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Cell. 2015 Mar 12;160(6):1111-24. doi: 10.1016/j.cell.2015.02.029.

Codon optimality is a major determinant of mRNA stability.

Author information

1
Center for RNA Molecular Biology, Case Western Reserve University, Cleveland, OH 44106, USA.
2
Statistical Science Core in the Center for Clinical Investigation, Case Western Reserve University, Cleveland, OH 44106, USA.
3
Department of Genetics and Developmental Biology, Institute for Systems Genomics, University of Connecticut Health Center, Farmington, CT 06030, USA.
4
Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, 94158, USA.
5
Center for RNA Molecular Biology, Case Western Reserve University, Cleveland, OH 44106, USA. Electronic address: jmc71@case.edu.

Abstract

mRNA degradation represents a critical regulated step in gene expression. Although the major pathways in turnover have been identified, accounting for disparate half-lives has been elusive. We show that codon optimality is one feature that contributes greatly to mRNA stability. Genome-wide RNA decay analysis revealed that stable mRNAs are enriched in codons designated optimal, whereas unstable mRNAs contain predominately non-optimal codons. Substitution of optimal codons with synonymous, non-optimal codons results in dramatic mRNA destabilization, whereas the converse substitution significantly increases stability. Further, we demonstrate that codon optimality impacts ribosome translocation, connecting the processes of translation elongation and decay through codon optimality. Finally, we show that optimal codon content accounts for the similar stabilities observed in mRNAs encoding proteins with coordinated physiological function. This work demonstrates that codon optimization exists as a mechanism to finely tune levels of mRNAs and, ultimately, proteins.

PMID:
25768907
PMCID:
PMC4359748
DOI:
10.1016/j.cell.2015.02.029
[Indexed for MEDLINE]
Free PMC Article

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