The glutaredoxin ATGRXS13 is required to facilitate Botrytis cinerea infection of Arabidopsis thaliana plants.
Identifieur interne : 000906 ( Main/Exploration ); précédent : 000905; suivant : 000907The glutaredoxin ATGRXS13 is required to facilitate Botrytis cinerea infection of Arabidopsis thaliana plants.
Auteurs : Sylvain La Camera [Allemagne] ; Floriane L'Haridon ; Jérémy Astier ; Mark Zander ; Eliane Abou-Mansour ; Gonzague Page ; Corinna Thurow ; David Wendehenne ; Christiane Gatz ; Jean-Pierre Métraux ; Olivier LamotteSource :
- The Plant journal : for cell and molecular biology [ 1365-313X ] ; 2011.
Descripteurs français
- KwdFr :
- ARN des plantes (génétique), Acide salicylique (métabolisme), Arabidopsis (enzymologie), Arabidopsis (génétique), Arabidopsis (microbiologie), Botrytis (pathogénicité), Clonage moléculaire (MeSH), Cyclopentanes (métabolisme), Données de séquences moléculaires (MeSH), Facteurs de transcription (métabolisme), Glutarédoxines (génétique), Glutarédoxines (métabolisme), Maladies des plantes (génétique), Maladies des plantes (microbiologie), Mutagenèse par insertion (MeSH), Oxylipines (métabolisme), Protéines d'Arabidopsis (génétique), Protéines d'Arabidopsis (métabolisme), Régulation de l'expression des gènes végétaux (MeSH), Résistance à la maladie (MeSH), Séquence d'acides aminés (MeSH), Séquençage par oligonucléotides en batterie (MeSH), Transduction du signal (MeSH), Épissage alternatif (MeSH).
- MESH :
- enzymologie : Arabidopsis.
- génétique : ARN des plantes, Arabidopsis, Glutarédoxines, Maladies des plantes, Protéines d'Arabidopsis.
- microbiologie : Arabidopsis, Maladies des plantes.
- métabolisme : Acide salicylique, Cyclopentanes, Facteurs de transcription, Glutarédoxines, Oxylipines, Protéines d'Arabidopsis.
- pathogénicité : Botrytis.
- Clonage moléculaire, Données de séquences moléculaires, Mutagenèse par insertion, Régulation de l'expression des gènes végétaux, Résistance à la maladie, Séquence d'acides aminés, Séquençage par oligonucléotides en batterie, Transduction du signal, Épissage alternatif.
English descriptors
- KwdEn :
- Alternative Splicing (MeSH), Amino Acid Sequence (MeSH), Arabidopsis (enzymology), Arabidopsis (genetics), Arabidopsis (microbiology), Arabidopsis Proteins (genetics), Arabidopsis Proteins (metabolism), Botrytis (pathogenicity), Cloning, Molecular (MeSH), Cyclopentanes (metabolism), Disease Resistance (MeSH), Gene Expression Regulation, Plant (MeSH), Glutaredoxins (genetics), Glutaredoxins (metabolism), Molecular Sequence Data (MeSH), Mutagenesis, Insertional (MeSH), Oligonucleotide Array Sequence Analysis (MeSH), Oxylipins (metabolism), Plant Diseases (genetics), Plant Diseases (microbiology), RNA, Plant (genetics), Salicylic Acid (metabolism), Signal Transduction (MeSH), Transcription Factors (metabolism).
- MESH :
- chemical , genetics : Arabidopsis Proteins, Glutaredoxins, RNA, Plant.
- enzymology : Arabidopsis.
- genetics : Arabidopsis, Plant Diseases.
- chemical , metabolism : Arabidopsis Proteins, Cyclopentanes, Glutaredoxins, Oxylipins, Salicylic Acid, Transcription Factors.
- microbiology : Arabidopsis, Plant Diseases.
- pathogenicity : Botrytis.
- Alternative Splicing, Amino Acid Sequence, Cloning, Molecular, Disease Resistance, Gene Expression Regulation, Plant, Molecular Sequence Data, Mutagenesis, Insertional, Oligonucleotide Array Sequence Analysis, Signal Transduction.
Abstract
Botrytis cinerea is a major pre- and post-harvest necrotrophic pathogen with a broad host range that causes substantial crop losses. The plant hormone jasmonic acid (JA) is involved in the basal resistance against this fungus. Despite basal resistance, virulent strains of B. cinerea can cause disease on Arabidopsis thaliana and virulent pathogens can interfere with the metabolism of the host in a way to facilitate infection of the plant. However, plant genes that are required by the pathogen for infection remain poorly described. To find such genes, we have compared the changes in gene expression induced in A. thaliana by JA with those induced after B. cinerea using genome-wide microarrays. We have identified genes that are repressed by JA but that are induced by B. cinerea. In this study, we describe one candidate gene, ATGRXS13, that encodes for a putative glutaredoxin and that exhibits such a crossed expression. In plants that are infected by this necrotrophic fungus, ATGRXS13 expression was negatively controlled by JA and TGA transcription factors but also through a JA-salicylic acid (SA) cross-talk mechanism as B. cinerea induced SA production that positively controlled ATGRXS13 expression. Furthermore, plants impaired in ATGRXS13 exhibited resistance to B. cinerea. Finally, we present a model whereby B. cinerea takes advantage of defence signalling pathways of the plant to help the colonization of its host.
DOI: 10.1111/j.1365-313X.2011.04706.x
PubMed: 21756272
Affiliations:
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Regulation, Plant (MeSH)</term><term>Glutaredoxins (genetics)</term><term>Glutaredoxins (metabolism)</term><term>Molecular Sequence Data (MeSH)</term><term>Mutagenesis, Insertional (MeSH)</term><term>Oligonucleotide Array Sequence Analysis (MeSH)</term><term>Oxylipins (metabolism)</term><term>Plant Diseases (genetics)</term><term>Plant Diseases (microbiology)</term><term>RNA, Plant (genetics)</term><term>Salicylic Acid (metabolism)</term><term>Signal Transduction (MeSH)</term><term>Transcription Factors (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>ARN des plantes (génétique)</term><term>Acide salicylique (métabolisme)</term><term>Arabidopsis (enzymologie)</term><term>Arabidopsis (génétique)</term><term>Arabidopsis (microbiologie)</term><term>Botrytis (pathogénicité)</term><term>Clonage moléculaire (MeSH)</term><term>Cyclopentanes (métabolisme)</term><term>Données de séquences moléculaires (MeSH)</term><term>Facteurs de transcription 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salicylique</term><term>Cyclopentanes</term><term>Facteurs de transcription</term><term>Glutarédoxines</term><term>Oxylipines</term><term>Protéines d'Arabidopsis</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Botrytis</term></keywords><keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Botrytis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Alternative Splicing</term><term>Amino Acid Sequence</term><term>Cloning, Molecular</term><term>Disease Resistance</term><term>Gene Expression Regulation, Plant</term><term>Molecular Sequence Data</term><term>Mutagenesis, Insertional</term><term>Oligonucleotide Array Sequence Analysis</term><term>Signal Transduction</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Clonage moléculaire</term><term>Données de séquences moléculaires</term><term>Mutagenèse par insertion</term><term>Régulation de l'expression des gènes végétaux</term><term>Résistance à la maladie</term><term>Séquence d'acides aminés</term><term>Séquençage par oligonucléotides en batterie</term><term>Transduction du signal</term><term>Épissage alternatif</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Botrytis cinerea is a major pre- and post-harvest necrotrophic pathogen with a broad host range that causes substantial crop losses. The plant hormone jasmonic acid (JA) is involved in the basal resistance against this fungus. Despite basal resistance, virulent strains of B. cinerea can cause disease on Arabidopsis thaliana and virulent pathogens can interfere with the metabolism of the host in a way to facilitate infection of the plant. However, plant genes that are required by the pathogen for infection remain poorly described. To find such genes, we have compared the changes in gene expression induced in A. thaliana by JA with those induced after B. cinerea using genome-wide microarrays. We have identified genes that are repressed by JA but that are induced by B. cinerea. In this study, we describe one candidate gene, ATGRXS13, that encodes for a putative glutaredoxin and that exhibits such a crossed expression. In plants that are infected by this necrotrophic fungus, ATGRXS13 expression was negatively controlled by JA and TGA transcription factors but also through a JA-salicylic acid (SA) cross-talk mechanism as B. cinerea induced SA production that positively controlled ATGRXS13 expression. Furthermore, plants impaired in ATGRXS13 exhibited resistance to B. cinerea. Finally, we present a model whereby B. cinerea takes advantage of defence signalling pathways of the plant to help the colonization of its host.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">21756272</PMID><DateCompleted><Year>2012</Year><Month>03</Month><Day>16</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1365-313X</ISSN><JournalIssue CitedMedium="Internet"><Volume>68</Volume><Issue>3</Issue><PubDate><Year>2011</Year><Month>Nov</Month></PubDate></JournalIssue><Title>The Plant journal : for cell and molecular biology</Title><ISOAbbreviation>Plant J</ISOAbbreviation></Journal><ArticleTitle>The glutaredoxin ATGRXS13 is required to facilitate Botrytis cinerea infection of Arabidopsis thaliana plants.</ArticleTitle><Pagination><MedlinePgn>507-19</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1365-313X.2011.04706.x</ELocationID><Abstract><AbstractText>Botrytis cinerea is a major pre- and post-harvest necrotrophic pathogen with a broad host range that causes substantial crop losses. The plant hormone jasmonic acid (JA) is involved in the basal resistance against this fungus. Despite basal resistance, virulent strains of B. cinerea can cause disease on Arabidopsis thaliana and virulent pathogens can interfere with the metabolism of the host in a way to facilitate infection of the plant. However, plant genes that are required by the pathogen for infection remain poorly described. To find such genes, we have compared the changes in gene expression induced in A. thaliana by JA with those induced after B. cinerea using genome-wide microarrays. We have identified genes that are repressed by JA but that are induced by B. cinerea. In this study, we describe one candidate gene, ATGRXS13, that encodes for a putative glutaredoxin and that exhibits such a crossed expression. In plants that are infected by this necrotrophic fungus, ATGRXS13 expression was negatively controlled by JA and TGA transcription factors but also through a JA-salicylic acid (SA) cross-talk mechanism as B. cinerea induced SA production that positively controlled ATGRXS13 expression. Furthermore, plants impaired in ATGRXS13 exhibited resistance to B. cinerea. Finally, we present a model whereby B. cinerea takes advantage of defence signalling pathways of the plant to help the colonization of its host.</AbstractText><CopyrightInformation>© 2011 The Authors. The Plant Journal © 2011 Blackwell Publishing Ltd.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>La Camera</LastName><ForeName>Sylvain</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Département de Biologie, Université de Fribourg, 10 chemin du Musée, CH-1700 Fribourg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>L'haridon</LastName><ForeName>Floriane</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Astier</LastName><ForeName>Jérémy</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Zander</LastName><ForeName>Mark</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Abou-Mansour</LastName><ForeName>Eliane</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Page</LastName><ForeName>Gonzague</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Thurow</LastName><ForeName>Corinna</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Wendehenne</LastName><ForeName>David</ForeName><Initials>D</Initials></Author><Author ValidYN="Y"><LastName>Gatz</LastName><ForeName>Christiane</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Métraux</LastName><ForeName>Jean-Pierre</ForeName><Initials>JP</Initials></Author><Author ValidYN="Y"><LastName>Lamotte</LastName><ForeName>Olivier</ForeName><Initials>O</Initials></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>2011</Year><Month>08</Month><Day>31</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Plant J</MedlineTA><NlmUniqueID>9207397</NlmUniqueID><ISSNLinking>0960-7412</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D029681">Arabidopsis Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D003517">Cyclopentanes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D054477">Glutaredoxins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D054883">Oxylipins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018749">RNA, Plant</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D014157">Transcription Factors</NameOfSubstance></Chemical><Chemical><RegistryNumber>6RI5N05OWW</RegistryNumber><NameOfSubstance UI="C011006">jasmonic acid</NameOfSubstance></Chemical><Chemical><RegistryNumber>O414PZ4LPZ</RegistryNumber><NameOfSubstance UI="D020156">Salicylic Acid</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D017398" MajorTopicYN="N">Alternative Splicing</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000595" MajorTopicYN="N">Amino Acid Sequence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017360" MajorTopicYN="N">Arabidopsis</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D029681" MajorTopicYN="N">Arabidopsis Proteins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020171" MajorTopicYN="N">Botrytis</DescriptorName><QualifierName UI="Q000472" MajorTopicYN="Y">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003517" MajorTopicYN="N">Cyclopentanes</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D060467" MajorTopicYN="N">Disease Resistance</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018506" MajorTopicYN="N">Gene Expression Regulation, Plant</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D054477" MajorTopicYN="N">Glutaredoxins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016254" MajorTopicYN="N">Mutagenesis, Insertional</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D020411" MajorTopicYN="N">Oligonucleotide Array Sequence Analysis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D054883" MajorTopicYN="N">Oxylipins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010935" MajorTopicYN="N">Plant Diseases</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018749" MajorTopicYN="N">RNA, Plant</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020156" MajorTopicYN="N">Salicylic Acid</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015398" MajorTopicYN="N">Signal Transduction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014157" MajorTopicYN="N">Transcription Factors</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="entrez"><Year>2011</Year><Month>7</Month><Day>16</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2011</Year><Month>7</Month><Day>16</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2012</Year><Month>3</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">21756272</ArticleId><ArticleId IdType="doi">10.1111/j.1365-313X.2011.04706.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country></list><tree><noCountry><name sortKey="Abou Mansour, Eliane" sort="Abou Mansour, Eliane" uniqKey="Abou Mansour E" first="Eliane" last="Abou-Mansour">Eliane Abou-Mansour</name><name sortKey="Astier, Jeremy" sort="Astier, Jeremy" uniqKey="Astier J" first="Jérémy" last="Astier">Jérémy Astier</name><name sortKey="Gatz, Christiane" sort="Gatz, Christiane" uniqKey="Gatz C" first="Christiane" last="Gatz">Christiane Gatz</name><name sortKey="L Haridon, Floriane" sort="L Haridon, Floriane" uniqKey="L Haridon F" first="Floriane" last="L'Haridon">Floriane L'Haridon</name><name sortKey="Lamotte, Olivier" sort="Lamotte, Olivier" uniqKey="Lamotte O" first="Olivier" last="Lamotte">Olivier Lamotte</name><name sortKey="Metraux, Jean Pierre" sort="Metraux, Jean Pierre" uniqKey="Metraux J" first="Jean-Pierre" last="Métraux">Jean-Pierre Métraux</name><name sortKey="Page, Gonzague" sort="Page, Gonzague" uniqKey="Page G" first="Gonzague" last="Page">Gonzague Page</name><name sortKey="Thurow, Corinna" sort="Thurow, Corinna" uniqKey="Thurow C" first="Corinna" last="Thurow">Corinna Thurow</name><name sortKey="Wendehenne, David" sort="Wendehenne, David" uniqKey="Wendehenne D" first="David" last="Wendehenne">David Wendehenne</name><name sortKey="Zander, Mark" sort="Zander, Mark" uniqKey="Zander M" first="Mark" last="Zander">Mark Zander</name></noCountry><country name="Allemagne"><noRegion><name sortKey="La Camera, Sylvain" sort="La Camera, Sylvain" uniqKey="La Camera S" first="Sylvain" last="La Camera">Sylvain La Camera</name></noRegion></country></tree></affiliations></record>Pour manipuler ce 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