Cao Zhenjie, He Mingwang, Chen Xiaojuan, Wang Shifeng, Cai Yan, Xie Zhenyu, Sun Yun, Zhou Yongcan
State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan University, China; Key Laboratory of Tropical Biological Resources of Ministry of Education, Hainan University, Haikou, Hainan 570228, China.
Hainan Provincial Key Laboratory for Tropical Hydrobiology and Biotechnology, College of Marine Science, Hainan University, Haikou, Hainan 570228, China.
Fish Shellfish Immunol. 2017 Aug;67:55-65. doi: 10.1016/j.fsi.2017.05.058. Epub 2017 May 26.
The classical major histocompatibility complex class I (MHC I) plays a vital role in the immune system. In this study, we cloned and identified golden pompano (Trachinotus ovatus) MHC Iα (Trov-MHC Iα), which encodes 351 amino acid residues including a leader peptide, α1, α2, α3 domain, a transmembrane region and a cytoplasmic domain. Twenty six different sequences, which encoded various numbers of amino acid residues ranging from 348 to 354, were obtained from 12 individuals. Highly genetic polymorphism was found in the Trov-MHC Iα, especially in the α1 and α2 domains. Meanwhile, in the α1 and α2 domains, 21 positive selected positions were revealed by site models, indicating the diversity of Trov-MHC Iα may be mainly generated by positive selection. Moreover, quantitative real-time reverse transcription PCR and western blotting analyses demonstrated that Trov-MHC Iα was ubiquitously expressed in the nine tested tissues and more highly expressed in intestine, head kidney, gill, and spleen. In the head kidney and spleen, Trov-MHC Iα was significantly upregulated under LPS or poly I:C stimulation. The results of this study provide valuable insight into molecular polymorphism, evolutionary mechanism, expression and function of MHC Iα in the immune system of golden pompano.
经典的主要组织相容性复合体I类(MHC I)在免疫系统中起着至关重要的作用。在本研究中,我们克隆并鉴定了卵形鲳鲹(Trachinotus ovatus)的MHC Iα(Trov-MHC Iα),其编码351个氨基酸残基,包括一个信号肽、α1、α2、α3结构域、一个跨膜区和一个胞质结构域。从12个个体中获得了26个不同的序列,这些序列编码的氨基酸残基数从348到354不等。在Trov-MHC Iα中发现了高度的遗传多态性,特别是在α1和α2结构域。同时,在位点模型中,在α1和α2结构域中发现了21个正选择位点,表明Trov-MHC Iα的多样性可能主要由正选择产生。此外,定量实时逆转录PCR和蛋白质印迹分析表明,Trov-MHC Iα在九个测试组织中普遍表达,在肠道、头肾、鳃和脾脏中表达更高。在头肾和脾脏中,Trov-MHC Iα在LPS或聚肌胞苷酸刺激下显著上调。本研究结果为卵形鲳鲹免疫系统中MHC Iα的分子多态性、进化机制、表达和功能提供了有价值的见解。