4.5 Article

Stop Codon Usage as a Window into Genome Evolution: Mutation, Selection, Biased Gene Conversion and the TAG Paradox

Journal

GENOME BIOLOGY AND EVOLUTION
Volume 14, Issue 8, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evac115

Keywords

stop codon usage; translation termination; translational read-through; stop codon read-through; molecular evolution; genome evolution

Funding

  1. European Research Council [669207]
  2. European Research Council (ERC) [669207] Funding Source: European Research Council (ERC)

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The usage of the TGA stop codon in protein coding genes is influenced by G + C content, while TAA may be the universally optimal stop codon. Despite being influenced by mutation bias and selection, G + C pressure is the main determinant of trends in TGA usage between different species.
Protein coding genes terminate with one of three stop codons (TAA, TGA, or TAG) that, like synonymous codons, are not employed equally. With TGA and TAG having identical nucleotide content, analysis of their differential usage provides an unusual window into the forces operating on what are ostensibly functionally identical residues. Across genomes and between isochores within the human genome, TGA usage increases with G + C content but, with a common G + C -> A + T mutation bias, this cannot be explained by mutation bias-drift equilibrium. Increased usage of TGA in G + C-rich genomes or genomic regions is also unlikely to reflect selection for the optimal stop codon, as TAA appears to be universally optimal, probably because it has the lowest read-through rate. Despite TAA being favored by selection and mutation bias, as with codon usage bias G + C pressure is the prime determinant of between-species TGA usage trends. In species with strong G + C-biased gene conversion (gBGC), such as mammals and birds, the high usage and conservation of TGA is best explained by an A + T -> G + C repair bias. How to explain TGA enrichment in other G + C-rich genomes is less clear. Enigmatically, across bacterial and archaeal species and between human isochores TAG usage is mostly unresponsive to G + C pressure. This unresponsiveness we dub the TAG paradox as currently no mutational, selective, or gBGC model provides a well-supported explanation. That TAG does increase with G + C usage across eukaryotes makes the usage elsewhere yet more enigmatic. We suggest resolution of the TAG paradox may provide insights into either an unknown but common selective preference (probably at the DNA/RNA level) or an unrecognized complexity to the action of gBGC.

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