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Organisme vivant modifié
(LMO)
L’image ci-dessous identifie l’OVM par son identificateur unique, son nom commercial et un lien vers cette page du Centre d’échange Cliquer dessus pour télécharger une plus grande image sur votre ordinateur Pour du soutien sur comment utiliser, aller dans la page de liens rapides OVM.
Droughtgard™ Maize
EN
MON 87460
Oui
MON-8746Ø-4
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Organisation :Monsanto Canada Inc. ()Téléphone :Télécopieur :E-mail :Site Web :
MON 87460 was developed through Agrobacterium-mediated transformation of conventional maize variety embryos and expresses cold shock protein B (CspB) from Bacillus subtilis and NptII from Tn5 of Escherichia coli. MON 87460 was developed to provide reduced yield loss under water-limited conditions compared to conventional maize.
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-246-6 Organisme Zea mays (Maize, Corn, MAIZE)Cultures
FR
PV-ZMAP595
EN
- Transgénèse par agrobacterium
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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-101416-7 Ti plasmid right border repeat | Agrobacterium tumefaciens (Agrobacterium)Plasmid vector
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BCH-GENE-SCBD-100364-5 Rice actin 1 gene promoter | Oryza sativa (Rice, ORYSA)Promoteur
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BCH-GENE-SCBD-100355-6 Rice actin 1, intron | Oryza sativa (Rice, ORYSA)Intron
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BCH-GENE-SCBD-103065-7 Cold shock protein gene | Bacillus subtilis (Bacillus, BACIU)Séquence codante de protéines | Tolérance au stress abiotique (Froid / chaleur, Sécheresse)
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BCH-GENE-SCBD-103067-9 Transcript 7 gene 3' untranslated region | Agrobacterium tumefaciens (Agrobacterium)Terminateur
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BCH-GENE-SCBD-103069-3 loxP recombination site | Bacteriophage P1 (Phage P1)recombination site
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BCH-GENE-SCBD-100287-7 CaMV 35S promoter | Cauliflower mosaic virus (CaMV)Promoteur
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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-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminateur
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BCH-GENE-SCBD-101415-9 Ti plasmid left border repeat | Agrobacterium tumefaciens (Agrobacterium)Plasmid vector
A disarmed Agrobacterium tumefaciens plant transformation system including the double-border, binary vector PV-ZMAP595 was used to transform LH59 embryos producing MON 87460.
The disarmed Agrobacterium tumefaciens transformation vector PV-ZMAP595 contains both left and right T-DNA border sequences facilitating the transformation. It was constructed using standard molecular biology techniques. The T-DNA region of this vector contains cspB and nptII expression cassettes and it is the portion that is integrated to maize genome during transformation event.
The genetic elements of PV-ZMAP595 intended for insertion into the maize genome comprised between the T-DNA borders are, from the right border region, promoter and leader from the rice actin gene (P-Ract1), a non-translated intron from the rice actin gene (I-Ract1), the cspB coding sequence (CS-cspB) and a polyadenylation sequence from the transcript 7 gene (T-tr7). These elements together constitute the cspB expression cassette which is followed by the nptII expression cassette. The latter is flanked by two loxP sites and constitutes of a transcriptional promoter (P-35S), the nptII coding sequence (CS-nptII), and a polyadenylation sequence from the nopaline synthase gene (T-nos).
MON 87460 contains one copy of the insert at a single insertion site hosting both cspB and nptII intact expression cassettes. No additional elements from the transformation vector PV-ZMAP595, linked or unlinked to the cspB and nptII expression cassettes, were detected in the genome of MON 87460. Additionally, backbone sequence from the plasmid PV-ZMAP595 was not detected.
EN
The disarmed Agrobacterium tumefaciens transformation vector PV-ZMAP595 contains both left and right T-DNA border sequences facilitating the transformation. It was constructed using standard molecular biology techniques. The T-DNA region of this vector contains cspB and nptII expression cassettes and it is the portion that is integrated to maize genome during transformation event.
The genetic elements of PV-ZMAP595 intended for insertion into the maize genome comprised between the T-DNA borders are, from the right border region, promoter and leader from the rice actin gene (P-Ract1), a non-translated intron from the rice actin gene (I-Ract1), the cspB coding sequence (CS-cspB) and a polyadenylation sequence from the transcript 7 gene (T-tr7). These elements together constitute the cspB expression cassette which is followed by the nptII expression cassette. The latter is flanked by two loxP sites and constitutes of a transcriptional promoter (P-35S), the nptII coding sequence (CS-nptII), and a polyadenylation sequence from the nopaline synthase gene (T-nos).
MON 87460 contains one copy of the insert at a single insertion site hosting both cspB and nptII intact expression cassettes. No additional elements from the transformation vector PV-ZMAP595, linked or unlinked to the cspB and nptII expression cassettes, were detected in the genome of MON 87460. Additionally, backbone sequence from the plasmid PV-ZMAP595 was not detected.
FR
- Nourriture
- Nourriture pour les animaux
- Biocombustible
- Event-specific Method for the Quantification of Maize MON87460 Using Real-time PCR [ English ]
- MON-8746Ø-4 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- MON-8746Ø-4 - CropLife International Detection Methods Database ( CropLife ) [ English ]
FR
FR
- MON 87460 - APHIS.pdf [ English ]
- MON87460 - OECD [ English ]
| Type de fichier | Champs | Fichier(s) : | |
|---|---|---|---|
| Décision de pays ou tout autre communication | Identification de l'OVM | 20 | |
| Évaluation des risques générée par un processus de réglementation | Organisme(s) vivant(s) modifié(s) | 20 | |
| Laboratoire pour la détection et d'identification des OVM | OVM(s) détectable(s) par le laboratoire | 7 | |
| Organisme vivant modifié | Organisme récepteur ou organismes parentaux | 46 | |
| Organisme vivant modifié | OVM connexe(s) | 1 | |