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Merck
CN

Mechanism of Virus Attenuation by Codon Pair Deoptimization.

Cell reports (2020-04-30)
Nicole Groenke, Jakob Trimpert, Sophie Merz, Andelé M Conradie, Emanuel Wyler, Hongwei Zhang, Orsalia-Georgia Hazapis, Sebastian Rausch, Markus Landthaler, Nikolaus Osterrieder, Dusan Kunec
摘要

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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Sigma-Aldrich
尿核甙, ≥99%
Sigma-Aldrich
单克隆抗-FLAG®, clone SIG1-25, ascites fluid
Sigma-Aldrich
5-溴尿苷, 98%
Sigma-Aldrich
牛IFNG /干扰素γELISA试剂盒, for serum, plasma and cell culture supernatants