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日本鳗鲡TBK-1基因的克隆及免疫刺激的表达模式

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利用PCR技术克隆了日本鳗鲡(Anguilla japonica)TBK-1基因(AjTBK-1),其开放阅读框为2193 bp,编码731个氨基酸.序列结构分析结果显示,AjTBK-1含有4个保守结构域,分别为氨基端激酶结构域,泛素样结构域和羧基端两个卷曲-螺旋结构域.系统发育分析表明,鱼类与四足类的TBK-1各自聚为一枝.实时定量PCR(qPCR)结果显示,AjTBK-1在日本鳗鲡各组织中均有表达.Poly Ⅰ:C刺激6h后,日本鳗鲡脾脏组织中AjTBK-1的上调倍数最高,为对照组的1.63倍;迟缓爱德华氏菌(Edwardsiella tarda)感染24h后,日本鳗鲡肝脏组织中AjTBK-1的上调倍数最高,为对照组的2.2倍:表明AjTBK-1参与了日本鳗鲡抗病毒、抗细菌免疫反应应答.
Cloning and Expression Pofile Analysis After Immune Stimulation of TBK-1 Gene in Japanese Eel(Anguilla japonica)
The TBK-1 gene from Japanese eel(Anguilla japonica)named AjTBK-1 was cloned using poly-merase chain reaction(PCR)technology,which has an open reading frame of 2193 bp encoding 731 amino acids.Sequence and structure analysis showed that AjTBK-1 contains four conserved domains,including an N-terminal kinase domain,a ubiquitin-like domain,and two coiled-coil domains at the C-terminus.Phyloge-netic analysis indicated that fish and tetrapod TBK-1 formed separate branches.qPCR results showed that AjT-BK-1 is expressed in various tissues of Japanese eel.After stimulation with Poly Ⅰ:C for 6 h,the maximal ex-pression of AjTBK-1 was detected in the spleen,which was 1.63-fold high than that of the control group.After infection with Edwardsiella tarda for 24 h,the maximal expression of AjTBK-1 was detected in the liver,which was 2.2-fold hign than that of the control group.Taken together,our results indicated that AjTBK-1 is involved in the antibacterial and antiviral immune responses of Japanese eel.

Japanese eel(Anguilla japonica)TBK-1 genesequence analysistranscriptional expression

赵歌洁、黄贝、黄文树

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集美大学水产学院,福建 厦门 361021

鳗鲡现代产业技术教育部工程研究中心,福建 厦门 361021

福建省水产生物育种与健康养殖工程研究中心,福建 厦门 361021

日本鳗鲡 TBK-1基因 序列分析 转录表达

福建省自然科学基金项目福建省自然科学基金项目国家自然科学基金项目

2021J020472020J0166632073011

2024

集美大学学报(自然科学版)
集美大学

集美大学学报(自然科学版)

影响因子:0.293
ISSN:1007-7405
年,卷(期):2024.29(1)
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