Cui Yu, Luo Shuai, Wu Baolan, Li Qiaoying, Han Fang, Wang Zhiyong
State Key Laboratory of Mariculture Breeding, Key Laboratory of Healthy Mariculture for the East China Sea, Fisheries College, Jimei University, Xiamen 361021, China.
Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.
Int J Mol Sci. 2024 Dec 20;25(24):13641. doi: 10.3390/ijms252413641.
Sphingosine kinases (SPHKs) are essential enzymes that catalyze the phosphorylation of sphingosine to produce sphingosine-1-phosphate (S1P), which plays pivotal roles in inflammation and immune regulation. In this study, genome-wide association analysis (GWAS) identified the gene as closely associated with the resistance of yellow drum () to . Structural prediction showed that YDSPHK1 contains a typical diacylglycerol kinase catalytic (DAGKc) domain (154-291 aa). By constructing and transfecting expression plasmids into yellow drum kidney cells, we found that YDSPHK1 is localized in the cytoplasm. Subsequent RNA-Seq analysis of an overexpression plasmid identified 25 differentially expressed genes (DEGs), including 13 upregulated and 12 downregulated. Notably, and were significantly upregulated, while and were downregulated. Promoter analysis indicated that the core regulatory regions of are located between -1931-1679 bp and -419+92 bp, with two predicted TFAP2A binding sites in the -419~+92 bp region. Further studies demonstrated that varying concentrations of TFAP2A significantly reduced promoter activity. These findings underscore the pivotal role of in regulating immune responses in yellow drum, particularly through its impact on key immune-related genes and pathways such as NF-κB signaling and ferroptosis. The identification of as a mediator of immune regulation provides valuable insights into the molecular mechanisms of immune defense and highlights its potential as a target for enhancing pathogen resistance in aquaculture practices. This study lays a strong foundation for future research aimed at developing innovative strategies for disease management in aquaculture species.
鞘氨醇激酶(SPHKs)是催化鞘氨醇磷酸化生成1-磷酸鞘氨醇(S1P)的关键酶,S1P在炎症和免疫调节中起关键作用。在本研究中,全基因组关联分析(GWAS)确定该基因与黄姑鱼()对的抗性密切相关。结构预测表明,YDSPHK1包含一个典型的二酰基甘油激酶催化(DAGKc)结构域(154-291氨基酸)。通过构建表达质粒并将其转染到黄姑鱼肾细胞中,我们发现YDSPHK1定位于细胞质中。随后对过表达质粒进行RNA测序分析,鉴定出25个差异表达基因(DEGs),其中13个上调,12个下调。值得注意的是,和显著上调,而和下调。启动子分析表明,的核心调控区域位于-1931-1679 bp和-419+92 bp之间,在-419~+92 bp区域有两个预测的TFAP2A结合位点。进一步研究表明,不同浓度的TFAP2A显著降低启动子活性。这些发现强调了在调节黄姑鱼免疫反应中的关键作用,特别是通过其对关键免疫相关基因和途径(如NF-κB信号通路和铁死亡)的影响。作为免疫调节介质的鉴定为免疫防御的分子机制提供了有价值的见解,并突出了其作为水产养殖实践中增强病原体抗性靶点的潜力。本研究为未来旨在开发水产养殖物种疾病管理创新策略的研究奠定了坚实基础。