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Michael Meacher Meets Scientists
Report on a Meeting of Molecular Biologists called by
Michael Meacher
on March 31st 1999
Prepared by Angela Ryan
In attendance:
The Right Honorable Michael Meacher, Minister for the Environment
Paul Burrows, Chemicals and Biotechnology division, DETR
Steven Tindale, Sustainable Development, DETR
Scientists
Professor Don Grierson, Plant Molecular Geneticist, Nottingham
University
Dr Mae-wan Ho, Geneticist and Biophysicist, Open University
Angela Ryan, Molecular Biologist and assistant to Dr Mae-wan Ho, Open
University
Dr Michael Antoniou, Gene Therapist, Guys Hospital, London
Dr Mark Bailey, NERC Molecular Ecology Lab, IVEM Oxford
Dr Andrew Lilley, NERC Molecular Ecology Lab, IVEM Oxford
Dr Ian Garner, PPL Therapuetics, Roslin Institute, Scotland. Member of
ACRE
Dr Phil Dale, John Innes Center, Norwich. Member of ACRE
The scientists were invited to the DETR by the Right Honorable Michael
Meacher. The agenda was set to discuss the special safety concerns raised
by the effects of random insertion of DNA vectors and horizontal gene
transfer.
Following formal introductions the minister asked the scientists: does
GM raise issues beyond conventional breeding practices?
Dr Phil Gale responded first and spoke of how GM was no different from
conventional breeding practices except that it is more precise. In
conventional breeding, seeds are irradiated to cause mutations at points
all along the germ line DNA. Following germination the seedlings undergo
analysis and selection protocols which eventually lead to the isolation of
varieties that can be used in farming. With GM a specific gene can be
inserted in a single copy so that a specific desired trait can be
introduced into an organism. The site of insertion is determined using
southern blotting and the chromosomal location is also determined using
fluorescent in situ hybridization (FISH). The expression pattern
of the insert is analysed over many generations to demonstrate that it is
completely stable and has become a constitutive part of that organism. GM
is much more precise and therefore safer than conventional breeding.
Dr. Mae-Wan Ho disagreed. GM technology is not at all precise. She
identified four special safety concerns arising from current transgenic
technologies.
1. The exotic genes and gene products introduced into the transgenic
organisms may be toxic. Antibiotic resistance marker genes are also often
left in the transgenic organisms.
2. Unintended, unexpected effects of random gene insertion and
interaction between foreign genes and host genes in the transgenic
organisms which could generate toxins and allergens.
3. The gene-constructs inserted into the transgenic organisms are also
novel. Foreign genes are typically introduced as 'gene expression
cassettes' each with a strong viral promoter/enhancer to boost expression
to very high levels. The trangenic organism is, in effect, under permanent
metabolic stress. The promoter most frequently used is from the
cauliflower mosaic virus (CaMV), which is closely related to human
hepatitis B virus, and less closely, to retroviruses such as the AIDS
virus. The CaMV promoter can drive the synthesis of related viruses. It is
active in all living systems from bacteria to higher plants. Two kinds of
potential hazards exist: the reactivation of dormant viruses, and
recombination between the CaMV promoter and other viruses, dormant or
otherwise, to generate new, super-infectious viruses or viruses with
broadened host-range.
4. The spread of transgenes and antibiotic resistance marker genes, not
only by ordinary cross-pollination , but especially by secondary,
horizontal gene transfer to unrelated species. The same mechanisms that
enable genes to insert into the genome can help them jump out again.
Integrases, enzymes catalyzing the integration, which exist in all
organisms from viruses to higher plants and animals, also act as disintegrases,
catalyzing the reverse reaction. There is already evidence suggesting that
the foreign genes inserted by vector in a transgenic plant may be up to 30
times more likely to escape than the same gene created by mutagenesis.
Horizontal gene transfer is well-documented in a special report
commissioned by the Norwegian Government Directorate of Nature Management
from independent virologist and genetic engineer, Terje Traavik, and
recently published in English.
Trangenic plants of the current generation are unpredictable, unstable,
do not breed true and do not perform consistently in the field. Molecular
analysis must be done to characterize the insert (s) and demonstrate
stability of the insert(s) at least over five successive generations. Such
data is often missing from applications for approval for field trials or
marketing.
Dr Michael Antonio explained the way in which genes work in genomes.
Genes do not function in isolation, they work in groups and are highly
integrated with one another. They are constantly interacting and are under
strict molecular control where genomic position is important. There are
regions of active transcription where genes are being transcribed and
there are silent regions where no transcription is taking place. A gene
vector can land in either region but in order for it to be actively
transcribed it must land in a region of active transcription. Random
insertion can cause insertion mutagenesis and it is well understood that
many viral induced cancers are caused in this way. Insertion may also
disrupt the gene regulation and natural groupings of the genes that are
functional in the region of insertion. The use of strong promoters and
enhancers in the vectors may cause metabolic stress to the transformants.
Both these factors may lead to the emergence of novel toxins or allergens
and there is no way to predict this at present for we are in the early
days of understanding gene function. In convention breeding, the natural
order or groupings of the genes is not disturbed. Point mutations may
result in changes to the amino acid sequence of the gene products but that
does not interfere with the natural groupings of the genes and alleles,
which we know to be vital to gene regulation. There are just too many
unknowns at present.
The Right Honorable Michael Meacher then made the point that novel
toxins and allergens may occur in organisms being produced via
conventional breeding as well and perhaps further scientific study should
have been done on organisms being produced in this way?
Dr Michael Antonio and Dr Mae-wan Ho both agreed that this is a very
valid point.
Dr Phil Dale reasserted his view that although the GM constructs are
inserted randomly at first, further analysis via southern blotting and
FISH isolates the precise region in the genome and on which chromosome the
insert has integrated.
Dr Michael Antonio replied and said that without further gene mapping
work it is impossible to understand how the act of insertion is affecting
the recipient genomes gene expression. The full extent of gene regulation
is yet to be elucidated and the effects of insertion on the recipient
genome will be largely unknown until we have gained a better understanding
of gene function. Knowing where an insert is on a southern blot and which
chromosome it is on, does not constitute knowing where it is in the
recipient genome’s gene regulation system. He then strongly
recommends further research in gene mapping in order to understand this
important safety aspect of GM.
Dr Ian Garner stated that it has been known for many years, from the
work of Barbara Maclintock, that genomes are fluid and dynamic. GM is
doing nothing more beyond what nature has been doing for millions of
years.
Dr Andrew Lilly added that the rate of evolution in bacteria is
incredibly rapid and that they are constantly changing their gene
expression. His colleague, Dr Mark Bailey reasserted that GM is merely
utilising an already well established natural system.
Dr Mae-wan Ho agreed that bacteria evolved rapidly and drew attention to
a paper by J. de Vries & W. Wackernagel, Mol. Gen.. Genet.. (1998)
257: 606-613 regarding transfer frequency from transgenic plant DNA to
soil bacteria. She pointed out that in transgenic potatoes, as little as
18 ng of potato DNA (2.5 x 10 3
genome equivalents, each with one copy of an the Kanamycin-resistant gene
npt11) was required to produce one kanamycin-resistant bacterial
transformant. She added that GM may greatly accelerate the rate of
horizontal gene transfer and enlarge it’s scope.
Dr Mark Bailey said he knew about this paper because he reviewed it and
he knows the authors personally. He warns we must be careful about
misinterpreting this paper. These experiments were conducted under strict
laboratory conditions and the plasmids were designed to have homology with
the Kanamycin-resistant gene within the transgenic plant DNA. This would
not occur normally in the wild in the absence of such specific homology.
Angela Ryan questioned this remark and stated that many gene constructs
used in GM do contain, to a greater or lesser degree, plasmid DNA, viral
DNA especially viral promoters e.g. CaMV promoter, long terminal repeats
(LTRs) and left and right borders, all of which are highly conserved and
may in theory find sequence homology in the wider environment.
Dr. Phil Dale remarked that just because it happens in the laboratory
does not mean it happens in nature.
Dr Mae-Wan Ho asked whether he could guarantee it will never take place
in nature, and added that although these experiments were conducted in the
laboratory the system used was actually adapted to natural transformation
and therefore could take place in the wild. Furthermore, homology is not
neccessary for successful horizontal gene transfer. Many insertions into
the genome happen without sequence homology, especially those involved in
making transgenic organisms.
The Right Honorable Michael Meacher then asked just how much evidence
will be needed before we can be sure that GMOs are safe? And how long will
it be until such time, five or maybe ten years?
Dr Mae-wan Ho responded and confirmed that there are many unanswered
questions surrounding GMOs and that is imperative that the precautionary
principle be applied. An inverse precautionary principle has been at work
regarding GMOs to date. She recommended an immediate ban on all commercial
plantings of GMO crops and called for a five year moratorium in order to
further identify the risks and conduct the necessary experimental
research. A full independent inquiry into the future of agriculture and
food security for all was also needed.
Dr Ian Garner and Dr Phil Dale said they did not believe a moratorium
was necessary.
Steven Tindale then asks about the CaMV promoter and its affects?
Dr Phil Dale said that we eat the CaMV all the time and it is present in
many of the vegetables that make up our staple diet. It does not have any
harmful effects.
Dr Mae-wan Ho refuted this remark and said that there is a great
difference between the CaMV we may eat everyday in vegetables and the CaMV
promoter used in GMOs. Viruses are protected in the environment by a
protein coat which also confers species specificity. The CaMV cannot enter
mammalian cells because it’s protein coat is specific to plant cells.
The CaMV promoter used in GMOs however, comes in the form of naked viral
DNA and naked DNA of any sort is highly infectious. The CaMV promoter is
also highly conserved and has been shown to have sequence homology with
other viruses. It is closely related to human Hepatitis B virus and also
to retroviruses like HIV. It is a very strong promoter, it shouts in a
recipient genome to be transcribed and that is why it is so widely used.
It may recombine with latent or infecting viruses within the host or
beyond and give rise to new super-viruses. The wide use of the CaMV
promoter alone carries enough risk to impose an immediate moratorium on
GMOs.
The Right Honorable Michael Meacher then asked the scientists for their
views on Dr Pusztai’s results?
Dr Ian Garner stated that we must be very careful not to take too
seriously experimental data that has not been peer reviewed.
Dr Mae-wan Ho refuted this remark and explained that Pusztai’s work
has been peer reviewed by 20 scientists who confirmed his results as
significant.
Dr Phil Dale added that lectins are well-known toxins and therefore the
result is not unusual considering this.
Dr Michael Antonio clarified this comment and said that the snowdrop
lectin had been specifically selected because it had no toxicity in
mammalian cells, it was only toxic to insects. He explained that the
transgenic potato contained the snowdrop lectin to confer insect
resistance.
Angela Ryan then added that Dr Pusztai’s experiments were designed
to develop new methods of testing GM food. He had worked for seven years
on this and was alarmed by the results he found. The symptoms observed in
the rats were consistent with viral infection.
Dr Phil Dale and Dr Ian Garner said they did not believe this.
Dr Mae-wan Ho confirmed that the rats had reduced weight in vital
organs, impairment of immunological responsiveness and signs suggestive of
viral infection.
Steven Tindale then asked if other feeding experiments have been
conducted?
Dr Phil Dale explained that because GM food is completely digested in
the gut, feeding experiments had been considered unnecessary, although he
wasn’t sure what had happened in America. Nobody had died yet from
eating GM food and he believes it to be perfectly safe.
Dr Mae-wan Ho confirmed that Dr Pusztai’s experiments were the
first comprehensive feeding experiments to be conducted. She refuted the
claim that GM food is completely digested in the gut and referred to
evidence which demonstrates that viral and plasmid DNA fed to mice had
been found to resist digestion in the gut. Large fragments passed into the
bloodstream and entered white blood cells, spleen and liver cells. It was
found attached to mouse DNA, suggesting integration, and when fed to
pregnant mice it was found in the nucleus of cells of the foetus and
new-born. She warned that if GM foods were having ill-effects on the
public we would not know about them as no one is monitoring for such
effects. She pointed to the catastrophic thalidomide incident in which
8000 babies with truncated limbs were born before thalidomide was admitted
as the harmful agent. Dr Pusztai’s work should be repeated and not be
dismissed in any way.
The Right Honorable Michael Meacher confirmed that the Government was
taking Dr Pusztai’s experiments very seriously and would certainly
not dismiss them.
At this point the meeting came to and end and Michael Meacher thanked
all the scientists for coming along and giving their time. He said he has
come to a better understanding of the complications regarding GMOs now,
and that he would welcome further help and advise.
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