Genetic science, animal exploitation,
and the challenge for democracy
Anyone who thinks that things will move slowly is being very
naive. –
Lee Silver, Molecular Biologist
As we move into a new millennium fraught with terror and danger,
a global
postmodern condition is unfolding in the midst of rapid evolutionary
and social
changes co-constructed by science, technology, and the restructuring
of global
capital. We are quickly morphing into a new biological and social
existence that
is ever-more mediated and shaped by computers, mass media, and
biotechnology,
all driven by the logic of capital and a powerful emergent techno-science.
In
this global context, science is no longer merely an interpretation
of the natural
and social worlds; rather it has become an active force in changing
them and the
very nature of life. In an era where life can be created and redesigned
in a
petridish, and genetic codes can be edited like a digital text,
the distinction
between ‘‘natural’’ and ‘‘artificial’’
has become greatly complexified. The new
techniques of manipulation call into question existing definitions
of life and
death, demand a rethinking of fundamental notions of ethics and
moral value,
and pose unique challenges for democracy.
As techno-science develops by leaps and bounds, and as genetics
rapidly
advances, the science–industrial complex has come to a point
where it is creating
new transgenic species and is rushing toward a posthuman culture
that unfolds
in the increasingly intimate merging of technology and biology.
The posthuman
involves both new conceptions of the ‘‘human’’
in an age of information and
communication, and new modes of existence, as flesh merges with
steel, circuitry,
and genes from other species. Exploiting more animals than ever
before,
techno-science intensifies research and experimentation into human
cloning.
This process is accelerated because genetic engineering and cloning
are developed
for commercial purposes, anticipating enormous profits on the
horizon for the biotech industry. Consequently, all natural reality—from
microorganisms and plants to animals and human beings—is
subject to genetic reconstruction in a commodified ‘‘Second
Genesis.’’
At present, the issues of cloning and biotechnology are being
heatedly debated
in the halls of science, in political circles, among religious
communities,
throughout academia, and more broadly in the media and public
spheres. Not
surprisingly, the discourses on biotechnology are polarized. Defenders
of biotechnology
extol its potential to increase food production and quality, and
to
cure diseases, endow us with ‘‘improved’’
human traits, and prolong human life.
Its critics claim that genetic engineering of food will produce
Frankenfoods,
which pollute the food supply with potentially harmful products
that could
devastate the environment, biodiversity, and human life itself;
that animal and
human cloning will breed monstrosities; that a dangerous new eugenics
is on the
horizon; and that the manipulation of embryonic stem cells violates
the principle
of respect for life and destroys a bona fide ‘‘human
being.’’
Interestingly, the same dichotomies that have polarized information-technology
discourses into one-sided technophobic and technophillic positions
are
reproduced in debates over biotechnology. Just as I believe that
critical theories
of technology are needed to produce more dialectical perspectives
that distinguish
between positive and negative aspects and effects of information
technology (Best and Kellner 2001), so too I would claim that
similar
approaches are required to articulate the potentially beneficial
and perhaps
destructive aspects of biotechnology. Indeed, current debates
over cloning and
stem cell research suggest powerful contradictions and ambiguities
in these
phenomena that render one-sided positions superficial and dangerous.
Parallels
and similar complexities in communication and biotechnology are
not surprising
given that information technology provides the infrastructure
to biotechnology
that has been constituted by computer-mediated technologies involved
in the
Human Genome Project, and, conversely, genetic science is being
used to push
the power and speed of computers through phenomena such as ‘‘gene
chips.’’
As the debates over cloning and stem cell research indicate,
issues raised by
biotechnology combine research into the genetic sciences, perspectives
and
contexts articulated by the social sciences, and the ethical and
anthropological
concerns of philosophy. Consequently, I argue that intervening
in the debates
over biotechnology require supra disciplinary critical philosophy
and social
theory to illuminate the problems and their stakes. In addition,
debates over
cloning and stem cell research raise exceptionally important challenges
to bioethics
and a democratic politics of communication. Biotechnology is thus
a
critical flashpoint for ethics and democratic theory and practice.
Contemporary
biotechnology underscores the need for more widespread knowledge
of important
scientific issues; participatory debate over science, technology,
values, and
our very concept of human life; and regulation concerning new
developments in
the biosciences, which have such high economic, political, and
social consequences.
New genetic technologies like stem cell research contain positive
potential for
medical advances that should not be blocked by problematic conservative
positions. Nonetheless, I believe that the entire realm of biotechnology
is fraught
with dangers and problems that require careful study and democratic
debate.
The emerging genomic sciences should thus be undertaken by scientists
with a
keen sense of responsibility and accountability, and be subject
to intense public
scrutiny and open discussion. Finally, in the light of the dangers
and potentially
deadly consequences of biotechnology, I maintain that the positive
potential of
biotechnology can be realized only in a new context of cultivating
new sensibilities
toward nature, engaging in ethical and political debate, and participating
in political struggles over biotechnology and its effects.
1 Brave new barnyard: the advent of animal cloning
The idea is to arrive at the ideal animal and repeatedly copy
it exactly as it is.– Dr. Mark
Hardy
From its entrenched standpoint of unqualified human superiority,
science,
typically first targets objects of nature and animals with its
analytic gaze and
instruments. The current momentous turn toward cloning is largely
undertaken
by way of animals, although some scientists have already directly
focused on
cloning human beings. While genetic engineering creates new ‘‘transgenic’’
species by inserting the gene from one species into another, cloning
replicates
cells to produce identical copies of a host organism by inserting
its DNA into an
enucleated egg. In a potent combination, genetic engineering and
cloning
technologies are used together in order, first, to custom design
a transgenic
animal to suit the needs of science and industry (the distinction
is irrevocably
blurred) and, second, to mass reproduce the hybrid creation endlessly
for
profitable peddling in medical and agricultural markets.
Cloning is a return to asexual reproduction and bypasses the
caprice of the
genetic lottery and random shuffling of genes. It dispenses with
the need to inject
a gene into thousands of newly fertilized eggs to get a successful
result. Rather,
much as the printing press replaced the scribe, cloning allows
mass reproduction
of a devised type, and thus opens genetic engineering to vast
commercial possibilities.
Life science companies are poised to make billions of dollars
in profits,
as numerous organizations, universities, and corporations move
toward cloning
animals and human stem cells, and patenting the methods and results
of their
research.
To date, science has engineered a myriad of transgenic animals
and has cloned
animals such as sheep, calves, goats, bulls, pigs, mice, and cats.
Although still far
from precise, cloning nevertheless has become routine. What is
radically new
and startling is not cloning itself, since from 1952 scientists
have replicated
organisms from embryonic cells. Rather, the new techniques of
cloning, or
‘‘nuclear somatic transfer,’’ from adult
mammal body cells constitute a new
form of animal reproduction. These methods accomplish what scientists
long
considered impossible—reverting adult (specialized) cells
to their original
(nonspecialized) embryonic state where they can be reprogrammed
to form a new
organism. In effect, this startling process creates the identical
twin of the adult
that provided the original donor cell. This technique was used
first to create
Dolly, the first mammal cloned from a cell from an adult animal,
and subsequently
all of her varied offspring.
2 Dolly and her progeny
Traditionally, scientists considered cloning beyond the reach
of human ingenuity.
But when Ian Wilmut and his associates from the Roslin Institute
near
Edinburgh, Scotland, announced their earth-shattering discovery
in March
1997, the ‘‘impossible’’ appeared in the
form of a sheep named Dolly, and a
‘‘natural law’’ had been broken. Dolly’s
donor cells came from a 6-year-old Finn
Dorset Ewe. Wilmut starved mammary cells in a low-nutrient tissue
culture
where they became quiescent and subject to reprogramming. He then
removed
the nucleus containing genetic material from an unfertilized egg
cell of a second
sheep, a Scottish Blackface, and, in a nice Frankenstein touch,
fused the two
cells with a spark of electricity. After 277 failed attempts,
the resulting embryo
was then implanted into a third sheep, a surrogate mother who
gave birth to
Dolly in July 1996.
Many critics said Dolly was either not a real clone or was just
a fluke. Yet, less
than 2 years after Dolly’s emergence, scientists had cloned
numerous species,
including mice, pigs, cows, and goats, and had even made clones
of clones of
clones, producing genetic simulacra in mass batches as in 1931
Huxley (1989a)
envisioned happening to human beings in Brave New World. The commercial
possibilities of cloning animals were dramatic and obvious for
all to behold. The
race was on to patent novel cloning technologies and the transgenic
offspring
they would engender.
Animals are being designed and bred as living drug and organ
factories, as
their bodies are disrupted, refashioned, and mutilated to benefit
meat and dairy
industries. Genetic engineering is employed in biomedical research
by infecting
animals with diseases that become a part of their genetic make
up and are
transmitted to their offspring, as in the case of researchers
trying to replicate the
effects of cystic fibrosis in sheep. Most infamously, Harvard
University, with
funding from Du Pont, has patented a mouse—OncoMouse —that
has human
cancer genes built into its genetic make up and are expressed
in its offspring
(Haraway 1997).
In the booming industry of ‘‘pharming’’
(pharmaceutical farming), animals
are genetically modified to secrete therapeutic proteins and medicines
in their
milk. The first major breakthrough came in January 1998, when
Genzyme
Transgenics created transgenic cattle named George and Charlie.
The result of
splicing human genes and bovine cells, they were cloned to make
milk that
contains human proteins such as the blood-clotting factor needed
by hemophiliacs.
Co-creator James Robl said, ‘‘I look at this as being
a major step
toward the commercialization of this [cloning] technology.’’1
In early January 2002, the biotech company PPL announced that
they had
just cloned a litter of pigs, which could aid in human organ transplants.
On the
eve of the publication of an article by another company, Immerge
Bio Therapeutics
claimed that they had achieved a similar breakthrough.2 The new
process
involved creation of the first ‘‘knockout’’
pigs, in which a single gene in pig
DNA is deleted to eliminate a protein that is present in pigs,
which is usually
violently rejected by the human immune system. This meant that
a big step
could be made in the merging of humans and animals, and creating
animals as
harvest-machines for human organs.
Strolling through the Brave New Barnyard, one can find incredible
beings that
appear normal, but in fact are genetic satyrs and chimera. Cows
generate lactoferrin,
a human protein useful for treating infections. Goats manufacture
antithrombin III, a human protein that can prevent blood clotting,
and serum
albumin, which regulates the transfer of fluids in the body. Sheep
produce alpha
antitrypsin, a drug used to treat cystic fibrosis. Pigs secrete
phytase, a bacterial
protein that enables them to emit less of the pollutant phosphorous
in their
manure, and chickens make lysozyme, an antibiotic, in their eggs
to keep their
own infections down.
‘‘BioSteel’’ presents an example of the
bizarre wonders of genetic technology
that points to the erasure of boundaries between animate and inanimate
matter,
as well as among different species. In producing this substance,
scientists have
implanted a spider gene into goats, so that their milk produces
a super-strong
material—BioSteel—that can be used for bulletproof
vests, medical supplies,
and aerospace and engineering projects. In order to produce vast
quantities of
BioSteel, Nexia Biotechnologies intend to house thousands of goats
in 15
weapons-storage buildings, confining them in small holding pens.3
As we see, animals are genetically engineered and cloned to produce
a stock of
organs for human transplants. Given the severe shortage of human
organs,
thousands of patients every year languish and die before they
can receive a
healthy kidney, liver, or heart. Rather than encouraging preventative
medicine
and finding ways to encourage more organ donations, medical science
has
turned to xeno-transplantation, and has begun breeding herds of
animals (with
pigs as a favored medium) to be used as organ sources for human
transplantation.
Clearly, this is a very hazardous enterprise due to the possibility
of animal
viruses causing new plagues and diseases in the human population
(a danger
which exists also in pharmaceutical milk). For many scientists,
however, the
main concern is that the human body rejects animal organs as foreign
and
destroys them within minutes. Researchers seek to overcome this
problem by
genetically modifying the donor organ so that they knock out markers
in pig
cells and add genes that make their protein surfaces identical
to those in humans.
Geneticists envision cloning entire herds of altered pigs and
other
transgenic animals so that an inexhaustible warehouse of organs
and tissues
would be available for human use. In the process of conducting
experiments
such as transplanting pig hearts modified with a human gene into
the bodies of
monkeys, companies such as Imutran have caused horrific suffering,
with no
evident value to be gained given the crucial differences among
species and
introducing the danger of new diseases into human populations.4
As if billions of animals were not already exploited enough in
laboratories,
factory farms, and slaughterhouses, genetic engineering and cloning
exacerbate
the killing and pain with new institutions of confinement and
bodily invasion
that demand billions of more captive bodies. Whereas genetic and
cloning
technologies in the cases described at least have the potential
to benefit human
beings, they have also been appropriated by the meat and dairy
industries for
purposes of increased profit through the exploitation of animals
and biotechnology.
It’s the nightmarish materialization of the H.G. Wells scenario
where, in
his prophetic 1904 novel The Food of the Gods, scientists invent
a substance that
prompts every living being that consumes it to grow to gargantuan
proportions
(Best and Kellner 2001). Having located the genes responsible
for regulating
growth and metabolism, university and corporate researchers immediately
exploited this knowledge for profit. Thus, for the glories of
carcinogenic carnivorous
consumption, corporations such as MetaMorphix and Cape Aquaculture
Technologies have created giant pigs, sheep, cattle, lobsters,
and fish that
grow faster and larger than the limits set by evolution.
Amidst the surreality of Wellsian gigantism, cattle and dairy
industries are
engineering and cloning designer animals that are larger, leaner,
and fastergrowing
value producers. With synthetic chemicals and DNA alteration,
pharmers
can produce pigs that mature twice as fast and provide at least
twice the
normal amount of sows per litter as they eat 25% less feed, and
cows that
produce at least 40% more milk. Since 1997, at least one country,
Japan, has
sold cloned beef to its citizens.5 But there is strong reason
to believe that U.S.
consumers—already a nation of guinea pigs in their consumption
of genetically
modified foods—have eaten cloned meat and dairy products.
For years, corporations
have cloned farmed animals with the express purpose of someday
introducing them to the market, and insiders claim many already
have been
consumed.6 The National Institute of Science and Technology has
provided two
companies, Origen Therapeutics of California, and Embrex of North
Carolina,with
almost $5 million to fund research into factory farming billions
of cloned
chickens for consumption.7 With the Food and Drug Administration
pondering
whether to regulate cloned meat and dairy products, it’s
a good bet they are
many steps behind an industry determined to increase their profits
through
biotechnology. The future to come seems to be one of cloned humans
eating
cloned animals.
While anomalies such as self-shearing sheep and broiler chickens
with fewer
feathers have already been assembled, some macabre visionaries
foresee engineering
pigs and chickens with flesh that is tender or can be easily microwaved,
and chickens that are wingless so they won’t need bigger
cages. The next step
would be to just create and replicate animal’s torsos—sheer
organ sacks—and
dispense with superfluous heads and limbs. In fact, scientists
have already created
headless embryos of mice and frogs in grotesque manifestations
of the
kinds of life they can now construct at will.
Clearly, there is nothing genetic engineers will not do to alter
or clone an
animal. Transgenic ‘‘artist’’ Eduardo
Kac, for instance, commissioned scientists
at the National Institute of Agronomic Research in France to create
Alba, a
rabbit that carries a fluorescent protein from a jellyfish and
thus glows in the
dark. This experiment enabled Mr. Kac to demonstrate his supremely
erudite
postmodern thesis that ‘‘genetic engineering [is]
in a social context in which the
relationship between the private and public spheres are negotiated.’’8
Although millions of healthy animals are euthanized every year
in U.S. animal
‘‘shelters,’’ corporations are working
to clone domestic animals, either to bring
them back from the dead, or to prevent them from ‘‘dying’’
(such as in the
Missyplicity Project, initiated by the wealthy ‘‘owners’’
of a dog who want to
keep her alive indefinitely).9 Despite alternatives to coping
with allergies problems
and the dangers with cloning animals, Transgenic Pets LLC is working
to
create transgenic cats that are allergen-free.10 In 2002, the
biotechnology company
Genetic Savings and Clone showcased the world’s first cloned
cat, named
CC, for Carbon Copy. Pandering to animal guardians’ misconceived
desires to
immortalize their cat, for a price of $50,000 each, Genetic Savings
since has
cloned additional cats, and hopes to cash in on what could be
a booming market
in feline simulacra at great risk for health problems and premature
aging.
3 Transgenic travesties
The agricultural use of genetics and cloning has produced horrible
monstrosities.
Transgenic animals often are born deformed and suffer from fatal
bleeding
disorders, arthritis, tumors, stomach ailments, kidney disease,
diabetes, inability
to nurse and reproduce, behavioral and metabolic disturbances,
high mortality
rates, and large offspring syndrome. In order to genetically engineer
animals for
maximal weight and profit, a Maryland team of scientists created
the infamous
‘‘Beltway pig’’ afflicted with arthritis,
deformities, and respiratory disease. Cows
engineered with bovine growth hormone (rBGH) have mastitis, hoof
and leg
maladies, reproductive problems, numerous abnormalities, and die
prematurely.
Giant supermice endure tumors, damage to internal organs, and
shorter life
spans. Numerous animals born from cloning are missing internal
organs such as
hearts and kidneys. A Maine lab specialized in breeding sick and
abnormal mice
that go by names such as Fathead, Fidget, Hairless, Dumpy, and
Greasy.
Similarly, experiments in the genetic engineering of salmon have
led to rapid
growth and various aberrations and deformities, with some growing
up to ten
times their normal body weight (see Fox 1999). Cloned cows are
ten times more
likely to be unhealthy as their natural counterparts. After 3
years of efforts to
clone monkeys, Dr. Tanja Dominko fled in horror from her well-funded
Oregon
laboratory. Telling cautionary tales of the ‘‘gallery
of horrors’’ she experienced,
Dominko said that 300 attempts at cloning monkeys produced nothing
but
freakishly abnormal embryos that contained cells either without
chromosomes
or with up to nine nuclei.11
For Dominko, a ‘‘successful’’ clone like
Dolly is the exception, not the rule.
But even Dolly became inexplicably overweight and arthritic, and
may have
been prematurely aging. In February 2003, suffering from progressive
lung
disease, poor Dolly was euthanized by her ‘‘creators,’’
bringing to a premature
end the first experiment with adult animal cloning and raising
questions concerning
its ethics.
A report from newscientists.com argues that genes are disrupted
when cultured
in a lab, and this explains why so many cloned animals die or
are grossly
abnormal. On this account, it is not the cloning or IVF process
that is at cause,
but the culturing of the stem cells in the lab, creating major
difficulties in cloning
since so far there is no way around cloning through cultured cells
in laboratory
conditions.
A team of U.S. scientists at the MIT Whitehead Institute examined
38 cloned
mice and learned that even clones which look healthy suffer genetic
maladies, as
mice cloned from embryonic stem cells had abnormalities in the
placenta, kidneys,
heart, and liver. Scientists feared that the defective gene functioning
in
clones could, wreak havoc with organs and trigger foul-ups in
the brain later in
life and that embryonic stem cells are highly unstable.13 ‘‘There
are almost no
normal clones,’’ study author and MIT biology professor
Rudolf Jaenisch, explained.
Jaenisch claims that only 1%–5% of all cloned animals survive,
and
even those that survive to birth often have severe abnormalities
and die prematurely.14
As I argue below, these risks make human cloning a deeply problematic
undertaking. Pro-cloning researchers claim that the ‘‘glitches’’
in animal cloning
eventually can be worked out. In January 2001, for example, researchers
at
Texas A&M University and the Roslin Institute claimed to have
discovered a
gene that causes abnormally large cloned fetuses, a discovery
they believe will
allow them to predict and prevent this type of mutation. It is
conceivable science
someday will work out the kinks, but for many critics this assumes
that science
can master what arguably are inherent uncertainties and unpredictable
variables
in the expression of genes in a developing organism. A recent
study showed that
some mouse clones seem to develop normally until an age the equivalent
of
30 years for a human being; then there is a spurt of growth and
they suddenly
become obese.15 Mark Westhusin, a cloning expert at Texas A&M,
points out
that the problem is not that of genetic mutation, but of ‘‘genetic
expression,’’
such that genes are inherently unstable and unpredictable in their
functioning.
Another report indicates that a few misplaced carbon atoms can
lead to cloning
failures.16 Thus, as suggested by chaos theory, small errors in
the cloning process
could lead to huge disasters, and the prevention of all such ‘‘small
errors’’ seems
to presume something close to omniscience.
Yet, while most scientists are opposed to cloning human beings
(rather than
stem cells), and decry it as ‘‘unacceptable,’’
few condemn the suffering caused to
animals or position animal cloning research itself as morally
problematic, and
many scientists aggressively defend animal cloning. Quite callously
and arbitrarily,
for example, Jaenisch proclaims, ‘‘You can dispose
of these animals, but
tell me—what do you do with abnormal humans?’’17
The attitude that animals
are disposable resources or commodities rather than subjects of
a life with
inherent value and rights is a good indication of the problems
inherent in the
mechanistic science that still prevails and a symptom of callousness
toward
human life that worries conservatives.
Despite the claims of its champions, the genetic engineering
of animals is a
radical departure from natural evolution and traditional forms
of animal
breeding. Genetic engineering involves manipulation of genes rather
than whole
organisms.Moreover, scientists engineer change at unprecedented
rates, and can
create novel beings across species boundaries that previously
were unbridgeable.
Ours is a world where cloned calves and sheep carry human genes,
human
embryo cells are merged with enucleated cows’ eggs, monkeys,
and rabbits are
bred with jellyfish DNA, a surrogate horse gives birth to a zebra,
a dairy cow
spawns an endangered gaur, and tiger cubs emerge from the womb
of an ordinary
housecat.
The ability to clone a desired genetic type brings the animal
kingdom into
entirely new avenues of exploitation and commercialization. From
the new
scientific perspective, animals are framed as genetic information
that can be
edited, transposed, and copied endlessly. Pharming and xenotransplantation
build on the system of factory farming that dates from the postwar
period and is
based on the confinement and intensive management of animals within
enclosed
buildings that are prison-houses of suffering.
The proclivity of the science-industrial complex to instrumentalize
animals as
nothing but resources for human use and profit intensifies in
an era in which
genetic engineering and cloning are perceived as a source of immense
profit and power. Still confined for maximal control, animals
are no longer seen as whole
species, but rather as fragments of genetic information to be
manipulated for
any purpose.
Weighty ethical and ecological concerns in the new modes of animal
appropriation
are largely ignored, as animals are still framed in the 17th century
Cartesian
worldview that sees them as non-sentient machines. As Rifkin (1998,
35) puts it, ‘‘Reducing the animal kingdom to customized,
mass-produced
replications of specific genotypes is the final articulation of
the mechanistic,
industrial frame of mind. A world where all life is transformed
into engineering
standards and made to conform to market values is a dystopian
nightmare, and
needs to be opposed by every caring and compassionate human being
who
believes in the intrinsic value of life.’’18
Patenting of genetically modified animals has become a huge industry
for
multinational corporations and chemical companies. The PPL Therapeutics,
Genzyme Transgenics, Advanced Cell Technology, and other enterprises
are
issuing broad patent claims on methods of cloning non-human animals.
The
PPL Therapeutics, the company that ‘‘invented’’
Dolly, has applied for the
patents and agricultural rights to the production of all genetically
altered
mammals that could secrete therapeutic proteins in their milk.
Nexia Biotechnologies
obtained exclusive rights to all results from spider silk research.
Patent
number 4,736,866 was granted to Du Pont for Oncomouse, which the
Patent
Office described as a new ‘‘composition of matter.’’
Infigen holds a U.S. patent
for activating human egg division through any means (mechanical,
chemical, or
otherwise) in the cloning process.
Certainly, genetics does not augur solely negative developments
for animals.
Given the reality of dramatic species extinction and loss of biodiversity,
scientists
are collecting the sperm and eggs of endangered species like the
giant panda
in order to preserve them in a ‘‘frozen zoo,’’
such as exists as San Diego Zoo. It
is indeed exciting to ponder the possibilities of a Jurassic Park
scenario of
reconstructing extinct species (as, for example, scientists recently
have uncovered
the well-preserved remains of a Tasmanian tiger and a woolly mammoth).
In
October 2001, European scientists cloned a seemingly healthy mouflon
lamb, a
member of an endangered species of sheep. In April 2003, ACT produced
the
first successful interspecies clone when a dairy cow gave birth
to a pair of
bantengs, a species of wild cattle, cloned from an animal that
died over 20 years
ago. One of the pair, however, was thereafter euthanized because
it was born
twice the normal size and was suffering. Currently, working with
preserved
tissue samples, ACT is working to bring back from extinction the
last bucardo
mountain goat, which was killed by a falling tree in January 2000.19
But critics dismiss these efforts as a misguided search for a
technofix that
distracts focus from the real problem of preserving habitat and
biodiversity.
Even if animals could be cloned, there is no way to replicate
habitats lost forever
to chainsaws, bulldozers and invading human armies. Moreover,
the behaviors
of cloned animals would unavoidably be altered and they would
end up in zoos
or exploitative entertainment settings, where they exist as spectacle
and simulacra.
Animals raised through interspecies cloning such as the gaur produced
by
ACT will not have the same disposition as if raised by their own
species and so,
for other reasons will not be less than ‘‘real.’’
Additionally, there is the likelihood
that genetic engineering and cloning would aggravate biodiversity
loss to
the extent it creates monolithic super breeds that could crowd
out other species
or be easily wiped out by disease. There is also great potential
for ecological
disaster when new beings enter an environment, and genetically
modified
organisms are especially unpredictable in their behavior and effects.
Still, cloning may prove a valuable tool in preserving what can
be salvaged
from the current extinction crisis. Moreover, advances in genetics
also may
bypass and obviate pharming and xenotransplantation through use
of stem cell
technologies that clone human cells, tissues, or perhaps even
entire organs and
limbs from human embryos or an individual’s own cells. Successful
stem cell
technologies could eliminate at once the problem of immune rejection
and the
need for animals. There is also the intriguing possibility of
developing medicines
and vaccines in plants, rather than animals, thus producing a
safer source of
pharmaceuticals and neutraceuticals and sparing animals’
tremendous suffering.
None of these promises, however, brighten the dark cloud cloning
casts over the
animal kingdom, or dispel the dangers of the dramatic alteration
of agriculture
and human life.
4 Deferring the brave new world: challenges for ethics
and democracy
Human history becomes more and more a race between education
and
catastrophe. – H.G. Wells
By summer of 2001, a technical and esoteric debate over stem
cells, confined
within the scientific community during the past years, had moved
to the headlines
to become the forefront of the ongoing science wars—battles
over the
cultural, ethical, and political implications of science. The
scientific debate over
stem cell research in large part is a disguised culture war, and
conservatives,
liberals, and radicals have all jumped into the fray. Coming from
a perspective
of critical theory and radical democratic politics, I reject conservative
theologies
and argue against conflations of religion and the state. Likewise,
I question neoliberal
acceptance of corporate capitalism and underscore the implications
of the
privatization of research and the monopolization of knowledge
and patents by
huge biotech corporations. In addition, I urge a deeper level
of public participation
in science debates than do conservatives or liberals and believe
that the
public can be adequately educated to have meaningful and intelligent
input into
technical issues such as cloning and stem cell research that have
tremendous
human and ethical implications.
As I have shown, numerous issues are at stake in the debate over
cloning,
having to do not only with science, but also with religion, politics,
economics,
democracy, ethics, and the meaning and nature of human beings,
and all life
forms as they undergo a process of genetic reconstruction. Thus,
my goal
throughout this paper has been to question the validity of the
cloning project,
particularly within the context of a global capitalist economy
and its profit
imperative, a modernist paradigm of reductionism, and a Western
sensibility
organized around the concept of the domination of nature. Until
science is
recontextualized within a new holistic paradigm informed by a
respect for living
processes, by democratic decision making, and by a new ethic toward
nature, the
genetic sciences on the whole are in the hands of those governed
by the
imperatives of profit. Moreover, politicians beholden to corporate
interests have
no grasp of the momentous issues involved, requiring that those
interested in
democratic politics and progressive social change must educate
and involve
themselves in the science and politics of biotechnology.
We have already entered a new stage of the postmodern adventure
in
which animal cloning is highly advanced and human cloning is on
the
horizon, if not now underway. Perhaps little human clones are
already
emerging, with failures being discarded, as were the reportedly
hundreds of
botched attempts to create Louise Brown, the first test-tube baby,
in 1978. At
this stage, human cloning is indefensible in the light of the
possibility of
monstrosities, dangers to the mother, burdens to society, failure
to reach a
consensus on the viability and desirability of cloning humans,
and the lack of
compelling reasons to warrant this fateful move. The case is much
different,
however, for therapeutic cloning, which is incredibly promising
and offers
new hope for curing numerous debilitating diseases. But even stem
cell research,
and the cloning of human embryos is problematic, in part because
it
is the logical first step toward reproductive cloning and mass
production of
desired types, which unavoidably brings about new (genetic) hierarchies
and
modes of discrimination.
We thus need to discuss the numerous issues involved in the shift
to a
posthuman, postbiological mode of existence where the boundaries
between our
bodies and technologies begin to erode as we morph toward a cyborg
state. Our
technologies are no longer extensions of our bodies, as Marshall
McLuhan
stated, but rather are intimately merging with our bodies, as
we implode with
other species through the genetic crossings of transgenic species.
In an era of
rapid flux, our genotypes, phenotypes, and identities are all
mutating. Under the
pressure of new philosophies and technological change, the humanist
mode of
understanding the self as a centered, rational subject has transformed
into new
paradigms of communication and intersubjectivity (Hayles 1999)
and information
and cybernetics (Habermas 1979, 1984, 1987).
Despite these shifts, it is imperative that elements of the modern
enlightenment
tradition be retained, as it is simultaneously radicalized. Now
more than
ever, as science embarks on the incredible project of manipulating
atoms and
genes through nanotechnology, genetic engineering, and cloning,
its awesome
powers must be measured and tempered through ethical, ecological,
and democratic
norms in a process of public debate and participation. The walls
between
‘‘experts’’ and ‘‘lay people’’
must be broken down along with the elitist norms
that form their foundation. Scientists need to enter into dialogical
relations with
the public to discuss the complexities of cloning and stem cell
research to make
their positions clear and accessible, as well as accountable and
responsible, while
public intellectuals and activists need to become educated in
biotechnology in
order to debate biotechnology issues in the media or public.
Scientists should recognize that their endeavors embody specific
biases and
value choices, subject them to critical scrutiny, and seek more
humane, life
enhancing, and democratic values to guide their work. Respect
for nature and
life, preserving the natural environment, and serving human needs
over corporate
profits should be primary values embedded in science.
This approach is quite unlike how science so far has conducted
itself in many
areas. Most blatantly, perhaps, scientists, hand in hand with
corporations, have
prematurely rushed the genetic manipulation of agriculture, animals,
and the
world’s food supply while ignoring important environmental,
health, and ethical
concerns. Immense power brings enormous responsibility, and it
is time for
scientists to be awake to this fact and make public accountability
integral to
their ethos and research. A schizoid modern science that rigidly
splits facts from
values must give way to a postmodern metascience that grounds
the production
of knowledge in a social context of dialogue and communication
with citizens.
The shift from a cold and detached ‘‘neutrality’’
to a participatory understanding
of life that deconstructs the modern subject/object dichotomy
derails
realist claims to unmediated access to the world and opens the
door to an
empathetic and ecological understanding of nature (Keller 1983;
Birke and
Hubbard 1995).
In addition, scientists need to take up the issue of democratic
accountability
and ethical responsibility in their work. As Bill Joy argued in
a much-discussed
Wired article in July 2000, uncontrolled genetic technology, artificial
intelligence,
and nanotechnology could create catastrophic disasters, as well
as utopian
benefits. Joy’s article set off a firestorm of controversy,
especially his call for
government regulation of new technology and ‘‘relinquishment’’
of development
of potentially dangerous new technologies, as he claimed biologists
called for in
the early days of genetic engineering, when the consequences of
the technology
were not yet clear.20 Arguing that scientists must assume responsibility
for their
productions, Joy warned that humans should be very careful about
the technologies
they develop, as they may have unforeseen consequences. Joy noted
that robotics was producing increasingly intelligent machines
that might generate
creative robots that could be superior to humans, produce copies
of
themselves, and assume control of the design and future of humans.
Likewise,
genetic engineering could create new species, some perhaps dangerous
to humans
and nature, while nanotechnology might build horrific ‘‘engines
of
destruction’’ as well as of the ‘‘engines
of creation’’ envisioned by Eric Drexler
(1987).
Science and technology, however, not only require responsibility
and
accountability on the part of scientists, but also regulation
by government and
democratic debate and participation by the public. Public need
to agree on rules
and regulations for cloning and stem cell research, and there
should be laws,
guidelines, and regulatory agencies open to public input and scrutiny.
To be
rational and informed, citizens must be educated about the complexities
of
genetic engineering and cloning, a process that can unfold through
vehicles such
as public forums, teach-ins, and creative use of the broadcast
media and Internet.
The Internet is a treasure-trove of information, ranging from
informative
sites such as the Council for Responsible Genetics (http://www.gene-watch.org)
and The Institute of Science in Society (http://www.i-sis.org.uk),
to lists serves
such as hosted by the Sierra Club and various weblogs.
But to publicize and politicize biotechnology issues, social
movements will have
to take up issues like the cloning and stem cell debate into their
public pedagogies
and struggles. Movements like the anti-nuclear coalitions and
organized struggles
against genetically modified foods have had major successes in
educating the
public, promoting debate, and influencing legislation and public
opinion. It will
not do, however, to simply let the market decide what technologies
will or will not
be allowed, nor should bans be accepted on technologies that can
benefit human
life. Instead, citizens and those involved in social movements
should engage issues
of biotechnology and aid in public education and debate.
An intellectual revolution is needed to remedy the deficiencies
in the education
of both scientists and citizens, as such that each can have, in
Habermas’
framework, ‘‘communicative competency’’
informed by sound value thinking,
skills in reasoning, and democratic sensibilities. A Deweyean
reconstruction of
education would have scientists take more humanities and philosophy
courses
and engage ethical and political issues involved in the development
and implementation
of science and technology, and would have students in other fields
take more science and technology courses to become literate in
some of the
major material and social forces of the epoch. C.P. Snow’s
analysis of the ‘‘two
cultures’’ problem provides a challenge for a democratic
reconstruction of
education to overcome in an increasing scientific and technological
age that
requires more and better knowledge of science and humanities.
Critical and self-reflexive scrutiny of scientific means, ends,
and procedures
should be a crucial part of the enterprise. ‘‘Critical,’’
in Haraway’s analysis,
signifies ‘‘evaluative, public, multiactor, multiagenda,
oriented to equality and
heterogeneous well-being (Haraway 1997, 95).’’ Indeed,
there should be debates
concerning precisely what values are incorporated into specific
scientific projects
and whether these serve legitimate ends and goals. In the case
of mapping the
human genome, for instance, enormous amounts of money and energy
are being
spent, but almost no resources are going to educating the public
about the
ethical implications of having a genome map. The Human Genome
Project
spent only 3%–5% of its $3 billion budget on legal, ethical,
and social issues,
and Celera spent even less.21
A democratic biopolitics and reconstruction of education would
involve the
emergence of new perspectives, understandings, sensibilities,
values, and paradigms
that put in question the assumptions, methods, values, and interpretations
of modern sciences, calling for a reconstruction of science.22
At the same time, as
science and technology co-construct each other, and both coevolve
in conjunction
with capitalist growth, profit, and power imperatives, science
is
reconstructing—not always for the better—the natural
and social worlds, as well
as our very identities and bodies. There is considerable ambiguity
and tension in
how science will play out given the different trajectories it
can take. Unlike the
salvationist promises of the techo scientific ideology and the
apocalyptic dystopias
of some of its critics, I see the future of science and technology
to be
entirely ambiguous, contested, and open. For now, the only certainty
is that the
juggernaut of the genetic revolution is rapidly advancing and
that in the name of
medical progress, animals are being victimized and exploited in
new ways, while
the replication and re-design of human beings is looming.
The human species is thus at a terribly difficult and complex
crossroads.
Whatever steps we take, it is imperative that we do not leave
the decisions to the
scientists, anymore than we would to the theologians (or corporate-hired
bioethicists
for that matter), for their judgment and objectivity is less than
perfect,
especially for the majority who are employed by biotechnology
corporations and
have a vested interest in the hastening and patenting of the brave
new world of
biotechnology.23 The issues involving genetics are so important
that scientific,
political, and moral debate must take place squarely within the
public sphere.
The fate of human beings, animals, and nature hangs in the balance,
thus it is
imperative that the public become informed on the latest developments
and
biotechnology and that lively and substantive democratic debate
take place
concerning the crucial issues raised by the new technosciences.
_______________________________________________________________________
Notes
1 Cited in Carey Goldberg, and Gina Kolata, ‘‘Scientists
Announce Births of Cows
Cloned in New Way.’’ The New York Times. January 21,
1998: A 14. Companies are
now preparing to sell milk from cloned cows; see Jennifer Mitol,
‘‘Got cloned milk?’’
http://www.abcnews.com/ July 16, 2001. For the story of Dolly
and animal cloning, see Kolata (1998).
2 See Sheryl Gay Stolberg, ‘‘Breakthrough in Pig
Cloning Could Aide Organ Transplants’’ (New
York Times, January 4, 2001). In July 2002, the Australian government
announced draft
guidelines that would regulate transplanting animal organs into
humans and anticipated research with pig organs translated into
humans within two years; see Benjamin Haslem, ‘‘Animal-to-human
transplants get nod,’’ The Australian, July 8, 2002:
A1
3 See http://abcnews.go.com/sections/DailyNews/biotechgoats.000618.html.
4 See Heather Moore, ‘‘The Modern-Day Island of Dr,
Moreau,’’
http://www.alternet.org/story.html?StoryID=11703, October 12,
2001. For a vivid description of the horrors of animal experimentation,
see Singer (1975); for an acute diagnosis of the unscientific
nature of vivisection,see Greek and Greek (2000).
5 See ‘‘In Test, Japanese Have No Beef With Cloned
Beef,’’
http://www.washingtonpost.com/wpsrv/inatl/daily/sept99/japan10.htm.
According to one report, it is more accurate to refer to this
beef as being produced by ‘‘embryo twinning,’’
and not the kind of cloning process that produced Dolly; see ‘‘‘Cloned’
Beef Scare Lacks Meat,’’ http://www.wired.com/news/technology/0,1282,19146,00.html.
As just one indicator of the corporate will to clone animals for
mass consumption, the National Institute of Science and Technology
has donated $4.7 million to two industries to fund research into
cloning chickens for food. See ‘‘Cloned chickens on
the menu,’’ New Scientist.com, August 15, 2001.
6 See Heather Moore, ‘‘The Modern-Day Island of Dr,
Moreau,’’ op. cit., and Sharon
Schmickle, ‘‘It’s what’s for dinner: milk
and meat from clones,’’
http://www.startribune.com/stories/462/868271.html, December 2,
2001.
7 ‘‘Clonefarm: Billions of identical chickens could
soon be rolling off production lines,’’
http://www.newscientist.com/hottopics/cloning/cloning.jsp?id=23040300,
August 18, 2001.
8 Cited in Heather Moore, ‘‘The Modern Day Island
of Dr. Moreau,’’ op. cit.
9 The Missyplicity Project boasts a strong code of bioethics;
see http://www.missyplicity.com/.
10 See http://www.transgenicpets.com/.
11 ‘‘In Cloning, Failure Far Exceeds Success,’’
Gina Kolata, http://www.nytimes.com/2001/12/11/science/11CLON.html.
12 See ‘‘Clones contain hidden DNA damage,’’
http://www.newscientist.com/news/news.-
jsp?id=ns9999982; see also the study published in Science (July
6, 2001), which discusses why so many clone pregnancies fail and
why some cloned animals suffer strange maladies in their hearts,
joints, and immune system.
13 ‘‘Clone Study Casts Doubt in Stem Cells: Variations
in Mice Raise Human Research Issues,’’ http://www.washingtonpost.com/ac2/wp-dyn/A23967-2001Jul5?language=
printer, July 6, 2001.
14 See ‘‘Scientists Warn of Dangers of Human Cloning,’’
http://www.abcnews.com/. See also the commentaries in Gareth Cook,
‘‘Scientists say cloning may lead to long-term ills,’’
The Boston Globe, July 6, 2001; Steve Connor, ‘‘Human
cloning will never be safe,’’ Independent, July 6,
2001; Carolyn Abraham, ‘‘Clone creatures carry genetic
glitches,’’ July 6, 2001; Connor cites Dolly-cloner
Ian Wilmut who noted: ‘‘It surely adds yet more evidence
that there should be a moratorium against copying people. How
can anybody take the risk of cloning a baby when its outcome is
so unpredictable?’’
15 See ‘‘Report Says Scientists See Cloning Problems‘‘,
http://abcnews.go.com/wire.US/reuters200103525_573.html.
16 The Westhusin quote is at http://abcnews.go.com/cloningflaw010705.htm;
the ‘‘misplaced carbons’’ quote is in
Philip Cohen, ‘‘Clone Killer,’’ http://www.newscientist.com/news.
17 ‘‘Human Clone Moves Sparks Global Outrage,’’
http://www.smh.com.au/, March 11, 2001.
18 Given this attitude, it is no surprise that in September,
2001, Texas AM University, the
same institution working on cloning cats and dogs, showed off
newly cloned pigs, who
joined the bulls and goat already cloned by the school, as part
of the ‘‘world’s first cloned
animal fair.’’
19 See ‘‘Back from the Brink: Cloning Endangered
Species,’’ Pamela Weintraub, http://
news.bmn.com/hmsbeagle/109/notes/ feature2, August 31, 2001. ‘‘Gene
Find No Small
Fetus,’’ http://www.wired.com/news/print/0,1294,41513,00.html
20 See the collection of responses to Joy’s article in
Wired 8.07 (July 2000). Agreeing with Joy that there need to be
firm guidelines regulating nanotechnology, the Foresight Institute
has written a set of guidelines for its development that take
into account problems such as commercialization, unjust distribution
of benefits, and potential dangers to the environment. See http://www.foresight.org/guidelines/current.html.
I encourage such critical dialog on both the benefits and dangers
of new technologies and hope to contribute to these debates with
our studies.
21 See http://www.wired.com/news/0,1294,36886,00.html.
22 On ‘‘new science’’ and ‘‘new
sensibilities,’’ see Herbert Marcuse, One-Dimensional
Man
(Beacon Press, Boston, 1964) and An Essay on Liberation (Beacon
Press, Boston 1969).
23 For a sharp critique of how bioethicists are bought off and
co-opted by corporations in their bid for legitimacy, see ‘‘Bioethicists
Fall Under Familiar Scrutiny,’’ http://www.nytimes.com/2001/08/02/health/genetics/02BIOE.html.
______________________________________________________________________________
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