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Living Modified Organism (LMO)
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Decisions on the LMO Risk Assessments  
last updated: 10 Jul 2026
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.
Herbicide-tolerant and insect-resistant cotton
EN
GHB811 × T304-40 × GHB119 × COT102
Yes
BCS-GH811-4 × BCS-GHØØ4-7 × BCS-GHØØ5-8 × SYN-IR1Ø2-7
The cotton (Gossypium hirsutum) was produced through cross‑breeding of modified parental varieties BCS-GH811-4, BCS-GHØØ4-7, BCS-GHØØ5-8, and SYN-IR1Ø2-7.
Cotton BCS-GH811-4 was modified for tolerance to glyphosate and isoxaflutole herbicides. To achieve isoxaflutole tolerance, the cotton expresses Pseudomonas fluorescens 4-hydroxyphenylpyruvate dioxygenase (HPPD), which contains a point mutation that confers reduced binding affinity to HPPD inhibitors. To achieve tolerance to glyphosate, the cotton expresses the Zea mays double mutant 5-enolpyruvylshikimate-3-phosphate synthase, which has a reduced binding affinity to the herbicide.
Cotton BCS-GHØØ4-7 was modified for resistance against lepidopteran insect pests and glufosinate-ammonium tolerance. To achieve resistance against Lepidoptera, the cotton expresses the cry1Ab gene from Bacillus thuringiensis subsp. kurstaki, which produces a crystal delta-endotoxin that binds to specific midgut receptors in the insect larva, forming pores that disrupt osmotic balance and cause fatal cell lysis. To achieve glufosinate tolerance, the cotton expresses Streptomyces hygroscopicus phosphinothricin N-acetyltransferase encoding pat gene, which inactivates the active compound L-phosphinothricin through acetylation of the primary amino group.
Cotton BCS-GHØØ5-8 was modified for lepidopteran insect pests and glufosinate-ammonium tolerance. To achieve resistance against Lepidoptera, the cotton expresses the cry2Ae gene from Bacillus thuringiensis, which produces a crystal delta-endotoxin Cry2Ae with a pore-forming mode of action in the midgut epithelium of feeding larvae. To achieve glufosinate tolerance, the cotton expresses the the bialaphos resistance gene from Streptomyces hygroscopicus to produce phosphinothricin N-acetyltransferase, which inactivates the herbicide by acetylating L-glufosinate ammonium.
Cotton SYN-IR1Ø2-7 was modified for resistance against lepidopteran insect pests such as the cotton bollworm (Helicoverpa zea), tobacco budworm (Heliothis virescens), pink bollworm (Pectinophora gossypiella), fall armyworm (Spodoptera frugiperd), beet armyworm (Spodoptera exigua), soybean looper (Pseudoplusia includens), cabbage looper (Trichoplusia ni), and cotton leaf perforator (Bucculatrix thurberiella). The LM cotton was also modified to express a selectable marker during transformation. To achieve lepidopteran resistance, the cotton expresses Bacillus thuringiensis vegetative insecticidal protein 3Aa (Vip3Aa), which causes gut paralysis and lysis of epithelium cells of feeding larvae. Vip3Aa is a vegetative insecticidal protein that binds to specific midgut receptors distinct from those recognized by Cry proteins and disrupts the integrity of epithelial cell membranes. For the selection marker, the cotton expresses Escherichia coli hygromycin-B phosphotransferase is also expressed.
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.
  • BCH-ORGA-SCBD-12080-6 Organism Gossypium hirsutum (Cotton)
    Crops
  • BCH-LMO-SCBD-113966-5 Living Modified Organism BCS-GH811-4 - Herbicide-tolerant cotton
    Bayer CropScience | Resistance to herbicides (Glyphosate)
  • BCH-LMO-SCBD-14992-10 Living Modified Organism SYN-IR1Ø2-7 - VIPCOT™ Cotton
    Syngenta | Resistance to antibiotics (Hygromycin), Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths)), Selectable marker genes and reporter genes
  • BCH-LMO-SCBD-101018-15 Living Modified Organism BCS-GHØØ4-7 - Herbicide-tolerant, insect-resistant cotton
    Bayer Crop Science K.K | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths), European corn borer (Ostrinia nubilalis)), Resistance to herbicides (Glufosinate)
  • BCH-LMO-SCBD-101898-7 Living Modified Organism BCS-GHØØ5-8 - Insect-protected and herbicide-tolerant cotton
    Bayer BioScience N.V. | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths), Cotton bollworm (Helicoverpa spp.), Fall armyworm (Spodoptera frugiperda)), Resistance to herbicides (Glufosinate)
Cultivar Coker 315 (for all events in this stacked LMO)
EN
Characteristics of the modification process
pTSIH09; pTDL008 derived from pGSV20; pTEM12; pCOT-1; PV-GHHT6997
EN
  • Cross breeding
 
0.000 kb
 
 
0.940 kb
 
 
1.850 kb
 
 
0.060 kb
 
 
1.040 kb
 
Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
  • BCH-GENE-SCBD-104647-3 Histone H4 gene Promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoter
  • BCH-GENE-SCBD-104648-2 Histone H3 Gene II intron 1 | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Intron
  • BCH-GENE-SCBD-101419-5 Optimized chloroplast transit peptide | Zea mays (Maize, Corn, MAIZE) | Helianthus annuus (Sunflower, HELAN)
    Transit signal
  • BCH-GENE-SCBD-46333-8 5-enolpyruvylshikimate-3-phosphate synthase | Zea mays (Maize, Corn, MAIZE)
    Protein coding sequence | Resistance to herbicides (Glyphosate)
  • BCH-GENE-SCBD-104646-4 Histone H4 gene 3' UTR | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Terminator
  • BCH-GENE-SCBD-101900-6 CsVMV promoter | Cassava vein mosaic virus (Cassava vein mosaic virus, CVMV, CsVMV)
    Promoter
  • BCH-GENE-SCBD-104793-3 4-hydroxyphenylpyruvate dioxygenase | Pseudomonas fluorescens (PSEFL)
    Protein coding sequence | Resistance to herbicides
  • BCH-GENE-SCBD-101416-7 Ti plasmid right border repeat | Agrobacterium tumefaciens (Agrobacterium)
    Plasmid vector
  • BCH-GENE-SCBD-101025-5 NADP-malic enzyme 1 gene 3'UTR and terminator | Flaveria bidentis (Coastal plain yellowtops, FLABI)
    Terminator
  • BCH-GENE-SCBD-14985-12 Cry1Ab | Bacillus thuringiensis (Bt, Bacillus, BACTU)
    Protein coding sequence | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths))
  • BCH-GENE-SCBD-104947-3 5'e1 Leader | Oryza sativa (Rice, ORYSA)
    Leader
  • BCH-GENE-SCBD-101021-3 Ps7s7 | Subterranean clover stunt virus (SCSV, Subterranean clover stunt virus)
    Promoter
  • BCH-GENE-SCBD-100287-7 CaMV 35S promoter | Cauliflower mosaic virus (CaMV)
    Promoter
  • BCH-GENE-SCBD-14972-12 Phosphinothricin N-acetyltransferase gene | Streptomyces hygroscopicus (STRHY)
    Protein coding sequence | Resistance to herbicides (Glufosinate)
  • BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)
    Terminator
  • BCH-GENE-SCBD-101415-9 Ti plasmid left border repeat | Agrobacterium tumefaciens (Agrobacterium)
    Plasmid vector
  • BCH-GENE-SCBD-101901-3 5' untranslated leader of chlorophyll a/b-binding protein | Petunia hybrida (Petunia, PETHY)
    Leader
  • BCH-GENE-SCBD-101902-5 Ribulose-1,5-bisphosphate carboxylase small subunit transit peptide | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Transit signal
  • BCH-GENE-SCBD-101895-8 Cry2Ae | Bacillus thuringiensis (Bt, Bacillus, BACTU)
    Protein coding sequence | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths), Cotton bollworm (Helicoverpa spp.), Fall armyworm (Spodoptera frugiperda))
  • BCH-GENE-SCBD-100290-6 CaMV 35S terminator | Cauliflower mosaic virus (CaMV)
    Terminator
  • BCH-GENE-SCBD-14991-8 Hygromycin B phosphotransferase gene | Escherichia coli (ECOLX)
    Protein coding sequence | Resistance to antibiotics (Hygromycin),Selectable marker genes and reporter genes
  • BCH-GENE-SCBD-101874-2 Ubiquitin gene 3 promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoter
  • BCH-GENE-SCBD-104517-2 Actin 2 promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoter
  • BCH-GENE-SCBD-14990-5 Vegetative insecticidal protein 3A | Bacillus thuringiensis (Bt, Bacillus, BACTU)
    Protein coding sequence | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths))
  • BCH-GENE-SCBD-104662-3 PCSV Promoter | Peanut chlorotic streak virus (PCSV, PClSV)
    Promoter
  • BCH-GENE-SCBD-104664-2 TEV 5' Untranslated Region | Tobacco etch virus (TEV)
    Leader
  • BCH-GENE-SCBD-100365-6 Chloroplast transit peptide 2 | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Transit signal
  • BCH-GENE-SCBD-100728-3 Dicamba monooxygenase gene | Stenotrophomonas maltophilia (S. maltophilia, Stenotrophomonas)
    Protein coding sequence | Resistance to herbicides
  • BCH-GENE-SCBD-105600-1 E6 gene terminator | Gossypium barbadense (Sea-island cotton, Egyptian cotton, GOSBA)
    Terminator
  • BCH-GENE-SCBD-100366-6 CaMV Enhanced 35S promoter | Cauliflower mosaic virus (CaMV)
    Promoter
  • BCH-GENE-SCBD-103901-2 HSP 70 5' untranslated leader sequence | Petunia hybrida (Petunia, PETHY)
    Leader
DNA insert from BCS-GH811-4 (vector pTSIH09)
The transforming plasmid for cotton BCS-GH811-4 contains two gene cassettes: Pseudomonas fluorescens 4-hydroxyphenylpyruvate dioxygenase (hppd) and Zea mays 5-enolpyruvylshikimate-3-phosphate synthase (2mepsps).
(1) The hppd gene is under control of a Cassava vein mosaic virus promoter and Arabidopsis thaliana histone H4 gene terminator (H4A748). A synthetic optimized N-terminal transit peptide was included to target the translated HPPD W336 protein to the chloroplast. High levels of expression are expected due to the nature of the viral promoter.
(2) The 2mepsps gene is under control of an A. thaliana histone H4 promoter and 3'untranslated region. An A. thaliana histone H3 intron was included to enhance the expression of 2mepsps and a synthetic optimized N-terminal transit peptide is also present to direct the protein to the chloroplasts.
Note
  • Molecular characterization of the event indicated that a single copy of the transfer DNA was inserted into the genome without the integration of vector backbone sequences.
  • The hppd sequence contains an amino acid substitution (glycine replacement for tryptophan) at position 336. The sequence was then codon-optimized for expression in plants.
  • The 2mepsps sequence contains two point mutations:  at position102 (substitution of threonine by isoleucine) and position 106 (substitution of proline by serine).
  • The optimized transit protein contains the sequence of the RuBisCO small subunit genes of Zea mays and Helianthus annuus with a tyrosine substitution at position 55 and cotton codon optimization. 

DNA insert from BCS-GHØØ4-7 (vector pTDL008 derived from pGSV20)
The transforming plasmid of cotton BCS-GHØØ4-7 contains two gene cassettes: Bacillus thuringiensis crystal protein cry1Ab and Streptomyces hygroscopicus phosphinothricin N-acetyltransferase (bar).
(1) The cry1Ab coding sequence is under the control of Subterranean clover stunt virus genome segment 7 (Ps7s7) promoter and Flaveria bidentis NADP-malic enzyme 1 terminator. The 5' leader sequence from Oryza sativa E1 gene was also included in the cassette to enhance the expression of cry1Ab. High levels of transcription is expected  due to the viral promoter.
(2) The bar coding sequence is under the control of a Cauliflower mosaic virus 35S promoter and Agrobacterium tumefaciens nopaline synthase terminator. High levels of transcription is expected  due to the viral promoter.
Note
  • The cry1Ab gene has been derived from Bacillus thuringiensis strain berliner 1715 (Genbank accession No. X04698).
  • Sequencing of the 9056 bp inserted transgenic construct and Southern blot analysis revealed a truncated T-DNA construct (with an incomplete me1 terminator) was inserted into the T304-40 LM cotton line in addition to: (1) a partial 3’me1 terminator; (2) a partial copy of the cry1Ab gene cassette, with a truncated Ps7s7 promoter, in a tail-to-tail orientation; (3) a partial copy of the bar gene cassette in which the nos terminator is truncated.
  • As a result of the transformation event, four new junctions were created (see Figure 4 in the attached file below), two being located at the 5’ and 3’ ends of the insert and two being located within the insert as a result of the rearrangement. 
  • Southern blot analysis of the genomic DNA from COT102 revealed the incorporation of single intact copies of the vip3Aa and hpt genes, along with intact copies of their respective regulatory sequences. Results of these analyses also demonstrated that none of the vector backbone sequences, including the streptomycin adenyltransferase (aadA) gene, were incorporated into the genomic DNA.

DNA insert from BCS-GHØØ5-8 (vector pTEM12 derived from pGSC1700)
The transforming plasmid for cotton BCS-GHØØ5-8 contains two gene cassettes: Streptomyces hygroscopicus phosphinothricin N-acetyltransferase encoding gene, also known as the bialaphos resistance gene (bar), and Bacillus thuringiensis cry2Ae gene.
(1) The bar coding sequence is under control of a Cassava vein mosaic virus promoter and an Agrobacterium tumefaciens nopaline synthase terminator. Due to the constitutive nature of the promoters, high levels of transcription from the bar gene cassettes are expected.
(2) The cry2Ae coding sequence is under control of a Cauliflower mosaic virus 35S promoter and terminator. Due to the constitutive nature of the promoters, high levels of transcription from the cry2Ae gene cassettes are expected.
Note
  • Southern Blot analysis indicated that a single copy of the insert is present in the GHB119 parental line and a configuration that correspond to that in the original vector. No insertion of plasmid backbone sequences were detected, however three ORF were present at the junctions of the integration site but do not have the required regulatory elements for functionality. 

DNA insert from SYN-IR1Ø2-7 (vector pCOT-1)
The transforming plasmid for cotton SYN-IR1Ø2-7 contains two gene cassettes: Escherichia coli hygromycin B phosphotransferase (hpt) and Bacillus thuringiensis vegetative insecticidal protein 3A (vip3Aa).
(1) Transcription of hpt is under control of the Arabidopsis thaliana ubiquitin 3 promoter and the Agrobacterium tumefaciens nopaline synthase (nos) terminator. The gene cassette is present in the counterclockwise orientation.
(2) The expression of Bacillus thuringiensis vip3Aa is under transcriptional control of the A. thaliana actin 2 promoter and the nos terminator.
Note
  • The coding sequence of the vip3Aa was optimized for expression in plant cells.
  • Transcription is expected to occur at elevated levels due to the constitutive nature of the promoters.
  • Southern blot analysis indicated the incorporation of a single copy of the transgene cassettes without the integration of the vector backbone sequences.
  • Western blot analysis confirmed the expression of the proteins. 

For additional information on this LMO, please refer to the records of the parental LMOs.
EN
LMO characteristics
EN
  • Feed
  • Fiber/textile
Additional Information
DNA insert from SYN-IR1Ø2-7 (vector pCOT-1)
  • This insect resistance is conferred by the vip3Aa gene, originally isolated from the common soil bacterium Bacillus thuringiensis strain AB88. The vip3Aa gene produces the insect control protein VIP3A in the plant tissues. VIP3A is a member of a class of recently discovered insecticidal proteins: VIP (vegetative insecticidal proteins) proteins are expressed by the bacterium during the vegetative stage, as well as during sporulation, the stage at which the delta-endotoxins (i.e., Cry proteins) are expressed. 
  • VIP proteins have an insecticidal mode of action similar to that of the delta-endotoxins: the ingestion by targeted insects leads to feeding cessation, loss of gut peristalsis, insect paralysis, and death. As with Cry proteins, VIP proteins also possess an active proteolytic core, which is activated by insect gut proteases, and binds to specific sites localized on the midgut lining of susceptible insect species. However, the VIP3A protein targets different molecules (i.e., receptors) in the mid-gut lining, and the binding results in the formation of ion channels distinct from those formed by delta endotoxins, such as Cry1Ab.
  • VIP proteins are not expected to affect other invertebrate and vertebrate organisms, including beneficial arthropods, birds and mammals. Only lepidopteran insect species possess VIP binding sites on the surface of their gut epithelia, therefore, livestock animals and humans are not susceptible to these proteins. Also, since only lepidopteran insect species are targeted by the VIP proteins, species of other insect orders, including beneficial and pest species, are not expected to be affected by this insecticidal protein. 
EN