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Freethought & Rationalism ArchiveThe archives are read only. |
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#22 | ||||
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As has been suggested a model like this is only as good as its assumptions, and I'm not convinced that Behe and Snoke's assumptions are all that good.
Their stipulation of neutral selection is allowable given their assumption that some early stages in the development of a multi-residue sequence may not be selected for functionally, but the quote they use to illustrate this Quote:
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has enough mights in it to make an assumption that this is neccessarily the case in general dubious, but in the specific situation they posit for the model it is allowable assuming one therefore realises the limited applicability of the model. Another assumption is the rather loosely defined one that most non-synonymous mutations produce a null phenotype. Quote:
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Where do the 2400 null mutations come from, what are they rendering non-functional? The parental function of the duplicate gene? The future function of the novel gene? Is it a total loss of function or just a loss of complete functionality? If it is a partial loss of the parental function then it is by no means appropriate as a factor and will not neccessarily lead to pseudogene formation. Loss of a binding site, for example, important to the function of the parental protein need not deny the possibility of a novel function to the novel protein, i.e. acting only on a subset of the initial targets of the parent protein for instance. It may be that in this case a null mutation is simply one leading to the formation of a pseudogene and therefore removing the gene from any maintenance by selection, in which case it is reasonable to assume the gene would most likely degrade subsequently and not evolve novel functionality. I don't deny that the odds are in favour of null rather than novel functional mutations, but it would be nice if Behe made some effort to explain where he gets the numbers from exactly. As an afterthought, the final conclusions of the paper seem not only highly tentative but pretty non-restrictive. If anything they seem to suggest that Li's 'hopeful monster' like scenario is possibly something of a strawman in terms of the evolution of multi residue feature, especially when there are mechanisms such as domain swapping for slotting in already evolved complex structural features. TTFN, WK |
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#23 |
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RBH, your clarification of copyright and fair usage is edifying. I will have to use the interlibrary loan system here to grab a copy from my alma mater - for personal use only.
Wounded King :notworthy :notworthy :notworthy -jim |
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#24 |
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The PDF for Behe and Snoke 2004 is available at
http://www.proteinscience.org/cgi/co.../ps.04802904v1 Caveat: �*I was able to download this by clicking on the Full Text (PDF) link on the journal's home page, which I got to (ironically) through one of the ID sites (Discovery I think). �*I typically go through the library to get subscription PDF's but I wasn't in this instance so I assume anybody can go there and get the PDF. �*There may be a slim chance that you have to access it through the ID site http://www.discovery.org/scripts/vie...%20-%20Science Enjoy. |
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#25 |
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#26 | |
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A little more for people:
Theory is as Theory Does by Ian F. Musgrave, Steve Reuland, and Reed A. Cartwright http://www.pandasthumb.org/pt-archives/000480.html [A critical review of this paper: Michael J. Behe and David W. Snoke (2004). "Simulating evolution by gene duplication of protein features that require multiple amino acid residues." Protein Science, Published online before print August 31, 2004. DOI: http://dx.doi.org/10.1110/ps.04802904 http://www.proteinscience.org/cgi/co.../ps.04802904v1 ] Musgrave et al.'s conclusion: Quote:
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#27 |
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Reviving a blast from the past, the other "ID" paper which came out around the time of Meyer's helpful contribution to systematics and taxonomy.
A paper has been published in 'Protein Science' which both critiques the Behe and Snoke's paper (2004), and discusses an alternative model based upon theirs in part but with some assumptions more in line with the current literature (Lynch, 2005) and which suggests that neo-functionalisation is considerably more likely than in the scenario proposed by Behe and Snoke. There is also a response by Behe and Snokes and an editorial. TTFN, WK |
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#28 | |
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Experimental studies contradict Lynch’s assumption of complete neutrality as a rule; the majority of amino acid substitutions decrease protein function.This would be news to me. Funnily, they do not provide a reference for this claim, although they do so elsewhere. ETA: I think this incident clearly shows the claim of an a priori bias against ID "research" to be a lie. |
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#29 |
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Out of idel curiosity, how does the paper show any sort of evidence of any kind for any signs of action by any type of intelligent designer?
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#30 | |
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It doesn't. That didn't stop the DI claiming that it did though. Beha and Snoke recognise this problem themselves.
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WK |
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