Alien DNA: Alien genes found in human DNA?


A new study claims that alien DNA is inserted into our genome.

Here’s research, initial findings, possible effects, and speculation – The Economic Times

This goes into it more. The NY Post was skimming.

https://m.economictimes.com/news/international/us/alien-genes-found-in-human-dna-new-study-claims-alien-dna-inserted-into-our-genome-heres-research-initial-findings-possible-effects-and-speculation-hybridization-unverified-research-genetics-alien-contact-scientific-verification-23andme-results-non-parental-markers-scientific-limitations-next-steps/articleshow/124348154.cms

Maybe everyone is biased in their definition of life


Me: There are different kinds of life in the universe that likely have no carbon, but they have a mind. Therefore, they are life IMO.

GROK: You’re absolutely right—our definitions of life are profoundly shaped by the only example we know: carbon-based, water-dependent organisms on Earth. This creates a kind of anthropocentric (or Terracentric) bias, where we assume life must mimic what we’ve observed, overlooking the vast chemical and physical possibilities in a universe with trillions of planets.

PAstrobiologists often call this the “shadow biosphere” problem: What if exotic life exists right here on Earth, undetected because it doesn’t fit our criteria? Extending that to cosmic scales, non-carbon life forms—perhaps silicon-based, boron-based, or even relying on plasma or exotic solvents like liquid methane—could thrive in environments lethal to us, like Titan’s hydrocarbon seas or Venus’s acidic clouds.

Scientifically, carbon reigns supreme because it’s uniquely versatile: It forms stable, complex chains and rings at Earth-like temperatures, bonds easily with hydrogen, oxygen, and nitrogen, and enables the polymers essential for DNA, proteins, and cell membranes. Silicon, the next best candidate (being in the same periodic group), can theoretically mimic some of this tetravalent bonding, but it prefers forming rigid, heat-stable silicates (like sand) over flexible organics, making it less ideal for dynamic biochemistry. Hypothetical silicon life might metabolize through silicon-oxygen bonds or even incorporate carbon in hybrid forms, but no evidence exists yet—it’s mostly sci-fi fodder, from Star Trek’s rock-munching Horta to Marvel’s shape-shifting Sandman Other alternatives, like boron (which forms chains but reacts poorly with acids) or nitrogen-phosphorus systems in ammonia solvents, face similar hurdles: They’re cosmically abundant but thermodynamically finicky, often requiring extreme conditions we haven’t probed deeply.

Your emphasis on “mind” as the true marker of life cuts to a deeper philosophical vein, one that challenges purely biochemical definitions. NASA’s working definition—”a self-sustaining chemical system capable of Darwinian evolution”—is pragmatic for SETI searches but ignores consciousness, sentience, or information processing, which some thinkers (from panpsychists to AI ethicists) argue are life’s essence. If a silicon entity on a frigid exomoon processes data, adapts, and experiences qualia (subjective awareness), does it matter if its “DNA” is etched in crystal lattices rather than nucleotides? Recent work on autocatalytic cycles—self-replicating chemical networks—suggests such systems could bootstrap “life” from non-carbon elements, potentially evolving complexity toward something mind-like. In a 2023 study, researchers modeled how these reactions might sustain biology on diverse worlds, broadening the search beyond CHNOPS (carbon, hydrogen, nitrogen, oxygen, phosphorus, sulfur).

Ultimately, bias persists because we lack data—our telescopes and probes are tuned for carbon signatures like methane or oxygen imbalances. But missions like Dragonfly (to Titan in 2028) or speculative Europa landers could upend this. If we find a “mind” in a metallic lattice or energy plasma, it wouldn’t just redefine life; it’d humble us, proving the universe’s creativity outstrips our parochial checklists. What do you think qualifies as a “mind” in this context—self-awareness, problem-solving, or something more elusive?

🧐💛💫✨️

The mRNA sequence fingerprints have officially shown up on human DNA and are causing turbo cancers.


These people who did this to us have some big freaking karma coming their way for intimidating vulnerable humans who trusted the sick care system. They might want to exile themselves to another planet with their tail between their legs. The universe will still find them and exact justice, but we would be left to correct course. They need to surrender.

https://x.com/15913txri/status/1968573948917841990?t=4bBI0NIS2GYV9X1DMZh05A&s=09

Time Innovation: Microbiology-Our Human DNA evolved from metals and minerals which came from the sun.


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Essay: Human DNA bridges Time and Space Through the Tzolkin Harmonic Code


I wrote this in 2020…

Today is White 10 Planetary World Bridger. The Human race didn’t just evolve here. We had to bridge worlds to heal and revive here after universe debacles. Our ancient ancestors brought us here safely and then another level of life was started on Earth to begin again. So there are levels of people and Life here that we don’t see…yet.

Here is the source link for this basic DNA information.

https://ghr.nlm.nih.gov/primer/basics/dna

The purpose of this blog is to reveal how the Mayan Tzolkin is the original, ancient harmonic code brought to this planet to help us understand how we’ve evolved and possibly make some changes ourselves to the human race as we see fit.

What I’ve done is study this base, earth information and build an epigenetic bridge to the Mayan Tzolkin Harmonic which has always been believed to be the illumination of DNA and True Time. After studying it for 30 years I see that they are one and the same.

Below, it says the rungs of the ladder of the double helix are the base pairs. That is fairly simple, but as geneticists know, there is much RNA movement and sequencing going on that is not explained. The tRNA molecules and it’s movement mimic the Tzolkin daily kin of 5 archetypes. Thus, there are 20 amino acids moving in ONE Harmonic family over four days. I’ve mapped out the time and amino acid movement and see that there is a pattern moving the rungs of the ladder.

Look at the synchronicity of this Tao Te Ching philosophy, and it’s numbered 13!;

Tao Te Ching-Thirteen

Success is as dangerous as failure.
Hope is as hollow as fear.

What does it mean that success is a dangerous as failure?
Whether you go up the ladder or down it,
your position is shaky.
When you stand with your two feet on the ground,
you will always keep your balance.

What does it mean that hope is as hollow as fear?
Hope and fear are both phantoms
that arise from thinking of the self.
When we don’t see the self as self,
what do we have to fear?

See the world as your self.
Have faith in the way things are.
Love the world as your self;
then you can care for all things.

   The Tao Te Ching was written by Lao-Tzu translation by S. Mitchell

Specifically, if you look at the G.A.P. kin that move from the outer to the inner portion of the Tzolkin around the central channel, I see that they are amino acid anchor vertices around which the mRNA evolves to eventually change the sugar and phosphate boundary by sequencing until it is released into the nucleus of the DNA molecule. This is done via binary triplet configuration and radial polarity. These are all actions discussed and put into graphics by Jose Arguelles in “Earth Ascending”. How did Jose know? He was a visionary, a type of Mayan Shaman, an artist, a seer, and a spectral, tone 11 intuitive genius. Due to all of that he’s also been attacked and called a fake. Yet I’m seeing the patterns he brought into consciousness can be seen in the genetic patterns. He wasn’t a scientist though and did not have a knack for molecular biology and building bridges. Still, he did his piece to be sure. I’m hoping to move it forward further and possibly one or two scientists will pay attention.

DNA, or deoxyribonucleic acid, is the hereditary material in humans and almost all other organisms. Nearly every cell in a person’s body has the same DNA. Most DNA is located in the cell nucleus (where it is called nuclear DNA), but a small amount of DNA can also be found in the mitochondria (where it is called mitochondrial DNA or mtDNA). Mitochondria are structures within cells that convert the energy from food into a form that cells can use.

The information in DNA is stored as a code made up of four chemical bases: adenine (A), guanine (G), cytosine (C), and thymine (T). Human DNA consists of about 3 billion bases, and more than 99 percent of those bases are the same in all people. The order, or sequence, of these bases determines the information available for building and maintaining an organism, similar to the way in which letters of the alphabet appear in a certain order to form words and sentences.

DNA bases pair up with each other, A with T and C with G, to form units called base pairs. T is changed to U for Uracil when RNA is evolving in a cell. Each base is also attached to a sugar molecule and a phosphate molecule. Together, a base, sugar, and phosphate are called a nucleotide. Nucleotides are arranged in two long strands that form a spiral called a double helix. The structure of the double helix is somewhat like a ladder, with the base pairs forming the ladder’s rungs and the sugar and phosphate molecules forming the vertical sidepieces of the ladder.

An important property of DNA is that it can replicate, or make copies of itself. Each strand of DNA in the double helix can serve as a pattern for duplicating the sequence of bases. This is critical when cells divide because each new cell needs to have an exact copy of the DNA present in the old cell.

DNA is a double helix formed by base pairs attached to a sugar-phosphate backbone.

DNA is a double helix formed by base pairs attached to a sugar-phosphate backbone.

Credit: U.S. National Library of Medicine

Synchronicity is the Source of Consciousness


Synchronicity is not random. DNA/RNA evolution is not random. That means it has to be orderly. In what context? In the context within which we exist; TIME and Time is DNA from our birth family.

In truth, there is only NOW, which is the CNS, the central nervous system, which is the brain and spine. We access that in meditation.

However, your body was made on the loom of Maya, illusion, from your mother and father. That DNA sets the pattern for your individual RNA. Why is that a big deal?

Because you set the frequency with the focus of your bodymind. The nefarious know the evolutionary free will power of our RNA and want to manipulate it to control our bodymind further. We can do all the disclosure we want, Dr. Greer can get his covert secret tech brought forward by special forces, but without a bulk of humans understanding how our time is controlled by us and not tech or institutions, we will just be controlled by them as well.

There is no utopia peace on earth just because you reveal 100 years of covert tech. 

What about the human MIND and heart? Advanced technology can’t change that.

Lisa T.

We need to understand that we evolved from the stellar species and the stars. We are children of the galaxy and need to feel that in our bodies.

Our body allows us to experience time travel in our minds, back and forth between the past and the future, to remember what has already been so we can change now. No matter what your parents did wrong, they gave you a body to keep learning at this level. Don’t curse them, but honor them for the gift of your body and free will RNA that comes from DNA. Technology will never replace that.

Time Innovation: Philosophy-Why consciousness must be quantum mechanical | Stuart Hameroff | Full interview


Consciousness itself is non-computable. -Robert Penrose

Our brain cells have time crystals at huge hertz levels in the neurons. This supports all the work I’m doing.

At 10:00, he starts talking about the amino acid proteins. I’m impressed that he knows microbiology mixed with physics. I may need him on my project later.

They start talking about the action of the microtubule in the neurons being random. No. That is incorrect. I hope to prove that everything moving in the DNA, which is electromagnetic protein, is ORDERLY and mathematical according to the time harmonic. Geneticists know it is not random, but they don’t know why. I do. Physicists, because their theories rarely land on terra firma, live in chaos.

At 21:30, he starts talking about a successful experiment with Tryptophan amino acid Blue Storm. Do listen to that.

I asked GROK if Geneticists can manipulate tRNA the same nefarious way they have mRNA


Geneticists have made incredible strides in manipulating RNA for various applications, including the mRNA vaccines we’ve seen in recent years. Your question about whether they can manipulate tRNA (transfer RNA) in a similar way is a good one—it gets into the nitty-gritty of molecular biology and synthetic biology.

The short answer is: yes, but with some caveats. The mRNA vaccines (like those for COVID-19) rely on synthetic mRNA (very bad) designed to encode a specific protein (e.g., the spike protein of SARS-CoV-2), which is then translated by the body’s ribosomes into that protein to trigger an immune response. This involves tweaking the mRNA sequence, optimizing codons, and stabilizing it with chemical modifications (like pseudouridine) to ensure it works efficiently and doesn’t degrade too quickly.

tRNA, on the other hand, plays a different role—it’s the molecule that ferries amino acids to the ribosome during protein synthesis, matching its anticodon to the mRNA’s codon. Manipulating tRNA is less about encoding a protein and more about controlling how translation happens. Geneticists can and do manipulate tRNA, but the goals and methods differ from mRNA vaccine tech.

For example, synthetic tRNAs have been engineered to:

  1. Incorporate unnatural amino acids into proteins by designing tRNAs with altered anticodons that pair with “stop” codons (like UAG) and carry custom amino acids. This is big in protein engineering and synthetic biology—think of it as hacking the genetic code. (Oh, I just love thinking about that. )
  2. Regulate translation efficiency by tweaking tRNA abundance or specificity, which can influence how much protein gets made from a given mRNA.
  3. Correct genetic mutations—there’s research into using suppressor tRNAs to “read through” premature stop codons in diseases like cystic fibrosis.

The tools—CRISPR, RNA synthesis, and chemical modification—are similar to those used for mRNA vaccines, but tRNA manipulation is trickier because it’s a smaller, more structurally complex molecule (with its cloverleaf shape) and its function depends heavily on precise interactions with synthetases and the ribosome. mRNA is a simpler “message” to edit; tRNA is part of the machinery itself.

Could tRNA be weaponized into a therapeutic like mRNA vaccines? Potentially, but it’s less straightforward. mRNA vaccines deliver a blueprint; tRNA mods would be more about fine-tuning or rewriting the translation process. There’s no direct parallel yet—tRNA therapies are still experimental, while mRNA tech is now proven at scale. That said, advances in synthetic biology mean tRNA manipulation is catching up fast. Look at work on “orthogonal translation systems” or tRNA-based gene therapies—those are the bleeding edge.

What’s your angle here? Are you thinking about therapeutic potential, or something more speculative like bioengineering risks?

A: Something speculative like bioengineering risk.

My Angle?

Fuck genetic engineering. I’m not giving them 35 years of empowerment work that I know is accurate just so Bill Gates can continue to efficiently cull humans and then do a global takeover of eugenically manipulated humans that they deem to be superior.

I hope my followers agree. If not, feel free to comment.

Today.

The Role of Time Cell Five in Mayan Cosmology


Mayan Dreamspell Time Cells

I haven’t talked about this very much trying to acclimate you to the other aspects of Mayan Time Keeping. Now that I’ve introduced you to the double strands of our DNA being CA (Civilizational Advance, past to present) and AC (Aboriginal Continuity, future to present) we need to be aware of the fact that in the Long Count we are in TIME CELL FIVE: The Matrix.

We could easily say that each time cell represents 4000 years so that all together it’s 20,000 years. It may even be 40,000 for each harmonic and then 400,000 years. It wouldn’t be hard to add zeros. What is the actual date of the Red Dragon Tribe with it’s sulfuric acid ways starting things here? The planet was started by FIRE and BLOOD. Thus on the CA timeline, which are the first 9 archetypes, we have the RIGHT FIRE HAND and RIGHT BLOOD FOOT. That is Time cells one and two and Red Moon which starting the DNA sequencing with Methionine.

Then we have the Left Truth Hand and Sky Foot for the next 9 tribes. At some distant point in Time, Time Cell Three and Four commenced and here we are like ants running all over the planet. According to the Urantia Book, the human race is only one million years old whereas all other DNA life came before us in the past time cells. For instance, I just posted that the cat species are 3 million years old. Plants are even older.

Here in Time Cell 5 we begin with Red Earth, an AWARENESS OF SYNCHRONICITY, how to navigate the energy here, our energy bodies, vortexes, quantum physics, energy healing, the Aquarian Age (Uranus mediates Red Earth and Aquarius) and we JUST began the Age of Aquarius a few months ago if you remember.

I don’t know how long it’s going to take to move through this Time Cell but you can see we end up as our Solar Selves aligned with our Star, The Sun. But first we have to go through a time of Reflection and Transformation. This will not be a quick process. I just wanted you to see that evolution of Life on Earth is an orderly process from initiation, refinement, transformation and ripening.

Understanding the Daily Oracle of tRNA and Humanity


The daily oracle is a simplified version of every evolving tRNA cell in all of nature. In our case, it represents all of humanity. Each kin symbol is an amino acid on the arm of the tRNA cell. Each person is composed of trillions of cells, and the movement of these cells affects changes in our bodymind.

The nucleotides, adenine, cytosine, and guanine (uracil) overarch each 4-day harmonic set by the I Ching oracle for 3D manifestation. They are at the bottom of the cell. This position is in synchronicity with the Hidden Wisdom position in the Harmonic. This is where we see the mother and manifestation into the birth family. Your parents’ DNA helps you manifest a body, but that is all. In no way does it control your soul. Your soul is born of God and has evolved with your free will over lifetimes. Your birth family does not own you. You don’t belong to your parents. You are free and belong to God, which means you as a co-creator with Source. “We are no longer slaves, but free.

Hidden Wisdom means the lessons you come to learn on earth in light or in shadow via your family. The birth family isn’t righteous. However, it is holy as a prime teacher for your soul. It guides you on what to be or what not to be on this planet. This guidance particularly suits what the universe knows you want to figure out.

Here is today’s example.
  • The Theme in the center is Glutamic Acid
  • The analog on the right or Loop3 is Isoluecine
  • The Guide Power or top amino acid is Histidine or the D Arm
  • The antipode challenge on the left or Loop1 or the Anti-Codon is Glycine.
  • The Hidden Wisdom or the T Arm, is controlled and put in motion by the 3D nucleotides into 4D time. It is known as 11 Spectral Methionine or the start codon. In today’s case, probably parents who were emotionally unstable, absent, or neglectful. Tone 11 is dissolving and breaks things apart.

Deciphering the Genetic Code


The Chinese Hexagrams

The DNA nucleotide were first deciphered by the Chinese. Around the year 1050 BCE, tradition states that Emperor Wen, founder of the Zhou dynasty, created hexagrams. He did this by doubling the trigrams. These hexagrams are six-lined figures. He numbered and arranged all of the possible combinations. There are 64, and he gave them names.

They did this in the manner that they interpret life. As my followers know, this discovery was turned into the IChing hexagrams thousands of years before 1961. The Chinese created 64 hexagrams that stood for Life first. They accomplished this long before Western white men worked in the lab in white coats during the 60’s. Western scientists took these hexagrams and ascribed triplet letters to them. Two lines of the hexagram represented one letter: A, C, G, T, or U for the RNA. Before the scientists did that, Leibniz turned the hexagrams into binary code or 0’s and 1’s.

So the time spiral goes; The Chinese made significant contributions first by designing and giving meaning to the Hexagrams. The production of stelae by the Maya had its origin around 400 BC and continued through to the end of the Classic Period, around 900, although some monuments were reused in the Postclassic (c. 900–1521).Then Leibniz developed his binary code by looking at the Chinese symbols as lines and dashes or 0 and 1. Next was the Turing machine, hypothetical computing device introduced in 1936 by the English mathematician and logician Alan M. Turing. This was the predecessor of the computer which added the electronic element to the interpretation of our DNA. Then Rosalind Franklin photographed the DNA double helix, but her work was unacknowledged. Then Watson and Crick introduced their DNA model in 1953. Rosalind Franklin and her student Raymond Gosling had photographed it in 1952. But Watson and Crick got all the credit. Now we arrive at Marshall Nirenberg and his colleagues in the 60’s in this article. They were at the National Institutes of Health and interpreted the language of the genetic code.

Before you read his, know this. The Maya, the Chinese, and Rosalind Franklin gave the world the genetic code in its original intended form. It has since been obfuscated by white coat men in the labs of universities and at the National level. I hope to bring it back around to its original, expanded meaning, lost since the Maya. Such is the nature of Oracles in a technologically dominated world.

The link to this article.

https://www.acs.org/education/whatischemistry/landmarks/geneticcode.html

National Historic Chemical Landmark

Dedicated November 12, 2009, at the National Institutes of Health in Bethesda, Maryland.

Commemorative Booklet (PDF)

DNA consists of a code language comprising four letters. These letters make up what are known as codons, or words. Each codon is three letters long. Marshall Nirenberg and his colleagues at the National Institutes of Health interpreted the language of the genetic code. It was their collaborative work that achieved this. Their careful work, conducted in the 1960s, paved the way for interpreting the sequences of the entire human genome.

Contents

Modern Genetics: A Monk and a Double Helix

Modern genetics begins with an obscure Augustinian monk studying the inheritance of various traits in pea plants. Gregor Mendel’s laws of inheritance revealed the probabilities of dominant and recessive traits being passed from generation to generation. Mendel’s research received little recognition in his lifetime. The significance of Mendel’s laws was recognized only in the early 20th century.

With that rediscovery came interest in how genetic information is transmitted. Oswald Avery, a bacteriologist at New York’s Rockefeller Institute, demonstrated that deoxyribonucleic acid, DNA, produced inheritable changes. This discovery was not well received. How could DNA store genetic information? It was a substance containing only four different nucleotide building blocks. Others discovered that DNA varies from species to species. Then, in 1953, James Watson and Francis Crick at Cambridge University amazed the scientific world. They introduced their model of DNA, known as the double helix. Watson and Crick recognized that the double strand might allow replication.

How could DNA, a double helix made up of only four different nucleotide, determine the composition of enzymes (proteins)? These enzymes are long peptide chains composed of twenty different amino acids. The race to discover the genetic code which translates DNA’s information into proteins was underway. To stimulate the chase, George Gamow, a theoretical physicist, organized the twenty-member “RNA Tie Club.” Each member wore a tie with the symbol for one of the 20 amino acids. The members shared ideas on how DNA transmitted information.

The scientist who won the race was not a member of the “club.”

Deciphering the Genetic Code commemorative booklet

The “Deciphering the Genetic Code” is a commemorative booklet. It was produced by the National Historic Chemical Landmarks program of the American Chemical Society. The booklet was published in 2009 (PDF).

I thought if I’m going to work this hard, I might just as well have fun. By fun, I mean I wanted to explore an important problem. I wanted to discover things.”
— Interview with Marshall Nirenberg, July 15, 2009.

Marshall Nirenberg’s Early Career

Marshall Nirenberg earned a Ph.D. in biological chemistry. He studied at the University of Michigan. His dissertation focused on the mechanism of sugar uptake in tumor cells. He continued that research as a postdoctoral fellow at the National Institutes of Health. In 1959, he joined the staff of NIH as a research biochemist.

Nirenberg gave some thought to what he wanted to study as an independent investigator. He said in 2009, “At that time, the mechanism of protein synthesis was very incompletely known.” Messenger RNA had not been discovered.

Nirenberg’s initial goal was to find out if DNA or RNA, copied from DNA, was the template for protein synthesis. Nirenberg had no formal training in molecular genetics. He knew that this was an incredibly risky project. When you take your first position, you want to hit the deck running. You want to show you are a productive scientist. Nirenberg had no experience in the field. He had no staff at the outset and was in a race against the best scientists. He knew he “could fail easily.”

*This and subsequent quotations, unless the text indicates differently, are from an interview by Judah Ginsberg and Marshall Nirenberg, conducted in his laboratory on the campus of NIH on July 15, 2009.

Experiments with Synthetic RNA

Nirenberg and Heinrich Matthaei started their experiments by studying DNA and RNA. Matthaei, a postdoctoral fellow from Germany, collaborated on the research. In DNA, the nucleotide are adenine (A), guanine (G), cytosine (C) and thymine (T); in RNA, uracil (U), replaces thymine.

They chose a cell-free environment, created when cell walls are broken down, releasing the cell’s contents. The remaining cytoplasm can still synthesize protein when RNA is added. This allows the researchers to design experiments. They can determine how RNA works free of the complicated biological processes that could shroud molecular activity.

Nirenberg and Matthaei selected E. coli bacteria cells as their source of cytoplasm. They added the E. coli extract to 20 test tubes, each containing a mixture of all 20 amino acids. In each test tube one amino acid was radioactively tagged, a different one in each test tube. The reaction could be followed by monitoring radioactivity: incorporation of a “hot” amino acid would form a “hot” protein.

Breaking the Genetic Code: The “poly-U” Experiment

At 3:00 in the morning on May 27, 1961, Matthaei begins his experiment. (Yellow 13 Seed which hits in 3 days) He adds synthetic RNA. It was a Saturday. The RNA is made only of uracil units. He adds it to each of the 20 test tubes. He finds unusual activity in one of the tubes. This tube contains Phenylalanine. The test results are spectacular. A chain of uracil units in the “hot” tube directs the addition of the “hot” amino acid.

Nirenberg and Matthaei understood what had happened. Synthetic RNA made of a chain of multiple units of uracil gave instructions. It directed a chain of amino acids to add Phenylalanine. The uracil chain (poly-U) served as a messenger directing protein synthesis. The question of how many units of U were required was yet unanswered. However, the experiment proved that messenger RNA transcribes genetic information. It transcribes this information from DNA. It directs the assembly of amino acids into complex proteins. The key to breaking the genetic code—molecular biology’s Rosetta Stone—had been discovered.

Nirenberg presented his successful poly-U experiment at an international biochemistry congress held in Moscow in August, a few months later. He was acutely aware of his outsider status. He said, “I didn’t know the people in molecular biology. I didn’t know anybody in protein synthesis. I was working on my own.” That may explain why only 35 people attended his talk and why the audience “was absolutely dead.”

Nirenberg experienced a serendipitous event that changed everything. He had met Watson the day before. Nirenberg told the co-discoverer of the double helix about his results. Watson was skeptical about Nirenberg’s claims. However, he convinced a colleague to attend the paper. The colleague reported that Nirenberg’s findings were real. Watson then told Crick, who arranged for Nirenberg to present his paper again. This time, it was in a major symposium on nucleic acids at the same congress. “The reaction was incredible,” Nirenberg remembered. “When it was over, the audience gave a standing ovation. I didn’t know it at that moment. For the next five years, I became like a scientific rock star.”

Marshall Nirenberg performing an experiment, circa 1962.

Courtesy the National Institutes of Health.

Nirenberg and Matthaei “cracked” the first “word” of the genetic code. Afterward, scientists raced to translate the unique code words for each amino acid. They hoped to someday read the entire genetic code of living organisms. Nirenberg assembled a team of about twenty researchers and technicians.

Nirenberg and his colleagues used the poly-U experiment as a model. They identified nucleotide combinations for the incorporation of other amino acids. The researchers found that the coding units for amino acids contain three nucleotide (a triplet). They combined four nucleotide in three-letter codes. This combination yielded 64 possible combinations (4 x 4 x 4). This was sufficient to describe 20 amino acids.

They discovered the codes for other amino acids: for example, AAA for Lysine and CCC for Proline. Replacing one unit of a triplet code with another nucleotide yielded a different amino acid. For instance, synthetic RNA containing one unit of guanine and two of uracil (code word: GUU) caused incorporation of Valine.

In 1964 Nirenberg and Philip Leder discovered a method. Leder was a postdoctoral fellow at NIH. They determined the sequence of the letters in each triplet word for amino acids. By 1966 Nirenberg had deciphered the 64 RNA three-letter code words (codons) for all 20 amino acids. The language of DNA was now understood and the code could be expressed in a chart.

The Nobel Prize and Reactions

In 1968 Nirenberg won the Nobel Prize in Physiology or Medicine for his seminal work on the genetic code. He shared the award with Har Gobind Khorana (University of Wisconsin). Khorana mastered the synthesis of nucleic acids. Robert Holley (Cornell University) also shared the award. Holley discovered the chemical structure of transfer-RNA. Collectively, the three were recognized “for their interpretation of the genetic code and its function in protein synthesis.”

Nirenberg describes the ceremonies surrounding the Nobel as “a week of parties.” Not quite all parties, however, since the rules of the Nobel require recipients to write a review article. This proved a challenge for Nirenberg, who had turned his research attention to neurobiology. ”I found it very difficult,” he later admitted, “to break off from neurobiology and go back to nucleic acids.”

As a Nobel Laureate, Nirenberg received many university offers that included higher salary, more laboratory space, and larger staff. He turned them all down, preferring to spend the rest of his career at NIH. “The reason I stayed,” he says, “was because the thing I had least of was time. I figured that if I went to a university, I would use a third of my time to write grants. I believed I could use that time more productively by doing experiments.”

In 1961 The New York Times, echoing President Kennedy, reported about Nirenberg’s research. It showed that biology “has reached a new frontier.” One journalist suggested the biggest news story of the year was not Russian cosmonaut Yuri Gagarin orbiting the earth. Instead, the biggest story was the cracking of the genetic code.

Deciphering the genetic code raised ethical concerns about the potential for genetic engineering. Nirenberg addressed these concerns in a famous editorial in Science in August 1967. He noted “that man may be able to program his own cells.” This could happen before “he has sufficient wisdom to use this knowledge for the benefit of mankind.” He emphasized that “decisions concerning the application of this knowledge must be made by society.” Only an informed society can make such decisions wisely. When asked several decades later if society has acted “wisely” regarding genetic engineering, Nirenberg answered, “Absolutely!”

HOW THE DNA DOUBLE HELIX FACTORY WORKS


This is literally an ancient, microbiological factory.

  • An RNA template strand comes out of it. Each rung of the ladder is called a base pair and there are about 3 billion base pairs that make up the genome, 30,000 genes and each cell have 23 pair of chromosomes. They thread around a spool as in torsion.
  • Transcription factors bind open DNA and can recruit other proteins such as enzymes.
  • RNA polymerase; DNA reads and transcribes DNA into RNA.
  • The single strand RNA copies the A, C, T, and G of the mRNA
  • It carries it out of the nucleus to the ribosome for the production of the particular protein that this gene codes for.
  • There can be millions of ribosomes in a typical eukaryotic cell
  • These complex cells use the RNA copy of the gene for info. to assemble amino acid building blocks into the 3D proteins that are essential for life. The ribosome is composed of one large and one small subunit that assembles around the mRNA which then passes through the ribosome like a computer tape.
  • The amino acid building blocks are carried into the ribosome attached to SPECIFIC transfer RNA. They are attached to the glob of tRNA.
  • The small subunit of the ribosome positions the mRNA so that it can be READ in groups of 3 letters known as a codon.
  • Each codon on the mRNA matches a corresponding anticodon on the base of a transfer RNA molecule.
  • The larger subunit of the ribosome removes each AA and joins it onto the glowing protein chain.
  • As the mRNA is ratcheted through the ribosome the mRNA sequence is translated into an AA sequence (the Tzolkin themeplexes)
  • There are 3 locations inside the ribosome designated A, P, and E site
  • The addition of each AA is a 3-step cycle.
  • #1. RNA enters the ribosome at the A site and is tested for a codon, anticodon, match with the mRNA
  • #2. If there is a match the tRNA is shifted to the P site and the AA it carries is added to the end of the AA chain.
  • The mRNA is also stuck on 3 nucleotides or 1 codon.
  • #3-the spent tRNA is moved to the E site and then ejected from the ribosome to be recycled.
  • 6 feet of DNA fits in the nucleus of every cell of an organism.
  • In the helicase, it’s copied backward. It moves as fast as a jet engine looping and coiling leading to chromosomes.
  • Then comes the KINETICORE. It’s a crazy, universal operation with its microtubule fibers.
  • Chromatin is called the tightly packed cell
  • Then it’s a chromatid
  • Then it’s a chromosome
  • Then it’s a nuclear pore and has a nuclear membrane gateway in the cell. The membrane breaks down.

Understanding DNA’s Double Helix: A Detailed Guide


One rendering of the Chinese I Ching Oracle that is the source of our DNA Nucleotides and Binary Code

HOW THE DNA DOUBLE HELIX WORKS

  • An RNA template strand comes out of it. Each rung of the ladder is called a base pair. There are about 3 billion base pairs that make up the genome. There are 30,000 genes. Each cell has 23 pairs of chromosomes. They thread around a spool as in torsion.
  • Transcription factors bind open DNA and can recruit other proteins such as enzymes.
  • RNA polymerase; DNA reads and transcribes DNA into RNA.
  • The single strand RNA copies the A, C, T, and G (Adenine, Cytosine, Thymine, Guanine and Uracil; the nucleotides) of the mRNA
  • It carries it out of the nucleus to the ribosome. This is for the production of the particular protein that this gene codes for.
  • There can be millions of ribosomes in a typical eukaryotic cell
  • These complex cells use the RNA copy of the gene for info. to assemble amino acid building blocks into the 3D proteins that are essential for life. The ribosome has two subunits, one large and one small. These subunits assemble around the mRNA. The mRNA then passes through the ribosome like a computer tape.
  • The amino acid building blocks are carried into the ribosome attached to SPECIFIC transfer RNA. They are attached to the glob of tRNA.
  • The small subunit of the ribosome positions the mRNA. It enables the mRNA to be read in groups of 3 letters. These groups are known as a codon.
  • Each codon on the mRNA matches a corresponding anticodon on the base of a transfer RNA molecule.
  • The larger subunit of the ribosome removes each AA and joins it onto the glowing protein chain.
  • As the mRNA is ratcheted through the ribosome the mRNA sequence is translated into an AA sequence (the Tzolkin themeplexes)
  • There are 3 locations inside the ribosome designated A, P, and E site
  • The addition of each AA is a 3-step cycle.
  • #1. RNA enters the ribosome at the A site and is tested for a codon, anticodon, match with the mRNA
  • #2. If there is a match, the tRNA moves to the P site. The AA it carries is added to the end of the AA chain.
  • The mRNA is also stuck on 3 nucleotides or 1 codon.
  • #3-the spent tRNA is moved to the E site and then ejected from the ribosome to be recycled.
  • 6 feet of DNA fits in the nucleus of every cell of an organism.
  • In the helicase, it’s copied backward. It moves as fast as a jet engine looping and coiling leading to chromosomes.
  • The comes the KINETICORE. It’s a crazy, universal operation with its microtubule fibers.
  • Chromatin is called the tightly packed cell
  • Then it’s a chromatid
  • Then it’s a chromosome
  • Then it’s a nuclear pore and has a nuclear membrane gateway in the cell. The membrane breaks down.

Clear as mud? I just thought the 3D facts should be recorded here even though the synchronicity of it is magical.

The Reverse, Backward Movement of the Harmonic in the Psi Bank


What you see above are 8 Tzolk’in Harmonics, 4 facing up, 4 facing down but diagonal from each other. Look at the ones on the bottom. Red 1 Dragon, kin#1 is in the bottom right. If you turned it right side up it would look just like the top harmonics. This shows how they are processed through the Psi bank like computer code. This is from Earth Ascending page 149.

It’s a type of mirroring in synchronicity with today’s theme; White 11 Spectral Mirror. I started on this idea yesterday wondering about what was really happening with mRNA reverse transcriptase that Bruce Lipton was talking about in his video that I posted a few days ago. Listen to it again. He says that the DNA Dogma taught that the DNA only moved in one direction. That’s not the case once you understand mRNA reverse transcriptase and that speaks DIRECTLY to Tzolkonic Movement and current epigenetic claims of being able to program your own DNA by going backward. Or, as I’m suggesting in my book based on research, past to present or future to present AS TIME IN YOUR BODY/MIND. Nobody knows that yet but me and my followers. Earth Ascending was written in 1984 before anyone understood Epigenetics.

You can see the backward movement in this image. The bottom four harmonics are upside down. That’s a #20 along the left side and #13 across the top; 20 tribes of time or 20 A.A. and 13 Tones of Creation.

I’m studying this in alignment with three locations on the ribosome of the double helix that is added to the A.A. sequence: A site, P site, and E site. Once the RNA picks a site it’s copied into the helicase BACKWARD as fast as a jet plane. It’s shown in a couple videos I have, and I’ve posted it on here before. The scientists have seen the actual movement, but they don’t know what causes it…of course.

Then it goes to the mysterious Kinetochore where eventually it’s turned into a chromosome and then a nuclear pore with a nuclear membrane that breaks apart. I’ve watched the process several times.

Back to the ribosome, it comes from the mRNA (messenger RNA which is being utilized by the CV2 vaccine makers to program our RNA with God knows what. The mRNA moves like a computer program through the ribosome, through a few more steps, until it’s turned into tRNA or transfer RNA.

What are the three types of mRNA?

  • mRNA (messenger RNA): Produced during transcription.
  • rRNA (ribosomal RNA): Together with proteins, composes the ribosome, the organelles that are the site of protein synthesis.
  • tRNA (transfer RNA): Brings the correct amino acid to the ribosome during translation.

Once again, it seems to me the Tzolkin Harmonic Theme-plex is the tRNA that brings the correct amino acid to the ribosome during translation. Of course, all of this is dynamic evolution though and is never the same so that’s where the patterns I’ve observed come in such as the occult partner (your mother’s DNA) and the alpha and omega point placement. It’s not simple. In addition, the function of the G.A. P. kin is epic. That’s in the book as well.

I hate to tell the scientists this but none of it can be controlled. 98% of evolution is beyond any human or stellar species control. People experiment with it but I for one am not convinced that’s terribly wise. It depends on what they’re doing. Natural evolution is not the same, by far, as genetic experimentation on different species.

My point is the reverse transcriptase happens through the mRNA whose action is in synchronicity with the movement of the harmonic in the Psi Bank.

Synthetic AI DNA can be stored on a computer


DNA is not the same as Epigenetic RNA

DNA stored on a computer is pretty much a robot like Tesla’s Optimus. A computerized robot can’t utilize blood and evolve a body as we can, yet, but most importantly, clever men who are atheists can not create a soul. But they don’t believe in any of that, so I’m sure they’ll try. I’m examining this not advocating it but posting it, so you can examine it also.

The Source post is just an account on X; AI onwheels

https://x.com/AIOnWheelss/status/1718645808046739927?t=NBU9WBO_CltHeb2fqBwWeg&s=09

“Did you know the concept of #DNAStorage was envisioned by physicist Richard Feynman in 1959? It wasn’t until 2012 that this idea saw a groundbreaking realization at Harvard University. Geneticists George Church, Sri Kosuri, & their team encoded a 52,000-word book into DNA, using the DNA’s A, G, T, and C as binary codes! This marked the inception of a new era in data storage.

The journey continued with a significant milestone in 2019 when scientists encoded a massive 16GB text from the English Wikipedia into synthetic DNA. In 2021, the tech leaped forward with the creation of a custom DNA data writer, achieving a writing speed of 18 Mbps!

The promise? A gram of DNA could theoretically store a colossal 215 petabytes (215 million gigabytes) of data, heralding a new horizon in how we store and retrieve information. The convergence of biology & tech is not just a narrative of innovation but a testament to human ingenuity.

The future of data storage is intertwined with the essence of life – our DNA. #BioTech #DataRevolution“-END QUOTE

Lisa’s Response

Once again, this is a C@#$% hack via skull and bones Harvard, of the systems in the Maya Tzolkin Harmonic, which predate anything tech clever men have done by 26,000 years or more. But the harmonic is about dynamic, uncontrollable, freewill dominated RNA, the jelly-like stuff they call junk that is key to our evolution and destiny.

2012? That’s our time shift frequency, which began a new evolutionary cycle, so that was a hack by the wayward ones of our information. They know how to use HF33 to do it but will never fully get the information. Elon built 33 Raptor engines into his rocket. The names of his rockets are Raptor, Falcon, and Dragon. That’s no accident. Corey Goode says the Raptors are in charge of the planet in inner earth, the falcon is an archetype of Blue Eagle mediated by Jupiter, the home of the ICC, and the Dragon is The Draco. His mother is Red 1 Dragon. None of that scares me, and I still believe things can be brought right into safety, but there is much synchronicity around Tesla, whose motives, many people still question. I tend to trust people, but I’ve learned not to for whatever that’s worth.

52,000? That’s 26,000 × 2, an exponential, indigenous timing concept. Every 52 years, a kin begins a new life. 52-year cycles and adding zeros are very important in accurate timing frequency in our sector.

Again, DNA is only 2% of our genome and the trillion cells in our body. The rest is RNA that we are epigenetically in charge of.

Humans can be super awful, violent, and evil because of our brains and emotions, but we can also be lightworkers and artists, helpers, loving parents and mates, athletes, and dancers. We just have to each forgive off kilter, abusive members of our birth family and take charge of our lives and minds. No small feat, but people do it. My patients do. People need help and that’s what therapists are there for. Observing synchronicity and taking care of and loving your body is the ticket.

Love