This is very interesting. I think some terms have been conflated or misunderstood. ID implies only the necessity of an intelligent designer, not how he acts. It could be by guided evolution, special creation, or a combination of unguided evolution, guided evolution, and special creation. Mix and match.
Swamidass has a point. He sees the signal in the genome for common descent as incontrovertible. Examples of de novo genes or incongruent gene trees or the extremely rare distribution of proteins in sequence space donāt matter. They would merely be acts of intervention against a background of common descent in Joshās view. Correct, @Josh? Even functional information translates to guided evolution on a background of common descent. Is there a point when the intervention outweighs common descent?
I donāt know how many of those potential interventions you would actually grant, but it appears to me that agreement on common descent is fundamental to you.
Weāve covered this here: Would God's Guidance Be DNA-Detectable?. Given what we know of population genetics, a priori we do not expect it would be detectable, even if we allowed every selectable mutation to have been inspired by God.
In principle, I agree with you. However, in practice, the immense amount of effort invested in arguing against common descent speaks something different with DIās actions.
You basically have it it right, though I wouldnāt say āincontrovertable.ā Remember, I have also made the case for a de novo Adam. Rather, Iād say it is very clear that God made us in a way that we looks like we share common ancestry with the great apes.
Given the evidence, the only viable argument against CD have to engage with theology. Not finding any contradiction between CD and Scripture, even if see teaching of a de novo Adam, there are no theological grounds for rejecting common descent. It looks like we share common descent with the apes, because we in fact did. Of course, Iām open to hearing other arguments, and I am happy to legitimize people taking different views, as long as they donāt justify themselves with anti-scientific arguments.
As for scientific evidence alone? The evidence, at most, could suggest Godās involvement. However, as I explained, we do not expect this would be detectable a prior. God could have been clear in the evidence. Imagine a world where humans-chimps had very different genomes, and archaic humans (e.g. Neanderthals) did not exist. Such a would would very much trouble or even disprove an evolutionary interpretation. That, however, is not the world we find. Instead, we see gobs of evidence that suggest common descent that need not exist unless we really did share ancestry with the apes.
That, in my view, is part of why the Genealogical Adam is so important. It makes space for the traditional account in the evolutionary story. It takes back ground that was lot. That should change the calculus for everyone.
I didnāt participate in that discussion, but I didnāt find it particularly convincing. Are you speaking of detecting guided point mutations? No, of course that canāt be detected. Even rearrangements or insertions and deletions canāt be individually identified as the result of design. But what about de novo genes? If it can be shown that non-coding DNA really doesnāt make functional protein without guidance, and that the probability of developing a promoter is exceedingly small, that would imply something unusual is responsible for all these de novo genes we are finding. And in that case we would have specific DNA changes to point to.
In the human genome, can you show any evidence of de novo genes that do not also have homology to non-coding DNA? @T.j_Runyon recently pointed to a paper on this, showing that the āde novoā genes in humans have such homology. Also, these genes are skewed to smaller proteins, consistent with random drift anyways.
I can grant if we found a large number of de novo genes that did not have an obvious mechanism, it would be suggestive. However, keep in mind that deletion in the great ape lineages will produce the appearance of a de novo gene, so that has to be ruled out too.
Though, keep in mind, we do not actually see de novo genes arises out of nothing. They all seem to arise out of homologues in non-coding DNA.
That being said, we agree here.
Iām just saying there does not appear to be any evidence that anything else was needed to produce the human genome from our common ancestor with the great apes. If you can show me evidence, that might be interesting. However, as I said, de novo genes in humans have homology to non-coding regions in apes. They are not really āde novo,ā in that critical sense. If one or two have no homology, that could be explained by gaps in the ape genomes, by deletions in the ape genomes, or possibly a rare horizontal transfer. There are not, however, many genes at all that this applies too.
It could have been another way. There could have been 100s or 1000s of de novo genes in the human genome, with no homologues in ape sequences. This would have been very clear evidence of something outside normal processes. This, however, is not what we find in our genomes.
@swamidass
I never said they had to arise out of nothing. In fact, what I said was, āIf it can be shown that non-coding DNA really doesnāt make functional protein without guidanceā, implying that de novo genes can come from non-coding DNA. It is the extreme unlikelihood of that that is in question.
Gosh, I never restricted it to humans and apes. The strongest evidence is in other taxa.
Not if you follow the evidence, which pretty much rules out special creation of any species. So we are left with guided and/or unquided evolution, period.
Now Joshuaās scenario is a special case, in which a couple of individuals of a previously existing, evolved species are specially created. That would be undetectable. But an entire specially created species would be undetectable only if god were being intentionally deceptive.
No, itās an inevitable inference from the idea of special creation thatās indistinguishable from common descent. Thereās no other credible motive than deception.
That is just the Texas Sharpshooter fallacy. What you need to do first is determine how many such adaptations are possible before you determine what is probable or improbable. This means finding all beneficial changes that are possible in any genome with respect to epistatis.
The other assumption is that such an adaptation is improbable. In order to make such a claim you have to know how many adaptations that require 4 specific mutations are possible. If there are billions and billions of such adaptations that are possible then such adaptations can easily occur through random changes to the genome.
It would appear that no ID researcher has determined how likely it is that beneficial proteins can emerge from non-coding DNA, so why is the ID community pushing orphan genes as a problem for evolution? Why is it even being brought up?
Not true. Bill Bessemer and John Sanford wrote a paper that could be applied here as it addresses the high probability of DNA breaking down with random change given the real ratio of deleterious mutations vs beneficial ones. This paper was discussed at TSZ.
If this the Mendelās Accountant stuff then it was refuted a long time ago. Sanfordās work predicted that species with short generations times, like rabbits and mice, should have gone extinct after just a few centuries.