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Phenotypic divergence of thermotolerance: Molecular basis and cold adaptive evolution related to intrinsic DNA flexibility of glacier‐inhabiting <i>Cryobacterium</i> strains

Qing Liu, Weizhi Song, Yu‐Guang Zhou, Xiuzhu Dong, Yu‐Hua Xin

2020Environmental Microbiology13 citationsDOI

Abstract

Summary The link between guanine–cytosine (GC) content and thermal adaptation is controversial. Here, we compared maximum growth temperature ( T MGT ) and genomics of 78 Cryobacterium strains to avoid unreliable conclusions resulting from distantly phylogenetic groups. Phylogenomic analysis revealed this taxon had much higher diversification than we knew. Interestingly, these strains showed thermotolerance divergence with phylogenetic cohesion. A significant difference was found between T MGT ≤ 20°C strains and T MGT &gt; 20°C strains in genomic GC content which mainly caused by variation of GC3. T MGT ≤ 20°C strains tended to use synonymous codons ended with A/U, but T MGT &gt; 20°C strains tended to use G/C. Lower GC content at synonymous sites (≈GC3) of T MGT ≤ 20°C strains could provide lower intrinsic DNA flexibility which strongly associated with optimal molecular dynamics, and then guarantee DNA function at lower growth temperatures. This analysis of codon bias revealed close relationships for thermal adaptation, GC content at synonymous sites (≈GC3), intrinsic DNA flexibility and optimal DNA dynamics. Natural selection was main force driving this codon bias; strains with lower T MGT endured stronger natural selection. Therefore, this study provided molecular basis for bacterial adaptive evolution from moderate temperature to low temperature.

Topics & Concepts

BiologyPhylogenetic treeNatural selectionAdaptation (eye)GeneticsDNACytosineCodon usage biasGC-contentComparative genomicsGenomicsGenomeGeneSelection (genetic algorithm)Computer scienceNeuroscienceArtificial intelligenceGenomics and Phylogenetic StudiesMicrobial Community Ecology and PhysiologyBacteriophages and microbial interactions
Phenotypic divergence of thermotolerance: Molecular basis and cold adaptive evolution related to intrinsic DNA flexibility of glacier‐inhabiting <i>Cryobacterium</i> strains | Litcius