转座因子                        
                
                                
                        
                            核糖核酸                        
                
                                
                        
                            生物                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            进化生物学                        
                
                                
                        
                            计算生物学                        
                
                                
                        
                            基因                        
                
                                
                        
                            基因组                        
                
                        
                    
            作者
            
                Hugo Vaysset,Chance Meers,Jean Cury,Aude Bernheim,Samuel H. Sternberg            
         
            
    
            
            标识
            
                                    DOI:10.1101/2024.06.21.599552
                                    
                                
                                 
         
        
                
            摘要
            
            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 transposases, which catalyze 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. Based on conservation in the protein primary sequence, domain architecture, and three-dimensional structure, as well as common architectural features of the non-coding RNA components, we propose that programmable RNA modification emerged via exaptation of components derived from IS110-like transposons. Alongside recent studies highlighting the origins of CRISPR-Cas9 and Cas12 in IS605-family transposons, these findings underscore how recurrent domestication events of transposable elements gave rise to complex RNA-guided biological mechanisms.
         
            
 
                 
                
                    
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