Loading...
You are viewing a DELETED record.
This record information is displayed for reference purpose only and should be not used.
This document has been updated. This is not the latest published version. Click here to view the latest version of the record.
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.
Insect-resistant sugarcane
EN
CTC-92015-7
Yes
CTC-92Ø15-7
-
Organization:CTC - Centro de Tecnologia Canavieira (CTC)Regional economic integration organizationFazenda Santo Antônio s/n, Caixa Postal 162Piracicaba, Sao Paulo
13400-970, BrazilPhone: +55 (11) 3429-8111,Fax: +55 (11) 3429-8111,Email: Wladecir.oliveira@ctc.com.br,Website: http://new.ctc.com.br/,
The sugarcane (Saccharum officinarum) event CTC-92015-7 expresses the Cry1Ac protein, which confers resistance to the sugarcane borer (Diatraea saccharalis), and the NPTII protein, used as a kanamycin selectable marker during transformation. This event uses sugarcane variety RB 92579 as the genetic background and thus differs from the other events developed by the Centro de Tecnologia Canavieira.
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-115592-1 Organism Saccharum officinarum L. (Sugarcane, Sugar cane)Crops
Variety RB 92579
EN
-
CTC-95Ø19-5 - Insect-resistant sugarcane| Dr Wladecir Salles Oliveira | Resistance to antibiotics (Kanamycin), Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths)), Selectable marker genes and reporter genes
pCTC146
EN
- Agrobacterium-mediated DNA transfer
|
0.000 kb
|
|
0.000 kb
|
|
0.000 kb
|
|
0.000 kb
|
|
0.000 kb
|
|
0.000 kb
|
|
0.000 kb
|
|
0.000 kb
|
Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
-
BCH-GENE-SCBD-14986-6 Cry1Ac | Bacillus thuringiensis (Bt, Bacillus, BACTU)Protein coding sequence | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths))
-
BCH-GENE-SCBD-100290-6 CaMV 35S terminator | Cauliflower mosaic virus (CaMV)Terminator
-
BCH-GENE-SCBD-100355-6 Rice actin 1, intron | Oryza sativa (Rice, ORYSA)Intron
-
BCH-GENE-SCBD-100354-6 5' untranslated leader from chlorophyll a/b-binding protein | Triticum aestivum (Wheat)Leader sequence
-
BCH-GENE-SCBD-100362-7 Ubiquitin gene promoter | Zea mays (Maize, Corn, MAIZE)Promoter
-
BCH-GENE-SCBD-15001-5 Neomycin Phosphotransferase II | Escherichia coli (ECOLX)Protein coding sequence | Resistance to antibiotics (Kanamycin)
-
BCH-GENE-SCBD-100269-8 Nopaline Synthase Gene Terminator | Agrobacterium tumefaciens (Agrobacterium)Terminator
-
BCH-GENE-SCBD-100366-6 CaMV Enhanced 35S promoter | Cauliflower mosaic virus (CaMV)Promoter
The modified sugarcane contains two gene cassettes: Bacillus thuringiensis crystal protein (cry1Ac) and Escherichia coli neomycin phosphotransferase II (nptII).
The cry1Ac coding sequence is under control of an enhanced Cauliflower mosaic virus 35S promoter and 35S terminator. The gene cassette additionally contains a Triticum aestivum 5' untranslated leader from chlorophyll a/b-binding protein and an Oryza sativa actin 1 intron for enhanced expression of cry1Ac. Due to the enhanced promoter and genetic elements, high levels of constitutive expression of Cry1Ac are expected.
The nptII coding sequence is under control of a Zea mays ubiquitin promoter and Agrobacterium tumefaciens nopaline synthase terminator. Expression of NPTII is expected in all plant tissues due to the nature of the ubiquitin promoter.
Note: The modified sugarcane event CTC-92015-7 expresses the same Cry1Ac and NPTII proteins, with 100% sequence homology, expressed by the reference CTC93209-4 modified sugarcane (see https://bch.cbd.int/en/database/record?documentID=115563).
The cry1Ac coding sequence is under control of an enhanced Cauliflower mosaic virus 35S promoter and 35S terminator. The gene cassette additionally contains a Triticum aestivum 5' untranslated leader from chlorophyll a/b-binding protein and an Oryza sativa actin 1 intron for enhanced expression of cry1Ac. Due to the enhanced promoter and genetic elements, high levels of constitutive expression of Cry1Ac are expected.
The nptII coding sequence is under control of a Zea mays ubiquitin promoter and Agrobacterium tumefaciens nopaline synthase terminator. Expression of NPTII is expected in all plant tissues due to the nature of the ubiquitin promoter.
Note: The modified sugarcane event CTC-92015-7 expresses the same Cry1Ac and NPTII proteins, with 100% sequence homology, expressed by the reference CTC93209-4 modified sugarcane (see https://bch.cbd.int/en/database/record?documentID=115563).
EN
- Food
EN
For more information on the genetic elements, see the pCTC146 vector map in the attached Chinese patent.
- CN114457088A.pdf [ Chinese ]
Loading...
