Abstract
Insertion sequences (ISs) are widespread prokaryotic transposable elements, often regarded as genomic parasites that primarily cause deleterious mutations. However, they can also promote adaptive changes. These antagonistic properties make their overall impact on prokaryotic evolution difficult to grasp. Here, we address this challenge by leveraging the framework of transposon ecology to analyze IS occurrences across and within 30,499 prokaryotic genomes. Combining phylogenomics with multi-scale genomic analysis, quantitative ecology, and mathematical modeling, we provide evidence that although genomes generally provide sufficient resources for IS coexistence, universal mechanisms shape their occurrence and chromosomal distribution across genomes. These include: (i) the preferential localization of ISs within highly variable and GC-heterogeneous chromosomal regions of genomic plasticity (RGPs), which act as the primary reservoir of IS niches; (ii) a linear scaling between IS abundance and niche size, with an average of 5.4 additional accessible insertion sites per IS; (iii) a dependence of IS occurrence on the presence of other ISs, suggesting a form of group behavior; (iv) the accumulation of AT-rich sequences in both coding and non-coding regions up to 100 kb surrounding ISs, indicative of ecological isolation; and (v) the spatial partitioning of mobile genetic elements around ISs, reminiscent of ecological niche differentiation. Besides these general principles, we also uncover niche specificities associated with particular IS families, hinting at regulatory mechanisms that modulate IS activity. Altogether, this comprehensive transposon ecology approach offers new insights and avenues for understanding IS-host interactions and genome evolution, moving beyond traditional host-centric perspectives.
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Abstract
Insertion sequences (ISs) are widespread prokaryotic transposable elements, often regarded as genomic parasites that primarily cause deleterious mutations. However, they can also promote adaptive changes. These antagonistic properties make their overall impact on prokaryotic evolution difficult to grasp. Here, we tackle this problem by leveraging the framework of transposon ecology to analyze IS occurrences across and within 30,409 prokaryotic genomes. Combining phylogenomics with multi-scale genomic analysis and modeling, we provide evidence for group behavior, whereby ISs collectively contribute to the construction of their own niche, whose spread is found to be limited within chromosomes. Niches are shared with other mobile genetic elements and exhibit spatial partitioning reminiscent of ecological niche differentiation. Our results further suggest both physical and ecological isolation, with up to 100 kb long niches characterized by particularly variable, heterogeneous, and AT-rich sequences. We also find evidence of functional roles of IS families, and of regulatory mechanisms modulating IS activity. Altogether, our comprehensive transposon ecology approach offers novel insights and new avenues for understanding IS-host interactions and genome evolution, moving beyond traditional host-centric perspectives.
Competing Interest Statement
The authors have declared no competing interest.
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