Wei Shu, Chen Yadong, Huang Lin, Ma Hui, Qi Longjiang, Wang Qian, Sun Mengjie, Zhang Xue, Sha Zhenxia
Institute of Biomedical Engineering, College of Life Sciences, Qingdao University, Qingdao, 266071, China.
Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, 266237, China; Key Laboratory for Sustainable Development of Marine Fisheries, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, 266071, China.
Dev Comp Immunol. 2021 Jul;120:104043. doi: 10.1016/j.dci.2021.104043. Epub 2021 Feb 20.
Long noncoding RNAs (lncRNAs) play a multifaceted role in transcriptional regulation and are important regulators of immune function. Scarce information is available regarding lncRNAs in fish. Peripheral blood mononuclear cells participate in the immune response of fish and aid resistance to infection with pathogenic microorganisms. Chitosan oligosaccharide can improve cellular and humoral immunity to enhance disease resistance in fish. In this study, we obtained peripheral blood leukocytes from half-smooth tongue sole and studied the effect of chitosan oligosaccharide on the lncRNA-mRNA expression profile of these cells using high-throughput sequencing and bioinformatics techniques. A total of 609 differentially expressed mRNAs and 50 differentially expressed lncRNAs were identified. The GO term enrichment analysis of the differentially expressed genes was annotated by 220 GO terms, 137 biological processes, 18 cellular components, and 65 molecular functions. Sixteen KEGG pathways, including immune signaling pathways, metabolism, and genetic information processing, were significantly enriched in differentially expressed genes. Thirty-six differentially expressed lncRNAs and 32 differentially expressed mRNAs produced a coexpression network containing 90 relationship pairs. The prediction of lncRNA target genes revealed 244 lncRNAs that potentially cis-regulated 294 differentially expressed mRNAs. qPCR verified that the expression levels of 17 differentially expressed lncRNAs and 15 differentially expressed mRNAs were consistent with the RNA-Seq results. Among them, 6 lncRNAs and 7 mRNAs were differentially expressed genes obtained from the prediction and analysis of lncRNA target genes, and 8 lncRNAs and 4 mRNAs were differentially expressed genes that participated in the construction of the coexpression network. In peripheral blood leukocytes after chitosan oligosaccharide treatment, as well as in peripheral blood and spleen after Vibrio anguillarum stimulation, lncRNAs and mRNAs showed significant differential expression. The results indicated that they may be related to the immune response, providing novel reference information for further research on the role of lncRNAs in immune regulation in half-smooth tongue sole.
长链非编码RNA(lncRNAs)在转录调控中发挥多方面作用,是免疫功能的重要调节因子。关于鱼类lncRNAs的信息稀缺。外周血单个核细胞参与鱼类的免疫反应,有助于抵抗病原微生物感染。壳寡糖可改善细胞免疫和体液免疫,增强鱼类抗病能力。在本研究中,我们从半滑舌鳎获取外周血白细胞,利用高通量测序和生物信息学技术研究壳寡糖对这些细胞lncRNA-mRNA表达谱的影响。共鉴定出609个差异表达的mRNA和50个差异表达的lncRNA。差异表达基因的GO术语富集分析由220个GO术语、137个生物学过程、18个细胞成分和65个分子功能注释。16条KEGG通路,包括免疫信号通路、代谢和遗传信息处理,在差异表达基因中显著富集。36个差异表达的lncRNA和32个差异表达的mRNA产生了一个包含90个关系对的共表达网络。lncRNA靶基因预测显示,244个lncRNA可能顺式调控294个差异表达的mRNA。qPCR验证了17个差异表达的lncRNA和15个差异表达的mRNA的表达水平与RNA-Seq结果一致。其中,6个lncRNA和7个mRNA是从lncRNA靶基因预测和分析中获得的差异表达基因,8个lncRNA和4个mRNA是参与共表达网络构建的差异表达基因。壳寡糖处理后的外周血白细胞以及鳗弧菌刺激后的外周血和脾脏中,lncRNA和mRNA均表现出显著差异表达。结果表明它们可能与免疫反应有关,为进一步研究lncRNA在半滑舌鳎免疫调节中的作用提供了新的参考信息。