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Living Modified Organism (LMO)
The image below identifies the LMO through its unique identifier, trade name and a link to this page of the BCH. Click on it to download a larger image on your computer. For help on how to use it go to the LMO quick-links page.
Droughtgard™ Maize
EN
MON 87460
Yes
MON-8746Ø-4
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Organization:Monsanto Canada Inc. ()Phone:Fax:Email:Website:
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.
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The term “Recipient organism” refers to an organism (either already modified or non-modified) that was subjected to genetic modification, whereas “Parental organisms” refers to those that were involved in cross breeding or cell fusion.
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BCH-ORGA-SCBD-246-6 Organism Zea mays (Maize, Corn, MAIZE)Crops
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PV-ZMAP595
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- Agrobacterium-mediated DNA transfer
0.356 kb
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0.923 kb
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0.476 kb
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0.203 kb
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0.507 kb
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0.033 kb
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0.292 kb
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0.794 kb
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0.252 kb
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0.033 kb
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0.441 kb
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Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
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BCH-GENE-SCBD-101416-6 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)Promoter
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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)Protein coding sequence | Tolerance to abiotic stress (Cold / Heat, Drought)
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BCH-GENE-SCBD-103067-9 Transcript 7 gene 3' untranslated region | Agrobacterium tumefaciens (Agrobacterium)Terminator
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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)Promoter
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BCH-GENE-SCBD-15001-5 Neomycin Phosphotransferase II | Escherichia coli (ECOLX)Protein coding sequence | Resistance to antibiotics (Kanamycin)
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BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminator
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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.
EN
- Food
- Feed
- Biofuel
- 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 ]
EN
EN
- MON 87460 - APHIS.pdf [ English ]
- MON87460 - OECD [ English ]
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