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Modified Organism
ACS-BNØØ3-6 × MON-ØØØ73-7 - Herbicide tolerant, male fertility restoring canola
Record information and status
Record ID
Date of creation
2021-09-27 20:01 UTC (austein.mcloughlin@cbd.int)
Date of publication
2021-09-27 20:01 UTC (austein.mcloughlin@cbd.int)

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.

LMO name
Herbicide tolerant, male fertility restoring canola
Transformation event
RF3 × RT73
Unique identifier
Bayer CropScience
Bayer CropScience Deutschland GmbH
Bayer CropScience AG
Alfred-Nobel-Str. 50
40789 Monheim am Rhein
Monheim am Rhein
Germany, 40789
Phone:+49 21 73 - 38-0
Url:Bayer CropScience
The modified canola (Brassica napus) was produced through the cross-breeding of modified parental lines for male fertility restoration and herbicide tolerance. The canola expresses Bacillus amyloliquefaciens barstar, an inhibitor of the ribonuclease barnase. In lines where barnase is expressed, barstar prevents the RNA degradation in the pollen tissues and thus restores male fertility (pollen development). For herbicide tolerance, the canola expresses Streptomyces hygroscopicus phosphinothricin acetyltransferase (glufosinate tolerance), Agrobacterium tumefaciens 5-enolpyruvylshikimate- 3-phosphate synthase (glyphosate tolerance) and Ochrobactrum anthropi glyphosate oxidoreductase (glyphosate tolerance).
Recipient Organism or Parental Organisms
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.
Brassica napus - Turnip, Rapeseed, Canola Plant, Oilseed Rape, Rape, BRANA
ACS-BNØØ3-6 - InVigor™ canola
Changes in physiology and/or production - Fertility restoration Resistance to herbicides - Glufosinate
Show detection method(s)
MON-ØØØ73-7 - Roundup Ready™ canola
Resistance to herbicides - Glyphosate
Show detection method(s)
Characteristics of the transformation process
pTHW118; PV-BNGT04
Techniques used for the modification
  • Cross breeding
Genetic elements construct
pTA29 pollen specific promoter
1.51 Kb
0.27 Kb
Barstar gene terminator
0.04 Kb
Nopaline Synthase Gene Terminator
0.26 Kb
rbcS Promoter
1.73 Kb
Phosphinothricin N-acetyltransferase gene
0.55 Kb
Transcript 7 gene 3' untranslated region
0.21 Kb
FMV 34S promoter
0.00 Kb
Chloroplast transit peptide 2
0.00 Kb
5-enolpyruvylshikimate-3-phosphate synthase gene
0.00 Kb
rbcS-E9 gene terminator
0.00 Kb
FMV 34S promoter
0.00 Kb
rbcS Transit Peptide
0.00 Kb
Glyphosate oxidoreductase gene
0.00 Kb
rbcS-E9 gene terminator
0.00 Kb
Further details
Notes regarding the genetic elements introduced or modified in this LMO
DNA insert from pTHW118 from RF3 (ACS-BNØØ3-6) canola
The DNA insert contains two gene cassettes: Bacillus amyloliquefaciens barstar and Streptomyces hygroscopicus phosphinothricin N-acetyltransferase (bar).

Barstar is under control of a Nicotiana tabacum TA29 pollen specific promoter and an Agrobacterium tumefaciens nopaline synthase terminator. An additional sequence, B. amyloliquefaciens barstar 3' untranslated region, which contributes to the polyadenylation of the coding sequence, can be found between the barstar coding sequence and nopaline synthase terminator.

Phosphinothricin N-acetyltransferase is under control of an Arabidopsis thaliana ribulose-1,5-bisphosphate carboxylase (Rubisco) small subunit promoter and A. tumefaciens transcript 7 3' untranslated region.

- The coding sequence of phosphinothricin N-acetyltransferase has the two N-terminal codons modified to ATG and GAC.
- Southern blot and PCR analysis indicated that the parental genome contains one complete copy of the transformation cassette arranged in an inverted repeat orientation to a second partial copy (comprising of a portion of the TA29 promoter, the barstar coding sequence, the nos terminator sequence and a non-initiation codon of the bar gene)  of the transformation cassette adjacent to the left T-DNA boundary.

DNA insert from PV-BNGT04 from RT73 (MON-ØØØ73-7) canola
The DNA insert contains two gene cassettes: Agrobacterium tumefaciens 5-enolpyruvylshikimate-3-phosphate synthase (cp4-epsps) and Ochrobactrum anthropic glyphosate oxidoreductase (gox).

The cp4-epsps coding sequence is under control of a Figwort mosaic virus 34S promoter and a Pisum sativum rubisco small subunit terminator. A transit peptide from ribulose-1,5-bisphosphate carboxylase (Rubisco) small subunit was included before the cp4-epsps coding sequence and contributes to a higher level of expression in leaf tissues.

- The genetic element sizes were not readily available at the time of this record's creation.
- The gox coding sequence differs from the wild-type version of the gene at 3 amino acid sites (G85S, R153K and R334H) and was designated as goxv247.
- The cp4-epsps sequence was optimized for expression in plants.
- PCR and southern blot analyses indicated that the parental genome contains a single insertion event containing one copy of the T-DNA from plasmid PV-BNGT04. No genetic elements from outside of the right and left borders of the plasmid were transferred into or are present in the genomic DNA of the LMO.

For more information, kindly refer to the parental LMO records.
LMO characteristics
Modified traits
  • Fertility restoration
Common use(s)
  • Food
  • Feed
Additional Information
Other relevant website address or attached documents

Records referencing this document (2)
2record(s) found
Country's Decision or any other Communication1 record
Risk Assessment1 record