Tang Xueying, Huang Baoyu, Zhang Linlin, Li Li, Zhang Guofan
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, Shandong 266071, China; University of Chinese Academy of Sciences, Beijing 100039, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, Shandong 266071, China; National & Local Joint Engineering Laboratory of Ecological Mariculture, Qingdao, Shandong 266071, China.
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, Shandong 266071, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, Shandong 266071, China; National & Local Joint Engineering Laboratory of Ecological Mariculture, Qingdao, Shandong 266071, China.
Fish Shellfish Immunol. 2016 Sep;56:330-335. doi: 10.1016/j.fsi.2016.07.011. Epub 2016 Jul 12.
As a benthic filter feeder of estuaries, the immune system of oysters provides one of the best models for studying the genetic and molecular basis of the innate immune pathway in marine invertebrates and examining the influence of environmental factors on the immune system. Here, the molecular function of molluscan TANK-binding kinase-1 (TBK1) (which we named CgTBK1) was studied in the Pacific oyster, Crassostrea gigas. Compared with known TBK1 proteins in other model organisms, CgTBK1 contains a conserved S-TKc domain and a coiled coil domain at the N- and C-terminals but lacks an important ubiquitin domain. Quantitative real-time PCR analysis revealed that the expression level of CgTBK1 was ubiquitous in all selected tissues, with highest expression in the gills. CgTBK1 expression was significantly upregulated in response to infections with Vibrio alginolyticus, ostreid herpesvirus 1 (OsHV-1 reference strain and μvar), and polyinosinic:polycytidylic acid sodium salt, suggesting its broad function in immune response. Subcellular localization showed the presence of CgTBK1 in the cytoplasm of HeLa cells, suggesting its potential function as the signal transducer between the receptor and transcription factor. We further demonstrated that CgTBK1 interacted with CgSTING in HEK293T cells, providing evidence that CgTBK1 could be activated by direct binding to CgSTING. In summary, we characterized the TBK1 gene in C. gigas and demonstrated its role in the innate immune response to pathogen infections.
作为河口的底栖滤食性动物,牡蛎的免疫系统为研究海洋无脊椎动物先天免疫途径的遗传和分子基础以及环境因素对免疫系统的影响提供了最佳模型之一。在此,我们对太平洋牡蛎(Crassostrea gigas)中软体动物TANK结合激酶-1(TBK1)(我们命名为CgTBK1)的分子功能进行了研究。与其他模式生物中已知的TBK1蛋白相比,CgTBK1在N端和C端包含一个保守的S-TKc结构域和一个卷曲螺旋结构域,但缺少一个重要的泛素结构域。定量实时PCR分析表明,CgTBK1的表达水平在所有选定组织中普遍存在,在鳃中表达最高。CgTBK1的表达在受到溶藻弧菌、牡蛎疱疹病毒1(OsHV-1参考菌株和μvar)以及聚肌苷酸:聚胞苷酸钠盐感染后显著上调,表明其在免疫反应中具有广泛功能。亚细胞定位显示CgTBK1存在于HeLa细胞的细胞质中,表明其作为受体和转录因子之间信号转导器的潜在功能。我们进一步证明CgTBK1在HEK293T细胞中与CgSTING相互作用,这为CgTBK1可通过直接结合CgSTING被激活提供了证据。总之,我们对太平洋牡蛎中的TBK1基因进行了表征,并证明了其在对病原体感染的先天免疫反应中的作用。