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Mechanism of Virus Attenuation by Codon Pair Deoptimization
Author(s) -
Nicole Groenke,
Jakob Trimpert,
Sophie Merz,
Andelé M. Conradie,
Emanuel Wyler,
Hongwei Zhang,
Orsalia-Georgia Hazapis,
Sebastian Rausch,
Markus Landthaler,
Nikolaus Osterrieder,
Dušan Kunec
Publication year - 2020
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2020.107586
Subject(s) - codon usage bias , cpg site , biology , genetics , genome , translation (biology) , gene , messenger rna , start codon , virus , computational biology , gene expression , dna methylation
Codon pair deoptimization is an efficient virus attenuation strategy, but the mechanism that leads to attenuation is unknown. The strategy involves synthetic recoding of viral genomes that alters the positions of synonymous codons, thereby increasing the number of suboptimal codon pairs and CpG dinucleotides in recoded genomes. Here we identify the molecular mechanism of codon pair deoptimization-based attenuation by studying recoded influenza A viruses. We show that suboptimal codon pairs cause attenuation, whereas the increase of CpG dinucleotides has no effect. Furthermore, we show that suboptimal codon pairs reduce both mRNA stability and translation efficiency of codon pair-deoptimized genes. Consequently, reduced protein production directly causes virus attenuation. Our study provides evidence that suboptimal codon pairs are major determinants of mRNA stability. Additionally, it demonstrates that codon pair bias can be used to increase mRNA stability and protein production of synthetic genes in many areas of biotechnology.

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