Silencing of PR-10-like proteins in Medicago truncatula results in an antagonistic induction of other PR proteins and in an increased tolerance upon infection with the oomycete Aphanomyces euteiches.
Identifieur interne : 000360 ( Main/Exploration ); précédent : 000359; suivant : 000361Silencing of PR-10-like proteins in Medicago truncatula results in an antagonistic induction of other PR proteins and in an increased tolerance upon infection with the oomycete Aphanomyces euteiches.
Auteurs : Frank Colditz [Allemagne] ; Karsten Niehaus ; Franziska KrajinskiSource :
- Planta [ 0032-0935 ] ; 2007.
Descripteurs français
- KwdFr :
- Aphanomyces (croissance et développement), Interférence par ARN (MeSH), Medicago truncatula (génétique), Medicago truncatula (microbiologie), Nodules racinaires de plante (microbiologie), Phénotype (MeSH), Protéines végétales (composition chimique), Protéines végétales (génétique), Racines de plante (composition chimique), Spectrométrie de masse (MeSH), Végétaux génétiquement modifiés (MeSH), Électrophorèse bidimensionnelle sur gel (MeSH).
- MESH :
- composition chimique : Protéines végétales, Racines de plante.
- croissance et développement : Aphanomyces.
- génétique : Medicago truncatula, Protéines végétales.
- microbiologie : Medicago truncatula, Nodules racinaires de plante.
- Interférence par ARN, Phénotype, Spectrométrie de masse, Végétaux génétiquement modifiés, Électrophorèse bidimensionnelle sur gel.
English descriptors
- KwdEn :
- Aphanomyces (growth & development), Electrophoresis, Gel, Two-Dimensional (MeSH), Mass Spectrometry (MeSH), Medicago truncatula (genetics), Medicago truncatula (microbiology), Phenotype (MeSH), Plant Proteins (chemistry), Plant Proteins (genetics), Plant Roots (chemistry), Plants, Genetically Modified (MeSH), RNA Interference (MeSH), Root Nodules, Plant (microbiology).
- MESH :
- chemical , chemistry : Plant Proteins.
- chemistry : Plant Roots.
- genetics : Medicago truncatula, Plant Proteins.
- growth & development : Aphanomyces.
- microbiology : Medicago truncatula, Root Nodules, Plant.
- Electrophoresis, Gel, Two-Dimensional, Mass Spectrometry, Phenotype, Plants, Genetically Modified, RNA Interference.
Abstract
Recent studies on the root proteome of Medicago truncatula (Gaertn.) showed an induction of pathogenesis-related (PR) proteins of the class 10 after infection with the oomycete pathogen Aphanomyces euteiches (Drechs.). To get insights into the function of these proteins during the parasitic root-microbe association, a gene knockdown approach using RNAi was carried out. Agrobacterium rhizogenes-mediated transformation of M. truncatula roots led to a knockdown of the Medicago PR10-1 gene in transgenic in vitro root cultures. Proteomic analyses of the MtPr10-1i root cultures showed that MtPr10-1 was efficiently knocked down in two MtPr10-1i lines. Moreover, five additional PR-10-type proteins annotated as abscisic acid responsive proteins (ABR17s) revealed also an almost complete silencing in these two lines. Inoculation of the root cultures with the oomycete root pathogen A. euteiches resulted in a clearly reduced colonization and thus in a suppressed infection development in MtPr10-1i roots as compared to that in roots of the transformation controls. In addition, MtPr10-1 silencing led to the induction of a new set of PR proteins after infection with A. euteiches including the de novo induction of two isoforms of thaumatin-like proteins (PR-5b), which were not detectable in A. euteiches-infected control roots. Thus, antagonistic induction of other PR proteins, which are normally repressed due to PR-10 expression, is supposed to cause an increased resistance of M. truncatula upon an A. euteiches in vitro infection. The results were also further confirmed by detecting increased PR-5b induction levels in 2-D gels of a previously analyzed M. truncatula line (F83.005-9) exhibiting increased A. euteiches tolerance associated with reduced PR-10 induction levels.
DOI: 10.1007/s00425-006-0466-y
PubMed: 17237953
Affiliations:
Links toward previous steps (curation, corpus...)
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an antagonistic induction of other PR proteins and in an increased tolerance upon infection with the oomycete Aphanomyces euteiches.</title><author><name sortKey="Colditz, Frank" sort="Colditz, Frank" uniqKey="Colditz F" first="Frank" last="Colditz">Frank Colditz</name><affiliation wicri:level="1"><nlm:affiliation>Department 7, Proteome and Metabolome Research, University of Bielefeld, Universitätsstrasse 25, 33615, Bielefeld, Germany. fcolditz@cebitec.uni-bielefeld.de</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Department 7, Proteome and Metabolome Research, University of Bielefeld, Universitätsstrasse 25, 33615, Bielefeld</wicri:regionArea><wicri:noRegion>33615, Bielefeld</wicri:noRegion><wicri:noRegion>33615, Bielefeld</wicri:noRegion><wicri:noRegion>Bielefeld</wicri:noRegion></affiliation></author><author><name sortKey="Niehaus, Karsten" sort="Niehaus, Karsten" uniqKey="Niehaus K" first="Karsten" last="Niehaus">Karsten Niehaus</name></author><author><name sortKey="Krajinski, Franziska" sort="Krajinski, Franziska" uniqKey="Krajinski F" first="Franziska" last="Krajinski">Franziska Krajinski</name></author></analytic><series><title level="j">Planta</title><idno type="ISSN">0032-0935</idno><imprint><date when="2007" type="published">2007</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aphanomyces (growth & development)</term><term>Electrophoresis, Gel, Two-Dimensional (MeSH)</term><term>Mass Spectrometry (MeSH)</term><term>Medicago truncatula (genetics)</term><term>Medicago truncatula (microbiology)</term><term>Phenotype (MeSH)</term><term>Plant Proteins (chemistry)</term><term>Plant Proteins (genetics)</term><term>Plant Roots (chemistry)</term><term>Plants, Genetically Modified (MeSH)</term><term>RNA Interference (MeSH)</term><term>Root Nodules, Plant (microbiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Aphanomyces (croissance et développement)</term><term>Interférence par ARN (MeSH)</term><term>Medicago truncatula (génétique)</term><term>Medicago truncatula (microbiologie)</term><term>Nodules racinaires de plante (microbiologie)</term><term>Phénotype (MeSH)</term><term>Protéines végétales (composition chimique)</term><term>Protéines végétales (génétique)</term><term>Racines de plante (composition chimique)</term><term>Spectrométrie de masse (MeSH)</term><term>Végétaux génétiquement modifiés (MeSH)</term><term>Électrophorèse bidimensionnelle sur gel (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Plant Proteins</term></keywords><keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Plant Roots</term></keywords><keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr"><term>Protéines végétales</term><term>Racines de plante</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Aphanomyces</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Medicago truncatula</term><term>Plant Proteins</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Aphanomyces</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Medicago truncatula</term><term>Protéines végétales</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Medicago truncatula</term><term>Nodules racinaires de plante</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Medicago truncatula</term><term>Root Nodules, Plant</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Electrophoresis, Gel, Two-Dimensional</term><term>Mass Spectrometry</term><term>Phenotype</term><term>Plants, Genetically Modified</term><term>RNA Interference</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Interférence par ARN</term><term>Phénotype</term><term>Spectrométrie de masse</term><term>Végétaux génétiquement modifiés</term><term>Électrophorèse bidimensionnelle sur gel</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Recent studies on the root proteome of Medicago truncatula (Gaertn.) showed an induction of pathogenesis-related (PR) proteins of the class 10 after infection with the oomycete pathogen Aphanomyces euteiches (Drechs.). To get insights into the function of these proteins during the parasitic root-microbe association, a gene knockdown approach using RNAi was carried out. Agrobacterium rhizogenes-mediated transformation of M. truncatula roots led to a knockdown of the Medicago PR10-1 gene in transgenic in vitro root cultures. Proteomic analyses of the MtPr10-1i root cultures showed that MtPr10-1 was efficiently knocked down in two MtPr10-1i lines. Moreover, five additional PR-10-type proteins annotated as abscisic acid responsive proteins (ABR17s) revealed also an almost complete silencing in these two lines. Inoculation of the root cultures with the oomycete root pathogen A. euteiches resulted in a clearly reduced colonization and thus in a suppressed infection development in MtPr10-1i roots as compared to that in roots of the transformation controls. In addition, MtPr10-1 silencing led to the induction of a new set of PR proteins after infection with A. euteiches including the de novo induction of two isoforms of thaumatin-like proteins (PR-5b), which were not detectable in A. euteiches-infected control roots. Thus, antagonistic induction of other PR proteins, which are normally repressed due to PR-10 expression, is supposed to cause an increased resistance of M. truncatula upon an A. euteiches in vitro infection. The results were also further confirmed by detecting increased PR-5b induction levels in 2-D gels of a previously analyzed M. truncatula line (F83.005-9) exhibiting increased A. euteiches tolerance associated with reduced PR-10 induction levels.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">17237953</PMID><DateCompleted><Year>2007</Year><Month>08</Month><Day>09</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0032-0935</ISSN><JournalIssue CitedMedium="Print"><Volume>226</Volume><Issue>1</Issue><PubDate><Year>2007</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Planta</Title><ISOAbbreviation>Planta</ISOAbbreviation></Journal><ArticleTitle>Silencing of PR-10-like proteins in Medicago truncatula results in an antagonistic induction of other PR proteins and in an increased tolerance upon infection with the oomycete Aphanomyces euteiches.</ArticleTitle><Pagination><MedlinePgn>57-71</MedlinePgn></Pagination><Abstract><AbstractText>Recent studies on the root proteome of Medicago truncatula (Gaertn.) showed an induction of pathogenesis-related (PR) proteins of the class 10 after infection with the oomycete pathogen Aphanomyces euteiches (Drechs.). To get insights into the function of these proteins during the parasitic root-microbe association, a gene knockdown approach using RNAi was carried out. Agrobacterium rhizogenes-mediated transformation of M. truncatula roots led to a knockdown of the Medicago PR10-1 gene in transgenic in vitro root cultures. Proteomic analyses of the MtPr10-1i root cultures showed that MtPr10-1 was efficiently knocked down in two MtPr10-1i lines. Moreover, five additional PR-10-type proteins annotated as abscisic acid responsive proteins (ABR17s) revealed also an almost complete silencing in these two lines. Inoculation of the root cultures with the oomycete root pathogen A. euteiches resulted in a clearly reduced colonization and thus in a suppressed infection development in MtPr10-1i roots as compared to that in roots of the transformation controls. In addition, MtPr10-1 silencing led to the induction of a new set of PR proteins after infection with A. euteiches including the de novo induction of two isoforms of thaumatin-like proteins (PR-5b), which were not detectable in A. euteiches-infected control roots. Thus, antagonistic induction of other PR proteins, which are normally repressed due to PR-10 expression, is supposed to cause an increased resistance of M. truncatula upon an A. euteiches in vitro infection. The results were also further confirmed by detecting increased PR-5b induction levels in 2-D gels of a previously analyzed M. truncatula line (F83.005-9) exhibiting increased A. euteiches tolerance associated with reduced PR-10 induction levels.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Colditz</LastName><ForeName>Frank</ForeName><Initials>F</Initials><AffiliationInfo><Affiliation>Department 7, Proteome and Metabolome Research, University of Bielefeld, Universitätsstrasse 25, 33615, Bielefeld, Germany. fcolditz@cebitec.uni-bielefeld.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Niehaus</LastName><ForeName>Karsten</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Krajinski</LastName><ForeName>Franziska</ForeName><Initials>F</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research 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MajorTopicYN="N">Medicago truncatula</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010641" MajorTopicYN="N">Phenotype</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D030821" MajorTopicYN="N">Plants, Genetically Modified</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D034622" MajorTopicYN="Y">RNA Interference</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D053204" 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sortKey="Colditz, Frank" sort="Colditz, Frank" uniqKey="Colditz F" first="Frank" last="Colditz">Frank Colditz</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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