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2001 |
“IRREDUCIBLE
COMPLEXITY OR REDUNDANT ASSEMBLY: AN
EVALUATION OF THE BIOCHEMICAL EVIDENCE FOR INTELLIGENT DESIGN” M.
Todd Tippetts Department of Chemistry, College of Mount St. Vincent |
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Throughout
the centuries that science has been a separate discipline, a dialogue
between science and religion has taken place.
This dialogue has ranged from a simple exchange of information,
to the use of religious principles for motivation in the study of
science, to the use of science to try and gain religious insights and
possibly even to “prove religion.”
This last aspect has been most commonly seen in a movement once
called Natural Theology. Natural
Theology uses science to look for the “footprints” or evidence of
God. By scientific
investigations, the natural theologian tries to find those facets of the
world which can seemingly only be explained by the existence of a
creator God. Before Darwin,
as scientists studied the wondrous diversity of life forms on earth, the
best explanation for the miracle of life was divine “intelligent
design.” In 1873 William
Paley (1873) proposed that, just as the existence of an obviously
designed watch implies the existence of a designer, the intricacies of
living organisms must also point toward the existence of a heavenly
designer. Charles
Darwin and his theory of evolution through natural selection, however,
has provided an equally adequate answer to the question of origins of
the great diversity of life, and one that is completely naturalistic.
Natural selection—a combination of random of variations, which
we now call mutations, with the selection power of an environment that
eliminates unfavorable change—can explain life’s design.
As long as there is enough time (and the four billion years that
there has been life on earth seems to be enough) natural selection can
accomplish the design of all the forms of life, without recourse to
the Divine, without any supernatural interventions. Even
before Darwin, Hume had addressed the Design Argument.
He pointed out that what we perceive to be design could only be
the appearance of it. Darwin
provided a mechanical, naturalistic mechanism by which the diversity of
life could arise without the help or input of a designer.
Natural Theology appeared to have been vanquished by Darwin’s
insights, but it just wouldn’t die.
Like the Hydra that fought with Hercules, every time one head was
cut off, two more grew in its place.
Natural Theology is alive and well and found in many forms today. One
current version of Natural Theology is called Intelligent Design Theory,
a movement that once again tries to use scientific knowledge to
“prove” the activity of God in the universe.
The basic strategy is as follows: Select and consider specific
aspects of life, using relevant knowledge from current natural science.
Then ask the question of whether one can, using the best
scientific knowledge of the day, construct a credible scenario in
which the particular life form came about in a gradualist, Darwinian
fashion. If not, then it
must be the outcome of not a mindless, naturalistic, evolutionary
process but rather a result of intelligent design. “The precise meaning of ‘intelligent design’ is not
always apparent, but it most often entails the combination of both
thoughtful conceptualization and the first assembly of a new form by
extra-natural means (Van Till, 1998, p. 345).”
Leaders of this movement would include Philip Johnson (1991),
William Dembski (1999) and the biochemist Michael Behe (1996).
Being trained in biochemistry and molecular biology myself, I
will primarily address the arguments of Michael Behe. Michael
Behe introduced what he claims to be evidence for an intelligent
designer: namely the presence of “irreducibly complex” systems.
Charles Darwin stated that “if it could be demonstrated that
any complex organ existed which could not possibly have been formed by
numerous, successive, slight modifications, my theory would absolutely
break down (1872, p. 154).” Behe
claims that irreducibly complex systems provide such a complex organ.
He (p. 39) describes such systems as follows: By
irreducibly complex, I mean a single system composed of several
well-matched, interacting parts that contribute to the basic function,
where in the removal of any one of the parts causes the system to
effectively cease functioning. An irreducibly complex system cannot be produced
directly...by slight, successive modifications of a precursor system,
because any precursor to an irreducibly complex system that is missing a
part is by definition nonfunctional.... Since natural selection can only
choose systems that are already working, then if a biological system
cannot be produced gradually it would have to arise an integrated unit,
in one fell swoop, for natural selection to have anything to work on. Behe
(p. 42) uses an analogy of a mousetrap to describe such irreducibly
complex systems: The
function of a mousetrap is to immobilize a
mouse....The mousetraps that my family used consist of a number
of parts: (1) a flat wooden platform to act as a base; (2) a metal
hammer, which does the actual job of crushing the little mouse; (3) a
spring with extended ends to press against the platform and the hammer
when the trap is charged; (4) a sensitive catch that releases when
slight pressure is applied; and (5) a metal bar that connects to the
catch and hold the hammer back when the trap is charged. Each
of these parts is necessary for a functional mousetrap.
A trap missing any one of these would not catch mice.
The trap, having no functional precursors, could not be an
improvement on an existing model (the hallmark of a system which
evolves). An isolated
spring, or trap without a spring, would be incapable of catching mice.
All parts of the mousetrap have to be assembled simultaneously
for any of them to be functional. Behe
then eloquently describes a series of cellular functions that are
remarkably complex, including the mechanisms for vision, blood clotting,
and the immune system. In
terms of making very complicated biochemical interactions understandable
to the layman, Behe does an admirable job.
These highly complex cellular systems can function as they do
only if all units are simultaneously present and
working closely together in an integrated function.
Gradual emergence, where these systems evolve one component at a
time, seems not to be able to explain the development of the system.
Just as the mousetrap won’t work with even one component
missing, cellular systems likewise cannot function in the absence of one
component. John Haught
(2000, p.4) summarizes Behe’s conclusion by saying: “....if the
cellular mechanism is not the product of gradual accumulation of small
changes, then, Behe concludes, the Darwinian explanation of life is
demonstrably erroneous.” According
to Behe, Darwinian or evolutionary explanations of such complex systems
are a “black box”—some hypothetical sequence of events and
mutations acted on by natural selection—and we are supposed to believe
that these events will explain the world without examining them all too
closely. Behe suggests that
rather than relying on a mysterious black box to explain the world, we
accept the more reasonable alternative of intelligent design. The
intelligent design proponents look at life and see it as too perfect for
it to have come about by chance. But
these people are betting on ignorance:
Because we cannot currently explain the evolution of complex
biochemical systems, they imply that it is impossible to explain them,
that the system could not have evolved and must have been designed.
This is, however, an example of “God of the Gaps” thinking,
which has proven problematic before.
When people explain the gaps in scientific knowledge by God’s
action, when the gap is later filled in by scientific progress, it seems
to eliminate the need for God. This
“leap of faith” to a conclusion that there must be a designer is
inspired by their belief in a God, and in the supernatural creation of
the world and of life itself. People
of faith, coming from this Weltanschauung, are very impressed
by Behe’s irreducibly complex systems.
To believers, both laymen and scholars, Behe’s thesis seems to
be compelling evidence for the existence of a designer God. According
to Behe, a system is irreducibly complex if all of its components are
essential to the function of the system.
Using his mousetrap example, a trap will not catch mice if it
is missing a spring, or the hammer or the wooden base.
No simpler version of the trap will be able to trap mice.
However, I remember in cartoons as a child seeing people catch
mice with a much simpler device, a box with one end raised and held up
by a stick, with a long string on the stick.
A person would hold the other end of the long string, waiting and
watching for a mouse to appear. When
a mouse was under the box, a tug on the string would pull out the stick,
and gravity caused the box to drop, trapping the mouse. This
trap could be improved by the addition of bait: a piece of cheese placed
under the box would attract mice, increasing the likelihood of the mouse
coming under the box, and being caught when the string was pulled.
In Boy Scouts they taught us to improve this trap once again by
automating it, and by making it more lethal.
A heavy board or log with a flat surface, which crushes the
little mouse against the ground, replaces the box.
This kills the mouse, rather than imprisons him, which precludes
the possibility of an escape. Rather
than a person sitting and watching to pull on the string, an arrangement
of notched sticks could both hold the bait and support the box.
When the bait is taken the sticks are disturbed and the heavy
board falls, killing the mouse. One
might make this trap more sturdy by fixing the parts to one another,
allowing them to move through the use of a hinge.
A firm board underneath replaces the ground which may be too soft
and yielding, and the falling board is attached to the base board by a
hinge. The trap has become
more efficient, more durable, and more lethal by the addition of these
components. So
far this trap is still powered by gravity.
One might be inspired by the spring and clip holding paper to a
clipboard, and the mousetrap takes a quantum leap forward.
Since the power of a coiled spring is much stronger than gravity,
one could replace the box with a bar and spring.
The top board now falls much faster, powered by the spring.
It would even be possible to decrease the size of the falling
board, since now it doesn’t require the heavy mass which was
accelerated by gravity. The
hammer of the modern mousetrap replaces the box, the spring replaces
gravity, and the bar holding back the hammer replaces the stick holding
up the box. The bait rigged
to the bar remains basically the same, with the catch of the modern trap
taking the place of my notched sticks. Behe
would argue (p. 44) that these variations of a dead fall mousetrap are
not physical precursors, but merely conceptual precursors.
They perform the same task, by a different means.
I have described how all the parts of the modern mousetrap were
represented in the primitive dead fall.
According to Behe, a physical precursor must be directly changed
into the modern mousetrap by gradual change or improvement, and
“...each change can be only a slight modification, duplication or
rearrangement of a pre-existing component, and the change must improve
the function....” Replacing
the box with a heavy board, and then the stick by a rod, hammer and
spring is not a direct duplication or improvement of a pre-existing
component, but rather an importation of components from outside the
system. The trap was
improved by substitution with or addition of components that existed in
another system, a clipboard. In
this very objection we see the problem with Behe’s logic.
He considers each biochemical system as an isolated system, cut
off from the rest of the cell, with no exchange of parts or materials
possible. The protein
components of each of these biochemical systems were not generated in
a vacuum, but rather resulted from the duplication or modification of
pre-existing proteins, which was used in another possibly related
system. These related
proteins constitute protein families and super-families.
Analysis of the DNA, the molecular instructions for protein
synthesis, gives us a clue as to the history and relatedness of
different proteins. Complex
tasks, performed by a seemingly irreducibly complex system can be
accomplished less elegantly by simpler means, as in my box mousetrap.
These simple systems can be improved by the appropriation of
other cellular components, which may add force, amplify a response, or
add regulation. The
modified system is clearly superior, and selectable by natural
selection. Once the new
components are optimally integrated into the system, it may appear to be
irreducibly complex, since now the removal of one of the components from
the system would render it non-functional. While
Behe does an admirable job of describing complex biochemical systems, he
ignores a great deal of biochemical and molecular biological evidence,
which does not support his idea of irreducible complexity.
We can see this more clearly by discussing the oxygen binding
protein, hemoglobin. Several
different α- like and β- like peptides can combine to form a
tetramer that constitutes the various functional hemoglobin molecules.
During human fetal development, up to eight weeks of gestation, the
embryonic hemoglobin expressed consists of two ζ (α- like) and
two ε (β- like) chains. This
embryonic hemoglobin is then gradually replaced by molecules consisting
of two adult α chains and two β- like chains Gα
or Gγ,
which make up fetal hemoglobin. While
the α peptide chains are produced throughout fetal and adult life,
the γ-globin chains are replaced by the adult β- like chains
β and δ during the first six months of life (Efstratis et. al,
1980). Most adult hemoglobin
consists of the α2β2
tetramer, but there is low level expression (about 1%) of the α2δ2
molecule as well (Voet et. al, 1999, p. 120).
These different combinations of globin chains produce hemoglobin
molecules particularly suited to their roles in human physiology.
For example, fetal hemoglobin containing either the Gα
and Gγ
peptide chain has a much higher affinity for the binding of oxygen than
adult hemoglobin. It can
therefore effectively extract oxygen from the maternal blood across the
placenta during gestation. On
the other hand, the adult hemoglobin is noted for the decrease in oxygen (Lodish
et al, 2000, p. 299). All of
these hemoglobin genes are also similar to myoglobin, an oxygen binding
protein expressed in muscles which facilitates oxygen diffusion through
the muscle. They likely arose from a common primordial oxygen storage
protein. Duplication of the
gene allowed the various globins to diverge from one another, and to take
on new physiological functions (Voet, 1999). Examination
of the genetic structure of these genes clearly shows their common
origins. The DNA coding for these molecules consists of identical
arrangements of exons (protein coding regions) and introns (DNA sequences
that are copied into RNA and then removed to form the functional mRNA
molecule, which directs protein synthesis.)
This gene structure is shown in figure 1.
Myoglobin, as well as all members of both the alpha and beta
globin families, shares not only amino acid similarity, but also this
basic genetic organization of exons and introns.
Figure
1 Genetic
Organization of the ß-Globin Gene (Lodish,
et al, 1995) The
similarity in amino acid sequence of the beta globin family is shown in
table 1 (at end of article). In
this table, the amino acid sequences of the members of the human beta
gene family (beta, epison, delta, Gγ and Gα) are aligned for
comparison. A consensus
sequence is determined, with absolutely conserved amino acids shown in
tan, conservative substitutions (replacement with a similar amino acid)
shown in gold, and non-conservative substitutions (replacement with a
chemically dissimilar amino acid shown in orange. As can be seen from table 1, the two human gamma globin genes
are the most similar, and the beta and delta genes likewise share many
common sequences. These
genes are arranged in clusters on the human chromosomes.
The alpha cluster is on chromosome 16 and is arranged as 5'- ζ2
- ζ1
- ψα1
- α2
-α1 - 3'. The beta cluster is on chromosome 11 and is arranged as 5' -
ψβ2
- ε - Gγ - Gα - ψβ1
- δ - β - 3' (Efstratiadis et al. 1980).
The ζ2
and ζ1
genes, as well as the α2
and α1 genes, yield proteins which are identical to one another in
amino acid sequence, although there are silent differences in nucleotide sequence. These
many related genes in the hemoglobin gene family are products of gene
duplication, a well-known process whereby a gene or region of DNA is
copied twice during replication of the genome.
One copy of the gene can continue to perform its existing function
(such as carrying oxygen in adult hemoglobin), while the duplicate copy
is available to evolve into new roles, such as the ability to bind oxygen
at the much lower concentrations available in fetal blood.
This duplicate copy may evolve into a functional gene, such as
those for fetal and embryonic hemoglobin; or it may evolve into a pseudogene,
which is designated in the figure with a ψ.
A pseudogene is a now useless variation that serves no
function, existing as an evolutionary artifact.
These genes are permanently silenced, never producing a protein
product. Rather than evolving
into a new function, they accumulate mutations which preclude the
production of a protein product. It seems that such relics of failed evolution are especially
incompatible with the notion of a divine designer.
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