Abstract

Although the genetic code is degenerate, synonymous codons for the same amino acid are not translated equally. Codon-specific translation is important for controlling gene expression and determining the proteome of a cell. At the molecular level, codon-specific translation is regulated by post-transcriptional epigenetic modifications of tRNA primarily at the wobble position 34 and at position 37 on the 3′-side of the anticodon. Modifications at these positions determine the quality of codon-anticodon pairing and the speed of translation on the ribosome. Different modifications operate in distinct mechanisms of codon-specific translation, generating a diversity of regulation that is previously unanticipated. Here we summarize recent work that demonstrates codon-specific translation mediated by the m1G37 methylation of tRNA at CCC and CCU codons for proline, an amino acid that has unique features in translation.

Highlights

  • Frontiers in GeneticsThe genetic code is degenerate, synonymous codons for the same amino acid are not translated

  • The redundancy of the genetic code offers an opportunity for fine-tuning of protein synthesis, virtually at every codon position

  • While we present one example in the regulation of bacterial Mg2+ homeostasis by the m1G37 modification of tRNA (Gall et al, 2016), there are increasing studies demonstrating the ability of post-transcriptional modifications in the anticodon region to alter protein expression

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Summary

Frontiers in Genetics

The genetic code is degenerate, synonymous codons for the same amino acid are not translated . Codon-specific translation is important for controlling gene expression and determining the proteome of a cell. Codonspecific translation is regulated by post-transcriptional epigenetic modifications of tRNA primarily at the wobble position 34 and at position 37 on the 3 -side of the anticodon. Modifications at these positions determine the quality of codon-anticodon pairing and the speed of translation on the ribosome. Different modifications operate in distinct mechanisms of codon-specific translation, generating a diversity of regulation that is previously unanticipated.

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