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In this post, I intend to outline only a few ways in which evolutionary biology has been providing practical benefits in medical research behind the scenes for at least the past several decades. These are by no means exhaustive, and others surely exist; however, they should suffice for a start.
"Ask, and ye shall receive..." For common descent, here's a few of the most obvious examples.
1. Evolutionary Genome Research
Background: comparing human and other genomes shows us which genes have been conserved or modified over the course of evolution; this allows us to hone in on specific genes that cause disease and perform vital functions much more efficiently than we could otherwise.
95% or so of the human genome consists of non-coding DNA (source). What that means is that, unlike ordinary genes, any function these sections of DNA possess is not dependent on specific sequence. Like filler in a wall, you can basically toss anything there without a negative effect.
This is evident by the fact most of these sections of DNA exhibit a high number of mutation-induced variation and polymorphisms even in the same species. Mutations that occur there, unlike ones in functional genes, will not disrupt anything, and so will not be weeded out by natural selection.
However, we're looking for coding DNA, the actual genes that make us tick and can cause major screwups if damaged. Without evolution, you would have to do some really tricky and time-consuming in vitro stuff to identify them, similar to the proverbial needle in a haystack fiasco.
So, what do we do? Compare genomes of different organisms, of course! If evolution is correct, mice and humans, as well as all other mammals, share a common ancestor.
And since mission-critical genes, like those most often associated with hereditary disease, are conserved in the population by natural selection more than other genes, they'll stand out like a sore thumb by having the largest number of similarities to homologous genes in distantly related species.
"The scientific designers of the HGP [human genome project] realized that evolution provides an important framework in which to interpret the human genome, and made provisions for simultaneous study of a number of model organisms. The model organisms contribute advantages missing from humans: smaller genome sizes, the availability of extensive collections of mutations, and the potential for experimental manipulation. Utilization of those features that are conserved through the course of evolution between humans and the model organisms has greatly facilitated the advancement of the functional goals of the HGP.
An example that illustrates the use of an evolutionary framework in genome analysis is the identification of the gene that is responsible for cystic fibrosis. Starting with a broad scale chromosomal localization for the gene, scientists used a 'zoo blot' (a DNA profile generated for many organisms) to concentrate their sequencing efforts to a smaller region of the chromosomal DNA." - Evolution as a Framework for Genome Analysis
Without the assumption of common descent, there would be no reason to assume mission-critical genes would be identifiable by evolutionary predictions (inferred from anatomical and other non-genomic data, no less!) to the exclusion of function or other likely design-oriented goals.
Coincidentally, if the genome of chimps was ordered in anything other than the specific and antecedently unlikely patterns common descent requires, we wouldn't achieve any success from using it as a paradigm for such research.
2. Yielding Insights into the Biochemistry of Chemical Side Effects
Evolution also guides research into understanding the underlying biochemical reasons for side effects from antibiotics and other toxic chemicals. We now know, for example, that the mitochondria organelles powering our cells were once free-living organisms.
By understanding the ways in which certain chemicals attack homologues to our mitochondria, ribosomes and other cellular organelles in other species, we can infer the best course of action to take in regards to preventing their nasty side effects.
"Mitochondria and the Antibiotic Connection
Is it of any practical significance to know that mitochondria are procaryotic in character? Yes: A tragic use of an antibiotic in medicine is linked to the mitochondrion. This antibiotic, chloramphenicol, was widely used in the early days of antibiotic therapy because it was thought to be nontoxic. However, infants and certain other groups turned out to be unusually sensitive to chloramphenicol, and a number of deaths due to blood anemia occurred before the general use of this antibiotic in medicine ceased. What was going on here? We now know that chloramphenicol specifically affects the ribosomes of procaryotic cells, thus inhibiting protein synthesis. In eukaryotes, the ribosomes in the cytoplasm are unaffected by chloramphenicol, but those in the mitochondria, being procaryotic in character, are attacked. Once the connection between chloramphenicol and the procaryotic ribosome was discerned, it made sense that under certain conditions, chloramphenicol might inhibit eukaryotic cells. The cells inhibited in eukaryotes by chloramphenicol are those that are multiplying rapidly, such as blood-forming cells of the bone marrow, where new mitochondria are being synthesized at a rapid rate. With this understanding of the connection between eukaryotic mitochondria and procaryotes, the use of chloramphenicol ceased, except for special cases where it is the only antibiotic that works. Many other antibiotics in clinical use, for example streptomycin, tetracycline, and erythromycin, also interfere specifically with 70S ribosome function, but since these antibiotics are not taken up by eukaryotic cells, mitochondrial ribosomes are unaffected." - Biology of Microorganisms, Fifth Edition, page 104
Note that this is an entirely counterintuitive factoid if one is disallowed the use of evolution as an explanatory framework, as there is little obvious reason why both mitochondrial and bacterial ribosomes should be affected by the same drug if they don't share a common ancestor.
3. Predicting Side Effects and Complications from Animal Models
Per common descent, if two different species that together split off from the general mammal lineage before humans, such as gorillas and chimpanzees, each have the same difficulty with a drug or surgical procedure, it stands to reason that humans will as well.
On the other hand, if only gorillas and, say, old world monkeys share the problem, but neither chimps nor bonobos (which are closer to us on the standard phylogeny) do, it also stands to reason the drug or procedure is safe for further evaluation in humans. While this is not an exact prediction in the line of the fossil record or ERVs, it's a surprisingly effective rule of thumb.
Note that this is entirely dependent on the assumption of common descent. Under any other explanatory framework, one has as much reason to suspect gorillas have many features closer to ours than chimps would; in fact, that's usually the way real-world designs are implemented, with modular reuse of components sorted by environment or other criteria other than historical constraint.
But as with everything else, animal models demonstrate the successful experimental consequences of evolution.
4. Identifying Damaged Elements in the Genome and Anatomy by Comparison of Non-Human Species
As noted in other topics, genomes of various species contain a large number of detritus such as ancient fragments left behind by botched viral infection. These things can, in some cases, be dangerous to our health and it's important to identify them.
Per common descent, if two different species that split off from the general mammal lineage before humans, such as gorillas and chimpanzees, have the same damaged retroelement, it stands to reason that humans will have, at one point, inherited it from the common ancestor as well.
The same applies for pseudogenes that code for everything from smell to vitamin C production. With evolution, we can predict the presence of a crippled gene in our genome if we find its identical presence in two or more of our closest relatives.
This also applies to gross anatomy; if the two species of ape closest to us share the same anatomical vestige, it's pretty much a guarantee we'll have the same thing or something very similar.
This allows us to identify, in advance, disease-prone elements, crippled genes, problematic areas of our anatomy and other things without actually conducting costly, inefficient and/or unethical experiments on humans.
Summary
Evolution is an indispensible theory that can guide research in everything from genetics to anatomy. As we gain more insights into the historical causes and constraints that impose disease and medical problems on our bodies, we'll be ever better equipped to counteract them.
Using it, we can:
There are many more examples of the practical effects of evolution, both in the medical field and others; these range from improved understanding about ecology to predicting findings in embryology and the fossil record well in advance of the event.
There are also genetic algorithms, evolutionary computer simulations used for everything from designing safer aircraft wings to plotting satellite orbits to chemically arranging more effective drugs to evolving radios out of ordinary circuits merely by allowing random mutation and natural selection to operate, etc.
However, for the purpose of this particular discussion, I decided to focus on the medical insights we've gleaned from having access to the paradigm of common descent itself.
Much as the assumptions of quantum mechanics are borne out by our successful utilization of solid-state electronics, which shouldn't work if it's incorrect, so too does the success of evolution as a guide into genome research and other areas lend us ever-increasing confidence in its validity.
Originally posted by bevets in the "What scientific accomplishments have scientists achieved with creationism?" thread
Your question assumes that evolution is science. It is not. Evolution is atheist mythology. Please give specific accomplisments that are a DIRECT result of evolutionary mythology.
"Ask, and ye shall receive..." For common descent, here's a few of the most obvious examples.
1. Evolutionary Genome Research
Background: comparing human and other genomes shows us which genes have been conserved or modified over the course of evolution; this allows us to hone in on specific genes that cause disease and perform vital functions much more efficiently than we could otherwise.
95% or so of the human genome consists of non-coding DNA (source). What that means is that, unlike ordinary genes, any function these sections of DNA possess is not dependent on specific sequence. Like filler in a wall, you can basically toss anything there without a negative effect.
This is evident by the fact most of these sections of DNA exhibit a high number of mutation-induced variation and polymorphisms even in the same species. Mutations that occur there, unlike ones in functional genes, will not disrupt anything, and so will not be weeded out by natural selection.
However, we're looking for coding DNA, the actual genes that make us tick and can cause major screwups if damaged. Without evolution, you would have to do some really tricky and time-consuming in vitro stuff to identify them, similar to the proverbial needle in a haystack fiasco.
So, what do we do? Compare genomes of different organisms, of course! If evolution is correct, mice and humans, as well as all other mammals, share a common ancestor.
And since mission-critical genes, like those most often associated with hereditary disease, are conserved in the population by natural selection more than other genes, they'll stand out like a sore thumb by having the largest number of similarities to homologous genes in distantly related species.
"The scientific designers of the HGP [human genome project] realized that evolution provides an important framework in which to interpret the human genome, and made provisions for simultaneous study of a number of model organisms. The model organisms contribute advantages missing from humans: smaller genome sizes, the availability of extensive collections of mutations, and the potential for experimental manipulation. Utilization of those features that are conserved through the course of evolution between humans and the model organisms has greatly facilitated the advancement of the functional goals of the HGP.
An example that illustrates the use of an evolutionary framework in genome analysis is the identification of the gene that is responsible for cystic fibrosis. Starting with a broad scale chromosomal localization for the gene, scientists used a 'zoo blot' (a DNA profile generated for many organisms) to concentrate their sequencing efforts to a smaller region of the chromosomal DNA." - Evolution as a Framework for Genome Analysis
Without the assumption of common descent, there would be no reason to assume mission-critical genes would be identifiable by evolutionary predictions (inferred from anatomical and other non-genomic data, no less!) to the exclusion of function or other likely design-oriented goals.
Coincidentally, if the genome of chimps was ordered in anything other than the specific and antecedently unlikely patterns common descent requires, we wouldn't achieve any success from using it as a paradigm for such research.
2. Yielding Insights into the Biochemistry of Chemical Side Effects
Evolution also guides research into understanding the underlying biochemical reasons for side effects from antibiotics and other toxic chemicals. We now know, for example, that the mitochondria organelles powering our cells were once free-living organisms.
By understanding the ways in which certain chemicals attack homologues to our mitochondria, ribosomes and other cellular organelles in other species, we can infer the best course of action to take in regards to preventing their nasty side effects.
"Mitochondria and the Antibiotic Connection
Is it of any practical significance to know that mitochondria are procaryotic in character? Yes: A tragic use of an antibiotic in medicine is linked to the mitochondrion. This antibiotic, chloramphenicol, was widely used in the early days of antibiotic therapy because it was thought to be nontoxic. However, infants and certain other groups turned out to be unusually sensitive to chloramphenicol, and a number of deaths due to blood anemia occurred before the general use of this antibiotic in medicine ceased. What was going on here? We now know that chloramphenicol specifically affects the ribosomes of procaryotic cells, thus inhibiting protein synthesis. In eukaryotes, the ribosomes in the cytoplasm are unaffected by chloramphenicol, but those in the mitochondria, being procaryotic in character, are attacked. Once the connection between chloramphenicol and the procaryotic ribosome was discerned, it made sense that under certain conditions, chloramphenicol might inhibit eukaryotic cells. The cells inhibited in eukaryotes by chloramphenicol are those that are multiplying rapidly, such as blood-forming cells of the bone marrow, where new mitochondria are being synthesized at a rapid rate. With this understanding of the connection between eukaryotic mitochondria and procaryotes, the use of chloramphenicol ceased, except for special cases where it is the only antibiotic that works. Many other antibiotics in clinical use, for example streptomycin, tetracycline, and erythromycin, also interfere specifically with 70S ribosome function, but since these antibiotics are not taken up by eukaryotic cells, mitochondrial ribosomes are unaffected." - Biology of Microorganisms, Fifth Edition, page 104
Note that this is an entirely counterintuitive factoid if one is disallowed the use of evolution as an explanatory framework, as there is little obvious reason why both mitochondrial and bacterial ribosomes should be affected by the same drug if they don't share a common ancestor.
3. Predicting Side Effects and Complications from Animal Models
Per common descent, if two different species that together split off from the general mammal lineage before humans, such as gorillas and chimpanzees, each have the same difficulty with a drug or surgical procedure, it stands to reason that humans will as well.
On the other hand, if only gorillas and, say, old world monkeys share the problem, but neither chimps nor bonobos (which are closer to us on the standard phylogeny) do, it also stands to reason the drug or procedure is safe for further evaluation in humans. While this is not an exact prediction in the line of the fossil record or ERVs, it's a surprisingly effective rule of thumb.
Note that this is entirely dependent on the assumption of common descent. Under any other explanatory framework, one has as much reason to suspect gorillas have many features closer to ours than chimps would; in fact, that's usually the way real-world designs are implemented, with modular reuse of components sorted by environment or other criteria other than historical constraint.
But as with everything else, animal models demonstrate the successful experimental consequences of evolution.
4. Identifying Damaged Elements in the Genome and Anatomy by Comparison of Non-Human Species
As noted in other topics, genomes of various species contain a large number of detritus such as ancient fragments left behind by botched viral infection. These things can, in some cases, be dangerous to our health and it's important to identify them.
Per common descent, if two different species that split off from the general mammal lineage before humans, such as gorillas and chimpanzees, have the same damaged retroelement, it stands to reason that humans will have, at one point, inherited it from the common ancestor as well.
The same applies for pseudogenes that code for everything from smell to vitamin C production. With evolution, we can predict the presence of a crippled gene in our genome if we find its identical presence in two or more of our closest relatives.
This also applies to gross anatomy; if the two species of ape closest to us share the same anatomical vestige, it's pretty much a guarantee we'll have the same thing or something very similar.
This allows us to identify, in advance, disease-prone elements, crippled genes, problematic areas of our anatomy and other things without actually conducting costly, inefficient and/or unethical experiments on humans.
Summary
Evolution is an indispensible theory that can guide research in everything from genetics to anatomy. As we gain more insights into the historical causes and constraints that impose disease and medical problems on our bodies, we'll be ever better equipped to counteract them.
Using it, we can:
- Find mission-critical genes among the mounds of irrelevant stuffing merely by comparing the genomes of different organisms.
- Gain insights into the biochemical and historical causes responsible for drug side effects.
- Successfully utilize animal models as a substitute for experimentation on humans.
- Find worn-out, crippled and problem-causing sections of our genome and body by focusing on the similarities, in damaged aspects, of related species.
- Do many additional things not listed here:
There are many more examples of the practical effects of evolution, both in the medical field and others; these range from improved understanding about ecology to predicting findings in embryology and the fossil record well in advance of the event.
There are also genetic algorithms, evolutionary computer simulations used for everything from designing safer aircraft wings to plotting satellite orbits to chemically arranging more effective drugs to evolving radios out of ordinary circuits merely by allowing random mutation and natural selection to operate, etc.
However, for the purpose of this particular discussion, I decided to focus on the medical insights we've gleaned from having access to the paradigm of common descent itself.
Much as the assumptions of quantum mechanics are borne out by our successful utilization of solid-state electronics, which shouldn't work if it's incorrect, so too does the success of evolution as a guide into genome research and other areas lend us ever-increasing confidence in its validity.