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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.
Glyphosate tolerant maize
EN
MON87427 × NK603
Oui
MON-87427-7 × MON-ØØ6Ø3-6
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Organisation :Monsanto ()800 North Lindbergh Blvd.St. Louis, MO
63167, États-Unis d'AmériqueTéléphone : + 1 314 694-1000,Télécopieur : +1 314 694-3080,E-mail :Site Web : http://www.monsanto.com,
The stacked maize line MON-87427-7 X MON-ØØ6Ø3-6 was obtained through the conventional cross breeding of each of the parental organisms, and exhibits tolerance to glyphosate.
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-LMO-SCBD-104758-3 Organisme vivant modifié MON-87427-7 - Maize modified for tissue selective glyphosate toleranceMonsanto | Résistance aux herbicides (Glyphosate)
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BCH-LMO-SCBD-14776-18 Organisme vivant modifié MON-ØØ6Ø3-6 - Roundup Ready™ maizeMonsanto | Résistance aux herbicides (Glyphosate)
FR
PV-ZMAP1043 and PV-ZMGT32
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-100366-6 CaMV Enhanced 35S promoter | Cauliflower mosaic virus (CaMV)Promoteur
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BCH-GENE-SCBD-100359-7 Hsp70 intron | Zea mays (Maize, Corn, MAIZE)Intron
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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-14979-7 5-enolpyruvylshikimate-3-phosphate synthase gene | Agrobacterium tumefaciens (Agrobacterium)Séquence codante de protéines | Résistance aux herbicides (Glyphosate)
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BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminateur
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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
Genetic elements introduced from PV-ZMAP1043:
The expression of Agrobacterium tumefaciens 5-enolpyruvylshikimate-3-phosphate synthase (cp4 epsps) is under the control of the Cauliflower Mosaic Virus 35S enhanced promoter (P-e35S) and the A. tumefaciens nopaline synthase (nos) terminator. The transcript contains the Zea Mays heatshock protein 70 intron (I-Hsp70) for improved in planta expression and the Arabidopsis thaliana chloroplast transit peptide 2 for targeting the protein to the chloroplast. I-Hsp70 is not translated. The cp4 epsps coding sequence is the codon optimized coding sequence of the aroA gene from A. tumefaciens strain CP4 encoding CP4 EPSPS.
Southern blot analyses indicate that a single copy of the T-DNA was inserted at a single site in the maize genome and no plasmid vector backbone sequences were detected to have been integrated. DNA sequencing analyses indicated that the expected T-DNA sequences were integrated.
Genetic elements introduced from PV-ZMGT32:
The plant expression plasmid vector, PV-ZMGT32 contains two adjacent plant gene expression cassettes each containing a single copy of the cp4 epsps. In the first (5' end) expression cassette, the cp4 epsps gene is under the regulation of the Oryza sativa actin promoter (P-Ract1) and the rice actin intron (I-Ract1). The second cassette, which is fused to the 3' end of the first, consists of the cp4epsps gene regulated by P-e35S and I-Hsp70. Both expression cassettes incorporate the 3'untranslated region of the nos for signal polyadenylation.
The vector also contains the nptII gene encoding kanamycin resistance allowing selection of bacteria containing the plasmid, and an origin of replication (ori) necessary for replicating the plasmid in Escherichia coli. For the transformation through particle bombardment, a fragment of the vector (obtained after digestion with the restriction enzyme MluI) was used which contains only the two cp4 epsps gene expression cassettes. Therefore, the nptII gene and the origin of replication were not inserted into NK603.
Corn NK603 contains one insertion site containing a single copy of the linear DNA of PV-ZMGT32 used for transformation. Both cp4 epsps gene cassettes within the single insert which are intact.
Note:
* P-e35S is a 0.61Kb long sequence containing the promoter and leader for the cauliflower mosaic virus (CaMV) 35S RNA containing the duplicated enhancer region. This modification was made to enhance the activity of this promoter in plants.)
** For more information, please refer to the parental LMO records.
EN
The expression of Agrobacterium tumefaciens 5-enolpyruvylshikimate-3-phosphate synthase (cp4 epsps) is under the control of the Cauliflower Mosaic Virus 35S enhanced promoter (P-e35S) and the A. tumefaciens nopaline synthase (nos) terminator. The transcript contains the Zea Mays heatshock protein 70 intron (I-Hsp70) for improved in planta expression and the Arabidopsis thaliana chloroplast transit peptide 2 for targeting the protein to the chloroplast. I-Hsp70 is not translated. The cp4 epsps coding sequence is the codon optimized coding sequence of the aroA gene from A. tumefaciens strain CP4 encoding CP4 EPSPS.
Southern blot analyses indicate that a single copy of the T-DNA was inserted at a single site in the maize genome and no plasmid vector backbone sequences were detected to have been integrated. DNA sequencing analyses indicated that the expected T-DNA sequences were integrated.
Genetic elements introduced from PV-ZMGT32:
The plant expression plasmid vector, PV-ZMGT32 contains two adjacent plant gene expression cassettes each containing a single copy of the cp4 epsps. In the first (5' end) expression cassette, the cp4 epsps gene is under the regulation of the Oryza sativa actin promoter (P-Ract1) and the rice actin intron (I-Ract1). The second cassette, which is fused to the 3' end of the first, consists of the cp4epsps gene regulated by P-e35S and I-Hsp70. Both expression cassettes incorporate the 3'untranslated region of the nos for signal polyadenylation.
The vector also contains the nptII gene encoding kanamycin resistance allowing selection of bacteria containing the plasmid, and an origin of replication (ori) necessary for replicating the plasmid in Escherichia coli. For the transformation through particle bombardment, a fragment of the vector (obtained after digestion with the restriction enzyme MluI) was used which contains only the two cp4 epsps gene expression cassettes. Therefore, the nptII gene and the origin of replication were not inserted into NK603.
Corn NK603 contains one insertion site containing a single copy of the linear DNA of PV-ZMGT32 used for transformation. Both cp4 epsps gene cassettes within the single insert which are intact.
Note:
* P-e35S is a 0.61Kb long sequence containing the promoter and leader for the cauliflower mosaic virus (CaMV) 35S RNA containing the duplicated enhancer region. This modification was made to enhance the activity of this promoter in plants.)
** For more information, please refer to the parental LMO records.
FR
- Nourriture
- Nourriture pour les animaux
- Biocombustible
- http://gmo-crl.jrc.ec.europa.eu/gmomethods/search?db=gmometh&q=ac:MON-87427-7 [ English ]
- http://gmo-crl.jrc.ec.europa.eu/gmomethods/query.do?db=gmometh&query=ac:MON-00603-6 [ English ]
- http://www.detection-methods.com/product/roundup-ready-2/ [ English ]
- MON-ØØ6Ø3-6 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- MON-87427-7 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- MON-87427-7 - CropLife International Detection Methods Database ( CropLife ) [ English ]
- MON-ØØ6Ø3-6 - CropLife International Detection Methods Database ( CropLife ) [ English ]
FR
FR
| Type de fichier | Champs | Fichier(s) : | |
|---|---|---|---|
| Décision de pays ou tout autre communication | Identification de l'OVM | 3 | |
| Évaluation des risques générée par un processus de réglementation | Organisme(s) vivant(s) modifié(s) | 3 | |