AgrobacTransV1, Main, Exploration, bibRecord, 000775

pSAT vectors: a modular series of plasmids for autofluorescent protein tagging and expression of multiple genes in plants.

Identifieur interne : 000775 ( Main/Exploration ); précédent : 000774; suivant : 000776

pSAT vectors: a modular series of plasmids for autofluorescent protein tagging and expression of multiple genes in plants.

Auteurs : Tzvi Tzfira [États-Unis] ; Guo-Wei Tian ; Benoît Lacroix ; Shachi Vyas ; Jianxiong Li ; Yael Leitner-Dagan ; Alexander Krichevsky ; Tamir Taylor ; Alexander Vainstein ; Vitaly Citovsky

Source :

Plant molecular biology [ 0167-4412 ] ; 2005.

RBID : pubmed:15821977

Descripteurs français

English descriptors

KwdEn :
- Base Sequence (MeSH), Cloning, Molecular (methods), Gene Expression (MeSH), Genetic Vectors (chemistry), Genetic Vectors (genetics), Green Fluorescent Proteins (genetics), Green Fluorescent Proteins (metabolism), Luminescent Proteins (genetics), Luminescent Proteins (metabolism), Microscopy, Confocal (MeSH), Molecular Sequence Data (MeSH), Mutation (MeSH), Plant Proteins (genetics), Plant Proteins (metabolism), Plants, Genetically Modified (MeSH), Plasmids (chemistry), Plasmids (genetics), Recombinant Fusion Proteins (genetics), Recombinant Fusion Proteins (metabolism), Rhizobium (genetics), Sequence Analysis, DNA (MeSH), Sequence Homology, Nucleic Acid (MeSH).
MESH :
- chemical , genetics : Green Fluorescent Proteins, Luminescent Proteins, Plant Proteins, Recombinant Fusion Proteins.
- chemistry : Genetic Vectors, Plasmids.
- genetics : Genetic Vectors, Plasmids, Rhizobium.
- chemical , metabolism : Green Fluorescent Proteins, Luminescent Proteins, Plant Proteins, Recombinant Fusion Proteins.
- methods : Cloning, Molecular.
- Base Sequence, Gene Expression, Microscopy, Confocal, Molecular Sequence Data, Mutation, Plants, Genetically Modified, Sequence Analysis, DNA, Sequence Homology, Nucleic Acid.

Abstract

Autofluorescent protein tags represent one of the major and, perhaps, most powerful tools in modern cell biology for visualization of various cellular processes in vivo. In addition, advances in confocal microscopy and the development of autofluorescent proteins with different excitation and emission spectra allowed their simultaneous use for detection of multiple events in the same cell. Nevertheless, while autofluorescent tags are widely used in plant research, the need for a versatile and comprehensive set of vectors specifically designed for fluorescent tagging and transient and stable expression of multiple proteins in plant cells from a single plasmid has not been met by either the industrial or the academic communities. Here, we describe a new modular satellite (SAT) vector system that supports N- and C-terminal fusions to five different autofluorescent tags, EGFP, EYFP, Citrine-YFP, ECFP, and DsRed2. These vectors carry an expanded multiple cloning site that allows easy exchange of the target genes between different autofluorescence tags, and expression of the tagged proteins is controlled by constitutive promoters, which can be easily replaced with virtually any other promoter of interest. In addition, a series of SAT vectors has been adapted for high throughput Gateway recombination cloning. Furthermore, individual expression cassettes can be assembled into Agrobacterium binary plasmids, allowing efficient transient and stable expression of multiple autofluorescently tagged proteins from a single vector following its biolistic delivery or Agrobacterium-mediated genetic transformation.

DOI: 10.1007/s11103-005-0340-5
PubMed: 15821977

Affiliations:

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 000794
to stream Main, to step Curation: 000794

Le document en format XML

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<term>Genetic Vectors (genetics)</term>
<term>Green Fluorescent Proteins (genetics)</term>
<term>Green Fluorescent Proteins (metabolism)</term>
<term>Luminescent Proteins (genetics)</term>
<term>Luminescent Proteins (metabolism)</term>
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<term>Molecular Sequence Data (MeSH)</term>
<term>Mutation (MeSH)</term>
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<term>Plant Proteins (metabolism)</term>
<term>Plants, Genetically Modified (MeSH)</term>
<term>Plasmids (chemistry)</term>
<term>Plasmids (genetics)</term>
<term>Recombinant Fusion Proteins (genetics)</term>
<term>Recombinant Fusion Proteins (metabolism)</term>
<term>Rhizobium (genetics)</term>
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<term>Sequence Homology, Nucleic Acid (MeSH)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Analyse de séquence d'ADN (MeSH)</term>
<term>Clonage moléculaire (méthodes)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Expression des gènes (MeSH)</term>
<term>Microscopie confocale (MeSH)</term>
<term>Mutation (MeSH)</term>
<term>Plasmides (composition chimique)</term>
<term>Plasmides (génétique)</term>
<term>Protéines de fusion recombinantes (génétique)</term>
<term>Protéines de fusion recombinantes (métabolisme)</term>
<term>Protéines luminescentes (génétique)</term>
<term>Protéines luminescentes (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Protéines à fluorescence verte (génétique)</term>
<term>Protéines à fluorescence verte (métabolisme)</term>
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<term>Vecteurs génétiques (génétique)</term>
<term>Végétaux génétiquement modifiés (MeSH)</term>
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<term>Protéines végétales</term>
<term>Protéines à fluorescence verte</term>
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<term>Mutation</term>
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<front><div type="abstract" xml:lang="en">Autofluorescent protein tags represent one of the major and, perhaps, most powerful tools in modern cell biology for visualization of various cellular processes in vivo. In addition, advances in confocal microscopy and the development of autofluorescent proteins with different excitation and emission spectra allowed their simultaneous use for detection of multiple events in the same cell. Nevertheless, while autofluorescent tags are widely used in plant research, the need for a versatile and comprehensive set of vectors specifically designed for fluorescent tagging and transient and stable expression of multiple proteins in plant cells from a single plasmid has not been met by either the industrial or the academic communities. Here, we describe a new modular satellite (SAT) vector system that supports N- and C-terminal fusions to five different autofluorescent tags, EGFP, EYFP, Citrine-YFP, ECFP, and DsRed2. These vectors carry an expanded multiple cloning site that allows easy exchange of the target genes between different autofluorescence tags, and expression of the tagged proteins is controlled by constitutive promoters, which can be easily replaced with virtually any other promoter of interest. In addition, a series of SAT vectors has been adapted for high throughput Gateway recombination cloning. Furthermore, individual expression cassettes can be assembled into Agrobacterium binary plasmids, allowing efficient transient and stable expression of multiple autofluorescently tagged proteins from a single vector following its biolistic delivery or Agrobacterium-mediated genetic transformation.</div>
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<Abstract><AbstractText>Autofluorescent protein tags represent one of the major and, perhaps, most powerful tools in modern cell biology for visualization of various cellular processes in vivo. In addition, advances in confocal microscopy and the development of autofluorescent proteins with different excitation and emission spectra allowed their simultaneous use for detection of multiple events in the same cell. Nevertheless, while autofluorescent tags are widely used in plant research, the need for a versatile and comprehensive set of vectors specifically designed for fluorescent tagging and transient and stable expression of multiple proteins in plant cells from a single plasmid has not been met by either the industrial or the academic communities. Here, we describe a new modular satellite (SAT) vector system that supports N- and C-terminal fusions to five different autofluorescent tags, EGFP, EYFP, Citrine-YFP, ECFP, and DsRed2. These vectors carry an expanded multiple cloning site that allows easy exchange of the target genes between different autofluorescence tags, and expression of the tagged proteins is controlled by constitutive promoters, which can be easily replaced with virtually any other promoter of interest. In addition, a series of SAT vectors has been adapted for high throughput Gateway recombination cloning. Furthermore, individual expression cassettes can be assembled into Agrobacterium binary plasmids, allowing efficient transient and stable expression of multiple autofluorescently tagged proteins from a single vector following its biolistic delivery or Agrobacterium-mediated genetic transformation.</AbstractText>
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pSAT vectors: a modular series of plasmids for autofluorescent protein tagging and expression of multiple genes in plants.

pSAT vectors: a modular series of plasmids for autofluorescent protein tagging and expression of multiple genes in plants.

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