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Genetic Entropy and Malarial Parasite P. falciparum

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The two most recent books I’ve read are Biochemistry Professor M.Behe’s Edge of Evolution and Cornell geneticist J.Sanford’s Genetic Entropy.

Edge of Evolution I found to be amazing. It presented a case history of a eukaryote (P.falciparum) that has replicated billions of trillions of times within a span of a few decades. More importantly this is one of the most well studied organisms in biology due to its huge toll on human lives. In the last decade we’ve gone beyond phenotype analysis of the bug and have completely sequenced its genotype. This represents the largest test of evolution that we can hope to observe. The result of random mutation + natural selection being given billions of trillions of opportunities to generate significant novel biological complexity was essentially nil. Except for biochemically (but medically important) trivial changes in genotype the bug went exactly nowhere. It’s still the same old P.falciparum as its great grandparents billions of trillions of generations removed. It neither progressed nor regressed in an evolutionary sense.

All the negative reviews I’ve read of EoE nitpick at minutae while dodging the big picture. The big picture is that P.falciparum under intense scrutiny for billions of trillions of generations did exactly what ID theorists predicted – next to nothing. In contrast the ID deniers tell us over and over that the same evolutionary mechanism (RM+NS), in orders of magnitude fewer generations, turned a lizard into a lemur. Of course that’s a wholly imaginary story because the transformation of reptiles into mammals took hundreds of millions of years so can’t be confirmed by genotype observation. All we have is phenotype evidence based on fossils. Clearly *something* caused the transformation from reptile to mammal but I’ve yet to see any reasonable explanation for the observed failure of P.faciparum to evolve while somehow the same mechanism with fewer opportunities is imagined to have caused reptiles to evolve into mammals. Non sequitur!

Genetic Entropy I found less amazing because its basic conclusion was already obvious to me and unlike EoE it didn’t really present anything I didn’t already know. That’s not meant to detract from Genetic Entropy as many of its readers probably haven’t figured out for themselves that genetic entropy is, outside of environmental catastrophe, the force majeure in the evolution of species (or better put the eventual extinction of species).

One major disagreement I had with Genetic Entropy was the rate Sanford gives for random mutation. In virtually all the scientific literature I’ve read on the subject the given rate of copy errors in eukaryote DNA replication is one in one billion nucleotides. Sanford proposes, with references which I admittedly didn’t fisk, that the rate is really at least one and possibly two orders of magnitude greater. The lower rate Sanford gives is about one in ten million errors per nucleotide.

It occured to me recently that Sanford’s projected rate of genetic decay doesn’t square with the observed performance of P.falciparum. P.falciparum‘s genome is about 23 million nucleotides. At Sanford’s lowest given rate of nucleotide copy errors that means each individual P.falciparum should have, on average, about 3 nucleotide errors compared to its immediate parent. If those are nearly neutral but slightly deleterious mutations (as the vast majority of eukaryote mutations appear to be) then the number should be quite sufficient to cause a genetic meltdown from their accumulation over the course of billions of trillions of replications. Near neutral mutations are invisible to natural selection but the accumulation of same will eventually become selectable. If all individuals accumulate errors the result is decreasing fitness and natural selection will eventually kill every last individual (extinction). Yet P.falciparum clearly didn’t melt down but rather demonstrated an amazing ability to keep its genome perfectly intact. How?

After thinking about it for a while I believe I found the answer – the widely given rate of eukaryote replication errors is correct. If P.falciparum individuals get an average DNA copy error rate of one in one billion nucleotides then it follows that approximately 97% of all replications result in a perfect copy of the parent genome. That’s accurate enough to keep a genome that size intact. An enviromental catastrophe such as an ice age which lowers temperatures even at the equator below the minimum of ~60F in which P.falciparum can survive would cause it to become extinct while genetic meltdown will not. Mammals however, with an average genome size 100 times that of P.falciparum, would have an average of 3 replication errors in each individual. Thus mammalian genomes would indeed be subject to genetic decay over a large number of generations which handily explains why the average length of time between emergence to extinction for mammals and other multicelled organisms with similar genome sizes is about 10 million years if the fossil and geological evidence paints an accurate picture of the past. I DO believe the fossil and geological records present us with an incontrovertible picture of progressive phenotype evolution that occured over a period of billions of years. I don’t disbelieve common ancestry and phenotype evolution by descent with modification – I question the assertion that random mutation is the ultimate source of modification which drove phylogenetic diversification.

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P.S. I would love to evolve a third hand out of my chest, (to hold the keys while I open the door to carry in my groceries.) But I can hardly count it as evolution if my gametic DNA doesn't mutate also. Let alone, getting a date in order to procreate the new 3rd hand race of humans.the wonderer
October 29, 2007
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Whenever I hear these numbers, I often wonder if the calculator's take into account that for evolution to occur, the mutations have to be in the gametes, not the body cells. (Assuming sexually reproducing organisms, duh.) Who cares if a a somatic cell mutates, that isn't evolution. I think that puts these numbers much more improbable than depicted.the wonderer
October 29, 2007
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DaveScot, A minor nitpick--I observed in a recent online discussion a scientist taking a neophyte to task for failing to observe the "rules" of binomial nomenclature in the scientific names of organisms. In particular, when dealing with fauna, the first word in the scientific name (the genus name)is always capitalized, and the whole name (genus + species) should be italicized or underlined. Thus the microbe in question here would be P. falciparum. I mention this only because I think we want to limit the Darwinists' opportunities for ad hominem responses.Mickey Bitsko
October 29, 2007
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I DO believe the fossil and geological records present us with an incontrovertible picture of progressive phenotype evolution that occured over a period of billions of years. I don’t disbelieve common ancestry and phenotype evolution by descent with modification - I question the assertion that random mutation is the ultimate source of modification which drove phylogenetic diversification.
The evidence does not support common descent, see Doolittle et al. Extant organisms can be very nicely arranged into nested hierarchies according to their DNA but defy forming any kind of meaningful phylogenetic tree. The same excuses are currently being made for the lack of evidence of a tree of life that have traditionally been made for lack of evidence of gradualism in the fossil record. With neither paleological nor genetic evidence of common descent, I would argue that the concept is patently false. For those of you that believe in common descent. What was the last common ancestor of the fish, the squid, and the horseshoe crab? When did it live? What did it look like? What is the evidence it ever existed?Jehu
October 29, 2007
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All the negative reviews I’ve read of EoE nitpick at minutae while dodging the big picture. This is a key point. The reviews blather on about a two-amino-acid change being approachable in two naturally selectable steps instead of one, as though this somehow salvages the grand Darwinian story. It’s like arguing that it should be possible to introduce two sequential random errors into a space shuttle computer program and still have it work okay, and therefore this explains where the space shuttle came from. Thus mammalian genomes would indeed be subject to genetic decay over a large number of generations which handily explains why the average length of time between emergence to extinction for mammals and other multicelled organisms with similar genome sizes is about 10 million years… Here’s the real mystery: Creatures go extinct as a result of progressive genetic decay, but then new creatures suddenly appear, fully formed, more complex, and with mysteriously rejuvenated genomes good for another 10-million-year round of decay. Something fishy is going on here.GilDodgen
October 29, 2007
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DaveScot, Excellent Summary! I hope you don't mind if I quote this article. I do have one small concern with this statement of yours: "I DO believe the fossil and geological records present us with an incontrovertible picture of progressive phenotype evolution that occurred over a period of billions of years." I have a concern for the fossil record shows more variety of phyla at the end of the Cambrian Explosion 540 million years ago than is present now! To me that indicates "overall" the fossil record is not as progressive as the evolutionary theory requires and is in fact a major blow to their "progressive" evolutionary scenario. But that is a small gripe, you did a fine job summarizing the books, and reconciling them to clear reasoning.bornagain77
October 29, 2007
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Thanks DaveScot While Behe shows the limits of evolution Sanford shows genetic degradation or entropy - i.e. "natural selection" going backwards. Combined, these are extremely difficult for any Darwinian theory to overcome. Of the two, I believe Sanford's results will eventually be shown to be more powerful though possibly more "obvious". If I understand your comments, you end up agreeing with Sanford, the difference being the size of the genome and the complexity of the systems. The very low rate of copying errors in both systems highlights the amazing features of: * highly selective copying * error detection and * error correction * error removal by sexual reproduction These show strong parallels to design of computer systems and are strong evidence for ID. As you noted, the more complex the genome, the more important these error correcting systems become and the more difficult they are for RM & NS to explain. Conversely with more complex systems it is easier to demonstrate ID and easier to develop an ID design theory for them.DLH
October 29, 2007
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DaveScot, thanks for the well-thought summary of these two texts. I fully agree with your conclusions. I have not found any evidence to reject common descent -- assuming that some guy is twiddling with creatures that are making babies. I have found no reason to reject nautral selection as a powerful preservative agent. Every bone in my body says that the maximum mutations an organism can take and be protected by natural selection is 1 (mutations in true "junk dna" excepted.) I have found no scientific case whatsoever to support random mutation as a constructive agent. I find Behe's "malaria" case to be compelling as a confirmation of this limitation.bFast
October 29, 2007
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