Efficient production of transgenic citrus plants using isopentenyl transferase positive selection and removal of the marker gene by site-specific recombination
Identifieur interne : 002468 ( Main/Exploration ); précédent : 002467; suivant : 002469Efficient production of transgenic citrus plants using isopentenyl transferase positive selection and removal of the marker gene by site-specific recombination
Auteurs : Alida Ballester [Espagne] ; Magdalena Cervera [Espagne] ; Leandro Pena [Espagne]Source :
- Plant cell reports : (Print) [ 0721-7714 ] ; 2007.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Production, Plante transgénique.
English descriptors
- KwdEn :
- Alkyl and Aryl Transferases (genetics), Alkyl and Aryl Transferases (metabolism), Base Sequence, Citrus, Citrus (genetics), Citrus (growth & development), Citrus sinensis (genetics), Citrus sinensis (growth & development), Gene, Genetic Markers, Genetic Vectors (genetics), Genetic transformation, Molecular Sequence Data, Plant Shoots (genetics), Plant Shoots (growth & development), Plants, Genetically Modified (genetics), Plants, Genetically Modified (growth & development), Production, Recombinases (genetics), Recombinases (metabolism), Recombination, Recombination, Genetic (genetics), Selection, Site specificity, Transferases, Transformation, Genetic, Transgenic plant, Vegetals.
- MESH :
- chemical , genetics : Alkyl and Aryl Transferases, Recombinases.
- chemical , metabolism : Alkyl and Aryl Transferases, Recombinases.
- genetics : Citrus, Citrus sinensis, Genetic Vectors, Plant Shoots, Plants, Genetically Modified, Recombination, Genetic.
- growth & development : Citrus, Citrus sinensis, Plant Shoots, Plants, Genetically Modified.
- Base Sequence, Genetic Markers, Molecular Sequence Data, Transformation, Genetic.
Abstract
The presence of marker genes conferring antibiotic resistance in transgenic plants represents a serious obstacle for their public acceptance and future commercialization. In citrus, selection using the selectable marker gene nptll, that confers resistance to the antibiotic kanamycin, is in general very effective. An attractive alternative is offered by the MAT system (Multi-Auto-Transformation), which combines the ipt gene for positive selection with the recombinase system R/RS for removal of marker genes from transgenic cells after transformation. Transformation with a MAT vector has been attempted in two citrus genotypes, Pineapple sweet orange (Citrus sinensis L. Osb.) and Carrizo citrange (C. sinensis L. Osb. x Poncirus trifoliata L. Raf.). Results indicated that the IPT phenotype was clearly distinguishable in sweet orange but not in citrange, and that excision was not always efficient and precise. Nevertheless, the easy visual detection of the IPT phenotype combined with the higher transformation efficiency achieved in sweet orange using this system open interesting perspectives for the generation of marker-free transgenic citrus plants.
Affiliations:
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Le document en format XML
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<term>Base Sequence</term>
<term>Citrus</term>
<term>Citrus (genetics)</term>
<term>Citrus (growth & development)</term>
<term>Citrus sinensis (genetics)</term>
<term>Citrus sinensis (growth & development)</term>
<term>Gene</term>
<term>Genetic Markers</term>
<term>Genetic Vectors (genetics)</term>
<term>Genetic transformation</term>
<term>Molecular Sequence Data</term>
<term>Plant Shoots (genetics)</term>
<term>Plant Shoots (growth & development)</term>
<term>Plants, Genetically Modified (genetics)</term>
<term>Plants, Genetically Modified (growth & development)</term>
<term>Production</term>
<term>Recombinases (genetics)</term>
<term>Recombinases (metabolism)</term>
<term>Recombination</term>
<term>Recombination, Genetic (genetics)</term>
<term>Selection</term>
<term>Site specificity</term>
<term>Transferases</term>
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<term>Recombinases</term>
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<term>Citrus sinensis</term>
<term>Genetic Vectors</term>
<term>Plant Shoots</term>
<term>Plants, Genetically Modified</term>
<term>Recombination, Genetic</term>
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<term>Citrus sinensis</term>
<term>Plant Shoots</term>
<term>Plants, Genetically Modified</term>
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<term>Genetic Markers</term>
<term>Molecular Sequence Data</term>
<term>Transformation, Genetic</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Production</term>
<term>Plante transgénique</term>
<term>Transferases</term>
<term>Sélection</term>
<term>Gène</term>
<term>Citrus</term>
<term>Site spécifique</term>
<term>Recombinaison</term>
<term>Transformation génétique</term>
<term>Végétal</term>
<term>Citrus sinensis Poncirus trifoliata</term>
<term>Isopentenyl transferase</term>
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<front><div type="abstract" xml:lang="en">The presence of marker genes conferring antibiotic resistance in transgenic plants represents a serious obstacle for their public acceptance and future commercialization. In citrus, selection using the selectable marker gene nptll, that confers resistance to the antibiotic kanamycin, is in general very effective. An attractive alternative is offered by the MAT system (Multi-Auto-Transformation), which combines the ipt gene for positive selection with the recombinase system R/RS for removal of marker genes from transgenic cells after transformation. Transformation with a MAT vector has been attempted in two citrus genotypes, Pineapple sweet orange (Citrus sinensis L. Osb.) and Carrizo citrange (C. sinensis L. Osb. x Poncirus trifoliata L. Raf.). Results indicated that the IPT phenotype was clearly distinguishable in sweet orange but not in citrange, and that excision was not always efficient and precise. Nevertheless, the easy visual detection of the IPT phenotype combined with the higher transformation efficiency achieved in sweet orange using this system open interesting perspectives for the generation of marker-free transgenic citrus plants.</div>
</front>
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