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Chapter 6 - Molecular Biology and Evolutionary Theory |
The
frontier of biological science is molecular biology and molecular genetics. The
fundamental assumption is that all biodesign information is contained in the genes and
that changes in genes produce evolutionary change in species. Therefore, molecular biology
should explain how evolution occurs.
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1. Has molecular biology explained development of the
embryo?
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Answer: In 1984
Nobel Laureate biologist Paul Berg of Stanford University said No:
At present, there is no general theory that can be formulated to explain development;
for example, the progress from a fertilized cell to an adult organism...
Another aspect of development that intrigues many people is trying to translate cell
phenomenology or organ morphology into molecular terms. For instance, what governs the
liver's growth and shape? What regulates the growth of cells? What triggers a cell into
the division cycle? All of these questions require molecular explanation. Ultimately they
will be defined in molecular and chemical terms.1
Take note of Prof. Berg's faith for the future.
Ten years later in of 1994 much progress has been made in
understanding the genetic control of embryonic development. However, the location of
designs for complex biological structures is still shrouded in much mystery. As we shall
see, neither the embryonic development nor the evolutionary origin of complex structures
and organs has yet been adequately explained.
Below under Question 6 we have quoted from an authority on
embryonic development and evolutionary theory, Prof. Lewis Wolpert. Take note of the fact
that in 1994 Lewis Wolpert affirmed the same faith in the future that Paul Berg did in
1984. We are still waiting for them to prove their case. They are still seeking their holy
grail, the origin of life without God the Creator.
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2. Has molecular biology explained speciation?
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Answer: No, the
process by which new species form is not well understood. Prof. Richard C. Lewontin of
Harvard University wrote in 1974, "...we know virtually nothing about the genetic
changes that occur in species formation."2
Eight years later Prof. Edward O. Wilson, also of Harvard, said, "It [molecular
biology] doesn't have much to say about speciation, about macroevolution or about rates of
evolution."3
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3. Has molecular biology explained embryonic
development and evolution?
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Answer:
Although much has been learned about this subject, the big questions are still unanswered. In Section 7 below we have quoted at some length from Lewis
Wolpert's 1994 survey of recent progress in the study of embryonic development. He makes
it clear that, at the level of molecular genetics, it is still not known why an egg
becomes a chicken in 21 days. If this be so, it is certain that evolutionary science
cannot explain how a microbe became a university professor in three billion years.
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4. Has molecular biology explained the evolution of new
complex organs or structures?
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Answer: No,
only limited variation has been partially explained. Two internationally respected
biologists, G. Ledyard Stebbins and Francisco J. Ayala, said No:
The most dramatic changes in thinking about evolution stem from new knowledge about
genetic processes at a molecular level, and yet the implications of that knowledge for
evolutionary theory remain obscure. The molecular pathways that lead from genes to visible
characteristics are long, complex, and as yet largely unexplored. Until the relation of
genes to development is better understood at a molecular level the full impact of
molecular biology on evolutionary theory cannot be assessed.4
A family of genes, homeobox genes, are found in many different organisms to have
important influence in the embryonic development of basic body plans. In 1992 Jean Marx
surveyed recent progress in the coordination of two fields of evolutionary biology,
embryonic development and molecular genetics. She observed that homeobox gene research,
...is starting to bring together developmental and evolutionary biologists, a merger
that is badly needed, considering the intractability of certain evolutionary puzzles, such
as the long-standing quandary of how the body plan of multi-celled organisms arose.
...While the final marriage of developmental biology and evolutonary theory is clearly
some way off, perhaps one day it will produce an offspring that can explain in satisfying
molecular detail, how new species evolved.5
By the term "new species" Marx actually refers to new organisms characterized
by new complex biological structures.
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5. Does molecular biology explain the origin of complex new
biochemical systems?
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Answer: No, such an
explanation has yet to be published. Biochemist Michael Behe has dealt with this question
very effectively in his 1996 book, Darwin's Black Box.6 He shows that the crucial issue at the molecular level is that of
"irreducible complexity." This is logically related to the principle of a
complex combination of complex interdependent parts that was outlined in Chapter 2 in our
consideration of the molecular rotary motors that power the flagellae of the microbe E.
coli. For example, the step-by-step sequence of
many biochemical reactions needed to synthesize one important molecule, adenosine
monophosphate (AMP), in a living cell is amazingly complex (pp. 142-161). The process
starts with a foundation molecule, ribose-6-phosphate. This foundation molecule is then
modified in a series of reaction steps that leads finally to the product, AMP. Could such
a complex biochemical system evolve step-by-step by a random process of mutations and
natural selection (M&NS)? Evolution is defined as a blind process that does not know
what its goal is. So what is NS selecting for? Each new intermediate step that is added by
evolution must make a product molecule that has some value to the organism that causes it
to be selected. Furthermore it presumably carries the process nearer to the AMP molecule
that is the unknown goal. Therefore, an evolutionary theorist trying to explain the
evolution of this chain of reactions leading to the desired amino acid must dream up some
benefit offered to the organism by each reaction step and its product molecule that
M&NS adds to the evolving series of reactions. And finally this unguided process
stumbles on the final product, AMP. Has such an explanation ever been published in the
biochemical literature? NO, not yet. And the principal reason for this failure is the fact
that the existing system of chemical reactions that produces AMP is useless if any one of
the reactions and its intermediate product is missing. If the complexity of the
biochemical system is reduced by deleting just a single step, the system is
non-functioning. The system as it exists for producing AMP is irreducibly complex.
Other irreducibly complex biochemical systems treated in
Prof. Behe's book include the chemistry of vision (pp. 18-25), Bombardier beetle's
artillery (pp. 31-36), cilia (pp. 59-69), bacterial flagellae (pp. 69-73), and the human
immune system(pp. 74-97). Prof. Behe made a thorough survey of the scientific literature
of molecular biology. He reports that the Journal of Molecular Biology in the past
25 years published about 100 papers per year on molecular evolution. Not a single paper
attempted to explain in any detailed scientific manner the evolution of any complex
biochemical system. The many hundreds of papers on this subject in the Proceedings of
the National Academy of Sciences yield the same zero result (pp. 165-179).
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6. Does not molecular biology prove that protein
molecules have evolved?
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Answer: The
comparison of amino acid sequences of corresponding proteins in different species has been
interpreted in terms of homology. It has been assumed, for example, that the cytochrome c
molecule has evolved with time as new species have evolved from pre-existing species.
However, a series of proteins with systematic differences and similarities no more proves
evolution than does a series of fossil skeletons or of living creatures. (See Chapter 10, sections 1 & 2) The
fundamental protein chain of cytochrome c contains 101 amino acid residues, and the amino
acid sequence (the order of the different amino acids along the chain) has been determined
for about a hundred species of plants, bacteria and animals. The differences have been
analyzed in terms of the assumption that the cytochrome c molecules have evolved by
mutations at a constant rate for years. If this were the case, then the number of
differences in the cytochrome c molecules from two different species should be
proportional to the length of time back to the separation of their two lines of descent
from a common ancestor. These times are obtained from the theory of evolution and the time
table of historical geology. Graphs of this relationship have been published which show a
fair straightline relationship, reflecting that the number of differences is proportional
to the time.7 This may be taken as circumstantial
evidence for the theory of molecular evolution.
On the other hand, :Michael Denton in his 1985 book, Evolution: A Theory In Crisis,
shows that the data can be interpreted in accord with the creation model of origins.7 The essential structure of the enzyme is the same for
all of the hundred or so species studied. For example, thirty-five of the 101 positions in
the chain are invariant, being filled by the same amino acids in all of the species. Also,
eleven of these unchangeable positions are together at the vital action center of the
molecule where its enzyme function is performed. All of the cytochrome c molecules from
the different species fold up into the same basic three-dimensional shape so that they can
do the same job in cell chemistry. This accords with the view that the design was created,
not evolved.
The differences in the amino acid sequences of the cytochrome c molecules of different
species may be understood as either the result of mutations, or created differences, or a
combination of these. The fewer differences generally observed between similar species is
in agreement with the creation model. Denton has shown that the differences in the
sequences, when arranged in a matrix, reveal that groups of similar species are separated
from other such groups.7 There are no
intermediates between the groups. These groups distinguished by the similarities of their
cytochrome c molecules correspond precisely to their traditional biological
classifications based on their bodily forms. And, finally, the molecular separations
between these groups correspond numerically to the degree of their differences. For
example, the difference between horse and dog (two mammals) is six percent, between horse
and turtle (2 vertebrates) is 11 percent, and between horse and fruit fly (vertebrate and
insect) 22 percent. The differences in cytochrome c molecules may in some cases be
necessary or advantageous in certain species.
Finally, the theory and the graphs mentioned earlier were sharply criticized by
prominent evolutionary scientists. It was charged that the time periods used in making the
graphs were not really in line with current geological theory.8
It has been pointed out that, in order to interpret the protein sequence data and get
results in line with current evolutionary theory, considerable computer
"massaging" of data is practiced.10
Christian Schwabe of the Department of Biochemistry, Medical University of South
Carolina, has raised serious questions about this theory. In 1986 he wrote an article
entitled, "On the validity of molecular evolution," in which he said:
...many exceptions exist to the orderly progression of species as determined by
molecular homologies; so many in fact that I think the exception, the quirks, may carry
the more important message.11
For example the data of different molecular homologies often, in the same set of
species, suggest different rates for the evolutionary "clock." It is not
uncommon for the data from the same protein studied in different species to lead to
ridiculous conclusions concerning the supposed evolutionary relationships of the species.
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7. What bold assertions can we make about the failure
of evolutionary biology?
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Answer: We can
assert that at the level of the molecular biology of the genes, where final explanations
are supposed to be found, there are today still no testable theories or demonstrable
mechanisms for biological inheritance, embryonic development, speciation, or the evolution
of anything new. Let us explain this sweeping claim. From the above quotations from
leading evolutionary scientists we see that it is not known how or where in the DNA the
design information is stored for the structures of organisms. Further, it is not known how
any such stored information is translated into biostructures as the embryo develops from
egg to adult. Biologists are struggling to solve this riddle. Humanly speaking, they might
succeed someday. But as long as we are ignorant of this basic information, it is clear
that we do not know how any new structures could be produced by evolution.
It is pretty well understood how genes are inherited, but just what the genes mean with
respect to the structures of the organism is not known. Most genes apparently code for
particular protein molecules, but it is not known what the proteins mean with respect to
biostructures of the organism. Therefore, when chromosomes and their genes are inherited,
we actually do not know what biostructures are being inherited. In other words, we really
have only a very incomplete theory of biological inheritance! The complexity ot he
situation is rendered almost infinite by the fact that most structural features of an
organism are influenced by many genes (called pleotropy), and many genes influence many
different structures in the organism.
Lewis Wolpert of the Department of Anatomy and Developmental Biology, University
College London, is a leading authority on molecular biology and developmental biology, and
their relation to evolutionary theory. In a brief survey of recent research published in
1994 he discussed findings in studies of the embryonic development of the fruitfly,
Drosophila, raising serious questions:
...How, for example, does the change in just one gene change the antenna of the fly
into a leg? It may well be that no general principles are involved in the control of
morphogenesis and cell differentiation. Even so, we do not yet have an example where we
understand in detail the development of a single adult organ. We remain largely ignorant
of timing mechanisms and how the size of different structures is controlled.
How many genes control development -- as distinct from providing the housekeeping
functions of the cell? The answer is not known, but one can guess. ...If one thinks of,
say, 100 genes for each multicellular structure in the adult, then 50 different structures
in Drosophila would require 5000 genes. For mammals, for which there are some 350 distinct
cell types, tens of thousands of genes might be needed. Understanding the function of so
many genes is made even more difficult by cases of apparent redundancy. that is, it is
possible to knock out certain genes in mice without there being any obvious effect on the
phenotype. It is likely that true redundancy is illusory and merely reflects the failure
to provide the correct test for an altered phenotype. It may thus be very difficult to
work out the true function of such genes.
Will the egg be computable? That is, given a total description of the fertilized egg --
the total DNA sequence and the location of all proteins and RNA -- could one predict how
the embryo will develop? This is a formidable task, for it implies that in computing the
embryo, it may be necessary to compute the behavior of all the constituent cells. ...
What will the next 20 years bring? ....We can also look forward to great progress in
the area of evolution and development. We may then see the solution to grand problems like
how basic body plans emerged, how they are conserved, and the origin of developmental
novelty. We will thus come to understand how development constrains and directs the form
of all multicellular organisms.12 (Developmental
novelty refers to new, complex biostructures.)
It is clear from Wolpert's discussion that biologists cannot explain why an egg becomes
a chicken in 21 days. He also makes it clear that the evolutionary origin of neither
general body plans nor of new complex organs(developmental novelty) has been explained
theoretically. But these are the primary, the most crucial problems for evolutionary
theory. If secularistic science cannot explain how an egg becomes a chicken in 21 days, in
it certain that a scientific explanation of how an amoeba could become a university
professor in 3 billion years is far from achievement. Why is it then that the public is
continually propagandized to believe that evolution is a fact and that science has it all
explained? Could it be that science and education is now dominated by unbelievers who are
falsely using science as a weapon against the God of creation?
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8. Can we even be sure that all biological
inheritance and all cellular activities are determined by the DNA of the genes in cells?
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Answer: No,
until it can be proved just where and how inherited information is stored in the genes, we
cannot be positive that the genes do determine all inheritance. To begin with, it is
definitely known that some important biological information is transmitted in the
structure of the plasma and outer cortex of the cell, not in DNA. This is the case both in
fertilized egg cells and in protozoans which produce new generations by cell division.13 And so long as we remain ignorant of where and how
the bulk of inherited information is stored in the genes, there is a possibility that
important biological information is not stored in physical structures of the cell at all.
In fact, it has been suggested that perhaps the genes cannot store enough information to
describe and construct an organism.14
Let us indulge in a far-out speculation. Perhaps the information which determines the
distinctive structures of the created kinds is provided through an immaterial channel, by
special divine providence! In the current state of scientific knowledge and ignorance, it
is not possible to prove that this speculation is false. Under this model for genetics,
the information carried in the chromosomes and their genes provides for fundamental
housekeeping in the cells and in the whole organism. This information would also provide
for limited genetic variation and adaptation to changing environments.
In Chapter 2, Section 3-d, we described
at length the mysterious construction of the Venus flowerbasket sponge by disconnected,
blind, brainless single cells. Then we described the mysterious ability of blind,
brainless amoeba-like arenacious foraminifera cells to build little houses from sponge
spicules found in the dark ooze on the sea floor. Scientists are helpless to explain how
DNA in genes can empower and direct these cells to accomplish their tasks. It is certain,
therefore, that scientists are also helpless to explain how these tiny creatures evolved
with their mysterious powers.
We conclude that Christians cannot be faulted on scientific grounds if they believe
that some aspects of living organisms are actively directed by special divine Providence.
The Scriptures suggest that God is actively involved in the lives of all of His creatures.
...These all wait for You, that You may give them their food in due season. What You
give them they gather in; You open Your hand, they are filled with good. You hide Your
face, they are troubled; You take away their breath, they die and return to their dust.
You send forth Your Spirit, they are created; and You renew the face of the earth. (Psalm 104: 27-30)
...If He should set His heart on it, if He should gather to Himself His Spirit and His
breath, all flesh would perish together, and man would return to dust. (Job 34:14-15)
As we said. we are offering a far-out speculation. But there is no law against
speculation in science. This idea is not a testable scientific hypothesis, because it
involves a supernatural element. But the definition of science does not prohibit a
scientist from believing in divine special creation and in a supernaturally imparted
aspect of living matter. These ideas can also be a part of his conceptual framework for
his scientific work. We have proposed here a type of divine "vitalism." Vitalism
is the idea that living matter possesses some character radically different from
non-living matter, something beyond the laws of physics and chemistry. This concept was
repudiated by most scientists after the mid-19th century, for two reasons. First, they had
begun to have some success in showing how living organisms function according to the laws
of physics and chemistry. Second, following Darwin, they were moving toward the belief
that everything in the universe has a completely materialistic cause and effect
explanation. But this view of the world has yet to be validated by science. A scientist
who believes in a created, divinely directed world is entirely free to do so, and the data
of science afford him much support for this belief.
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References
1 Berg, Paul in Chemical &
Engineering News, 62, 13 Aug. 1984, p. 62.
2 Lewontin, Richard C., The
Genetic Basis of Evolutionary Change (Columbia Univ. Press, New York, 1974), p. 159.
3 Wilson, Edward O. in Lewin,
Roger, "Molecules Come to Darwin's Aid," Science, 216, 4 June 1982, p.
1092.
4 Stebbins, G. Ledyard, and Ayala,
Francisco J., Scientific American, 253, July 1985, p. 72.
5 Marx, Jean, "Homeobox Genes
Go Evolutionary," Science, 255, 24 Jan. 1992, pp. 309, 401.
6 Behe, Michael J., Darwin's
Black Box the Biochemical Challenge to Evolution (Free Press, Simon & Schuster
Inc., New York, 1996)
7 Dickerson, Richard E., ibid.,
226, April 1972, pp. 58-72.
8 Denton, Michael, Evolution:
A Theory in Crisis (Adler & Adler, Bethesda, MD, 1986), pp. 274-307; see also
Kofahl, Robert E. and Kelly L. Segraves, The
Creation Explanation (Harold Shaw Publishers, Wheaton, IL, 1975, pp. 165-169.
9 Crowson, R.A., Nature,
254, 3 April 1975, p. 464.
10 Dwinell, Mark, Origins
Research, 8, No. 2, Fall/Winter 1985, p. 10.
11 Schwabe, Christian, Trends
in Biochemical Sciences, 11, July 1986, p. 280.
12 Wolpert, Lewis, "Do We
Understand Development," Science, 266, 28 October 1994, pp. 571-572.
13 Sonnenborn, T.M., "Gene
Action in Development," Proc. Royal Soc. London. B. 176, 1970, pp.347-366; Jones,
A.J., Creation Research Soc. Quarterly, 19, June 1982, pp. 13-18.
14 Bremmerman, Hans, Progress
in Theor. Biol., 1, 1967, pp. 70-72.
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