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GP on the Origin of Body Plans [OoBP] challenge

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. . . here (at 194) in his amazing engineering thread as he responds to Dionisio:

>>Dionisio:

Thank you for summarizing that interesting discussion.

I will summarize it even more.

1) Nobody knows how morphogenesis is controlled and guided.

2) Moran is no exception to that.

3) “Experts” are no exception to that.

4) However, according to Moran (and, unfortunately, he is probably quite right): “experts do not see a need to encode body plans and brain in our genome”

5) You and I, and probably some more sensible people, do see that need.

6) So, it seems, the problem is not about what we know, but about what we see as a need.

Now, I notice that Moran says:

“experts do not see a need to encode body plans and brain in our genome” (emphasis mine)

OK, that can mean two very different things:

a) Experts do not see a need to encode body plans and brain in our genome, but they think that body plans and the brain are encoded elsewhere

OR

b) Experts do not see a need to encode body plans and brain anywhere.

I will not ask Moran what he really meant, because I think it unlikely that he would respond. So, I can only guess.

I would say that he means b). Why? Because, if he means a), I could probably partially agree, and that is a rather unlikely situation, IMO.

Now, a) just means that the procedures are encoded elsewhere. That is probably true, at least in part. That “elsewhere can still mean two different things:

a1) At some epigenetic level, that we can imagine

a2) In some other way, that at present we cannot even imagine

Well, I believe that all of that is true. The procedures are encoded in the genome, both at the level of proteome (see my OP here, for that) and at the level of non coding DNA (Ouch! Moran will not like that). And they are also encoded at many epigenetic levels. And they are also encoded at other levels that at present we cannot imagine.

But there is one certainty, for me: they are encoded somewhere.

Because, you see, most neo darwinists would rather go with b): they really believe that those things are not encoded anywhere.

Now, while you and I certainly find that idea completely absurd, let’s try to understand what they think.

The best, and most honest, admission about that, in my memory, was made by Piotr, some time ago, in a discussion that was exactly about the procedures for cell (and tissue, and organ, and body) development. He said, if I remember well:

“I think it’s just the memory of what worked”.

OK, that’s a very honest statement of a neo darwinian perspective. But, as it is honest, it includes a precious little word: memory.

Now, you and I, having some love for informatics and programming, know all too well that “memory” is not a vague concept.

Memory of information must be stored to survive and be available. And that requires, in our human experience, some storage medium. Usually some physical (and often expensive) storage medium.

IOWs, no memory storage medium, no party.

So, I would like to ask Piotr (if he still reads this blog, that is unlikely), or Moran (if he likes to answer, that is unlikely), or anyone else:

Where and how are the procedure for cell (and tissue, and organ, and body) development stored?

Because, you see, they are certainly available in some way, otherwise how could the embryo of any organism generate the full body?

I suppose that the most likely argument of any neo darwinist, at this point, would be that those procedures must, after all, be very simple. A few HARs, a few hundred, at best a few thousand, nucleotides, and the deed is done.

Done? The human body plan? The human brain and nervous system? The whole immunology network? And so on, and so on?

You and I, having some love for informatics and programming, know all too well a very basic truth: very simple programs require some limited memory to be stored, but very complex programs require a lot of memory.

So, is the information for human brain really so simple? Is it like squeezing, say, Windows 10 in 1-2 KB at most?

OK, we know that the biological designer must be very good, but so good?

Ah, but I forgot: neo darwinian evolution can do practically anything: even miracles, provided we don’t call them miracles! >>

He goes on, in 201:

>>By the way, let’s comment some more on this interesting issue of development, always in the light of the results presented in this OP.

Vertebrates are considered as a subphylum of chordates: chordates with backbones.

So, in a sense, the basic body plan is set up in chordates, with the appearance of the notochord, and other features.

As we know, phyla correspond to basic body plans. But, strangely enough, they all appear very “suddenly”, during the so called “Cambrian explosion” (approximately 541 – 520 million years ago).

We know well all the debates about that amazing event. Of course, neo darwinist have tried their best to hypothesize that the explosion is not an explosion at all, and that the true information for all those new body plans was being “manufactured” more gradually during the previous times. And so on.

But the evidence of the fossils remains what it is, and I don’t think that our “polite dissenters” have succeeded in explaining away the “almost miracle” of the Cambrian events.

However, with vertebrates we are apparently observing an event slightly later than the Cambrian explosion itself. The emergence of a very important (for future developments) subphylum in the well established phylum of chordata.

That allows to localize better the emergence of the new information, to somewhat later than the Cambrian, but anyway well more than 400 million years ago.

Now, if we judge from the following natural history, it seems that the emergence of vertebrates was a very successful innovation: indeed, chordates not vertebrates are a rather small bunch of organisms today, while vertebrates are, in comparison, one of the main representative groups of animals, from many points of view, even if we don’t consider the side aspect that we, as humans, are part of it.

So, it is rather interesting to observe, according to the data presented in the OP, that the transition to vertebrates was a very exceptional “jump” from the point of view of some specific functional information in the proteome, certainly the biggest step we can observe in the accumulation of human conserved protein information. In that sense, it is a much bigger step than the simple appearance of the phylum chordata, with the appearence of more than twice human conserved information (3,708,977 bits vs 1,685,550, not corrected for redundancy).

If we want to make hypotheses about that interesting fact, we could probably reason that the new body plan of vertebrates includes at least two major innovations that will be very important in all the future natural history of that branch:

1) Cephalization, and in particular the gradual development of the brain, and therefore of all new functiona connected to that

2) Adaptive immunity, which appears for the first time in jawed vertebrates.

Both these innovations have a common denominator: they are linked to the appearance and development of two very complex regulatory systems, both aimed to a very complex and nuanced interaction with the outer environment.

IOWs, they are both, in different ways, complex systems that process information from the outer world.

That is an important concept, because it bears a fundamental implication:

If the bulk of the huge informational jump that appears in the vertebrate proteome is really linked to the premises for the development of the central nervous system and the brain and of the adaptive immune system, then it is perfectly reasonable to think that much of that new information must be strongly connected, as one can expect in any big and complex system that mainly processes information and reacts to it in very complex and nuanced modalities.

Another way to say it is that, in that huge informational jump, a great part of the total information can be expected to be irreducibly complex.>>

Sobering issues, well worth headlining and inviting further discussion. Let’s see if objectors to design thought have a good, cogent and plausible counter-case that is suitably empirically well-grounded in actual observations rather than ideologically loadesd reconstructions of the inherently unobservable remote past of origins. END

PS: I have been very busy RW.

Comments
Origenes @ 74 / Eric Anderson @ 75: I've spent some time rewriting/expanding interdependent code. In my experience it usually requires you to build parallel structures that simply imitate the original, which involves writing the code you want, then writing even more code to make it act exactly like what you have; then, once you have covered the whole of what you want to change, you can start removing the code that makes it act like what you had, locally, though you have to make sure to keep the neighboring adaptation code compatible with each local removal. Basically, a multi-staged, neutrally at best (though surely negatively with any practical expectation) selected process that requires complete, top-down knowledge of the code structure and function, with complexity growth being something more than linear. Of course, chasing after a modification that produces some desirable result is always a terrible idea that practically always leads to a circular route, most often of small radius but perhaps even more often as a singular point phenomenon. This is what Darwin thought ultimately built everything from germs to super computers, as well as any program ever written. I never tried such a process from the onset; but landing close to the solution after your careful plans prove insufficient, you sometimes flail and thrash about; and even then it doesn't ever get you there, and more often than not will carry you away and you can actually ruin your code if you don't get back to the drawing board. Start overs from backups aren't an option for critters whose ancestors aren't maintaining a benevolent stasis.LocalMinimum
April 3, 2017
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InVivoVeritas: Well, that's a rather big number! And I was so proud of my 1.7 million bits for the vertebrate proteome... :)gpuccio
April 3, 2017
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bill cole: "Could knowledge of the function of TE’s be the end of evolutionary theory as we know it?" That would be a very safe bet. But I am rather sure that neo darwinists will do their best to imagine new "solutions", "theories", fairy tales and so on... :)gpuccio
April 3, 2017
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The Origin of the Body Plans is a very interesting Challenge for materialists/naturalists and for ID skeptics. The topic Extremely Difficult Engineering Problems are Brilliantly Solved in Living Organisms presented on 25 February 2017 at AM-NAT BIOLOGY CONFERENCE - and soon to be available on youtube - touched this problem as a tangible, undeniable super-function of organisms: sexual reproduction, problem that cannot be resolved but only through exceptionally engineered elements: information, processes and procedures, i.e. through Super, Exceptional, Transcendental Intelligent Design. Below are two slides from that AM-NAT presentation that seem related to the topic of this blog. Problem: Construct a Body through cellular divisions Here are the empirical assumptions for this problem that is solved brilliantly by all organisms that replicate through sexual reproduction: * The body construction is driven and controlled by information * The information that controls the body development and construction is supplied in the fecundated female egg that develops in female body (placenta) until the baby is delivered Here are questions and challenges that are raised when considering how this body develops from the single fecundated female egg – one single cell: * What is the estimated amount of information needed to drive body construction through cellular division? * What is the nature and format of this information; how is this information coded and physically represented in the original cell and in the descendent cells? Is the body development process centrally controlled (let’s say from the original cell) or is a distributed process: i.e. are there many, control centers that develop during body growth through cellular division? * How is the information copied and distributed (if it happens) from the original cells to all or some of the descended cells? * We are going to consider and analyze each of the above question separately on the next slides Q: What is the estimated amount of information needed to drive body construction through cellular division?? We are going to consider this question for the human species. Here are some primary facts on which will base the computation for our estimate. * There is an estimate of 37*10^12 (10^12 means 10 power 12) cells in an adult human body * We are assuming that a human baby at the moment of delivery will have 37 times fewer cells, i.e. a count of 10^12 cells. * We calculated x = number of cellular divisions to reach from the single fecundated ovum cell to a count of 10^12 cells in the delivered baby by solving the equation below logarithmically: 2^x = 10^12 and found out that Number of Divisions ND is about: ND = x = 42 * The number of distinct cell types in the human body is estimated to be 200 .............. We do not show the Slides with computation of Information Estimate. We may add them later. But we show below the amount of Estimated Information in the Conclusion Slide for this computation: .............. Estimated amount of information -Conclusions We concluded that a conservative estrimate for the baby construction plan is an unimaginable huge number: INFO’ = 10 ^661,971,970,618 i.e. a 1 followed by over 600 billion zeroes. The literature estimate for the number of atoms in a cell is 10^14 atoms. Let’s assume that the actual number for a fecundated female ovum is one million times larger than that, i.e. 10^20 Still we cannot comprehend that the unimaginable large information for body construction plan quantified in INFO’ above can be contained, codified in the 10^20 atoms of the originating cell.InVivoVeritas
April 3, 2017
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gpuccio @66: Can the informational jumps for PAX-6 and SATB2 be considered combined as a requirement for the transition that you described? Are there more protein information jumps that could be considered in combination with PAX-6 and SATB2?Dionisio
April 3, 2017
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Origines @74: Meyer:
This generates a dilemma: major changes are not viable; viable changes are not major.
Welcome to real-world engineering. This is always true for complex functional systems. Only in fantasy-world Darwinian thought does the evolutionary paradigm stand a chance.Eric Anderson
April 3, 2017
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Bob O’H, Stephen Meyer on the ideas of evo-devo advocates such as Sean B. Carroll (the author of ‘Endless Forms Most Beautiful’, 2006) and Jeffrey Schwartz:
Despite the enthusiasm surrounding the field, evo-devo fails, and for an obvious reason: its main proposal, that early-acting developmental mutations can cause stably heritable, large-scale changes in animal body plans, contradicts the results of one hundred years of mutagenesis experiments.13 As we saw in Chapter 13, the experiments of scientists such as Nüsslein-Volhard and Wieschaus have shown definitively that early-acting body-plan mutations invariably generate embryonic lethals—dead animals incapable of further evolution. The results of these experiments have generated the dilemma for evolutionary biologists that geneticist John McDonald aptly described as the “great Darwinian paradox.” Recall that McDonald noted that early-acting regulatory mutations do not produce viable alterations in form that will persist in populations, as evolution absolutely requires. Instead, these mutations are eliminated immediately by natural selection because of their invariably destructive consequences. On the other hand, later-acting mutations can generate viable changes in the features of animals, but these changes do not affect global animal architectures. This generates a dilemma: major changes are not viable; viable changes are not major. In neither case do the kinds of mutation that actually occur produce viable major changes of the kind necessary to build new body plans. [Stephen Meyer, ‘Darwin’s Doubt’, Ch. 16]
Origenes
April 3, 2017
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GP
I believe that the growth of non coding DNA (especially TEs) in mammals and humans has a meaning. I don’t believe that it is only a passive effect of the accumulation of “errors”.
I agree, this is a very likely prediction :-) If we have an ancestor shared with the puffer fish millions of years ago why would our lineage start to accumulate useless junk in our genome? Could knowledge of the function of TE's be the end of evolutionary theory as we know it?bill cole
April 3, 2017
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bill cole: At present, we don't understand how body plans are really controlled. Until we do, reasonings like Moran's are really arbitrary and pointless. I do believe TEs have an important role in information development (I have many times expressed the idea that transposons are optimal tools for design), and probably in cell development. But we really don't know, yet. I believe that the growth of non coding DNA (especially TEs) in mammals and humans has a meaning. I don't believe that it is only a passive effect of the accumulation of "errors". But the field is still open. Let's see what happens.gpuccio
April 3, 2017
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Eric Anderson: "I presume you mean the latter, but just wanted to confirm" I presume too, probably mainly epigenetic states transmitted through the egg's cytoplasm (and, of course, also the epigenetic state of the egg's nucleus).gpuccio
April 3, 2017
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Origenes Here is Dr Morans answer.
Which do you think is more likely? Here’s a hint. The pufferfish genome is only about 12% of the size of our genome but pufferfish have bodies and brains. Clearly, they don’t need a lot of extra DNA to make their bodies. Humans don’t need it either.
Human body plans appear to be more complex than pufferfish. The difference appears to be TE"s. Are TE's critical to the mammal lineage? If so, then Larry's argument is incorrect. Thoughts?bill cole
April 3, 2017
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Bob O'H @45: Bob, can you comment on this further:
. . . the mother provides some of the information for development to occur correctly.
When you say the mother provides "information" are you talking about information in the autosomal DNA, information in the X chromosome, information in the mitochondrial DNA, or information located elsewhere in the egg cell? I presume you mean the latter, but just wanted to confirm. Thanks, -----
As with most of biology, it’s more complicated than we’d wish.
Yes, it is absolutely more complicated than the fanciful stories about mutations resulting in this or that outcome, or claims of "plasticity" or general assertions of "change over time," or naive ideas that once gene products exist in the cell they just come together in the right way by virtue of chemistry and physics. This is why scientists with simplistic notions keep getting surprised. On the other hand, if we approach biology from an engineering standpoint, we can anticipate a lot of the complexity. To be sure, we are noobs at this type of engineering and will still be surprised at the complexity, but there is a great deal of coordinated complexity and engineering that can be foreseen if we are willing to look for it.Eric Anderson
April 3, 2017
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rvb8 @22 and @27: Great literature bluff. Coupled with this kind of attitude:
No! If you can’t, or won’t read it I can’t and won’t make you. But these two parts are full of links you can and, no doubt with the curiosity inherrant in ID folk, will ignore.
C'mon, rvb8, we've asked over and over again. Just a paragraph or two, in your own words, describing the key points. You are the one claiming you have found an explanation. Well, let's hear it. Otherwise, don't bother throwing at the wall the results of your quick Google/Wikipedia search to find something to that kinda, sorta, has a title that might, perhaps, be relevant to the fundamental questions on the table.Eric Anderson
April 3, 2017
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Origenes @6: Thanks for reminding us about that laughable assertion that 340 mutations could turn an ape-like creature into a human being. ----- And anyone who thinks an organism will self-assemble once the various DNA gene products are produced (because they influence each other and so forth) is both unaware of the chemistry involved and incredibly naive about systems engineering.Eric Anderson
April 3, 2017
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Dionisio: PAX 6 is a Master Regulator, specially involved in the embrional development of the eye and the brain. Here is a recent paper about its role: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706819/ It interacts with lots of proteins. I have rapidly checked just a few: some are strongly engineered in the vertebrate transition, other not specially. Just anecdotically, I mention here one that is particularly extreme: DNA-binding protein SATB2 (Q9UPW6) From UNIPROT: "Binds to DNA, at nuclear matrix- or scaffold-associated regions. Thought to recognize the sugar-phosphate structure of double-stranded DNA. Transcription factor controlling nuclear gene expression, by binding to matrix attachment regions (MARs) of DNA and inducing a local chromatin-loop remodeling. Acts as a docking site for several chromatin remodeling enzymes and also by recruiting corepressors (HDACs) or coactivators (HATs) directly to promoters and enhancers. Required for the initiation of the upper-layer neurons (UL1) specific genetic program and for the inactivation of deep-layer neurons (DL) and UL2 specific genes, probably by modulating BCL11B expression. Repressor of Ctip2 and regulatory determinant of corticocortical connections in the developing cerebral cortex. May play an important role in palate formation. Acts as a molecular node in a transcriptional network regulating skeletal development and osteoblast differentiation." Length: 733 AAs This protein practically "appears" in cartilaginous fish: Cnidaria: 0.0893588 Cephalopoda: 0.1251023 Deuterostomia (not vertebrates): 0.1705321 (jump here) Cartilaginous fish: 1.568895 Bony fish: 1.450205 Amphibia: 1.754434 Crocodylia: 1.869031 Marsupialia: 2.024557 Afrotheria: 2.050477 Jump in cartilaginous fish: 1.398363 baa However, the behaviour of specific groups of proteins will be the theme of a next OP. :)gpuccio
April 3, 2017
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Bob O’H: … a major theme of Endless Forms Most Beautiful, and indeed the evo-devo revolution, is that a lot of evolution in development is due to changes in the control of gene expression (i.e. epigenetics is involved, in one form or another).
Yes, it’s undeniable, and the ‘beyond genes’ aspect of epigenetics constitutes a tremendous problem for neo-darwinism and/or neutral theory. Of course Larry Moran wants none of it:
Moran: We're only going to cover epigenetics for a few minutes in today's class because there aren't any serious arguments in favor of changing our view of evolution because of epigenetics. However, we are going to spend a lot more time learning that evo-devo is just as stupid because there are some seriously misled developmental biologists who think that discoveries in their field change how we should view evolution. :-)
- - - - - - //
Bob O’H: I can’t comment on what Larry Moran meant (partly because I’m too lazy to try to find the original quote) …
Here you can find the original quote.Origenes
April 3, 2017
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gpuccio: I officially add myself to the folks that have encouraged you to gather all this research work you have done and compile it into a book. I would like to ask you for an autograph on my copy before other buyers start lining up for the book signing session at the bookstore! That would give me another valid excuse to travel to Italy! Can the eBooks be autographed by the authors? :)Dionisio
April 3, 2017
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gpuccio: Does pax-6 work alone or in conjunction with another protein? Did the other protein also experience any jump around the same timeframe? Are there other cases of proteins that could be analyzed in conjunction?Dionisio
April 3, 2017
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gpuccio: @61: I have not been able to keep up with all this research information avalanche. The whole thing is getting overwhelming with every new discovery. I'm told to start wrapping up the research part so I can move on to the next phase of the project, but I'm dragging my feet unable to resist the temptation to look at what is next. It's like watching those TV serials with adventures for kids and waiting for the next episode.Dionisio
April 3, 2017
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Dionisio: By the way, Circular RNAs are really interesting. And fashionable, I believe! :) Another tier of information that emerges from non coding DNA (I have really stopped counting).gpuccio
April 3, 2017
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Dionisio: "This seems to be the “cuore” of this topic, right?" Yes. It's an old concept of mine. In the proteome, I believe that a lot of functional information is underestimated, because it is less conserved throughout evolutionary history: but the reason why it is less conserved is that it is "branch specific", or "organism specific". IOWs, "taxonomically restricted". Therefore, very functional. I think that there are ways to clearly show that. My reasoning about PAX 6 here is an example. A similar reasoning is applied in this older OP, which was not very popular at the time, probably because it is rather technical: https://uncommondescent.com/intelligent-design/information-jumps-again-some-more-facts-and-thoughts-about-prickle-1-and-taxonomically-restricted-genes/ Of course, I do believe that a relevant part of protein sequences that are not conserved are not functional, or at least not essential to the function. Neutral variation does act on protein sequences, and we know that well. The problem is that, while for sequences that are always conserved we can easily assume function, for sequences that change two possibilities remain: non relevant function (and therefore neutral variation) or function that changes. There is no immediate way to distinguish the two, but I believe that reasonable comparisons and analyses, such as the ones I have proposed, can really help.gpuccio
April 3, 2017
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Dionisio: "Wow! I see your point. Had you read about this observation somewhere else before? Are you the first to point at this?" Maybe. As far as I know...gpuccio
April 3, 2017
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Dionisio: "The term “Human Conserved Information (HCI)” seems key in this and your previous OP that triggered this one. Did you coin that term?" I suppose so. And then, out of mere laziness, the acronym. :) However, the term derives immediately from the methodology I have used in the analysis.gpuccio
April 3, 2017
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gpuccio @47:
[...] probably because it is functionally tweaked to different final functions.
This seems to be the "cuore" of this topic, right? I think you've hit the target right in its center. Don't expect any objection to your clear reasoning on this. By now the politely-dissenting interlocutors are running for the doors. :)Dionisio
April 3, 2017
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gpuccio @47:
These two parts of the molecule (not corresponding to recognizable domains), when compared to the human protein, are almost completely different in Drosophila (and, in general, in pre-vertebrates), while they are almost identical already in Cartilaginous fish, and so they remain, almost unchanged, throughout the following natural evolutionary history (more than 400 million years). So, not only a big jump, but a very specific, targeted jump.
Wow! I see your point. Had you read about this observation somewhere else before? Are you the first to point at this?Dionisio
April 3, 2017
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gpuccio @47:
[...] the homology found in Drosophila (or, say, in all protostomia and non vertebrate dueterostomia) is strictly confined to two well defined regions of the sequence: 1) The Paired Box domain (AAs 4 – 128) 2) The Homeobox domain (AAs 211 – 266)
Hmm... Very interesting...Dionisio
April 3, 2017
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gpuccio: The term "Human Conserved Information (HCI)" seems key in this and your previous OP that triggered this one. Did you coin that term?Dionisio
April 3, 2017
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gpuccio @47: While looking at your post, saw this quote from Wikipedia:
The field is characterised by some key concepts, which took biologists by surprise.
Still don't quite understand why they are surprised so often? :) Still reading through your insightful comment. Thanks.Dionisio
April 3, 2017
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KF and GP: Sorry for bringing up this off-topic info, but I thought you would like to see it too:
Circular RNAs (circRNAs) comprise a family of noncoding RNAs (ncRNAs) that have drawn intense interest in the last few years. Although they were first discovered in 1979 by electron microscopy, they were thought to be byproducts of splicing and did not receive much attention due to their low abundance and lack of known functions.
Emerging roles and context of circular RNAs. Panda AC, Grammatikakis I, Munk R, Gorospe M, Abdelmohsen K. Wiley Interdiscip Rev RNA. 8(2). doi: 10.1002/wrna.1386.
Dionisio
April 3, 2017
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Bob O'H: Of course, one can always read more and better. However, what I meant, and in the rush did not express well, is that IMO many new regulatory functions will be found in the bulk of non coding DNA, that part that almost all still consider junk. I was giving for granted the parts that we already know of, enhancers, miRNAs, lncRNAs for which funtions have already been described, and so on. That said, I am still interested in your opinion about my OP about engineering in the vertebrate proteome, and about my notes here regarding TFs and PAX 6 in particular. If you find the time, of course.gpuccio
April 3, 2017
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