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Correlation between Shine--Dalgarno sequence conservation and codon usage of bacterial genes.
1Laboratory for Bioinformatics, Keio University, 5322 Endo, Fujisawa, 252-8520, Japan.
Journal of Molecular Evolution
|March 7, 2001
Summary
This study reveals a link between codon usage bias and Shine-Dalgarno sequence conservation in prokaryotes. Higher codon adaptation index (CAI) values correlate with more conserved SD sequences, impacting translation efficiency.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- Codon usage bias influences gene expression.
- Shine-Dalgarno (SD) sequences are crucial for translation initiation in prokaryotes.
- Understanding the relationship between codon bias and SD sequence conservation can elucidate translation regulation.
Purpose of the Study:
- To investigate the correlation between codon usage bias and SD sequence conservation across nine prokaryotic genomes.
- To determine if this correlation varies among different prokaryotic species.
Main Methods:
- Calculated codon usage bias using the codon adaptation index (CAI).
- Assessed SD sequence conservation by aligning predicted SD motifs with 5' untranslated region (5'UTR) sequences.
- Analyzed complete genome sequences of nine prokaryotes.
Main Results:
- A clear correlation between CAI values and SD sequence conservation was observed in *Escherichia coli*, *Bacillus subtilis*, *Haemophilus influenzae*, *Archaeoglobus fulgidus*, *Methanobacterium thermoautotrophicum*, and *Methanococcus jannaschii*.
- Genes with higher CAI values showed more conserved SD sequences in these organisms.
- No significant relationship was found in *Mycoplasma genitalium*, *Mycoplasma pneumoniae*, and *Synechocystis*.
Conclusions:
- Codon usage bias and SD sequence conservation are linked in many prokaryotes, suggesting a co-evolutionary relationship.
- This correlation likely impacts translation initiation and overall translation efficiency.
- Species-specific variations in this correlation highlight diverse regulatory strategies in prokaryotic gene expression.