# Forbidden codon combinations in error-detecting circular codes

**Authors:** Elena Fimmel, Hadi Saleh, Lutz Strüngmann

PMC · DOI: 10.1007/s12064-024-00431-6 · Theory in Biosciences · 2024-12-15

## TL;DR

This paper introduces a new software tool to construct special genetic codes called circular codes, using mathematical theorems to exclude certain codon combinations.

## Contribution

A novel software tool for constructing self-complementary circular codes using mathematical theorems to exclude forbidden codon combinations.

## Key findings

- A systematic approach using two mathematical theorems to exclude codons in constructing circular codes.
- The software provides an efficient method for building self-complementary C³-codes of maximum size.
- The approach sheds light on the mathematical foundations of these codes.

## Abstract

Circular codes, which are considered as putative remnants of primaeval comma-free codes, have recently become a focal point of research. These codes constitute a secondary type of genetic code, primarily tasked with detecting and preserving the normal reading frame within protein-coding sequences. The identification of a universal code present across various species has sparked numerous theoretical and experimental inquiries. Among these, the exploration of the class of 216 self-complementary \documentclass[12pt]{minimal}
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				\begin{document}$$C^3$$\end{document}C3-codes of maximum size 20 has garnered significant attention. However, the origin of the number 216 lacks a satisfactory explanation, and the mathematical construction of these codes remains elusive. This paper introduces a new software designed to facilitate the construction of self-complementary \documentclass[12pt]{minimal}
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				\begin{document}$$C^3$$\end{document}C3-codes (of maximum size). The approach involves a systematic exclusion of codons, guided by two fundamental mathematical theorems. These theorems demonstrate how codons can be automatically excluded from consideration when imposing requirements such as self-complementarity, circularity or maximality. By leveraging these theorems, our software provides a novel and efficient means to construct these intriguing circular codes, shedding light on their mathematical foundations and contributing to a deeper understanding of their biological significance.

## Full-text entities

- **Genes:** DOCK11 (dedicator of cytokinesis 11) [NCBI Gene 139818] {aka ACG, ADMIDX, ZIZ2, bB128O4.1}, CAT (catalase) [NCBI Gene 847]
- **Chemicals:** Cytosine (MESH:D003596), Poly-U (MESH:D011072), acids (MESH:D000143), phenylalanine (MESH:D010649), Guanine (MESH:D006147), AGC (-), Thymine (MESH:D013941), amino acids (MESH:D000596), U (MESH:D014501), Uracil (MESH:D014498), Adenine (MESH:D000225)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC11802632/full.md

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Source: https://tomesphere.com/paper/PMC11802632