MON-ØØ81Ø-6 - YieldGard™ maize | BCH-LMO-SCBD-14750 | Living Modified Organism | Biosafety Clearing-House

Loading...
  |  

Living Modified Organism (LMO)

Decisions on the LMO Risk Assessments  
last updated: 24 May 2013
Living Modified Organism identity
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.
YieldGard™ maize
EN
MON810
MON-ØØ81Ø-6
  • - Organization: Monsanto () | BCH-CON-SCBD-14925-3
    Organization
    Monsanto ()
    800 North Lindbergh Blvd.
    St. Louis, MO
    63167, United States of America
    Phone: + 1 314 694-1000,
    Fax: +1 314 694-3080,
    Email:
Insect-resistant maize produced by inserting the cry1Ab gene from Bacillus thuringiensis subsp. kurstaki HD-1. The genetic modification affords resistance to attack by the European corn borer (ECB), Ostrinia nubilalis.
EN
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.
EN
  • PH-MON8Ø9-2 - Insect-resistant maize MON809
    | Resistance to antibiotics - Kanamycin Resistance to diseases and pests - Insects - Lepidoptera (butterflies and moths) Resistance to herbicides - Glyphosate
  • Insect Resistant Maize MON801
    | Resistance to antibiotics - Kanamycin Resistance to diseases and pests - Insects - Lepidoptera (butterflies and moths) Resistance to herbicides - Glyphosate
Characteristics of the modification process
PV-ZMBK07 and PV-ZMGT10
EN
  • Biolistic / Particle gun
 
0.610 kb
 
 
0.800 kb
 
 
3.460 kb
 
Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
The transgenic maize line MON810 was genetically engineered to resist ECB by producing its own insecticide. This line was developed by introducing a synthetic version of the cry1Ab gene, isolated from the soil bacterium Bacillus thuringiensis (Bt) which was modified to enhance the expression of the Cry1Ab protein in plants, however the resulting amino acid sequence is identical to the native protein.

Molecular studies demonstrated that a single truncated copy of the cryIAb coding sequence was integrated into the corn genome along with the enhanced cauliflower mosaic virus 35S promoter (P-e35S), and the hsp 70 intron (I-Hsp70).  The nos terminator was not integrated into MON810 due to a truncation of the 3’ end of the gene cassette.  Western analysis confirmed that a truncated Cry1Ab protein of approximately 91 kD (native Cry1Ab had a molecular weight of approximately 131 kD) was inserted into the genome. 

Corn event MON 810 was produced by microprojectile bombardment of embryogenic corn tissue with plasmids PVZMBK07 and PV-ZMGT10. However plasmid vector PV-ZMGT10 was not integrated into the plant genome. Further Southern blot analysis indicated that the genes for glyphosate tolerance (CP4 EPSPS) and antibiotic resistance (neo) were not transferred to line MON 810 and the absence of the CP4 EPSPS and gox gene products was also confirmed by Western blotting. The CP4 EPSPS and GOX protein encoding genes were presumed to have been inserted into the initial transformant at a separate genetic loci from the cry1Ab gene and then subsequently lost through segregation during the crossing events leading to line MON810.

Southern analysis confirms that the nptII gene (originally present in PVZMBK07 and PV-ZMGT10) is not present in MON 810.
EN
LMO characteristics
EN
  • Food
  • Feed
  • Biofuel
Records referencing this document Show in search
Record type Field Record(s)
Living Modified Organism Recipient Organism” or “Parental Organisms 29
Living Modified Organism Related LMO(s) 2
Risk Assessment generated by a regulatory process Living modified organism(s) 42
Country's Decision or any other Communication Living modified organism(s) 44
Laboratory for detection and identification of LMOs LMO(s) detectable by the laboratory 38