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Notification report


General information

Notification Number
B/FR/05/02/02

Member State to which the notification was sent
France

Date of acknowledgement from the Member State Competent Authority
07/01/2005

Title of the Project
Testage de maïs génétiquement modifiés tolérants à un herbicide

Proposed period of release:
01/04/2005 to 30/11/2008

Name of the Institute(s) or Company(ies)
Biogemma, ;


3. Is the same GMPt release planned elsewhere in the Community?
No

Has the same GMPt been notified elsewhere by the same notifier?
No

Genetically modified plant

Complete name of the recipient or parental plant(s)
Common NameFamily NameGenusSpeciesSubspeciesCultivar/breeding line
maizepoaceaezeazea maysmaysA188 line

2. Description of the traits and characteristics which have been introduced or modified, including marker genes and previous modifications:
Improvement of growing performances under drought conditions
Transgenic plants contain the bar gene conferring resistance to glufosinate.


Genetic modification

3. Type of genetic modification:
Insertion;

In case of insertion of genetic material, give the source and intended function of each constituent fragment of the region to be inserted:
CsVMV promoter: Cassava vein mosaic virus non coding regulatory sequence
Asr1: Zea mays coding sequence
Actin1 promoter &first intron:Oryza sativa non coding regulatory sequence
bar: Streptomyces hygroscopicus coding sequence
nos 3’: Agrobacterium tumefaciens non coding regulatory sequence
Ds 5’ / Ds 3’: Zea mays non coding sequence
RB / LB: Agrobacterium tumefaciens non-coding sequence


6. Brief description of the method used for the genetic modification:
Agrobacterium tumefaciens mediated transformation.

7. If the recipient or parental plant is a forest tree species, describe ways and extent of dissemination and specific factors affecting dissemination:
Non applicable

Experimental Release

1. Purpose of the release:
Production of plant and grain under agronomic conditions (irrigation) and in dry conditions (low or no irrigation).
Total biomass production evaluation under different irrigation conditions.
Functional gene validation.


2. Geographical location of the site:
Center of France (Puy-de-Dôme, Auvergne)
South-west of France (Haute-Garonne, Midi-Pyrénées)
West of France (Charente Maritime, Poitou Charente)
South-East of France


3. Size of the site (m2):
Auvergne 1 500 sq mt (2005 to 2008, border rows not included)
Midi-Pyrénées 1 500 sq mt (2005 to 2008, border rows not included)
Poitou Charente 1 500 sq mt (2005 to 2008, border rows not included)
South-East of France 1 500 sq mt (2005 to 2008, border rows not included)


4. Relevant data regarding previous releases carried out with the same GM-plant, if any, specifically related to the potential environmental and human health impacts from the release:
First release for these transformation events.

Environmental Impact and Risk Management

Summary of the potential environmental impact from the release of the GMPts:
None of the introduced traits has potential effects to modify the plant persistency in the environment. There is no wild relatives of corn in Europe and outcrossing are not possible. In this experiment, there is no modification of the direct or indirect interactions between the modified plants and target or non-target organisms. There is no expected effects on human health and on animal health. Plants will not be used as food. There is no short-term possible effect on specific cultivation management and harvesting techniques.
Potential environmental impact considered minimal, given the conditions of the field trial (location, absence of pollen production or field isolation, minimal contacts with fauna and flora, absence of wild relatives of maize species in the release areas...).


Brief description of any measures taken for the management of risks:
Release sites located in intensive agriculture areas. Collection of seeds, destruction of plant vegetative material.
Monitoring and destruction of volunteers during one year following the end of experiment.


Summary of foreseen field trial studies focused to gain new data on environmental and human health impact from the release:
Non applicable

Final report
-

European Commission administrative information

Consent given by the Member State Competent Authority:
Yes
27/04/2005 00:00:00
Remarks: