Mutations in DMI3 and SUNN modify the appressorium-responsive root proteome in arbuscular mycorrhiza.
Identifieur interne : 003183 ( Main/Corpus ); précédent : 003182; suivant : 003184Mutations in DMI3 and SUNN modify the appressorium-responsive root proteome in arbuscular mycorrhiza.
Auteurs : Nardjis Amiour ; Ghislaine Recorbet ; Franck Robert ; Silvio Gianinazzi ; Eliane Dumas-GaudotSource :
- Molecular plant-microbe interactions : MPMI [ 0894-0282 ] ; 2006.
English descriptors
- KwdEn :
- Electrophoresis, Gel, Two-Dimensional (methods), Genes, Plant (genetics), Mass Spectrometry (methods), Medicago truncatula (genetics), Medicago truncatula (metabolism), Medicago truncatula (microbiology), Mutation (genetics), Mycorrhizae (growth & development), Plant Proteins (analysis), Plant Roots (genetics), Plant Roots (metabolism), Plant Roots (microbiology), Proteome (analysis), Proteomics (methods), Symbiosis (physiology), Time Factors (MeSH).
- MESH :
- chemical , analysis : Plant Proteins, Proteome.
- genetics : Genes, Plant, Medicago truncatula, Mutation, Plant Roots.
- growth & development : Mycorrhizae.
- metabolism : Medicago truncatula, Plant Roots.
- methods : Electrophoresis, Gel, Two-Dimensional, Mass Spectrometry, Proteomics.
- microbiology : Medicago truncatula, Plant Roots.
- physiology : Symbiosis.
- Time Factors.
Abstract
Modification of the Medicago truncatula root proteome during the early stage of arbuscular mycorrhizal symbiosis was investigated by comparing, using two-dimensional electrophoresis, the protein patterns obtained from non-inoculated roots and roots synchronized for Glomus intraradices appressorium formation. This approach was conducted in wild-type (J5), mycorrhiza-defective (TRV25, dmi3), and autoregulation-defective (TR122, sunn) M. truncatula genotypes. The groups of proteins that responded to appressorium formation were further compared between wild-type and mutant genotypes; few overlaps and major differences were recorded, demonstrating that mutations in DMI3 and SUNN modified the appressorium-responsive root proteome. Except for a chalcone reductase, none of the differentially displayed proteins that could be identified using matrix-assisted laser desorption ionization time-of-flight mass spectrometry previously was known as appressorium responsive. A DMI3-dependent increased accumulation of signal transduction-related proteins (dehydroascorbate reductase, cyclophilin, and actin depolymerization factor) was found to precede mycorrhiza establishment. Differences in the accumulation of proteins related to plant defense reactions, cytoskeleton rearrangements, and auxin signaling upon symbiont contact were recorded between wild-type and hypermycorrhizal genotypes, pointing to some putative pathways by which SUNN may regulate very early arbuscule formation.
DOI: 10.1094/MPMI-19-0988
PubMed: 16941903
Links to Exploration step
pubmed:16941903Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Mutations in DMI3 and SUNN modify the appressorium-responsive root proteome in arbuscular mycorrhiza.</title><author><name sortKey="Amiour, Nardjis" sort="Amiour, Nardjis" uniqKey="Amiour N" first="Nardjis" last="Amiour">Nardjis Amiour</name><affiliation><nlm:affiliation>Unité Mixte de Recherche Plante-Microbe-Environnement INRA 1088, CNRS 5184, Université de Bourgogne, INRA-CMSE, BP 86510, 21065 Dijon, France.</nlm:affiliation></affiliation></author><author><name sortKey="Recorbet, Ghislaine" sort="Recorbet, Ghislaine" uniqKey="Recorbet G" first="Ghislaine" last="Recorbet">Ghislaine Recorbet</name></author><author><name sortKey="Robert, Franck" sort="Robert, Franck" uniqKey="Robert F" first="Franck" last="Robert">Franck Robert</name></author><author><name sortKey="Gianinazzi, Silvio" sort="Gianinazzi, Silvio" uniqKey="Gianinazzi S" first="Silvio" last="Gianinazzi">Silvio Gianinazzi</name></author><author><name sortKey="Dumas Gaudot, Eliane" sort="Dumas Gaudot, Eliane" uniqKey="Dumas Gaudot E" first="Eliane" last="Dumas-Gaudot">Eliane Dumas-Gaudot</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2006">2006</date><idno type="RBID">pubmed:16941903</idno><idno type="pmid">16941903</idno><idno type="doi">10.1094/MPMI-19-0988</idno><idno type="wicri:Area/Main/Corpus">003183</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">003183</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Mutations in DMI3 and SUNN modify the appressorium-responsive root proteome in arbuscular mycorrhiza.</title><author><name sortKey="Amiour, Nardjis" sort="Amiour, Nardjis" uniqKey="Amiour N" first="Nardjis" last="Amiour">Nardjis Amiour</name><affiliation><nlm:affiliation>Unité Mixte de Recherche Plante-Microbe-Environnement INRA 1088, CNRS 5184, Université de Bourgogne, INRA-CMSE, BP 86510, 21065 Dijon, France.</nlm:affiliation></affiliation></author><author><name sortKey="Recorbet, Ghislaine" sort="Recorbet, Ghislaine" uniqKey="Recorbet G" first="Ghislaine" last="Recorbet">Ghislaine Recorbet</name></author><author><name sortKey="Robert, Franck" sort="Robert, Franck" uniqKey="Robert F" first="Franck" last="Robert">Franck Robert</name></author><author><name sortKey="Gianinazzi, Silvio" sort="Gianinazzi, Silvio" uniqKey="Gianinazzi S" first="Silvio" last="Gianinazzi">Silvio Gianinazzi</name></author><author><name sortKey="Dumas Gaudot, Eliane" sort="Dumas Gaudot, Eliane" uniqKey="Dumas Gaudot E" first="Eliane" last="Dumas-Gaudot">Eliane Dumas-Gaudot</name></author></analytic><series><title level="j">Molecular plant-microbe interactions : MPMI</title><idno type="ISSN">0894-0282</idno><imprint><date when="2006" type="published">2006</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Electrophoresis, Gel, Two-Dimensional (methods)</term><term>Genes, Plant (genetics)</term><term>Mass Spectrometry (methods)</term><term>Medicago truncatula (genetics)</term><term>Medicago truncatula (metabolism)</term><term>Medicago truncatula (microbiology)</term><term>Mutation (genetics)</term><term>Mycorrhizae (growth & development)</term><term>Plant Proteins (analysis)</term><term>Plant Roots (genetics)</term><term>Plant Roots (metabolism)</term><term>Plant Roots (microbiology)</term><term>Proteome (analysis)</term><term>Proteomics (methods)</term><term>Symbiosis (physiology)</term><term>Time Factors (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>Plant Proteins</term><term>Proteome</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Genes, Plant</term><term>Medicago truncatula</term><term>Mutation</term><term>Plant Roots</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Medicago truncatula</term><term>Plant Roots</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Electrophoresis, Gel, Two-Dimensional</term><term>Mass Spectrometry</term><term>Proteomics</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Medicago truncatula</term><term>Plant Roots</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Symbiosis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Time Factors</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Modification of the Medicago truncatula root proteome during the early stage of arbuscular mycorrhizal symbiosis was investigated by comparing, using two-dimensional electrophoresis, the protein patterns obtained from non-inoculated roots and roots synchronized for Glomus intraradices appressorium formation. This approach was conducted in wild-type (J5), mycorrhiza-defective (TRV25, dmi3), and autoregulation-defective (TR122, sunn) M. truncatula genotypes. The groups of proteins that responded to appressorium formation were further compared between wild-type and mutant genotypes; few overlaps and major differences were recorded, demonstrating that mutations in DMI3 and SUNN modified the appressorium-responsive root proteome. Except for a chalcone reductase, none of the differentially displayed proteins that could be identified using matrix-assisted laser desorption ionization time-of-flight mass spectrometry previously was known as appressorium responsive. A DMI3-dependent increased accumulation of signal transduction-related proteins (dehydroascorbate reductase, cyclophilin, and actin depolymerization factor) was found to precede mycorrhiza establishment. Differences in the accumulation of proteins related to plant defense reactions, cytoskeleton rearrangements, and auxin signaling upon symbiont contact were recorded between wild-type and hypermycorrhizal genotypes, pointing to some putative pathways by which SUNN may regulate very early arbuscule formation.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16941903</PMID><DateCompleted><Year>2006</Year><Month>10</Month><Day>27</Day></DateCompleted><DateRevised><Year>2006</Year><Month>11</Month><Day>15</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0894-0282</ISSN><JournalIssue CitedMedium="Print"><Volume>19</Volume><Issue>9</Issue><PubDate><Year>2006</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Molecular plant-microbe interactions : MPMI</Title><ISOAbbreviation>Mol Plant Microbe Interact</ISOAbbreviation></Journal><ArticleTitle>Mutations in DMI3 and SUNN modify the appressorium-responsive root proteome in arbuscular mycorrhiza.</ArticleTitle><Pagination><MedlinePgn>988-97</MedlinePgn></Pagination><Abstract><AbstractText>Modification of the Medicago truncatula root proteome during the early stage of arbuscular mycorrhizal symbiosis was investigated by comparing, using two-dimensional electrophoresis, the protein patterns obtained from non-inoculated roots and roots synchronized for Glomus intraradices appressorium formation. This approach was conducted in wild-type (J5), mycorrhiza-defective (TRV25, dmi3), and autoregulation-defective (TR122, sunn) M. truncatula genotypes. The groups of proteins that responded to appressorium formation were further compared between wild-type and mutant genotypes; few overlaps and major differences were recorded, demonstrating that mutations in DMI3 and SUNN modified the appressorium-responsive root proteome. Except for a chalcone reductase, none of the differentially displayed proteins that could be identified using matrix-assisted laser desorption ionization time-of-flight mass spectrometry previously was known as appressorium responsive. A DMI3-dependent increased accumulation of signal transduction-related proteins (dehydroascorbate reductase, cyclophilin, and actin depolymerization factor) was found to precede mycorrhiza establishment. Differences in the accumulation of proteins related to plant defense reactions, cytoskeleton rearrangements, and auxin signaling upon symbiont contact were recorded between wild-type and hypermycorrhizal genotypes, pointing to some putative pathways by which SUNN may regulate very early arbuscule formation.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Amiour</LastName><ForeName>Nardjis</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Unité Mixte de Recherche Plante-Microbe-Environnement INRA 1088, CNRS 5184, Université de Bourgogne, INRA-CMSE, BP 86510, 21065 Dijon, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Recorbet</LastName><ForeName>Ghislaine</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Robert</LastName><ForeName>Franck</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Gianinazzi</LastName><ForeName>Silvio</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Dumas-Gaudot</LastName><ForeName>Eliane</ForeName><Initials>E</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></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Mol Plant Microbe Interact</MedlineTA><NlmUniqueID>9107902</NlmUniqueID><ISSNLinking>0894-0282</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020543">Proteome</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D015180" MajorTopicYN="N">Electrophoresis, Gel, Two-Dimensional</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017343" MajorTopicYN="N">Genes, Plant</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013058" MajorTopicYN="N">Mass Spectrometry</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D046913" MajorTopicYN="N">Medicago truncatula</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009154" MajorTopicYN="N">Mutation</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020543" MajorTopicYN="N">Proteome</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="Y">analysis</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D040901" MajorTopicYN="N">Proteomics</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013559" MajorTopicYN="N">Symbiosis</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>9</Month><Day>1</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>10</Month><Day>28</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>9</Month><Day>1</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16941903</ArticleId><ArticleId IdType="doi">10.1094/MPMI-19-0988</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Bois/explor/MycorrhizaeV1/Data/Main/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003183 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd -nk 003183 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Bois
|area= MycorrhizaeV1
|flux= Main
|étape= Corpus
|type= RBID
|clé= pubmed:16941903
|texte= Mutations in DMI3 and SUNN modify the appressorium-responsive root proteome in arbuscular mycorrhiza.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Corpus/RBID.i -Sk "pubmed:16941903" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd \
| NlmPubMed2Wicri -a MycorrhizaeV1
| This area was generated with Dilib version V0.6.37. |  |