The astonishing language written on microtubules, amazing evidence of design

The astonishing language written on microtubules, amazing evidence of design

Argument from cell communication
Proof of the signals in the neurons

  1. A reflex signal from a bump on your knee needs to go in the direction of the controlling muscle and on to the brain, not any which way. What directs the placement of “one way” signs in nerve cells? According to a press release from the University of Georgia, it’s the enzyme MEC-17.
  2. The MEC-17, which they studied in roundworms, zebrafish and human cancer cells, is responsible for placing the traffic signs, called acetylation marks, on the cellular highways made of microtubules. The paths with lots of these marks are on the sending end, and the paths with few of them are on the receiving end. When the marks are not set properly, bad things happen: zebrafish develop neuromuscular defects, and humans are subject to debilitating neural diseases like Parkinson’s, Alzheimer’s and Huntington’s. This discovery may lead to new treatment strategies by enhancing or inhibiting the action of MEC-17.
  3. By noticing that MEC-17 works identically in animals as diverse as roundworms, fish and humans, the researchers deduced that “this microtubule acetylation process using MEC-17 is an evolutionarily conserved function.” Conserved means un-evolved.
  4. The following important question however the researchers did not answer:
    a. What controls MEC-17, and what would happen to the living beings without having this enzyme fully developed from the beginning.
    b. If this enzyme puts up the signs, who is the foreman?
  5. We don’t control anything within our bodies. Many different processes happen without our knowledge.
  6. If we are not in control of the processes in our bodies than who was the designer of those processes?
  7. The infinite regress question is: who is the designer of the designer? However, the hierarchy of design must eventually stop at a Designer who is omniscient and omnipotent and that is God. Aristotle already taught us in his “on the motion of animals” about the Unmoved Mover; No mouse can climb a hill of grain, since it has no basis.
  8. Hence God exists.

Following information is truly mind boggling. Take your time to read all through, and check the links. The creator of life has left a wealth of evidence for his existence in creation. A treasure grove to evidence intelligent design is every living cell. Its widely known that DNA is a advanced information storage device, encoding complex specified information to make proteins and directing many highly complex processes in the cell. What is less known, is that there are several other code systems as well, namely the histone binding code, transcription factor binding code, the splicing code, and the RNA secondary structure code. And there is another astonishing code system, called the tubuline code, which is being unravelled in recent scientific research. It is known so far that amongst other things, it directs and signals Kinesin and Myosin motor proteins precisely where and when to disengage from nanomolecular superhighways and deliver their cargo.

Recent research helds that this code in a amazing manner even stores our memories in the brain and makes them available on the long therm.

For cells to function properly, they must organize themselves and interact mechanically with each other and with their environment. They have to be correctly shaped, physically robust, and properly structured internally. Many have to change their shape and move from place to place. All cells have to be able to rearrange their internal components as they grow, divide, and adapt to changing circumstances. These spatial and mechanical functions depend on a remarkable system of filaments called the cytoskeleton. The cytoskeleton’s varied functions depend on the behavior of three families of protein filaments—actin filaments, microtubules, and intermediate filaments. Microtubules are very important in a number of cellular processes. They are involved in maintaining the structure of the cell and provide a platform for intracellular macromolecular assemblies through dynein and kinesin motors. They are also involved in chromosome separation (mitosis and meiosis), and are the major constituents of mitotic spindles, which are used to pull apart eukaryotic chromosomes. Mitotic cell division is the most fundamental task of all living cells. Cells have intricate and tightly regulated machinery to ensure that mitosis occurs with appropriate frequency and high fidelity. If someone wants to explain the origin of eukaryotic cells, the arise of mitosis and its mechanism and involved cell organelles and proteins must be elucidated. The centrosome plays a crucial role : it functions as the major microtubule-organizing center and plays a vital role in guiding chromosome segregation during mitosis. In the centrosome, two centrioles reside at right angles to each other, connected at one end by fibers.
These architecturally perfect structures are essential in many animal cells and plants (though not in flowering plants or fungi, or in prokaryotes). They help organize the centrosomes, whose spindles of microtubules during cell division reach out to the lined-up chromosomes and pull them into the daughter cells.

α- and β-tubulin heterodimers are the structural subunits of microtubules. The structure is divided in the amino-terminal domain containing the nucleotide-binding region, an intermediate domain containing the Taxol-binding site, and the carboxy-terminal domain, which probably constitutes the binding surface for motor proteins. Unless all 3 functional domais were fully functional right from the beginning, tubulins would have no useful function. There would be no reason for the Taxol-binding site to be without motor proteins existing. Dynamic instability, the stochastic switching between growth and shrinkage, is essential for microtubule function.

Microtubule dynamics inside the cell are governed by a variety of proteins that bind tubulin dimers or microtubules. Proteins that bind to microtubules are collectively called microtubule-associated proteins, or MAPs.The MAP family includes large proteins like MAP-1A, MAP-1B, MAP-1C, MAP-2, and MAP-4 and smaller components like tau and MAP-2C.

This is highly relevant. Microtubules depend on microtubule-associated proteins for proper function. Interdependence is a hallmark of intelligent design, and strong evidence that both, microtubules, and MAP’s had to emerge together, at the same time, since one depends on the other for proper function. But more than that. Microtubules are essential to form the cytoskeleton, which is essential for cell shape and structure. In a few words, No MAP’s, no proper function of microtubules. No microtubules, no proper function of the cytoskeleton. No cytoskeleton, no proper functioning cell. Evidence is very strong, that all these elements had to arise together at once. Kinesin and Dynein belong to MAP proteins. Kinesin-13 proteins contribute to microtubule depolymerizing activity to the centrosome and centromere during mitosis. These activities have been shown to be essential for spindle morphogenesis and chromosome segregation. A step-wise evolutionary emergence of eukaryotic cells is not feasable since several parts of the call can only work if interacting together in a interlocked fully developed system.

When incorporated into microtubules, tubulin accumulates a number of post-translational modifications, many of which are unique to these proteins. These modifications include detyrosination, acetylation, polyglutamylation, polyglycylation,phosphorylation, ubiquitination, sumoylation, and palmitoylation. The α- and β-tubulin heterodimer undergoes multiple post-translational modifications (PTMs). The modified tubulin subunits are non-uniformly distributed along microtubules. Analogous to the model of the ‘histone code’ on chromatin, diverse PTMs are proposed to form a biochemical ‘tubulin code’ that can be ‘read’ by factors that interact with microtubules .

This is a relevant and amazing fact , and raises the question of how the " tubulin code " beside the several other codes in the cell emerged. In my view, once more this shows that intelligence was required to create these amazing biomolecular structures; formation of coded information has always shown to be able only to be produced by intelligent minds. What good would the tubulin code be for, if no specific goal was forseen, that is, it acts as emitter of information , and if there is no destination and receiver of the information, there is no reason of the code to arise in the first place. So both, sender and receiver, must exist first as hardware, that is the microtubules with the post transcriptional modified tubulin units in a specified coded conformation, and the the receiver, which can be MAP’s in general, or Kinesin or Myosin motor proteins, which are directed to the right destination to fullfill specific tasks, or other proteins directed for specific jobs.

Taken together, multiple and complex tubulin PTMs provide a myriad of combinatorial possibilities to specifically ‘tag’ microtubule subpopulations in cells, thus destining them for precise functions. How this tubulin or microtubule code allows cells to divide, migrate, communicate and differentiate in an ordered manner is an exciting question that needs to be answered in the near future. Initial insights have already revealed the potential roles of tubulin PTMs in a number of human pathologies, like cancer, neurodegeneration and ciliopathies. This raises the question : If PTM’s are not precise and fully functioning, they cause deseases. What about if the MAP’s are not fully specified and evolved ? There is a threshold , a dividing line between a non functional protein - amino acid sequence that is non functional, and when it has enough residues to fold properly and become functional. How proteins arose in the first place is a mistery for proponents of natural mechanisms… Not only does it have to be elucidated how this tubulin or microtubule code allows cells to do all these tasks, but also what explains best its arising and encoding. Most of these enzymes are specific to tubulin and microtubule post translational modifications. They have only use if microtubules exist. Microtubules however require these enzymes to modify their structures. It can therefor be concluded that they are interdependent and could not arise independently by natural evolutionary mechanisms.

An emerging hypothesis is that tubulin modifications specify a code that dictates biological outcomes through changes in higher-order microtubule structure and/or by recruiting and interacting with effector proteins. This hypothesis is analogous to the histone code hypothesis ‑ that modifications on core histones, acting in a combinatorial or sequential fashion, specify multiple functions of chromatin such as changes in higher-order chromatin structure or selective activation of transcription. The apparent parallels between these two types of structural frameworks, chromatin in the nucleus and microtubules in the cytoplasm, are intriguing

Isn’t that striking evidence of a common designer that invented both codes ?

Microtubules are typically nucleated and organized by dedicated organelles called microtubule-organizing centres (MTOCs). Contained within the MTOC is another type of tubulin, γ-tubulin, which is distinct from the α- and β-subunits of the microtubules themselves. The γ-tubulin combines with several other associated proteins to form a lock washer-like structure known as the γ-tubulin ring complex" (γ-TuRC). This complex acts as a template for α/β-tubulin dimers to begin polymerization; it acts as a cap of the (−) end while microtubule growth continues away from the MTOC in the (+) direction. The γ-tubulin small complex (γTuSC) is the conserved, essential core of the microtubule nucleating machinery, and it is found in nearly all eukaryotes.

This γ-tubulin ring complex is a striking example of purposeful design which is required to nucleate the microtubules into the right shape. There would be no function for the γ-tubulin ring complex to emerge without microtubules, since it would have no function by its own. Furthermore, it is made of several subunits which are indispensable for proper use, that is for example the attachment factors, accessory proteins, and γ-tubulins, which constitute a irreducible γ-tubulins ring complex, made of several interlocked parts, which could not emerge by natural selection. The complex has only purposeful function when microtubules have to be asssembled. So the, γ-tubulins ring complex and microtubules are interdependent.

See its striking structure here :

Here’s an Incredible Idea For How Memory Works

Cytoskeletal Signaling: Is Memory Encoded in Microtubule Lattices by CaMKII Phosphorylation?

how the brain could store information long-term has been something of a mystery. But now researchers have developed a very interesting idea of how the brain’s neurons could store information using, believe it or not, a binary encoding scheme based on phosphorylation:

Memory is attributed to strengthened synaptic connections among particular brain neurons, yet synaptic membrane components are transient, whereas memories can endure. This suggests synaptic information is encoded and ‘hard-wired’ elsewhere, e.g. at molecular levels within the post-synaptic neuron. In long-term potentiation (LTP), a cellular and molecular model for memory, post-synaptic calcium ion (Ca2+) flux activates the hexagonal Ca2±calmodulin dependent kinase II (CaMKII), a dodacameric holoenzyme containing 2 hexagonal sets of 6 kinase domains.
This enzyme has a astonishing and remarkable configuration and functionality :

Each kinase domain can either phosphorylate substrate proteins, or not (i.e. encoding one bit). Thus each set of extended CaMKII kinases can potentially encode synaptic Ca2+ information via phosphorylation as ordered arrays of binary ‘bits’. Candidate sites for CaMKII phosphorylation-encoded molecular memory include microtubules (MTs), cylindrical organelles whose surfaces represent a regular lattice with a pattern of hexagonal polymers of the protein tubulin. Using molecular mechanics modeling and electrostatic profiling, we find that spatial dimensions and geometry of the extended CaMKII kinase domains precisely match those of MT hexagonal lattices. This suggests sets of six CaMKII kinase domains phosphorylate hexagonal MT lattice neighborhoods collectively, e.g. conveying synaptic information as ordered arrays of six “bits”, and thus “bytes”, with 64 to 5,281 possible bit states per CaMKII-MT byte. Signaling and encoding in MTs and other cytoskeletal structures offer rapid, robust solid-state information processing which may reflect a general code for MT-based memory and information processing within neurons and other eukaryotic cells.

Size and geometry of the activated hexagonal CaMKII holoenzyme and the two types of hexagonal lattices (A and B) in MTs are identical. 6 extended kinases can interface collectively with 6 tubulins

Is the precise interface matching striking coincidence, or purposeful design ? Either a intelligent , goal oriented creator made the correct size, where CaMKII would fit and match the hexagonal lattices, or that is the result of unguided, random, evolutionary processes. What explanation makes more sense ?

The electrostatic pattern formed by a neighborhood of tubulin dimers on a microtubule ( MT ) surface shows highly negative charged regions surrounded by a less pronounced positive background, dependent on the MT lattice type . These electrostatic fingerprints are complementary to those formed by the 6 CaMKII holoenzyme kinase domains making the two natural substrates for interaction. Alignment of the CaMKII holoenzyme with tubulin dimers in the A-lattice MT arrangement yields converging electric field lines indicating a mutually attractive interaction.

So additionally to the precise interface matching significant association of the CaMKII holoenzyme with the MT through electrostatic forces indicates cumulative evidence of design.

there are 26 possible encoding states for a single CaMKII-MT interaction resulting in the storage of 64 bits of information. This case, however, only accounts for either α- or β-tubulin phosphorylation, not both. In the second scenario each tubulin dimer is considered to have three possible states – no phosphorylation (0), β-tubulin phosphorylation (1), or α-tubulin phosphorylation (2) (see Figure 5 B). These are ternary states, or ‘trits’ (rather than bits). Six possible sites on the A-lattice yield 36 = 729 possible states. The third scenario considers the 9-tubulin B-lattice neighborhood with ternary states. As in the previous scenarios the central dimer is not considered available for phosphorylation. In this case, 6 tubulin dimers out of 8 may be phosphorylated in three possible ways. The total number of possible states for the B lattice neighborhood is thus 36–28−8(27) = 5281 unique states.

So thirdly we have here a advanced encoding mechanism of information, which adds to the precise interface and electrostatic force interactions, which adds further cumulative evidence of design.

Motor proteins dynein and kinesin move along microtubules (using ATP as fuel) to transport and deliver components and precursors to specific synaptic locations. While microtubules are assumed to function as passive guides, like railroad tracks for motor proteins, the guidance mechanism seems to be through CaMKII kinase enzymes which “write” on microtubules through phosphorylation and encode the way to regulate motor protein transport along microtubules directly, and signal motor proteins precisely where and when to disengage from microtubules and deliver their cargo. There needs to be programming all the way along. Programming to make the specific enzymes, and how they have to operate. That constitutes in my view another amazing argument for intelligent design.

It’s evolutionarily conserved and un-evolved?


If evolution is “change” - - ANY change in the gene pool… then a CONSERVED function is one that has not changed.

It doesn’t mean that there hasn’t been any other evolution for the creature … only that this function is not one of the things that has evolved.


Evolution conserves it. So if it changes then natural selection eliminates it.

I never said that. My point was to point out the contradiction I mentioned. but if you can shed more light on the microtubule acetylation process and how it was conserved, by all means have a go at it.

Don’t some things change even if natural selection is neutral about the change?


Yes you are right. There is genetic drift.

And I’ll go ahead and mention the obvious: genetic draft. As selection dynamics favor particular alleles, others adjacent to them in the genome tend to “tag along” and see their allele frequencies similarly increased in the population. Of course, the classic textbook example of that happened when fox farms inevitably selected for foxes which could tolerate confinement and human activity around them. Silver fur became more and more common due to those genes being selected indirectly as the “domestication-tolerating genes” were selected.

Seriously? Please define your use of the word “un-evolved”.

Edie, No. “Change in allele frequency” and “descent with modification” are in no way contradictory nor in any kind of conflict. (And one more time: nobody claims that natural selection CREATES what came about by mutation. Evolution does not involve just one process, despite the infamous “skeptics of evolution” petition that still makes its round online on creationist websites.) I’m getting the very strong impression, again, that you do not have a solid grasp of evolutionary processes. As so often happens, people focus on some one aspect of evolution and assume it an either/or false dichotomy when compared to all others which scientists discuss. I would encourage you to start with an introductory evolutionary biology textbook and gain a systematic familiarity with the topic. It sounds like your view of the Theory of Evolution is based on a hodge-podge of popular denialist arguments based on popular myths and misunderstandings of how evolution operates. (Your misunderstanding of the genetic draft example in thinking that you had found some major problem which all of the scientists had missed is part of a pattern in your comments that illustrates how you are trying to approach the topic without a solid foundation of the basics.)

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Ah yes, the very famous Belyaev domesticated foxes!! And he also bred a line of extremely aggressive foxes! Belyaev was a very careful scientist, and he put himself in peril for not following the official Soviet thinking on genetics.

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A few comments addressed to Eddie.

  1. “Change in allele frequency” is a demarcation criterion for evolution. It is not, and was never intended to be (as far as I know), a complete description of evolution.

  2. Casting debates within evolutionary theory as a generational conflict is at best incomplete, and may be thoroughly misleading. Look at those you describe as leading the charge against neo-Darwinism: Gould has been dead for years, Margulis is dead, Shapiro is no spring chicken, the structuralists represent a long-running, fruitful research program, not upstart youth. There are lots of controversies within evolutionary biology, and the field is changing constantly, but there is no particular changing of the guard going on that I can see.

  3. It would be helpful if you would distinguish between different kinds of ideas that run counter to neo-Darwinism. Genetic drift, whole genome duplication and the constraints imposed by developmental programs, for example, are consensus biology at this point, even though they weren’t envisioned by the neo-Darwinian synthesizers. On the other hand, most evolutionary biologists (I think) view Shapiro’s natural genetic engineering concept as pushing valid ideas too far, while some of Margulis’s later ideas are just viewed as nuts. You are contributing as much confusion as enlightenment by contrasting a neo-Darwinian orthodoxy (which nowhere exists today) with such diverse ideas.

  4. You might be well served by spending less time reading on evolutionary theory (especially reading the most polemical stuff in the field), and more time talking to working biologists. This would give you a better feel for where real controversies and disagreements lie. Speaking as a population geneticist, I have to say that your description of pop-gen-centered evolutionary biology bears little relation to how I or anyone I know thinks.



I suspect that @Otangelo_Grasso merely equates “un-evolved” with the term “un-changed”. I don’t think that is a problem.

What is more intriguing is the likelihood of a species having evolved significantly … while looking quite un-changed.

For example, modern day crocodiles may look quite a bit like very ancient crocodiles … but this doesn’t mean the genetic configuration is completely unchanged.

There is a very real chance (though more or less untestable) that a modern crocodile would not be able to mate with an ancient crocodile and produce fertile offspring. Genetic configuration is like a rotating crystal … with constantly changing features.

Given enough time, any two identical groups of specimens would eventually create two sets of descendants that are virtually incompatible sexually.

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