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Updated: Mar 21, 2026

ACT1-CUP1 Assays Determine the Substrate-Specific Sensitivities of Spliceosomal Mutants in Budding Yeast
Published on: June 30, 2022
A novel nuclear genetic code alteration in yeasts and the evolution of codon reassignment in eukaryotes
Stefanie Mühlhausen1, Peggy Findeisen1, Uwe Plessmann2
1Group Systems Biology of Motor Proteins, Department of NMR-Based Structural Biology, Max-Planck-Institute for Biophysical Chemistry, 37077 Göttingen, Germany;
The yeast Pachysolen tannophilus reassigns the CUG codon to translate as alanine instead of leucine. This genetic code evolution discovery in yeast offers a new mechanism for nuclear genetic code alterations.
Area of Science:
- Molecular Biology
- Genetics
- Evolutionary Biology
Background:
- The genetic code translates nucleotide sequences into amino acid sequences.
- Changes to sense codons are typically detrimental, but rare codon reassignment events demonstrate code evolution.
- Existing models for nuclear genetic code alteration lack resolution.
Purpose of the Study:
- To investigate a novel sense codon reassignment in the yeast Pachysolen tannophilus.
- To elucidate the mechanism behind this genetic code alteration.
Main Methods:
- Proteomics data generation.
- Transfer RNA (tRNA) sequence comparisons.
- Analysis of tRNA anticodon mutations and recognition sites.
Main Results:
- Pachysolen tannophilus translates CUG codons as alanine, not leucine.
- The yeast possesses an anticodon-mutated tRNA(Ala) (tRNACAG) responsible for CUG decoding.
- A tRNA loss-driven mechanism is proposed for CUG codon reassignment in yeasts.
Conclusions:
- A novel sense codon reassignment (CUG to alanine) was identified in Pachysolen tannophilus.
- The findings support a tRNA loss-driven mechanism for nuclear genetic code evolution.
- This mechanism provides a framework for understanding past and predicting future codon reassignments.
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