Network of GRAS transcription factors involved in the control of arbuscule development in Lotus japonicus.
Identifieur interne : 001470 ( Main/Exploration ); précédent : 001469; suivant : 001471Network of GRAS transcription factors involved in the control of arbuscule development in Lotus japonicus.
Auteurs : Li Xue [États-Unis] ; Haitao Cui [États-Unis] ; Benjamin Buer [États-Unis] ; Vinod Vijayakumar [États-Unis] ; Pierre-Marc Delaux [États-Unis] ; Stefanie Junkermann [États-Unis] ; Marcel Bucher [États-Unis]Source :
- Plant physiology [ 1532-2548 ] ; 2015.
Descripteurs français
- KwdFr :
- Analyse de profil d'expression de gènes (MeSH), Facteurs de transcription (métabolisme), Glucuronidase (métabolisme), Gènes de plante (MeSH), Liaison aux protéines (MeSH), Loteae (génétique), Loteae (microbiologie), Mutagenèse par insertion (MeSH), Mutation (MeSH), Mycorhizes (croissance et développement), Mycorhizes (métabolisme), Phylogenèse (MeSH), Phénotype (MeSH), Protéines végétales (métabolisme), Régulation de l'expression des gènes végétaux (MeSH), Régulation positive (génétique), Réseaux de régulation génique (MeSH), Spécificité d'organe (MeSH), Symbiose (MeSH), Transcription génétique (MeSH).
- MESH :
- croissance et développement : Mycorhizes.
- génétique : Loteae, Régulation positive.
- microbiologie : Loteae.
- métabolisme : Facteurs de transcription, Glucuronidase, Mycorhizes, Protéines végétales.
- Analyse de profil d'expression de gènes, Gènes de plante, Liaison aux protéines, Mutagenèse par insertion, Mutation, Phylogenèse, Phénotype, Régulation de l'expression des gènes végétaux, Réseaux de régulation génique, Spécificité d'organe, Symbiose, Transcription génétique.
English descriptors
- KwdEn :
- Gene Expression Profiling (MeSH), Gene Expression Regulation, Plant (MeSH), Gene Regulatory Networks (MeSH), Genes, Plant (MeSH), Glucuronidase (metabolism), Lotus (genetics), Lotus (microbiology), Mutagenesis, Insertional (MeSH), Mutation (MeSH), Mycorrhizae (growth & development), Mycorrhizae (metabolism), Organ Specificity (MeSH), Phenotype (MeSH), Phylogeny (MeSH), Plant Proteins (metabolism), Protein Binding (MeSH), Symbiosis (MeSH), Transcription Factors (metabolism), Transcription, Genetic (MeSH), Up-Regulation (genetics).
- MESH :
- chemical , metabolism : Glucuronidase, Plant Proteins, Transcription Factors.
- genetics : Lotus, Up-Regulation.
- growth & development : Mycorrhizae.
- metabolism : Mycorrhizae.
- microbiology : Lotus.
- Gene Expression Profiling, Gene Expression Regulation, Plant, Gene Regulatory Networks, Genes, Plant, Mutagenesis, Insertional, Mutation, Organ Specificity, Phenotype, Phylogeny, Protein Binding, Symbiosis, Transcription, Genetic.
Abstract
Arbuscular mycorrhizal (AM) fungi, in symbiosis with plants, facilitate acquisition of nutrients from the soil to their host. After penetration, intracellular hyphae form fine-branched structures in cortical cells termed arbuscules, representing the major site where bidirectional nutrient exchange takes place between the host plant and fungus. Transcriptional mechanisms underlying this cellular reprogramming are still poorly understood. GRAS proteins are an important family of transcriptional regulators in plants, named after the first three members: GIBBERELLIC ACID-INSENSITIVE, REPRESSOR of GAI, and SCARECROW. Here, we show that among 45 transcription factors up-regulated in mycorrhizal roots of the legume Lotus japonicus, expression of a unique GRAS protein particularly increases in arbuscule-containing cells under low phosphate conditions and displays a phylogenetic pattern characteristic of symbiotic genes. Allelic rad1 mutants display a strongly reduced number of arbuscules, which undergo accelerated degeneration. In further studies, two RAD1-interacting proteins were identified. One of them is the closest homolog of Medicago truncatula, REDUCED ARBUSCULAR MYCORRHIZATION1 (RAM1), which was reported to regulate a glycerol-3-phosphate acyl transferase that promotes cutin biosynthesis to enhance hyphopodia formation. As in M. truncatula, the L. japonicus ram1 mutant lines show compromised AM colonization and stunted arbuscules. Our findings provide, to our knowledge, new insight into the transcriptional program underlying the host's response to AM colonization and propose a function of GRAS transcription factors including RAD1 and RAM1 during arbuscule development.
DOI: 10.1104/pp.114.255430
PubMed: 25560877
PubMed Central: PMC4348782
Affiliations:
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Le document en format XML
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<author><name sortKey="Delaux, Pierre Marc" sort="Delaux, Pierre Marc" uniqKey="Delaux P" first="Pierre-Marc" last="Delaux">Pierre-Marc Delaux</name>
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<author><name sortKey="Junkermann, Stefanie" sort="Junkermann, Stefanie" uniqKey="Junkermann S" first="Stefanie" last="Junkermann">Stefanie Junkermann</name>
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<placeName><region type="state">Wisconsin</region>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Gene Expression Profiling (MeSH)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Gene Regulatory Networks (MeSH)</term>
<term>Genes, Plant (MeSH)</term>
<term>Glucuronidase (metabolism)</term>
<term>Lotus (genetics)</term>
<term>Lotus (microbiology)</term>
<term>Mutagenesis, Insertional (MeSH)</term>
<term>Mutation (MeSH)</term>
<term>Mycorrhizae (growth & development)</term>
<term>Mycorrhizae (metabolism)</term>
<term>Organ Specificity (MeSH)</term>
<term>Phenotype (MeSH)</term>
<term>Phylogeny (MeSH)</term>
<term>Plant Proteins (metabolism)</term>
<term>Protein Binding (MeSH)</term>
<term>Symbiosis (MeSH)</term>
<term>Transcription Factors (metabolism)</term>
<term>Transcription, Genetic (MeSH)</term>
<term>Up-Regulation (genetics)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Facteurs de transcription (métabolisme)</term>
<term>Glucuronidase (métabolisme)</term>
<term>Gènes de plante (MeSH)</term>
<term>Liaison aux protéines (MeSH)</term>
<term>Loteae (génétique)</term>
<term>Loteae (microbiologie)</term>
<term>Mutagenèse par insertion (MeSH)</term>
<term>Mutation (MeSH)</term>
<term>Mycorhizes (croissance et développement)</term>
<term>Mycorhizes (métabolisme)</term>
<term>Phylogenèse (MeSH)</term>
<term>Phénotype (MeSH)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Régulation positive (génétique)</term>
<term>Réseaux de régulation génique (MeSH)</term>
<term>Spécificité d'organe (MeSH)</term>
<term>Symbiose (MeSH)</term>
<term>Transcription génétique (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Glucuronidase</term>
<term>Plant Proteins</term>
<term>Transcription Factors</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>Lotus</term>
<term>Up-Regulation</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Mycorrhizae</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Loteae</term>
<term>Régulation positive</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Mycorrhizae</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Loteae</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Lotus</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Facteurs de transcription</term>
<term>Glucuronidase</term>
<term>Mycorhizes</term>
<term>Protéines végétales</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Plant</term>
<term>Gene Regulatory Networks</term>
<term>Genes, Plant</term>
<term>Mutagenesis, Insertional</term>
<term>Mutation</term>
<term>Organ Specificity</term>
<term>Phenotype</term>
<term>Phylogeny</term>
<term>Protein Binding</term>
<term>Symbiosis</term>
<term>Transcription, Genetic</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Analyse de profil d'expression de gènes</term>
<term>Gènes de plante</term>
<term>Liaison aux protéines</term>
<term>Mutagenèse par insertion</term>
<term>Mutation</term>
<term>Phylogenèse</term>
<term>Phénotype</term>
<term>Régulation de l'expression des gènes végétaux</term>
<term>Réseaux de régulation génique</term>
<term>Spécificité d'organe</term>
<term>Symbiose</term>
<term>Transcription génétique</term>
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<front><div type="abstract" xml:lang="en">Arbuscular mycorrhizal (AM) fungi, in symbiosis with plants, facilitate acquisition of nutrients from the soil to their host. After penetration, intracellular hyphae form fine-branched structures in cortical cells termed arbuscules, representing the major site where bidirectional nutrient exchange takes place between the host plant and fungus. Transcriptional mechanisms underlying this cellular reprogramming are still poorly understood. GRAS proteins are an important family of transcriptional regulators in plants, named after the first three members: GIBBERELLIC ACID-INSENSITIVE, REPRESSOR of GAI, and SCARECROW. Here, we show that among 45 transcription factors up-regulated in mycorrhizal roots of the legume Lotus japonicus, expression of a unique GRAS protein particularly increases in arbuscule-containing cells under low phosphate conditions and displays a phylogenetic pattern characteristic of symbiotic genes. Allelic rad1 mutants display a strongly reduced number of arbuscules, which undergo accelerated degeneration. In further studies, two RAD1-interacting proteins were identified. One of them is the closest homolog of Medicago truncatula, REDUCED ARBUSCULAR MYCORRHIZATION1 (RAM1), which was reported to regulate a glycerol-3-phosphate acyl transferase that promotes cutin biosynthesis to enhance hyphopodia formation. As in M. truncatula, the L. japonicus ram1 mutant lines show compromised AM colonization and stunted arbuscules. Our findings provide, to our knowledge, new insight into the transcriptional program underlying the host's response to AM colonization and propose a function of GRAS transcription factors including RAD1 and RAM1 during arbuscule development. </div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">25560877</PMID>
<DateCompleted><Year>2016</Year>
<Month>01</Month>
<Day>19</Day>
</DateCompleted>
<DateRevised><Year>2018</Year>
<Month>12</Month>
<Day>02</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1532-2548</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>167</Volume>
<Issue>3</Issue>
<PubDate><Year>2015</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Plant physiology</Title>
<ISOAbbreviation>Plant Physiol</ISOAbbreviation>
</Journal>
<ArticleTitle>Network of GRAS transcription factors involved in the control of arbuscule development in Lotus japonicus.</ArticleTitle>
<Pagination><MedlinePgn>854-71</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1104/pp.114.255430</ELocationID>
<Abstract><AbstractText>Arbuscular mycorrhizal (AM) fungi, in symbiosis with plants, facilitate acquisition of nutrients from the soil to their host. After penetration, intracellular hyphae form fine-branched structures in cortical cells termed arbuscules, representing the major site where bidirectional nutrient exchange takes place between the host plant and fungus. Transcriptional mechanisms underlying this cellular reprogramming are still poorly understood. GRAS proteins are an important family of transcriptional regulators in plants, named after the first three members: GIBBERELLIC ACID-INSENSITIVE, REPRESSOR of GAI, and SCARECROW. Here, we show that among 45 transcription factors up-regulated in mycorrhizal roots of the legume Lotus japonicus, expression of a unique GRAS protein particularly increases in arbuscule-containing cells under low phosphate conditions and displays a phylogenetic pattern characteristic of symbiotic genes. Allelic rad1 mutants display a strongly reduced number of arbuscules, which undergo accelerated degeneration. In further studies, two RAD1-interacting proteins were identified. One of them is the closest homolog of Medicago truncatula, REDUCED ARBUSCULAR MYCORRHIZATION1 (RAM1), which was reported to regulate a glycerol-3-phosphate acyl transferase that promotes cutin biosynthesis to enhance hyphopodia formation. As in M. truncatula, the L. japonicus ram1 mutant lines show compromised AM colonization and stunted arbuscules. Our findings provide, to our knowledge, new insight into the transcriptional program underlying the host's response to AM colonization and propose a function of GRAS transcription factors including RAD1 and RAM1 during arbuscule development. </AbstractText>
<CopyrightInformation>© 2015 American Society of Plant Biologists. All Rights Reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Xue</LastName>
<ForeName>Li</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.).</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Cui</LastName>
<ForeName>Haitao</ForeName>
<Initials>H</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.).</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Buer</LastName>
<ForeName>Benjamin</ForeName>
<Initials>B</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.).</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Vijayakumar</LastName>
<ForeName>Vinod</ForeName>
<Initials>V</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.).</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Delaux</LastName>
<ForeName>Pierre-Marc</ForeName>
<Initials>PM</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.).</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Junkermann</LastName>
<ForeName>Stefanie</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.).</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Bucher</LastName>
<ForeName>Marcel</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Botanical Institute, Cologne Biocenter, Cluster of Excellence on Plant Sciences, University of Cologne, D-50674 Cologne, Germany (L.X., B.B.,V.V., S.J., M.B.);Department of Plant-Microbe Interactions, Max Planck Institute for Plant Breeding Research, D-50829 Cologne, Germany (H.C.); andDepartment of Agronomy, University of Wisconsin, Madison, Wisconsin 53706 (P.-M.D.) m.bucher@uni-koeln.de.</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>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2015</Year>
<Month>01</Month>
<Day>05</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Plant Physiol</MedlineTA>
<NlmUniqueID>0401224</NlmUniqueID>
<ISSNLinking>0032-0889</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D014157">Transcription Factors</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 3.2.1.31</RegistryNumber>
<NameOfSubstance UI="D005966">Glucuronidase</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018506" MajorTopicYN="N">Gene Expression Regulation, Plant</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D053263" MajorTopicYN="Y">Gene Regulatory Networks</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017343" MajorTopicYN="N">Genes, Plant</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005966" MajorTopicYN="N">Glucuronidase</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000070116" MajorTopicYN="N">Lotus</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D016254" MajorTopicYN="N">Mutagenesis, Insertional</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009154" MajorTopicYN="N">Mutation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName>
<QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009928" MajorTopicYN="N">Organ Specificity</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010641" MajorTopicYN="N">Phenotype</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011485" MajorTopicYN="N">Protein Binding</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013559" MajorTopicYN="N">Symbiosis</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014157" MajorTopicYN="N">Transcription Factors</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014158" MajorTopicYN="N">Transcription, Genetic</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015854" MajorTopicYN="N">Up-Regulation</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
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<affiliations><list><country><li>États-Unis</li>
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<name sortKey="Cui, Haitao" sort="Cui, Haitao" uniqKey="Cui H" first="Haitao" last="Cui">Haitao Cui</name>
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