Proteomic analysis of Pteris vittata fronds: two arbuscular mycorrhizal fungi differentially modulate protein expression under arsenic contamination.
Identifieur interne : 002634 ( Main/Exploration ); précédent : 002633; suivant : 002635Proteomic analysis of Pteris vittata fronds: two arbuscular mycorrhizal fungi differentially modulate protein expression under arsenic contamination.
Auteurs : Elisa Bona [Italie] ; Chiara Cattaneo ; Patrizia Cesaro ; Francesco Marsano ; Guido Lingua ; Maria Cavaletto ; Graziella BertaSource :
- Proteomics [ 1615-9861 ] ; 2010.
Descripteurs français
- KwdFr :
- Analyse de variance (MeSH), Arsenic (analyse), Arsenic (pharmacologie), Caroténoïdes (analyse), Caroténoïdes (métabolisme), Chlorophylle (analyse), Chlorophylle (métabolisme), Feuilles de plante (composition chimique), Feuilles de plante (métabolisme), Mycorhizes (métabolisme), Mycorhizes (physiologie), Phosphore (analyse), Phosphore (pharmacologie), Protéines végétales (composition chimique), Protéines végétales (métabolisme), Protéomique (méthodes), Pteris (microbiologie), Pteris (métabolisme), Racines de plante (composition chimique), Racines de plante (métabolisme), Spectrométrie de masse en tandem (MeSH), Stress physiologique (MeSH), Symbiose (physiologie).
- MESH :
- analyse : Arsenic, Caroténoïdes, Chlorophylle, Phosphore.
- composition chimique : Feuilles de plante, Protéines végétales, Racines de plante.
- microbiologie : Pteris.
- métabolisme : Caroténoïdes, Chlorophylle, Feuilles de plante, Mycorhizes, Protéines végétales, Pteris, Racines de plante.
- méthodes : Protéomique.
- pharmacologie : Arsenic, Phosphore.
- physiologie : Mycorhizes, Symbiose.
- Analyse de variance, Spectrométrie de masse en tandem, Stress physiologique.
English descriptors
- KwdEn :
- Analysis of Variance (MeSH), Arsenic (analysis), Arsenic (pharmacology), Carotenoids (analysis), Carotenoids (metabolism), Chlorophyll (analysis), Chlorophyll (metabolism), Mycorrhizae (metabolism), Mycorrhizae (physiology), Phosphorus (analysis), Phosphorus (pharmacology), Plant Leaves (chemistry), Plant Leaves (metabolism), Plant Proteins (chemistry), Plant Proteins (metabolism), Plant Roots (chemistry), Plant Roots (metabolism), Proteomics (methods), Pteris (metabolism), Pteris (microbiology), Stress, Physiological (MeSH), Symbiosis (physiology), Tandem Mass Spectrometry (MeSH).
- MESH :
- chemical , analysis : Arsenic, Carotenoids, Chlorophyll, Phosphorus.
- chemical , chemistry : Plant Proteins.
- chemical , metabolism : Carotenoids, Chlorophyll, Plant Proteins.
- chemical , pharmacology : Arsenic, Phosphorus.
- chemistry : Plant Leaves, Plant Roots.
- metabolism : Mycorrhizae, Plant Leaves, Plant Roots, Pteris.
- methods : Proteomics.
- microbiology : Pteris.
- physiology : Mycorrhizae, Symbiosis.
- Analysis of Variance, Stress, Physiological, Tandem Mass Spectrometry.
Abstract
Arbuscular mycorrhizae (AM) are the most widespread mutualistic symbioses between the roots of most land plants and a phylum of soil fungi. AM are known to influence plant performance by improving mineral nutrition, protecting against pathogens and enhancing resistance or tolerance to biotic and abiotic stresses. The aim of this study was to investigate the frond proteome of the arsenic hyperaccumulator fern Pteris vittata in plants that had been inoculated with one of the two AM fungi (Glomus mosseae or Gigaspora margarita) with and without arsenic treatment. A protective role for AM fungi colonisation in the absence of arsenic was indicated by the down-regulation of oxidative damage-related proteins. Arsenic treatment of mycorrhizal ferns induced the differential expression of 130 leaf proteins with specific responses in G. mosseae- and Gi. margarita-colonised plants. Up-regulation of multiple forms of glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, and enolase, primarily in G. mosseae-inoculated plants, suggests a central role for glycolytic enzymes in arsenic metabolism. Moreover, a putative arsenic transporter, PgPOR29, has been identified as an up-regulated protein by arsenic treatment.
DOI: 10.1002/pmic.200900436
PubMed: 20957753
Affiliations:
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xml:lang="fr"><term>Protéomique</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Arsenic</term><term>Phosphore</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Mycorhizes</term><term>Symbiose</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Mycorrhizae</term><term>Symbiosis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Analysis of Variance</term><term>Stress, Physiological</term><term>Tandem Mass Spectrometry</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Analyse de variance</term><term>Spectrométrie de masse en tandem</term><term>Stress physiologique</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Arbuscular mycorrhizae (AM) are the most widespread mutualistic symbioses between the roots of most land plants and a phylum of soil fungi. AM are known to influence plant performance by improving mineral nutrition, protecting against pathogens and enhancing resistance or tolerance to biotic and abiotic stresses. The aim of this study was to investigate the frond proteome of the arsenic hyperaccumulator fern Pteris vittata in plants that had been inoculated with one of the two AM fungi (Glomus mosseae or Gigaspora margarita) with and without arsenic treatment. A protective role for AM fungi colonisation in the absence of arsenic was indicated by the down-regulation of oxidative damage-related proteins. Arsenic treatment of mycorrhizal ferns induced the differential expression of 130 leaf proteins with specific responses in G. mosseae- and Gi. margarita-colonised plants. Up-regulation of multiple forms of glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, and enolase, primarily in G. mosseae-inoculated plants, suggests a central role for glycolytic enzymes in arsenic metabolism. Moreover, a putative arsenic transporter, PgPOR29, has been identified as an up-regulated protein by arsenic treatment.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20957753</PMID><DateCompleted><Year>2011</Year><Month>02</Month><Day>28</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1615-9861</ISSN><JournalIssue CitedMedium="Internet"><Volume>10</Volume><Issue>21</Issue><PubDate><Year>2010</Year><Month>Nov</Month></PubDate></JournalIssue><Title>Proteomics</Title><ISOAbbreviation>Proteomics</ISOAbbreviation></Journal><ArticleTitle>Proteomic analysis of Pteris vittata fronds: two arbuscular mycorrhizal fungi differentially modulate protein expression under arsenic contamination.</ArticleTitle><Pagination><MedlinePgn>3811-34</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1002/pmic.200900436</ELocationID><Abstract><AbstractText>Arbuscular mycorrhizae (AM) are the most widespread mutualistic symbioses between the roots of most land plants and a phylum of soil fungi. AM are known to influence plant performance by improving mineral nutrition, protecting against pathogens and enhancing resistance or tolerance to biotic and abiotic stresses. The aim of this study was to investigate the frond proteome of the arsenic hyperaccumulator fern Pteris vittata in plants that had been inoculated with one of the two AM fungi (Glomus mosseae or Gigaspora margarita) with and without arsenic treatment. A protective role for AM fungi colonisation in the absence of arsenic was indicated by the down-regulation of oxidative damage-related proteins. Arsenic treatment of mycorrhizal ferns induced the differential expression of 130 leaf proteins with specific responses in G. mosseae- and Gi. margarita-colonised plants. Up-regulation of multiple forms of glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, and enolase, primarily in G. mosseae-inoculated plants, suggests a central role for glycolytic enzymes in arsenic metabolism. Moreover, a putative arsenic transporter, PgPOR29, has been identified as an up-regulated protein by arsenic treatment.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bona</LastName><ForeName>Elisa</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Department of Environmental and Life Sciences, University of Piemonte Orientale A. Avogadro, Alessandria, Novara, Vercelli, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cattaneo</LastName><ForeName>Chiara</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Cesaro</LastName><ForeName>Patrizia</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Marsano</LastName><ForeName>Francesco</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Lingua</LastName><ForeName>Guido</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Cavaletto</LastName><ForeName>Maria</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Berta</LastName><ForeName>Graziella</ForeName><Initials>G</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>Germany</Country><MedlineTA>Proteomics</MedlineTA><NlmUniqueID>101092707</NlmUniqueID><ISSNLinking>1615-9853</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>1406-65-1</RegistryNumber><NameOfSubstance UI="D002734">Chlorophyll</NameOfSubstance></Chemical><Chemical><RegistryNumber>27YLU75U4W</RegistryNumber><NameOfSubstance UI="D010758">Phosphorus</NameOfSubstance></Chemical><Chemical><RegistryNumber>36-88-4</RegistryNumber><NameOfSubstance UI="D002338">Carotenoids</NameOfSubstance></Chemical><Chemical><RegistryNumber>N712M78A8G</RegistryNumber><NameOfSubstance UI="D001151">Arsenic</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000704" MajorTopicYN="N">Analysis of Variance</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001151" MajorTopicYN="N">Arsenic</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002338" MajorTopicYN="N">Carotenoids</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002734" MajorTopicYN="N">Chlorophyll</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010758" MajorTopicYN="N">Phosphorus</DescriptorName><QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018517" MajorTopicYN="N">Plant Roots</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D040901" MajorTopicYN="N">Proteomics</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D032495" MajorTopicYN="N">Pteris</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013312" MajorTopicYN="N">Stress, Physiological</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013559" MajorTopicYN="N">Symbiosis</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D053719" MajorTopicYN="N">Tandem Mass Spectrometry</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate 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M" first="Maria" last="Cavaletto">Maria Cavaletto</name><name sortKey="Cesaro, Patrizia" sort="Cesaro, Patrizia" uniqKey="Cesaro P" first="Patrizia" last="Cesaro">Patrizia Cesaro</name><name sortKey="Lingua, Guido" sort="Lingua, Guido" uniqKey="Lingua G" first="Guido" last="Lingua">Guido Lingua</name><name sortKey="Marsano, Francesco" sort="Marsano, Francesco" uniqKey="Marsano F" first="Francesco" last="Marsano">Francesco Marsano</name></noCountry><country name="Italie"><noRegion><name sortKey="Bona, Elisa" sort="Bona, Elisa" uniqKey="Bona E" first="Elisa" last="Bona">Elisa Bona</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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