The identification, evolutionary analysis, and immune roles of Rab family members in red swamp crayfish, Procambarus clarkii

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
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:276: 133606-133606 被引量:2
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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