» Articles » PMID: 23262490

Evolutionary Conservation of Codon Optimality Reveals Hidden Signatures of Cotranslational Folding

Overview
Date 2012 Dec 25
PMID 23262490
Citations 261
Authors
Affiliations
Soon will be listed here.
Abstract

The choice of codons can influence local translation kinetics during protein synthesis. Whether codon preference is linked to cotranslational regulation of polypeptide folding remains unclear. Here, we derive a revised translational efficiency scale that incorporates the competition between tRNA supply and demand. Applying this scale to ten closely related yeast species, we uncover the evolutionary conservation of codon optimality in eukaryotes. This analysis reveals universal patterns of conserved optimal and nonoptimal codons, often in clusters, which associate with the secondary structure of the translated polypeptides independent of the levels of expression. Our analysis suggests an evolved function for codon optimality in regulating the rhythm of elongation to facilitate cotranslational polypeptide folding, beyond its previously proposed role of adapting to the cost of expression. These findings establish how mRNA sequences are generally under selection to optimize the cotranslational folding of corresponding polypeptides.

Citing Articles

The ribosome as a platform to coordinate mRNA decay.

Muller M, Becker T, Denk T, Hashimoto S, Inada T, Beckmann R Nucleic Acids Res. 2025; 53(4).

PMID: 39921564 PMC: 11806357. DOI: 10.1093/nar/gkaf049.


Modeling coding sequence design for virus-based expression in tobacco.

Burghardt M, Tuller T Synth Syst Biotechnol. 2025; 10(2):337-345.

PMID: 39802156 PMC: 11718241. DOI: 10.1016/j.synbio.2024.12.002.


Transfer RNA Levels Are Tuned to Support Differentiation During Drosophila Neurogenesis.

Wint R, Cleary M Genes (Basel). 2025; 15(12.

PMID: 39766869 PMC: 11675937. DOI: 10.3390/genes15121602.


Predicting gene sequences with AI to study codon usage patterns.

Sidi T, Bahiri-Elitzur S, Tuller T, Kolodny R Proc Natl Acad Sci U S A. 2024; 122(1):e2410003121.

PMID: 39739812 PMC: 11725940. DOI: 10.1073/pnas.2410003121.


Pulling Forces Differentially Affect Refolding Pathways Due to Entangled Misfolded States in SARS-CoV-1 and SARS-CoV-2 Receptor Binding Domain.

Lan P, OBrien E, Li M Biomolecules. 2024; 14(10).

PMID: 39456260 PMC: 11505858. DOI: 10.3390/biom14101327.


References
1.
Gupta S, Majumdar S, Bhattacharya T, Ghosh T . Studies on the relationships between the synonymous codon usage and protein secondary structural units. Biochem Biophys Res Commun. 2000; 269(3):692-6. DOI: 10.1006/bbrc.2000.2351. View

2.
Alexandrov A, Chernyakov I, Gu W, Hiley S, Hughes T, Grayhack E . Rapid tRNA decay can result from lack of nonessential modifications. Mol Cell. 2006; 21(1):87-96. DOI: 10.1016/j.molcel.2005.10.036. View

3.
Takyar S, Hickerson R, Noller H . mRNA helicase activity of the ribosome. Cell. 2005; 120(1):49-58. DOI: 10.1016/j.cell.2004.11.042. View

4.
Zhang F, Saha S, Shabalina S, Kashina A . Differential arginylation of actin isoforms is regulated by coding sequence-dependent degradation. Science. 2010; 329(5998):1534-7. PMC: 2941909. DOI: 10.1126/science.1191701. View

5.
Dos Reis M, Savva R, Wernisch L . Solving the riddle of codon usage preferences: a test for translational selection. Nucleic Acids Res. 2004; 32(17):5036-44. PMC: 521650. DOI: 10.1093/nar/gkh834. View