muaxiong said:R-i-g-h-t. Knowing in detail the exact order of the blood clotting cascade has little to do with the hypothesis of how such an elaborate process came to be. Knowing the steps of the krebs cycle does little in showing why evolution favored the citric acid cycle as the dominant process for metabolism. In fact knowing anything about biology doesn't give anyone a single clue as it its origin via the goo to you method! But since creationists are such ignoramouses when it comes to biology in terms of evolution - why don't you school us.
Understanding how the process evolved actually helps us understand how things can go wrong and how one might treat it and find new treatments. For example, different animals have different clotting factors, but by looking at the evolutionary relationiships between the animals, we can understand more about how blood clotting works. Or do you believe that discovering about how things evolved gives us no useful information about now? If so, that's extremely short sighted and extremely anti-science.
EDIT TO ADD: Here's an example of using evolutionary theory to look for how blood clotting may have orginiated, by Ken Miller
Even a general scheme, like the one I've just presented, leads to a number of very specific predictions, each of which can be tested. First, the scheme itself is based on the use of well-known biochemical clues. For example, most of the enzymes involved in clotting are serine proteases, protein-cutting enzymes so-named because of the presence of a highly reactive serine in their active sites, the business ends of the protein. Now, what organ produces lots of serine proteases? The pancreas, of course, which releases serine proteases to help digest food. The pancreas, as it turns out, shares a common embryonic origin with another organ: the liver. And, not surprisingly, all of the clotting proteases are made in the liver. So, to “get” a masked protease into the serum all we'd need is a gene duplication that is turned on in the pancreas' “sister” organ. Simple, reasonable, and supported by the evidence.
Next, if the clotting cascade really evolved the way I have suggested, then the clotting enzymes would have to be near-duplicates of a pancreatic enzyme and of each other. As it turns out, they are. Not only is thrombin homologous to trypsin, a pancreatic serine protease, but the 5 clotting proteases (prothrombin and Factors X, IX, XI, and VII) share extensive homology as well. This is consistent, of course, with the notion that they were formed by gene duplication, just as suggested. But there is more to it than that. We could take one organism, humans for example, and construct a branching “tree” based on the relative degrees of similarity and difference between each of the five clotting proteases. Now, if the gene duplications that produced the clotting cascade occurred long ago in an ancestral vertebrate, we should be able to take any other vertebrate and construct a similar tree in which the relationships between the five clotting proteases match the relationships between the human proteases. This is a powerful test for our little scheme because it requires that sequences still undiscovered should match a particular pattern. And, as anyone knows who has followed the work in Doolittle's lab over the years, it is also a test that evolution passes in one organism after another.
There are many other tests and predictions that can be imposed on the scheme as well, but one of the boldest was made by Doolittle himself more than a decade ago. If the modern fibrinogen gene really was recruited from a duplicated ancestral gene, one that had nothing to do with blood clotting, then we ought to be able to find a fibrinogen-like gene in an animal that does not possess the vertebrate clotting pathway. In other words, we ought to be able to find a non-clotting fibrinogen protein in an invertebrate. That's a mighty bold prediction, because if it could not be found, it would cast Doolittle's whole evolutionary scheme into doubt.
Not to worry. In 1990, Xun Yu and Doolittle won their own bet, finding a fibrinogen-like sequence in the sea cucumber, an echinoderm. The vertebrate fibrinogen gene, just like genes for the other proteins of the clotting sequence, was formed by the duplication and modification of pre-existing genes.
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