Then I agree with your hypothesis that a longer random sequence is more likely to find some of these structures.
Apologies, but I don’t fully grok the comment system here yet, and I seem to have fouled things up. Will fix it if I can?
DE: That would seem to be a reasonable prediction for evolved proteins, yes.
BC: You’re assuming your conclusion here.
DE: I don’t understand how you mean that. I think that interdependencies among proteins are not an unexpected product of evolution. Allow me to re-phrase: “I am (was “we are”) not surprised at interdependencies among proteins.”
DE: I’m a statistician not a biologist, but I’ve tinkered with genetic search algorithms, and I do not see how it would be possible to stop such interdependencies from forming if it favors fitness.
BC:Do the genetic search algorithms you worked with include a target sequence?
DE: That is not the setting where I applied GA. This was just a side project I did for fun, setting up a complex optimization problem with a simple fitness function and letting it fly.
DE: I am admittedly making a naive claim based on my limited experience with GA. BUT given what I know, if there exists the potential for protein dependencies, I am not surprised that genetic search is able to find them. GA is a very efficient search method (“big Oh” O[n*log(n)])!
DE: Depending on where we draw the line for “life”, I wouldn’t necessarily require cell division, only a sustainable process that reproduces itself.
BC: I am not sure how you can have a sustainable process that reproduces itself without cell division. Can you describe something here that is testable?
DE: At a minimum - A self-reproducing protein, perhaps a chain-molecule that lengthens itself with occasional errors, and periodically breaks into two pieces, both piece continuing the process.
DE: Now I’m going to hedge a bit, because that minimal molecule might not have all the qualities of life. Call it a pre-biotic molecule if you like. The essential quality is the ability to reproduce imperfectly, allowing natural selection to come into play.
DE: Can I test that? No, not personally. Dr. S has a better answer here.
Is that testable? As I understand, a molecule with such properties is an object of current research into abiogenesis.
If you can write one without a sequence target over 50 english letter characters you will be the first that I know of.
The evolutionary problem is that proteins are sequence dependent. From Szostak’s work the binding of ATP (the power molecule) requires 10^10 trials for a 70 Amino acid protein. How could a random process build a structure that required 13 proteins to bind together and produce a coordinated function?
He is cleaver but his solution requires life to exist already. The origin of life including the origin of proteins is a monster problem. First you assume matter exists then you need something that can sustain itself through reproduction and obtain energy on its own. The closest thing we can observe now to what is OOL is a bacteria. You need DNA that is organized to obtain around 500 proteins to have an energy consuming reproducing organism. To maintain these proteins you need to produce hundreds if not thousands of AA s per hour. After they are produced initially they can be recycled but again this requires proteins.
In order to do this you need enzymes that can produce the AA’s. You also need proteins for the process of turning DNA into proteins. The chickens and the eggs need to show up at the same time This is why I think the simple to complex model is broken. It started with complexity.
70 amino acids is a really small protein. I have to wonder what the chances would be for “regular” sized proteins.
By starting with two proteins that bind together and produce a coordinated function.
That’s not very close. All bacteria we have now are the product of 3.5 billion years of evolution. You might as well claim that the first human civilizations had build BMW’s in order to survive.
There was no target sequence in my application, only a function to optimize, which it did in some interesting ways. Likewise, if we consider a (hypothetical) function for evolutionary fitness, there is no target, only some interesting ways in which it might be optimized.
We are at risk of talk past each other - I think you missed the significance of the efficiency of genetic algorithms. “Big O of N times log(N)” is about as good as any search algorithm can do (see Burjorjee, 2015). Given a fitness function with the input of “50 english letter characters”, a GA should be able to reach a near optimal solution in ~K*200 generations, for some constant K. Given reasonable computing resources for the task that should not be too difficult. K in a practical application would depend on the actual function and parameters.
I don’t know enough about the Szostak example to try to frame that for a GA. Can you give me a reference?
OOL has not been the context of this discussion to this point. Please do not move the goalposts.
Burjorjee, K. M. (2015, January). Hypomixability elimination in evolutionary systems. In Proceedings of the 2015 ACM Conference on Foundations of Genetic Algorithms XIII (pp. 163-175). ACM.
How do we get those?
You are speculating. Show a simpler life form is possible. This is what the Venter lab is trying to do and they are claiming between 400 and 500 proteins required for a living organism.
I looked briefly at your reference and I would have to spend time with it. Apologize for moving the goal posts I mistakenly thought that was where you were going.
To simulate a protein search we need to estimate how many functional sequence exist inside the 50 letters. Lets call function a coherent sentence that we could recognize meaning from. For argument purposes lets assume one million or 10^6 sentences we could recognize. So your algorithm has to find one of these in about 28^46 search space to functional space ratio. Dawkins created a program to do this with a single target. Given the size of the search space this seems like a very difficult problem without a target.
That reference is very technical. I gave it to show that I wasn’t just making up this “Big O” stuff.
Now we are progressing into a discussion of fitness landscapes, which is more than I can attempt tonight, or maybe this week. I would need to review the topic myself, and you might do better to read about it on your own. I suggest we take a break for a few days, and consider starting a new topic so others might join in.
The answer to the problem you pose, however, depends on the smoothness of the fitness landscape. I’ll leave it at that.
I have had lots of discussions on this subject and it is part of the discussion in Hunts article. I am happy to discuss this when you are ready.
The same way we get proteins now. Transcription, translation, mutation, selection . . .
You are speculating that modern bacteria are the simplest life possible.
It is the only evidence we have at this point.
I don’t see how it can be evidence at all for how simple life can be. Bacteria are the product of 3.5 billion years of evolution which has continually added dependencies and contingencies into its systems. You might as well start pulling out parts from your car until it stops running and then proclaim that this is the simplest car possible. Doesn’t work that way.
Again you’re speculating without evidence. You’re thinking is also circular assuming bacteria evolved.
Not really. This is related to appearance of affirming the consequent in scientific thinking. Have you learned about this yet?
No, I’m not speculating.
I have not. Thank you for the citation.
Just citing a paper is not helpful. Please state your case and show how the paper supports your case.
It’s 29+ tests for common ancestry and evolution. I don’t see how you can say that evolution is speculation when it is trivially simple to use Google and find the evidence and scientific tests.
I think my claim was that evolution by random mutation was speculation. This paper does not support your claim. It supports common descent independent of mechanism. The weakness of this paper is that it highlights the similarities but does not give a detailed account of the differences.
That’s what the tests do, test for evolution by random mutation.
Please explain this. Why aren’t these tests for random mutations as the cause for differences between lineages?