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Updated: May 22, 2025

Identifying Amino Acid Overproducers Using Rare-Codon-Rich Markers
Published on: June 24, 2019
Genomic AT Bias Coupled with Amino Acid Metabolism Modulates Codon Usage.
Lucio Aliperti Car1, Ignacio E Sánchez2
1Instituto de Química Biológica de La Facultad de Ciencias Exactas y Naturales (IQUIBICEN), Facultad de Ciencias Exactas y Naturales, Laboratorio de Fisiología de Proteínas, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires, Argentina.
This study introduces a simplified model for genome evolution, explaining codon and amino acid proportions using GC content and metabolic costs. The model reveals an entropy-cost trade-off influencing genomic features across diverse organisms.
Area of Science:
- Genomics
- Evolutionary Biology
- Bioinformatics
Background:
- Genome evolution results in specific codon and amino acid proportions.
- Genomic GC (guanine + cytosine) content influences these proportions.
Purpose of the Study:
- To develop a simplified maximum entropy model for predicting codon and amino acid abundances.
- To account for genomic GC content and metabolic costs in genome evolution.
Main Methods:
- A maximum entropy model was created, grouping codons by GC content and amino acid.
- The model incorporates codon cost based on genomic GC content and amino acid metabolic cost.
- Analysis was performed on over 50,000 genomes using seven interpretable parameters.
Main Results:
- Both codon and amino acid costs are crucial for accurate abundance predictions.
- The optimal model suggests a universal equilibrium genomic GC content below 50%.
- Amino acids were grouped based on Watson-Crick base pairing strength (GC vs. AU), indicating differential GC-dependent selection.
Conclusions:
- An entropy-cost trade-off explains how organisms solve the genome encoding problem for a given GC content.
- Empirical boundaries of this trade-off suggest minimum amino acid and codon entropies.
- These findings may impose limits on the GC content observed in natural genomes.
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