Abstract

BackgroundFungal and animal mitochondrial genomes typically have one tRNA for each synonymous codon family. The codon-anticodon adaptation hypothesis predicts that the wobble nucleotide of a tRNA anticodon should evolve towards maximizing Watson-Crick base pairing with the most frequently used codon within each synonymous codon family, whereas the wobble versatility hypothesis argues that the nucleotide at the wobble site should be occupied by a nucleotide most versatile in wobble pairing, i.e., the tRNA wobble nucleotide should be G for NNY codon families, and U for NNR and NNN codon families (where Y stands for C or U, R for A or G and N for any nucleotide).ResultsWe here integrate these two traditional hypotheses on tRNA anticodons into a unified model based on an analysis of the wobble costs associated with different wobble base pairs. This novel approach allows the relative cost of wobble pairing to be qualitatively evaluated. A comprehensive study of 36 fungal genomes suggests very different costs between two kinds of U:G wobble pairs, i.e., (1) between a G at the wobble site of a tRNA anticodon and a U at the third codon position (designated MU3:G) and (2) between a U at the wobble site of a tRNA anticodon and a G at the third codon position (designated MG3:U).ConclusionIn general, MU3:G is much smaller than MG3:U, suggesting no selection against U-ending codons in NNY codon families with a wobble G in the tRNA anticodon but strong selection against G-ending codons in NNR codon families with a wobble U at the tRNA anticodon. This finding resolves several puzzling observations in fungal genomics and corroborates previous studies showing that U3:G wobble is energetically more favorable than G3:U wobble.

Highlights

  • Fungal and animal mitochondrial genomes typically have one tRNA for each synonymous codon family

  • The wobble versatility hypothesis [1,2,3,4,5,6], abbreviated as WVH, states that the wobble site of tRNA anticodon should have G for NNY codons because G can pair with both C and U in RNA, and should have U for NNR to pair with both A and G

  • The codon-anticodon adaptation hypothesis, or CAAH for short, invokes the codon usage bias as a determining factor, i.e., the wobble site of tRNA anticodon should co-evolve with codon usage so that the nucleotide in the wobble site of tRNA anticodon should match the most abundant codon in a synonymous codon family [6,13,14,15]

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Summary

Introduction

Fungal and animal mitochondrial genomes typically have one tRNA for each synonymous codon family. The codon-anticodon adaptation hypothesis predicts that the wobble nucleotide of a tRNA anticodon should evolve towards maximizing Watson-Crick base pairing with the most frequently used codon within each synonymous codon family, whereas the wobble versatility hypothesis argues that the nucleotide at the wobble site should be occupied by a nucleotide most versatile in wobble pairing, i.e., the tRNA wobble nucleotide should be G for NNY codon families, and U for NNR and NNN codon families (where Y stands for C or U, R for A or G and N for any nucleotide). The wobble versatility hypothesis [1,2,3,4,5,6], abbreviated as WVH, states that the wobble site of tRNA anticodon should have G for NNY codons (where Y stands for C or U and N for any nucleotide) because G can pair with both C and U in RNA, and should have U for NNR to pair with both A and G. The two traditional hypotheses, CAAH and WVH, will be shown to be special forms of WCH

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