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Organisme vivant modifié
(LMO)
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Liberty Link™ Bollgard II™ cotton
EN
LLCotton25 x MON15985
Oui
ACS-GHØØ1-3 × MON-15985-7
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Organisation :Bayer CropScience ()Téléphone :Télécopieur :E-mail :Site Web : http://www.bayercropscience.com,
A stacked insect-resistant and herbicide-tolerant cotton derived from conventional cross-breeding of ACS-GHØØ1-3 with MON-15985-7. Tolerance to the herbicide glufosinate ammonium was produced by inserting a modified phosphinothricin acetyltransferase (PAT) encoding gene (bar) from Streptomyces hygroscopicus, and resistance to lepidoptera insects is conferred from the cry1Ac gene and the cry2Ab gene from Bacillus thuringiensis.
EN
Le terme « organisme récepteur » désigne un organisme (non modifié ou déjà modifié) ayant fait l'objet d'une modification génétique, tandis que les « organismes parentaux » désignent les organismes impliqués dans un croisement ou une fusion cellulaire pour générer un organisme modifié.
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BCH-ORGA-SCBD-12080-6 Organisme Gossypium hirsutum (Cotton)Cultures
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BCH-LMO-SCBD-14851-8 Organisme vivant modifié ACS-GHØØ1-3 - Liberty Link™ cottonBayer CropScience | Résistance aux herbicides (Glufosinate)
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BCH-LMO-SCBD-14774-19 Organisme vivant modifié MON-15985-7 - Bollgard II™ cottonMonsanto | Résistance aux antibiotiques (Kanamycine, Néomycine), Résistance aux maladies et aux parasites (Insectes, Chenille tisseuse (papillons et mites)), Gènes marqueurs et gènes rapporteurs sélectables
FR
pGSV71, PV-GHBK11 and PV-GHBK04
EN
- Croisement
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Certains de ces éléments génétiques peuvent être présents sous forme de fragments ou sous forme tronquée. Veuillez consulter les notes ci-dessous, s’il y a lieu.
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BCH-GENE-SCBD-14986-6 Cry1Ac | Bacillus thuringiensis (Bt, Bacillus, BACTU)Séquence codante de protéines | Résistance aux maladies et aux parasites (Insectes, Chenille tisseuse (papillons et mites))
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BCH-GENE-SCBD-14988-7 Cry2Ab2 | Bacillus thuringiensis (Bt, Bacillus, BACTU)Séquence codante de protéines | Résistance aux maladies et aux parasites (Insectes, Chenille tisseuse (papillons et mites))
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BCH-GENE-SCBD-14972-12 Phosphinothricin N-acetyltransferase gene | Streptomyces hygroscopicus (STRHY)Séquence codante de protéines | Résistance aux herbicides (Glufosinate)
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BCH-GENE-SCBD-100366-6 CaMV Enhanced 35S promoter | Cauliflower mosaic virus (CaMV)Promoteur
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BCH-GENE-SCBD-103901-2 HSP 70 5' untranslated leader sequence | Petunia hybrida (Petunia, PETHY)Leader
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BCH-GENE-SCBD-100365-6 Chloroplast transit peptide 2 | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)Séquence signal
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BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminateur
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BCH-GENE-SCBD-103856-6 α' subunit of β-conglycinin gene terminator | Glycine max (Soybean, Soya bean, Soya, SOYBN)Terminateur
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BCH-GENE-SCBD-15001-5 Neomycin Phosphotransferase II | Escherichia coli (ECOLX)Séquence codante de protéines | Résistance aux antibiotiques (Kanamycine)
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BCH-GENE-SCBD-46004-7 Beta-glucuronidase coding sequence | Escherichia coli (ECOLX)Séquence codante de protéines | Gènes marqueurs et gènes rapporteurs sélectables
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BCH-GENE-SCBD-100287-7 CaMV 35S promoter | Cauliflower mosaic virus (CaMV)Promoteur
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BCH-GENE-SCBD-15033-8 3"(9)-O-aminoglycoside adenyltransferase | Escherichia coli (ECOLX)Séquence codante de protéines | Résistance aux antibiotiques (Streptomycine)
DNA insert from MON-15985-7 vectors PV-GHBK11 and PV-GHBK04
Event 15985 (tradename Bollgard II®) was derived from the retransformation of transgenic cotton line MON 531. As a result of these two transformation events, MON15985 contains the cry1Ac gene and the cry2Ab conferring resistance to lepidopteran pests as well as copies of the nptII and uidA and aadA genes.
DNA insert from LLCotton25 vector pGSV71
The T-DNA cassette from teh LLCotton25 line contined the coding sequence for the bar gene which confers tolerance to the glufosinate herbicide.
For additional information on this LMO, please refer to the records of the parental LMO.
EN
Event 15985 (tradename Bollgard II®) was derived from the retransformation of transgenic cotton line MON 531. As a result of these two transformation events, MON15985 contains the cry1Ac gene and the cry2Ab conferring resistance to lepidopteran pests as well as copies of the nptII and uidA and aadA genes.
DNA insert from LLCotton25 vector pGSV71
The T-DNA cassette from teh LLCotton25 line contined the coding sequence for the bar gene which confers tolerance to the glufosinate herbicide.
For additional information on this LMO, please refer to the records of the parental LMO.
FR
- Nourriture
- Nourriture pour les animaux
- Fibre / textile
- ACS-GHØØ1-3 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) [ English ]
- MON-15985-7 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) [ English ]
- ACS-GHØØ1-3 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- MON-15985-7 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- ACS-GHØØ1-3 - CropLife International Detection Methods Database ( CropLife ) [ English ]
- MON-15985-7 - CropLife International Detection Methods Database ( CropLife ) [ English ]
FR
The stacked cotton line ACS-GHØØ1-3 x MON-15985-7 expresses three novel proteins: the enzyme phosphinothricin acetyl-transferase (PAT) and the delta-endotoxins Cry1Ac and Cry2Ab, both of which confer resistance to the lepidopteran pests of cotton, such as the cotton bollworm, pink bollworm and tobacco budworm.
The insecticidal proteins Cry1Ac and Cry2Ab are produced by the cry1Ac and cry2Ab genes respectively, both of which were originally isolated from the soil bacterium Bacillus thuringiensis and are derived from MON-15985-7. The bar gene, which codes for the production of PAT, is derived from ACS-GHØØ1-3. This enzyme renders glufosinate ammonium inactive in the plant. The expression of the bar gene allows the plant to survive the otherwise lethal application of glufosinate ammonium. The bar gene was isolated from Streptomyces hygroscopius, a gram-positive soil bacterium. The novel traits of each parental line have been combined, through traditional plant breeding, to produce this new cotton line.
For a full description of each parental line please refer to the individual descriptions for the parent organisms.
This plant is a product of traditional plant breeding, and therefore is not automatically subject to regulation in all jurisdictions as are transgenic plants resulting from recombinant DNA technologies. Certain jurisdictions may request notification in advance of the release of a stacked hybrid, or may request information to conduct an environmental and food safety assessment.
EN
The insecticidal proteins Cry1Ac and Cry2Ab are produced by the cry1Ac and cry2Ab genes respectively, both of which were originally isolated from the soil bacterium Bacillus thuringiensis and are derived from MON-15985-7. The bar gene, which codes for the production of PAT, is derived from ACS-GHØØ1-3. This enzyme renders glufosinate ammonium inactive in the plant. The expression of the bar gene allows the plant to survive the otherwise lethal application of glufosinate ammonium. The bar gene was isolated from Streptomyces hygroscopius, a gram-positive soil bacterium. The novel traits of each parental line have been combined, through traditional plant breeding, to produce this new cotton line.
For a full description of each parental line please refer to the individual descriptions for the parent organisms.
This plant is a product of traditional plant breeding, and therefore is not automatically subject to regulation in all jurisdictions as are transgenic plants resulting from recombinant DNA technologies. Certain jurisdictions may request notification in advance of the release of a stacked hybrid, or may request information to conduct an environmental and food safety assessment.
- CERA GM Database [ English ]
| Type de fichier | Champs | Fichier(s) : | |
|---|---|---|---|
| Organisme vivant modifié | Related LMO(s) | 2 | |
| Évaluation des risques générée par un processus de réglementation | Organisme(s) vivant(s) modifié(s) | 4 | |
| Décision de pays ou tout autre communication | Identification de l'OVM | 4 | |
| Laboratoire pour la détection et d'identification des OVM | OVM(s) détectable(s) par le laboratoire | 1 | |