首页|黄喉拟水龟ISG15基因cDNA序列克隆及其表达特征分析

黄喉拟水龟ISG15基因cDNA序列克隆及其表达特征分析

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[目的]克隆黄喉拟水龟(Mauremys mutica)干扰素刺激基因15(ISG15)并分析其表达特征,为探究ISG15蛋白在黄喉拟水龟抗病原微生物侵袭过程中的免疫功能和作用机制提供理论依据。[方法]应用RACE克隆黄喉拟水龟ISG15基因(MmISG15)cDNA全长序列,进行生物信息学分析,采用实时荧光定量PCR检测MmISG15基因在健康黄喉拟水龟不同组织中的表达情况,并检测黄喉拟水龟受脂多糖(LPS)、多肌胞苷酸[Poly(I∶C)]和肺炎克雷伯氏菌刺激后,MmISG15基因的表达变化,以PBS为对照。[结果]MmISG15基因cDNA序列全长1274 bp,5'端非编码区(5'-UTR)与3'端非编码区(3'-UTR)分别为126和650 bp,开放阅读框(ORF)为498 bp,编码165个氨基酸残基,蛋白分子量为15。3 kD,理论等电点(pI)为7。70。MmISG15蛋白N端存在2个泛素样结构域(UBD),C端含有1段高度保守的LRLRGG基序。MmISG15氨基酸序列与其他爬行动物ISG15氨基酸序列相似性为55。57%~95。54%,与鱼类和哺乳动物的相似性分别为34。09%~49。02%及38。64%~48。25%。系统发育进化树显示,MmISG15和其他爬行动物ISG15聚为一支,其中与乌龟(Mauremys reevesii)亲缘关系最近。实时荧光定量PCR检测结果表明,MmISG15基因在健康黄喉拟水龟8种组织中均有表达,在脾脏组织中相对表达量最高,其次是肝脏,在前肠、后肠、肾脏、肺和肌肉组织中的相对表达量较低,而在脑组织中的相对表达量最低;LPS刺激后黄喉拟水龟脾脏和肝脏组织中MmISG15基因相对表达量与对照无显著差异(P>0。05);Poly(I∶C)刺激后6 h脾脏和肝脏组织中MmISG15基因相对表达量极显著上调(P<0。01,下同)并在刺激后12 h达最大值;肺炎克雷伯氏菌刺激后12 h脾脏和肝脏组织中MmISG15基因相对表达量极显著上调并在刺激后48 h达最大值。[结论]MmISG15属于典型泛素样蛋白,MmISG15基因主要在黄喉拟水龟脾脏和肝脏组织中表达。Poly(I∶C)和肺炎克雷伯氏菌刺激能提高脾脏和肝脏中MmISG15基因的相对表达量,推测MmISG15基因参与黄喉拟水龟抵抗病毒和细菌侵袭的免疫反应,其编码蛋白发挥重要免疫功能。
Cloning of cDNA sequence and expression characteristics analysis of ISG15 gene in Mauremys mutica
[Objective]To clone the interferon-stimulated gene 15(ISG15)in Mauremys mutica,analyze its expres-sion characteristics,which could provide theoretical basis for exploring the immune function and mechanism of ISG15 protein during the invasion of disease-resistant microorganism in M.mutica.[Method]Using RACE technology,the full-length cDNA sequence of the ISG15 gene from M.mutica(MmISG15)was cloned.Bioinformatics analysis was con-ducted,and the expression of MmISG15 gene in various tissues of healthy M.mutica was assessed using real-time fluores-cence quantitative PCR.Additionally,the expression changes of the MmISG15 gene were monitored following stimula-tion with lipopolysaccharide(LPS),polycytidylic acid[Poly(I∶C)]and Klebsiella pneumoniae,with PBS serving as the control.[Result]The full-length cDNA sequence of MmISG15 gene was 1276 bp,including 5'untranslated regions(5'-UTR)and 3'untranslated regions(3'-UTR)of 126 and 650 bp respectively,and an open reading frame(ORF)of 498 bp,encoding 165 amino acid residues with protein molecular mass and isoelectric point(pI)of 15.3 kD and 7.70 respectively.The N-terminus of MmISG15 protein contained 2 ubiquitin-like domains(UBD),and the C-terminus con-tained a highly conserved LRLRGG sequence.Homology analysis revealed that the amino acid sequence of MmISG15 shared 55.57%-95.54%similarity with ISG15 amino acid sequence of other reptiles,and 34.09%-49.02%and 38.64%-48.25%similarity with mammals and fish respectively.Phylogenetic analysis showed that MmISG15 clustered with ISG15 from other reptiles,and the most closely related to turtles(Mauremys reevesii).Real-time fluorescence quantita-tive PCR results indicated that MmISG15 gene was expressed in all 8 examined tissues of healthy M.mutica,with the highest relative expression in the spleen,followed by liver.Lower relative expressions were observed in the foregut,hind-gut,kidney,lung and muscle tissues,with the lowest in brain tissue.Following LPS stimulation,there was no significant difference in the relative expression of MmISG15 gene in the spleen and liver tissues compared to the control(P>0.05).Post-stimulation with Poly(I∶C),extremly significant up-regulation of MmISG15 gene was observed at 6 h in the spleen and liver tissues(P<0.01,the same below),reaching a peak at 12 h.Following stimulation with K.pneumoniae,ex-tremely significant up-regulation in MmISG15 gene expression was noted at 12 h in the spleen and liver tissues,reaching the highest level at 48 h post-stimulation.[Conclusion]MmISG15 is a classical ubiquitin-like protein,MmISG15 gene primarily expresses in the spleen and liver tissues of M.mutica.Stimulation with Poly(I∶C)and K.pneumoniae up-regulates the expression levels of the MmISG15 gene in spleen and liver,indicating that MmISG15 gene plays an impor-tant role in the immune response of M.mutica against virus and bacterial invasion,with its encoded protein playing impor-tant immunological role.

Mauremys muticaISG15disease resistance immunitytissue expressionRACEreal-time fluores-cence quantitative PCR

陈铭曲、彭文、韩鹏夫、纪月鑫、陆专灵、韦友传

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广西大学动物科学技术学院/广西高校水生生物健康养殖与营养调控重点实验室,广西 南宁 530004

广西水产科学研究院/广西水产遗传育种与健康养殖重点实验室,广西 南宁 530021

黄喉拟水龟 ISG15 抗病免疫 组织表达 RACE 实时荧光定量PCR

2024

南方农业学报
广西壮族自治区农业科学院

南方农业学报

CSTPCD北大核心
影响因子:0.83
ISSN:2095-1191
年,卷(期):2024.55(11)