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General Conclusion
Due to the very incomplete knowledge about DNA, it is neither possible to reliably
predict the influence of a gene transferred to a foreign context nor the effect of any other
genetic manipulation. Molecular biology has predicted and verified that unforeseeable
metabolic disturbances may occur due to gene transfer. But, in addition to this, it cannot
be ruled out that there might occur complications, the nature of which cannot even be
predicted because of the incompleteness of knowledge.
Thus, there is no basis today for excluding that so far unforeseen consequences of gene
transfer may add to known risks that may make GE organsims unsuitable or even harmful
as food. And it cannot be excluded that the abnormality introduced into DNA through
gene transfer may make such genes harmful to the environment in ways that cannot be
imagined presently.
An important consequence of this is that geneticists and molecular biologists don't have
the knowledge and methods required to realistically judge the effects of genetic
engineering.
"We know far less than one per cent of what will be
known about biology, human physiology, and
medicine.
Source: "The Genome Warrior", The New Yorker Magazine, June 12, 2000.
Contents
Already several decades ago, some scientists pointed out that a key feature
of life processess is the great interdependence of the parts. This means that
no part, no detail can be fully understood without reference to all other
parts. They also pointed out that in such systems, the interactions of the
parts leads to the emergence of properties that cannot be deduced from
knowledge of the parts. You will find an excellent overview of this issue
in the book "The Web of Life" by Fritjof Capra (Harper Collins, London,
UK, 1996).
When these two approaches are combined with the central insight
of living systems theory — that of the ceaseless flux of matter — it
offers a radically new way of conceiving reality, according to
Capra. Pattern, structure, and process are three different but
inseparable perspectives of the phenomenon of life.
In effect, this means that to understand any living system, one must
answer three questions: what is its structure? What is its pattern of
organization? And what is the process of life? In Capra's view, this
new approach overcomes two conceptual problems that have
plagued science for centuries. First, the interdependence of pattern
and structure overcomes the traditional division between the
organic and the inorganic, between the living and the nonliving.
And second, the interdependence of process and structure
overcomes the Cartesian split between mind and matter. Source:
"Book review" by Scott London.
In the last decade, there has been a growing realization in bioscience that
the above criticism is justified. For example, the leading science journal
"Science Magazine" devoted a whole issue already to this question, see
Science, April 04 1999. Its introductory article has the title "Beyond
Reductionism". There, the term "complex systems" is applied to designate
systems whose properties are not fully explained by an understanding of
its parts. Examples of successful applications of a complex system
approach are presented including a study of "emergent" properties.
This means that geneticists and molecular biologists dont have the
knowledge and methods required to correctly judge the effects of genetic
engineering.. Yet they have an almost exclusively dominant position in
the national and international bodies that evaluate the safety of genetic
engineering.
One reason why quantum physics has been largely left out in Molecular
Biology is that its major focus has so far been on DNA coding. This does
not require quantum physics. Another reason is that quantum physical
theory has so far not provided workable mathematical models for handling
the wave mechanics of aggregates of particles.
This research has generated seeds to entirely new theories about the DNA
regulation of cellular processes. This research is just in the very beginning
and has already revealed huge "white areas" of ignorance about DNA.
This lends further support to our opinion that we know far too little to
be able to manipulate DNA without the risk of completely
unpredictable consequences.
Molecular biology has advanced far in describing the structural genes that
determine the properties of the bodily parts. These are the simplest part of the
genetic system. But knowledge about the important regultory genes that regulate
the activity of all the structural genes is incomplete. The codes of these genes are
only partially known.
Altogether, the genes constitute less than 2% of all DNA. The rest, more than
98% of all DNA was long called "Junk DNA" by molecular biologists, as they
were unable to ascribe any function to it. Recently it has been found that the it
seems that this "Junk" is structured in an orderly way resembling a language. But
the meaning of this language is completely unknown. The last few years some
experimental observations indicate that the part of DNA that does not consist
of genes may have various functions including regulation of the activity of
genes. But little is yet known about it. (see also "Junk DNA").
In any case, this indicates that a very large part of DNA, over 98% may have
important, yet to a very large extent unkown functions.
One more dimension of the "domain of ignorance" about DNA is the histone
system. Histones are protein structures that are associated with the DNA string.
They were formerly believed to function only as a scaffold making it possible to
pack DNA tightly. However, in recent years increasing evidence have appeared
indicating that they play an important role in the expression of genes. They may
also be involved a/o in DNA repair, replication and recombination.
Increasing evidence indicate that the 98% of DNA has an important regulatory
function, the nature of which is very little nknown. Moreover the histones
surrounding DNA seem also to have important regulatory functions. There exists
no knowledge how the insertion of a foreign gene can influence the regulatory
function of these elements and how they, in turn, can influence the inserted gene.
This is an additional reason why the consequences of gene insertion is
unpredictable.
"These findings demonstrate the fragmentary nature of current
knowledge of genome structure and function and regulation of gene
expression in general, and the limited understanding of several
physiological, ecological, agronomical and toxicological aspects
relevant to present-day and planned genetic modifications of crops."
When genetic engineering was conceived over 30 years ago, it was believed that
genes are carriers of single traits - stable units, that govern the activities of the cell
unidirectionally and without any influence from the neighbouring genes.
But this is not the case - Genes are variable, changing their behavior and even
their structure because of influences from other genes or because of influences
from the conditions in the cell and the environment. So genes are not stable
carriers of well defined properties as was believed when genetic engineering was
invented. For further details, see "The new understanding of genes" at
http://www.psrast.org/newgen.htm.
Because of this, a foreign gene may have unexpected effects, not appearing in its
normal context. There are experimental observations verifying unexpected effects,
see http://www.psrast.org/molbeng.htm. Recently, the National Academy of
Science in the US has warned that because of this, there may occur unintentional
"comopositional changes" including the appearance of unexpected harmful
substances, see National Research Council, "Genetically Modified Pest-protected
Plants", URL: http://books.nap.edu/books/0309069300/html/63.html#page_top.
This doctrine is outdated. It has been well established that the effects of a gene is
dependent on interaction with its context. The insertion of a gene into a foreign
context therefore has unpredictable effects that may be of significant importance
for the safety of the organisms as food as well as for the stability and functioning
of the GMO. For more see "Human Genome research has confirmed the fallacy of
the one gene - one property doctrine", footnote 2.
General conclusion
General Conclusion
Due to the very incomplete knowledge about DNA, it is neither possible to reliably
predict the influence of a gene transferred to a foreign context nor the effect of any other
genetic manipulation. Molecular biology has predicted and verified that unforeseeable
metabolic disturbances may occur due to gene transfer. But, in addition to this, it cannot
be ruled out that there might occur complications, the nature of which cannot even be
predicted because of the incompleteness of knowledge.
Thus, there is no basis today for excluding that so far unforeseen consequences of gene
transfer may add to known risks that may make GE organsims unsuitable or even harmful
as food. And it cannot be excluded that the abnormality introduced into DNA through
gene transfer may make such genes harmful to the environment in ways that cannot be
imagined presently.
An important consequence of this is that geneticists and molecular biologists don't have
the knowledge and methods required to realistically judge the effects of genetic
engineering.
In July 2007 a consortium of 35 groups of leading scientists published the conclusion that
single genes are not carriers of isolated traits after a four year coordinated research effort.
See "Genetech is based on an outdated understanding"
This definitely confirms the point, stated in the article above, that the one-gene-one-trait
concept is wrong.
Although already more than ten years ago there was important evidence supporing this
point, there has been a long period of scientifically ill-founded resistance from scientists
sponsored by the biotech companies, see "Dysfunctional science". The conclusion of this
authoritative consortium definitely puts an end to this pseudodebate that has confused
politicians and postponed and adequate policy for safety assessment of GE foods.
This underscores our conclusion that gene technology is so unpredictable that its
commercial implementation can only be described as seriously irresponsible application
of science and technology with unpredictable, potentially dangerous outcomes.
Therefore it has to be stopped before a major disaster - a "Chernobyl" occurs - we have
most likely already had the "Harrisburg" of genetic engineering, see the Showa Denko
Tryptophan disaster.
Footnote 1.
This footnote has been moved to a separate page: "Quantum phenomena in Biology"
We are happy to find that the results of the Human Genome project research now
strongly support what we have stated about the fallacy of the one gene - one property
doctrine which is the very basis of biotechnology. In February 2001, Dr. Craig Venter,
world leading expert on Human Genome research said:
"In everyday language the talk is about a gene for this and a gene for that.
We are now finding that that is rarely so. The number of genes that work
in that way can almost be counted on your fingers, because we are just not
hard-wired in that way."
Source: Times, Monday February 12, 2001 "Why you can't judge a man
by his genes" http://www.thetimes.co.uk/article/0,,2-82213,00.html
The important connotation of this is that now it can be said with certainty that artificial
insertion of genes is unlikely to yield exactly the "desired effect" of the inserted gene.
Deviations from the desired effect along with unexpected other effects are likely to be the
rule rather than the exception. Such unpredictable effects may include the appearance of
harmful substances difficult to detect.
Richard Strohman, Professor Emeritus of Molecular and Cell Biology at the Berkeley
untiversity makes similar conclusions in his article about the present status of the
understanding of genetic regulation and the results of the Human Genome Project. See
Toward a new paradigm for life - Beyond genetic determinism
Excerpt:
If the announcements from the HGP tell us anything, they tell us that we
do not now how organisms make themselves. We are still, as many
developmental biologists have said, in the dark ages about how
organisms regulate their genomes to produce adults.
It is no more justified to assert that genetic engineering is high-tech science mastering its
results. Rather it is groping in the dark - a roulette game with seriously incomplete
knowledge of the consequences. This the key reason why PSRAST demands that genetic
engineering of every kind should be strictly confined within laboratory walls until science
knows enough about DNA to understand what it is doing - which probably will take
several decades and might even reach into the next century.