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Author Topic:   molecular genetic proof against random mutation (1)
derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 220 of 274 (20498)
10-22-2002 11:48 AM


quote:
Originally posted by peter borger:
PB:
quote:----------------------------------------------------------------
Originally posted by peter borger:
The ZFX gene has about 20% neutral positions on third codon position. No variation in these position during 20 million years simply overturns molecular evolution. Today is just another bad day for evolutionism, I guess.
----------------------------------------------------------------------
SLP: So Peter B. thinks that evolution is overturned becasue about 80 nucleotides in 'neutral' positions did not exhibit substitution in 20 million years.
Of course, where is Borger's evidence that there were no back mutations?
MY RESPONSE:
If there were, it would only confirm non-random mutations. I don't mind non-random mutations. That is what I am telling you all the time.
Only if one were to employ your naive 'definition' of non-random. Why you keep ignoring the fact that you do not seem to understand what 'random' means in terms of genbetics is beyond me.
quote:
YOU SAY:
No, if there were an intergenic locus of 5kb that showed no change between species in 20 million years, I would be a bit suspicious. But nothing in 300+ bps? Chance alone can probably explain that...
I SAY:
Chance alone? Calculate a bit on it, please. Demonstrate the odds.
Mutation rate estimates are along the lines of 1 mutation per 10^9 bps per generation. At a 20 year generation time, that amounts to 1 million mutations in 20 million years. So any given site in a 3.2 billion bp genome has about a 0.03125% chance of 'suffering' a mutation in that time frame. That works out to less than 1 in 300 bases.
Very rough estimate and calculation, but it demonstrates my point.
How about you - lets see your calculations.
quote:
But....
That is about 0.0000025 % of the genome.
I guess we should ignore the fact that most of the remaining 99.9999975% doesn't show anything out of the ordinary (at least according to asthma guy creationist Borger).
"ASTMA GUY CREATIONIST BORGER" RESPONSE:
As a matter of fact within a species the major part of the DNA sequences do not change at all. So, in contrast to what evolutionism requires (change), DNA sequences are stable. Stability of DNA sequences is the rule, not the exception.
So I have to wonder why you have tried to make such a big deal out of this. It looks to me like you just contradicted your original hyperbole.

Replies to this message:
 Message 236 by Fred Williams, posted 10-31-2002 4:33 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 222 of 274 (20583)
10-23-2002 1:16 PM
Reply to: Message 221 by peter borger
10-22-2002 10:23 PM


quote:
Originally posted by peter borger:
You write:
quote:
----------------------------------------------------------------------
Originally posted by peter borger:
I didn't forget about this reference. I read it last weekend and the content of the article simply doesn't rebut my observation that the ZFX gene is completely stable during '20 million' years.
----------------------------------------------------------------------
I think I see the problem - Peter B - Do you know the difference between a gene and an exon?
It is an honest question. After all, a PhD-holding creationist once appeared on a discussion board, claiming that his doctorate was in microbiology and genetics, and launched into a diatribe about the human genome having 3 billion codons...
MY RESPONSE:
Dr Page I am always so impressed by your honest questions. (Does it implicate that your other questions are dishonest questions?)
You did not answer the question. The reader can draw his or her own conclusions. And hey - I liked that snide redirect....
quote:
I have the opinion --honestly-- that evolutionism is an outdated theory and I mentioned that several times.
Yes I know you have that opinion. You and every other creationist.
quote:
Why do I have this opinion? In my discussion over the last couple of years I discovered that most evolutionist do not know anything on contemporary biology besides their own field.
But YOU do, right? it is amazing at how well-rounded creationist scientists are. Why, not only are they 'experts' in their own fields, but they can speak with authority on nearly ANY field of science! It is amazing.
quote:
Contemporary biology demonstrates that the complexity of life is beyond any expectation and it is simply not known (remember aditinal DNA associated codes I mentioned before) or denied (common habit throughout this site).
Denied? Don't you mean exposed? Or perhaps refuted?
quote:
In looking for truth I discovered that evolutionism does not provide anything close to solutions except just-so stories.
Just-so stories? You mean like how all those articles demonstrating that directed mutations are artifacts of genome-wide hypermutation were claimed ot be evidence FOR directed mutations? Something like that?
quote:
Example, recently I looked into the origin of the invariable histons H3 and H4 (human, trout and chicken have exacly the same), ubuiquinon, TCR (T cell receptor) and ribunucleases since they seem to drop out of the sky and stay unchanged for 1.000.000.000 years or so. Explanation: birth-and-death-evolution, or another just-so story. (It used to be concerted evolution, but that vision has been abondoned recently).
Creationists like those 'anomalies'. After all, they PROVE evolution wrong... Right?
quote:
I don't believe these stories any more. I prefer creaton interactions with matter in a morphogenetic field, abbreviated: creation. It is not a better or worse explanation you provide me with in evolutionism. So, in my example of unchanged proteins it is B-a-D evolution versus Creation. I prefer creatons.
Of course you 'prefer' creations. That is what creationists do. They prefer to posit a miracle rather than try to find out a real answer.
quote:
Now, regarding your question whether I know the difference between exons and introns.
That was not my question. My question was do you know the difference between an exon and a gene. I asked that because you keep referring to the ZFX/ZFY as 'genes' when the papers you cite deal with only the sequence from one exon of around 300 bps - the exon that encodes the portion of the protein that is the binding site, i.e., the protion that is under great selective constraint. You apparently totally ignored the alignment I took the time to make for you, as the creationist is wont to do, as well as the other references provided (that you just blew off or twisted around).
quote:
I often wonder whether evolutionary biologist know about the difference, since the simply compare them to assess neutral evolution in genes. They have the tacit assumption that introns do not serve functions and are able to change over time with a neutral rate.
Now you are just blowing more smoke. Going off on a tangent of your own creation to try to prove some vacuous point. To claim that evolutionists think that introns serve no function is to display YOUR ignorance, not ours.[quote] So, my question to you do you know the difference/similarities between introns and exons?? [QUOTE] Yes I do. You did not answer my question, and you deigned not to respond to anything else you 'requested' of me before. Typical.
Do you get your information on what 'evolutionists' know from evolutionists, or creationists?
The answer to that question will clear several things up.

This message is a reply to:
 Message 221 by peter borger, posted 10-22-2002 10:23 PM peter borger has replied

Replies to this message:
 Message 223 by peter borger, posted 10-23-2002 7:57 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 224 of 274 (20722)
10-24-2002 3:08 PM
Reply to: Message 223 by peter borger
10-23-2002 7:57 PM


quote:
Originally posted by peter borger:
Dear Dr Page,
You wonder:
"Do you get your information on what 'evolutionists' know from evolutionists, or creationists?"
I say:
You should know by now that I am perfectly able to read scientific manuscripts and analyse the data by myself. I don't require either creationists or evolutionists opinions on science. Ever heard of objective unbiased data analysis?
Best wishes,
Peter

Well, I know how you analyze papers.
Oh - I wasn't aware that locus control regions had genes in them...
Citation please?

This message is a reply to:
 Message 223 by peter borger, posted 10-23-2002 7:57 PM peter borger has replied

Replies to this message:
 Message 225 by peter borger, posted 10-24-2002 9:23 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 229 of 274 (20941)
10-28-2002 10:47 AM
Reply to: Message 225 by peter borger
10-24-2002 9:23 PM


quote:
Originally posted by peter borger:
Dear Dr Page,
Often I have the feeling that I am waisting my time here on this board. If you for instance started to look up the papers I refer to, it certainly would improve our discussion.
Weeks and weeks ago I referred to a Nature paper on the gene in LCR16a region. You even commented on it, and now I have to inform you again on the same topic. But, for the purposes of discussion, you can find the reference in: Nature 2001, volume 413, pp514-519.
The paper is on the morpheus gene family and the authors conclude:
...some genes emerge and evolve very rapidly, generating copies that bear little similarity to their ancestral precursors. Consequently, a small fraction of human genes may not possess discernible orthologues within genomes of model organisms.
Random mutation and selection?
I don't think so, the odds are against it.
Best wishes,
Peter

Funny you should feel that way - YOU mentioned the LCR, THEn went on about a gene.
If YOU could keep your claims straight, then there would not be so much confusion.
I take it hten that you have conceded the point on the LCRs?
I will look at the Nature paper later.

This message is a reply to:
 Message 225 by peter borger, posted 10-24-2002 9:23 PM peter borger has not replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 235 of 274 (21186)
10-31-2002 11:54 AM
Reply to: Message 233 by peter borger
10-31-2002 5:28 AM


PB:
"But evidence is at close hands (see Dr Page's mailing: Cairns excerpt. I invite also Dr Page to rediscuss this topic since I discovered some 'strange stuff' in this mailing). "
No you didn't. You just used that laughable creationist interpretation to try to claim the opposite of what the evidence indicates.

This message is a reply to:
 Message 233 by peter borger, posted 10-31-2002 5:28 AM peter borger has replied

Replies to this message:
 Message 237 by peter borger, posted 10-31-2002 9:10 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 239 of 274 (21268)
11-01-2002 12:43 PM
Reply to: Message 237 by peter borger
10-31-2002 9:10 PM


quote:
Originally posted by peter borger:
dear Dr Page,
Is this an invitation to discuss the paper again?
Please let me know, and I will expose evolutionism as one big idee fix.
best wishes,
Peter

Yes it is.
Your overconfidene is noted.
Common psychological trait among the pseudocertain.
Ask Fred.

This message is a reply to:
 Message 237 by peter borger, posted 10-31-2002 9:10 PM peter borger has not replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 241 of 274 (21272)
11-01-2002 1:54 PM
Reply to: Message 236 by Fred Williams
10-31-2002 4:33 PM


Ahh yes, thew Lord of Delusion makes an appearance....
quote:
Originally posted by Fred Williams:
quote:
----------------------------------------------------------------------
YOU SAY:
No, if there were an intergenic locus of 5kb that showed no change between species in 20 million years, I would be a bit suspicious. But nothing in 300+ bps? Chance alone can probably explain that...
I SAY:
Chance alone? Calculate a bit on it, please. Demonstrate the odds.
----------------------------------------------------------------------
SLP: Mutation rate estimates are along the lines of 1 mutation per 10^9 bps per generation. At a 20 year generation time, that amounts to 1 million mutations in 20 million years. So any given site in a 3.2 billion bp genome has about a 0.03125% chance of 'suffering' a mutation in that time frame. That works out to less than 1 in 300 bases.
Very rough estimate and calculation, but it demonstrates my point.
----------------------------------------------------------------------
ROTFL! Very ROUGH indeed! This is bogus beyond words. First, it’s 1 million generations, not mutations.
The stupidity and eagerness of the creationist to 'prove their mettle' is beyond words.
The young earth creationist electrician apparently overlooked this:
"Very rough estimate and calculation, but it demonstrates my point. "
Very rough - I made a simple math error.
In a genome of ~3 billion bp, an error rate of 1 per billion per generation works out to 3 million mutations in 20 million years, not 1 million.
Williams the young earth creationist - who believes that 8000 Kinds on the ark hyperevolved to produce the extant diversity of today via magical evidence-free 'non-random mutations' - laughs at many things. I laugh at someone that actually thinks that the bible is literally true - indeed, I am still waiting for the evidence that leprosy can be ured by killing a couple of pigeons over running water and binding their wings with red thread...
quote:
Second, the rate you cite is way too low; your source must be either deleterious only, or rate/year, not generation. Estimates I’ve seen for *all* mutations (harmful through neutral through beneficial) runs at roughly 100 per diploid/generation, or 3 x 10^-8 bps/generation.
My source explains that the estimates are generalzed estimates that have been seen to be applicable to populations of mice as well as fruit flies (for example).
They go on to break it down to one mutation per gene in the germ line every 200,000 years.
Using that extrapolation, it works out to about 100 changes in 20 million years in the average gene.
The ZFX/ZFY genes are well over 1000 bp in length, not including introns. We can say that therefore, being generous, that about 1 in 10 bps should have 'changed' in 20 million years in this gene.
Of course, 1 in 10 is an average - it does not mean that, literally, every tenth site should have suffered a mutation.
But more importantly - and this is something that I should have picked up on before, Borger's original claim is bogus anyway.
It is the Ks value ("In contrast, the Ks value between human and hominoid primates for the ZFX gene was 0.008 for each comparison") - Ks being synonymous substitutions - that is the same, NOT the exact nucleotide sequence!
The species exhibiting identical nucleotide sequences for a partial exon in ZFX (~400 bp) did not infact diverge 20 million years ago. 18 million is a better value. In addition, looking at the last intron of both the ZFX and ZFY genes rveals a healthy amount of difference - 35/1229 between human and orang in ZFX, for example.
Tells me that the coding regions are under selective constraints.
****
And of course your sources are always right about everything. Like ReMine, for example. ReMine the creationist magician and engineer says that Haldane's model is beyond reproach and that 1667 fixed beneficial mutations is too many to account for human evolution so it MUST be true.
My source is "Molecular Cell Biology, 3rd Ed.,p. 242-3. Alberts et al. 1994.
My source goes on to say:
"...a single gene that encodes an average sized protein (containing about 10^3 coding base pairs) would suffer a mutation once in about 10^6 cell generations."
How does that bode for Borger's insistance that a particular 300+ bp exon, that is under selective constraint, within a gene must have accrued some mutation in that time span?
Funny how you don't address that.
11th Commandmant and all that, I suppose...
quote:
Finally, last and certainly not least, you assume a constant population size of 1 through that entire 20 million years! I didn’t realize we were asexual, and that there really was no Eve, ever. Just Adam, Adam Jr, Adam III, etc! ROTFL!
Yes, ROFTL!
Do you not assume a conststant population size when you hawk Haldane's dilemma?
Or is there some sort of double standard going on here?
Or is it some sort of scientific naievete being displayed by a creationist that is out to 'prove' his ancient religious text literally true?[/quote]
Granted this isn’t a straightforward computation. It’s an interesting problem. Here’s my rough estimate:
Let’s first try to calculate the number of organisms after 20 million years who should have a mutation at a specific neutral site. Assume 3x10^-8 bps/generation, and a population size of 1M. Also assume 20 year/generation. In 20 million years this is 1M generations. So, after 20 million years we will roughly have 3x10^-8 * 10^12 = 31,250 organisms with a mutation at a specific site. This is a rough estimate and will actually be lower because 1) duplicate hits are not accounted for, 2) it assumes the mutation is always inherited. Number 1 is negligible and can be ignored, number two however impacts the number by roughly 50% (due to mendelian genetics). So, that leaves 31,250/2 = 15,625. Out of a population of 1M, after 20 million years 1.6% have the mutation at a specific site.
Now we need to know what the odds are that 80 bps will avoid the mutation. This is given by:
P = 1 - [(100 — f)/100]^N, where f = frequency, N is number of attempts. In our example,
P = 1-[(100 — 1.6)/100]^80 = .725.
This means there is a 72.5% chance that at least one of the 80 neutral sites should have been mutated. Or, there is a 1 in 3.6 chance we would not see a mutation within the 80bp window.
For 300 sites, we get P = .992, or 99.2% chance, which means the odds are 1 in 125 we do not see a mutation within a 300bp window.
These odds obviously do not favor evolution, but they are also not near significant enough to declare the ZFX sequence anomaly a nail-in-the-coffin evidence against the theory. Still 1 in 125 chance IMO refutes your claim that chance alone can explain it. Maybe you got lucky, again. Evolution always gets lucky! LOL!
BTW, it does get really bad if the sequence were 5Kb. Better hope we don’t find one like that. The number becomes P = 9*10^-36![/quote]
Oh boy!
You are really on top of things, aren't you!
Off top class now - will comment on the rest later....

This message is a reply to:
 Message 236 by Fred Williams, posted 10-31-2002 4:33 PM Fred Williams has replied

Replies to this message:
 Message 244 by Fred Williams, posted 11-01-2002 7:12 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 248 of 274 (21515)
11-04-2002 9:53 AM
Reply to: Message 244 by Fred Williams
11-01-2002 7:12 PM


quote:
Originally posted by Fred Williams:
[B]
quote:
Very rough - I made a simple math error.
You made several errors, and they were huge. [/quote]
Right - I forgot that in addition ot being an expert on the bible, genetics, and of course Information Theory, you are also an expert in statistics.
quote:
You still don’t recognize one of them:
quote:
Fred: Finally, last and certainly not least, you assume a constant population size of 1 through that entire 20 million years! I didn’t realize we were asexual, and that there really was no Eve, ever. Just Adam, Adam Jr, Adam III, etc! ROTFL!
Yes, ROFTL!
Do you not assume a conststant population size when you hawk Haldane's dilemma?
Or is there some sort of double standard going on here?
Assuming a constant population is fine, ye ole dimbulb.
Please explain WHY assuming a constant population size in fine, creationist.
I am sorry, but an assertion form you is hardly worth banking on. You - and your , um, 'intellectual' mentors have a history of not being able to suppoort assertions.
quote:
What isn't fine is assuming a constant population size of ONE through the generations!
Who did that? Are you fogetting your Kimura? Oh, wait, you never knew your Kiumura - as per your much belated 'admission', you simply cribbed quotes from documented misquoter ReMine's silly book.
quote:
Adam begot Adam Jr, begot Adam III, begot Adam IV Somewhere along the line a female mutated from the male.
Adam? Who is Adam? What is the EVIDENCE that this 'Adam' existed?
quote:
But wait! We can’t do that, because Scott is assuming a population size of ONE throughout the generations! ROTFL indeed! Its not Adam & Eve, or Adam & Steve, its Adam and, well NOBODY!
Your stupidity is surpassed only by your ignorance-based overconfidence.
As one proclaiming his scientific knowledge as unassailabale, you should recall that according to the NT, neutral mutations can fix in a population regardless of its size at a rate equal to the mutation rate.
ROFTLMAO.
Indeed.
quote:
Williams the young earth creationist - who believes that 8000 Kinds on the ark hyperevolved to produce the extant diversity of today via magical evidence-free 'non-random mutations' - laughs at many things. I laugh at someone that actually thinks that the bible is literally true - indeed, I am still waiting for the evidence that leprosy can be ured by killing a couple of pigeons over running water and binding their wings with red thread...
First, there could easily have been 30K kinds or more.
Evidence?
quote:
Second, I never claimed non-random mutations were the only possible solution, and in fact have stated that I recently (within last 6 months) can see other mechanisms that can exmplain the rapid diversification in 5K years (in fact we see many examples in nature, such as Darwin’s finches).
True, but you claim they were a big part and yet cannot produce any actual evidence that these mutations even occur! There is a good reason that you yourself claimed to be a 'proselytizer' of that myth.
quote:
You ignore this though I’ve told it to you before. It is because you are the internet king of misrepresentation.
I don't recall you 'telling' me anything. We all know the creationiost tendency to cry 'misrepresentation!' at the drop of a hat.
This is called 'projection.' You do it all the time - even to your own words. You usually try to pawn off your errors on "the shortcomings of the medium" or some such ego-saving lie, but thats your style.
quote:
I also never said leprosy can be cured in the manner *you* prescribed.
Oh, so you DON'T believe the bible is "100%" accurate and error free... You heathen unbeliever!
Hope you don't eat shrimp, either....
quote:
It is the Ks value ("In contrast, the Ks value between human and hominoid primates for the ZFX gene was 0.008 for each comparison") - Ks being synonymous substitutions - that is the same, NOT the exact nucleotide sequence!
That is why I gave a number for 80 bps (and later one for 300 bps). I haven’t had time to check the papers or look up the sequence of these genes. I was just doing calculations on your’s and Peter’s claims.
Really? Where was your , um, refutation of Borger?
quote:
Even for 80 bps sequence, we would have expected to see some variation, but not to an extent that offers compelling evidence against evolution, as I stated. There still could also be something wrong with my analysis, particularly since I had to make some assumptions that may be flawed.
Imagine that...
Of course, being an expert in math and all, I assume that you realize that 'expectations' (probabilities) are not certainties, right?
And I hope that YOU know that an exon is not a gene.
Though I suspect you still link to Luke Randall's site.
You remember Luke Randall, right? The creationist microbiologist/geneticist that claimed that the human genome has 3 billion codons?

This message is a reply to:
 Message 244 by Fred Williams, posted 11-01-2002 7:12 PM Fred Williams has replied

Replies to this message:
 Message 250 by Fred Williams, posted 11-05-2002 6:46 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 253 of 274 (21679)
11-06-2002 8:31 AM
Reply to: Message 250 by Fred Williams
11-05-2002 6:46 PM


[QUOTE]Originally posted by Fred Williams:
[B][quote]You remember Luke Randall, right? The creationist microbiologist/geneticist that claimed that the human genome has 3 billion codons?[/b]
Yes, it's one of your favorite stored chestnuts you like to bring out every couple weeks or so.[/quote]
Every couple of weeks? that is a grotesque misrepresenations. Typical..
quote:
Hmm, I also remember a certain PhD biologist who admitted to not taking a SINGLE class in pop genetics, yet is now developing a class at his university called evolutionary biology, which according to books I have on the topic is mostly pop genetics!
What books DO you have? Lets see, I know you have "Biotic Message". B ut that is really about ReMine telling everyone how much smarter than everyone else he thinks he is... And of course "Not by Chance"... Also a creationist tome....
Did I leave any out?
Well, anyway, that is why the class is being developed. In fact, I have not even started it yet.
Of course, I will not present myself as an 'expert' in it, as I am not a pompous, pseudocertain simpleton that continues to ignore straightforward challenges and questions.
quote:
I hope this certain biologist now knows that SNP means single nucleotide polymorphism, and therefore cannot represent a fixed alelle (key word polymorphism).
I realized that a long time ago. That biologist, however, never went on month long tirades blabbering about how "informed creationists" know that I am right blah blah blah, only to months later claimn to have knowin it all along...
No - that was a certain non-biologist engineer creationist who laughably claims to be an "expert" in Information theory...
quote:
I also hope he now realizes that when a mutant allele reaches fixation in a population then it follows that the original wild-type is no longer present in the same population.
I always did. I also realized - and informed cretins also should - that a mutatnt dominant phenotype can be 'fixed' in a population before the genotype. Inbformed, intelligent cretins also realize that there is technically no such thing as an allele that is fixed in 100% of a population, as borne out by HGP data.
quote:
I also hope this certain biologist realizes that sound math above the hasbro-level is crucial to population genetics.
Shame that internet pseudogeniuses actually believe that off-the-cuff internet discussion board posts are representative of one's abilities. Well, actually, I guess they are representative of the creationsts abilities - observe how a certain creationist ignores questions relating DIRECTLY to many of his claims, abandons threads in which he is getting quashed, only to pop up in a new thread (which itself is sure to soon be abandoned)...
Yes, Fred, shame that creationits don't seem to realize that arguing fossils, genetics, anatomy, cosmology, etc. really taskes more than reading a few creationist books, an ancient religious text, and having an ego the size of Texass...
Just think of what even your fellow creationists must think of you...
Mr.Hyssop oil....
Mr.Banner of uncomfoprtable truths...
Moderator 3...

This message is a reply to:
 Message 250 by Fred Williams, posted 11-05-2002 6:46 PM Fred Williams has not replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 265 of 274 (22216)
11-11-2002 9:03 AM
Reply to: Message 255 by peter borger
11-06-2002 7:54 PM


quote:
Originally posted by peter borger:
Dear Buddika,
You write:
Comments on Borger's opening message:
Borger seems to indicate that he is a big fan of Lee Spetner, who is not a biologist or a geneticist, but a physicist, but Spetner's work is flawed:
http://home.wxs.nl/~gkorthof/kortho36.htm
MY RESPONSE:
I know Korthof's work. He writes book reviews related to evolutionism-creationism. I recommend you to read his discussion with Spetner. It can be found here:
http://home.wxs.nl/~gkorthof/kortho36a.htm
Best wishes,
Peter

Yes, I recommend reading that exchange too. Spetner comes off looking like a desperate, egomaniacal, backpeddaling, red herring-spewing, minutiae-monger...
No wonder Borger recommends it...

This message is a reply to:
 Message 255 by peter borger, posted 11-06-2002 7:54 PM peter borger has replied

Replies to this message:
 Message 267 by peter borger, posted 11-11-2002 6:02 PM derwood has replied

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 266 of 274 (22261)
11-11-2002 2:10 PM


quote:
Originally posted by Fred Williams:
Maybe Scott is ready to shatter the world with the example he implies he has in his hand. Let’s see if he plays the card, or keeps us all in suspense!
What example? Oh yes - an example of a gene duplication and subsequent mutation that conferred a benefit to the population.
The series of gene duplications in what we now call the beta globin gene cluster, a group of 5 genes and a pseudogene. Epsilon-globin, which is expressed in the embryo, has a higher affinity for oxygen than does the adult-expressed beta and delta globin, thereby making it easier for an embryo to gets its 'fair share' of oxygen. Epsilon arose via a duplication from other genes starting with proto-beta.
Healthy embryos make for healthy offspring, and healthy offspring are beneficial to the population.
What about an insertion that confers pesticide resistence?
A Single P450 Allele Associated with Insecticide Resistance in Drosophila
P. J. Daborn,1 J. L. Yen,1 M. R. Bogwitz,2 G. Le Goff,1 E. Feil,1 S. Jeffers,3 N. Tijet,4 T. Perry,2 D. Heckel,2 P. Batterham,2 R. Feyereisen,5 T. G. Wilson,3 R. H. ffrench-Constant1*
Science 297:2253-7.
Some interesting findings:
From the abstract:
"Transgenic analysis of Cyp6 1 shows that overtranscription
of this gene alone is both necessary and sufficient for resistance. Resistance and up-regulation in Drosophila populations are associated wit a single Cyp6 1 allele that has spread globally. The is allele is characterized by the insertion of an Accord transposable element into the 5' end of the Cyp6 1 gene."
From the paper:
"First, resistance to DDT was wide-spread, as expected, and second, resistance can persist in laboratory strains in the absence
of pesticide selection, which suggests that little or no fitness cost is associated with this mechanism."
"The observation that the nucleotide sequence around the first intron in Cyp6g1 (291 bp away from the site of the insertion) is identical in all the resistant alleles supports the concept of this global spread and suggests strong linkage disequilibrium or hitchhiking of nucleotide variation with the spread of DDT resistance."
I was especially interested in your Information Theory expertise on this, because: there is no change in the expressed protein, just more of it, and this confers an advantage. Is this 'new information'? If not, why not? If it is, how is so when the expressed protein has not changed?
The ref for how Gene duplication can result in altered phenotype is at the office, will post that later.
But I did come across this pertinent ref (pay attention Freddie and Borger), emphases mine:
*************************************************
Amplification-mutagenesis: evidence that "directed" adaptive mutation and general hypermutability result from growth with a selected gene amplification.
Proc Natl Acad Sci U S A 2002 Feb 19;99(4):2164-9
Hendrickson H, Slechta ES, Bergthorsson U, Andersson DI, Roth JR.
Department of Biology, University of Utah, Salt Lake City, UT 84112, USA.
When a particular lac mutant of Escherichia coli starves in the presence of lactose, nongrowing cells appear to direct mutations preferentially to sites that allow growth (adaptive mutation). This observation suggested that growth limitation stimulates mutability. Evidence is provided here that this behavior is actually caused by a standard Darwinian process in which natural selection acts in three sequential steps. First, growth limitation favors growth of a subpopulation with an amplification of the mutant lac gene; next, it favors cells with a lac(+) revertant allele within the amplified array. Finally, it favors loss of mutant copies until a stable haploid lac(+) revertant arises and overgrows the colony. By increasing the lac copy number, selection enhances the likelihood of reversion within each developing clone. This sequence of events appears to direct mutations to useful sites. General mutagenesis is a side-effect of growth with an amplification (SOS induction). The F' plasmid, which carries lac, contributes by stimulating gene duplication and amplification. Selective stress has no direct effect on mutation rate or target specificity, but acts to favor a succession of cell types with progressively improved growth on lactose. The sequence of events--amplification, mutation, segregation--may help to explain both the origins of some cancers and the evolution of new genes under selection.
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Looks like the ball is in William's court now.
Let the hand waving, insults, backpedalling, and story-telling begin!

derwood
Member (Idle past 1906 days)
Posts: 1457
Joined: 12-27-2001


Message 269 of 274 (22352)
11-12-2002 11:02 AM
Reply to: Message 267 by peter borger
11-11-2002 6:02 PM


quote:
Originally posted by peter borger:
Dear Dr Page,
You write:
Yes, I recommend reading that exchange too. Spetner comes off looking like a desperate, egomaniacal, backpeddaling, red herring-spewing, minutiae-monger...
No wonder Borger recommends it...
I say:
.........I am always so impressed by your 'scientific' replies and rebuttals.
Best wishes,
Peter

What was to rebut? You were engaging in hero-worship, I point out your delusions.
I have yet to see you post anything scientific, frankly - using scientific words, posting citations to the literature, etc. are not necessarily scientific, especially when one considers the degree of delusion inherent in your interpretations.

This message is a reply to:
 Message 267 by peter borger, posted 11-11-2002 6:02 PM peter borger has not replied

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