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首页> 外文期刊>Toxins >Aberrant Expressional Profiling of Known MicroRNAs in the Liver of Silver Carp ( Hypophthalmichthys molitrix ) Following Microcystin-LR Exposure Based on samllRNA Sequencing
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Aberrant Expressional Profiling of Known MicroRNAs in the Liver of Silver Carp ( Hypophthalmichthys molitrix ) Following Microcystin-LR Exposure Based on samllRNA Sequencing

机译:基于SamllRNA测序的微囊藻酸钠曝光后,银鲤鱼肝脏肝脏中已知微小RNA的异常表征性探讨

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Microcystin-LR (MC-LR) poses a serious threat to human health due to its hepatotoxicity. However, the specific molecular mechanism of miRNAs in MC-LR-induced liver injury has not been determined. The aim of the present study was to determine whether miRNAs are regulated in MC-LR-induced liver toxicity by using high-throughput sequencing. Our research demonstrated that 53 miRNAs and 319 miRNAs were significantly changed after 24 h of treatment with MC-LR (50 and 200 μg/kg, respectively) compared with the control group. GO enrichment analysis revealed that these target genes were related to cellular, metabolic, and single-organism processes. Furthermore, KEGG pathway analysis demonstrated that the target genes of differentially expressed miRNAs in fish liver were primarily involved in the insulin signaling pathway, PPAR signaling pathway, Wnt signaling pathway, and transcriptional misregulation in cancer. Moreover, we hypothesized that 4 miRNAs (miR-16, miR-181a-3p, miR-451, and miR-223) might also participate in MC-LR-induced toxicity in multiple organs of the fish and play regulatory roles according to the qPCR analysis results. Taken together, our results may help to elucidate the biological function of miRNAs in MC-LR-induced toxicity.
机译:由于其肝毒性,微阴囊蛋白-LR(MC-LR)对人类健康构成严重威胁。然而,未确定MIRNA在MC-LR诱导的肝损伤中的特定分子机制。本研究的目的是通过使用高通量测序来确定MIRNA是否在MC-LR诱导的肝脏毒性中调节。我们的研究表明,与对照组的MC-LR(50和200μg/ kg)治疗24小时后,53 miRNA和319 miRNA显着改变。致富集分析显示,这些靶基因与细胞,代谢和单生体过程有关。此外,Kegg途径分析证明了鱼肝中差异表达miRNA的靶基因主要参与胰岛素信号通路,PPAR信号通路,WNT信号传导途径和癌症的转录错误测定。此外,我们假设4 miRNA(miR-16,miR-181a-3p,miR-451和miR-223)也可以参与鱼类的多个器官中的MC-LR诱导的毒性,并根据该毒性QPCR分析结果。在一起,我们的结果可能有助于阐明MIRNA在MC-LR诱导的毒性中的生物学功能。

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