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Author Topic:   Evolution Requires Reduction in Genetic Diversity
Faith 
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Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 478 of 1034 (758009)
05-18-2015 2:12 PM
Reply to: Message 470 by RAZD
05-17-2015 6:52 PM


Re: RAZD pt 3 Pelycodus
So let's try to break it down verbally.
The bottom horizontal line represents a population (Pelycodus ralstoni) with variations in the size of individuals in the population, and the predominant size is represented by the thicker section of the line.
So this is all about the size of the creature.
The original chart gives what sound like the names of locations on the left margin. Were these fossils found scattered in many locations, or in roughly the same geographical area or even in a column one layer above another? Or do the names designate the layers themselves. And does it matter how many fossils were found in each layer?
I'm going to have to comment as I go if only because I interpret this sort of thing differently than you do. so I can't just let evolutionist interpretations stand.
Other lines represent populations of the same species at later times, as they are embedded in layers above the bottom layer, the higher they are the younger they are.
OK, but that of course is evolutionist theory. A simple description of the phenomena would be something like: "Such and such number of this fossil were found in such and such layer at such and such geographical area. This layer is usually dated to such and such MYA. The many collections of these fossils found in various layers appear to differ in average size from one layer to the next. The measured sizes are such and such." And the dates each was found could be handy, as well as who found them etc.Instead of simple description we get theory. Why is that?
The ages are relativistic based on the geological layers and the law of superposition.
No problem with superposition of course, tells the order they were buried in which might have something to do with their size though it might not; but geological time is always problematic.
Each of the fossil lines overlap the lines of the layer below and the layer above and thus they show continuity of the species from one line to the next.
Again this is of course evolutionist theory. If they were simply buried all at once in a one-time catastrophe the only continuity would be that they are clearly the same species that got sorted into different burial locations for one reason or another. Did anyone differentiate between adult and young individuals or male and female?
The variable in question is size. What we see is that size in each population differs in distribution from one layer to the next, and this would be due to the alleles that govern body size.
It could. Since four subspecies/races are noted the sizes could reflect the range of genetic diversity for size in each population, which I think is what you have in mind. But again I'd like to know if the size could be related to age or sex and if that was taken into account.
There is an overall general trend from the original smaller fossils to larger fossils as you rise from the bottom layer to Pelycodus trigonodus, about half-way up the chart, and at this point all the fossils at this level are larger than all the fossils of the bottom original population layer. This is shown by the vertical line marked by the 1's in the diagram.
OK, I'm getting that now, thanks to your writing it out more clearly this time.
This trend continues through Pelycodus jarrovii, about 3/4ths up the chart and up to the red line. At this point the population divides, with one population continuing the trend to larger fossils up to the top of the chart with N.venticolis.
The vertical line marked with the 2's shows that these top larger fossils are all larger than the Pelycodus trigonodus population, which are all larger than the original population at the bottom. None of the Pelycodus trigonodus population are the same size as either the top or the bottom, so the size of the fossils in N.venticolis are twice removed from the size of the original population.
But the population at the red line splits and forms two populations with different sizes:
the ones to the right keep the larger fossils size and the trend to larger fossils in higher\newer layers
the other population takes the small size from the red line and reverses the trend, and instead trends to smaller fossil sizes in the higher\newer layers.
Line 3 is a vertical line from the left end of Pelycodus jarrovii, and following it down we see that all the original base population were smaller than the smallest fossil at the Pelycodus jarrovii level -- so all of those alleles should be lost to the species at this point according to your hypothesis.
But as we follow the line up we see the second population trending smaller crosses this line and continues to get smaller up to N.nunienus, when all of the fossils are to the left of line 3 ... when alleles for these sizes should not be available anymore, having been lost. In fact ~half of N.nunienus are the same size as Pelycodus ralstoni.
First, of course I dispute the whole evolutionist interpretation that says the populations genetically diverged from each other over time as represented by the layers, which I guess would make P. ralstoni the ancestral population. My interpretation is that they are certainly all related and may be different subpopulations but that they would have been contemporaneous with each other, probably inhabiting different locations. If some are subpopulations of others there is no reason to think they lived in different time periods anyway, or that the higher in the strata are necessarily the offspring of the lower: it could be the other way around.
But for the sake of argument, accepting the evolutionist interpretation that the higher descended from the lower over time, and that size was the main variable from population to population, while there should always be a trend to loss of genetic diversity as a new subpopulation develops its new gene frequencies, there's no way to know, especially from fossils, whether the alleles for the other trait completely disappeared from the new population. If they still exist in the collective genome, further population splits could select those alleles, and two separate populations branching off could select alleles for each end of the spectrum, which would be reflected in the size differences between the two groups at the top. Or those two populations could reflect incompletely inbred genes, since the first stage of the expression of new gene frequencies is likely to bring out a motley collection of traits, possibly including the extremes, which would work through the population through many recombinations over time until a general phenotype emerges.
So there would have been a reduction in genetic diversity if these really were subpopulations formed over time, but complete loss of alleles for different traits doesn't necessarily always occur. It's a TREND I'm trying to highlight, that only becomes expressed in complete genetic depletion at the end of a series of subpopuloations.
I don't think that is what happened though because of course I don't accept the whole evolutionist interpretation that these fossils represent different populations that formed at separate times from the one lower in the strata.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 480 of 1034 (758019)
05-18-2015 3:28 PM
Reply to: Message 476 by Admin
05-18-2015 7:04 AM


Re: No 'new functions'
The Lenski E. coli example addresses your main point (that evolution is driven by reductions in genetic diversity) more directly than any other.
All bacteria have to do to adapt is generate one mutation that is then copied many times and becomes the characteristic of a new population. It's pretty specialized at that point though, having lost all its other genetic information, which doesn't sound like it's even particularly a good thing for bacteria. I'm sure this is way too simplistic but I'll have to come back to it later if it's too far out of the ballpark.
In sexually reproducing creatures a mutation has to occur in the right place at the right time with the right characteristics even to get passed on, and then you'll only have this one mutation that can only affect the phenotype if it's dominant; if it's recessive it has to continue to get passed on until it pairs up with another copy of itself in order to be expressed in the phenotype. I don't think there is really any valid comparison with bacteria and in fact I think even if beneficial mutations did occur the chances of their contributing anything to the organism is pretty iffy. Again I'm sure this is way too simplistic but I'll have to come back to it some other time.
I believe junk DNA is genes that died over the millennia as a result of the Fall,...
...
The only thing I suggest is that genes died as a result of all those people and animals dying in the Flood,...
Your hypothesis contains an apparent contradiction, since first you state that genes dying are a long term result of the Fall, but then you state it was a result of the Flood.
OK, I'll spell it out. Death started at the Fall, and all the disease processes, but we can tell from the fact that people normally lived hundreds of years up until the Flood that there was still a great deal of vitality in the genome of human beings; and most likely animals too since they were also taken onto the ark in very small numbers, from which all species since then descended, showing enormous genetic diversity and vitality compared to now.
But the Flood was a one-time catastrophic death of human beings and animals both. a massive fulfillment of the effects of the Fall which would have wiped out not only the creatures but their genetic information.
But my main concern is that you understand that your main responsibility is providing evidence for your hypothesis. For example, people will reasonably expect that evidence will be forthcoming for genes dying around 6500 years ago (the Fall) and 4700 years ago (the Flood).
But I barely have the hypothesis worked out and where is the evidence going to come from? I can offer reasoning to support the hypothesis but how on earth could I prove it beyond that, especially since genetic studies are always interpreted through evolutionist theory. Emphasis on "interpreted" because it really isn't any more evidence for evolution than for Flood theory, it's mainly a difference in interpretation.
I think the fact that it's a reasonable interpretation of junk DNA that fits the known facts ought to be treated as evidence.
So where is the evidence for the evolutionist interpretation of the fossil record? It's all interpretation of facts that are open to other interpretations. RAZD just spelled out the typical evolutionist interpretation of different populations of species being found in separate layers, treating it as known fact. It's not, the Flood offers a whole other interpretive system. Other "evidence" includes nested hierarchies. But this is based completely on subjective assessment of similarity of traits. Similarity of traits can bei\ interpreted as design factors; there's no actual evidence for descent, it's simply assumed. I've also offered a whole other interpretative system for new traits emerging from microevolution: Darwin and followers explain it as environmental pressures or natural selection changing the organism to accommodate to the envifronment. You find this even in discussions of speciation where simple random migration with subsequent change in gene frequencies is taken seriously. But actual natural selection is really quite rare. Pocket mice and peppered moths come to mind. But Darwin's Galapagos turtles that look different from their mainland progenitors don't fit the natural selection model; they fit the migration model which brings out new traits simply through the new gene frequencies in the Galapagos population. Same with Darwin's finch beaks. Migration is enough to explain these variations through simple change in gene frequencies too, and natural selection would be enormously costly since all the "wrong" or unfitted beaks \for a particular food would have to be eliminated from the population; but when the new beak is there first the finch simply finds the food it's suited for.
Then a couple years ago on another thread there was the example of the surprisingly rapid evolution of a lizard that was isolated on an island in Croatia, that was found after thirty years of isolation to have developed a very large head that fitted it to a different diet from its ancestral population. In a mere thirty years did the food bring about the change in the head size? More likely didn't the head size emerge as a result of the new gene frequencies caused by the smaller numbers of individuals inbreeding for thirty years, and then finding new food that it could now handle? There is no more EVIDENCE for the random gene frequencies theory than the evolutionist natural selection theory, except the time factor and common sense. And then there was the example of the Jutland cattle that developed four completely different subpopulations in a very short period of time, not time enough for natural selection to change them, besides which it was supposedly genetic drift and no change in the environment that made the difference anyway.
There's no EVIDENCE for natural selection in these cases, but there is again reason or common sense that supports the random genetic change theory over natural selection. In other words you are asking me for a kind of evidence that isn't even available for evolution. Almost any particular offering of evidence for evolution can be interpreted from a completely different but just as reasonable a point of view, and more reasonable in many cases.
And they'll expect that evidence will be forthcoming for how a mass die-off by drowning can affect genomes.
Well I've thought about this and have the beginnings of a reasoned argument, but not hard evidence if you insist on that.
Genomes are "specialized" to use Denisova's term, for the trait combinations of the subpopulations they govern. If a trait is governed by ten different genes then the different combinations of the alleles for those genes will determine differences between races or breeds; and if there are many alleles for those genes as well, which is still in question, the combinations can vary almost astronomically. So the people and animals on the ark would have carried their own particular combinations of genetic material and that's what would have survived to generate all further subspecies from then on. They would not have had junk DNA except perhaps a tiny percentage reflecting death since the Fall, but as these few humans and animals started reproducing after the Flood, some of the limited availability of alleles would start pairing up and becoming fixed loci and some of those would eventually find nothing to pair up with and the gene would die, and the dead gene would continue to be passed on and that's the source of junk DNA. Again I'm being terrifically simplistic and I'll have to work on it more. I've been clearer on this at least to myself.
All I meant in my message is that you must understand that issuing hypotheses is accompanied by an obligation to support those hypotheses with facts. A statement that they're consistent with what is already known is not evidence, plus in this case that must remain an open question (at a minimum) since the evidence from ancient DNA contradicts your claims.
Based on bogus dates but yes. So if you want to demand evidence of a kind I can't produce and a coherent statement of an alternative hypothesis and different system of interpretations isn't enough I'll have to leave.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 482 of 1034 (758023)
05-18-2015 3:49 PM
Reply to: Message 481 by herebedragons
05-18-2015 3:31 PM


Re: Moderator Introduced Definitions
"Junk DNA" was a very unfortunate term coined in the early days of genetic sequencing when it was thought that DNA --> Protein was the major player. It is now known that it is not anywhere near that simplistic. We now suspect that the majority of "non-coding" sequences actually have a function. Even spacer DNA that is 1000's of bases long serves an important function even though they don't "do" anything other than keep two segments seperated. The term "junk DNA" really needs to completely fall out of usage.
All based on "suspecting" that it has a function you want to throw out a concept that makes good sense in the Flood theory.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 485 of 1034 (758031)
05-18-2015 7:51 PM
Reply to: Message 483 by Dr Jack
05-18-2015 6:20 PM


Re: Moderator Introduced Definitions
.
There are bits and pieces of signal among the noise but the majority of it has no function at all. The differential rates of mutation between Junk DNA and coding DNA across evolutionary time should be sufficient to convince you of that.
And what are those differential rates of mutation?

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 486 of 1034 (758032)
05-18-2015 7:53 PM
Reply to: Message 481 by herebedragons
05-18-2015 3:31 PM


Re: Moderator Introduced Definitions
I suspect that most evolutionary change is due to regulatory changes rather than changes in protein coding sequences. Changes in proteins probably come after the gene regulation has been altered.
I didn't know what you meant by this at first; now I gather it's another way of talking about junk DNA. Right? All those "regions" that affect diversity but don't code for proteins are what is usually called Junk DNA, right? Leaving that 2% you said do code for proteins.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 487 of 1034 (758034)
05-18-2015 7:58 PM
Reply to: Message 484 by Denisova
05-18-2015 7:16 PM


Re: Moderator Introduced Definitions
But the number of genes cannot drop that much. Because all individuals in questions are of the same species. Species do not vary genetically much. Max. 1, 2 or 3% genetic diversity. Otherwise you would get a different species!
So in your view what are all those dead genes in the genomes of so many species? 95% or more. If you said in your post, I didn't get it.
I'm intending to get to all your neglected posts next.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 488 of 1034 (758035)
05-18-2015 8:09 PM
Reply to: Message 416 by Denisova
05-14-2015 12:21 PM


Re: Replaced from other thread to here
OK, yes, that is what I meant. I think the original genome could have had more genes per trait, meaning five or six where now there are three or four. Yes I believe there has been a great loss of genes and genetic diversithy in human AND ANIMAL genomes since Adam and Eve, but more since the huge bottleneck of the Flood that wiped out most living creatures, which I suggest is most likely the source of junk DNA. And more genes per trait is one way the earlier genome was probably fuller than it is now.
Very well then, so may I have the empirical evidence for it?
Where in the scientific literature can we find evidence for the claim that the original genomes had more genetic diversity than today?
No, because the scientific literature is in thrall to the evolutionist paradigm and assumes the opposite. Assumes I say, it is not evidenced, it's an interpretation imposed on all the data.
So, that leaves only this part of your contention intact:
....and also observations about both mutations and the loss of genetic diversity in evolutionary processes.
Yes, that's exactly what I asked for.
Now, where may we find those observations in the genetic literature?
I picked it up here and there from internet sites. I'm sure you can find it without my help.
And you will not find this answer by explaining how skin colour in extant humans (of whom we know the genome) is related to 4 genes.
We do not have the gene sequence of Adam and Eve.
But we DO have the gene sequence of Homo Neanderthalis, Homo Denisovia and Homo Heidelbergensis. And the genome sequence of many specimens of archaic Homo sapiens as well.
Or we may retrieve information from DNA of old human remains and compare them to modern human DNA. Or just look for genetic evidence in the extant human genome by smart comparison.
It's all there.
In that case you really need to spell it all out here.
I just realized there wasn't much point in answering this post. Well, on to the next one.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 489 of 1034 (758037)
05-18-2015 8:41 PM
Reply to: Message 417 by Denisova
05-14-2015 12:25 PM


Re: Replaced from other thread to here
I am still awaiting your response on the points I made:
1. there is no overall loss in genetic diversity, it's only parcelled out in two isolated genomes - the evolutionary requirement for initial gain in genetic diversity is met.
Assertion without evidence. Don't demand evidence of me if you aren't giving any of your own.
However, being "parceled out in two isolated genomes" doesn't provide a gain at all, where do you get that? The two together retain the original genetic diversity though, at least until the new gene frequencies have been worked through them. But my contention is that EACH new subpopulation is where we see the reduction in genetic diversity-- the alleles remain in the other population. The idea is that these populations are actively evolving because of their new gene frequencies and that's where reduced genetic diversity occurs.
2. the fact that after the split into two genetically isolated genomes, both of those sub-genomes take away only a subset of the original, total genome DOES NOT detract ANYTHING of the simple fact that there was an initial gain in genetic diversity BEFORE the split, which is what evolution theory ACTUALLY requires.
You have yet to show this actually happens, and there is certainly no reason why it should happen. What could possibly bring about this "initial gain? Mutations see the split coming and jump on the bandwagon?
3. evolution theory DOES NOT require each of the subset genomes AFTER the split to retain all the initial genetic diversity at the moment of the split. As a matter of fact, evolution theory predicts those two sub-genomes to be SPECIALISED due to different environmental conditions. And specialization implies the reinforcement of some traits, mostly at the expense of other ones. If you think otherwise, show me the papers by evolutionists who say so. So your rendition of evolution theory on this is flawed.
This actually sounds like what I'm saying happens, in different words, so I don't "think otherwise." I THINK I know what you mean by "specialized" but I could be wrong. In my system it wouldn't apply to the subpopulations at the split but after a period of inbreeding in which the new gene frequencies get worked through the whole population. That changes combinations sometimes drastically enough all by itself to prevent the reintroduction of gene flow between the two populations.
|
However, I haven't found discussions anywhere of how genetic diversity is lost in these splits so if you know where to find them please provide links. But I see by your next point that I must be misreading you anyway.
5. In other words, the evolutionary requirement for a gain in genetic diversity has been met.
By what where? You haven't said one thing to show where this would come from, you just keep saying it.
A POSSIBLE loss of genetic diversity in any of the sub-genomes AFTER the split is NOT an evolutionary requirement.
It depends on the numbers that form the new subpopulations whether there will be an apparent loss in genetic diversity or not, though that will always be the trend; but one thing there won't be is an increase. I guess you think you are dealing with this by insisting on it as a done deal before the split occurs but again there's no reason to think this occurs and you haven't offered any.
MORE THAN THAT, it is the thing for evolution theory TO EXPLAIN ("speciation", which is a split into two genetically isolated sub-genomes). Hence, it is the CONSEQUENCE of the evolutionary processes as conceived. And you CAN'T take the consequence of a process as its own requirement.
So you keep saying but in this case you have to have reduced genetic diversity, which is, yes, also a consequence of splitting the populations, in order to get the new traits brought about by the new gene frequencies. You can't have new traits without this trend to reduction, though it doesn't have to be a big reduction at first; so it IS a requirement as well as a consequence.
The OBJECT of evolution theory is to explain speciation. When speciation occurs, there MUST be an initial gain in genetic diversity.
Nope. Speciation is really only the formation of a subpopulation that has lost its ability to interbreed with the former population. This requires no increase and must very often result from the decrease which soon renders it a genetic mismatch with the former population. Are "new species" tested for genetic diversity? I didn't think so. At the end of a series of subspecies one that speciates must have lost so much diversity there's little left for any further formation of subpopulations.
>>>This requirement has been met<<<.
Again, I ask, by what? How?
There also MIGHT be a SUBSEQUENT loss in genetic diversity in any of the diverted sub-genomes AFTER THE SPLIT but that's a CONSEQUENCE of and the THING TO BE EXPLAINED by evolution theory.
I hope you acknowledge that you cannot take THE THING TO BE EXPLAINED as a REQUIREMENT for a scientific theory. That would be circular reasoning.
See above.
6. MOREOVER, I EVEN hardly doubt any of the resulting sub-genomes after the split ACTUALLY to have smaller genetic diversity than the original overall genome before the split, as I tried to explain in the elaborated example in my post #163.
Perhaps I missed it. Will check.
ABE: You did not write post 163 on this thread. /abe
None of these points but #1. were addressed by you.
Hope they now are.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 490 of 1034 (758038)
05-18-2015 8:49 PM
Reply to: Message 430 by Denisova
05-15-2015 3:59 AM


Re: genetic diversity
All you are doing in this post is saying I haven't addressed your posts. I just addressed two so if that isn't enough you'll have to provide links to any others that exist.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 491 of 1034 (758039)
05-18-2015 9:03 PM
Reply to: Message 473 by PaulK
05-18-2015 2:00 AM


Pseudogenes
PaulK writes:
. How do genes "die" ? They certainly can't be "killed" just by a bottleneck. How does this hypothesis explain the quantity of junk DNA ? What evidence is there that all junk DNA is "dead" genes ?
The Wikipedia article on Pseudogenes describes very well what I have in mind except for the parts about how it may have a function, which I doubt:
Pseudogenes are dysfunctional relatives of genes that have lost their protein-coding ability or are otherwise no longer expressed in the cell.[1] Pseudogenes often result from the accumulation of multiple mutations within a gene whose product is not required for the survival of the organism. ...
Because pseudogenes are generally thought of as the last stop for genomic material that is to be removed from the genome,[5] they are often labeled as junk DNA. We can define a pseudogene operationally as a fragment of nucleotide sequence that resembles a known protein's domains but with stop codons or frameshifts mid-domain. Nonetheless, pseudogenes contain fascinating biological and evolutionary histories within their sequences. This is due to a pseudogene's shared ancestry with a functional gene:...
And here it goes into evolutionist interpretations I don't share. But otherwise the description and analysis are very much what I have in mind.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 495 of 1034 (758043)
05-18-2015 9:50 PM
Reply to: Message 494 by Taq
05-18-2015 9:40 PM


Re: Pseudogenes
What you would need to explain is why psuedogenes share sequence homology with functional genes in other species.
Most creatures have similar design features, one creature happens to lose a gene to junk DNA that remains alive in another.
And here it goes into evolutionist interpretations I don't share.
What evidence do you have that would refute that interpretation?
Same evidence evolution has for its interpretation: None, or really, same facts, different interpretation. It's an interpretation.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 497 of 1034 (758045)
05-18-2015 9:55 PM
Reply to: Message 493 by Taq
05-18-2015 9:37 PM


Re: Moderator Introduced Definitions
This makes sense overall.
These mutations will be selected against.
Is there evidence for this? It just sounds like another unevidenced evolutionist assumption.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 499 of 1034 (758050)
05-18-2015 10:14 PM
Reply to: Message 496 by Taq
05-18-2015 9:54 PM


Re: Pseudogenes
Most creatures share design features in common, one creature happens to lose a gene to junk DNA that remains alive in another.
If that function were important, then the loss of that gene would reduce the fitness of that individual.
Well, I assume that any loss of a gene to junk DNA reduces the individual's fitness. I suppose most such losses aren't particularly important, since there are so many of them and we go on surviving. Like having a dysfunctional appendix. Some losses are surely important though, and the accumulated total loss definitely must have reduced the fitness of all species that possess so much junk DNA, but since we can't imagine a really fit healthy state it's hard to measure the loss.
Those with the mutation that knocked out the gene would be outcompeted by individuals with the functional allele.
Depends on what the allele is for. It may be for something that seems quite minor in the overall range of traits so its loss wouldn't make much difference, especially if other traits are possessed that are lost to others, which should also be the case. We notice people's different strengths and weaknesses anyway as just expressions of individuality.
This would eliminate the pseudogene from the population.
It would have to be positively lethal for that to happen, wouldn't it?
It would seem to me that pseudogenes occur when there is a lack of negative selection against mutations in a gene, meaning that the function isn't needed in that gene.
I'm sure that's what the ToE would suggest, but while living things seem to do OK without all those genes in junk DNA, the way we seem to do OK without a functioning appendix and without a gall bladder and tonsils too since they are easily dispensed with, my guess would be that we'd be a lot healthier and stronger if they were still functioning.
Same evidence evolution has for its interpretation: None, or really, same facts, different interpretation. It's an interpretation.
How does your interpretation match up better with the evidence than the evolutionary interpretation?
I think it makes more sense to assume nature wouldn't allow for so much death and disease in the normal course of things as the ToE takes for granted, so it has to be a degeneration from a formerly healthy state, but as I said there's really no actual evidence to put one interpretation above the other.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 496 by Taq, posted 05-18-2015 9:54 PM Taq has not replied

  
Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 519 of 1034 (758119)
05-19-2015 7:33 PM
Reply to: Message 506 by Denisova
05-19-2015 7:21 AM


Pseudogenes caused by bottleneck
But the number of genes cannot drop that much. Because all individuals in questions are of the same species. Species do not vary genetically much. Max. 1, 2 or 3% genetic diversity. Otherwise you would get a different species!
So in your view what are all those dead genes in the genomes of so many species? 95% or more. If you said in your post, I didn't get it.
In the first place your answer does no relate to the point I made. I was not talking about junk DNA in that particular point. I was saying that in a population bottleneck it is impossible for the number of genes to drop dramatically.
Then let me try to clarify. I don't mean to be saying that the genes became junk DNA IN the bottleneck but as a result of it due to the loss of so many alleles for so many traits. This should have an effect on the genome over the generations afterward, not immediately. It's basically the same as my general argument in this thread. Severe bottlenecks today operate similarly except that they start from less genetic diversity. The bottlenecked population's genes aren't changed, it's only as they inbreed for a few generations that the loss of alleles becomes apparent and we find many fixed loci developing for lack of alternative alleles. This is the case for instance with the cheetah and with the elephant seal. Then in the formation of breeds and small subpopulations in the wild which we've been discussing, the reduced genetic diversity should also trend to an increase in fixed loci due to its loss of alleles that remain in the larger general population. In the case of domestic breeding the more fixed loci the more "pure" the breed. Even a reduction in alleles without a total loss would trend in this direction, and the fewest would eventually drop out of the population altogether.
Apparently you wanted me to answer your comment, but it wasn't a question so I wouldn't have known that. Since you seemed to be saying that most junk DNA isn't really nonfunctioning genes I wanted to know what you think it is. I think I know now so it's no longer a question.
Now let's examine what happens when the vast majority of a population gets extinct by such an alleged event like the Flood. You imply that the great majority of the genes are silenced or just passed away along with their owners, leaving only the small subpopulation of Noah and his crew with their subset of genes and alleles.
Such an extinction event will delete many alleles from the original, common genome, without any doubt. They will be GONE because all the unfortunate ones that died throughout the flood took those alleles with them to their inundated graves.
That means that there will be NO REMNANTS of THOSE alleles in the genomes of Noah and his crew. Noah can't just take away with him the alleles of OTHER persons who just died. Not even in the junk parts of his genome.
All true.
Now what about the genes themselves?
Are there genes within individuals who belong to the very same species that may not exist in other members of that species? Without any doubt they will. But not much I think. Because too much of non-shared genes will imply interspecies rather than intraspecies differences.
I'm not sure what point you are making here. I'm not expecting any difference in numbers of genes between individuals in a population. I have in mind that if enough alleles are lost in such a huge bottleneck then the genes themselves would eventually be compromised as well, but not immediately.
When, as you imply, most of the original genes are silenced by an extinction event, it must be those ones that disappeared along with their deceased owners. In that case, again, Noah and his crew just can't "take over" those genes. When their owners died due to the Flood, those genes will be lost for eternity.
Apparently I haven't been clear. I don't expect the effect on Noah's family to be immediate but something that would occur among his descendants in the following generations due to the reduction in genetic diversity, i.e., the great loss of alleles for many traits. Noah and his descendants would have all the same genes but those genes would have fewer alleles (still haven't worked out the question of new alleles forming or how many would have been in the reproducing pairs on the ark, the three human pairs.) Many genes would eventually be reduced to fixed loci and come to characterize the subpopulations that migrated to different parts of the planet.
I did have in mind that simply the existence of many fixed loci could result eventually in the loss of function of many of those genes, but right now I'm thinking there is no real reason why that would be so: destructive mutations would have to occur for that to happen, and destructive mutations should have been on the rise after the Flood too.
In other words, junk DNA in extant humans CANNOT be explained by extinction events by definition and sheer logic.
Not if you're thinking it would occur immediately, but down the generations as I've explained above it could, and especially, as I now think, if mutations are involved.
[From Wikipedia: "Pseudogenes often result from the accumulation of multiple mutations within a gene whose product is not required for the survival of the organism."]
Moreover, when MOST of the genes ("95% junk DNA") are lost, the original human genome must have comprised thousands of genes more than today. BECAUSE all these genes originally were in the individuals that were killed during the Flood, there must have been an ENORMOUS genetic divergence between the unhappy mortals that died and the surviving Noah crew. I don't think that ANY definition of a biological species can be compatible with such an ENORMOUS genetic diversity within just the very same species.
It is enormous, for sure, but it does seem to be what happened. To my mind it speaks to the far more enormous original genetic diversity all species had. The loss is incalculable, but here we are. If some junk DNA isn't just disabled genes it would be much less of an effect but the vast majority do seem to be formerly functioning genes.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 506 by Denisova, posted 05-19-2015 7:21 AM Denisova has replied

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 520 of 1034 (758137)
05-20-2015 5:50 AM
Reply to: Message 506 by Denisova
05-19-2015 7:21 AM


genes lost in bottleneck?
Taking another look at this. I think I really don't get what you're trying to say.
But the number of genes cannot drop that much. Because all individuals in questions are of the same species. Species do not vary genetically much. Max. 1, 2 or 3% genetic diversity. Otherwise you would get a different species!
So in your view what are all those dead genes in the genomes of so many species? 95% or more. If you said in your post, I didn't get it.
The reason I asked about junk DNA was that you seem to be implying that junk DNA can't have many nonfunctioning genes because there's only a few percent genetic diversity in a species anyway. I really don't know what you are saying and I should have asked. More than that and you'd "get a different species?" This really makes no sense.
In the first place your answer does no relate to the point I made. I was not talking about junk DNA in that particular point. I was saying that in a population bottleneck it is impossible for the number of genes to drop dramatically.
This too is hard to decipher. I didn't say genes dropped at all in the bottleneck. So again the only relevance is my claim that junk DNA was a result of the Flood, but that didn't happen immediately so that's why I answered as I did above. Loss of genes to junk DNA would have happened due to new combinations that lead to fixed loci through generations, and mutations that wipe out those alleles.
I think the rest of my post addresses the topic.

This message is a reply to:
 Message 506 by Denisova, posted 05-19-2015 7:21 AM Denisova has replied

Replies to this message:
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