克氏原螯虾                        
                
                                
                        
                            拉布                        
                
                                
                        
                            生物                        
                
                                
                        
                            GTP酶                        
                
                                
                        
                            白斑综合征                        
                
                                
                        
                            基因                        
                
                                
                        
                            基因家族                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            病菌                        
                
                                
                        
                            蛋白质家族                        
                
                                
                        
                            保守序列                        
                
                                
                        
                            细胞生物学                        
                
                                
                        
                            小龙虾                        
                
                                
                        
                            肽序列                        
                
                                
                        
                            基因表达                        
                
                                
                        
                            生态学                        
                
                        
                    
            作者
            
                Lei Zhu,Zhengyan Du,Yiming Kong,Xinru Wang,Hao Li,Libo Hou,Xianghui Kong            
         
                    
        
    
            
            标识
            
                                    DOI:10.1016/j.ijbiomac.2024.133606
                                    
                                
                                 
         
        
                
            摘要
            
            The Rab GTPase constitutes the largest family of small GTPases that regulate intracellular trafficking. Different eukaryotes possess varying numbers of Rab paralogs. However, limited knowledge exists regarding the evolutionary pattern of Rab family in most major eukaryotic supergroups. This study cloned 24 Rab genes from transcriptome data of Procambarus clarkii haemocytes. The multiple sequence alignment and phylogenetic tree analysis revealed a relatively high degree of conservation for PcRab. Furthermore, PcRab exhibited similarities in motif composition with all members showing presence of G, PM, RabF, and RabSF motifs. The tertiary structure indicated that PcRab proteins mainly consisted of α-helices and β-strands, and most PcRab proteins shared similar tertiary structures, and it was indicated that they have similar protein characteristics. Protein-protein interaction prediction identified a total of 20 interacting proteins involved in vesicle trafficking, phagocytosis, and signal transduction with 193 interactions. Expression analysis showed wide expression patterns for PcRab in P. clarkii organs. Upon infection by white spot syndrome virus and Aeromonas veronii, significant induction was observed for PcRab gene expression levels, indicating their involvement in pathogen response mechanisms. The present study represents the pioneering effort in comprehensively identifying and cloning the Rab family genes in crustacean, followed by a systematic investigation into their evolutionary patterns and immune response upon pathogen infection. The results provided valuable insights for further investigation into the molecular mechanism underlying the response of P. clarkii to pathogen infection.
         
            
 
                 
                
                    
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