Abstract

AbstractAmong eubacteria and archeabacteria, amino acid composition is correlated with habitat temperatures. In particular, species living at high temperatures have proteins enriched in the amino acids E-R-K and depleted in D-N-Q-T-S-H-A. Here, we show that this bias is a proteome-wide effect in prokaryotes, and that the same trend is observed in fully sequenced mammals and chicken compared to cold-blooded vertebrates (Reptilia, Amphibia and fish). Thus, warm-blooded vertebrates likely experienced genome-wide weak positive selection on amino acid composition to increase protein thermostability.

Highlights

  • Evolutionary molecular biology is mostly concerned with the forces affecting individual genes

  • The ribosomal RNAs and transfer RNAs of prokaryotes living at high temperatures contain a much larger Guanine and Cytosine (GC)-fraction in their stem regions compared to prokaryotes living at more moderate temperatures, likely because G-C pairs are more stable to thermal fluctuations than A-T pairs

  • Despite large variation in amino acid composition within mesophiles (Fig. 1), we still see a significant correlation of ERK with optimal growth temperature among prokaryotes living at temperatures between 8°C and 50°C (Pearson’s R=0.23, p=0.0017; Spearman’s R=0.21, p=0.0045)

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Summary

Introduction

Evolutionary molecular biology is mostly concerned with the forces affecting individual genes. In the case of vertebrates, it was argued convincingly that the ‘isochore’ structure of high- and low-GC regions is not due to selection, but reflects varying fixation bias of GC over AT in the presence of recombination. A clear picture emerges only in the study of structured RNAs. The ribosomal RNAs and transfer RNAs of prokaryotes living at high temperatures contain a much larger GC-fraction in their stem regions compared to prokaryotes living at more moderate temperatures , likely because G-C pairs (with three hydrogen bonds) are more stable to thermal fluctuations than A-T pairs (with only two hydrogen bonds). In organisms living at elevated temperatures, RNAs that require a specific threedimensional structure to perform their function appear to be under selection for increased thermostability

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