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Codon usage patterns in Escherichia coli, Bacillus subtilis, Saccharomyces cerevisiae, Schizosaccharomyces pombe, Drosophila melanogaster and Homo sapiens; a review of the considerable within-species diversity

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TLDR
These trends for codon usage are illustrated for six species whereCodon usage has been examined in detail, by presenting the pooled codon used for the 10% of genes at either end of the major trend.
Abstract
The genetic code is degenerate, but alternative synonymous codons are generally not used with equal frequency. Since the pioneering work of Grantham's group it has been apparent that genes from one species often share similarities in codon frequency; under the "genome hypothesis" there is a species-specific pattern to codon usage. However, it has become clear that in most species there are also considerable differences among genes. Multivariate analyses have revealed that in each species so far examined there is a single major trend in codon usage among genes, usually from highly biased to more nearly even usage of synonymous codons. Thus, to represent the codon usage pattern of an organism it is not sufficient to sum over all genes as this conceals the underlying heterogeneity. Rather, it is necessary to describe the trend among genes seen in that species. We illustrate these trends for six species where codon usage has been examined in detail, by presenting the pooled codon usage for the 10% of genes at either end of the major trend. Closely-related organisms have similar patterns of codon usage, and so the six species in Table 1 are representative of wider groups. For example, with respect to codon usage, Salmonella typhimurium closely resembles E. coli, while all mammalian species so far examined (principally mouse, rat and cow) largely resemble humans.

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Journal ArticleDOI

Synonymous codon usage in Cryptosporidium parvum: identification of two distinct trends among genes.

TL;DR: The usage of alternative synonymous codons in the apicomplexan Cryptosporidium parvum has been investigated and 15 of the 18 codons identified as optimal are more G+C-rich than the otherwise common codons, so that codon selection associated with translation opposes the general mutation bias.
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Enhanced expression of codon optimized interferon gamma in CHO cells.

TL;DR: Experimental results suggested that codon context is relatively more effective parameter for improving recombinant IFN-γ expression in CHO cells.
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Studies of spectral properties of short genes using the wavelet subspace Hilbert–Huang transform (WSHHT)

TL;DR: In this paper, a wavelet subspace Hilbert-Huang transform (WSHHT) algorithm was used to identify spectral patterns of very short genes (below 70 bp) in DNA sequences.
Journal ArticleDOI

DNA sequence of the yeast transketolase gene.

TL;DR: This is the first transketolase gene of the pentose phosphate shunt to be sequenced from any source and the Molecular mass of the proposed translated protein is in good agreement with the observed molecular mass of about 75,000 daltons.
Journal ArticleDOI

Analysis of codon usage in Newcastle disease virus

TL;DR: It is suggested that more than one genotype of NDV circulates in waterfowl in USA; and gene length has no significant effect on the variations of synonymous codon usage in these virus genes.
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