Maximal Genetic Code Symmetry Is a Physicochemical Purine-Pyrimidine Symmetry Language for Transcription and Translation in the Flow of Genetic Information from DNA to Proteins.

Until now, research has not taken into consideration the physicochemical purine-pyrimidine symmetries of the genetic code in the transcription and translation processes of proteinogenesis. Our Supersymmetry Genetic Code table, developed in 2022, is common and unique for all RNA and DNA living species. Its basic structure is a purine-pyrimidine symmetry net with double mirror symmetry. Accordingly, the symmetry of the genetic code directly shows its organisation based on the principle of nucleotide Watson-Crick and codon-anticodon pairing. The maximal purine-pyrimidine symmetries of codons show that each codon has a strictly defined and unchangeable position within the genetic code. We discovered that the physicochemical symmetries of the genetic code play a fundamental role in recognising and differentiating codons from mRNA and the anticodon tRNA and aminoacyl-tRNA synthetases in the transcription and translation processes. These symmetries also support the wobble hypothesis with non-Watson-Crick pairing interactions between the translation process from mRNA to tRNA. The Supersymmetry Genetic Code table shows a specific arrangement of the second base of codons, according to which it is possible that an anticodon from tRNA recognises whether a codon from mRNA belongs to an amino acid with two or four codons, which is very important in the purposeful use of the wobble pairing process. Therefore, we show that canonical and wobble pairings essentially do not lead to misreading and errors during translation, and we point out the role of physicochemical purine-pyrimidine symmetries in decreasing disorder according to error minimisation and preserving the integrity of biological processes during proteinogenesis.

The Evolution of Life Is a Road Paved with the DNA Quadruplet Symmetry and the Supersymmetry Genetic Code.

Symmetries have not been completely determined and explained from the discovery of the DNA structure in 1953 and the genetic code in 1961. We show, during 10 years of investigation and research, our discovery of the Supersymmetry Genetic Code table in the form of 2 × 8 codon boxes, quadruplet DNA symmetries, and the classification of trinucleotides/codons, all built with the same physiochemical double mirror symmetry and Watson-Crick pairing. We also show that single-stranded RNA had the complete code of life in the form of the Supersymmetry Genetic Code table simultaneously with instructions of codons' relationship as to how to develop the DNA molecule on the principle of Watson-Crick pairing. We show that the same symmetries between the genetic code and DNA quadruplet are highly conserved during the whole evolution even between phylogenetically distant organisms. In this way, decreasing disorder and entropy enabled the evolution of living beings up to sophisticated species with cognitive features. Our hypothesis that all twenty amino acids are necessary for the origin of life on the Earth, which entirely changes our view on evolution, confirms the evidence of organic natural amino acids from the extra-terrestrial asteroid Ryugu, which is nearly as old as our solar system.

Novel look at DNA and life-Symmetry as evolutionary forcing.

After explanation of the Chargaff´s first parity rule in terms of the Watson-Crick base-pairing between the two DNA strands, the Chargaff´s second parity rule for each strand of DNA (also named strand symmetry), which cannot be explained by Watson-Crick base-pairing only, is still a challenging issue already fifty years. We show that during evolution DNA preserves its identity in the form of quadruplet A+T and C+G rich matrices based on purine-pyrimidine mirror symmetries of trinucleotides. Identical symmetries are present in our classification of trinucleotides and the genetic code table. All eukaryotes and almost all prokaryotes (bacteria and archaea) have quadruplet mirror symmetries in structural form and frequencies following the principle of Chargaff's second parity rule and Natural symmetry law of DNA creation and conservation. Some rare symbionts have mirror symmetry only in their structural form within each DNA strand. Based on our matrix analysis of closely related species, humans and Neanderthals, we find that the circular cycle of inverse proportionality between trinucleotides preserves identical relative frequencies of trinucleotides in each quadruplet and in the whole genome. According to our calculations, a change in frequencies in quadruplet matrices could lead to the creation of new species. Violation of quadruplet symmetries is practically inconsistent with life. DNA symmetries provide a key for understanding the restriction of disorder (entropy) due to mutations in the evolution of DNA.

Codon and Reverse Codon: A Theoretical Approach to Reinterpret the Genetic Code Table.

The genetic code table represents a fundamental scheme to translate a genetic code into a sequence of amino acids and, therefore, the possibility of operating the synthesis of all the proteins necessary for the life of organisms. Unfortunately, the various biological mechanisms are not fully clear. Hence, in this report, we analyzed the genetic code table and the amino acids codified by codons with an original theoretical and statistical approach based on the concept of permutations. We found an interesting reinterpretation of many codons, as reverse codons, which could help clarify some as-yet-unknown aspects in the field of protein folding.

Arguments against the stereochemical theory of the origin of the genetic code.

I support the hypothesis that stereochemical theory is unnatural because it is based on artificial and not simple mechanisms as required for a good theory. Indeed, for stereochemical theory the origin of the genetic code requires, in the first place, a primary interaction, for example, between a codon and an amino acid on a proto-tRNA. But this interaction is a necessary but not sufficient condition, because the evolution of the mRNA molecule, which would really define the genetic code, is still necessary for the complete origin of the genetic code. In other words, the need for two molecules, tRNA and mRNA, to define the genetic code, with their at least partial independence would testify to an artificial mechanism typical of stereochemical theory because it would not guarantee that amino acid-codon (or -anticodon) assignments realized in the first phase of the origin of the genetic code, would necessarily be maintained also in the second phase of its completion. Furthermore, the genetic code encodes for amino acids but amino acids are not the truly functional aspect, they are only intermediaries, of their final products, proteins, which are the only true entities actually coded by genes. Therefore, it would not be immediately clear from the point of view of stereochemical theory, to say why it is the amino acids and not the proteins that are involved in the primary stereochemical interactions that would have led to the origin of the genetic code. Hence, at least some of the stereochemical theory models would be not very credible, not being able to say much about the coding of proteins by genes. Finally, I inspected the genetic code table following the logic that more closely similar amino acids should - according to stereochemical theory - be coded by highly similar codons, finding that only a few pairs of amino acids actually satisfy this logic, further discretizing the stereochemical theory.