Chitinase-resistant hydrophilic symbiotic factors secreted by Frankia activate both Ca(2+) spiking and NIN gene expression in the actinorhizal plant Casuarina glauca.
Identifieur interne : 001306 ( Main/Corpus ); précédent : 001305; suivant : 001307Chitinase-resistant hydrophilic symbiotic factors secreted by Frankia activate both Ca(2+) spiking and NIN gene expression in the actinorhizal plant Casuarina glauca.
Auteurs : Mireille Chabaud ; Hassen Gherbi ; Elodie Pirolles ; Virginie Vaissayre ; Joëlle Fournier ; Daniel Moukouanga ; Claudine Franche ; Didier Bogusz ; Louis S. Tisa ; David G. Barker ; Sergio SvistoonoffSource :
- The New phytologist [ 1469-8137 ] ; 2016.
English descriptors
- KwdEn :
- Bacterial Proteins (genetics), Bacterial Proteins (metabolism), Calcium (metabolism), Chitinases (metabolism), Frankia (genetics), Frankia (physiology), Gene Expression Regulation, Plant (MeSH), Genes, Reporter (MeSH), Hydrophobic and Hydrophilic Interactions (MeSH), Luminescent Proteins (genetics), Luminescent Proteins (metabolism), Magnoliopsida (genetics), Magnoliopsida (microbiology), Mycorrhizae (physiology), Plant Proteins (genetics), Plant Proteins (metabolism), Plant Root Nodulation (MeSH), Plant Roots (genetics), Plant Roots (microbiology), Plants, Genetically Modified (MeSH), Recombinant Proteins (genetics), Recombinant Proteins (metabolism), Symbiosis (MeSH).
- MESH :
- chemical , genetics : Bacterial Proteins, Luminescent Proteins, Plant Proteins, Recombinant Proteins.
- chemical , metabolism : Bacterial Proteins, Calcium, Chitinases, Luminescent Proteins, Plant Proteins, Recombinant Proteins.
- genetics : Frankia, Magnoliopsida, Plant Roots.
- microbiology : Magnoliopsida, Plant Roots.
- physiology : Frankia, Mycorrhizae.
- Gene Expression Regulation, Plant, Genes, Reporter, Hydrophobic and Hydrophilic Interactions, Plant Root Nodulation, Plants, Genetically Modified, Symbiosis.
Abstract
Although it is now well-established that decorated lipo-chitooligosaccharide Nod factors are the key rhizobial signals which initiate infection/nodulation in host legume species, the identity of the equivalent microbial signaling molecules in the Frankia/actinorhizal association remains elusive. With the objective of identifying Frankia symbiotic factors we present a novel approach based on both molecular and cellular pre-infection reporters expressed in the model actinorhizal species Casuarina glauca. By introducing the nuclear-localized cameleon Nup-YC2.1 into Casuarina glauca we show that cell-free culture supernatants of the compatible Frankia CcI3 strain are able to elicit sustained high frequency Ca(2+) spiking in host root hairs. Furthermore, an excellent correlation exists between the triggering of nuclear Ca(2+) spiking and the transcriptional activation of the ProCgNIN:GFP reporter as a function of the Frankia strain tested. These two pre-infection symbiotic responses have been used in combination to show that the signal molecules present in the Frankia CcI3 supernatant are hydrophilic, of low molecular weight and resistant to chitinase degradation. In conclusion, the biologically active symbiotic signals secreted by Frankia appear to be chemically distinct from the currently known chitin-based rhizobial/arbuscular mycorrhizal signaling molecules. Convenient bioassays in Casuarina glauca are now available for their full characterization.
DOI: 10.1111/nph.13732
PubMed: 26484850
Links to Exploration step
pubmed:26484850Le document en format XML
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</affiliation>
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</affiliation>
<affiliation><nlm:affiliation>Laboratoire Commun de Microbiologie, Institut de Recherche pour le Développement/Institut Sénégalais des Recherches Agricoles/Université Cheikh Anta Diop, BP 1386, Dakar, Sénégal.</nlm:affiliation>
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<term>Bacterial Proteins (metabolism)</term>
<term>Calcium (metabolism)</term>
<term>Chitinases (metabolism)</term>
<term>Frankia (genetics)</term>
<term>Frankia (physiology)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Genes, Reporter (MeSH)</term>
<term>Hydrophobic and Hydrophilic Interactions (MeSH)</term>
<term>Luminescent Proteins (genetics)</term>
<term>Luminescent Proteins (metabolism)</term>
<term>Magnoliopsida (genetics)</term>
<term>Magnoliopsida (microbiology)</term>
<term>Mycorrhizae (physiology)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Plant Root Nodulation (MeSH)</term>
<term>Plant Roots (genetics)</term>
<term>Plant Roots (microbiology)</term>
<term>Plants, Genetically Modified (MeSH)</term>
<term>Recombinant Proteins (genetics)</term>
<term>Recombinant Proteins (metabolism)</term>
<term>Symbiosis (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Bacterial Proteins</term>
<term>Luminescent Proteins</term>
<term>Plant Proteins</term>
<term>Recombinant Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Bacterial Proteins</term>
<term>Calcium</term>
<term>Chitinases</term>
<term>Luminescent Proteins</term>
<term>Plant Proteins</term>
<term>Recombinant Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Frankia</term>
<term>Magnoliopsida</term>
<term>Plant Roots</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Magnoliopsida</term>
<term>Plant Roots</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Frankia</term>
<term>Mycorrhizae</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Gene Expression Regulation, Plant</term>
<term>Genes, Reporter</term>
<term>Hydrophobic and Hydrophilic Interactions</term>
<term>Plant Root Nodulation</term>
<term>Plants, Genetically Modified</term>
<term>Symbiosis</term>
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<front><div type="abstract" xml:lang="en">Although it is now well-established that decorated lipo-chitooligosaccharide Nod factors are the key rhizobial signals which initiate infection/nodulation in host legume species, the identity of the equivalent microbial signaling molecules in the Frankia/actinorhizal association remains elusive. With the objective of identifying Frankia symbiotic factors we present a novel approach based on both molecular and cellular pre-infection reporters expressed in the model actinorhizal species Casuarina glauca. By introducing the nuclear-localized cameleon Nup-YC2.1 into Casuarina glauca we show that cell-free culture supernatants of the compatible Frankia CcI3 strain are able to elicit sustained high frequency Ca(2+) spiking in host root hairs. Furthermore, an excellent correlation exists between the triggering of nuclear Ca(2+) spiking and the transcriptional activation of the ProCgNIN:GFP reporter as a function of the Frankia strain tested. These two pre-infection symbiotic responses have been used in combination to show that the signal molecules present in the Frankia CcI3 supernatant are hydrophilic, of low molecular weight and resistant to chitinase degradation. In conclusion, the biologically active symbiotic signals secreted by Frankia appear to be chemically distinct from the currently known chitin-based rhizobial/arbuscular mycorrhizal signaling molecules. Convenient bioassays in Casuarina glauca are now available for their full characterization. </div>
</front>
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<Month>09</Month>
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<Title>The New phytologist</Title>
<ISOAbbreviation>New Phytol</ISOAbbreviation>
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<ArticleTitle>Chitinase-resistant hydrophilic symbiotic factors secreted by Frankia activate both Ca(2+) spiking and NIN gene expression in the actinorhizal plant Casuarina glauca.</ArticleTitle>
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<Abstract><AbstractText>Although it is now well-established that decorated lipo-chitooligosaccharide Nod factors are the key rhizobial signals which initiate infection/nodulation in host legume species, the identity of the equivalent microbial signaling molecules in the Frankia/actinorhizal association remains elusive. With the objective of identifying Frankia symbiotic factors we present a novel approach based on both molecular and cellular pre-infection reporters expressed in the model actinorhizal species Casuarina glauca. By introducing the nuclear-localized cameleon Nup-YC2.1 into Casuarina glauca we show that cell-free culture supernatants of the compatible Frankia CcI3 strain are able to elicit sustained high frequency Ca(2+) spiking in host root hairs. Furthermore, an excellent correlation exists between the triggering of nuclear Ca(2+) spiking and the transcriptional activation of the ProCgNIN:GFP reporter as a function of the Frankia strain tested. These two pre-infection symbiotic responses have been used in combination to show that the signal molecules present in the Frankia CcI3 supernatant are hydrophilic, of low molecular weight and resistant to chitinase degradation. In conclusion, the biologically active symbiotic signals secreted by Frankia appear to be chemically distinct from the currently known chitin-based rhizobial/arbuscular mycorrhizal signaling molecules. Convenient bioassays in Casuarina glauca are now available for their full characterization. </AbstractText>
<CopyrightInformation>© 2015 The Authors. New Phytologist © 2015 New Phytologist Trust.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chabaud</LastName>
<ForeName>Mireille</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Laboratory of Plant-Microbe Interactions, Institut National de la Recherche Agronomique (UMR 441), Centre National de la Recherche Scientifique (UMR 2594), F-31320, Castanet-Tolosan, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Gherbi</LastName>
<ForeName>Hassen</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Unité Mixte de Recherche Diversité Adaptation et Développement des Plantes (IRD/Université Montpellier), F-34394, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratoire des Symbioses Tropicales et Méditerranéennes (IRD/INRA/CIRAD/Université Montpellier/Supagro), 34398, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Pirolles</LastName>
<ForeName>Elodie</ForeName>
<Initials>E</Initials>
<AffiliationInfo><Affiliation>Unité Mixte de Recherche Diversité Adaptation et Développement des Plantes (IRD/Université Montpellier), F-34394, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratoire des Symbioses Tropicales et Méditerranéennes (IRD/INRA/CIRAD/Université Montpellier/Supagro), 34398, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Vaissayre</LastName>
<ForeName>Virginie</ForeName>
<Initials>V</Initials>
<AffiliationInfo><Affiliation>Unité Mixte de Recherche Diversité Adaptation et Développement des Plantes (IRD/Université Montpellier), F-34394, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Fournier</LastName>
<ForeName>Joëlle</ForeName>
<Initials>J</Initials>
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</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Moukouanga</LastName>
<ForeName>Daniel</ForeName>
<Initials>D</Initials>
<AffiliationInfo><Affiliation>Unité Mixte de Recherche Diversité Adaptation et Développement des Plantes (IRD/Université Montpellier), F-34394, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Franche</LastName>
<ForeName>Claudine</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Unité Mixte de Recherche Diversité Adaptation et Développement des Plantes (IRD/Université Montpellier), F-34394, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bogusz</LastName>
<ForeName>Didier</ForeName>
<Initials>D</Initials>
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</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Tisa</LastName>
<ForeName>Louis S</ForeName>
<Initials>LS</Initials>
<AffiliationInfo><Affiliation>Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH, 03824-2617, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Barker</LastName>
<ForeName>David G</ForeName>
<Initials>DG</Initials>
<AffiliationInfo><Affiliation>Laboratory of Plant-Microbe Interactions, Institut National de la Recherche Agronomique (UMR 441), Centre National de la Recherche Scientifique (UMR 2594), F-31320, Castanet-Tolosan, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Svistoonoff</LastName>
<ForeName>Sergio</ForeName>
<Initials>S</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0001-8554-2922</Identifier>
<AffiliationInfo><Affiliation>Unité Mixte de Recherche Diversité Adaptation et Développement des Plantes (IRD/Université Montpellier), F-34394, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratoire des Symbioses Tropicales et Méditerranéennes (IRD/INRA/CIRAD/Université Montpellier/Supagro), 34398, Montpellier Cedex 5, France.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratoire Mixte International Adaptation des Plantes et Microorganismes Associés aux Stress Environnementaux, Centre de Recherche de Bel Air, CP 18524, Dakar, Sénégal.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Laboratoire Commun de Microbiologie, Institut de Recherche pour le Développement/Institut Sénégalais des Recherches Agricoles/Université Cheikh Anta Diop, BP 1386, Dakar, Sénégal.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
<PublicationType UI="D013486">Research Support, U.S. Gov't, Non-P.H.S.</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2015</Year>
<Month>10</Month>
<Day>20</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>New Phytol</MedlineTA>
<NlmUniqueID>9882884</NlmUniqueID>
<ISSNLinking>0028-646X</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001426">Bacterial Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008164">Luminescent Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D011994">Recombinant Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C507867">yellow cameleon 2.1</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.2.1.14</RegistryNumber>
<NameOfSubstance UI="D002688">Chitinases</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>SY7Q814VUP</RegistryNumber>
<NameOfSubstance UI="D002118">Calcium</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D001426" MajorTopicYN="N">Bacterial Proteins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002118" MajorTopicYN="N">Calcium</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002688" MajorTopicYN="N">Chitinases</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D040161" MajorTopicYN="N">Frankia</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018506" MajorTopicYN="Y">Gene Expression Regulation, Plant</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017930" MajorTopicYN="N">Genes, Reporter</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D057927" MajorTopicYN="N">Hydrophobic and Hydrophilic Interactions</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008164" MajorTopicYN="N">Luminescent Proteins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D019684" MajorTopicYN="N">Magnoliopsida</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D055170" MajorTopicYN="N">Plant Root Nodulation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D030821" MajorTopicYN="N">Plants, Genetically Modified</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011994" MajorTopicYN="N">Recombinant Proteins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013559" MajorTopicYN="N">Symbiosis</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Frankia culture supernatant</Keyword>
<Keyword MajorTopicYN="N">NIN gene expression</Keyword>
<Keyword MajorTopicYN="N">actinorhiza</Keyword>
<Keyword MajorTopicYN="N">chitinase-resistance</Keyword>
<Keyword MajorTopicYN="N">nuclear Ca2+ spiking</Keyword>
<Keyword MajorTopicYN="N">plant-microbe signaling</Keyword>
<Keyword MajorTopicYN="N">transgenic Casuarina glauca</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="received"><Year>2015</Year>
<Month>08</Month>
<Day>03</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted"><Year>2015</Year>
<Month>09</Month>
<Day>27</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2015</Year>
<Month>10</Month>
<Day>21</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed"><Year>2015</Year>
<Month>10</Month>
<Day>21</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>2016</Year>
<Month>9</Month>
<Day>28</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">26484850</ArticleId>
<ArticleId IdType="doi">10.1111/nph.13732</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>
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