Department of Marine Life Sciences & Fish Vaccine Research Center, Jeju National University, Jeju Self-Governing Province, 63243, Republic of Korea.
Department of Marine Life Sciences & Fish Vaccine Research Center, Jeju National University, Jeju Self-Governing Province, 63243, Republic of Korea; Marine Science Institute, Jeju National University, Jeju Self-Governing Province, 63333, Republic of Korea.
Fish Shellfish Immunol. 2019 Jan;84:158-168. doi: 10.1016/j.fsi.2018.09.078. Epub 2018 Oct 2.
The structural and evolutionary linkage between tumor necrosis factor (TNF) and the globular C1q (gC1q) domain defines the C1q and TNF-related proteins (CTRPs), which are involved in diverse functions such as immune defense, inflammation, apoptosis, autoimmunity, and cell differentiation. In this study, red-lip mullet (Liza haematocheila) CTRP4-like (MuCTRP4-like), CTRP5 (MuCTRP5), CTRP6 (MuCTRP6), and CTRP7 (MuCTRP7) were identified from the red-lip mullet transcriptome database and molecularly characterized. According to in silico analysis, coding sequences of MuCTRP4-like, MuCTRP5, MuCTRP6, and MuCTRP7 consisted of 1128, 753, 729, and 888 bp open reading frames (ORF), respectively and encoded 375, 250, 242, and 295 amino acids, respectively. All CTRPs possessed a putative C1q domain. Additionally, MuCTRP5, MuCTRP6, and MuCTRP7 consisted of a collagen region. Phylogenetic analysis exemplified that MuCTRPs were distinctly clustered with the respective CTRP orthologs. Tissue-specific expression analysis demonstrated that MuCTRP4-like was mostly expressed in the blood and intestine. Moreover, MuCTRP6 was highly expressed in the blood, whereas MuCTRP5 and MuCTRP7 were predominantly expressed in the muscle and stomach, respectively. According to the temporal expression in blood, all MuCTRPs exhibited significant modulations in response to polyinosinic:polycytidylic acid (poly I:C) and Lactococcus garvieae (L. garvieae). MuCTRP4-like, MuCTRP5, and MuCTRP6 showed significant upregulation in response to lipopolysaccharides (LPS). The results of this study suggest the potential involvement of Mullet CTRPs in post-immune responses.
肿瘤坏死因子 (TNF) 与球状 C1q (gC1q) 结构域之间的结构和进化联系定义了 C1q 和 TNF 相关蛋白 (CTRPs),它们参与多种功能,如免疫防御、炎症、细胞凋亡、自身免疫和细胞分化。在这项研究中,从红鳍东方鲀转录组数据库中鉴定出了红鳍东方鲀 CTRP4 样 (MuCTRP4-like)、CTRP5 (MuCTRP5)、CTRP6 (MuCTRP6) 和 CTRP7 (MuCTRP7),并对其进行了分子特征分析。根据计算机分析,MuCTRP4-like、MuCTRP5、MuCTRP6 和 MuCTRP7 的编码序列分别由 1128、753、729 和 888 bp 的开放阅读框 (ORF) 组成,并分别编码 375、250、242 和 295 个氨基酸。所有 CTRPs 都具有一个假定的 C1q 结构域。此外,MuCTRP5、MuCTRP6 和 MuCTRP7 包含胶原区。系统进化分析表明,MuCTRPs 与相应的 CTRP 直系同源物明显聚类。组织特异性表达分析表明,MuCTRP4-like 主要在血液和肠道中表达。此外,MuCTRP6 在血液中高表达,而 MuCTRP5 和 MuCTRP7 分别在肌肉和胃中高表达。根据血液中的时间表达,所有 MuCTRPs 对聚肌胞苷酸 (poly I:C) 和迟缓爱德华氏菌 (L. garvieae) 均表现出显著的调节作用。MuCTRP4-like、MuCTRP5 和 MuCTRP6 对脂多糖 (LPS) 的反应呈显著上调。本研究结果表明,东方鲀 CTRPs 可能参与了免疫后反应。