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Synonymous but not silent: functional codon bias reveals decoupled mitonuclear evolution in parasitic worms
Kanhu Charan Das1, Ruchishree Konhar2, Devendra Kumar Biswal1,2
1Department of Zoology, North-Eastern Hill University, Shillong, Meghalaya, 793022, India.
Codon usage bias in parasites is shaped by mutation and selection. Mitochondrial genomes favor AT-rich codons, while nuclear genomes optimize codons for efficient protein production, especially in essential genes.
Area of Science:
- Evolutionary Biology
- Genomics
- Parasitology
Background:
- Codon usage bias arises from a balance between mutational pressure and translational selection.
- The distinct evolutionary pressures on mitochondrial and nuclear genomes regarding codon bias are not fully understood.
Purpose of the Study:
- To comparatively analyze codon usage bias drivers in mitochondrial and nuclear genomes of parasitic helminths.
- To investigate the interplay of mutational and selection forces on synonymous codon usage in parasites.
Main Methods:
- Comparative genomic analysis of 120 parasitic helminths (Platyhelminthes and Nematoda).
- Integration of mitochondrial genome data with matched nuclear transcriptome data.
- Analysis of codon optimization patterns in relation to gene expression and functional importance (e.g., oxidative phosphorylation subunits).
Main Results:
- Mitochondrial genes show an AT-rich bias driven by mutational factors.
- Nuclear codon preferences correlate with gene expression, favoring optimal codons in highly expressed genes.
- Selection for codon optimization is evident in essential oxidative phosphorylation genes across both genomes, with variations indicating lineage-specific strategies.
Conclusions:
- Synonymous codon usage in parasites reflects functional adaptation relevant to parasite biology and control.
- Parasites exhibit diverse evolutionary strategies for respiratory system assembly, involving both mitonuclear coadaptation and compartmental decoupling.
- Understanding codon usage bias provides insights into parasite evolution and potential targets for control.
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