Molecular Mechanism of traf6 like Gene in Innate Immunity of Procambarus clarkii
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摘要:
目的 深入研究克氏原螯虾(Procambarus clarkia)traf6 like基因参与先天免疫调节的功能。 方法 以Pc-traf6 like基因为研究对象,利用RNAi技术干扰目的基因表达量之后,进行细菌模拟刺激,并且通过实时荧光定量PCR(qRT-PCR)检测细胞凋亡相关基因表达量的变化情况。 结果 干扰Pc-traf6 like基因,通过干扰效果检测,显示48 h时干扰效果良好,可用于后续试验。在目的基因干扰后,进行金黄色葡萄球菌(Staphylococcus aureus)刺激,检测表明促凋亡基因Bax、抗凋亡基因Bcl 2、细胞凋亡关键基因Caspase 3不同程度上调表达;在目的基因干扰后,进行鲶爱德华氏菌(Edwardsiella ictaluri )刺激,检测表明促凋亡基因Bax、抗凋亡基因Bcl 2、细胞凋亡关键基因Caspase 3不同程度上调表达。 结论 Pc-traf6 like基因被干扰,机体在受到金黄色葡萄球菌及鲶爱德华氏菌刺激后,Bax、Bcl 2和Caspase 3基因的相对表达量上调,推测Pc-traf6 like基因通过调控细胞凋亡参与了先天免疫反应。 Abstract:Objective Role of traf6 like gene in innate immunity regulation of Procambarus clarkia(Pc-traf6 like) was investigated. Methods RNAi technology was employed to interfere the expression of Pc-traf6 like gene. Bacterial simulation was performed to determine the changes of apoptosis-related gene expression by real-time quantitative PCR (qRT-PCR). Result The interference on the gene was effective after 48 h for the subsequent experiments. The interference-induced pro-apoptotic gene Bax, anti-apoptotic gene Bcl 2, and apoptotic protease Caspase 3 were upregulated in varying degrees with the stimulation of Staphylococcus aureus or Edwardsiella ictaluri. Conclusion After the Pc-traf6 like gene was effectively interfered, the relative expressions of Bax, Bcl 2, and Caspase 3 were upregulated after the P. clarkia was stimulated by either S. aureus or E. ictaluri indicating an involvement of Pc-traf6 like gene in the innate immune response by the regulating apoptosis. -
Key words:
- Procambarus clarkii /
- RNA interference /
- apoptosis /
- innate immunity
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图 2 Pc-traf6 like基因双链RNA干扰效果检测
18S RNA作为内参对照。不同字母表示不同时间点同一处理组差异显著(P<0.05);*、**表示同一时间点不同处理组之间差异显著(P<0.05)或极显著(P<0.01)。图3、4同。
Figure 2. Detection of interference on double-stranded RNA of Pc-traf6 like gene
18S RNA was used as inner control; data with different letters indicate significant difference in same group at times (P<0.05); * or ** indicates significant difference between treatment groups at 0.05 or 0.01 level. Same for Figs. 3 and 4.
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