Abstract

BackgroundGC pairs are generally more stable than AT pairs; GC-rich genomes were proposed to be more adapted to high temperatures than AT-rich genomes. Previous studies consistently showed positive correlations between growth temperature and the GC contents of structural RNA genes. However, for the whole genome sequences and the silent sites of the codons in protein-coding genes, the relationship between GC content and growth temperature is in a long-lasting debate.ResultsWith a dataset much larger than previous studies (681 bacteria and 155 archaea with completely assembled genomes), our phylogenetic comparative analyses showed positive correlations between optimal growth temperature (Topt) and GC content both in bacterial and archaeal structural RNA genes and in bacterial whole genome sequences, chromosomal sequences, plasmid sequences, core genes, and accessory genes. However, in the 155 archaea, we did not observe a significant positive correlation of Topt with whole-genome GC content (GCw) or GC content at four-fold degenerate sites. We randomly drew 155 samples from the 681 bacteria for 1000 rounds. In most cases (> 95%), the positive correlations between Topt and genomic GC contents became statistically nonsignificant (P > 0.05). This result suggested that the small sample sizes might account for the lack of positive correlations between growth temperature and genomic GC content in the 155 archaea and the bacterial samples of previous studies. Comparing the GC content among four categories (psychrophiles/psychrotrophiles, mesophiles, thermophiles, and hyperthermophiles) also revealed a positive correlation between GCw and growth temperature in bacteria. By including the GCw of incompletely assembled genomes, we expanded the sample size of archaea to 303. Positive correlations between GCw and Topt appear especially after excluding the halophilic archaea whose GC contents might be strongly shaped by intense UV radiation.ConclusionsThis study explains the previous contradictory observations and ends a long debate. Prokaryotes growing in high temperatures have higher GC contents. Thermal adaptation is one possible explanation for the positive association. Meanwhile, we propose that the elevated efficiency of DNA repair in response to heat mutagenesis might have the by-product of increasing GC content like that happens in intracellular symbionts and marine bacterioplankton.

Highlights

  • GC pairs are generally more stable than AT pairs; GC-rich genomes were proposed to be more adapted to high temperatures than AT-rich genomes

  • Consistent with numerous previous studies, we found positive correlations between the GC contents of structural RNA genes ­(GCtRNA, ­GC5S, ­GC16S, and ­GC23S) and the growth temperatures (Tmax, the optimal growth temperature (Topt), and Minimal growth temperature (Tmin)) in bacteria and archaea (Table 2)

  • We presented the relationships of optimal growth temperature with the GC contents of the whole genome, fourfold degenerate sites, tRNA, 5S rRNA, 16S rRNA, and 23S rRNA as (A), (B), (C), (D), (E), and (F) in this figure and those of the protein-coding sequences and the non-coding DNA were deposited in Additional file 3: Fig. S1

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Summary

Introduction

GC pairs are generally more stable than AT pairs; GC-rich genomes were proposed to be more adapted to high temperatures than AT-rich genomes. GC content, i.e., the percentage of G + C, is widely used to measure genomic nucleotide composition. Hu et al BMC Genomics (2022) 23:110 trait ranging from 8 to 75% [1,2,3] This genomic trait has been widely studied, and its evolution has been proposed to be associated with numerous mutational and selective forces driven by genetic, metabolic, and ecological factors [4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19]. Bernardi and Bernardi [24] proposed that high GC content is a thermal adaptation of warm-blooded animals

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