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Organisme vivant modifié (LMO)
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Décisions sur l’OVM Évaluations des risques  
published: 18 sept. 2013 last updated: 01 sept. 2026
Identité de l’organisme vivant modifié
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Enlist E3™ Soybean-
EN
DAS-44406-6
Oui
DAS-444Ø6-6
The soybean (Glycine max) was modified for glyphosate, 2,4-Dichlorophenoxyacetic acid (2,4-D) and glufosinate herbicide tolerance. To achieve glyphosate tolerance, the soybean expresses modified Zea mays enzyme 5-enolpyruvylshikimate-3-phosphate synthase, which has reduced binding affinity for glyphosate and allows continued synthesis of aromatic amino acids through the shikimate pathway in the presence of the herbicide. To achieve tolerance to aryloxyalkanoate herbicides, including 2,4-dichlorophenoxyacetic acid, the soybean expresses aryloxyalkanoate dioxygenase (AAD-12), which degrades these herbicides into non-herbicidal compounds. To achieve tolerance to glufosinate, the soybean expresses the gene from Streptomyces viridochromogenes encoding phosphinothricin N-acetyltransferase encoding gene, which inactivates the active compound L-phosphinothricin through acetylation of the primary amino group.
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.
FR
Caractéristiques du processus de modification
pDAB8264
EN
  • Transgénèse par agrobacterium
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.
  • BCH-GENE-SCBD-104802-5 Polyubiquitin10 gene promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoteur
  • BCH-GENE-SCBD-104805-2 Aryloxyalkanoate dioxygenase gene | Delftia acidovorans (DELAC)
    Séquence codante de protéines | Résistance aux herbicides
  • BCH-GENE-SCBD-104806-3 ORF23 3' Untranslated region | Agrobacterium tumefaciens (Agrobacterium)
    Terminateur
  • BCH-GENE-SCBD-101900-6 CsVMV promoter | Cassava vein mosaic virus (Cassava vein mosaic virus, CVMV, CsVMV)
    Promoteur
  • BCH-GENE-SCBD-15002-5 Phosphinothricin N-acetyltransferase | Streptomyces viridochromogenes (STRVR)
    Séquence codante de protéines | Résistance aux herbicides (Glufosinate)
  • BCH-GENE-SCBD-104807-2 ORF1 3' Untranslated region | Agrobacterium tumefaciens (Agrobacterium)
    Terminateur
  • BCH-GENE-SCBD-104795-4 RB7 matrix attachment region | Nicotiana tabacum (Tobacco, TOBAC )
    Enhancer
  • BCH-GENE-SCBD-104646-4 Histone H4 gene 3' UTR | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Terminateur
  • BCH-GENE-SCBD-46333-8 5-enolpyruvylshikimate-3-phosphate synthase | Zea mays (Maize, Corn, MAIZE)
    Séquence codante de protéines | Résistance aux herbicides (Glyphosate)
  • BCH-GENE-SCBD-101419-5 Optimized chloroplast transit peptide | Zea mays (Maize, Corn, MAIZE) | Helianthus annuus (Sunflower, HELAN)
    Séquence signal
  • BCH-GENE-SCBD-104647-3 Histone H4 gene Promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoteur
  • BCH-GENE-SCBD-104648-2 Histone H3 Gene II intron 1 | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Intron
Information of the inserted DNA sequences
The transforming plasmid pDAB8264 contained a transfer DNA region comprising three gene cassettes expressing the proteins 2mEPSPS (modified 5-enolpyruvylshikimate-3-phosphate synthase gene) derived from Zea mays, aryloxyalkanoate dioxygenase (AAD-12) from Delftia acidovorans, and phosphinothricin N-acetyltransferase (PAT) from Streptomyces viridochromogenes. Transformation of soybean was achieved through Agrobacterium tumefaciens-mediated transformation.

(1) Transcription of the 2mepsps coding sequence is directed by H4 histone (H4A748) promoter together with the 5′ untranslated region and an intron from the histone 3 gene from Arabidopsis thaliana. The coding region includes an optimized chloroplast transit peptide derived from Zea mays and Helianthus annuus RuBisCO sequences to direct the expressed protein to the chloroplast. Transcription is terminated by the 3′ untranslated region of the H4A748 gene from Arabidopsis thaliana. A matrix attachment region from the Nicotiana tabacum rb7 gene is also present to increase gene expression. Expression of this cassette results in production of the 2mEPSPS protein containing two amino acid substitutions that confer reduced sensitivity to glyphosate, thereby allowing continued synthesis of aromatic amino acids through the shikimate pathway in the presence of the herbicide.

(2) Transcription of the aad-12 coding sequence is directed by the promoter together with the 5′ untranslated region and intron from the polyubiquitin 10 gene from Arabidopsis thaliana. Transcription is terminated by the 3' untranslated region (3' UTR) of open reading frame 23 (ORF23) of plasmid pTi15955 from Agrobacterium tumefaciens. Expression of this cassette results in production of the AAD-12 protein, an alpha-ketoglutarate-dependent dioxygenase that metabolically inactivates herbicides of the aryloxyalkanoate family, including 2,4-dichlorophenoxyacetic acid (2,4-D).

(3) Transcription of the pat coding sequence is directed by the promoter together with the 5′ untranslated region from the Cassava Vein Mosaic virus. Transcription is terminated by the 3' UTR of the ORF1 of plasmid pTi15955 from Agrobacterium tumefaciens. Expression of this cassette results in production of the PAT protein, a phosphinothricin acetyltransferase that inactivates glufosinate through acetylation.

Note
  • Molecular characterization by Southern blot analysis indicated that a single, intact copy of the intended T-DNA insertion containing the aad-12, 2mepsps and pat expression cassettes was integrated into the soybean genome.
  • Southern blot analysis confirmed the absence of integrated plasmid backbone DNA.
  • The integrity of the inserted DNA was demonstrated over five breeding generations. Segregation analyses confirmed the expected Mendelian inheritance pattern, indicating stable inheritance during conventional breeding.
  • No evidence of rearrangement or instability of the inserted genetic material was reported.
EN
Caractéristiques de l’OVM
FR
  • Nourriture pour les animaux
  • Nourriture
Méthode(s) de détection
FR
Informations supplémentaires
FR
Les fichiers qui font référence à ce document Montré dans la recherche
Type de fichier Champs Fichier(s) :
Organisme vivant modifié Organisme récepteur ou organismes parentaux 3
Décision de pays ou tout autre communication Identification de l'OVM 18
Évaluation des risques générée par un processus de réglementation Organisme(s) vivant(s) modifié(s) 23
Laboratoire pour la détection et d'identification des OVM OVM(s) détectable(s) par le laboratoire 5
Soumissions RECORDS 1