Vectors for RNAi technology in poplar.
Identifieur interne : 004135 ( Main/Exploration ); précédent : 004134; suivant : 004136Vectors for RNAi technology in poplar.
Auteurs : S. Meyer [Allemagne] ; K. Nowak ; V K Sharma ; J. Schulze ; R R Mendel ; R. H NschSource :
- Plant biology (Stuttgart, Germany) [ 1435-8603 ]
Descripteurs français
- KwdFr :
- Amorces ADN (génétique), Glucuronidase (génétique), Gènes rapporteurs (MeSH), Interférence par ARN (MeSH), Populus (génétique), Protéines recombinantes (génétique), Rhizobium (génétique), Séquence nucléotidique (MeSH), Transformation génétique (MeSH), Vecteurs génétiques (MeSH), Végétaux génétiquement modifiés (MeSH).
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : DNA Primers, Glucuronidase, Recombinant Proteins.
- genetics : Populus, Rhizobium.
- Base Sequence, Genes, Reporter, Genetic Vectors, Plants, Genetically Modified, RNA Interference, Transformation, Genetic.
Abstract
The potential of double-stranded RNA interference (RNAi) technology was studied for down-regulation of gene expression in poplar. A set of vectors was constructed generating RNAs capable of duplex formation of sequences specific for the beta-glucuronidase (GUS) reporter gene system. These gene cassettes are driven by the CaMV-35S promoter. To address the question of gene silencing, we tested the functionality of these vectors, both in transient assays by transforming protoplasts with the RNAi constructs, and in stably transformed GUSexpressing poplar plants. Agrobacterium-mediated transformation of those GUS-expressing plants with a GUS-specific RNAi construct showed a strong down-regulation of the reporter gene. From these results we conclude that RNAi is also functional in poplar.
DOI: 10.1055/s-2004-815729
PubMed: 15095140
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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<wicri:regionArea>Institut für Pflanzenbiologie, Technische Universität Braunschweig, Braunschweig</wicri:regionArea>
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<author><name sortKey="Nowak, K" sort="Nowak, K" uniqKey="Nowak K" first="K" last="Nowak">K. Nowak</name>
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<author><name sortKey="Schulze, J" sort="Schulze, J" uniqKey="Schulze J" first="J" last="Schulze">J. Schulze</name>
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<author><name sortKey="Mendel, R R" sort="Mendel, R R" uniqKey="Mendel R" first="R R" last="Mendel">R R Mendel</name>
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<term>DNA Primers (genetics)</term>
<term>Genes, Reporter (MeSH)</term>
<term>Genetic Vectors (MeSH)</term>
<term>Glucuronidase (genetics)</term>
<term>Plants, Genetically Modified (MeSH)</term>
<term>Populus (genetics)</term>
<term>RNA Interference (MeSH)</term>
<term>Recombinant Proteins (genetics)</term>
<term>Rhizobium (genetics)</term>
<term>Transformation, Genetic (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Amorces ADN (génétique)</term>
<term>Glucuronidase (génétique)</term>
<term>Gènes rapporteurs (MeSH)</term>
<term>Interférence par ARN (MeSH)</term>
<term>Populus (génétique)</term>
<term>Protéines recombinantes (génétique)</term>
<term>Rhizobium (génétique)</term>
<term>Séquence nucléotidique (MeSH)</term>
<term>Transformation génétique (MeSH)</term>
<term>Vecteurs génétiques (MeSH)</term>
<term>Végétaux génétiquement modifiés (MeSH)</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>DNA Primers</term>
<term>Glucuronidase</term>
<term>Recombinant Proteins</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Populus</term>
<term>Rhizobium</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Amorces ADN</term>
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<term>Genetic Vectors</term>
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<term>RNA Interference</term>
<term>Transformation, Genetic</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Gènes rapporteurs</term>
<term>Interférence par ARN</term>
<term>Séquence nucléotidique</term>
<term>Transformation génétique</term>
<term>Vecteurs génétiques</term>
<term>Végétaux génétiquement modifiés</term>
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<front><div type="abstract" xml:lang="en">The potential of double-stranded RNA interference (RNAi) technology was studied for down-regulation of gene expression in poplar. A set of vectors was constructed generating RNAs capable of duplex formation of sequences specific for the beta-glucuronidase (GUS) reporter gene system. These gene cassettes are driven by the CaMV-35S promoter. To address the question of gene silencing, we tested the functionality of these vectors, both in transient assays by transforming protoplasts with the RNAi constructs, and in stably transformed GUSexpressing poplar plants. Agrobacterium-mediated transformation of those GUS-expressing plants with a GUS-specific RNAi construct showed a strong down-regulation of the reporter gene. From these results we conclude that RNAi is also functional in poplar.</div>
</front>
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<DateCompleted><Year>2004</Year>
<Month>05</Month>
<Day>19</Day>
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<DateRevised><Year>2008</Year>
<Month>01</Month>
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<JournalIssue CitedMedium="Print"><Volume>6</Volume>
<Issue>1</Issue>
<PubDate><MedlineDate>2004 Jan-Feb</MedlineDate>
</PubDate>
</JournalIssue>
<Title>Plant biology (Stuttgart, Germany)</Title>
<ISOAbbreviation>Plant Biol (Stuttg)</ISOAbbreviation>
</Journal>
<ArticleTitle>Vectors for RNAi technology in poplar.</ArticleTitle>
<Pagination><MedlinePgn>100-3</MedlinePgn>
</Pagination>
<Abstract><AbstractText>The potential of double-stranded RNA interference (RNAi) technology was studied for down-regulation of gene expression in poplar. A set of vectors was constructed generating RNAs capable of duplex formation of sequences specific for the beta-glucuronidase (GUS) reporter gene system. These gene cassettes are driven by the CaMV-35S promoter. To address the question of gene silencing, we tested the functionality of these vectors, both in transient assays by transforming protoplasts with the RNAi constructs, and in stably transformed GUSexpressing poplar plants. Agrobacterium-mediated transformation of those GUS-expressing plants with a GUS-specific RNAi construct showed a strong down-regulation of the reporter gene. From these results we conclude that RNAi is also functional in poplar.</AbstractText>
</Abstract>
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<ForeName>S</ForeName>
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