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暗纹东方鲀肾脏组织 Poly(I:C)应激转录组分析

Transcriptome Analysis of the Kidney of Obscure Puffer, , Challenged with Poly(I:C).

机构信息

College of Oceanography, Hohai University, Nanjing, Jiangsu 210098, China.

College of Oceanography, Hohai University, Nanjing, Jiangsu 210098, China,

出版信息

Zoolog Sci. 2022 Apr;39(2):198-205. doi: 10.2108/zs210070.

Abstract

Obscure puffer, , is an important aquaculture species in China, but the disease problem of this species seriously affects its production and causes huge economic losses. In order to reveal the molecular mechanism of disease resistance, polyinosinic-polycytidylic acid [poly(I:C)] was used to stimulate obscure puffer. At 0, 12, and 48 h (named To0, To12, and To48) after poly(I:C) challenge, the kidneys from obscure puffer were collected for transcriptome sequencing. A total of 54,816 transcripts was generated. Pairwise comparison of the sequencing libraries of tissue samples at these three time points revealed that the number of differentially expressed genes (DEGs) at To12 vs To0, To48 vs To0, and To48 vs To12 were 2039, 776, and 2579, respectively. Gene Ontology (GO) function classification analysis revealed that some DEGs were annotated to GO items for membrane, biological process, molecular function, and metabolic process. Kyoto Encyclopedia of Genes and Genomes pathway (KEGG) analysis of DEGs demonstrated that they mainly presented in immune-related pathways, such as Toll-like receptor signaling pathway, Retinoic acid-inducible gene-I-like receptor signaling pathway and NOD-like receptor signaling pathway. Then, eight genes were randomly selected from immune-related genes for real-time quantitative reverse transcription PCR verification (RT-qPCR), and 22 key immune DEGs were used to construct network functions. This study has obtained a large number of information resources about the transcriptome of obscure puffer, which can provide references for further research on the anti-virus response of obscure puffer.

摘要

暗纹东方鲀是中国重要的水产养殖品种,但该品种的疾病问题严重影响其生产,造成巨大的经济损失。为了揭示抗病的分子机制,用聚肌胞苷酸[poly(I:C)]刺激暗纹东方鲀。在聚肌胞苷酸刺激后 0、12 和 48 小时(分别命名为 To0、To12 和 To48),采集暗纹东方鲀肾脏进行转录组测序。共产生了 54816 个转录本。对这三个时间点的组织样本测序文库进行两两比较,结果表明 To12 与 To0、To48 与 To0、To48 与 To12 的差异表达基因(DEGs)数量分别为 2039、776 和 2579 个。基因本体(GO)功能分类分析显示,一些 DEGs 被注释到膜、生物过程、分子功能和代谢过程的 GO 项。DEGs 的京都基因与基因组百科全书(KEGG)通路分析表明,它们主要存在于免疫相关通路中,如 Toll 样受体信号通路、视黄酸诱导基因 I 样受体信号通路和 NOD 样受体信号通路。然后,从免疫相关基因中随机选择了 8 个基因进行实时定量逆转录 PCR 验证(RT-qPCR),并构建了 22 个关键免疫 DEGs 的网络功能。本研究获得了大量暗纹东方鲀转录组信息资源,可为进一步研究暗纹东方鲀抗病毒反应提供参考。

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