Serveur d'exploration sur le peuplier

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A multi-omics approach reveals function of Secretory Carrier-Associated Membrane Proteins in wood formation of​ ​​Populus​​ ​trees.

Identifieur interne : 001075 ( Main/Exploration ); précédent : 001074; suivant : 001076

A multi-omics approach reveals function of Secretory Carrier-Associated Membrane Proteins in wood formation of​ ​​Populus​​ ​trees.

Auteurs : Ogonna Obudulu [Suède] ; Niklas M Hler [Suède, Norvège] ; Tomas Skotare [Suède] ; Joakim Bygdell [Suède] ; Ilka N. Abreu [Suède] ; Maria Ahnlund [Suède] ; Madhavi Latha Gandla [Suède] ; Anna Petterle [Suède] ; Thomas Moritz [Suède] ; Torgeir R. Hvidsten [Suède, Norvège] ; Leif J. Jönsson [Suède] ; Gunnar Wingsle [Suède] ; Johan Trygg [Suède] ; Hannele Tuominen [Suède]

Source :

RBID : pubmed:29298676

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English descriptors

Abstract

BACKGROUND

Secretory Carrier-Associated Membrane Proteins (SCAMPs) are highly conserved 32-38 kDa proteins that are involved in membrane trafficking. A systems approach was taken to elucidate function of SCAMPs in wood formation of Populus trees. Phenotypic and multi-omics analyses were performed in woody tissues of transgenic Populus trees carrying an RNAi construct for Populus tremula x tremuloides SCAMP3 (PttSCAMP3; Potri.019G104000).

RESULTS

The woody tissues of the transgenic trees displayed increased amounts of both polysaccharides and lignin oligomers, indicating increased deposition of both the carbohydrate and lignin components of the secondary cell walls. This coincided with a tendency towards increased wood density as well as significantly increased thickness of the suberized cork in the transgenic lines. Multivariate OnPLS (orthogonal projections to latent structures) modeling of five different omics datasets (the transcriptome, proteome, GC-MS metabolome, LC-MS metabolome and pyrolysis-GC/MS metabolome) collected from the secondary xylem tissues of the stem revealed systemic variation in the different variables in the transgenic lines, including changes that correlated with the changes in the secondary cell wall composition. The OnPLS model also identified a rather large number of proteins that were more abundant in the transgenic lines than in the wild type. Several of these were related to secretion and/or endocytosis as well as both primary and secondary cell wall biosynthesis.

CONCLUSIONS

Populus SCAMP proteins were shown to influence accumulation of secondary cell wall components, including polysaccharides and phenolic compounds, in the woody tissues of Populus tree stems. Our multi-omics analyses combined with the OnPLS modelling suggest that this function is mediated by changes in membrane trafficking to fine-tune the abundance of cell wall precursors and/or proteins involved in cell wall biosynthesis and transport. The data provides a multi-level source of information for future studies on the function of the SCAMP proteins in plant stem tissues.


DOI: 10.1186/s12864-017-4411-1
PubMed: 29298676
PubMed Central: PMC5753437


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<title xml:lang="en">A multi-omics approach reveals function of Secretory Carrier-Associated Membrane Proteins in wood formation of​ ​​Populus​​ ​trees.</title>
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<nlm:affiliation>Present address: Department of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, 40530, Gothenburg, Sweden.</nlm:affiliation>
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<name sortKey="M Hler, Niklas" sort="M Hler, Niklas" uniqKey="M Hler N" first="Niklas" last="M Hler">Niklas M Hler</name>
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<nlm:affiliation>Faculty of Chemistry, Biotechnology and Food Science, Norwegian, University of Life Sciences, 1432, Ås, Norway.</nlm:affiliation>
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<name sortKey="Hvidsten, Torgeir R" sort="Hvidsten, Torgeir R" uniqKey="Hvidsten T" first="Torgeir R" last="Hvidsten">Torgeir R. Hvidsten</name>
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<nlm:affiliation>Faculty of Chemistry, Biotechnology and Food Science, Norwegian, University of Life Sciences, 1432, Ås, Norway.</nlm:affiliation>
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<wicri:regionArea>Faculty of Chemistry, Biotechnology and Food Science, Norwegian, University of Life Sciences, 1432, Ås</wicri:regionArea>
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<name sortKey="Jonsson, Leif J" sort="Jonsson, Leif J" uniqKey="Jonsson L" first="Leif J" last="Jönsson">Leif J. Jönsson</name>
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<nlm:affiliation>Department of Chemistry, Umeå University, 90187, Umeå, Sweden.</nlm:affiliation>
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<name sortKey="Wingsle, Gunnar" sort="Wingsle, Gunnar" uniqKey="Wingsle G" first="Gunnar" last="Wingsle">Gunnar Wingsle</name>
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<affiliation wicri:level="1">
<nlm:affiliation>Computational life science cluster (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.</nlm:affiliation>
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<author>
<name sortKey="Tuominen, Hannele" sort="Tuominen, Hannele" uniqKey="Tuominen H" first="Hannele" last="Tuominen">Hannele Tuominen</name>
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<nlm:affiliation>Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, 90187, Umeå, Sweden. hannele.tuominen@umu.se.</nlm:affiliation>
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<series>
<title level="j">BMC genomics</title>
<idno type="eISSN">1471-2164</idno>
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<date when="2018" type="published">2018</date>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Biosynthetic Pathways (genetics)</term>
<term>Cell Wall (metabolism)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Membrane Proteins (genetics)</term>
<term>Membrane Proteins (metabolism)</term>
<term>Membrane Proteins (physiology)</term>
<term>Metabolome (MeSH)</term>
<term>Metabolomics (MeSH)</term>
<term>Monosaccharides (metabolism)</term>
<term>Multigene Family (MeSH)</term>
<term>Phenols (metabolism)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Plant Proteins (physiology)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
<term>Proteomics (MeSH)</term>
<term>Trees (MeSH)</term>
<term>Wood (genetics)</term>
<term>Wood (metabolism)</term>
<term>Xylem (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Arbres (MeSH)</term>
<term>Bois (génétique)</term>
<term>Bois (métabolisme)</term>
<term>Famille multigénique (MeSH)</term>
<term>Métabolome (MeSH)</term>
<term>Métabolomique (MeSH)</term>
<term>Oses (métabolisme)</term>
<term>Paroi cellulaire (métabolisme)</term>
<term>Phénols (métabolisme)</term>
<term>Populus (génétique)</term>
<term>Populus (métabolisme)</term>
<term>Protéines membranaires (génétique)</term>
<term>Protéines membranaires (métabolisme)</term>
<term>Protéines membranaires (physiologie)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Protéines végétales (physiologie)</term>
<term>Protéomique (MeSH)</term>
<term>Voies de biosynthèse (génétique)</term>
<term>Xylème (métabolisme)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Membrane Proteins</term>
<term>Plant Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Biosynthetic Pathways</term>
<term>Populus</term>
<term>Wood</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Bois</term>
<term>Populus</term>
<term>Protéines membranaires</term>
<term>Protéines végétales</term>
<term>Voies de biosynthèse</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Cell Wall</term>
<term>Membrane Proteins</term>
<term>Monosaccharides</term>
<term>Phenols</term>
<term>Plant Proteins</term>
<term>Populus</term>
<term>Wood</term>
<term>Xylem</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Bois</term>
<term>Oses</term>
<term>Paroi cellulaire</term>
<term>Phénols</term>
<term>Populus</term>
<term>Protéines membranaires</term>
<term>Protéines végétales</term>
<term>Xylème</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Protéines membranaires</term>
<term>Protéines végétales</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en">
<term>Membrane Proteins</term>
<term>Plant Proteins</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Gene Expression Profiling</term>
<term>Metabolome</term>
<term>Metabolomics</term>
<term>Multigene Family</term>
<term>Proteomics</term>
<term>Trees</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de profil d'expression de gènes</term>
<term>Arbres</term>
<term>Famille multigénique</term>
<term>Métabolome</term>
<term>Métabolomique</term>
<term>Protéomique</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Secretory Carrier-Associated Membrane Proteins (SCAMPs) are highly conserved 32-38 kDa proteins that are involved in membrane trafficking. A systems approach was taken to elucidate function of SCAMPs in wood formation of Populus trees. Phenotypic and multi-omics analyses were performed in woody tissues of transgenic Populus trees carrying an RNAi construct for Populus tremula x tremuloides SCAMP3 (PttSCAMP3; Potri.019G104000).</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The woody tissues of the transgenic trees displayed increased amounts of both polysaccharides and lignin oligomers, indicating increased deposition of both the carbohydrate and lignin components of the secondary cell walls. This coincided with a tendency towards increased wood density as well as significantly increased thickness of the suberized cork in the transgenic lines. Multivariate OnPLS (orthogonal projections to latent structures) modeling of five different omics datasets (the transcriptome, proteome, GC-MS metabolome, LC-MS metabolome and pyrolysis-GC/MS metabolome) collected from the secondary xylem tissues of the stem revealed systemic variation in the different variables in the transgenic lines, including changes that correlated with the changes in the secondary cell wall composition. The OnPLS model also identified a rather large number of proteins that were more abundant in the transgenic lines than in the wild type. Several of these were related to secretion and/or endocytosis as well as both primary and secondary cell wall biosynthesis.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>Populus SCAMP proteins were shown to influence accumulation of secondary cell wall components, including polysaccharides and phenolic compounds, in the woody tissues of Populus tree stems. Our multi-omics analyses combined with the OnPLS modelling suggest that this function is mediated by changes in membrane trafficking to fine-tune the abundance of cell wall precursors and/or proteins involved in cell wall biosynthesis and transport. The data provides a multi-level source of information for future studies on the function of the SCAMP proteins in plant stem tissues.</p>
</div>
</front>
</TEI>
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<DateCompleted>
<Year>2018</Year>
<Month>07</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Electronic">
<Journal>
<ISSN IssnType="Electronic">1471-2164</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>19</Volume>
<Issue>1</Issue>
<PubDate>
<Year>2018</Year>
<Month>01</Month>
<Day>03</Day>
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</JournalIssue>
<Title>BMC genomics</Title>
<ISOAbbreviation>BMC Genomics</ISOAbbreviation>
</Journal>
<ArticleTitle>A multi-omics approach reveals function of Secretory Carrier-Associated Membrane Proteins in wood formation of​ ​​Populus​​ ​trees.</ArticleTitle>
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<MedlinePgn>11</MedlinePgn>
</Pagination>
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<Abstract>
<AbstractText Label="BACKGROUND">Secretory Carrier-Associated Membrane Proteins (SCAMPs) are highly conserved 32-38 kDa proteins that are involved in membrane trafficking. A systems approach was taken to elucidate function of SCAMPs in wood formation of Populus trees. Phenotypic and multi-omics analyses were performed in woody tissues of transgenic Populus trees carrying an RNAi construct for Populus tremula x tremuloides SCAMP3 (PttSCAMP3; Potri.019G104000).</AbstractText>
<AbstractText Label="RESULTS">The woody tissues of the transgenic trees displayed increased amounts of both polysaccharides and lignin oligomers, indicating increased deposition of both the carbohydrate and lignin components of the secondary cell walls. This coincided with a tendency towards increased wood density as well as significantly increased thickness of the suberized cork in the transgenic lines. Multivariate OnPLS (orthogonal projections to latent structures) modeling of five different omics datasets (the transcriptome, proteome, GC-MS metabolome, LC-MS metabolome and pyrolysis-GC/MS metabolome) collected from the secondary xylem tissues of the stem revealed systemic variation in the different variables in the transgenic lines, including changes that correlated with the changes in the secondary cell wall composition. The OnPLS model also identified a rather large number of proteins that were more abundant in the transgenic lines than in the wild type. Several of these were related to secretion and/or endocytosis as well as both primary and secondary cell wall biosynthesis.</AbstractText>
<AbstractText Label="CONCLUSIONS">Populus SCAMP proteins were shown to influence accumulation of secondary cell wall components, including polysaccharides and phenolic compounds, in the woody tissues of Populus tree stems. Our multi-omics analyses combined with the OnPLS modelling suggest that this function is mediated by changes in membrane trafficking to fine-tune the abundance of cell wall precursors and/or proteins involved in cell wall biosynthesis and transport. The data provides a multi-level source of information for future studies on the function of the SCAMP proteins in plant stem tissues.</AbstractText>
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<LastName>Obudulu</LastName>
<ForeName>Ogonna</ForeName>
<Initials>O</Initials>
<AffiliationInfo>
<Affiliation>Umeå Plant Science Centre, Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences, 90183, Umeå, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Computational life science cluster (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Present address: Department of Microbiology and Immunology, Institute of Biomedicine, University of Gothenburg, 40530, Gothenburg, Sweden.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Mähler</LastName>
<ForeName>Niklas</ForeName>
<Initials>N</Initials>
<AffiliationInfo>
<Affiliation>Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, 90187, Umeå, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Faculty of Chemistry, Biotechnology and Food Science, Norwegian, University of Life Sciences, 1432, Ås, Norway.</Affiliation>
</AffiliationInfo>
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<LastName>Skotare</LastName>
<ForeName>Tomas</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Chemistry, Umeå University, 90187, Umeå, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
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<ForeName>Joakim</ForeName>
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<AffiliationInfo>
<Affiliation>Department of Chemistry, Umeå University, 90187, Umeå, Sweden.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Computational life science cluster (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.</Affiliation>
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<ForeName>Ilka N</ForeName>
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<ForeName>Torgeir R</ForeName>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Faculty of Chemistry, Biotechnology and Food Science, Norwegian, University of Life Sciences, 1432, Ås, Norway.</Affiliation>
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<ForeName>Gunnar</ForeName>
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<LastName>Trygg</LastName>
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<Affiliation>Computational life science cluster (CLiC), Department of Chemistry, Umeå University, Umeå, Sweden.</Affiliation>
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<AffiliationInfo>
<Affiliation>Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, 90187, Umeå, Sweden. hannele.tuominen@umu.se.</Affiliation>
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<Grant>
<GrantID>232-2009-1698</GrantID>
<Agency>Svenska Forskningsrådet Formas</Agency>
<Country>International</Country>
</Grant>
<Grant>
<GrantID>RBP14-0011</GrantID>
<Agency>Stiftelsen för Strategisk Forskning</Agency>
<Country>International</Country>
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<Grant>
<GrantID>2015-02290</GrantID>
<Agency>VINNOVA (SE)</Agency>
<Country>International</Country>
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<Grant>
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