School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, PR China.
Department of Zoology and Fisheries, University of Agriculture, Faisalabad 38000, Pakistan.
Fish Shellfish Immunol. 2017 Dec;71:423-433. doi: 10.1016/j.fsi.2017.10.030. Epub 2017 Oct 19.
The RNA-sequencing followed by de novo assembly generated 61,912 unigene sequences of P. clarkii hepatopancreas. Comparison of gene expression between LPS challenged and PBS control samples revealed 2552 differentially expressed genes (DEGs). Of these sequences, 1162 DEGs were differentially up-regulated and 1360 DEGs differentially down-regulated. The DEGs were then annotated against gene ontology (GO) database and Kyoto Encyclopedia of Genes and Genomes (KEGG) database. Some immune-related pathways such as PPAR signaling pathway, lysosome, Chemical carcinogenesis, Peroxisome were predicted by canonical pathways analysis. The reliability of transcriptome data was validated by quantitative real time polymerase chain reaction (qRT-PCR) for the selected genes. The data presented here shed light into antibacterial immune responses of crayfish. In addition, these results suggest that transcriptomic data provides valuable sequence resource for immune-related gene identification and helps to understand P. clarkii immune functions.
RNA 测序和从头组装生成了 61912 条中华绒螯蟹肝胰腺的 unigene 序列。对 LPS 刺激和 PBS 对照样品之间的基因表达进行比较,发现了 2552 个差异表达基因(DEGs)。在这些序列中,1162 个 DEGs 上调,1360 个 DEGs 下调。然后将这些 DEGs 注释到基因本体(GO)数据库和京都基因与基因组百科全书(KEGG)数据库中。通过通路分析预测了一些与免疫相关的通路,如过氧化物酶体、PPAR 信号通路、溶酶体、化学致癌作用。通过对选定基因进行定量实时聚合酶链反应(qRT-PCR)验证了转录组数据的可靠性。本研究结果为中华绒螯蟹的抗菌免疫反应提供了新的见解。此外,这些结果表明转录组数据为免疫相关基因的鉴定提供了有价值的序列资源,并有助于理解中华绒螯蟹的免疫功能。