The Genetic Code and Protein Synthesis: by Chance, Mutations, Natural Selection, or Intelligence?

 

Since the introduction of cell theory in 1838, our understanding of biological cells and their functions has expanded significantly. Ongoing research has revealed critical insights into cellular components such as proteins, biological machines, DNA structure, the genetic code and its involvement in protein synthesis, RNA and its roles, protective mechanisms, and cell signaling. The complexity inherent in these systems raises a fundamental question about their origins. Part 1 will address the genetic code and the process of protein synthesis, while Part 2 will consider whether random events, mutation, natural selection, or intelligence provide the most plausible explanation for the emergence of such complexity. This discussion excludes evolutionary hypotheses that lack substantive evidential support.

Part 1 – The Genetic Code and Protein Synthesis

Proteins and the genetic code

Proteins are vital components of all living organisms, playing indispensable roles in nearly every biological process, such as cell division, the synthesis of other proteins, structural support of cells and tissues, digestion, speeding up chemical reactions, cell signaling, the immune system, channels to allow particular substances in and out of the cell, and transport of things within and between cells. [1][2][3][4] Each protein is encoded by DNA and RNA through a nearly universal genetic code conserved in all organisms, with few exceptions. [5][6][7] Structurally, proteins are formed of extensive chains of amino acids joined by peptide bonds. Notably, only 20 distinct amino acids of the roughly 500 amino acids in nature [8] are routinely found in protein molecules. Of these 20 amino acids, 11 are synthesized endogenously by the human body; the remaining 9 either cannot be produced in adequate amounts or at all, needing their acquisition through dietary intake. [9] Chirality, which will be addressed in detail later in this article, plays a vital role in the structure and function of proteins and other biomolecules.[10]

The precise number of different protein types present in the human body is still uncertain, though prevailing estimates range from approximately 20,000 to over 100,000. [11][12] Titin, recognized as the largest protein in humans, includes more than 34,000 amino acids and plays a critical role in muscle elasticity, functionality, and stability. [13][14][15] In comparison, the smallest protein in the human body has 44 amino acids. [16] Proteins typically are 300 to 500 amino acids in length. [17] The largest documented protein, found in the golden algae Prymnesium parvum, consists of 45,212 amino acids. [18]

Chromosomes, DNA and RNA

A chromosome is a thread-like structure made of a single molecule of deoxyribonucleic acid (DNA) coiled around proteins. All animal and plant cells have chromosomes - the number, size and shape vary among organism types. Humans normally have 23 pairs of linear chromosomes, each made up of lengthy DNA strands that are coiled tightly around histone proteins.

DNA has a double helix structure, resembling a twisted ladder. Its sides are made of alternating deoxyribose sugar and phosphate, while its rungs are composed of paired bases. A nucleotide is a subunit of DNA or RNA composed of one sugar, one phosphate group, and one base. DNA has four bases: adenine (A), thymine (T), cytosine (C), and guanine (G). Adenine pairs only with thymine, and cytosine pairs only with guanine, which supports the molecule's stability. In total, there are approximately 3.2 billion bases in the human genome. [19] Histones are essential for the structural organization of DNA – compaction to fit in the cell, gene expression.

Ribonucleic Acid (RNA), unlike DNA, consists of a single strand, uses ribose sugar instead of deoxyribose, has uracil (U) in place of thymine, and is not coiled around proteins. Because of these differences, RNA is structurally much less stable than DNA.

In animal, plant, fungal, and protist cells, DNA is almost exclusively housed within a specialized compartment - the nucleus. [20] RNA resides both in nucleus and cytoplasm of biological cells.

The Genome and the Genetic Code

The genome encompasses all genetic material contained within an organism's DNA. In humans, approximately 1–2% of this DNA, known as coding DNA, handles encoding proteins via the genetic code, while the remaining 98–99%, referred to as non-coding DNA, does not directly code for proteins or use the genetic code. Non-coding DNA instead contributes significantly to the regulation of gene expression, supports RNA synthesis, and maintains the structural integrity of the genome. According to research by ENCODE published in September 2012, 80.4% of the human genome shows functionality in at least one cell type. [21] [22] ENCODE’s leading analyst coordinator, Ewan Birney, said “it’s likely that 80 percent will go to 100 percent.” [23] Various biological science entities define "functional" in diverse ways.

The genetic code provides the directives for the order in which amino acids are assembled into proteins. In the code, each nucleotide is denoted by one of the bases — C, A, G, T, or U. Sequences of three nucleotides, known as codons, specify individual amino acids or serve as stop signals during protein synthesis. For instance, the codons UUA, UUG, CUU, CUC, CUA, and CUG all specify leucine, while AUG exclusively encodes methionine, which typically starts protein synthesis but may be cleaved later.[24] The stop codons UAG, UAA, and UGA serve as termination signals in translation, marking the end of polypeptide elongation rather than coding for amino acids.

How is the genetic code transcribed to messenger RNA?

“Transcription is highly regulated through promoter sequences, enhancers, repressors, transcription factors, and epigenetic modifications.” [25]

Before the genetic code is translated into a protein, it must first undergo transcription into messenger RNA (mRNA). This process is helped by an RNA polymerase enzyme, with support from a transcription factor protein and a helicase enzyme. Initially, RNA polymerase binds to the gene’s promoter region, found at once upstream of the coding sequence; however, transcription cannot begin until both the transcription factor and helicase are properly positioned. The transcription factor ensures that transcription initiates at the correct site on the gene and regulates gene expression in response to various signals. Upon receiving an activation signal, helicase begins unwinding and separating the DNA into coding and template strands moving in the 5’ to 3’ direction. [a] RNA polymerase then follows on the template strand in the 5’ to 3’ direction, synthesizing a complementary precursor mRNA strand from the exposed template strand, substituting uracil (U) for thymine (T). [b] While transcription proceeds, the coding and template strands rejoin behind. As it transcribes, RNA polymerase not only adds complementary nucleotides to the growing RNA strand but also employs several mechanisms to proofread and correct any errors. It continues this process until it meets a terminator sequence that marks the end of transcription.

The direction of transcription is critical as transcription in the reverse direction will reverse the letters in the genetic code. In most cases, this will cause the wrong amino acid to be placed in the wrong position in the protein chain. For example, UCC codes for serine but CCU codes for proline. [26]

Right after precursor mRNA is synthesized, a 5’ cap is added to shield it from enzymes that could break it down and provide crucial binding to the ribosome. The next step is splicing. Some genes in nuclear cells have introns, which are noncoding regions situated between exons, the segments that code for proteins. When the mRNA is created, these introns are transcribed along with the exons into the precursor mRNA and must be removed; otherwise, the genetic information will not translate accurately. Splicing removes the introns. Splicing takes place inside the nucleus through a series of reactions conducted by the spliceosome, which consists of small nuclear ribonucleoproteins (snRNPs). [27] There are also some introns that can splice themselves. [28] Then, precursor mRNA is finished into mature mRNA with the addition of a polyadenine tail on the 3’ end to protect it from degrading enzymes.

Protein synthesis is an energy demanding process. Adenosine Triphosphate (ATP) and Guanosine Triphosphate (GTP) are the primary sources of this energy.

How is mRNA translated to proteins?

Once a mature mRNA has been synthesized, it is transported (through a nuclear pore in eukaryotes) to a ribosome, a large molecular machine, where translation takes place.

The ribosome forms around the start codon (AUG) during initiation of translation and the first tRNA carrying the amino acid methionine binds to the start codon. Ribosomes translate the mRNA codons in the 5’ to 3’ direction. As the ribosome moves along the mRNA strand, each transfer RNA (tRNA) molecule—carrying both its specific amino acid and an anticodon loop—recognizes and binds to matching codons on the mRNA. [29] (Typically, there are 20 different tRNA molecules, one for each amino acid.) In this way, tRNAs deliver their amino acids in the precise order specified by the mRNA's codon sequence. [30] Before continuing to the next codon, the ribosome facilitates a peptide bond between the amino acids. Translation proceeds in this manner until meeting a stop codon and after a short pause, the tRNAs and the completed protein are cleaved off into the cytoplasm.[31]

In nucleated cells, up to ten million ribosomes may exist within the cytoplasm. [32] Ribosomes themselves typically consist of three or four ribosomal RNA molecules, along with approximately 40 to 80 distinct ribosomal proteins. [33]

A subset of proteins emerges from the ribosome requiring further conformational modification to achieve functionality. This final folding process is helped by molecular chaperones, which are themselves proteins that rely on ATP for energy. Various chaperone molecules are used depending on the specific protein and the cellular environment.

 

Part 2 – Evaluating the Evidence

Did the genetic code result from intelligence?

Codes are generated through deliberate and intelligent actions designed to achieve specific goals. Some examples of this include:

1.   Language can be conceptualized as a system of codes, using words or characters as symbols to stand for ideas, objects, or actions.[34] It is governed by grammatical rules that decide how these symbols may be structured to convey meaning. Communication through language entails encoding thoughts into linguistic forms and then decoding them by the listener or reader to extract meaning. [35]The origins of language are debated, but most agree it appeared through cognitive processes rather than chance. In biblical accounts, God spoke creation into existence, Adam and Eve used language, and all people originally shared a single language before the Tower of Babel.

2.    International Morse code, a system of dots, dashes, and spaces used in telecommunications to encode Latin letters and Indo-Arabic numerals was preliminarily proposed by Samuel Morse, developed by Alfred Vail, and revised by Friedrich Gerke. [36][37]

3.    During World War II, Nazi Germany used an advanced cipher machine with rotating wheels and a plugboard to encrypt and decrypt messages by turning plain text into code. This machine was conceived, designed, and constructed by intelligent people.

4.    Password and ID generators do not rely solely on chance; they are purposefully crafted through thoughtful design and development. Even though many programming languages offer built-in functionalities for generating random codes, these capabilities are the result of deliberate work by skilled professionals.

5.   Artificial intelligence (AI) does not always require human intelligence to function, but it could not exist without planning, coding algorithms by programmers, gathering of data, and training models. [38]   

Also, the genetic code holds information necessary for synthesis of proteins, the building blocks of all life. And information according to information laws requires an intelligent sender. [39][40][41] 

Why is there a genetic code and what are its implications?

The genetic code plays a vital role in the complex cellular processes that generate the many proteins essential for life. It holds instructions to create potentially over 100,000 different proteins, with at least one chain composed of tens of thousands of amino acids. However, these instructions depend on specific biological systems to transcribe, transmit, and translate them; without this machinery, the information is ineffective. Constructing such a system required planning and anticipation, qualities defined as the ability to foresee and prepare for future requirements [42]. Chemicals alone lack the capacity for foresight or thought. Achieving this level of complexity is possible only through cognitive reasoning by an intelligent designer.

The chirality problem

Chiral molecules are characterized by their inability to align perfectly with their mirror images. These two unique, non-superimposable forms are called enantiomers and are categorized as “left-handed” (L) and “right-handed” (D) types of chirality.

All types of biomolecules display homochirality, which means they have consistent handedness. This applies to amino acids (except glycine), proteins/enzymes, sugars, and nucleotides. In living systems, most amino acids are L-chiral, with glycine being the exception because it is not chiral. Proteins are built from these L-chiral amino acids. Sugars usually have D-chirality, with only a few exceptions, and nucleotides also generally show D-chirality. However, during transcription, nucleotides can temporarily shift to L-chirality due to torsional strain. [43]Homochirality “is essential for the proper functioning of biological processes.” [44] Some ways that chirality affects biological processes:

1.      Chirality plays an essential role in biological systems by allowing molecules to align precisely with specific binding sites, such as those within enzymes that help biochemical reactions. This exact correspondence contributes to the accuracy and efficiency of vital biological processes, including metabolism and genetic information transfer. [45]

2.     Except for glycine, all amino acids used in proteins have D-chirality. “If a protein were built with a mix of L- and D- amino acids, it would be unable to fold into the precise three-dimensional shape necessary for biological function.” [46] Glycine, being achiral, allows proteins to fold with sharper turns. Additionally, the precise order of amino acids decides both how accurately a protein folds and its biological effectiveness.

3.      “DNA could not be stabilized in a helix if even a single wrong-handed monomer were present, so it could not form long chains. This means it could not store much information, so it could not support life.”[47]

4.      D-chiral sugars are vital for enzyme and receptor recognition affecting metabolism. [48]

“It is a scientifically verifiable fact that a random chance process, which forms a chiral product, can only be a 50/50 mixture of the two optical isomers. There are no exceptions.” [49] The origin of homochirality in living things continues to be an important topic for evolutionary scientists. The possibility that intelligence engaged in creating homochirality cannot be eliminated.

Is it possible for all proteins essential to life to originate by chance?

While experiential evidence suggests that highly improbable events may occur, the likelihood of some outcomes is so minimal that it is reasonable for rational individuals to disregard them in their deliberations.

“(I)f every event in the universe over its entire history were devoted to producing combinations of amino acids of the correct length in a prebiotic soup” there would be “roughly 1 out of a trillion trillion - of the total number of events needed to have a 50 percent chance of generating … any functional protein of modest length.” [50]

A cell forming by chance requires “at least one hundred functional proteins” forming “simultaneously in one place.”   An estimated probability of this happening is 1/102000 [51]

The probability of all essential proteins for an organism arising by random processes is exceedingly small, which shows that their presence may be attributable to alternative factors.

Was the genetic code formed through natural selection or mutation?

Natural selection has no consciousness and therefore no foresight. It only functions by selecting among the genetic information that is already there to adapt to environments. In the process no added information is available, but some information is lost.

Mutations do not lead to evolution but devolution where information is corrupted which usually results in decreased functions.

“For any conceivable favorable mutation, a species must pay the price or bear the burden of more than 1000 harmful mutations of the gene... As mutational load increases with time, the survival of the species will be threatened as matings produce a greater percentage of offspring carrying serious genetic defects.” [52]

Since genetic information is continually degraded or lost, it's logical to think that it was once in a better state, like how a wound-up clock gradually runs down over time. Mechanisms exist to protect the genetic code from mutations.

What cellular mechanisms exist to safeguard genetic information, and what are the broader implications of these protective processes?

Corrupted genetic information can lead to genetic disorders including cancers. The cell employs various mechanisms to protect its genetic information and remove errors and replace them with the correct components including:

1.      The genetic code is “arranged to minimize error in protein sequences and structure.” [53]

2.      Cells use strategies to exclude molecules with incorrect chirality, such as L-chiral sugars and D- chiral amino acids, from their internal processes.

3.     During replication, DNA polymerase conducts proofreading to detect errors and stops while errors are being corrected before continuing.

4.      In eukaryotes (cells with a nucleus), the genetic material in the nucleus is protected by a double membrane, while nuclear pores control the passage of molecules between the cytoplasm and nucleoplasm.

5.     DNA repair incorporates a collection of cellular mechanisms dedicated to finding and correcting damage in DNA molecules that encode the genome [54]. Each cell daily experiences 10,000 to 1,000,000 individual molecular lesions in its DNA. [55] [56] DNA repair is therefore needed constantly during the life of the cell.

6.      During transcription, RNA polymerase employs various mechanisms to proofread and correct errors.

7.      Messenger RNA undergoes capping and receives a polyadenine tail to safeguard it from enzymatic degradation.

8.    The genetic code has degeneracy whereby multiple codons code for the same amino acid. This redundancy adds an added layer of protection as certain codon errors will not cause the wrong amino acid to be substituted into the protein chain.

The creation of cellular mechanisms that safeguard genetic information involve foresight as their existence results from the anticipation of future harm unless certain actions are prepared and started. Foresight, as said earlier, requires intelligence.

Which originated first: proteins, the genetic code, or were both set up simultaneously?

Currently, genetic information encoded in DNA is transcribed by proteins into messenger RNA (mRNA), which is then conveyed to ribosomes—complexes composed of ribosomal proteins and ribosomal RNA—for translation into proteins with the aid of transfer RNA. The synthesis of proteins today requires homochirality, the genetic code, DNA, RNA, pre-existing proteins, the right amino acids, and energy. For functional protein synthesis to take place in the distant past, all the necessary components had to be present. If these components were added gradually over billions of years as some evolutionists hypothesize, no biological proteins would form until every part was available; thus, it is argued that all components must have come together simultaneously, suggesting intelligent design. It is also important to note that needing existing proteins to form the first protein seems contradictory and almost impossible to explain scientifically—it could even be considered a miracle.

What does a nearly universal genetic code for proteins across all organisms today imply?

The fact that there is a nearly universal genetic code, with few exceptions, does not imply that all organisms have a common ancestor; that is merely an evolutionary assumption. [57][58][59] Considering the evidence that codes come from intelligence, what should be clear is that all organisms had a common intelligent designer who varied the code in those few cases where it was helpful.

Conclusions

The genetic code has been proposed as evidence of an intelligent origin, based on arguments that information-bearing codes are exclusively the product of intelligent entities. Additionally, it is suggested that the complexity of protein synthesis requires foresight, defined as the ability to anticipate and plan for future requirements, which entails cognitive processes typically associated with intelligence. Mechanisms such as random chance, mutation, and natural selection are regarded as lacking foresight and, therefore, considered inadequate for independently assembling all necessary components for protein synthesis.

Effective protein synthesis mandates the simultaneous presence of homochirality in biological chemicals, DNA, RNA, the genetic code, various proteins, appropriately matched amino acids, biological machinery for transcription, transportation, and translation of the genetic code into proteins, protective systems against errors, and sufficient energy sources all within a single location. The absence of any one part prevents the occurrence of protein synthesis, challenging theories that support incremental evolutionary development over lengthy periods. Moreover, the intricate biological mechanisms and processes involved in protein synthesis often require more than intelligence alone; they present a paradox wherein existing proteins are needed to produce new proteins, prompting inquiry into how first protein formation could occur without significant intervention.

 

Notes:

[a] The 5’ end is the end with a phosphate group and the 3’ end is the end with a hydroxyl group.

[b] The U for T substitution in mRNA performs an important function as it aids in the breakdown of the messenger RNA after translation.

Picture:

(a) By Zephyris - Own work, CC BY-SA 3.0, via Wikipedia Commons

References:

[1] “Human Nutrition: 2020 Edition, Defining Protein,” Press Books, viewed internet December 31, 2025

[2] “Cell signaling,” Wikipedia, viewed on internet January 20, 2026

[3] Alikiotis, A, “Protein Power: Fighting Disease And Building Health, MedShun, March 27, 2025

[4] “What is the function of proteins?” Cleveland Clinic, viewed on internet December 19, 2025

[5] “The Genetic Code,” lumen, viewed on internet January 16, 2026

[6] Lisle, J, “Creation 101: Genetics, Biblical Science Institute, September 8, 2017

[7] “Genetic code,” Wikipedia, viewed on internet January 30, 2026

[8] “Amino Acids: The Building Blocks OF Proteins,” MedShum, March 30, 2025

[9] “Human Nutrition: 2020 Edition, Defining Protein,” Press Books, viewed internet December 31, 2025

[10] Biochemistry Den, “Chirality of Amino Acids: Enantiomers, Differences, and Importance in Biology, Biochem Den, February 20,2025

[11] “Protein,” Wikipedia, viewed on internet January 23, 2026

[12] “Human Nutrition: 2020 Edition, Defining Protein”

[13] “Molecule of the Month: Titan,” PDB-101, viewed on internet October 13, 2025

[14] “The Largest Protein’s Amino Acid Composition,” MedShum, April 2, 2025

[15] “Titin Protein Structure and Its Role in Muscle Function,” biologyinsights.com, July 30, 2025

[16] “The Largest Protein’s Amino Acid Composition”

[17] Ibid.

[18] “Massive genes allow golden algae to synthesize its toxin,” U.S. National Science Foundation, August 8, 2024

[19] “DNA repair,” Wikipedia, viewed on internet January 27, 2026

[20] “Can DNA Leave the Nucleus? The Exceptions Explained,” biologyinsights.com, August 18, 2025

[21] “Encode,” Wikipedia, viewed on internet February 1, 2026

[22] “Biochemical functions for most of human genome identified: New map finds genetic regulatory elements account for 80 percent of our DNA,” ScienceDaily, source Massachusetts Institute of Technology, September 5, 2012

[23] Tomkins, J, “Pervasive Genome Functionality Destroys the Myth of Junk DNA,” The Institute for Creation Research, August 29, 2025

[24] Thomas, D, “Evolution’s fatal problem of non-standard genetic codes,” creation.com, viewed on internet November 26, 2025

[25] Helmenstine, A, “Transcription in Biology – Steps, Functions, Regulation,” Science Notes, updated December 2, 2025

[26] Thomas

[27] “RNA splicing,” Wikipedia, viewed on internet December 29. 2025

[28] Ibid.

[29] “What Happens to mRNA After It Completes Transcription?” biologyinsights.com, September 1, 2025

[30] Ibid.

[31] “The End of Translation: stop codons looking for something they cannot find,” Passel, University of Nebraska, viewed internet January 21, 2026

[32] “ribosome.” Britannica, viewed on internet December 29, 2025

[33] Ibid.

[34] From information gathered by copilot.

[35] From information gathered by copilot.

[36] “Morse code,” Wikipedia, viewed on internet, January 29, 2026

[37] “Morse code,” Britannica, viewed on internet, January 29, 2026

[38] Shah, S, “How is AI Created? Unveiling the Secrets Behind Algorithms, Data, and Real-World Applications,” Yeti AI, viewed on internet.

[39] Gitt, W, “Life Requires a Source of Information,” Answers in Genesis, viewed on internet January 29, 2026

[40] Helmenstine, A, “Transcription in Biology – Steps, Functions, Regulation,” Science Notes, updated December 2, 2025

[41] “DNA Was Created as a Reservoir for the Information of Life,” Institute for Creation Research, viewed on internet December 6, 2025

[42] Oxford American Dictionary, Heald College Edition, (New York, New York, Avon Books, 1980)

[43] “What Is DNA Chirality? Right-Handed vs. Left-Handed,” Scienceinsights, November 10,2025

[44] “What is a Chiral Molecule and Why Does It Matter?” biologyinsights.com, July 31, 2025

[45] Ibid.

[46] “What is Chirality and Why Does it Matter?” Scienceinsights, viewed on internet October 14, 2025

[47] Sarfati, J, “Origin of life: the chirality problem,” Creation.com, September 24, 2024

[48] Mukhopadhyay, M, “Carbohydrate Stereochemistry: A Complete Guide for Students,” Bio Tech Beacons, September 3, 2025

[49] McCombs, C, “Evolution Hopes You Don’t Know Chemistry: The Problem with Chirality,” The Institute for Creation Research, May 1, 2004

[50] Meyer, Stephen C., Signature in the Cell, (New YorkHarperCollins Publishers, 2009), 218

[51] Denton, Michael, Evolution: A Theory in Crisis (Maryland: Adler & Adler, Publishers, Inc.,1985), 323

[52] Parker, G, EdD, “Creation, Mutation, and Variation,” The Institute of Creation Research, November 1, 1980

[53] “DNA Was Created as a Reservoir for the Information of Life,” Institute for Creation Research, viewed on internet December 6, 2025

[54] “DNA repair”

[55] Ibid.

[56] Alhmoud, J., Woolley, J, et al., “DNA Damage/ Repair Management in Cancers,” NLM, April 23, 2020, internet

[57] Thomas

[58] Lisle

[59] “Understanding the Universality of the Genetic Code – Key Insights into the Fundamental Principles of Life,” Science of Bio Genetics, December 20, 2023

 

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