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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.
Herbicide tolerant maize
EN
MZHG0JG
Yes
SYN-ØØØJG-2
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Organization:Syngenta Seeds GmbH ()Private sector (business and industry)Syngenta Seeds GmbH Zum Knipkenbach 20Bad Salzuflen,
32107, GermanyPhone: +49 52 22 5308-0,Fax: +49 52 22 5308-12,Email: info.seeds@syngenta.com,Website: http://www.syngenta-seeds.de/de/,
MZHG0JG corn was genetically modified to tolerate herbicides containing glyphosate and glufosinate-ammonium with the insertion of the transgene mepsps-02, which encodes the enzyme modified 5-enol pyruvylshikimate-3-phosphate synthase (mEPSPS), and the transgene pat-09, which encodes the enzyme phosphinothricin acetyltransferase (PAT).
Note: SYN-ØØØJG-2, is also referred to with the UID SYN-ØØØJG-3.
EN
Note: SYN-ØØØJG-2, is also referred to with the UID SYN-ØØØJG-3.
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
EN
pSYN18857
EN
- Agrobacterium-mediated DNA transfer
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0.102 kb
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0.293 kb
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3.988 kb
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0.068 kb
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0.372 kb
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1.338 kb
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1.000 kb
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0.521 kb
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0.552 kb
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0.253 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-105196-2 FMV 35S Enhancer | Figwort mosaic virus (Figwort mottle virus, FMV, CMoVb)Leader
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BCH-GENE-SCBD-105197-2 CaMV 35S Enhancer | Cauliflower mosaic virus (CaMV)Leader
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BCH-GENE-SCBD-100362-7 Ubiquitin gene promoter | Zea mays (Maize, Corn, MAIZE)Promoter
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BCH-GENE-SCBD-104820-3 Omega 5' untranslated leader | Tobacco mosaic virus (TMV)Leader
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BCH-GENE-SCBD-101419-5 Optimized chloroplast transit peptide | Zea mays (Maize, Corn, MAIZE) | Helianthus annuus (Sunflower, HELAN)Transit signal
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BCH-GENE-SCBD-46333-8 5-enolpyruvylshikimate-3-phosphate synthase | Zea mays (Maize, Corn, MAIZE)Protein coding sequence | Resistance to herbicides (Glyphosate)
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BCH-GENE-SCBD-110612-2 Ubiquitin gene terminator | Zea mays (Maize, Corn, MAIZE)Terminator
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BCH-GENE-SCBD-100287-7 CaMV 35S promoter | Cauliflower mosaic virus (CaMV)Promoter
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BCH-GENE-SCBD-15002-5 Phosphinothricin N-acetyltransferase | Streptomyces viridochromogenes (STRVR)Protein coding sequence | Resistance to herbicides (Glufosinate)
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BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminator
Genetic characterization studies demonstrated that MZHG0JG corn contains, at a single locus within the corn genome, a single copy of each of the following functional elements: mepsps-02, pat-09, FMV-05 enhancer, 35S-05 enhancer, OTP-02 transit peptide, Ubi158-02 promoter, TMV-03 enhancer, Ubi158-02 terminator, 35S-19 promoter, and NOS-05-01 terminator. It does not contain any extraneous DNA fragments of these functional elements elsewhere in the MZHG0JG corn genome, and it does not contain the plasmid backbone sequence from transformation plasmid pSYN18857.
Nucleotide sequence analysis determined that the MZHG0JG insert consists of the intact T-DNA region of the pSYN18857 plasmid vector. The results of the Southern blot analyses are consistent with the results of the nucleotide sequence analysis.
Sequence analysis of the MZHG0JG insertion site demonstrated that 22 bp from the corn genomic sequence were deleted during the integration of the MZHG0JG insert, and 43 bp of DNA were inserted into the integration site; a 4-bp DNA sequence was present at the junction between the MZHG0JG insert and the 5ʹ flanking region and a 39-bp DNA sequence was present at the junction between the MZHG0JG insert and the 3ʹ flanking region. BLASTN analyses comparing the corn genomic sequence flanking the MZHG0JG insert with sequences in public databases indicated that the insert does not disrupt any known endogenous corn gene.
EN
Nucleotide sequence analysis determined that the MZHG0JG insert consists of the intact T-DNA region of the pSYN18857 plasmid vector. The results of the Southern blot analyses are consistent with the results of the nucleotide sequence analysis.
Sequence analysis of the MZHG0JG insertion site demonstrated that 22 bp from the corn genomic sequence were deleted during the integration of the MZHG0JG insert, and 43 bp of DNA were inserted into the integration site; a 4-bp DNA sequence was present at the junction between the MZHG0JG insert and the 5ʹ flanking region and a 39-bp DNA sequence was present at the junction between the MZHG0JG insert and the 3ʹ flanking region. BLASTN analyses comparing the corn genomic sequence flanking the MZHG0JG insert with sequences in public databases indicated that the insert does not disrupt any known endogenous corn gene.
EN
- Food
- Feed
- SYN-ØØØJG-2 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
EN
EN
- SYN-ØØØJG-2 - APHIS [ English ]
- SYN-ØØØJG-2 - OECD [ English ]
- SYN-ØØØJG-3 - OECD [ English ]
- SYN-ØØØJG-2 - ISAAA [ English ]
| Record type | Field | Record(s) | |
|---|---|---|---|
| Country's Decision or any other Communication | LMO identification | 11 | |
| Risk Assessment generated by a regulatory process | Living modified organism(s) | 11 | |
| Laboratory for detection and identification of LMOs | LMO(s) detectable by the laboratory | 4 | |
| Risk Assessment generated by an independent or non-regulatory process | Living modified organism(s) | 1 | |