecular tiers with a role in
<i>Populus</i>
-fungal mutualistic associations and provides a set of potential molecular targets for future enhancement.</div>
</front>
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<ArticleTitle>Identification of
<i>Populus</i>
Small RNAs Responsive to Mutualistic Interactions With Mycorrhizal Fungi,
<i>Laccaria bicolor</i>
and
<i>Rhizophagus irregularis</i>
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<AbstractText>Ecto- and endo-mycorrhizal colonization of
<i>Populus</i>
roots have a positive impact on the overall tree health and growth. A complete molecular understanding of these interactions will have important implications for increasing agricultural or forestry sustainability using plant:microbe-based strategies. These beneficial associations entail extensive morphological changes orchestrated by the genetic reprogramming in both organisms. In this study, we performed a comparative analysis of two
<i>Populus</i>
species (
<i>Populus deltoides</i>
and
<i>P. trichocarpa</i>
) that were colonized by either an arbuscular mycorrhizal fungus (AmF),
<i>Rhizophagus irregularis</i>
or an ectomycorrhizal fungus (EmF),
<i>Laccaria bicolor</i>
, to describe the small RNA (sRNA) landscape including small open reading frames (sORFs) and micro RNAs (miRNAs) involved in these mutualistic interactions. We identified differential expression of sRNAs that were, to a large extent, (1) within the genomic regions lacking annotated genes in the
<i>Populus</i>
genome and (2) distinct for each fungal interaction. These sRNAs may be a source of novel sORFs within a genome, and in this regard, we identified potential sORFs encoded by the sRNAs. We predicted a higher number of differentially-expressed miRNAs in
<i>P. trichocarpa</i>
(4 times more) than in
<i>P. deltoides</i>
(conserved and novel). In addition, 44 miRNAs were common in
<i>P. trichocarpa</i>
between the EmF and AmF treatments, and only 4 miRNAs were common in
<i>P. deltoides</i>
between the treatments. Root colonization by either fungus was more effective in
<i>P. trichocarpa</i>
than in
<i>P. deltoides</i>
, thus the relatively few differentially-expressed miRNAs predicted in
<i>P. deltoides</i>
might reflect the extent of the symbiosis. Finally, we predicted several genes targets for the plant miRNAs identified here, including potential fungal gene targets. Our findings shed light on additional molecular tiers with a role in
<i>Populus</i>
-fungal mutualistic associations and provides a set of potential molecular targets for future enhancement.</AbstractText>
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<ForeName>Ritesh</ForeName>
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</AffiliationInfo>
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<LastName>Yin</LastName>
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<AffiliationInfo>
<Affiliation>State Key Laboratory of Tree Genetics and Breeding, Research Institute of Subtropical Forestry, Chinese Academy of Forestry, Fuyang, China.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<AffiliationInfo>
<Affiliation>INRA, UMR 1136 INRA-University of Lorraine, Interactions Arbres/Microorganismes, Laboratory of Excellence ARBRE, INRA-Nancy, VandIJuvre-lès-Nancy, France.</Affiliation>
</AffiliationInfo>
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<ForeName>Jessy L</ForeName>
<Initials>JL</Initials>
<AffiliationInfo>
<Affiliation>Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, United States.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Yang</LastName>
<ForeName>Xiaohan</ForeName>
<Initials>X</Initials>
<AffiliationInfo>
<Affiliation>Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN, United States.</Affiliation>
</AffiliationInfo>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Laccaria</Keyword>
<Keyword MajorTopicYN="N">Populus</Keyword>
<Keyword MajorTopicYN="N">Rhizophagus</Keyword>
<Keyword MajorTopicYN="N">arbuscular mycorrhizal fungus</Keyword>
<Keyword MajorTopicYN="N">ectomycorrhizal fungus</Keyword>
<Keyword MajorTopicYN="N">microRNA</Keyword>
<Keyword MajorTopicYN="N">mutualistic symbiosis</Keyword>
<Keyword MajorTopicYN="N">small RNA</Keyword>
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<Month>04</Month>
<Day>08</Day>
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<Month>02</Month>
<Day>28</Day>
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