Vaysset Hugo, Meers Chance, Cury Jean, Bernheim Aude, Sternberg Samuel H
Molecular Diversity of Microbes Lab, CNRS UMR3525, Institut Pasteur, Paris, France.
AgroParisTech, Université Paris-Saclay, Paris, France.
Nat Microbiol. 2025 Jan;10(1):20-27. doi: 10.1038/s41564-024-01889-2. Epub 2025 Jan 2.
Transposase genes are ubiquitous in all domains of life and provide a rich reservoir for the evolution of novel protein functions. Here we report deep evolutionary links between bacterial IS110-family transposases, which catalyse RNA-guided DNA recombination using bridge RNAs, and archaeal/eukaryotic Nop5-family proteins, which promote RNA-guided RNA 2'-O-methylation using C/D-box snoRNAs. On the basis of conservation of protein sequence, domain architecture, three-dimensional structure and non-coding RNA features, alongside phylogenetic analyses, we propose that programmable RNA modification emerged through the exaptation of components derived from IS110-like transposons. These findings underscore how recurrent domestication events of transposable elements have driven the evolution of RNA-guided mechanisms.
转座酶基因在生命的所有领域中普遍存在,为新蛋白质功能的进化提供了丰富的资源库。在此,我们报告了细菌IS110家族转座酶与古菌/真核生物Nop5家族蛋白之间深层次的进化联系,前者利用桥接RNA催化RNA引导的DNA重组,后者利用C/D盒小核仁RNA促进RNA引导的RNA 2'-O-甲基化。基于蛋白质序列、结构域结构、三维结构和非编码RNA特征的保守性,以及系统发育分析,我们提出可编程RNA修饰是通过对源自IS110样转座子的成分进行功能改变而出现的。这些发现强调了转座元件的反复驯化事件如何推动了RNA引导机制的进化。