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Fig. 2 | Genome Biology

Fig. 2

From: Post-translational buffering leads to convergent protein expression levels between primates

Fig. 2

Transcriptional regulation contributes significantly more to protein level divergence compared to translational regulation. a Inter-species divergence in translation efficiency. A scatter plot comparing translation efficiency (TE) between human and chimpanzee. Each data point represents a gene, position along each axis indicates log2 translation efficiency of each species, and the color of each data point indicates whether the gene is significantly diverged between species in translation efficiency at a significance cut-off of FWER 0.05 (blue: significant, gray: not significant). b An example gene, Profilin 1 (PFN1), which shows human–chimpanzee divergence in translation efficiency. Level of protein translation (blue) and RNA transcription (red) are shown in log2RPKM. Each data point represents an individual human or chimpanzee sample. c Divergence between human and chimpanzee at the transcript level occurs more frequently than that of translation efficiency. Quantile-quantile plot of –log10(p values) derived from testing for divergence between human and chimpanzee for each trait of interest (RNA: transcript level, TE: translation efficiency). For each molecular trait, observed p value (y-axis) is plotted against the null expectation (i.e. uniform distribution of p values) (x-axis). The red line marks the expected results from a scenario where no divergence is observed. d Divergence between human and chimpanzee at the transcript level is greater than that of translation efficiency. Boxplots comparing effect size (absolute log2 ratio) of human-chimpanzee divergence (RNA: transcript level, TE: translation efficiency). Only genes that are diverged in protein levels were considered in this analysis. e Between human and chimpanzee, inter-species divergence in translation efficiency contributes little to inter-species divergence in protein level. Proportion of inter-species divergence propagated from translation level to the protein level (y-axis) was estimated using coefficient of determination (r2) between translation level divergence and protein level divergence. Each r2 was calculated for a subset of genes each defined by an FDR cut-off (x-axis) for divergence in protein level. These coefficients (r2) were calculated either with (red) or without (black) accounting for the effects from the transcript level

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