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Influence of Populus genotype on gene expression by the wood decay fungus Phanerochaete chrysosporium.

Identifieur interne : 000312 ( Main/Exploration ); précédent : 000311; suivant : 000313

Influence of Populus genotype on gene expression by the wood decay fungus Phanerochaete chrysosporium.

Auteurs : Jill Gaskell [États-Unis] ; Amber Marty [États-Unis] ; Michael Mozuch [États-Unis] ; Philip J. Kersten [États-Unis] ; Sandra Splinter Bondurant [États-Unis] ; Grzegorz Sabat [États-Unis] ; Ali Azarpira [États-Unis] ; John Ralph [États-Unis] ; Oleksandr Skyba [Canada] ; Shawn D. Mansfield [Canada] ; Robert A. Blanchette [États-Unis] ; Dan Cullen [États-Unis]

Source :

RBID : pubmed:25015893

Descripteurs français

English descriptors

Abstract

We examined gene expression patterns in the lignin-degrading fungus Phanerochaete chrysosporium when it colonizes hybrid poplar (Populus alba × tremula) and syringyl (S)-rich transgenic derivatives. A combination of microarrays and liquid chromatography-tandem mass spectrometry (LC-MS/MS) allowed detection of a total of 9,959 transcripts and 793 proteins. Comparisons of P. chrysosporium transcript abundance in medium containing poplar or glucose as a sole carbon source showed 113 regulated genes, 11 of which were significantly higher (>2-fold, P < 0.05) in transgenic line 64 relative to the parental line. Possibly related to the very large amounts of syringyl (S) units in this transgenic tree (94 mol% S), several oxidoreductases were among the upregulated genes. Peptides corresponding to a total of 18 oxidoreductases were identified in medium consisting of biomass from line 64 or 82 (85 mol% S) but not in the parental clone (65 mol% S). These results demonstrate that P. chrysosporium gene expression patterns are substantially influenced by lignin composition.

DOI: 10.1128/AEM.01604-14
PubMed: 25015893
PubMed Central: PMC4178610


Affiliations:


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Le document en format XML

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<term>Carbon (metabolism)</term>
<term>Chromatography, Liquid (MeSH)</term>
<term>Culture Media (chemistry)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Gene Expression Regulation, Fungal (MeSH)</term>
<term>Genotype (MeSH)</term>
<term>Lignin (metabolism)</term>
<term>Microarray Analysis (MeSH)</term>
<term>Phanerochaete (genetics)</term>
<term>Phanerochaete (growth & development)</term>
<term>Phanerochaete (metabolism)</term>
<term>Populus (genetics)</term>
<term>Tandem Mass Spectrometry (MeSH)</term>
<term>Wood (metabolism)</term>
<term>Wood (microbiology)</term>
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<term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Analyse sur microréseau (MeSH)</term>
<term>Bois (microbiologie)</term>
<term>Bois (métabolisme)</term>
<term>Carbone (métabolisme)</term>
<term>Chromatographie en phase liquide (MeSH)</term>
<term>Génotype (MeSH)</term>
<term>Lignine (métabolisme)</term>
<term>Milieux de culture (composition chimique)</term>
<term>Phanerochaete (croissance et développement)</term>
<term>Phanerochaete (génétique)</term>
<term>Phanerochaete (métabolisme)</term>
<term>Populus (génétique)</term>
<term>Régulation de l'expression des gènes fongiques (MeSH)</term>
<term>Spectrométrie de masse en tandem (MeSH)</term>
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<term>Lignin</term>
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<term>Milieux de culture</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Phanerochaete</term>
<term>Populus</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en">
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Phanerochaete</term>
<term>Populus</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Phanerochaete</term>
<term>Wood</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr">
<term>Bois</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Wood</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Bois</term>
<term>Carbone</term>
<term>Lignine</term>
<term>Phanerochaete</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Chromatography, Liquid</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Fungal</term>
<term>Genotype</term>
<term>Microarray Analysis</term>
<term>Tandem Mass Spectrometry</term>
</keywords>
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<term>Analyse de profil d'expression de gènes</term>
<term>Analyse sur microréseau</term>
<term>Chromatographie en phase liquide</term>
<term>Génotype</term>
<term>Régulation de l'expression des gènes fongiques</term>
<term>Spectrométrie de masse en tandem</term>
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<div type="abstract" xml:lang="en">We examined gene expression patterns in the lignin-degrading fungus Phanerochaete chrysosporium when it colonizes hybrid poplar (Populus alba × tremula) and syringyl (S)-rich transgenic derivatives. A combination of microarrays and liquid chromatography-tandem mass spectrometry (LC-MS/MS) allowed detection of a total of 9,959 transcripts and 793 proteins. Comparisons of P. chrysosporium transcript abundance in medium containing poplar or glucose as a sole carbon source showed 113 regulated genes, 11 of which were significantly higher (>2-fold, P < 0.05) in transgenic line 64 relative to the parental line. Possibly related to the very large amounts of syringyl (S) units in this transgenic tree (94 mol% S), several oxidoreductases were among the upregulated genes. Peptides corresponding to a total of 18 oxidoreductases were identified in medium consisting of biomass from line 64 or 82 (85 mol% S) but not in the parental clone (65 mol% S). These results demonstrate that P. chrysosporium gene expression patterns are substantially influenced by lignin composition. </div>
</front>
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<Day>08</Day>
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<Title>Applied and environmental microbiology</Title>
<ISOAbbreviation>Appl Environ Microbiol</ISOAbbreviation>
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<ArticleTitle>Influence of Populus genotype on gene expression by the wood decay fungus Phanerochaete chrysosporium.</ArticleTitle>
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<Abstract>
<AbstractText>We examined gene expression patterns in the lignin-degrading fungus Phanerochaete chrysosporium when it colonizes hybrid poplar (Populus alba × tremula) and syringyl (S)-rich transgenic derivatives. A combination of microarrays and liquid chromatography-tandem mass spectrometry (LC-MS/MS) allowed detection of a total of 9,959 transcripts and 793 proteins. Comparisons of P. chrysosporium transcript abundance in medium containing poplar or glucose as a sole carbon source showed 113 regulated genes, 11 of which were significantly higher (>2-fold, P < 0.05) in transgenic line 64 relative to the parental line. Possibly related to the very large amounts of syringyl (S) units in this transgenic tree (94 mol% S), several oxidoreductases were among the upregulated genes. Peptides corresponding to a total of 18 oxidoreductases were identified in medium consisting of biomass from line 64 or 82 (85 mol% S) but not in the parental clone (65 mol% S). These results demonstrate that P. chrysosporium gene expression patterns are substantially influenced by lignin composition. </AbstractText>
<CopyrightInformation>Copyright © 2014, American Society for Microbiology. All Rights Reserved.</CopyrightInformation>
</Abstract>
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<LastName>Gaskell</LastName>
<ForeName>Jill</ForeName>
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<LastName>Marty</LastName>
<ForeName>Amber</ForeName>
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<Affiliation>Department of Bacteriology, University of Wisconsin, Madison, Madison, Wisconsin, USA.</Affiliation>
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