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Published on: November 12, 2012
Same-strand overlapping genes in bacteria: compositional determinants of phase bias
Niv Sabath1, Dan Graur, Giddy Landan
1Department of Biology and Biochemistry, University of Houston, Houston, TX 77204, USA. nsabath@uh.edu
A compositional model explains the phase bias in same-strand overlapping genes, showing initiation codon frequencies, not selection, drive this phenomenon. This provides a null model for studying gene evolution.
Area of Science:
- Genomics
- Molecular Biology
- Evolutionary Biology
Background:
- Same-strand overlapping genes exhibit a bias, with more phase-1 overlaps than phase-2 overlaps in bacterial genomes.
- Previous explanations involving genomic location or selection have limitations.
- A purely compositional model offers a more parsimonious explanation for this observed phase bias.
Purpose of the Study:
- To investigate whether codon composition explains the observed phase bias in same-strand overlapping genes.
- To test the hypothesis that frequencies of initiation and termination codons influence the number of overlapping genes.
Main Methods:
- Analysis of initiation- and termination-codon frequencies in bacterial genomes across different phases.
- Examination of amino acid frequencies and their relation to start codon formation.
- Correlation analysis between overlapping gene frequencies, codon usage, and genomic GC content.
Main Results:
- Initiation codons are significantly more abundant in phase 1 compared to phase 2.
- Termination codon frequencies do not significantly differ between phases.
- Amino acid frequencies and species-specific codon usage determine start codon frequencies, explaining the phase bias and correlating with GC content.
Conclusions:
- Compositional factors, specifically initiation codon frequencies, parsimoniously explain the phase bias in same-strand overlapping genes.
- The proposed model serves as a null model for neutral evolution, useful for testing selection hypotheses.
- This finding advances our understanding of the evolutionary mechanisms shaping gene organization.
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