Abstract

BackgroundCodon bias is believed to play an important role in the control of gene expression. In Escherichia coli, some rare codons, which can limit the expression level of exogenous protein, have been defined by gene engineering operations. Previous studies have confirmed the existence of codon pair's preference in many genomes, but the underlying cause of this bias has not been well established. Here we focus on the patterns of rarely-used synonymous codons. A novel method was introduced to identify the rare codons merely by codon pair bias in Escherichia coli.ResultsIn Escherichia coli, we defined the "rare codon pairs" by calculating the frequency of occurrence of all codon pairs in coding sequences. Rare codons which are disliked in genes could make great contributions to forming rare codon pairs. Meanwhile our investigation showed that many of these rare codon pairs contain termination codons and the recognized sites of restriction enzymes. Furthermore, a new index (Frare) was developed. Through comparison with the classical indices we found a significant negative correlation between Frare and the indices which depend on reference datasets.ConclusionsOur approach suggests that we can identify rare codons by studying the context in which a codon lies. Also, the frequency of rare codons (Frare) could be a useful index of codon bias regardless of the lack of expression abundance information.

Highlights

  • Codon bias is believed to play an important role in the control of gene expression

  • From early investigations in Escherichia coli[1], it was found that usage of preferred codons in genes was positively correlated with their respective major isoacceptor tRNA levels, and this was explained as an adaptation of highly expressed genes to translational efficiency

  • Identification of rare codons of Escherichia coli based on codon pairs preference 1

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Summary

Introduction

In Escherichia coli, some rare codons, which can limit the expression level of exogenous protein, have been defined by gene engineering operations. There is still no final verdict on the formation mechanism, codon bias has been widely used to estimate and compare the expression level of endogenous genes, From early investigations in Escherichia coli[1], it was found that usage of preferred codons in genes was positively correlated with their respective major isoacceptor tRNA levels, and this was explained as an adaptation of highly expressed genes to translational efficiency. One long accepted principle of this theory is that highly expressed gene must show high codon usage bias. With the development of high throughput technology for gene sequencing and expression level detection, doubts over this theory have increased gradually[1,19,20,21,22,23,24,25,26]

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