GE Free New Zealand
GE Free New Zealand PRESS RELEASE –7.12.03
Veil of Secrecy for GE Constructs Prompts Ombudsman Appeal
GE Free New Zealand (in food and environment) is to appeal to the ombudsman after ERMA - the Environmental Risk
Management Authority- refused an Official Information Act request to identify the gene constructs used in an application
for GE onions.
In a letter rejecting the request ERMA have cited the information would both 'unreasonably prejudice' and 'damage' the
commercial position of Seminis Seeds and Crop and Food.
But GE Free New Zealand is concerned that ERMA have seen fit not to allow this information to be released in the public
interest when international research has revealed genetic constructs used in commercial crops have fragmented and
Instead ERMA are unfairly allowing corporate interests to make the rules and are keeping hidden information that is
vital for independent scientists to contribute advice.
"We are worried that ERMA are setting a precedent with this veil of secrecy in the face of alarming new findings of
genetic instability", says Jon Carapiet from GE Free NZ in food and environment.
It is deeply concerning that ERMA will be the only body 'in the know' about gene constructs to be used in the New
Zealand environment in future.
The decision must be appealed to the ombudsman or it will create a situation where no independent scientific advice or
viewpoints will be taken into account.
Since ERMA are a quasi judicial body that cannot be held responsible for their decisions under the law GE Free New
Zealand feel this is wholly unreasonable.
The whole basis of patenting and approving GE organisms is dependent on specified gene maps, but these are now being
found to have changed from the original after release. The discovery indicates an intrinsic instability that calls into
question the validity of both the science used to develop and approve the organism and the patents.
Biotech companies know that these crops are unstable and without transparency and openness from ERMA companies will find
it easier to hide the fact.
Once again the promises made by government about the "new improved" ERMA process are being revealed to be part of a
regulatory sham designed to promote biotech commercial interests over those of the public and sound peer-reviewed
"We have no option but to appeal to the ombudsman against ERMA's secrecy," says Mr Carapiet.
Jon Carapiet - 09 815 3370
See below - ISIS Press Release 03/12/03
Unstable Transgenic Lines Illegal
ISIS Press Release 03/12/03
Unstable Transgenic Lines Illegal
Further evidence that most if not all commercially approved transgenic lines are genetically unstable and non-uniform
has come to light. The transgenic lines fail to satisfy the current EU Directive requirements for proof of genetic
stability and uniformity, and are hence illegal. Dr. Mae-Wan Ho reports.
In a recent study  on five commercially approved transgenic lines carried out by two French laboratories , all
five transgenic inserts were found to have rearranged, not just from the construct used in transformation, but also from
the original structure reported by the company. This was clear evidence that all the lines were genetically unstable.
Further evidence has come to light since. The Service of Biosafety and Biotechnology (SBB) of the Scientific Institute
of Public Health (IPH) in Brussels has published on its website (http://biosafety.ihe.be/TP/MGC.html) reports on the
molecular characterisation of the genetic map of six transgenic lines, four of which overlap with those analysed by the
French laboratories: Bt 176 maize (Syngenta), Mon 810 maize (Monsanto), T25 maize (Bayer CropScience) and GTS 40-3-2
The IPH is a Scientific Institute of the State, linked to the Belgian Federal Ministry of Social Affairs, Public Health
and the Environment.
The Brussels reports are an overview of data presented at a meeting of the Belgian Biosafety Advisory Council. The data
come from different scientific institutions, the applicants and from published papers. The reports found evidence of
genetic instability similar to those described in the French study.
However, there are small and large discrepancies when the two sets of data are compared. In one case, Bt 176, there may
even have been a misreporting or misidentification of the Bt transgene present, which the company claimed to be crylAb.
Comparison with the public database revealed that the transgene has only 65% homology with the native crylAb, but 94%
homology with crylAc. Bt toxins are potential allergens and immunogens; crylAc, in particular, was identified as a
potent systemic and mucosal immunogen, as potent as cholera toxin .
The studies also revealed a discrepancy in regulatory practice. UK’s Advisory Committee on Novel Foods and Processes
(ACNFP) and the Belgian authority both appear to have allowed Monsanto to submit new molecular data on Roundup Ready
soybean when independent analysis revealed its insert had rearranged.
Most of the discrepancies involve the structure of the insert, the number of insert(s) and locations within the genome;
suggesting that the transgenic lines are not only unstable but also non-uniform. Consequently, the results of the
molecular characterisation could differ from sample to sample of the same transgenic line. In other words, the
transgenic lines may well not pass the DUS (distinctness, uniformity and stability) test, which is required by European
The new EU Directive 2001/18/EC on deliberate release of GMOs also requires information documenting genetic stability
(Annex IIIB) as a condition for market approval. Genetic stability can only be demonstrated by ‘event specific’
molecular data of the kind carried out in the two studies. In view of the finding that practically every transgenic
insert has rearranged from that reported in the company’s original dossier, it would indicate that the transgenic lines
have failed the test of genetic stability, and are no longer the same lines that were risk assessed, and in some cases,
placed on the market. This has important safety implications. Rearrangements and deletions are signs of structural
instability, which enhances horizontal gene transfer and recombination, with all the attendant risks . This is
particularly relevant as the molecular analyses have so far revealed a strong tendency for transgenic inserts to land in
mobile genetic elements, such as retrotransposons and repeat sequences. Four out of six transgenic inserts analysed for
flanking sequences identified repeat or retrotransposon sequences.
For either or both those reasons, it would be illegal, under European legislation, to grant those transgenic lines
commercial approval; and the lines that have been approved must surely now be withdrawn.
The detailed comparisons on the findings in the four transgenic lines from the two studies are presented below, followed
by comments on the additional transgenic lines investigated separately in the two studies.
Transgenic lines analysed in both studies
Bt 176 maize (Syngenta)
The Bt176 maize dossier was first submitted in 1994 by Ciba Geigy (Novartis) and approved under the old EU Directive for
growing, seed production, import, processing and food/feed purposes since 23 January 1997 . It was modified for
tolerance to the herbicide glufosinate, male sterility and insect resistance. Two constructs were used to transform
maize (see below).
Only the simpler construct was analysed. Company data showed single insert containing the cauliflower mosaic virus
(CaMV) 35S promoter (hereafter referred to as P35S) driving the bar gene (glufosinate tolerance) terminated by the CaMV
35S terminator (hereafter referred to as T35S) followed by the ampicillin resistance (bla) gene plus a bacterial
promoter, and the plasmid origin of replication, ori.
Analysis revealed several fragments, all containing P35S: one with P35S joined to T35S, a second with P35S joined to an
unknown sequence, and a third with P35S joined to the bar gene, with the T35S deleted (that means P35S could drive the
expression of downstream maize genes).
At least three insertion sites were found for this construct.
This study  describes the line as being obtained by microprojective bombardment into immature embryos of inbred corn
line CG00526 (Zea mays L.) using two different transforming plasmids. The plasmid pCIB4431 contains two copies of a
synthetic truncated crylA(b) gene, having approximately 65% homology at nucleotide level with the native gene of
Bacillus thuringiensis subsp. kurstaki strain HD1. The first copy is under the regulation of the maize
phosphenlopyruvate caboxylase (PEPC) promoter (PPEPC) and the T35S. The second copy is under the regulation of the maize
calcium-dependent protein kinase (CDPK) promoter(PCDPK), resulting in pollen-specific expression, and terminated with
T35S. In addition, both copies were combined with the intron #9 derived from the maize PEPC gene to enhance expression
in maize. The plasmid pCIB3064 contains the bar gene derived from Streptomyces hygroscopicus under the regulation of
P35S and T35S. Both plasmids also contain a copy of the bla gene for amipicillin resistance under the control of a
There are still uncertainties about the copy number of the insert in event Bt176. Published results from Koziel et al
 indicated that there may be as many as five copies of the crylA(b) gene present.
Data from Centrum Landbouwkundig Onderzoek, Mell, Belgium (CLO) revealed that the cry coding sequence showed 94%
similarity with Genbank accession no. AF537267 for synthetic construct of crylAc gene. In comparison, the cry transgene
showed only 65% homology at nucleotide level with the native gene of Bacillus thuringiensis subsp. kurstaki strain HD1.
This suggests the company may have misreported or misidentified the transgene present.
The company’s dossier claimed one single copy of transgene insert (P35S-bar-T35S), and gave no information on 5’ or 3’
flanking sequences. For the second transgene insert (T35S-int#9-crylAb-PPEPC-PCPDK- cry1Ab-int#9-T35S), it claimed 2 to
5 copies were present, but no information on flanking sequences was provided.
Other sources report that first transgene insert is present in at least 4 truncated copies, and depending on the source,
the number of truncated copies differs. This is an indication of non-uniformity of the transgenic line as well as
genetic instability. The second transgene insert is present in at least 5 copies.
There are basic agreements between the two studies on the rampant rearrangements that have occurred. There is also
evidence of non-uniformity from the Brussels study.
Mon 810 (Monsanto)
Mon 810, modified for resistance to lepidopteran insects (butterflies & moths), was submitted by Monsanto in 1995 and approved under the old Directive for growing, import, seed production and
processing into animal feeding stuffs and industrial purposes since 22 April 1998 . In December 1997 food and food
ingredients derived from Mon 810 maize were notified under Article 5 of the Regulation (EC) 238/97 (for novel foods).
Several hybrids of Mon810 are still pending approval for marketing:
T25 x Mon810 submitted under the old directive in April 1999. The Scientific Committee gave a favourable opinion on 6
Mon810 x K603 submitted 15 Jan 2003 under the new Directive 2001/18/EC for import and use in feed and industrial
Mon863x Mon 810 submitted under the new Directive 7 Feb. 2003 for import and use of grain and grain products. On 29
August 2002, the application was submitted under Regulation (EC) 258/97.
MaisGard/RR (Mon810and GA21) submitted under the new Directive 13 Feb 2003 for import and use in feed and industrial
processing. On 16 March 2000, maize application was submitted under Regulation (EC) 258/97.
Company data showed that the insert has a P35S driving a crylAb synthetic gene with terminator T-nos. Maize heat shock
protein intron is located between P35S and crylAb. Analysis revealed however, that T-nos and part of the 3’ (tail) end
of the crylAb gene have been deleted. T-nos is detected elsewhere in the genome, indicating that it may have moved from
its original position.
The 5’ (head) end of the insertion site shows homology to the long terminal repeats (LTR) of the maize alpha Zein gene
cluster, but no homology to the maize genome was detected at the 3’ site, indicating that there had been scrambling of
the maize genome at the insertion site. The strong P35S promoter could therefore be driving the transcription of an
unknown gene downstream.
Mon 810 was produced by transforming maize genotype HiII with two plasmid vectors, pV-ZMBK07 and pV-ZMGT10. The plasmid
pV-ZMVK07 contains the crylAb gene isolated from Bacillus thuringiensis ssp. kurstaki, placed under control of the
enhanced CaMV 35S promoter (e35S) and the T-nos. An intron from the maize heat-shock protein (hsp70) is located between
the e35S promoter and the crylAb gene. The second plasmid pV-ZMGT10 contains the CP4 EPSPS gene from Agrobacterium
strain CP4 and the gox gene cloned from Achromobacter strain LBAA. Both plasmids contain the nptII gene under control of
a bacterial promoter. Molecular analysis by Monsanto showed that the nptII gene and the backbone sequences of pV-ZMBK07
are not integrated and that none of the DNA sequences from vector pV-ZMGT10 are present.
According to the company dossier, Mon 810 contains a single copy of the e35S promoter, the hsp70 intron and the crylAb
gene. The absence of the 3’T-nos sequence was confirmed by CLO.
CLO determined the 5’ junction, upstream from the e35S, and found that the DNA shows 88% identity with the 22kDa alpha
Zein gene of maize.
The rearrangement of the insert was confirmed in both studies. A potentially serious discrepancy is that the French
study found the insert flanked by the LTR of the Zein gene cluster at its 5’end, and not by the Zein gene, as found in
the Brussels study. A minor discrepancy is in the P35S reported in the French study as opposed to e35S in the Brussels
study, and the detecting of T-nos elsewhere in the maize genome in the French study.
T25 maize (Bayer)
Liberty-link maize event T25, modified for tolerance to the herbicide glufosinate, was submitted by AgrEvo (Bayer
CropScience) in 1995 and approved for marketing since 22 April 1998 . Products derived from T25 have been notified
under Article 5 of the Regulation (EC) 258/97 on 21 October 1999.
A hybrid of T25, still pending approval for marketing, T25 x Mon 810, was submitted 29 April under the old Directive,
and the Scientific Committee gave a favourable opinion on the dossier 6 June 2000.
Company data showed that the insert includes a truncated ampicillin resistance bla gene in the plasmid vector pUC18, a
P35S driving a synthetic pat gene (glufosinate tolerance) terminated by T35S. On analysis, the insert was found to have
undergone further rearrangement, so that a second, truncated and rearranged P35S has been joined to the 5’ (left, or
head) end of the insert, while additional pUC18 sequences were found at the 3’ (right, or tail) end.
Edges flanking the insert show homologies (similarities) with Huck retrotransposons (a class of mobile genetic elements)
in the maize genome.
T25 was obtained by protoplast transformation of the parental line He/89 using plasmid pUC/Ac containing the pat gene
from S. viridochromogenes Tu494 and controlled by P35S and T35S. The plasmid includes the bla gene for ampicillin
The company dossier claimed there was a single insert, and this was confirmed by CLO’s analysis. The pat gene is
"surrounded" by sequences from the plasmid vector pUC18. According to the dossier, a 2187 bp pUC fragment is present
upstream of P35S. This fragment ends up in the bla gene followed by a 353bp fragment of the P35S, probably resulting
from a duplication/recombination event. CLO confirmed these data, except that a shorter, 298 bp P35S promoter fragment
was found. According to both the applicant and CLO, a fragment from pUC plasmid was found at the 3’ end downstream of
35S terminator; but differences in length were reported.
Aventis submitted data that describe the host flanking sequences of the T25 line. A 151p(5’) and a 121 bp (3’) fragment
show homology (94% identity) to maize alcohol dehydrogenase adh1 gene. This differs from the findings of the French
study, which detected flanking sequences homologous with Huck retrotransposons.
Apart from this discrepancy, the nature of the rearrangement in the insert was confirmed in both studies.
GTS 40-3-2 (Monsanto)
This line was modified for tolerance to the herbicide glyphosate (Roundup Ready variety). According to UK’s Advisory
Committee for Novel Foods and Processes (ACNFP) , the Committee considered Monsanto’s RR soybeans line 40-3-2 under
its "voluntary scheme" in 1994 and gave it clearance for food safety on 20 February 1995. The event has been approved
for planting and/or consumption in a number of countries worldwide and products from it consumed for a number of years.
The company’s original data showed a single insert with P35S driving a composite gene containing the N-terminal
chloroplast transit peptide (CPT4) joined to modified EPSPS gene with T-nos terminator. Analysis provided by the
Ministry of Midclass and Agriculture, Belgium, published by Windels et al  revealed that a 254bp piece of DNA
homologous to the EPSPS gene and 534bp of unknown DNA have been joined to the 3’end of the insert.
It was not possible to identify the insertion site, indicating that substantial genome scrambling or deletion had taken
place at the insertion site.
This study merely referred out to the ACNFP website. It appears that Monsanto was allowed to submit new data in 2000,
and again in 2002. The first confirming that a 254bp piece of the EPSPS gene has been joined to the 3’ end of the
insert, the second claiming that "large portions" (29bp + 420bp) of the 543bp of unknown DNA found by Windels et al 
was identical to soybean genomic DNA from the company’s own "proprietary database", that has undergone rearrangement.
While the French study emphasized the rearrangement of the insert, both the UK ACNFP and the Brussel report have
accepted Monsanto’s new data and not questioned why they should differ so substantially from those presented in the
company’s original dossier.
Transgenic lines analysed in one study only
GA 21 maize (Monsanto) – French study
The line was modified for tolerance to the herbicide glyphosate (Roundup Ready). Company data indicated that the insert
contains multiple copies of the cassette with the rice actin gene promoter (P-ract) driving the composite gene
containing the N-terminal chloroplast transit peptide (CPT4) joined to modified EPSPS gene and T-nos. There were three
complete cassettes flanked by a cassette with P-ract partially deleted at the 5’ end, and one cassette with 3’ deletion
of EPSPS plus a lone P-ract at the 3’end. Analysis found partial deletion of P-ract and deletion of T-nos in two
The insertion site at the 3’end is flanked by sequences of pol polyprotein gene belonging to a PREM2-retrotransposon.
On 15 September 2003, Monsanto informed the European Commission that it was withdrawing its application for GA21 Roundup
Ready maize and GA21 x MON810 MaisGard/Roundup Ready maize, for "commercial reasons".
Bt 11 maize (Syngenta) – Brussels study
This was notified in 1996 and approved under the old Directive for import and processing since 22 April 1998 . The
notifications for cultivation submitted in 1996 and 1998 are still pending. On 30 November 2000, the EU Scientific
Committee on Plants gave a favourable opinion for cultivation. Up till now, the Commission has not received an updated
version of these two notifications according to the requirements of Directive 2001/18/EC. In February 1999, Novartis
submitted a new application, which is still pending. On 13 March 2002, the SCP gave a favourable opinion.
Food and food ingredient products derived from Bt11 crossed with the Northup King Company inbred line #2044 maize were
notified on 20 Jan. 1998.
The plasmid used for transformation contains a synthetic truncated crylAb, isolated from Bacillus thuringiensis spp.
kurstaki HDI, and a synthetic pat gene, isolated from Streptomyces viridochromogenes Tu494. Both coding sequences were
placed under the regulation of P35S and the T-nos terminator from Agrobacterium tumefaciens. In addition, the promoter
sequences of the pat and cry1Ab gene were combined with respectively intron Int II and Int VI derived from maize alcohol
dehydrogenase adh1S gene to enhance expression. The event Bt11 maize was obtained by protoplast transformation with
plasmid pZ01502 after digestion with restriction enzyme Not1 to remove the bla gene encoding ampicillin resistance.
The whole sequence of the insert was determined by TEPRAL, Strasbourg, France. The insert consists of a single copy of
the vector fragment carrying both the crylAb and pat gene. "It was found that rearrangements have taken place into the
insert compared to the original insert and that several parts of the plasmid have been truncated or unexpected inserted,
e.g., t35S sequences….The presence of t35S fragments into the insert was confirmed by INRA."
Sequence analysis done by CLO with PCR using P35S specific primer in combination with a 3’T-nos specific primer, proved
that the DNA segment present in between the two expression cassettes of the Bt11 insert is similar to the pUC vector
Zimmermann et al  showed that next to the 5’ P35S border of the crylAb, a maize 180bp knob-specific repeat sequence
is present. In addition, CLO analysed the sequence that is present between the P35S sequence and the maize plant and
demonstrated that a 1099 bp segment is present, homologous to the pUC backbone sequence and contains part of the lacZ
The junction regions at the 3’ T- nos terminator border were amplified by CLO using a specific anchor primer. A 244 bp
junction was amplified that contains 149 bp plant DNA that on BLAST sequence analysis, showed similarity to the maize
180bp knob associated tandem repeat. Independently from CLO, the 3’ T-nos border region was also amplified by Ronning et
al , confirming this finding. The remaining part of the amplified 3’T-nos junction is homologous with the pUC
These data provide evidence that the Bt11 insert is integrated in the Zea mays 180bp knob associated tandem repeat
locus. At the P35S border, an extensive piece 1099 bp of pUC backbone DNA was observed between the plant DNA and the
P35S promoter, while at the 3’nos border only a small stretch of pUC backbone DNA is present.
According to TEPRAL, it is not certain if only one copy of the insert is present.
Preliminary data of INRA showed that a set of primers designed on the edge fragment of Bt 176 amplified sequences from
both Bt176 and Bt11. These data were obtained on six different Bt11 plant seeds received by Syngenta, suggest
contamination of Bt11 by Bt176.
Bt 11 is therefore neither genetically stable nor uniform, and should on no account be approved.
Event Ms8xRf3 canola (Aventis, Bayer)
This ‘event’ is really a composite of two different transformations, and was first notified in 1996 (C/BE/96/01) from
PGS (now Bayer Cropscience) under the old Directive 90/220/EEC for cultivation, import, seed production and processing
into animal feed stuffs and industrial purposes . On 24 Jan 2003, the European Commission received an updated
version according to the requirements of the new Directive 2001/18/EC. Oil derived from Ms8xRf3 products has been
notified under Article 5 of the Regulation (EC 258/97) on 21 October 1999.
It is not clear whether the company’s data were provided in the original 1996 dossier or in the updated version
submitted 24 January 2003.
Ms8 was produced by Agrobacterium mediated transformation using plasmid pTHW107. This plasmid contains the barnase gene
derived from Bacillus amyloliquefaciens and the bar gene derived from Streptomyces hygroscopicus. Barnase under
regulation of a tapetum specific promoter PTA29 isolated from Nicotiana tabacum and the T- nos terminator of
Agrobacterium tumefaciens. The bar gene is regulated by the PSsuAra promoter isolated from Arabidopsis thaliano and by
the 3’ end of the T-DNA gene 7 of A. tumefaciens.
The transgenic fertility restorer line Rf3 was obtained using plasmid pTHW118 containing a barstar gene derived from
Bacillus amyloliquefaciens under regulation of the PTA29 promoter and the T-nos together with the same bar cassette as
described for pTHW107.
According to the company dossier, the Ms8 insertion contains a single T-DNA copy. At the left border (3’end of the
T-DNA) a 357 bp host sequence was retrieved. At the right border junction (5’ of the TDNA) an 864 bp host sequence was
retrieved. PCR amplification from the parental line showed co-linearity with the sequences found on both sides of the
T-DNA insert. Molecular analysis done by the CLO confirmed that the adjacent DNA is plant DNA. Search in the database
showed that part of the 5’ flanking regions has over 82% similarity with Arabidopsis sequences.
Determination of the pre-insertion site was done by the applicant using DNA isolated from wild type oilseed rape.
Alignment of wildtype sequence with the Rf3 transgene locus revealed that a fragment of 51 bp is present at the wildtype
locus but missing from the transgene locus. At the right border 5 nucleotides (filler-DNA) are inserted. Alignment of
the wildtype sequence with the Ms8 transgenic locus revealed that 19bp are missing at the target site. At right border
junction 3 nucleotides of unknown origin are inserted.
Both Rf3 line and Ms8 line transgene is integrated in a single genetic locus. But the Rf3 event resulted in the
insertion of one-TDNA copy arranged in an inverted repeat structure with a second incomplete T-DNA copy. Event Ms8
contains an intact single T-DNA copy. During insertion, typical rearrangements have occurred at the pre-insertion site.
In both lines, the dossier claimed, the inserts are flanked by plant DNA showing high similarity with Arabidopsis DNA.
CLO analysis confirms data in dossier (1996) for the right border (RB) of the Rf3 insert, but no data were available for
the truncated left border (LB) and the plant DNA rearrangement. For Ms8, CLO confirms data in dossier.
I cannot ascertain from the report whether rearrangement had occurred in the original inserts in the two events Ms8 and
Rf3, as it is unclear if the company’s data were provided in the original 1996 dossier or in the updated version
submitted 24 January 2003. The characteristic inversions, duplications and deletions, insertions and scrambling of host
genome DNA at the sites of insertions are evident.
We have explained why this line is unacceptable in other respects  and should not be approved for commercial
release. This is a ‘terminator’ crop, engineered for male sterility, ostensibly to prevent transgene escape, but in
reality to protect patented herbicide tolerant trait. It also prevents farmers from saving seeds, compelling them to buy
the fertile hybrid every year. In reality, the crop spreads both the male sterility ‘suicide’ gene barnase in its pollen
– which is highly toxic to all cells, mammalian included - as well as the herbicide tolerance trait, with potentially
large impacts on agricultural and natural biodiversity including the soil biota. The results of UK government-sponsored
Farm Scale Evaluations, recently released, have documented negative impacts on biodiversity from growing this transgenic
1. "Transgenic lines proven unstable" by Mae-Wan Ho, ISIS Report, 23 October 2003 www.i-sis.org.uk
2. Collonier C, Berthier G, Boyer F, Duplan M-N, Fernandez S, Kebdani N, Kobilinsky A, Romanuk M, Bertheau Y.
Characterization of commercial GMO inserts: a source of useful material to study genome fluidity. Poster presented at
ICPMB: International Congress for Plant Molecular Biology (n°VII), Barcelona, 23-28th June 2003. Poster courtesy of Pr.
Gilles-Eric Seralini, Président du Conseil Scientifique du CRII-GEN, www.crii-gen.org
3. Vázquez-Padrón RI, Moreno-Fierros L, Neri-Bazán L, de la Riva G and López-Revilla R. Intragastric and intraperitoneal
administration of CrylAC protoxin from Bacillus thuringiensis induce systemic and mucosal antibody response in mice.
Life Sciences 1999, 64, 1897-1912.
4. Ho MW, Lim LC et al. The Case of a GM-Free Sustainable World, Report of the Independent Science Panel on Genetic
Modification, TWN and ISIS, Penang and London, 2003.
5. Report on the molecular characterisation of the genetic map of event Bt176, 16 June 2003, Scientific Institute of
Public Health, Service of Biosafety and Biotechnology IPH/1520/SBB/03-0408.
6. Koziel MG et al. Field performance of elite transgenic maize plants expressing an insecticidal protein derived from
Bacillus thuringiensis. Bio/Technology 1993, 11, 194-200.
7. Report on the molecular characterisation of the genetic map of event Mon 810, 16 June 2003, Scientific Institute of
Public Health, Service of Biosafety and Biotechnology IPH/1520/SBB/03-0409.
8. Report on the molecular characterisation of the genetic map of event T25, 16 June 2003, Scientific Institute of
Public Health, Service of Biosafety and Biotechnology IPH/1520/SBB/03-0407.
10. Windels P, Tavenier I, Depicker A, Van Bockstaele E and De Loose M. Characterisation of the Roundup Ready soy
insert. Eur Food Res and Tech 2001, 213, 107-12.
11. Report on the molecular characterisation of the genetic map of event Bt11, 16 June 2003, Scientific Institute of
Public Health, Service of Biosafety and Biotechnology IPH/1520/SBB/03-0325.
12. Zimmerman A, Luthy J and Pauli U. Event specific transgene detection in Bt11 corn by quantitative PCR at the
integration site. Lebensm Wiss u Technol 2000, 33, 210-6.
13. Rønning SB, Vaitlingom M, Berdal KG and Holst-Jensen A. Event specific real-tiime quantitative PCR for genetically
modified Bt11 maize (Zea mays). Euro Food Res Technol 2003, DOI 10.1007/s00217-002-0653-4.
14. Report on the molecular characterisation of the genetic map of event Ms8 xRf3, 16 June 2003, Scientific Institute of
Public health, Service of Biosafety and Biotechnology IPH/1520/SBB/03-0406.
15. Ho MW and Cummins J. Chronicle of an ecological disaster foretold. Science in Society 2003, 18, 26-7 (Fully
referenced version enclosed).
16. Lim LC. GM crops harm wildlife, Science in Society 20, Autumn/Winter
2003, 4-6, www.i-sis.org.uk