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Scatter plot of CAI with Axis 1 CAI and codon usage variation: role of gene expressivity Codon Adaptation Index (CAI) has been extensively used as a measure of gene expression level in organisms. Within T. elongatus genome, CAI showed positive correlation with the positions of genes along axis 1 and GC3s ( r = 0.274 and r= 0.229 respectively, P<0.01) (Figure 4) but was negatively correlated with Nc (r =0.389). This has reflected the effect of gene expression level on codon selection pattern in T. elongatus. Data suggested that genes with higher expression level exhibing a greater degree of codon usage bias were distributed at right side of the first axis and prefered to use G-or C-ending codons. This result indicated a role of expression levels of genes in codon usage variation along with compositional constraints and supported the argument of presence of additional factors along with compositional constraint in shaping the codon usage bias in this genome. Furthermore, CAI showed a positive correlation with C3s (r = 0.605, P <0.01) whereas negative correlation with G3s (r =-0.243, P <0.01) supporting our hypothesis that the influence of mutational bias is reflected in the choice of bases in the third codon position and thus, favor translational selection. 

Scatter plot of CAI with Axis 1 CAI and codon usage variation: role of gene expressivity Codon Adaptation Index (CAI) has been extensively used as a measure of gene expression level in organisms. Within T. elongatus genome, CAI showed positive correlation with the positions of genes along axis 1 and GC3s ( r = 0.274 and r= 0.229 respectively, P<0.01) (Figure 4) but was negatively correlated with Nc (r =0.389). This has reflected the effect of gene expression level on codon selection pattern in T. elongatus. Data suggested that genes with higher expression level exhibing a greater degree of codon usage bias were distributed at right side of the first axis and prefered to use G-or C-ending codons. This result indicated a role of expression levels of genes in codon usage variation along with compositional constraints and supported the argument of presence of additional factors along with compositional constraint in shaping the codon usage bias in this genome. Furthermore, CAI showed a positive correlation with C3s (r = 0.605, P <0.01) whereas negative correlation with G3s (r =-0.243, P <0.01) supporting our hypothesis that the influence of mutational bias is reflected in the choice of bases in the third codon position and thus, favor translational selection. 

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Analysis of synonymous codon usage pattern in the genome of a thermophilic cyanobacterium, Thermosynechococcus elongatus BP-1 using multivariate statistical analysis revealed a single major explanatory axis accounting for codon usage variation in the organism. This axis is correlated with the GC content at third base of synonymous codons (GC3s) in...

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... for translational accuracy is predicted to have a positive correlation between codon bias and gene length [15]. From the plot drawn with gene length against Nc (Figure 2), it is clear that shorter genes have a much wider variance in Nc values and vice versa for longer genes. Lower Nc values of longer genes may be expected due to the direct effect of translation time on fitness or to the extra energy cost associated with longer translational timing. Correlation analyses between gene length and gene position on axis 1, GC3s and Nc values (r = 0.158, 0.170 and -0.173, respectively, P< 0.01) were all significantly correlated. The observed significant correlation in T. elongatus genome revealed that gene length influences codon usage of this organism. Gene length was negatively correlated with Nc (r = -0.173) but it showed positive correlation with GC3s (r = 0.170). Therefore, codon bias is lower in longer genes than in shorter ones (Figure 3). It is meaningful that up to certain extent, translational accuracy also plays a role in dictating the codon usage variation in this genome. (Figure 4) but was negatively correlated with Nc (r =0.389). This has reflected the effect of gene expression level on codon selection pattern in T. elongatus. Data suggested that genes with higher expression level exhibing a greater degree of codon usage bias were distributed at right side of the first axis and prefered to use G-or C-ending codons. This result indicated a role of expression levels of genes in codon usage variation along with compositional constraints and supported the argument of presence of additional factors along with compositional constraint in shaping the codon usage bias in this genome. Furthermore, CAI showed a positive correlation with C3s (r = 0.605, P <0.01) whereas negative correlation with G3s (r = -0.243, P <0.01) supporting our hypothesis that the influence of mutational bias is reflected in the choice of bases in the third codon position and thus, favor translational ...

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... In most of the species a significant negative correlation between Nc and GC3 was depicted, a trend well in line with the standard notion of Nc-GC3 relationship (Hassan et al., 2009;Pandit and Sinha, 2011;Prabha et al., 2012;Malakar et al., 2016Malakar et al., , 2019Song et al., 2017b). The results of the correlation analysis is shown in Supplementary Table 3. ...
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Soil is a diversified and complex ecological niche, home to a myriad of microorganisms particularly bacteria. The physico-chemical complexities of soil results in a plethora of physiological variations to exist within the different types of soil dwelling bacteria, giving rise to a wide variation in genome structure and complexity. This serves as an attractive proposition to analyze and compare the genome of a large number soil bacteria to comprehend their genome complexity and evolution. In this study a combination of codon usage and molecular phylogenetics of the whole genome and key housekeeping genes like infB (translation initiation factor 2), trpB (tryptophan synthase, beta subunit), atpD (ATP synthase, beta subunit), and rpoB (RNA polymerase, beta subunit) of 92 soil bacterial species spread across the entire eubacterial domain and residing in different soil types was performed. The results indicated the direct relationship of genome size with codon bias and coding frequency in the studied bacteria. The codon usage profile demonstrated by the gene trpB was found to be relatively different from the rest of the housekeeping genes with a large number of bacteria having a greater percentage of genes with Nc values less than the Nc of trpB. The results from the overall codon usage bias profile also depicted that the codon usage bias in the key housekeeping genes of soil bacteria was majorly due to selectional pressure and not mutation. The analysis of hydrophobicity of the gene product encoded by the rpoB coding sequences demonstrated tight clustering across all the soil bacteria suggesting conservation of protein structure for maintenance of form and function. The phylogenetic affinities inferred using 16S rRNA gene and the housekeeping genes demonstrated conflicting signals with trpB gene being the noisiest one. The housekeeping gene atpD was found to depict the least amount of evolutionary change in the soil bacteria considered in this study except in two Clostridium species. The phylogenetic and codon usage analysis of the soil bacteria consistently demonstrated the relatedness of Azotobacter chroococcum with different species of the genus Pseudomonas.
... One of the objectives of this study is to investigate the codon usage in the genomes of different cyanobacterial species that belong to diverse habitats and present different physiological and morphological characteristics. Although some studies have been conducted on the codon usage in certain closely related cyanobacterial genomes (Campbell and Gowri, 1990;Prabha et al., 2012;Yu et al., 2012;Xu et al., 2013), a comprehensive genome-wide analysis representing major taxonomic groups of cyanobacteria is lacking. We analyzed codon usage bias and codon context patterns among 41 sequenced cyanobacterial genomes representing five different taxonomic orders. ...
... All the 16 cyanobacterial genomes with Nc higher than 50 were associated with GC3s ranging between 0.3 and 0.6 (Fig. 2). Nc plot indicated that factors other than the compositional bias are also influencing codon usage bias of the genes as suggested by Hassan et al. (2009) and Prabha et al. (2012). It also revealed that many cyanobacteria, majority of which are members of Prochlorales lied very close to expected curve supporting that compositional constraint is major factor in shaping codon usage bias of these organisms. ...
... Study of codon usage is valuable due to its importance in the perception of the molecular basics plus potential utilization as a molecular marker for typifying molecular evolution. Oligonucleotide probes and DNA primers can also be designed for catching genes of interest based on this knowledge as well (Prabha et al., 2012). Likely selection patterns due to varying environmental factors effect gene expressivity and codon usage trend among genes in different species of bacteria (McInerney, 1997). ...
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... Closely related species, living in distinct environments may exhibit considerable genomic diversity (Paul et al. 2010) that lead to differences in factors behind diversification of SCU patterns. Mutational pressure was found to be the major factor, influencing SCU pattern across PCG in strictly thermophilic cyanobacterium Thermosynechococcus elongatus BP-1 (Prabha et al. 2012) which is less adaptive to other temperature ranges as growth of thermophiles is restricted to particular environment at specific temperature (Botzman and Margalit 2011). These reports support our finding that SCU pattern of P. chromatophora and S. elongatus is dictated by mutational pressure due to their less adaptation to varying environments. ...
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Comparative study of synonymous codon usage variations and factors influencing its diversification in α - cyanobacterial descendant Paulinella chromatophora and β - cyanobacterium Synechococcus elongatus PCC6301 has not been reported so far. In the present study, we investigated various factors associated with synonymous codon usage in the genomes of P. chromatophora and S. elongatus PCC6301 and findings were discussed. Mutational pressure was identified as the major force behind codon usage variation in both genomes. However, correspondence analysis revealed that intensity of mutational pressure was higher in S. elongatus than in P. chromatophora. Living habitats were also found to determine synonymous codon usage variations across the genomes of P. chromatophora and S. elongatus. Whole genome sequencing of α-cyanobacteria in the cyanobium clade would certainly facilitate the understanding of synonymous codon usage patterns and factors contributing its diversification in presumed ancestors of photosynthetic endosymbionts of P. chromatophora.
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